WorldWideScience

Sample records for catalytic water co-existing

  1. Catalytic water co-existing with a product peptide in the active site of HIV-1 protease revealed by X-ray structure analysis.

    Directory of Open Access Journals (Sweden)

    Vishal Prashar

    Full Text Available BACKGROUND: It is known that HIV-1 protease is an important target for design of antiviral compounds in the treatment of Acquired Immuno Deficiency Syndrome (AIDS. In this context, understanding the catalytic mechanism of the enzyme is of crucial importance as transition state structure directs inhibitor design. Most mechanistic proposals invoke nucleophilic attack on the scissile peptide bond by a water molecule. But such a water molecule coexisting with any ligand in the active site has not been found so far in the crystal structures. PRINCIPAL FINDINGS: We report here the first observation of the coexistence in the active site, of a water molecule WAT1, along with the carboxyl terminal product (Q product peptide. The product peptide has been generated in situ through cleavage of the full-length substrate. The N-terminal product (P product has diffused out and is replaced by a set of water molecules while the Q product is still held in the active site through hydrogen bonds. The position of WAT1, which hydrogen bonds to both the catalytic aspartates, is different from when there is no substrate bound in the active site. We propose WAT1 to be the position from where catalytic water attacks the scissile peptide bond. Comparison of structures of HIV-1 protease complexed with the same oligopeptide substrate, but at pH 2.0 and at pH 7.0 shows interesting changes in the conformation and hydrogen bonding interactions from the catalytic aspartates. CONCLUSIONS/SIGNIFICANCE: The structure is suggestive of the repositioning, during substrate binding, of the catalytic water for activation and subsequent nucleophilic attack. The structure could be a snap shot of the enzyme active site primed for the next round of catalysis. This structure further suggests that to achieve the goal of designing inhibitors mimicking the transition-state, the hydrogen-bonding pattern between WAT1 and the enzyme should be replicated.

  2. Catalytic Water Co-Existing with a Product Peptide in the Active Site of HIV-1 Protease Revealed by X-Ray Structure Analysis

    OpenAIRE

    Prashar, Vishal; Bihani, Subhash; Das, Amit; Ferrer, Jean-Luc; Hosur, Madhusoodan

    2009-01-01

    Background It is known that HIV-1 protease is an important target for design of antiviral compounds in the treatment of Acquired Immuno Deficiency Syndrome (AIDS). In this context, understanding the catalytic mechanism of the enzyme is of crucial importance as transition state structure directs inhibitor design. Most mechanistic proposals invoke nucleophilic attack on the scissile peptide bond by a water molecule. But such a water molecule coexisting with any ligand in the active site has not...

  3. Heterogeneous water supply affects growth and benefits of clonal integration between co-existing invasive and native Hydrocotyle species

    Science.gov (United States)

    Wang, Yong-Jian; Bai, Yun-Fei; Zeng, Shi-Qi; Yao, Bin; Wang, Wen; Luo, Fang-Li

    2016-01-01

    Spatial patchiness and temporal variability in water availability are common in nature under global climate change, which can remarkably influence adaptive responses of clonal plants, i.e. clonal integration (translocating resources between connected ramets). However, little is known about the effects of spatial patchiness and temporal heterogeneity in water on growth and clonal integration between congeneric invasive and native Hydrocotyle species. In a greenhouse experiment, we subjected severed or no severed (intact) fragments of Hydrocotyle vulgaris, a highly invasive species in China, and its co-existing, native congener H. sibthorpioides to different spatial patchiness (homogeneous and patchy) and temporal interval (low and high interval) in water supply. Clonal integration had significant positive effects on growth of both species. In the homogeneous water conditions, clonal integration greatly improved the growth in fragments of both species under low interval in water. However, in the patchy water conditions, clonal integration significantly increased growth in both ramets and fragments of H. vulgaris under high interval in water. Therefore, spatial patchiness and temporal interval in water altered the effects of clonal integration of both species, especially for H. vulgaris. The adaptation of H. vulgaris might lead to invasive growth and potential spread under the global water variability. PMID:27439691

  4. Heterogeneous water supply affects growth and benefits of clonal integration between co-existing invasive and native Hydrocotyle species.

    Science.gov (United States)

    Wang, Yong-Jian; Bai, Yun-Fei; Zeng, Shi-Qi; Yao, Bin; Wang, Wen; Luo, Fang-Li

    2016-01-01

    Spatial patchiness and temporal variability in water availability are common in nature under global climate change, which can remarkably influence adaptive responses of clonal plants, i.e. clonal integration (translocating resources between connected ramets). However, little is known about the effects of spatial patchiness and temporal heterogeneity in water on growth and clonal integration between congeneric invasive and native Hydrocotyle species. In a greenhouse experiment, we subjected severed or no severed (intact) fragments of Hydrocotyle vulgaris, a highly invasive species in China, and its co-existing, native congener H. sibthorpioides to different spatial patchiness (homogeneous and patchy) and temporal interval (low and high interval) in water supply. Clonal integration had significant positive effects on growth of both species. In the homogeneous water conditions, clonal integration greatly improved the growth in fragments of both species under low interval in water. However, in the patchy water conditions, clonal integration significantly increased growth in both ramets and fragments of H. vulgaris under high interval in water. Therefore, spatial patchiness and temporal interval in water altered the effects of clonal integration of both species, especially for H. vulgaris. The adaptation of H. vulgaris might lead to invasive growth and potential spread under the global water variability. PMID:27439691

  5. Catalytic distillation water recovery subsystem

    Science.gov (United States)

    Budininkas, P.; Rasouli, F.

    1985-01-01

    An integrated engineering breadboard subsystem for the recovery of potable water from untreated urine based on the vapor phase catalytic ammonia removal was designed, fabricated and tested. Unlike other evaporative methods, this process catalytically oxidizes ammonia and volatile hydrocarbons vaporizing with water to innocuous products; therefore, no pretreatment of urine is required. Since the subsystem is fabricated from commercially available components, its volume, weight and power requirements are not optimized; however, it is suitable for zero-g operation. The testing program consists of parametric tests, one month of daily tests and a continuous test of 168 hours duration. The recovered water is clear, odorless, low in ammonia and organic carbon, and requires only an adjustment of its pH to meet potable water standards. The obtained data indicate that the vapor phase catalytic ammonia removal process, if further developed, would also be competitive with other water recovery systems in weight, volume and power requirements.

  6. Glycol-Water Interactions and co-existing phases and Temperature Dependent Solubility. An Example Of Carbon-Hydrogen Chemistry In Water

    CERN Document Server

    Michael, Fredrick

    2010-01-01

    Recently there has been great interest in Glycol-Water chemistry and solubility and temperature dependent phase dynamics. The Glycol-Water biochemistry of interactions is present in plant biology and chemistry, is of great interest to chemical engineers and biochemists as it is a paradigm of Carbon-Hydrogen Water organic chemistry. There is an interest moreover in formulating a simpler theory and computation model for the Glycol-Water interaction and phase dynamics, that is not fully quantum mechanical yet has the high accuracy available from a fully quantum mechanical theory of phase transitions of fluids and Fermi systems. Along these lines of research interest we have derived a Lennard-Jones -like theory of interacting molecules-Water in a dissolved adducts of Glycol-Water system interacting by Hydrogen bonds whose validity is supported at the scale of interactions by other independent molecular dynamics investigations that utilize force fields dependent on their experimental fittings to the Lennard-Jones ...

  7. Biogeochemical redox cycling of arsenic in mine-impacted lake sediments and co-existing pore waters near Giant Mine, Yellowknife Bay, Canada

    Energy Technology Data Exchange (ETDEWEB)

    Andrade, C.F. [Queen' s University, Department of Geological Sciences and Geological Engineering, Kingston, K7L 3N6 (Canada); Jamieson, H.E., E-mail: jamieson@geol.queensu.ca [Queen' s University, Department of Geological Sciences and Geological Engineering, Kingston, K7L 3N6 (Canada); Kyser, T.K. [Queen' s University, Department of Geological Sciences and Geological Engineering, Kingston, K7L 3N6 (Canada); Praharaj, T.; Fortin, D. [University of Ottawa, Department of Earth Sciences, Ottawa, K1A 3N5 (Canada)

    2010-02-15

    Lacustrine sediments, submerged tailings, and their pore waters have been collected at several sites in Yellowknife Bay, Great Slave Lake, Canada, in order to investigate the biogeochemical controls on the remobilization of As from mining-impacted materials under different depositional conditions. Radiometric dating confirms that a mid-core enrichment of Pb, Zn, Cu and Sb corresponds to the opening of a large Au mine 60 a ago. This was evident even in a relatively remote site. Arsenic was enriched at mid-core, coincident with mining activity, but clearly exhibited post-depositional mobility, migrating upwards towards the sediment water interface (SWI) as well as down-core. Deep-water (15 m) Yellowknife Bay sediments that contain buried mine waste are suboxic, relatively organic-rich and abundant in microbes with As in pore waters and sediments reaching 585 {mu}g/L and 1310 mg/kg, respectively. Late summer pore waters show equal proportions of As(III) and As(V) (16-415 {mu}g/L) whereas late winter pore waters are dominated by As(III) (284-947 {mu}g/L). This can be explained by As(III) desorption mechanisms associated with the conversion of FeS to FeS{sub 2} and the reduction of As(V) to As(III) through the oxidation of dissolved sulfide, both microbially-mediated processes. Processes affecting As cycling involve the attenuating efficiency of the oxic zone at the SWI, sediment redox heterogeneity and the reductive dissolution of Fe(hydr)oxides by labile organic matter, temporarily and spatially variable.

  8. Silver nanocluster catalytic microreactors for water purification

    Science.gov (United States)

    Da Silva, B.; Habibi, M.; Ognier, S.; Schelcher, G.; Mostafavi-Amjad, J.; Khalesifard, H. R. M.; Tatoulian, M.; Bonn, D.

    2016-07-01

    A new method for the elaboration of a novel type of catalytic microsystem with a high specific area catalyst is developed. A silver nanocluster catalytic microreactor was elaborated by doping a soda-lime glass with a silver salt. By applying a high power laser beam to the glass, silver nanoclusters are obtained at one of the surfaces which were characterized by BET measurements and AFM. A microfluidic chip was obtained by sealing the silver coated glass with a NOA 81 microchannel. The catalytic activity of the silver nanoclusters was then tested for the efficiency of water purification by using catalytic ozonation to oxidize an organic pollutant. The silver nanoclusters were found to be very stable in the microreactor and efficiently oxidized the pollutant, in spite of the very short residence times in the microchannel. This opens the way to study catalytic reactions in microchannels without the need of introducing the catalyst as a powder or manufacturing complex packed bed microreactors.

  9. Co-existence of agricultural production systems.

    Science.gov (United States)

    Jank, Bernhard; Rath, Johannes; Gaugitsch, Helmut

    2006-05-01

    Strategies and best practices for the co-existence of GM and non-GM crops need to be developed and implemented with the participation of farmers and other stakeholders. According to the principle of 'subsidiarity', decisions should be made by the lowest authority possible. When applying this concept to the case of GM crops, the affected society should determine their use and management in a regional decision-making process. Public participation is better accomplished at a lower level, and democratic deficits in decision-making on GMOs are better resolved, enabling farmers to manage or avoid GM crops. Ultimately, voluntary GMO-free zones might be a tool for sustainable co-existence and GM-free production and GMO-free zones might create a specific image for marketing regional products and services, such as tourism. PMID:16545877

  10. Catalytic hydrothermal liquefaction of water hyacinth.

    Science.gov (United States)

    Singh, Rawel; Balagurumurthy, Bhavya; Prakash, Aditya; Bhaskar, Thallada

    2015-02-01

    Thermal and catalytic hydrothermal liquefaction of water hyacinth was performed at temperatures from 250 to 300 °C under various water hyacinth:H2O ratio of 1:3, 1:6 and 1:12. Reactions were also carried out under various residence times (15-60 min) as well as catalytic conditions (KOH and K2CO3). The use of alkaline catalysts significantly increased the bio-oil yield. Maximum bio-oil yield (23 wt%) comprising of bio-oil1 and bio-oil2 as well as conversion (89%) were observed with 1N KOH solution. (1)H NMR and (13)C NMR data showed that both bio-oil1 and bio-oil2 have high aliphatic carbon content. FTIR of bio-residue indicated that the usage of alkaline catalyst resulted in bio-residue samples with lesser oxygen functionality indicating that catalyst has a marked effect on nature of the bio-residue and helps to decompose biomass to a greater extent compared to thermal case. PMID:25240515

  11. Water recovery by catalytic treatment of urine vapor

    Science.gov (United States)

    Budininkas, P.; Quattrone, P. D.; Leban, M. I.

    1980-01-01

    The objective of this investigation was to demonstrate the feasibility of water recovery on a man-rated scale by the catalytic processing of untreated urine vapor. For this purpose, two catalytic systems, one capable of processing an air stream containing low urine vapor concentrations and another to process streams with high urine vapor concentrations, were designed, constructed, and tested to establish the quality of the recovered water.

  12. Catalytic Behavior of Dense Hot Water

    Energy Technology Data Exchange (ETDEWEB)

    Wu, C J; Fried, L E; Yang, L H; Goldman, N; Bastea, S

    2008-06-05

    Water is known to exhibit fascinating physical properties at high pressures and temperatures. Its remarkable structural and phase complexity suggest the possibility of exotic chemical reactivity under extreme conditions, though this remains largely unstudied. Detonations of high explosives containing oxygen and hydrogen produce water at thousands of K and tens of GPa, similar to conditions of giant planetary interiors. These systems thus provide a unique means to elucidate the chemistry of 'extreme water'. Here we show that water plays an unexpected role in catalyzing complex explosive reactions - contrary to the current view that it is simply a stable detonation product. Using first-principles atomistic simulations of the detonation of high explosive pentaerythritol tetranitrate (PETN), we discovered that H{sub 2}O (source), H (reducer) and OH (oxidizer) act as a dynamic team that transports oxygen between reaction centers. Our finding suggests that water may catalyze reactions in other explosives and in planetary interiors.

  13. Degradation of Organic Pollutants in Water by Catalytic Ozonation

    Institute of Scientific and Technical Information of China (English)

    LI Xin; YAO Jun-hai; QI Jing-yao

    2007-01-01

    Different series of transition metal catalysts supported on Al2O3 were prepared by the impregnation method. The catalytic activity was measured in a batch reactor with ozone as the oxidizing reagent. The experimental results indicate that Cu/Al2O3 has a very effective catalytic activity during the ozonation of organic pollutants in water. The optimum conditions for preparing Cu/Al2O3 were systematically investigated with the orthogonal testing method. Furthermore, the results also show that the surface properties of catalyst are not compulsory for effective oxidation.

  14. On channel selection and shape co-existence

    International Nuclear Information System (INIS)

    Ambivalence with respect to a favoured shape is emerging as a ubiquitous phenomenon in nuclei. Multiple minima in the nuclear potential well occur because of the delicate balance in nuclei between the long and short-range properties of the nuclear force and the contribution specific particle orbitals make in forcing the nucleus to a decision. Exploration of the dependence of the resulting shape co-existence on particle number and orbital is a prominent area of research. Experimental aspects of spectroscopy studies using heavy ion fusion, evaporation reactions and channel selection are discussed, with focus on shape co-existence in the light Os-Pt-Hg-Pb region. 42 refs., 8 figs

  15. Co-existence of Organic and GM Agriculture

    OpenAIRE

    Boelt, Birte

    2004-01-01

    The Danish Minister for Food, Agriculture and Fisheries presented in spring 2004 a bill on co-existence of genetically modified, conventional and organic crops in support of the free choice of consumers and to ensure development possibilities for new and existing production forms. The bill contains a framework for regulation based on crop specific control measures, communication among farmers and mandatory courses in GM cultivation. The identification of control measures is based on the repor...

  16. Co-existence of Bronchiectasis and Chronic Obstructive Pulmonary Disease.

    Science.gov (United States)

    Goel, Nitin; Gupta, Pawan; Singh, Abhijeet; Prasad, Rajendra

    2015-01-01

    We present the case of a 56-year-old male who presented with cough and breathlessness. Chest radiograph (postero-anterior view) showed bulla and signs of hyperinflation in the right upper zone with cystic shadows in the left lower zone. Spirometry showed severe irreversible airflow obstruction with restriction and decreased diffusion capacity for carbon monoxide. On high resolution computed tomography (HRCT), right upper lobe bulla with emphysematous changes and left lower lobe cystic bronchiectasis were seen. Considering its rarity of occurrence and paucity of data in literature regarding co-existence of bronchiectasis with emphysema, this case is being reported. PMID:26591975

  17. Water detritiation: better catalysts for liquid phase catalytic exchange

    International Nuclear Information System (INIS)

    Fusion reactors are our hope for a clean nuclear energy. But as they shall handle huge amounts of tritium, 1.5 1019 Bq GWth-1 a-1 or about 50 000 times more tritium than light water fission reactors, they need detritiation. Most tritium losses can be trapped as or can easily be transformed into tritiated water. Water detritiation is preferably based on the multiplication of the large equilibrium isotope effect during the exchange reaction of tritium between hydrogen gas and liquid water in a counter current trickle bed reactor. Such LPCE (Liquid Phase Catalytic Exchange) requires an efficient hydrophobic catalyst. SCK-CEN invented and developed such a catalyst in the past. In combination with an appropriate packing, different batches of this catalyst performed very well during years of extensive testing, allowing to develop the ELEX process for water detritiation at inland reprocessing plants. The main objectives of this study were to reproduce and possibly improve the SCK-CEN catalyst for tritium exchange between hydrogen and liquid water; and to demonstrate the high overall exchange rate and thus high detritiation factors that can be realized with it in a small and simple LPCE column under typical but conservative operating conditions

  18. Nuclear power generation and co-existence with local area

    International Nuclear Information System (INIS)

    In addition to originally strong anxiety and unreliability on nuclear power generation, frequent accidents and troubles in the old Nuclear Reactor and Fuels Development Incorporation (the new Nuclear Fuel Cycle Development Incorporation), a fact that numbers of opposition group was over a half at citizen's vote conducted first in Japan and at Maki-machi in Niigata prefecture in August, 1996 on location of a nuclear power generation of the Tohoku Electric Co., Ltd., and so forth, affects some ripple effects to make difficult to form consensus on new location of a nuclear power generation. On making consensus of such location, every electric companies practise good communication with location areas, communication and other organizations, and so forth, promote positive information supplies and conversation type understanding works, and effort to acquire reliability for people of the location areas. Together with such efforts, they accumulate steadily safe operation results of the present nuclear power plants and develop nuclear PA (public acceptance) actions, local area promotion supporting countermeasures, and so forth. Here was introduced on a part of actions aiming at assistance to and co-existence with local areas promoted by every electric companies on various forms. (G.K.)

  19. Catalytic hydrolysis for the degradation of organophosphorus pesticides in water

    International Nuclear Information System (INIS)

    The kinetic studies of catalytic hydrolysis revealed that the concentration of two kinds of organophosphorus pesticides (omethoate and methidathion) in solution apparently decays according to the second order reaction. It was found that the rate constant value was highest at strong acidic conditions and it continued to decrease as the pH of the solution was increased. At basic conditions the rate constant value decreased to minimum. Manganese dioxide under acidic conditions converted into Mn/sup 2+/ ions and then these ions in water form hexaaquomanganese (II) ion. This hexaaquomanganese (II ion then adsorbed itself on the S or O atom of the organophosphorus compound and thus weakens the bond between P-S. This reaction facilitated the attack of H/sub 2/O or OH/sup -/ ion and thus enhanced the efficiency of hydrolysis. It was studied that methidathion hydrolyzed more efficiently than omethoate The rate constants of catalytic hydrolysis were increased with increasing the amount of MnO/sub 2/. It was found that the pesticides had undergone adsorption on catalyst in the first few minutes and there was the rapid drop of total phosphorus concentration. The decrease of total phosphorus adsorption with increasing pH was also observed. After the addition of alkaline earth metal cations (Ca/sup 2+/ and Mg/sup 2+/) along with magnesium, the enhancement in the efficiency of hydrolysis at near neutral conditions occurred. (author)

  20. Combined Electrolysis and Catalytic Exchange (CECE) upgraders - an alternative to Water Distillation (DW) heavy water upgraders

    International Nuclear Information System (INIS)

    All operating CANDU stations are equipped with Water Distillation (DW) systems for heavy water upgrading. An alternative process, Combined Electrolysis and Catalytic Exchange (CECE), is being considered for use in future CANDU stations. The CECE process has several operating advantages over DW systems, including lower emissions and heavy water losses. Changes in nuclear standards may change seismic requirements and classification of upgrader systems. These changes will likely increase the cost of heavy water upgraders, but the cost increase will be smaller for a CECE upgrader. Research at Chalk River Labs has identified materials for use in the CECE process that will not chemically or mechanically degrade when exposed to highly tritiated water. (author)

  1. Experimental studies on catalytic hydrogen recombiners for light water reactors

    International Nuclear Information System (INIS)

    In the course of core melt accidents in nuclear power plants a large amount of hydrogen can be produced and form an explosive or even detonative gas mixture with aerial oxygen in the reactor building. In the containment atmosphere of pressurized water reactors hydrogen combines a phlogistically with the oxygen present to form water vapor even at room temperature. In the past, experimental work conducted at various facilities has contributed little or nothing to an understanding of the operating principles of catalytic recombiners. Hence, the purpose of the present study was to conduct detailed investigations on a section of a recombiner essentially in order to deepen the understanding of reaction kinetics and heat transport processes. The results of the experiments presented in this dissertation form a large data base of measurements which provides an insight into the processes taking place in recombiners. The reaction-kinetic interpretation of the measured data confirms and deepens the diffusion theory - proposed in an earlier study. Thus it is now possible to validate detailed numeric models representing the processes in recombiners. Consequently the present study serves to broaden and corroborate competence in this significant area of reactor technology. In addition, the empirical knowledge thus gained may be used for a critical reassessment of previous numeric model calculations. (orig.)

  2. Hydrogen production by catalytic gasification of cellulose in supercritical water

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Cellulose,one of the important components of biomass,was gasified in supercritical water to produce hydrogen-rich gas in an autoclave which was operated batch-wise under high-pressure.K2CO3 and Ca(OH)2 were selected as the catalysts (or promoters).The temperature was kept between 450℃ and 500℃ while pressure was maintained at 24-26 MPa.The reaction time was 20 min.Experimental results showed that the two catalysts had good catalytic effect and optimum amounts were observed for each catalyst.When 0.2 g K2CO3 was added,the hydrogen yield could reach 9.456 mol.kg-1 which was two times of the H2 amount produced without catalyst.When 1.6 g Ca(OH)2 was added,the H2 yield was K2CO3 as catalyst but is still 1.7 times that achieved without catalyst.Comparing with the results obtained using KaCO3 or Ca(OH)2 alone,the use of a combination of K2CO3 and Ca(OH)2 could increase the H2 yield by up to 2.5 times that without catalyst and 25% and 45% more than that obtained using K2CO3 and Ca(OH)2 alone,respectively.It was found that methane was the dominant product at relatively low temperature.When the temperature was increased,the methane reacts with water and is converted to hydrogen and carbon dioxide.

  3. The effect of temperature on the catalytic conversion of Kraft lignin using near-critical water

    DEFF Research Database (Denmark)

    Nguyen, Thi Dieu Huyen; Maschietti, Marco; Åmand, Lars-Erik;

    2014-01-01

    The catalytic conversion of suspended LignoBoost Kraft lignin was performed in near-critical water using ZrO2/K2CO3 as the catalytic system and phenol as the co-solvent and char suppressing agent. The reaction temperature was varied from 290 to 370 C and its effect on the process was investigated...

  4. Catalytic hydrogenation of naphthalene through water gas shift reaction in supercritical water

    Energy Technology Data Exchange (ETDEWEB)

    Okazaki, S.; Kurosawa, S.; Adschiri, T.; Arai, K. [Tohoku University, Sendai (Japan). Dept. of Chemical Engineering

    1998-07-01

    The catalytic hydrogenation of naphthalene through water-gas shift reaction in supercritical water (SCW) was studied with batch experiments. A comparative study of catalytic hydrogenation of naphthalene with NiMo/Al{sub 2}O{sub 3} at 673 K and water density of 0.3 g/cm{sup 3} (30 MPa) was conducted in various atmospheres. Higher conversion of naphthalene to tetralin was obtained in CO-SCW, and H{sub 2}-CO{sub 2}-SCW than in H{sub 2}-SCW. The results clearly indicate that the water-gas shift reaction in SCW produces species which can hydrogenate naphthalene more effectively than H{sub 2} gas in SCW. The effect of water density (0.1-0.5 g/cm{sup 3}) on the hydrogenation in H{sub 2}-SCW and in CO-SCW was also studied. In H{sub 2}-SCW, naphthalene conversion gradually decreased with increasing water density. In CO-SCW, naphthalene conversion first increased and then gradually decreased with increasing water density. 8 refs., 2 figs.

  5. Energy Conservation:Challenges and Opportunities Co-existing

    Institute of Scientific and Technical Information of China (English)

    Sun; Yongjian

    2006-01-01

      Yang Zhenhuai, Chairman, China Energy Conservation Association:China such has a large population,but natural resources as infields, water, oil and gas, etc.,are in comparative scarce. The zoology environment is comparatively weak. During the past 20 years, the economic growth has been realized mainly on through resource exploitation, heavy pollution and expansion, the environmental pollution and zoological destruction have developed to a very serious extent.……

  6. Energy Conservation:Challenges and Opportunities Co-existing

    Institute of Scientific and Technical Information of China (English)

    Sun Yongjian

    2006-01-01

    @@ Yang Zhenhuai, Chairman, China Energy Conservation Association:China such has a large population,but natural resources as infields, water, oil and gas, etc.,are in comparative scarce. The zoology environment is comparatively weak. During the past 20 years, the economic growth has been realized mainly on through resource exploitation, heavy pollution and expansion, the environmental pollution and zoological destruction have developed to a very serious extent.

  7. Single-chain folding of polymers for catalytic systems in water.

    Science.gov (United States)

    Terashima, Takaya; Mes, Tristan; De Greef, Tom F A; Gillissen, Martijn A J; Besenius, Pol; Palmans, Anja R A; Meijer, E W

    2011-04-01

    Enzymes are a source of inspiration for chemists attempting to create versatile synthetic catalysts. In order to arrive at a polymeric chain carrying catalytic units separated spatially, it is a prerequisite to fold these polymers in water into well-defined compartmentalized architectures thus creating a catalytic core. Herein, we report the synthesis, physical properties, and catalytic activity of a water-soluble segmented terpolymer in which a helical structure in the apolar core is created around a ruthenium-based catalyst. The supramolecular chirality of this catalytic system is the result of the self-assembly of benzene-1,3,5-tricarboxamide side chains, while the catalyst arises from the sequential ruthenium-catalyzed living radical polymerization of the different monomers followed by ligand exchange. The polymers exhibit a two-state folding process and show transfer hydrogenation in water. PMID:21405022

  8. Radiation-catalytical properties of natural zeolite of mordenite type during radiolysis of water

    International Nuclear Information System (INIS)

    Radiation-catalytic properties of natural zeolite of mordenite type in cation Na+, K+, Ca2+, Ba2+ forms during radiolysis of water molecules were investigated with the use of 60Co γ-radiation (6 Gy/s). Kinetic parameters of radiolysis of water molecules in the presence of these zeolite samples were determined. It was revealed that zeolite of mordenite type catalyzes the radiolysis water molecules, its catalytic activity growing with decrease in ionic radius of the cation in the zeolite composition

  9. Optimal conditions for the catalytic and non-catalytic pyrolysis of water hyacinth

    International Nuclear Information System (INIS)

    Highlights: • Particle size, temperature and catalyst affect greatly the water hyacinth pyrolysis. • <200 μm is the optimal particle size for water hyacinth to produce syngas. • There are more porosity, surface area and crystalline at a higher temperature. • 900 °C is the best pyrolysis temperature for water hyacinth to produce syngas. • The syngas production can be greatly promoted by catalysts, and KCl is the best one. - Abstract: Water hyacinth pyrolysis was carried out in a quartz tube reactor. Different particle sizes, pyrolysis temperatures and catalysts were tested. The product fractional yields, gaseous products, surface morphology and crystal structure were analyzed in order to obtain the optimal pyrolysis condition for producing syngas (CO + H2) from water hyacinth. The results indicated that particle size had a significant impact on water hyacinth pyrolysis and among four particle sizes in this paper dp < 200 μm was the optimal particle size for syngas production. Moreover, active surface area, porosity level and crystalline materials increased as the temperature rose and the results showed that among five temperatures in this study 900 °C was the best pyrolysis temperature for producing syngas. In addition, the syngas production levels can be improved if a suitable catalyst is used. The best catalyst was KCl, followed by CaO and MgO

  10. Osteomalacia and coxa vara. An unusual co-existence for femoral neck stress fracture

    Directory of Open Access Journals (Sweden)

    Kerim Sariyilmaz

    2015-01-01

    Conclusion: Joint and bone pain without any trauma should be investigated and bone metabolism disorders should be kept in mind. There might be co-existing factors related with stress fractures, and they must be treated simultaneously.

  11. Co-existence of classical and alternative activation programs in macrophages responding to Toxoplasma gondii

    OpenAIRE

    Patil, Veerupaxagouda; Zhao, Yanlin; Shah, Suhagi; Fox, Barbara A.; Rommereim, Leah M.; Bzik, David J.; Yap, George S.

    2013-01-01

    Pro-inflammatory M1 macrophages are critical for defense against intracellular pathogens while alternatively-activated M2 macrophages mediate tissue homeostasis and repair. Whether these distinct activation programs are mutually exclusive or can co-exist within the same cell is unclear. Here, we report the co-existence of these programs in Toxoplasma gondii-elicited inflammatory macrophages. This is independent of parasite expression of the virulence factor ROP16 and host cell expression of s...

  12. Co-existence of Sarcina Organisms and Helicobacter pylori Gastritis/Duodenitis in Pediatric Siblings

    OpenAIRE

    Sauter, Jennifer L.; Nayar, Suresh K.; Anders, Paige D.; D’Amico, Michael; Butnor, Kelly J.; Wilcox, Rebecca L.

    2013-01-01

    Sarcina are gram-positive anaerobic bacteria found to be associated with delayed gastric emptying and gastric outlet obstruction. We describe two cases of Sarcina co-existing with Helicobacter pylori organisms in pediatric siblings presenting within four months of each other with pyloric obstruction secondary to severe gastritis/duodenitis. The co-existence of Sarcina and Helicobacter pylori has not, to our knowledge, been previously reported. Its characteristic tetrad packeted morphology per...

  13. Catalytical degradation of relevant pollutants from waters using magnetic nanocatalysts

    Science.gov (United States)

    Nadejde, C.; Neamtu, M.; Schneider, R. J.; Hodoroaba, V.-D.; Ababei, G.; Panne, U.

    2015-10-01

    The catalytic efficiency of two magnetically responsive nanocatalysts was evaluated for the degradation of Reactive Black 5 (RB5) and Reactive Yellow 84 (RY84) azo dyes using hydrogen peroxide as oxidant under very mild conditions (atmospheric pressure, room temperature). In order to obtain the nanocatalysts, the surface of magnetite (Fe3O4) nanoparticles, prepared by a co-precipitation method, was further modified with ferrous oxalate, a highly sensitive non-hazardous reducing agent. The sensitized nanomaterials were characterized by X-ray diffraction, scanning and transmission electron microscopy, energy-dispersive X-ray spectroscopy and vibrating sample magnetometry, and used in the catalytic wet hydrogen peroxide oxidation (CWHPO) of RB5 and RY84, in laboratory-scale experiments. The effect of important variables such as catalyst dosage, H2O2 concentration, and contact time was studied in the dye degradation kinetics. The results showed that it was possible to remove up to 99.7% dye in the presence of 20 mM H2O2 after 240 min of oxidation for a catalyst concentration of 10 g L-1 at 25 °C and initial pH value of 9.0. CWHPO of reactive dyes using sensitized magnetic nanocatalysts can be a suitable pre-treatment method for complete decolorization of effluents from textile dyeing and finishing processes, once the optimum operating conditions are established.

  14. The ISS Water Processor Catalytic Reactor as a Post Processor for Advanced Water Reclamation Systems

    Science.gov (United States)

    Nalette, Tim; Snowdon, Doug; Pickering, Karen D.; Callahan, Michael

    2007-01-01

    Advanced water processors being developed for NASA s Exploration Initiative rely on phase change technologies and/or biological processes as the primary means of water reclamation. As a result of the phase change, volatile compounds will also be transported into the distillate product stream. The catalytic reactor assembly used in the International Space Station (ISS) water processor assembly, referred to as Volatile Removal Assembly (VRA), has demonstrated high efficiency oxidation of many of these volatile contaminants, such as low molecular weight alcohols and acetic acid, and is considered a viable post treatment system for all advanced water processors. To support this investigation, two ersatz solutions were defined to be used for further evaluation of the VRA. The first solution was developed as part of an internal research and development project at Hamilton Sundstrand (HS) and is based primarily on ISS experience related to the development of the VRA. The second ersatz solution was defined by NASA in support of a study contract to Hamilton Sundstrand to evaluate the VRA as a potential post processor for the Cascade Distillation system being developed by Honeywell. This second ersatz solution contains several low molecular weight alcohols, organic acids, and several inorganic species. A range of residence times, oxygen concentrations and operating temperatures have been studied with both ersatz solutions to provide addition performance capability of the VRA catalyst.

  15. Recycle attuned catalytic exchange (RACE) for reliable and low inventory processing of highly tritiated water

    International Nuclear Information System (INIS)

    The detritiation of highly tritiated water by liquid phase catalytic exchange needs dilution of the feed with water to tritium concentrations suitable for catalyst and safety rules and to assure flow rates large enough for wetting the catalyst. Dilution by recycling detritiated water from within the exchange process has three advantages: the amount and concentration of the water for dilution is controlled within the exchange process, there is no additional water load to processes located downstream RACE, and the ratio of gas to liquid flow rates in the exchange column could be adjusted by using several recycles differing in amount and concentration to avoid an excessively large number of theoretical separation stages. In this paper, the flexibility of the recycle attuned catalytic exchange (RACE) and its effect on the cryogenic distillation are demonstrated for the detritiation of the highly tritiated water from a tritium breeding blanket

  16. Catalytic Conversion of Glucose into 5-Hydroxymethylfurfural by Hf(OTf4 Lewis Acid in Water

    Directory of Open Access Journals (Sweden)

    Junjie Li

    2015-12-01

    Full Text Available A series of Lewis acidic metal salts were used for glucose dehydration to 5-hydroymethylfurfural (HMF in water. Effect of valence state, ionic radii of Lewis acidic cation, and the type of anions on the catalytic performance have been studied systematically. The experimental results showed that the valence state played an important role in determining catalytic activity and selectivity. It was found that a higher glucose conversion rate and HMF selectivity could be obtained over high valent Lewis acid salts, where the ionic radii of these Lewis acidic metal salts are usually relatively small. Analysis on the effect of the anions of Lewis acid salts on the catalytic activity and the selectivity suggested that a higher glucose conversion and HMF selectivity could be readily obtained with Cl−. Furthermore, the recyclability of high valence state Lewis acid salt was also studied, however, inferior catalytic performance was observed. The deactivation mechanism was speculated to be the fact that high valence state Lewis acid salt was comparatively easier to undergo hydrolysis to yield complicated metal aqua ions with less catalytic activity. The Lewis acidic activity could be recovered by introducing a stoichiometric amount of hydrochloric acid (HCl to the catalytic before the reaction.

  17. Catalytic Response and Stability of Nickel/Alumina for the Hydrogenation of 5-Hydroxymethylfurfural in Water.

    Science.gov (United States)

    Perret, Noémie; Grigoropoulos, Alexios; Zanella, Marco; Manning, Troy D; Claridge, John B; Rosseinsky, Matthew J

    2016-03-01

    The catalytic response of Ni on Al2O3 obtained from Ni-Al layered double hydroxides was studied for the liquid-phase hydrogenation of hydroxymethyl furfural to tetrahydrofuran-2,5-diyldimethanol (THFDM) in water. The successive calcination and reduction of the precursors caused the removal of interlayer hydroxyl and carbonate groups and the reduction of Ni(2+) to Ni(0). Four reduced mixed oxide catalysts were obtained, consisting of different amount of Ni metal contents (47-68 wt%) on an Al-rich amorphous component. The catalytic activity was linked to Ni content whereas selectivity was mainly affected by reaction temperature. THFDM was formed in a stepwise manner at low temperature (353 K) whereas 3-hydroxymethyl cyclopentanone was generated at higher temperature. Coke formation caused deactivation; however, the catalytic activity can be regenerated using heat treatment. The results establish Ni on Al2O3 as a promising catalyst for the production of THFDM in water. PMID:26870940

  18. Photocatalytic Water-Splitting Reaction from Catalytic and Kinetic Perspectives

    KAUST Repository

    Hisatomi, Takashi

    2014-10-16

    Abstract: Some particulate semiconductors loaded with nanoparticulate catalysts exhibit photocatalytic activity for the water-splitting reaction. The photocatalysis is distinct from the thermal catalysis because photocatalysis involves photophysical processes in particulate semiconductors. This review article presents a brief introduction to photocatalysis, followed by kinetic aspects of the photocatalytic water-splitting reaction.Graphical Abstract: [Figure not available: see fulltext.

  19. Session 6: Catalytic Dechlorination Reaction of Chlorinated Hydrocarbons with Water Using nano-structured Alumina

    Energy Technology Data Exchange (ETDEWEB)

    Abbas, Khaleel [United Arab Emirates Univ., Dept. of Chemistry, Al-Ain (United States)

    2004-07-01

    Herein, we report our recent results from a study on the catalytic dechlorination reactions of 1,2-dichloroethane (DCE) and carbon tetrachloride (CTC) with water using HSA-Al{sub 2}O{sub 3} as the catalyst. The obtained experimental results are explained. (O.M.)

  20. Spacecraft Water Regeneration by Catalytic Wet Air Oxidation Project

    Data.gov (United States)

    National Aeronautics and Space Administration — The objective of this project is to develop advanced catalysts for a volatile removal assembly used to purify spacecraft water. The innovation of the proposed...

  1. GMO neighbourhoods - will co-existence be a geographically realistic possibility?

    DEFF Research Database (Denmark)

    Qvist, H. Witt; Lundsgaard, H.; Brandt, Jesper

    2006-01-01

    of the precautionary principle adopted in the Maastricht treaty from 1992 by the EU (Andersen, 2000). We concretised these rules in relation to actual landscape practices among primary producers of sugar beet in Denmark, we simulated the co-existence of GM and conventional sugar beet in an area of...... after the study took place. It is concluded that although the farmers are positive towards the possibility of introducing GM sugar beet, it is not realistic to expect the rules of co-existence to be observed, which makes the risk assessment behind the new rules unrealistical. Further studies of social...... practice in relation to trends and geographical variations in the distribution of structure, size and fragmentation of agricultural holdings are recommended in order to investigate possibilities for realistic co-existence....

  2. Conserved water-mediated H-bonding dynamics of catalytic Asn 175 in plant thiol protease

    Indian Academy of Sciences (India)

    Tapas K Nandi; Hridoy R Bairagya; Bishnu P Mukhopadhyay; K Sekar; Dipankar Sukul; Asim K Bera

    2009-03-01

    The role of invariant water molecules in the activity of plant cysteine protease is ubiquitous in nature. On analysing the 11 different Protein DataBank (PDB) structures of plant thiol proteases, the two invariant water molecules W1 and W2 (W220 and W222 in the template 1PPN structure) were observed to form H-bonds with the Ob atom of Asn 175. Extensive energy minimization and molecular dynamics simulation studies up to 2 ns on all the PDB and solvated structures clearly revealed the involvement of the H-bonding association of the two water molecules in fixing the orientation of the asparagine residue of the catalytic triad. From this study, it is suggested that H-bonding of the water molecule at the W1 invariant site better stabilizes the Asn residue at the active site of the catalytic triad.

  3. Tritiated water processing using liquid phase catalytic exchange and solid oxide electrolyte cell

    International Nuclear Information System (INIS)

    Liquid phase catalytic exchange (LPCE) is an effective method for enrichment and removal of tritium from tritiated water. Combined electrolysis catalytic exchange (CECE) process is an attractive application of a LPCE column. We proposed a new process that improves the CECE process. Using a solid oxide electrolyte (SOE) cell for electrolysis makes the CECE process more energy efficient and eliminates other disadvantages such as large tritium inventory and extremely slow system response. When the cell is used for recombination, the system becomes even more simple, efficiently, reliable and safe. 21 refs., 9 figs

  4. Valorization of horse manure through catalytic supercritical water gasification.

    Science.gov (United States)

    Nanda, Sonil; Dalai, Ajay K; Gökalp, Iskender; Kozinski, Janusz A

    2016-06-01

    The organic wastes such as lignocellulosic biomass, municipal solid waste, sewage sludge and livestock manure have attracted attention as alternative sources of energy. Cattle manure, a waste generated in surplus amounts from the feedlot, has always been a chief environmental concern. This study is focused on identifying the candidacy of horse manure as a next generation feedstock for biofuel production through supercritical water gasification. The horse manure was gasified in supercritical water to examine the effects of temperature (400-600°C), biomass-to-water ratio (1:5 and 1:10) and reaction time (15-45min) at a pressure range of 23-25MPa. The horse manure and resulting biochar were characterized through carbon-hydrogen-nitrogen-sulfur (CHNS), inductively coupled plasma-mass spectrometry (ICP-MS), thermogravimetric analysis (TGA), Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy and scanning electron microscopy (SEM). The effects of alkali catalysts such as NaOH, Na2CO3 and K2CO3 at variable concentrations (1-2wt%) were investigated to maximize the hydrogen yields. Supercritical water gasification of horse manure with 2wt% Na2CO3 at 600°C and 1:10 biomass-to-water ratio for 45min revealed maximum hydrogen yields (5.31mmol/g), total gas yields (20.8mmol/g) with greater carbon conversion efficiency (43.1%) and enhanced lower heating value of gas products (2920kJ/Nm(3)). The manure-derived biochars generated at temperatures higher than 500°C also demonstrated higher thermal stability (weight loss 70wt%) suggesting their application in enhancing soil fertility and carbon sequestration. The results propose that supercritical water gasification could be a proficient remediation technology for horse manure to generate hydrogen-rich gas products. PMID:27067100

  5. Children with burns referred for child abuse evaluation: Burn characteristics and co-existent injuries.

    Science.gov (United States)

    Pawlik, Marie-Christin; Kemp, Alison; Maguire, Sabine; Nuttall, Diane; Feldman, Kenneth W; Lindberg, Daniel M

    2016-05-01

    Intentional burns represent a serious form of physical abuse that must be identified to protect children from further harm. This study is a retrospectively planned secondary analysis of the Examining Siblings To Recognize Abuse (ExSTRA) network data. Our objective was to describe the characteristics of burns injuries in children referred to Child Abuse Pediatricians (CAPs) in relation to the perceived likelihood of abuse. We furthermore compare the extent of diagnostic investigations undertaken in children referred to CAPs for burn injuries with those referred for other reasons. Within this dataset, 7% (215/2890) of children had burns. Children with burns were older than children with other injuries (median age 20 months vs. 10 months). Physical abuse was perceived as likely in 40.9% (88) and unlikely in 59.1% (127). Scalds accounted for 52.6% (113) and contact burns for 27.6% (60). Several characteristics of the history and burn injury were associated with a significantly higher perceived likelihood of abuse, including children with reported inflicted injury, absent or inadequate explanation, hot water as agent, immersion scald, a bilateral/symmetric burn pattern, total body surface area ≥10%, full thickness burns, and co-existent injuries. The rates of diagnostic testing were significantly lower in children with burns than other injuries, yet the yield of skeletal survey and hepatic transaminases testing were comparable between the two groups. This would imply that children referred to CAPs for burns warrant the same level of comprehensive investigations as those referred for other reasons. PMID:27088728

  6. Catalytic combustion of styrene over copper based catalyst: inhibitory effect of water vapor.

    Science.gov (United States)

    Pan, Hongyan; Xu, Mingyao; Li, Zhong; Huang, Sisi; He, Chun

    2009-07-01

    The effects of water vapor on the activity of the copper based catalysts with different supports such as CuO/gamma-Al2O3, CuO/SiO2 and CuO/TiO2 for styrene combustion were investigated. The catalytic activity of the catalysts was tested in the absence of and presence of water vapor and the catalysts were characterized. Temperature programmed desorption (TPD) experiments and diffuse reflectance infrared fourier transform spectroscopy (DRIFTS) measurements were conducted in order to estimate and explain the water effects. Results showed that the existence of water vapor had a significant negative effect on the catalytic activity of these copper based catalysts due to the competition adsorption of water molecule. DRIFTS studies showed that the catalyst CuO/gamma-Al2O3 had the strongest adsorption of water, while the catalyst CuO/TiO2 had the weakest adsorption of water. H2O-TPD studies also indicated that the order of desorption activation energies of water vapor on the catalysts or the strength of interactions of water molecules with the surfaces of the catalysts was CuO/gamma-Al2O3>CuO/SiO2>CuO/TiO2. As a consequence of that, the CuO/TiO2 exhibited the better durability to water vapor, while CuO/gamma-Al2O3 had the poorest durability to water vapor among these three catalysts. PMID:19427660

  7. COAL CONVERSION WASTEWATER TREATMENT BY CATALYTIC OXIDATION IN SUPERCRITICAL WATER; FINAL

    International Nuclear Information System (INIS)

    Wastewaters from coal-conversion processes contain phenolic compounds in appreciable concentrations. These compounds need to be removed so that the water can be discharged or re-used. Catalytic oxidation in supercritical water is one potential means of treating coal-conversion wastewaters, and this project examined the reactions of phenol over different heterogeneous oxidation catalysts in supercritical water. More specifically, we examined the oxidation of phenol over a commercial catalyst and over bulk MnO(sub 2), bulk TiO(sub 2), and CuO supported on Al(sub 2) O(sub 3). We used phenol as the model pollutant because it is ubiquitous in coal-conversion wastewaters and there is a large database for non-catalytic supercritical water oxidation (SCWO) with which we can contrast results from catalytic SCWO. The overall objective of this research project is to obtain the reaction engineering information required to evaluate the utility of catalytic supercritical water oxidation for treating wastes arising from coal conversion processes. All four materials were active for catalytic supercritical water oxidation. Indeed, all four materials produced phenol conversions and CO(sub 2) yields in excess of those obtained from purely homogeneous, uncatalyzed oxidation reactions. The commercial catalyst was so active that we could not reliably measure reaction rates that were not limited by pore diffusion. Therefore, we performed experiments with bulk transition metal oxides. The bulk MnO(sub 2) and TiO(sub 2) catalysts enhance both the phenol disappearance and CO(sub 2) formation rates during SCWO. MnO(sub 2) does not affect the selectivity to CO(sub 2), or to the phenol dimers at a given phenol conversion. However, the selectivities to CO(sub 2) are increased and the selectivities to phenol dimers are decreased in the presence of TiO(sub 2) , which are desirable trends for a catalytic SCWO process. The role of the catalyst appears to be accelerating the rate of formation of

  8. Catalytic wet air oxidation of organic pollutants in waste waters

    OpenAIRE

    Gomes, Helder; Figueiredo, José; Boaventura, Rui; Faria, Joaquim

    2001-01-01

    Organic compounds are involved iii the manufacture of a wide variety of chemical products, generating in the process different kinds of liquid effluents with high chemical oxygen demand (COD) and high toxicity. Discharge of these waters without treatment into a river course is unacceptable, due to the toxic potential of some organic compounds or to depletion of the dissolved oxygen level, which can decrease below the level considered necessary to support aquatic life.

  9. The catalytic oxidation of manganese in water treatment clarification processes

    OpenAIRE

    Lloyd, A.

    1982-01-01

    The removal of dissolved manganese in water treatment floc blanket clarifiers has been studied. The removal mechanisms may be broadly classed as adsorption and oxidation. Adsorption of manganese (II) occurs rapidly and is completed in less than five minutes under conditions prevailing in a floe blanket clarifier. The extent of adsorption is determined by pH, iron and manganese concentrations. Manganese adsorption is relatively insensitive to the concentration of other cations and anions prese...

  10. Metal nanoparticles in catalytic polymer membranes and ion-exchange systems for advanced purification of water from molecular oxygen

    International Nuclear Information System (INIS)

    Methods of synthesis of metal nanoparticles and metal/polymer nanocomposites including ion-exchange materials are considered. The effect of the composition and size of nanoparticles on their catalytic activity is analyzed. Attention is focused on the composites used in catalytic processes, namely, catalytic membranes and ion-exchange systems. The problems associated with the removal of dissolved oxygen from water by means of such composites are discussed. The bibliography includes 225 references.

  11. Carbon and oxygen isotopes in apatite CO2 and co-existing calcite

    International Nuclear Information System (INIS)

    Carbon and oxygen isotopes were analyzed in carbonate apatite CO2 and in co-existing calcite. Both C and O in apatite CO2 are enriched in the respective light isotopes relative to calcite. These results confirm the proposition that carbonate is part of the apatite structure

  12. Shape and rotational co-existence of N=Z nuclei around A ≅ 72 region

    International Nuclear Information System (INIS)

    It was observed that the shape isomerism in N=Z nucleus which at the same time supports the predicted scenario of oblate prolate shape co-existence in the medium mass region. 72Kr seems to be one of the rarer nuclei with a rather pure oblate deformed ground state and the oblate-prolate shape mixing found in the Kr isotopes

  13. Frequency of co-existence of dengue and malaria in patients presenting with acute febrile illness

    International Nuclear Information System (INIS)

    To find out the frequency of co-existence of malaria and dengue fever in patients presenting with acute febrile illness. Methods: The descriptive cross-sectional study was conducted at the Military Hospital Rawalpindi from June to November 2012. A total of 500 patients with complaint of acute febrile illness were selected after applying the inclusion and exclusion criteria. Preliminary data was collected on a pretested proforma. Blood samples of patients were tested for dengue serology and malaria parasite. Results were entered in respective proforma. Co-existence was considered present when a patient had both dengue serology and malaria parasite slide positive. SPSS 20 was used for data analysis. Result: Of the total, 349 (69.8%) were males and 151 (30.2%) females. Dengue serology was positive in 16 (3.2%); 81(16.2%) had malaria parasite slide positive; 403 (80.4%) had none of the two findings. Co-existence of both dengue and malaria was nil among the whole sample. In males, 67 (13.4%) had malaria, while 11 (2.2%) had dengue. In females, 14 (2.8%) had malaria, while 5 (1%) suffered from dengue fever. Conclusion: Co-existence of dengue and malaria was zero per cent in 500 patients visiting Military Hospital Rawalpindi. More studies shall be conducted to find out whether the reason of having zero per cent co-existence is that dengue or/and malaria epidemic did not occur in 2012 or whether there are some other factors involved. (author)

  14. Heterogeneous catalytic ozonation of ciprofloxacin in water with carbon nanotube supported manganese oxides as catalyst

    International Nuclear Information System (INIS)

    Highlights: ► Ciprofloxacin in water was degraded by heterogeneous catalytic ozonation. ► MnOx were supported on MWCNTs to serve as catalyst for ozonation. ► MnOx/MWCNT exhibited highly catalytic activity on ozonation of ciprofloxacin in water. ► MnOx/MWCNT resulted in effective antibacterial activity inhibition on ciprofloxacin. ► MnOx/MWCNT promoted the generation of hydroxyl radicals. - Abstract: Carbon nanotube-supported manganese oxides (MnOx/MWCNT) were used as catalysts to assist ozone in degrading ciprofloxacin in water. Manganese oxides were successfully loaded on multi-walled carbon nanotube surfaces by simply impregnating the carbon nanotube with permanganate solution. The catalytic activities of MnOx/MWCNT in ciprofloxacin ozonation, including degradation, mineralization effectiveness, and antibacterial activity change, were investigated. The presence of MnOx/MWCNT significantly elevated the degradation and mineralization efficiency of ozone on ciprofloxacin. The microbiological assay with a reference Escherichia coli strain indicated that ozonation with MnOx/MWCNT results in more effective antibacterial activity inhibition of ciprofloxacin than that in ozonation alone. The effects of catalyst dose, initial ciprofloxacin concentration, and initial pH conditions on ciprofloxacin ozonation with MnOx/MWCNT were surveyed. Electron spin resonance trapping was applied to assess the role of MnOx/MWCNT in generating hydroxyl radicals (HO·) during ozonation. Stronger 5,5-dimethyl-1-pyrroline-N-oxide–OH signals were observed in the ozonation with MnOx/MWCNT compared with those in ozonation alone, indicating that MnOx/MWCNT promoted the generation of hydroxyl radicals. The degradation of ciprofloxacin was studied in drinking water and wastewater process samples to gauge the potential effects of water background matrix on MnOx/MWCNT catalytic ozonation.

  15. Heterogeneous catalytic ozonation of ciprofloxacin in water with carbon nanotube supported manganese oxides as catalyst

    Energy Technology Data Exchange (ETDEWEB)

    Sui, Minghao, E-mail: suiminghao.sui@gmail.com [State Key Laboratory of Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Tongji University, 1239 Siping Road, Shanghai 200092 (China); Xing, Sichu; Sheng, Li; Huang, Shuhang; Guo, Hongguang [State Key Laboratory of Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Tongji University, 1239 Siping Road, Shanghai 200092 (China)

    2012-08-15

    Highlights: Black-Right-Pointing-Pointer Ciprofloxacin in water was degraded by heterogeneous catalytic ozonation. Black-Right-Pointing-Pointer MnOx were supported on MWCNTs to serve as catalyst for ozonation. Black-Right-Pointing-Pointer MnOx/MWCNT exhibited highly catalytic activity on ozonation of ciprofloxacin in water. Black-Right-Pointing-Pointer MnOx/MWCNT resulted in effective antibacterial activity inhibition on ciprofloxacin. Black-Right-Pointing-Pointer MnOx/MWCNT promoted the generation of hydroxyl radicals. - Abstract: Carbon nanotube-supported manganese oxides (MnOx/MWCNT) were used as catalysts to assist ozone in degrading ciprofloxacin in water. Manganese oxides were successfully loaded on multi-walled carbon nanotube surfaces by simply impregnating the carbon nanotube with permanganate solution. The catalytic activities of MnOx/MWCNT in ciprofloxacin ozonation, including degradation, mineralization effectiveness, and antibacterial activity change, were investigated. The presence of MnOx/MWCNT significantly elevated the degradation and mineralization efficiency of ozone on ciprofloxacin. The microbiological assay with a reference Escherichia coli strain indicated that ozonation with MnOx/MWCNT results in more effective antibacterial activity inhibition of ciprofloxacin than that in ozonation alone. The effects of catalyst dose, initial ciprofloxacin concentration, and initial pH conditions on ciprofloxacin ozonation with MnOx/MWCNT were surveyed. Electron spin resonance trapping was applied to assess the role of MnOx/MWCNT in generating hydroxyl radicals (HO{center_dot}) during ozonation. Stronger 5,5-dimethyl-1-pyrroline-N-oxide-OH signals were observed in the ozonation with MnOx/MWCNT compared with those in ozonation alone, indicating that MnOx/MWCNT promoted the generation of hydroxyl radicals. The degradation of ciprofloxacin was studied in drinking water and wastewater process samples to gauge the potential effects of water background matrix on

  16. [Beta-blockers usage in cardio-vascular diseases co-existing with COPD].

    Science.gov (United States)

    Walczak, Dorota; Kowal, Aneta; Jankowska, Renata

    2012-12-01

    Chronic obstructive pulmonary disease (COPD) is one of the most frequent chronic diseases. Slightly reversable and progressive decrease in airflow through the airways is characteristic for the disease. It has been brought up last years that COPD course influences not only pulmonary system status but also many co-existing diseases in the eldery, especially cardio-vascular diseases, such as: ischaemic heart disease, hypertension, heart arrythmias, heart infarction. Wide usage and established position in the treatment of cardio-vascular diseases have the antagonists of beta-adrenergic receptors (beta-blockers). The aim of this work was the combination of the studies results quoted in the literature about the usage of beta-blockers in cardiovascular diseases co-existing with COPD. Conclusions. Nowadays there are no unambiguous recommendations for the usage of beta-blocker in patients with COPD and the decision about including them into treatment depends on the individually estimated risk of complications. PMID:23437704

  17. Co-existence of classical and alternative activation programs in macrophages responding to Toxoplasma gondii.

    Science.gov (United States)

    Patil, Veerupaxagouda; Zhao, Yanlin; Shah, Suhagi; Fox, Barbara A; Rommereim, Leah M; Bzik, David J; Yap, George S

    2014-02-01

    Pro-inflammatory M1 macrophages are critical for defense against intracellular pathogens while alternatively-activated M2 macrophages mediate tissue homeostasis and repair. Whether these distinct activation programs are mutually exclusive or can co-exist within the same cell is unclear. Here, we report the co-existence of these programs in Toxoplasma gondii-elicited inflammatory macrophages. This is independent of parasite expression of the virulence factor ROP16 and host cell expression of signal transducer and activator of transcription 6 (STAT6). Furthermore, this observation was recapitulated by IFN-γ and IL-4 treated bone marrow-derived macrophages in vitro. These results highlight the multi-functionality of macrophages as they respond to diverse microbial and endogenous stimuli. PMID:24083945

  18. Co-Existence of Peri-Ampullary Carcinoma with Peripancreatic Tuberculous Lymphadenopathy

    Directory of Open Access Journals (Sweden)

    Shah S

    2004-05-01

    Full Text Available CONTEXT: Pancreatic tuberculosis and peripancreatic tuberculous lymphadenitis are rare, mimicking various pathologies of the pancreas. The coexistence of peri-ampullary malignancy with peripancreatic tuberculous lymphadenitis has not been reported. CASE REPORT: We present the case of a young woman who had been operated on with a preoperative diagnosis of peri-ampullary adenocarcinoma in whom a frozen section of regional lymph nodes revealed tuberculosis. The final pathology confirmed the co-existence of tuberculosis with malignancy. The patient made an uneventful recovery. CONCLUSION: In countries with high endemicity for tuberculosis, the co-existence of malignancy and tuberculosis should be considered and resection, which is the only chance for cure, should not be abandoned due to observations based solely on frozen sections.

  19. Pancreatic insulinoma co-existing with gastric GIST in the absence of neurofibromatosis-1

    Directory of Open Access Journals (Sweden)

    O'Sullivan Brendan

    2009-02-01

    Full Text Available Abstract Background Gastrointestinal stromal tumours (GIST frequently occur in patients with neurofibromatosis type 1 (NF-1. It has been reported that GIST may co-exist with pancreatic endocrine tumors but this has only been in association with NF-1. Case presentation A 76 year old woman presented with a 12 month history of hypoglycaemia symptoms. Abdominal CT scan demonstrated a 13 mm insulinoma localized in the tail of her pancreas. She was commenced on diazoxide and later underwent surgery for enucleation of insulinoma when a small ( Conclusion This is the first case report of a pancreatic insulinoma co-existing with a GIST in a patient without NF-1. In addition, we make the first report of rapidly growing cystic GIST recurrence following resection of a primary GIST tumour.

  20. Co-existing institutional logics and agency among top-level public servants

    DEFF Research Database (Denmark)

    Bjerregaard, Toke

    2011-01-01

    basis for both coping and more proactive strategies in pluralistic public administrations. Findings illustrate the role of public servants' practical sense of realizable opportunities that inform such strategies of handling co-existing institutional logics. Implications for institutional studies of......While institutional organization research to some extent has neglected the micro agency of organization members, parts of the strategy-as-practice research have tended to bracket off wider societal environments shaping the practices-in-use of top-level strategy practitioners. This article attempts...... to address parts of this void. This study examines the agency exerted by top-level public servants through their everyday strategy and policy work in face of co-existing logics of public administration. The findings illustrate how their action strategies span from more passive strategies of coping...

  1. Genetically modified and non-genetically modified food supply chains : co-existence and traceability

    OpenAIRE

    Bertheau, Yves

    2013-01-01

    In the European Union nations, and other countries including Japan, Australia and Malaysia, it is a legal requirement that food products containing genetically modified organism (GMO) materials are labelled as such in order that customers may make informed purchasing decisions. For manufacturers and consumers to be confident about these assertions, systems must be in place along the entire food chain which support the co-existence of GM and non GM materials whilst maintaining a strict segrega...

  2. Co-existence with GM crops: grasses, clover and fodder beet

    OpenAIRE

    Jørgensen, R. B.; Løjtnant, C.; Andersen, N.S.; Andersen, B.A.

    2007-01-01

    Co-existence with GM crops: grasses, clover and fodder beet In 2006 the global cultivation of genetically modified crops increased with 13% and reached 102 million hectares. The GM crops cultivated are mainly soybean, maize, cotton and oilseed rape, but other modified crops are appearing, e.g. in 2006 herbicide tolerant alfalfa was commercialized in US. Also in Europe, GM crop cultivation is increasing with the largest areas in Rumania and Spain followed by Portugal, France, Germany, Czec...

  3. Pharmaceutical and Industrial Traits in Genetically Modified Crops: Co-Existence with Conventional Agriculture

    OpenAIRE

    Moschini, GianCarlo

    2006-01-01

    This paper discusses the implications of using genetically modified crops to biomanufacture pharmaceuticals and industrial compounds from the perspective of their co-existence with conventional agriculture. Such plant-made pharmaceuticals and plant-made industrial products rely on exciting scientific and technological breakthroughs and promise new opportunities for the agricultural sector, but they also entail novel risks. The management of the externalities and of the possible unintended eco...

  4. Unusual case of bancroftian filariasis co-existing with chronic myeloid leukemia

    OpenAIRE

    Mallika Kinger; Preeti Rihal Chakrabarti; Surabhi Sharma; Priyanka Kiyawat

    2014-01-01

    Filariasis, a tropical parasite infection, is a common public health problem in the Indian sub-continent. Occurrence of filariasis with chronic myeloid leukemia (CML) is unusual though there are case reports of leishmaniasis, malaria, and other vector-borne diseases seen in association with leukemias. Filariasis co-existing with CML has not been documented to the best of our knowledge and hence definitely needs a space in literature. We report an incidental finding of bancroftian filariasis i...

  5. Pancreatic insulinoma co-existing with gastric GIST in the absence of neurofibromatosis-1

    OpenAIRE

    O'Sullivan Brendan; Bramhall Simon; Alabraba Edward; Mahon Brinder; Taniere Philippe

    2009-01-01

    Abstract Background Gastrointestinal stromal tumours (GIST) frequently occur in patients with neurofibromatosis type 1 (NF-1). It has been reported that GIST may co-exist with pancreatic endocrine tumors but this has only been in association with NF-1. Case presentation A 76 year old woman presented with a 12 month history of hypoglycaemia symptoms. Abdominal CT scan demonstrated a 13 mm insulinoma localized in the tail of her pancreas. She was commenced on diazoxide and later underwent surge...

  6. Catalytic oxidation of water and alcohols by a robust iron(iii) complex bearing a cross-bridged cyclam ligand.

    Science.gov (United States)

    Tan, Peng; Kwong, Hoi-Ki; Lau, Tai-Chu

    2015-08-01

    An iron(iii) complex bearing a cross-bridged cyclam ligand (4,11-dimethyl-1,4,8,11-tetraazabicyclo[6.6.2]hexadecane) is an efficient catalyst for the oxidation of both water and alcohols using sodium periodate as the oxidant. In catalytic water oxidation a maximum turnover number (TON) of 1030 is achieved, while in catalytic alcohol oxidation >95% conversions and yields can be obtained. PMID:26126521

  7. Iron-doped Pt-TiO2 nanotubes for photo-catalytic water splitting

    International Nuclear Information System (INIS)

    In this work we report on the photo-catalytic performance of phase-pure and iron-doped anatase and rutile nanotubes, produced via a sol-gel process using pristine carbon nanotubes as templates. The encapsulated iron residues can be used to in situ dope the TiO2 nanotubes without phase separation. The anatase and rutile nanotubes were further impregnated with platinum crystals with a uniform dispersion and an average size of ∼2 nm. The materials showed dramatically improved activities for the photo-catalytic splitting of water compared to commercial TiO2 with similar surface area (up to two orders of magnitudes), due to their higher illumination area, extended absorption range and reduced electron-hole recombination rate. The homogeneous dispersion of platinum nanoparticles further increased the hydrogen evolution rate for anatase nanotubes by a factor of seven in comparison to that for the pristine material, thus proving the great potential for commercial applications.

  8. A feasibility study of catalytic reduction method for tritium recovery from tritiated water

    International Nuclear Information System (INIS)

    Feasibility of catalytic reduction method for the application to the tritium recovery process in the fusion fuel cleanup system and the blanket tritium recovery system was studied by experimental work and the thermodynamic analysis. Reduction experiments of H2O vapor with Ar carrier were carried out under the following conditions: temperature; 350 -- 650 K, H2O vapor concentration in feed gas; 103 -- 104 ppm, mole ratio of CO to H2O; 1 -- 10, space velocity; 2 x 102 -- 2 x 104 hr-1. Catalyst was the mixture of CuO, ZnO and Cr2O3, which has been used as the catalyst for the water-gas shift reaction H2O(g) + CO(g) reversible H2(g) + CO2(g). Relations between the conversion factor for H2O vapor and the operating conditions such as temperature, feed composition and feed flow rate were obtained by the experiments. Catalytic reaction rate equation and the rate constants, which can be used for designing a practicable catalytic reduction bed, were also determined by the treatment of the second order reaction. Advantages of the tritium recovery system composed of the reduction bed and palladium diffusers were verified by the present experiments and the study of several tritium recovery systems. Very high recovery ratio will be obtained at low operation temperature by the systems. (author)

  9. A study on the photo catalytic decomposition reactions of organics dissolved in water (II)

    International Nuclear Information System (INIS)

    Experiments on aqueous TiO2 photo catalytic reaction of nitrogen containing organic compounds such as ethylamine, phenylhydrazine, pyridine, urea and EDTA were carried out. Based on the values calculated for the distribution of ionic species and atomic charge, the characteristics of their photo catalytic decomposition were estimated. It was shown that the decomposition characteristics was linearly proportional to nitrogen atomic charge value. On the other hand, the effects of aqueous pH, oxygen content and concentration on the TiO2 photo catalytic characteristics of EDTA, EDTA-Cu(II) and EDTA-Fe(III) were experimentally investigated. All EDTA systems were decomposed better in the pH range of 2.5-3.0 and with more dissolved oxygen. These results could be applied to construction of a process for removal of organic impurities dissolved in a source of system water, or for treatment of EDTA-containing liquid waste produced by a chemical cleaning in the domestic NPPs. (author)

  10. A study on the photo catalytic decomposition reactions of organics dissolved in water (II)

    Energy Technology Data Exchange (ETDEWEB)

    Sung, K.W.; Na, J. W.; Cho, Y. H.; Chung, H. H

    2000-01-01

    Experiments on aqueous TiO{sub 2} photo catalytic reaction of nitrogen containing organic compounds such as ethylamine, phenylhydrazine, pyridine, urea and EDTA were carried out. Based on the values calculated for the distribution of ionic species and atomic charge, the characteristics of their photo catalytic decomposition were estimated. It was shown that the decomposition characteristics was linearly proportional to nitrogen atomic charge value. On the other hand, the effects of aqueous pH, oxygen content and concentration on the TiO{sub 2} photo catalytic characteristics of EDTA, EDTA-Cu(II) and EDTA-Fe(III) were experimentally investigated. All EDTA systems were decomposed better in the pH range of 2.5-3.0 and with more dissolved oxygen. These results could be applied to construction of a process for removal of organic impurities dissolved in a source of system water, or for treatment of EDTA-containing liquid waste produced by a chemical cleaning in the domestic NPPs. (author)

  11. Advanced aerogel materials for photo catalytic detoxification of cyanide wastes in water

    International Nuclear Information System (INIS)

    Ultraviolet (UV) - irradiated TiO2 - SiO2 aerogels were used in the study as catalysts for oxidation of cyanide species (CN-) in water to CO2 and N2. TiO2-SiO2 aerogel catalysts were prepared by the sol-gel and supercritical drying techniques. Three types of this aerogel were prepared with different SiO2 content (i.e., TiO2 molar ratio = 1:1.3, 1:2.6 and 1:3.9). It was observed that with increasing SiO2 content, shrinkage and apparent density decreased, however, translucency increased. This resulted in higher photo catalytic activity for oxidation of CN- in dilute solutions (1000 and 522 Ppm) of ferric cyanide. Compared with TiO2 powder (i.e., anatase with TiO 2 > 98% and particle diameter 2 content has higher efficiency in the photo catalytic oxidation of CN- at similar experimental conditions. This aerogel catalyst was completely recovered and reused several times to check the activity loss. No significant change in the photo catalytic activity was observed. 6 figs., 2 tabs

  12. Cost of GMO-related co-existence and traceability systems in food production in Germany

    OpenAIRE

    Menrad, Klaus; Gabriel, Andreas; Zapilko, Marina

    2009-01-01

    In contrast to the increasing use of GM plants in world-wide agriculture, the acceptance of GM food is still low in the European Union (EU). In order to ensure freedom of choice for consumers and users of GM and non-GM products, GM food and feed products have to be labeled in case a tolerance threshold of 0.9 % is exceeded for EU authorized GMOs. This paper aims to quantify the cost of traceability and co-existence systems for GM food from the seed to the food level for sugar, wheat starch an...

  13. The Co-existence between Oreochromis niloticus and Lates niloticus in Lake Victoria (Kenya Sector).

    OpenAIRE

    Ogari, J.

    1990-01-01

    The present study was undertaken to try and find out why Lates niloticus and Oreochromis niloticus have managed to co-exist in Lake Victoria (Kenya sector). The study is considered to be of tremendous scientific value not only because lates has been accused of preying on the cichlid stocks in L.Victoria but also for considering suitable management approaches to maintain viable fishery resources on long-term basis. The results presented are preliminary and the final detailed results will be pr...

  14. The co-existence between Oreochromis niloticus and Lates niloticus in Lake Victoria (Kenya sector)

    OpenAIRE

    Ogari, J.

    1990-01-01

    The present study was undertaken to try and find out why Lates niloticus and Oreochromis nilolicus have managed to co-exist in Lake Victoria (Kenya sector). The study is considered to be of tremendous scientific value not only because Lates has been accused of preying on the cichlid stocks in L.Victoria but also for considering suitable management approaches to maintain viable fishery resources on long-term basis. The results presented are preliminary and the final detailed results will be pr...

  15. Network competition - the co-existence of hub-and-spoke and point-to-point

    OpenAIRE

    Alderighi, Marco; Cento, Alessandro; Nijkamp, Peter; Rietveld, Piet

    2005-01-01

    Airlines network choices are analysed to describe the co-existence of alternative business models: the full service model based on the hub-and-spoke (HS) system and the low cost model based on point-to-point (PP) system. The analysis is carried on both theoretically and empirically. In the theoretical part, we show that the rise of the low costs business model can be the consequence of a simple two-player game. When two carriers compete in designing their network configurations (HS or PP), as...

  16. Organising co-existence in cyberspace: Content regulation and privacy compared

    OpenAIRE

    Engel, Christoph

    2002-01-01

    The Internet globalizes the world. National regulatory autonomy shrinks. Transferring data from one country to another is almost costless. Foreign content is just a click away. Why is it that states have been able to re-install co-existence in some policy areas, and not in others? In data protection, the safe-harbour compromise between the US and the EU found a way out. In the area of content regulation, transnational conflict is no less pronounced. The Europeans are preoccupied with Nazi pub...

  17. WISA vs. WLAN: Co-existence challenges : - A tool for WLAN performance testing

    OpenAIRE

    Strand, Erlend Barstad

    2007-01-01

    Wireless Interface for Sensors and Actuators (WISA) is ABB's proprietary wireless protocol for industrial automation on the factory floor. It operates in the 2.4GHz ISM band. Wireless Local Area Networks (WLANs), which typically occupy a fixed portion of the same 2.4GHz ISM band, are becoming more and more common on the factory floor. This raises a question of co-existence and how the performance of traffic over WLAN is affected when interfered by WISA. This report is a result of the developm...

  18. Implications of co-existing national and multinational geological repository development programmes in Europe - 59118

    International Nuclear Information System (INIS)

    The aim of this paper is to identify interactions between national and multi-national geological repository programmes that are potentially either beneficial or problematic, so as to avoid any unintended negative impacts on national or multinational programmes and to maximise mutual benefits wherever possible. Regional, multi-national cooperation on geological disposal is a topical issue at present at the IAEA and also in the EU, which has produced a new proposed Directive that explicitly allows agreements on sharing. Two extended tables in the paper identify and comment briefly on historic and current positive and negative perceptions of co-existing national and multinational geological disposal programmes. It would, we believe, be a positive message to the global nuclear community to know that leading national disposal programmes are interacting constructively with regional initiatives. The extensive experience already gained in national programmes could be very beneficial to new nuclear countries. In particular, it is crucial for all nuclear programmes that the new entrants develop credible, long-term waste management programmes, whether these be national, regional or dual-track. For global safety and security reasons, the nuclear community must move towards a situation where both national and shared programmes will co-exist and interact symbiotically. (authors)

  19. Co-existence of shapes in nuclei at high angular momentum

    International Nuclear Information System (INIS)

    Recent strides in the gamma spectroscopy have revealed spectacular co-existence of shapes in nuclei. For example, transitional nuclei between the double closed shell, Z=64 and N=82 have several interesting properties. At spins below 40 h, there is known to be (1,2) a competition among several shapes. This is found to be due to small shifts in the particle alignment frequencies, which shifts in the particle alignment frequencies, which produces dramatic difference in band behaviour. For such 'soft' nuclei even the neighbours (e.g. isotones) can show strikingly different band structure at high spins. A study of such nuclei using an array of Compton-suppressed Ge detectors leads to interesting physics: mechanism of nuclear shape change, extent to which different shapes co-exist and quenching of pairing correlations with increasing spin. Some recent studies in the spherical region has revealed a collective behaviour for yrast states in these nuclei. Deformed, rotational like bands have been observed. Further the rotational inertia was found to remain constant at higher spins, something which is characteristic of good rotors. Much interest is focussed on these aspects. An axis ratio of 2 to 1 is recognised as corresponding to a superdeformed shape. A global hunt is on to identify and study superdeformed shape exhibited by nuclei. Pairing forces play a paradoxical role in the description of superdeformed rotational bands. (author). 5 refs., 6 figs

  20. Respiratory Distress Secondary to Rhabdomyosarcoma of the Tongue and Co-existent Choanal Atresia.

    Science.gov (United States)

    Chatopadhayay, Rahul; Tiwari, Preeti; Gangopadhyay, A N; Pandey, Vaibhav

    2016-07-01

    Whilst rhabdomyosarcoma (RMS) is the third most common solid tumour in children, congenital RMS of the tongue is extremely rare and usually present as painless progressive mass since birth (Dagher and Helman in Oncologist 4:34-44, 1999; Childs and Goudy in Int J Pediatr Otorhinolaryngol 5:126-128, 2010). In neonates, presentation with respiratory distress is unexpected as neonates are preferential nasal breathers and restricted oral breathing due to tumour usually poses no problem. We herein report a case of rhabdomyosarcoma of the tongue with co-existent unilateral choanal atresia, presenting with respiratory distress. The baby developed upper respiratory tract infection following which developed severe respiratory distress. Airway symptoms were precipitated as there was combined obstruction of both the nostrils due to infection or adenoid enlargement and unilateral chonal atresia. Treatment of respiratory distress in the presence of RMS and bilateral nasal pathology must first prioritise the security of the airway, before taking a multi-factorial approach to the therapy of the lingual mass (Childs and Goudy in Int J Pediatr Otorhinolaryngol 5:126-128, 2010). This case illustrates the importance of vigilance with respect to co-existent nasal pathology, in order to avoid the occurrence of complete airway obstruction. We therefore feel that any diagnosis of lingual RMS should warrant a formal examination of both nasal cavities. PMID:27408448

  1. Co-existence and interaction between myxomycetes and other organisms in shared niches

    Directory of Open Access Journals (Sweden)

    Irina O. Dudka

    2013-12-01

    Full Text Available The ecology of myxomycetes co-existing with the Latridiidae (Coleoptera, bryophytes and ascomycetous, basidiomycetous and anamorphic fungi were studied in Crimea and at different locations on the left bank of Ukraine. Results from the left bank indicate that the Latridiidae feed on myxomycetes. Colonies of the most common 13 myxomycete species (which included Stemonitis axifera (Bull. Macbr., S. fusca Roth, S. splendens Rost., Fuligo septica (L. Wigg. and Mucilago crustacea Wigg. were inhabited by 5 species of the Latridiidae. Myxomycete spores were present in guts of 19 of the 25 beetle specimens investigated. Beetles Latridius hirtus, Enicmus rugosus and E fungicola seem to be obligate myxomycete feeders, while Corticarina truncatella was clearly facultative. 13 species of myxomycetes were recorded on 9 species of moss and 3 species of liverwort developing on decaying wood or bark in the Crimean Nature Reserve. Relations between myxomycetes and bryophytes on woody substrata are spatial rather than trophic, and are possibly regulated by specific microclimatic conditions inside bryophyte thallomes. 69 species of myxomycetes were found co-existing with 36 species of ascomycetes, 21 species of basidiomycetes and 9 species of anamorphic fungi in the Crimean Nature Reserve. Associations formed by myxomycetes and fungi on different woody substrata are analyzed.

  2. Spatiotemporal Co-existence of Female Thyroid and Breast Cancers in Hangzhou, China

    Science.gov (United States)

    Fei, Xufeng; Christakos, George; Lou, Zhaohan; Ren, Yanjun; Liu, Qingmin; Wu, Jiaping

    2016-06-01

    Thyroid and breast cancers (TC, BC) are common female malignant tumors worldwide. Studies suggest that TC patients have a higher BC risk, and vice versa. However, it has not been investigated quantitatively if there is an association between the space-time TC and BC incidence distributions at the population level. This work aims to answer this question. 5358 TC and 8784 BC (female) cases were diagnosed in Hangzhou (China, 2008–2012). Pearson and Spearman rank correlation coefficients of the TC and BC incidences were high, and their patterns were geographically similar. The spatiotemporal co-existence of TC and BC distributions was investigated using the integrative disease predictability (IDP) criterion: if TC-BC association is part of the disease mapping knowledge bases, it should yield improved space-time incidence predictions. Improved TC (BC) incidence predictions were generated when integrating both TC and BC data than when using only TC (BC) data. IDP consistently demonstrated the spatiotemporal co-existence of TC and BC distributions throughout Hangzhou (2008–2012), which means that when the population experiences high incidences of one kind of cancer attention should be paid to the other kind of cancer too. The strength of TC-BC association was measured by the IDP coefficients and incidence prediction accuracy.

  3. Development of an Experimental Model of Diabetes Co-Existing with Metabolic Syndrome in Rats.

    Science.gov (United States)

    Suman, Rajesh Kumar; Ray Mohanty, Ipseeta; Borde, Manjusha K; Maheshwari, Ujwala; Deshmukh, Y A

    2016-01-01

    Background. The incidence of metabolic syndrome co-existing with diabetes mellitus is on the rise globally. Objective. The present study was designed to develop a unique animal model that will mimic the pathological features seen in individuals with diabetes and metabolic syndrome, suitable for pharmacological screening of drugs. Materials and Methods. A combination of High-Fat Diet (HFD) and low dose of streptozotocin (STZ) at 30, 35, and 40 mg/kg was used to induce metabolic syndrome in the setting of diabetes mellitus in Wistar rats. Results. The 40 mg/kg STZ produced sustained hyperglycemia and the dose was thus selected for the study to induce diabetes mellitus. Various components of metabolic syndrome such as dyslipidemia {(increased triglyceride, total cholesterol, LDL cholesterol, and decreased HDL cholesterol)}, diabetes mellitus (blood glucose, HbA1c, serum insulin, and C-peptide), and hypertension {systolic blood pressure} were mimicked in the developed model of metabolic syndrome co-existing with diabetes mellitus. In addition to significant cardiac injury, atherogenic index, inflammation (hs-CRP), decline in hepatic and renal function were observed in the HF-DC group when compared to NC group rats. The histopathological assessment confirmed presence of edema, necrosis, and inflammation in heart, pancreas, liver, and kidney of HF-DC group as compared to NC. Conclusion. The present study has developed a unique rodent model of metabolic syndrome, with diabetes as an essential component. PMID:26880906

  4. Mechanisms Leading to Co-Existence of Gas Hydrate in Ocean Sediments [Part 1 of 2

    Energy Technology Data Exchange (ETDEWEB)

    Bryant, Steven; Juanes, Ruben

    2011-12-31

    In this project we have sought to explain the co-existence of gas and hydrate phases in sediments within the gas hydrate stability zone. We have focused on the gas/brine interface at the scale of individual grains in the sediment. The capillary forces associated with a gas/brine interface play a dominant role in many processes that occur in the pores of sediments and sedimentary rocks. The mechanical forces associated with the same interface can lead to fracture initiation and propagation in hydrate-bearing sediments. Thus the unifying theme of the research reported here is that pore scale phenomena are key to understanding large scale phenomena in hydrate-bearing sediments whenever a free gas phase is present. Our analysis of pore-scale phenomena in this project has delineated three regimes that govern processes in which the gas phase pressure is increasing: fracturing, capillary fingering and viscous fingering. These regimes are characterized by different morphology of the region invaded by the gas. On the other hand when the gas phase pressure is decreasing, the corresponding regimes are capillary fingering and compaction. In this project, we studied all these regimes except compaction. Many processes of interest in hydrate-bearing sediments can be better understood when placed in the context of the appropriate regime. For example, hydrate formation in sub-permafrost sediments falls in the capillary fingering regime, whereas gas invasion into ocean sediments is likely to fall into the fracturing regime. Our research provides insight into the mechanisms by which gas reservoirs are converted to hydrate as the base of the gas hydrate stability zone descends through the reservoir. If the reservoir was no longer being charged, then variation in grain size distribution within the reservoir explain hydrate saturation profiles such as that at Mt. Elbert, where sand-rich intervals containing little hydrate are interspersed between intervals containing large hydrate

  5. Mechanisms Leading to Co-Existence of Gas Hydrate in Ocean Sediments [Part 2 of 2

    Energy Technology Data Exchange (ETDEWEB)

    Bryant, Steven; Juanes, Ruben

    2011-12-31

    In this project we have sought to explain the co-existence of gas and hydrate phases in sediments within the gas hydrate stability zone. We have focused on the gas/brine interface at the scale of individual grains in the sediment. The capillary forces associated with a gas/brine interface play a dominant role in many processes that occur in the pores of sediments and sedimentary rocks. The mechanical forces associated with the same interface can lead to fracture initiation and propagation in hydrate-bearing sediments. Thus the unifying theme of the research reported here is that pore scale phenomena are key to understanding large scale phenomena in hydrate-bearing sediments whenever a free gas phase is present. Our analysis of pore-scale phenomena in this project has delineated three regimes that govern processes in which the gas phase pressure is increasing: fracturing, capillary fingering and viscous fingering. These regimes are characterized by different morphology of the region invaded by the gas. On the other hand when the gas phase pressure is decreasing, the corresponding regimes are capillary fingering and compaction. In this project, we studied all these regimes except compaction. Many processes of interest in hydrate-bearing sediments can be better understood when placed in the context of the appropriate regime. For example, hydrate formation in sub-permafrost sediments falls in the capillary fingering regime, whereas gas invasion into ocean sediments is likely to fall into the fracturing regime. Our research provides insight into the mechanisms by which gas reservoirs are converted to hydrate as the base of the gas hydrate stability zone descends through the reservoir. If the reservoir was no longer being charged, then variation in grain size distribution within the reservoir explain hydrate saturation profiles such as that at Mt. Elbert, where sand-rich intervals containing little hydrate are interspersed between intervals containing large hydrate

  6. Papillary thyroid microcarcinoma co-exists with Hashimoto's thyroiditis: Is strain elastography still useful?

    Science.gov (United States)

    Li, Yi; Wang, Yan; Wu, Qiong; Hu, Bing

    2016-05-01

    To study the performance of strain elastography in differentiating papillary thyroid microcarcinoma (PTMC) combined with Hashimoto's thyroiditis (HT), conventional ultrasound scan (US) and strain elastography (SE) were performed on 558 nodules smaller than 10mm by one examiner before surgeries. Serum concentrations of thyroid peroxidase antibody (TPO-Ab) (normal range: 0-60U/ml) were measured. Continuous variables were analyzed by independent t test. Receiver operating characteristics (ROC) curve analysis was applied to calculate the cut-off values of strain ratio (SR) and elastography score (ES). The comparison of AUCs is performed by Z test. 482 nodules were diagnosed as PTMC and there were 181 nodules co-existed with HT. SR measurements were lower in PTMC co-existed with HT when comparing to those without HT. (7.292±6.581 vs 11.319±13.155, p2.58. When taking the data from 181 PTMC with HT, the best cut-off was SR>2.10. The diagnostic value of SR>2.1 were higher than ES>3, conventional US and combining US and SE (z=3.595, 4.876, 4.420, p2.1 did not show significant enhancement of diagnostic value compared to SR>2.58 (z=0.439, p=0.8903>0.001) in PTMC with HT. There is a negative relation between SR and titer of TPO-Ab (r=-0.650, pTPO-Ab (>1000) titer presented lower SR (5.972±4.118 vs 8.379±9.172, p=0.009). Although SR measurements were lower in nodules co-existed with HT when comparing those without HT, using a regular ES and cut-off of SR measurement would not influence the diagnosing performance. SE is still very useful for diagnosing PTMC with HT. PTMC with high TPO-Ab titer might require a lower cut-off of SR. PMID:26945905

  7. Co-existence of Insulin Dependent Diabetes and Graves’ Disease in a Patient with Down Syndrome

    Directory of Open Access Journals (Sweden)

    Ayşe Kubat Üzüm

    2010-05-01

    Full Text Available Down’s syndrome is the most common genetic disorder. It is well established that there is an increased risk of autoimmune endocrine diseases in Down’s syndrome. Defect of a gene located on chromosome 21q22.3 causes autoimmune polyglandular syndrome type 1 and this might be related with susceptibility to autoimmune diseases in patients with Down’s syndrome. We reported a 20-year-old male with Down’s syndrome who was brought to emergency room by his family and had a diagnose of diabetic ketoacidosis and Graves’ disease. Underlying mechanisms in co-existing of autoimmune diseases in Down’s syndrome, management of such patients and the importance of making the family to be aware of the symptoms of possible subsequent components of the autoimmune polyglandular syndrome are discussed. Turk Jem 2010; 14: 17-9

  8. A rare case of breast carcinoma co-existing with axillary mantle cell lymphoma

    Directory of Open Access Journals (Sweden)

    Scally John

    2003-12-01

    Full Text Available Abstract Background Mantle cell lymphoma (MCL is a rare variety of non-Hodgkin's lymphoma which originates from CD5+ B-cell population in the mantle zones of lymphoid follicles. Coexistence of such tumours in the axillary lymph nodes with invasive breast cancers without prior history of adjuvant chemotherapy or radiotherapy has not been previously reported in literature. Case report We report a rare case of breast cancer co-existing with stage I mantle cell lymphoma of the ipsilateral axillary lymph node detected fortuitously by population screening. Conclusion Though some studies have tried to prove breast carcinomas and lymphomas to share a common molecular or viral link, more research needs to be done to establish whether such a link truly exists.

  9. Co-existing ericaceous plant species in a subarctic mire community share fungal root endophytes

    DEFF Research Database (Denmark)

    Kjøller, Rasmus; Olsrud, Maria; Michelsen, Anders

    2010-01-01

    the fungal composition in roots of co-existing ericaceous plants is scarce. In the present paper, the fungal community in roots of four ericaceous plant species, Empetrum hermaphroditum, Andromeda polifolia, Vaccinium uliginosum and Vaccinium vitis-idaea which often dominate subarctic heaths and mires......, was studied. From each of these plants, in each of five plots, clone libraries were established using fungal specific ITS-PCR followed by cloning, PCR–RFLP and sequencing. The clone libraries were dominated by potential ericoid mycorrhizal fungi, particularly Rhizoscyphus ericae, fungi belonging...... to the Sebacinales group B, and Capronia-like fungi. Additionally, the results showed that while ericaceous plant species growing within the same 15 × 15 cm blocks shared a common fungal community, plots just 2–3 m away harboured a significantly different fungal community. The possible functional implications of co...

  10. Azathioprine Induced Pancreatitis in a Patient with Co-Existing Autoimmune Pancreatitis and Hepatitis

    Directory of Open Access Journals (Sweden)

    Preethi GK Venkatesh

    2011-05-01

    Full Text Available Context Azathioprine induced pancreatitis usually runs a benign self limited course with rapid disappearance of signs and symptoms upon with drawl of the drug. Azathioprine is used in treating relapses in patients with autoimmune pancreatitis and maintenance of remission in autoimmune hepatitis. Acute pancreatitis complicated by symptomatic pseudocysts requiring drainage is not usually associated with drug induced pancreatitis. The risk of azathioprine use in patients with underlying disease of pancreas including autoimmune pancreatitis is unclear. Case report We report here a case of an African American patient with co-existing autoimmune pancreatitis and autoimmune hepatitis who developed azathioprine induced acute pancreatitis complicated by a large symptomatic pseudocyst compressing the duodenum requiring a cystoduodenostomy. Conclusions Future studies to investigate the risk of azathioprine induced pancreatitis in the presence of underlying disease of the pancreas including autoimmune pancreatitis are required to further understand the safety of azathioprine in this sub group of patients.

  11. First-principles quantum-mechanical investigations: The role of water in catalytic conversion of furfural on Pd(111)

    Science.gov (United States)

    Xue, Wenhua; Borja, Miguel Gonzalez; Resasco, Daniel E.; Wang, Sanwu

    2015-03-01

    In the study of catalytic reactions of biomass, furfural conversion over metal catalysts with the presence of water has attracted wide attention. Recent experiments showed that the proportion of alcohol product from catalytic reactions of furfural conversion with palladium in the presence of water is significantly increased, when compared with other solvent including dioxane, decalin, and ethanol. We investigated the microscopic mechanism of the reactions based on first-principles quantum-mechanical calculations. We particularly identified the important role of water and the liquid/solid interface in furfural conversion. Our results provide atomic-scale details for the catalytic reactions. Supported by DOE (DE-SC0004600). This research used the supercomputer resources at NERSC, of XSEDE, at TACC, and at the Tandy Supercomputing Center.

  12. A supramolecular ruthenium macrocycle with high catalytic activity for water oxidation that mechanistically mimics photosystem II

    Science.gov (United States)

    Schulze, Marcus; Kunz, Valentin; Frischmann, Peter D.; Würthner, Frank

    2016-06-01

    Mimicking the ingenuity of nature and exploiting the billions of years over which natural selection has developed numerous effective biochemical conversions is one of the most successful strategies in a chemist's toolbox. However, an inability to replicate the elegance and efficiency of the oxygen-evolving complex of photosystem II (OEC-PSII) in its oxidation of water into O2 is a significant bottleneck in the development of a closed-loop sustainable energy cycle. Here, we present an artificial metallosupramolecular macrocycle that gathers three Ru(bda) centres (bda = 2,2‧-bipyridine-6,6‧-dicarboxylic acid) that catalyses water oxidation. The macrocyclic architecture accelerates the rate of water oxidation via a water nucleophilic attack mechanism, similar to the mechanism exhibited by OEC-PSII, and reaches remarkable catalytic turnover frequencies >100 s–1. Photo-driven water oxidation yields outstanding activity, even in the nM concentration regime, with a turnover number of >1,255 and turnover frequency of >13.1 s–1.

  13. A supramolecular ruthenium macrocycle with high catalytic activity for water oxidation that mechanistically mimics photosystem II.

    Science.gov (United States)

    Schulze, Marcus; Kunz, Valentin; Frischmann, Peter D; Würthner, Frank

    2016-06-01

    Mimicking the ingenuity of nature and exploiting the billions of years over which natural selection has developed numerous effective biochemical conversions is one of the most successful strategies in a chemist's toolbox. However, an inability to replicate the elegance and efficiency of the oxygen-evolving complex of photosystem II (OEC-PSII) in its oxidation of water into O2 is a significant bottleneck in the development of a closed-loop sustainable energy cycle. Here, we present an artificial metallosupramolecular macrocycle that gathers three Ru(bda) centres (bda = 2,2'-bipyridine-6,6'-dicarboxylic acid) that catalyses water oxidation. The macrocyclic architecture accelerates the rate of water oxidation via a water nucleophilic attack mechanism, similar to the mechanism exhibited by OEC-PSII, and reaches remarkable catalytic turnover frequencies >100 s(-1). Photo-driven water oxidation yields outstanding activity, even in the nM concentration regime, with a turnover number of >1,255 and turnover frequency of >13.1 s(-1). PMID:27219702

  14. Effect of zinc and copper additions on catalytic response of noble metal alloyed 304 SS in high temperature water

    International Nuclear Information System (INIS)

    The effect of zinc (Zn) and copper (Cu) additions on the catalytic behavior of noble metal alloyed 304 stainless steel (SS) in 288 C water understoichiometric excess hydrogen was studied. It was observed that an increase in the Zn or Cu content of the water increased the electrochemical corrosion potential (ECP) of noble metal alloyed 304 SS by ∼ 30 to 50 mV and decreased the recombination efficiency of oxygen (O2)and hydrogen (H2) by ∼ 10%. The change in the ECP and recombination rate was correlated with incorporation of zinc and copper in the oxide film, which, by covering catalytic sites, would alter the redox reaction rate

  15. Session 6: Water depollution from aniline and phenol by air oxidation and adsorptive-catalytic oxidation in liquid phase

    Energy Technology Data Exchange (ETDEWEB)

    Dobrynkin, N.M.; Batygina, M.V.; Noskov, A.S. [Boreskov Institute of Catalysis of Siberian Branch of Russian Academy of Sciences, Pr. Ak. Lavrentieva (Russian Federation)

    2004-07-01

    This paper is devoted to development of carbon catalysts and application of catalytic wet air oxidation for deep cleaning of polluted waters. The described catalysts and method are solving the problem of development environmentally reliable method for fluids treatment and allow carrying out the adsorption of pollutants on carbon CAPM (catalytically active porous material) with following regeneration of the CAPM without the loss of adsorptive qualities. The experiments have shown a principal capability simultaneously to use carbon CAPM as adsorbent and either as catalyst, or as a catalyst support for oxidation of aniline and phenol in water solutions. (authors)

  16. Mobile Communication Networks and Digital Television Broadcasting Systems in the Same Frequency Bands – Advanced Co-Existence Scenarios

    OpenAIRE

    L. Polak; Kaller, O.; L. Klozar; J. Sebesta; T. Kratochvil

    2014-01-01

    The increasing demand for wireless multimedia services provided by modern communication systems with stable services is a key feature of advanced markets. On the other hand, these systems can many times operate in a neighboring or in the same frequency bands. Therefore, numerous unwanted co-existence scenarios can occur. The aim of this paper is to summarize our results which were achieved during exploration and measurement of the co-existences between still used and upcoming mobile networks ...

  17. An FTIR study on the catalytic effect of water molecules on the reaction of CO successive hydrogenation at 3 K

    International Nuclear Information System (INIS)

    Graphical abstract: This work highlights a selective catalytic action of water molecules on the reaction of CO hydrogenation at 3 K. Research highlights: → [CO/H2O] and [H/H2] are coinjected at 3 K. → H2 molecules condense rapidly at 3 K and screen the reaction mostly at the 1st step. → The observed catalytic effects on CO hydrogenation increase with water concentration. - Abstract: The reaction of successive CO hydrogenation has been performed at 3 K by coinjecting CO molecules and H atoms. The concentration of CO has been progressively reduced and replaced by water molecules to create two different environments where CO and H2O are successively the dominant species in the binary (CO/H2O) mixture. The catalytic effect of water molecules on CO hydrogenation appears clearly since the early times of the experiment and evolves with the formation of the CO/H2/H2O mixed-matrix. The process of CO hydrogenation, initially frozen at the first step of the reaction, is brought to completion through water influence. Water molecules guide the reaction toward the formation of CH3OH and promote different reaction steps depending on water concentration. Water molecules increase the probability of reactive to encounter H atoms either physically, by introducing structural changes in the matrix, or chemically, by raising the number of chemical pathways.

  18. Kinetic and Phase Behaviors of Catalytic Cracking Dry Gas Hydrate in Water-in-Oil Emulsion

    Institute of Scientific and Technical Information of China (English)

    MA Qinglan; HUANG Qiang; CHEN Guangjin; WANG Xiulin; SUN Changyu; YANG Lanying

    2013-01-01

    The systematic experimental studies were performed on the hydrate formation kinetics and gas-hydrate equilibrium for a simulated catalytic cracking gas in the water-in-oil emulsion.The effect of temperature,pressure and initial gas-liquid ratio on the hydrate formation was studied,respectively.The data were obtained at pressures ranging from 3.5 to 5 MPa and temperatures from 274.15 to 277.15 K.The results showed that hydrogen and methane can be separated from the C2+ fraction by forming hydrate at around 273.15 K which is much higher temperature than that of the cryogenic separation method,and the hydrate formation rate can be enhanced in the water-in-oil emulsion compared to pure water.The experiments provided the basic data for designing the industrial process,and setting the suitable operational conditions.The measured data of gas-hydrate equilibria were compared with the predictions by using the Chen-Guo hydrate thermodynamic model.

  19. Co-existence of dual intracranial pathology clinical relevance of proton MRS.

    Directory of Open Access Journals (Sweden)

    Tripathi R

    2000-10-01

    Full Text Available The co-existence of neuro-cysticercosis (NCC and intracranial neoplasm in an individual is a rare entity. Atypical presentation of cerebral cysticercosis may mimic glioma, metastasis, cerebral abscess or vice versa. The dual existence of these two lesions have led to several postulates which may have clinical impact in due course of time i.e. NCC as an oncogenetic factor for glioma or similarity of antigen found in glioma and NCC etc. An adequate management of such cases poses a challenge to both imageologists as well as clinicians. Thus, a proper diagnostic evaluation is essential for successful management of such cases. MR spectroscopy (MRS, although still a clinical research tool, may be extremely useful for exclusion or confirmation of neoplastic lesions in such a clinical scenario. The findings of MRS in collaboration with imaging parameters may increase the diagnostic yield of a MR investigation. The authors encountered five cases of dual intracranial pathologies i.e. neurocysticercosis and glioma. MR spectroscopy was useful to arrive at a definitive diagnosis in such a situation.

  20. UNIVERSITY OF WISCONSIN - PHOTO ELECTRO CATALYTIC DEGRADATION AND REMOVAL OFORGANIC AND INORGANIC CONTAMINANTS IN GROUND WATERS: SITE DOC

    Science.gov (United States)

    SITE DOC NRMRL-CIN-1338 Gallardo*, V. University of Wisconsin - Photo Electro Catalytic Degradation and Removal of Organic and Inorganic Contaminants in Ground Waters. 2001. EPA/540/R-01/502, http://www.epa.gov/ORD/SITE. 02/22/2001 Photocatalytic oxidation offers a means of...

  1. Novel Fe-Pd/SiO2 catalytic materials for degradation of chlorinated organic compounds in water

    Science.gov (United States)

    Novel reactive materials for catalytic degradation of chlorinated organic compounds in water at ambient conditions have been prepared on the basis of silica-supported Pd-Fe nanoparticles. Nanoscale Fe-Pd particles were synthesized inside porous silica supports using (NH4

  2. Co-existence of multiple strains of porcine circovirus type 2 in the same pig from China

    Directory of Open Access Journals (Sweden)

    Zhai Shao-Lun

    2011-11-01

    Full Text Available Abstract Pigs are often co-infected by different viral strains from the same virus. Up to now, there are few reports about co-existence of different porcine circovirus type 2 (PCV2 strains in China. The aim of this study was to evaluate it in Chinese swine herds. 118 PCV2 positive DNAs isolated from diseased pigs identified by classic PCR were re-detected using a modified differential PCR assay. The results indicated that co-existence rates of PCV2 were 32.2% (38/118 in diseased pigs and 0% (0/41 in asymptomatic pigs. Four PCV2 complete genomes were cloned from two co-infected samples and their nucleotide (nt identities were 95%-97.3%. The phylogenetic analysis showed that four PCV2 strains were divided into different genotypes, PCV2a, PCV2b, PCV2d and PCV2e, respectively. In addition, co-existence were not detected in 41 serum samples from healthy pigs but PCV2 single infection (31.7%, 13/41 existed. These data revealed that the co-existence of different strains of PCV2 might contribute to the development of more severe clinical symptoms for pigs. This is the first report confirming the co-existence of different PCV2 strains in Chinese swine herds. Meanwhile, this study could help us to understand new infection and prevalence forms of PCV2 clinically.

  3. Co-existence of multiple strains of porcine circovirus type 2 in the same pig from China

    OpenAIRE

    Zhai Shao-Lun; Chen Sheng-Nan; Wei Zu-Zhang; Zhang Jian-Wu; Huang Lv; Lin Tao; Yue Cheng; Ran Duo-Liang; Yuan Shi-Shan; Wei Wen-Kang; Long Jin-Xue

    2011-01-01

    Abstract Pigs are often co-infected by different viral strains from the same virus. Up to now, there are few reports about co-existence of different porcine circovirus type 2 (PCV2) strains in China. The aim of this study was to evaluate it in Chinese swine herds. 118 PCV2 positive DNAs isolated from diseased pigs identified by classic PCR were re-detected using a modified differential PCR assay. The results indicated that co-existence rates of PCV2 were 32.2% (38/118) in diseased pigs and 0%...

  4. Phenomenological modeling and study of a catalytic membrane reactor for water detritiation

    International Nuclear Information System (INIS)

    Tritium is produced in light and heavy water reactor fuel by ternary fission or neutron activation. This by-product is used as fuel in fusion fuel reactors such as JET in Culham or ITER in Cadarache (France). The growing interest of this research area will make the tritium fluxes increase; it is then worth addressing the question of its future whether it will be used or flushed out from liquid and gaseous effluents or waste. This thesis studies the recovery of tritium as fuel for fusion machines by means of packed bed membrane reactor (PBMR). Such a reactor combines catalytic conversion of tritiated water thanks to isotope exchange with hydrogen according to the reversible reaction Q2O+H2↔H2O+Q2 (Q=H,D or T) and selective permeation of Q2 through Pd-based membrane. In fact, palladium has the ability to bond with hydrogen isotopes, creating a selective permeation barrier. In the PBMR, thanks to the reaction products withdrawal, these permeation fluxes drive the heavy water conversion rate, to higher values than those reached in conventional fixed bed reactors (Le Chatelier's law). In order to study PBMRs, the CEA has built a test bench, using deuterium instead of tritium, allowing the analysis of their conversion and separation performances at the laboratory scale. An in-house method has been developed to determine simultaneously hydrogen and water isotopologues content by mass spectrometer analysis. It was experimentally shown that the activity of Ni-based catalyst used in this study was sufficient to allow the isotope exchange reactions to reach their thermodynamic equilibrium in a very short time. In addition, hydrogen permeation flux was shown to follow a Richardson's law. Sensitivity studies performed on the PBMR's main operating parameters revealed that its global performance (i.e. de-deuteration factor) increases with the temperature, the transmembrane pressure difference, the sweep gas flow rate and the residence time in the catalyst

  5. Reactivity of Ir(III) carbonyl complexes with water: alternative by-product formation pathways in catalytic methanol carbonylation

    OpenAIRE

    Haynes, A.; Elliott, P. I. P.; Haak, S; Meijer, A.J.H.M.; Sunley, G.J

    2013-01-01

    The reactions of water with a number of iridium(III) complexes relevant to the mechanism for catalytic methanol carbonylation are reported. The iridium acetyl, [Ir(CO)2I3(COMe)]−, reacts with water under mild conditions to release CO2 and CH4, rather than the expected acetic acid. Isotopic labeling and kinetic experiments are consistent with a mechanism involving nucleophilic attack by water on a terminal CO ligand of [Ir(CO)2I3(COMe)]− to give an (undetected) hydroxycarbonyl spec...

  6. Co-Existence of Tuberous Sclerosis and the Fanconi Syndrome in Two Saudi Male Siblings: Report on Two Cases

    International Nuclear Information System (INIS)

    In this report, we present two cases of familial tuberous sclerosis co-existing with the Fanconi Syndrome. Both cases presented with history of failure to thrive and mental retardation associated with hypokalemic metabolic acidosis. To our knowledge, the association between tuberous sclerosis and the Fanconi Syndrome has not been reported previously. (author)

  7. Long-term monitoring of GM winter oilseed rape volunteers and its implications for co-existence

    Czech Academy of Sciences Publication Activity Database

    Rakouský, S.; Hraška, M.; Bříza, Jindřich; Psota, B.

    Montpellier: Agropolis Productions, 2005 - (Messéan, A.), s. 89-91 [Int. Conf. on Co-existence Between GM and Non-GM Based Agricultural Supply Chains /2./. Montpellier (FR), 14.11.2005-15.11.2005] Institutional research plan: CEZ:AV0Z5051902 Keywords : GMO Subject RIV: EB - Genetics ; Molecular Biology

  8. Polyurethane foams doped with stable silver nanoparticles as bactericidal and catalytic materials for the effective treatment of water

    OpenAIRE

    Domènech Garcia, Berta; Ziegler Benítez, Kharla; Vigués Frantzen, Núria; Olszewski, Wojciech; Marini, Carlo; Mas Gordi, Jordi; Muñoz Tapia, Maria; Muraviev, Dmitri N; Macanás de Benito, Jorge

    2016-01-01

    The development of reusable dual-purpose nanocomposite foams for catalytic and bactericidal water treatment is reported. Small non-aggregated silver nanoparticles were made using Intermatrix Synthesis inside a polyurethane foam, which was chosen as a suitable polymeric matrix due to its high chemical and mechanical stability and industrial applicability. The antibacterial activity of the obtained nanocomposites was evaluated against suspensions of Gram-negative bacteria (E. coli), showing ide...

  9. Catalytic hydrodechlorination of PCDD/Fs from condensed water with Pd/γ-Al2O3.

    Science.gov (United States)

    Liu, Mei-Chen; Chang, Shu-Hao; Chang, Moo-Been

    2016-07-01

    A continuous pyrolysis system (CPS) with effective air pollution control devices (APCDs) is designed and constructed to remediate the soil containing high-concentration PCDD/Fs. The quench tower of the APCDs system can capture the pollutants of high boiling points from the flue gas of CPS and produces condensed water of high PCDD/Fs concentration (16-44 ng I-TEQ/L), and needs further treatment. First, the result of activated carbon adsorption test displays the PCDD/Fs toxicity concentration of effluents meet the regulatory standards as the liquid to solid ratio is controlled at 3: 1. However, large amount of activated carbon need to achieve the high removal efficiency leads to high cost, so catalytic hydrodechlorination technology with Pd/Al2O3 as catalyst is applied to treat the condensed water. The PCDD/Fs mass removal efficiency achieved without the reducing agent is 53.21% with the operating time of 180 min. As 5% reducing agent (methanol) is added, the removal efficiency increases to 71.86%. In addition, to better understand the differences between molecular hydrogen and hydrogen donor, the condensed water was pre-aerated with hydrogen and catalytic hydrodechlorination test with palladium as catalyst was conducted. The results show that the PCDD/Fs mass removal efficiency increases to 97.34% with the operating time of 180 min, demonstrating the high PCDD/Fs removal efficiency of catalytic hydrodechlorination. PMID:27088535

  10. Catalytic membrane reactors for tritium recovery from tritiated water in the ITER fuel cycle

    International Nuclear Information System (INIS)

    Palladium and palladium-silver permeators have been obtained by coating porous ceramic tubes with a thin metal layer. Three coating techniques have been studied and characterized: chemical electroless deposition (PdAg film thickness of 10 μm), ion sputtering (about 1 μm) and rolling of thin metal sheets (50 μm). The Pd-ceramic membranes have been used for manufacturing catalytic membrane reactors (CMR) for hydrogen and its isotopes recovering and purifying. These composite membranes and the CMR have been studied and developed for a closed-loop process with reference to the design requirements of the international thermonuclear experimental reactor (ITER) blanket tritium recovery system in the enhanced performance phase of operation. The membranes and CMR have been tested in a pilot plant equipped with temperature, pressure and flow-rate on-line measuring and controlling devices. The conversion value for the water gas shift reaction in the CMR has been measured close to 100% (always above the equilibrium one, 80% at 350 deg. C): the effect of the membrane is very clear since the reaction is moved towards the products because of the continuous hydrogen separation. The rolled thin film membranes have separated the hydrogen from other gases with a complete selectivity and exhibited a slightly larger mass transfer resistance with respect to the electroless membranes. Preliminary tests on the sputtered membranes have also been carried out with a promising performance. Considerations on the use of different palladium alloy in order to improve the performances of the membranes in terms of permeation flux and mechanical strength, such as palladium/yttrium, are also reported

  11. Effect of Water Vapour on the Acidity of ZSM-5Zeolite Used for Catalytic Cracking of Naphtha to Manufacture Ethylene and Propylene

    Institute of Scientific and Technical Information of China (English)

    Ma Guangwei; Xiao Jingxian; ZhangHuining; Xie Zaiku

    2008-01-01

    The change in acidity of the ZSM-5 zeolite was investigated after it was treated with water vapour,and its capability on ammonia adsorption was also studied after having adsorbed water vapour.The effect of water vapour on products distribution was studied during catalytic cracking of naphtha,the changes in the adsorption ability and catalytic performance of the ZSM-5 zeolite was investigated after the catalyst was loaded with phosphorus species.These results all indicated that water vapour could reduce the acid strength and acid density of ZSM-5 zeolite and affect the capability of ZSM-5 on adsorption of gases,therefore the activated energy contributed by the ZSM-5 zeolite to the catalytic cracking reaction would be low to prevent the feedstock from deepened catalytic cracking and coke formation.

  12. Principles of water oxidation and O2-based hydrocarbon transformation by multinuclear catalytic sites

    Energy Technology Data Exchange (ETDEWEB)

    Musaev, Djamaladdin G [Chemistry, Emory University; Hill, Craig L [Chemistry, Emory University; Morokuma, Keiji [Chemistry, Emory University

    2014-10-28

    Abstract The central thrust of this integrated experimental and computational research program was to obtain an atomistic-level understanding of the structural and dynamic factors underlying the design of catalysts for water oxidation and selective reductant-free O2-based transformations. The focus was on oxidatively robust polyoxometalate (POM) complexes in which a catalytic active site interacts with proximal metal centers in a synergistic manner. Thirty five publications in high-impact journals arose from this grant. I. Developing an oxidatively and hydrolytically stable and fast water oxidation catalyst (WOC), a central need in the production of green fuels using water as a reductant, has proven particularly challenging. During this grant period we have designed and investigated several carbon-free, molecular (homogenous), oxidatively and hydrolytically stable WOCs, including the Rb8K2[{Ru4O4(OH)2(H2O)4}(γ-SiW10O36)2]·25H2O (1) and [Co4(H2O)2(α-PW9O34)2]10- (2). Although complex 1 is fast, oxidatively and hydrolytically stable WOC, Ru is neither abundant nor inexpensive. Therefore, development of a stable and fast carbon-free homogenous WOC, based on earth-abundant elements became our highest priority. In 2010, we reported the first such catalyst, complex 2. This complex is substantially faster than 1 and stable under homogeneous conditions. Recently, we have extended our efforts and reported a V2-analog of the complex 2, i.e. [Co4(H2O)2(α-VW9O34)2]10- (3), which shows an even greater stability and reactivity. We succeeded in: (a) immobilizing catalysts 1 and 2 on the surface of various electrodes, and (b) elucidating the mechanism of O2 formation and release from complex 1, as well as the Mn4O4L6 “cubane” cluster. We have shown that the direct O-O bond formation is the most likely pathway for O2 formation during water oxidation catalyzed by 1. II. Oxo transfer catalysts that contain two proximal and synergistically interacting redox active metal

  13. Study on Influence to Waste Water Treatment Plant’s Sludge by Low-carbon Catalytic Combustion Furnace of Natural Gas

    OpenAIRE

    Ren TianQi; Fang Kai; Zhang Shihong

    2016-01-01

    There are two parts in this experiment. One of is about the concentration of Variation of exhaust gas while heating sludge of waste water treatment plant. The other one is about introduce the problems of the traditional incineration processes of sludge of waste water treatment as compared between the sludge heated by natural gas catalytic combustion furnace and the tradition’s. We can see that natural gas low-carbon catalytic combustion furnace realize the near-zero emission of contaminates.

  14. Dynamical co-existence of excitons and free carriers in perovskite probed by density-resolved fluorescent spectroscopic method

    CERN Document Server

    Wang, Wei; Wang, Xiangyuan; Lv, Yanping; Wang, Shufeng; Wang, Kai; Shi, Yantao; Xiao, Lixin; Chen, Zhijian; Gong, Qihuang

    2016-01-01

    Using transient fluorescent spectra at time-zero, we develop a density-resolved fluorescent spectroscopic method for investigating photoproducts in CH3NH3PbI3 perovskite and related photophysics. The density dependent dynamical co-existence of excitons and free carriers over a wide density range is experimentally observed for the first time. The exciton binding energy (EB) and the effective mass of electron-hole pair can be estimated based on such co-existence. No ionic polarization is found contributing to photophysical behavior. It also solves the conflict between the large experimentally measured EB and the small predicted values. The spectroscopic method also helps to detect the true free carrier density under continuous illumination without the interference of ionic conductivity. Our methods and results profoundly enrich the study and understanding of the photophysics in perovskite materials for photovoltaic applications.

  15. Mobile Communication Networks and Digital Television Broadcasting Systems in the Same Frequency Bands – Advanced Co-Existence Scenarios

    Directory of Open Access Journals (Sweden)

    L. Polak

    2014-04-01

    Full Text Available The increasing demand for wireless multimedia services provided by modern communication systems with stable services is a key feature of advanced markets. On the other hand, these systems can many times operate in a neighboring or in the same frequency bands. Therefore, numerous unwanted co-existence scenarios can occur. The aim of this paper is to summarize our results which were achieved during exploration and measurement of the co-existences between still used and upcoming mobile networks (from GSM to LTE and digital terrestrial television broadcasting (DVB systems. For all of these measurements and their evaluation universal measurement testbed has been proposed and used. Results presented in this paper are a significant part of our activities in work package WP5 in the ENIAC JU project “Agile RF Transceivers and Front-Ends for Future Smart Multi-Standard Communications Applications (ARTEMOS”.

  16. Co-existence of a rare dyspnea with pericardial diaphragmatic rupture and pericardial rupture: a case report

    OpenAIRE

    Öz, Necdet; Kargı, Ahmet Bülent; Zeybek, Arife

    2015-01-01

    Pericardial-diaphragmatic rupture is a rare condition which occurs after blunt trauma and involves the herniation of abdominal organs into the pericardium. A 77-year-old female patient presenting with complaints of palpitation and difficulty in breathing was admitted to the emergency room. Left lateral thoracotomy revealed the herniation of abdominal organs into the thorax. A pericardial-diaphragmatic rupture and a pericardial rupture were found to co-exist. The diaphragm and the pericardium ...

  17. COMPETITIVE ADVANTAGES OF POLISH ORGANIC SECTOR IN LIGHT OF CO-EXISTANCE BETWEEN GMO AND NON-GM PRODUCTS

    OpenAIRE

    Maciejczak, Mariusz

    2008-01-01

    The perfect segregation of the different agricultural production types, namely conventional, organic or based on genetically modified organisms is not possible in practice. But the side by side functioning of this systems in agricultural production and further on of the products on the shelves requires suitable measures during cultivation, harvest, transport, storage, and processing to ensure co-existence. Consumers, food and feed industry, as well as wholesalers and retailers in European Uni...

  18. Co-existence of Phenylketonuria and Fabry disease on a 3 year-old boy: case report

    Directory of Open Access Journals (Sweden)

    Bonapace Giuseppe

    2010-05-01

    Full Text Available Abstract Background The co-existence of two genetically distinct metabolic disorders in the same patient has rarely been reported. Phenylketonuria (PKU is an inborn error of the metabolism resulting from a phenylalanine hydroxylase deficiency. Fabry disease (FD is an X-linked lysosomal storage disorder due to a deficiency of the enzyme alpha-galactosidase A. Case presentation We report a case of a 3 year- old boy affected by classic PKU and FD, both confirmed by molecular data. The FD was suspected at the age of 21 months on the presence of non-specific GI symptoms (severe abdominal pain and periodically appearance of not specific episodes of gastroenteritis apparently non related to PKU. Conclusion This is the first report of co-existence of FD and PKU, two different congenital inborn of metabolism and in consideration of the prevalence of each disease this chance association is a very unusual event. The co-existence of this diseases made very difficult the correct interpretation of clinical symptoms as lack of appetite, severe abdominal pain and non-specific gastroenteritis episodes. Furthermore, this case report helps to define the early clinical phenotype of FD.

  19. Preparation of Molecular Sieve Catalyst and Application in the Catalytic Oxidation Treatment of Waste Water

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    @@ Citric acid is an important additive in foods, cosmetics, medicine and so on, but it discharges about 10 ton of factory effluent when 1 ton of citric acid is produced. The COD of the factory effluent is near 20000 mg/L. The treatment of citric acid factory effluent is a serious problem in environmental chemistry. It is found that molecular sieve support metal complexes have high catalytic activity in aerobic oxidation of alkene [1,2]. In this paper, a kind of molecular sieve catalyst was prepared. The catalyst was used for the treatment of citric acid factory effluent by method of catalytic oxygen oxidation.

  20. Inactive commissioning of a micro channel catalytic reactor for highly tritiated water production in the CAPER facility of TLK

    International Nuclear Information System (INIS)

    Highlights: ► In a DT fusion machine several events will generate highly tritiated water (HTW). ► PERMCAT appears a promising process to recover tritium from HTW. ► In order to perform R and D activity on HTW processing with PERMCAT, such water has to be produced on purpose. ► A tritium compatible micro-channel catalytic reactor (μCCR) has been designed and manufactured to produce up to 10 mL min−1 of HTW with very high specific tritium activity. ► The paper presents the inactive commissioning of the μCCR required before the integration in CAPER facility. ► The combination of the μCCR with the O2 sensor represents a reliable system able to produce HTW in a safe way and without radioactive waste. - Abstract: In future DT fusion machines, several events will generate highly tritiated water (HTW). Among potential techniques for HTW processing, isotopic swamping in a catalytic membrane reactor (PERMCAT) appears promising. The experimental demonstration of PERMCAT for HTW processing has started in the CAPER facility at the Tritium Laboratory of Karlsruhe (TLK). Without any HTW source, such water has to be produced on purpose. Catalytic HT oxidation would ensure clean operation but could be critical for operation due to possible occurrence of explosive mixture. A tritium compatible micro-channel catalytic reactor (μCCR) has been designed and manufactured to produce up to 10 mL min−1 of HTW with very high specific tritium activity (stoichiometric DTO: 5.2 × 1016 Bq kg−1). Prior to its integration in CAPER for tritium operation, this reactor has been commissioned at different feed flow rates, gas composition (air or Helium), and temperature. The results demonstrate the good performances of the μCCR in producing water. The combination of the μCCR with the O2 sensor represents a reliable system able to produce HTW in a safe way and without radioactive waste. Accordingly, the CAPER facility can be upgrade in order to continue the R and D activity on

  1. Leaf Growth and Photosynthetic Performance of Two Co-existing Oak Species in Contrasting Growing Seasons

    Directory of Open Access Journals (Sweden)

    SZŐLLŐSI, Erzsébet

    2007-01-01

    Full Text Available Ecophysiological investigations of Quercus petraea and Quercus cerris were performed atthe Sikfkút research site in the dry and humid growing seasons of 2003 and 2004. The resultssuggested that leaf growth and the photosynthetic apparatus of Q. petraea exhibited higher sensitivityto drought in 2003 than that of Q. cerris. In leaves of Q. petraea, chlorophyll content showed largerinter-annual and within-canopy variability than in those of Q. cerris. Fully developed leaves ofQ petraea showed lower SLM which indicated higher leaf cell wall elasticity allowing them tomaintain a water spending strategy, while high specific leaf mass (SLM values reflected a watersaving strategy for Q. cerris. Water use efficiency of Q. cerris was higher than in the case ofQ. petraea, which may provide an advantage for this species in dry periods. In the contrasting yearsthe final leaf area and leaf mass of both species were determined by the amount of rainfall andtemperature conditions during the period of early exponential phase of leaf growth. As indicated bythe low values of the Fv/Fm chlorophyll fluorescence parameter the photosynthetic apparatus of bothspecies exhibited high susceptibility to abiotic stress factors in early spring. A large VAZ cycle poolindicated that zeaxanthin dependent heat dissipation was the main contributor to photoprotection ofphotosynthetic apparatus in young leaves but in fully developed leaves the relatively high lightsaturated ETR and low Pmax as well as the maintenance of high Fv/Fm even in severe dry periodsreflected the potential involvement of photorespiratory electron transport in photoprotection of bothspecies in summer. Drought in 2003 may have resulted in serious depletion of dry matter reservesinfluencing the vitality of trees in following year. Q. petraea showed lower photochemical activity inthe successive vegetation period after the dry year than Q. cerris which suggested lower tolerance todrought in the long term.

  2. Applications of the water--gas shift reaction. II. Catalytic exchange of deuterium for hydrogen at saturated carbon

    International Nuclear Information System (INIS)

    Previous studies on the homogeneous catalysis of the water-gas shift reaction by metal complexes of groups 6 and 8 had been carried out using aqueous alcoholic solutions of group 8 metal carbonyl complexes made basic with KOH. Substitution of triethylamine (Et3N) for KOH as base and alcohol for solvent led to the discovery that Et3N in the presence of D2O, CO, and Rh6(CO)16 at 1500C undergoes an unusual catalytic exchange of deuterium for hydrogen. A suggested mechanism for this reaction is given and includes activation of hydrogen at a saturated carbon

  3. Non-Catalytic and MgSO4 - Catalyst based Degradation of Glycerol in Subcritical and Supercritical Water Media

    Directory of Open Access Journals (Sweden)

    Mahfud Mahfud

    2011-02-01

    Full Text Available This research aims to study the glycerol degradation reaction in subcritical and supercritical water media. The degradation of glycerol into other products was performed both with sulphate salt catalysts and without catalyst. The reactant was made from glycerol and water with the mass ratio of 1:10. The experiments were carried out using a batch reactor at a constant pressure of 250 kgf/cm2, with the temperature range of 200-400oC, reaction time of 30 minutes, and catalyst mol ratio in glycerol of 1:10 and 1:8. The products of the non-catalytic glycerol degradation were acetaldehyde, methanol, and ethanol. The use of sulphate salt as catalyst has high selectivity to acetaldehyde and still allows the formation alcohol product in small quantities. The mechanism of ionic reaction and free radical reaction can occur at lower temperature in hydrothermal area or subcritical water. Conversion of glycerol on catalytic reaction showed a higher yield when compared with the reaction performed without catalyst

  4. Preparation of Molecular Sieve Catalyst and Application in the Catalytic Oxidation Treatment of Waste Water

    Institute of Scientific and Technical Information of China (English)

    WANG; RongMin

    2001-01-01

    Citric acid is an important additive in foods, cosmetics, medicine and so on, but it discharges about 10 ton of factory effluent when 1 ton of citric acid is produced. The COD of the factory effluent is near 20000 mg/L. The treatment of citric acid factory effluent is a serious problem in environmental chemistry.  It is found that molecular sieve support metal complexes have high catalytic activity in aerobic oxidation of alkene [1,2]. In this paper, a kind of molecular sieve catalyst was prepared. The catalyst was used for the treatment of citric acid factory effluent by method of catalytic oxygen oxidation.  ……

  5. Co-existence of Phenylketonuria (PKU) and beta-Thalassemia Major in a 16 Years Old Girl: A Case Report

    OpenAIRE

    Hossein Karami; Mehrnoush Kosaryan; Aili Aliasgharian; Ali Abbaskhanian; Rayka Sharifian; Mehrdad Taghipour

    2012-01-01

    While thalassemia major (TM) used to be a prevalent genetic disease in the past, however, (PKU) is quite rare in spite of consanquiness marriage rate of about 40% in the region. Preventive efforts for TM started >20 years ago but neonatal screening for PKU started since 2007. This is the first report of co-existence of thalassemia and PKU in Middle East and in consideration of the prevalence of each genes, this chance association is a very unusual event. We report a case of having PKU and TM

  6. FREQUENCY CATASTROPHE AND CO-EXISTING ATTRACTORS IN A CELL Ca2+ NONLINEAR OSCILLATION MODEL WITH TIME DELAY*

    Institute of Scientific and Technical Information of China (English)

    应阳君; 黄祖洽

    2001-01-01

    Frequency catastrophe is found in a cell Ca2+ nonlinear oscillation model with time delay. The relation of the frequency transition to the time delay is studied by numerical simulations and theoretical analysis. There is a range of parameters in which two kinds of attractors with great frequency differences co-exist in the system. Along with parameter changes, a critical phenomenon occurs and the oscillation frequency changes greatly. This mechanism helps us to deepen the understanding of the complex dynamics of delay systems, and might be of some meaning in cell signalling.

  7. Co-existence of a rare dyspnea with pericardial diaphragmatic rupture and pericardial rupture: a case report.

    Science.gov (United States)

    Öz, Necdet; Kargı, Ahmet Bülent; Zeybek, Arife

    2015-06-01

    Pericardial-diaphragmatic rupture is a rare condition which occurs after blunt trauma and involves the herniation of abdominal organs into the pericardium. A 77-year-old female patient presenting with complaints of palpitation and difficulty in breathing was admitted to the emergency room. Left lateral thoracotomy revealed the herniation of abdominal organs into the thorax. A pericardial-diaphragmatic rupture and a pericardial rupture were found to co-exist. The diaphragm and the pericardium were repaired primarily. The case is presented here because herniation of abdominal organs into the pleural cavity through the pericardium is a rare condition. PMID:26336505

  8. Elucidating molecular iridium water oxidation catalysts using metal-organic frameworks: a comprehensive structural, catalytic, spectroscopic, and kinetic study.

    Science.gov (United States)

    Wang, Cheng; Wang, Jin-Liang; Lin, Wenbin

    2012-12-01

    As a new class of porous, crystalline, molecular materials, metal-organic frameworks (MOFs) have shown great promise as recyclable and reusable single-site solid catalysts. Periodic order and site isolation of the catalytic struts in MOFs facilitate the studies of their activities and reaction mechanisms. Herein we report the construction of two highly stable MOFs (1 and 2) using elongated dicarboxylate bridging ligands derived from Cp*Ir(L)Cl complexes (L = dibenzoate-substituted 2,2'-bipyridine, bpy-dc, or dibenzoate-substituted 2-phenylpyridine, ppy-dc) and Zr(6)O(4)(OH)(4)(carboxylate)(12) cuboctahedral secondary building units (SBUs) and the elucidation of water oxidation pathways of the Cp*Ir(L)Cl catalysts using these MOFs. We carried out detailed kinetic studies of Ce(4+)-driven water oxidation reactions (WORs) catalyzed by the MOFs using UV-vis spectroscopy, phosphorescent oxygen detection, and gas chromatographic analysis. These results confirmed not only water oxidation activity of the MOFs but also indicated oxidative degradation of the Cp* rings during the WOR. The (bpy-dc)Ir(H(2)O)(2)XCl (X is likely a formate or acetate group) complex resulted from the oxidative degradation process was identified as a competent catalyst responsible for the water oxidation activity of 1. Further characterization of the MOFs recovered from WORs using X-ray photoelectron, diffuse-reflectance UV-vis absorption, luminescence, and infrared spectroscopies supported the identity of (bpy-dc)Ir(H(2)O)(2)XCl as an active water oxidation catalyst. Kinetics of MOF-catalyzed WORs were monitored by Ce(4+) consumptions and fitted with a reaction-diffusion model, revealing an intricate relationship between reaction and diffusion rates. Our work underscores the opportunity in using MOFs as well-defined single-site solid catalytic systems to reveal mechanistic details that are difficult to obtain for their homogeneous counterparts. PMID:23136923

  9. Preparation and Catalytic Application of Novel Water Tolerant Solid Acid Catalysts of Zirconium Sulfate/HZSM-5

    Institute of Scientific and Technical Information of China (English)

    JIANG Ya-jie; JUAN Joon Ching; MENG Xiu-juan; CAO Wei-liang; YARMO Mohd Ambar; ZHANG Jing-chang

    2007-01-01

    Esterification of acrylic acid(AA) to produce AA esters has widespread application in the chemical industry. A series of water tolerant solid acid catalysts was prepared, and characterized by XRD, nitrogen adsorption, TGA-DTA, XPS, and ammonia adsorption FTIR. The effects of Si/Al ratio, zirconium sulfate(ZS) loading on HZSM-5 and calcination temperature on the esterification were investigated. When 20%(mass fraction) ZS is loaded on HZSM-5, the conversion of AA reaches 100%. XRD analysis indicates that ZS is highly dispersed on HZSM-5 because no crystalline structure assigned to ZS is found. Catalytic activity and hydrophobicity of ZS supported on HZSM-5 are higher compared with those of parent ZS or HZSM-5. Results show that this kind of novel catalysts is an efficient water tolerant solid acid catalyst for esterification reactions.

  10. On the study of catalytic membrane reactor for water detritiation: Membrane characterization

    International Nuclear Information System (INIS)

    Highlights: ► Catalytic palladium based membrane reactor is studied for ITER tritium waste management. ► Concentration polarization effect was highlighted by two-dimensional mass transfer model. ► Mass transfer resistance due to concentration polarization is reduced by the increase of fluid velocity. ► Concentration polarization phenomenon is enhanced by the decrease of non-permeable species content in the feed stream. -- Abstract: Tritium waste recycling is a real economic and ecological issue. Generally under the non-valuable Q2O form (Q = H, D or T), waste can be converted into fuel Q2 for a fusion machine (e.g. JET, ITER) by isotope exchange reaction Q2O + H2 = H2O + Q2. Such a reaction is carried out over Ni-based catalyst bed packed in a thin wall hydrogen permselective membrane tube. This catalytic membrane reactor can achieve higher conversion ratios than conventional fixed bed reactors by selective removal of reaction product Q2 by the membrane according to Le Chatelier's Law. This paper presents some preliminary permeation tests performed on a catalytic membrane reactor. Permeabilities of pure hydrogen and deuterium as well as those of binary mixtures of hydrogen, deuterium and nitrogen have been estimated by measuring permeation fluxes at temperatures ranging from 573 to 673 K, and pressure differences up to 1.5 bar. Pure component global fluxes were linked to permeation coefficient by means of Sieverts’ law. The thin membrane (150 μm), made of Pd–Ag alloy (23 wt.%Ag), showed good permeability and infinite selectivity toward protium and deuterium. Lower permeability values were obtained with mixtures containing non permeable gases highlighting the existence of gas phase resistance. The sensitivity of this concentration polarization phenomenon to the composition and the flow rate of the inlet was evaluated and fitted by a two-dimensional model

  11. Hydrothermal synthesis of Yttrium Orthovanadate (YVO4) and its application in photo catalytic degradation of sewage water

    International Nuclear Information System (INIS)

    In this paper; YVO4 powder was successfully synthesized from Vanadium Pentaoxide (V2O5), Yttrium Oxide (Y2O3) and ethyl acetate as a mineralizer by hydrothermal method at a low temperature (T=.230degreeC, and P=100 bars). The as-prepared powders were characterized by X-ray Diffraction, Fourier Transform Infrared Spectroscopy, Scanning Electron Microscopy, UV-V Spectroscopy and Chemical Oxygen Demand of the sewage water, respectively. The results show that hydrothermal method can greatly promote the crystallization and growth of YVO4 phase. X-ray Diffraction pattern clearly indicates the tetragonal structure and crystallinity. An fourier transform infrared spectrum of the YVO4 shows the presence of Y-O and V-O bond, respectively. The presence of these two peaks indicates that yttrium vanadate has been formed. UV-V is absorption spectra suggesting that YVO4 particles have stronger UV absorption than natural sunlight and subsequent photo catalytic degradation data also confirmed their higher photo catalytic activity.

  12. A broad spectrum catalytic system for removal of toxic organics from water by deep oxidation. 1998 annual progress report

    International Nuclear Information System (INIS)

    'Toxic organics and polymers pose a serious threat to the environment, especially when they are present in aquatic systems. The objective of the research is the design of practical procedures for the removal and/or recycling of such pollutants by oxidation. This report summarizes the work performed in the first one and half years of a three year project. The authors had earlier described a catalytic system for the deep oxidation of toxic organics, such as benzene, phenol and substituted phenols, aliphatic and aromatic halogenated compounds, organophosphorus, and organosulfur compounds [1]. In this system, metallic palladium was found to catalyze the oxidation of the substrate by dioxygen in aqueous medium at 80--100 C in the presence of carbon monoxide. For all the substrates examined, deep oxidation to carbon monoxide, carbon dioxide, and water occurred in high yields, resulting in up to several hundred turnovers over a 24 h period. Because of a pressing need for new procedures for the destruction of chemical warfare agents, the authors have examined in detail the deep oxidation of appropriate model compounds containing phosphorus-carbon and sulfur-carbon bonds using the same catalytic system. The result is the first observation of the efficient catalytic oxidative cleavage of phosphorus-carbon and sulfur-carbon bonds under mild conditions, using dioxygen as the oxidant [2]. In addition to the achievements described above, they have unpublished results in several other areas. For example, they have investigated the possibility of using dihydrogen rather than carbon monoxide as a coreductant in the catalytic deep oxidation of substrates. Even more attractive from a practical standpoint is the possibility of using a mixture of carbon monoxide and dihydrogen (synthesis gas). Indeed, experiments indicated that it is possible to substitute carbon monoxide by dihydrogen or synthesis gas. Significantly, in the case of nitro compounds, the deep oxidation in fact proceeded

  13. Study on Influence to Waste Water Treatment Plant’s Sludge by Low-carbon Catalytic Combustion Furnace of Natural Gas

    Directory of Open Access Journals (Sweden)

    Ren TianQi

    2016-01-01

    Full Text Available There are two parts in this experiment. One of is about the concentration of Variation of exhaust gas while heating sludge of waste water treatment plant. The other one is about introduce the problems of the traditional incineration processes of sludge of waste water treatment as compared between the sludge heated by natural gas catalytic combustion furnace and the tradition’s. We can see that natural gas low-carbon catalytic combustion furnace realize the near-zero emission of contaminates.

  14. Does Co-Existing Lumbar Spinal Canal Stenosis Impair Functional Outcomes and Activity Levels after Primary Total Hip Arthroplasty?

    Science.gov (United States)

    Jauregui, Julio J; Banerjee, Samik; Issa, Kimona; Cherian, Jeffrey J; Mont, Michael A

    2015-09-01

    Degenerative lumbar spinal stenosis (LSS) is a cause for substantial morbidity in the elderly population: many often undergo total hip arthroplasty for associated hip arthritis. With a matched cohort we investigated the effect of co-existing LSS on aseptic survivorship, functional outcomes, activity levels, overall subjective physical and mental health status, and satisfaction rates in patients undergoing primary THA. The aseptic-implant survivorship was similar in LSS and non-stenosis cohort. Although both cohorts significantly improved, the LSS cohort achieved lower improvements in HHS, UCLA, SF-36 physical, and satisfaction rates than the matched non-stenotic cohort. Surgeons should consider cautioning patients with LSS that although they can expect relief of their arthritic symptoms following THA, they may continue to expect limitations in function, physical-status, activity-levels, and satisfaction rates. PMID:25865814

  15. The co-existence of a myxoid liposarcoma and leiomyoma in the same ovarian mass of a dog.

    Science.gov (United States)

    Shiwa, Nozomi; Boonsriroj, Hassadin; Kimitsuki, Kazunori; Shimatsu, Taichi; Park, Chun-Ho

    2016-04-01

    A 15-year-old, female mixed-breed dog presented with abdominal distention. An exploratory laparotomy revealed a large left ovarian mass (20 × 15 × 12 cm). Histopathological examination of the mass revealed a mixed myxoid liposarcoma and a well-differentiated leiomyoma. Four months after surgical removal of the mass, the dog died due to multiorgan metastasis. The metastasis was composed solely of the liposarcoma component. The liposarcoma component was Alcian Blue- and Oil red O-positive, and demonstrated immunoreactivity with S-100, adipophilin and vimentin. Electron microscopy revealed that the tumor cell cytoplasms were packed with lipid vacuoles and dilated rough endoplasmic reticulum. To our knowledge, this is the first report of myxoid liposarcoma and leiomyoma co-existing in a canine ovary. PMID:26522811

  16. Co-existence of wind seas and swells along the west coast of India during non-monsoon season

    Directory of Open Access Journals (Sweden)

    R. Rashmi

    2012-10-01

    Full Text Available Wave data collected along the west coast of India (off Goa, Ratnagiri and Dwarka during non-monsoon season have been analysed to study the co-existence of wind seas and swells. Diurnal variation in wind and wave parameters is noticeable along the central west coast of India (off Goa and Ratnagiri, and this is not present along the northwest coast of India (off Dwarka. Swells are predominantly mature (91% and old (88% during late pre-monsoon and post-monsoon seasons, respectively. Sea Swell Energy Ratio quantifies wind sea, swell and mixed seas prevailing in the regions during non-monsoon season. Intermodal Distance (ID between the energy peaks is moderately separated during non-monsoon season, whereas, during the shamal events, energy peaks are very close to each other (ID ~ 0. However, pure wind seas (ID ~ 1 are found to co-exist with the swells during non-monsoon season. Wind seas are growing, when wind and wind seas are opposite to swell direction. Wind seas have minimum angular spreads in multimodal state. Under low winds, the interaction between wind sea and swell dominates and thereby the multimodal state reduces to unimodal state. The fetch available for the evolution of the wind sea spectrum has been estimated, and it is found to be less than 150 km. For the fetch limited condition, a non-dimensional empirical relation has been derived relating the significant wind sea height in terms of wind speed and peak wind sea period, and this relation fits for the west coast of India.

  17. Co-existence of wind seas and swells along the west coast of India during non-monsoon season

    Science.gov (United States)

    Rashmi, R.; Aboobacker, V. M.; Vethamony, P.; John, M. P.

    2013-03-01

    An attempt has been made to understand the co-existence of wind seas and swells along the west coast of India during non-monsoon season. Wave data were collected in different years during non-monsoon season (off Goa during May 2005, off Ratnagiri during January-February 2008 and off Dwarka during December 2007-January 2008), which is fairly a calm weather season along these regions. Diurnal variation in wave parameters is noticeable along the central west coast of India (off Goa and Ratnagiri), which is due to the interaction of multidirectional waves (both wind seas and swells) of varying magnitudes and frequencies. Swells are predominantly mature (91%) and old (88%) during late pre-monsoon and post-monsoon seasons, respectively. Sea Swell Energy Ratio quantifies wind sea, swell and mixed seas prevailing in these regions during non-monsoon season. Intermodal distance (ID) between the energy peaks is moderately separated during non-monsoon season, whereas, during the shamal events, energy peaks are very close to each other (ID ∼ 0). However, pure wind seas (ID ∼ 1) are weakly present and found to co-exist with the swells almost all the time during non-monsoon season. Wind sea growth has been found while the swell propagates opposite to the direction of the wind and wind sea. Wind seas have minimum angular spreads in multimodal state. Under low winds, the interaction between wind sea and swell dominates and thereby the multimodal state reduces to unimodal state. The fetch available for the evolution of the wind sea spectrum has been estimated, and it is found to be less than 150 km. For the fetch limited condition, a non-dimensional empirical relation has been derived relating the significant wind sea height in terms of wind speed and peak wind sea period, and this relation fits for the west coast of India.

  18. Bayesian risk maps for Schistosoma mansoni and hookworm mono-infections in a setting where both parasites co-exist

    Directory of Open Access Journals (Sweden)

    Giovanna Raso

    2007-11-01

    Full Text Available There is growing interest in the use of Bayesian geostatistical models for predicting the spatial distribution of parasitic infections, including hookworm, Schistosoma mansoni and co-infections with both parasites. The aim of this study was to predict the spatial distribution of mono-infections with either hookworm or S. mansoni in a setting where both parasites co-exist. School-based cross-sectional parasitological and questionnaire surveys were carried out in 57 rural schools in the Man region, western Côte d’Ivoire. A single stool specimen was obtained from each schoolchild attending grades 3-5. Stool specimens were processed by the Kato-Katz technique and an ether concentration method and examined for the presence of hookworm and S. mansoni eggs. The combined results from the two diagnostic approaches were considered for the infection status of each child. Demographic data (i.e. age and sex were obtained from readily available school registries. Each child’s socio-economic status was estimated, using the questionnaire data following a household-based asset approach. Environmental data were extracted from satellite imagery. The different data sources were incorporated into a geographical information system. Finally, a Bayesian spatial multinomial regression model was constructed and the spatial patterns of S. mansoni and hookworm mono-infections were investigated using Bayesian kriging. Our approach facilitated the production of smooth risk maps for hookworm and S. mansoni mono-infections that can be utilized for targeting control interventions. We argue that in settings where S. mansoni and hookworm co-exist and control efforts are under way, there is a need for both mono- and co-infection risk maps to enhance the cost-effectiveness of control programmes.

  19. Co-existence of wind seas and swells along the west coast of India during non-monsoon season

    Directory of Open Access Journals (Sweden)

    R. Rashmi

    2013-03-01

    Full Text Available An attempt has been made to understand the co-existence of wind seas and swells along the west coast of India during non-monsoon season. Wave data were collected in different years during non-monsoon season (off Goa during May 2005, off Ratnagiri during January–February 2008 and off Dwarka during December 2007–January 2008, which is fairly a calm weather season along these regions. Diurnal variation in wave parameters is noticeable along the central west coast of India (off Goa and Ratnagiri, which is due to the interaction of multidirectional waves (both wind seas and swells of varying magnitudes and frequencies. Swells are predominantly mature (91% and old (88% during late pre-monsoon and post-monsoon seasons, respectively. Sea Swell Energy Ratio quantifies wind sea, swell and mixed seas prevailing in these regions during non-monsoon season. Intermodal distance (ID between the energy peaks is moderately separated during non-monsoon season, whereas, during the shamal events, energy peaks are very close to each other (ID ∼ 0. However, pure wind seas (ID ∼ 1 are weakly present and found to co-exist with the swells almost all the time during non-monsoon season. Wind sea growth has been found while the swell propagates opposite to the direction of the wind and wind sea. Wind seas have minimum angular spreads in multimodal state. Under low winds, the interaction between wind sea and swell dominates and thereby the multimodal state reduces to unimodal state. The fetch available for the evolution of the wind sea spectrum has been estimated, and it is found to be less than 150 km. For the fetch limited condition, a non-dimensional empirical relation has been derived relating the significant wind sea height in terms of wind speed and peak wind sea period, and this relation fits for the west coast of India.

  20. Effects of hydrophobic carrier and packing on the mass transfer capabilities in hydrogen-water liquid phase catalytic exchange bed

    International Nuclear Information System (INIS)

    Hydrogen-water liquid phase catalytic exchange bed was packed with 'sandwich' layers of the catalyst and the packing, and the effects of catalyst carrier, inert packing and their filled ratio on the overall mass transfer coefficient (Kya) were investigated experimentally. The results show that C-PTFE is suitable for hydrophobic catalyst. Kya of the bed with catalyst-stainless steel mini-spiral packing is better than that with stainless steel θ-packing, and the active Al2O3 is not suitable for the exchange bed. Moreover, if the stainless steel mini-spiral packing is etched in aqua regia, the operating flexibility and overall mass transfer capability of exchange bed are improved notably. The preferable packing ratio (catalyst/packing) is 1:4. (authors)

  1. Beta radiation effect on catalytic activity of BASF K-3-10 catalyst in low-temperature water vapour conversion of carbon monoxide

    International Nuclear Information System (INIS)

    The CuO-ZnO-Cr2O3 based K-3-10 catalyst manufactured by BASF allows the conversion of CO with water vapour during the industrial production of hydrogen to be conducted at a relatively low temperature of 420 to 500 K. The effect of beta radiation on catalytic activity was studied in a troughflow tube reactor operating in integral mode. The effect of radiation was observed using the value of relative catalytic activity expressed as the ratio of reaction rate conctants during irradiation and without irradiation. Two cases were studied: a) preliminary irradiation of 8 samples of catalysts with a 90Sr-90Y source with doses of 1.7 to 3524 kGy, b) the incorporation of the 32P radionuclide in the catalytic bed of 6 samples such that the dose absorbed bz the catalyst during the experiment was 19.1 to 687.8 Gy. For preliminary irradiation, a non-monotonous increase was found in the catalytic activity amounting to 28 - 83 % (reaching maximum at a dose of 125.9 kGy.). Radioactive bed experiments showed a monotonous increase in catalytic activity with bed radioactivity; the highest achieved increase in activity was 72 %. Differences were found in the stability in time of radiation modified catalytic activity showing that effects induced by the two methods have a different character. A probable explanation of observed dependences is suggested. (A.K.)

  2. The effect of the nano-silica support on the catalytic reduction of water by gold, silver and platinum nanoparticles--nanocomposite reactivity.

    Science.gov (United States)

    Zidki, T; Bar-Ziv, R; Green, U; Cohen, H; Meisel, D; Meyerstein, D

    2014-08-01

    Pt°-NPs, prepared by the reduction of Pt(IV) salts with borohydride, do not catalyse the reduction of water in the presence of the strongly-reducing ˙C(CH3)2OH radicals. However, supporting the same metal nanoparticles (M°-NPs) with SiO2 alters the catalytic properties enabling the reaction. This effect depends both on the nature of M° and concentration of the composite nanoparticles. At low nanocomposite concentration: for M = Au nearly no effect is observed; for M = Ag the support decreases the catalytic reduction of water and for M = Pt the support initiates the catalytic process. At high nanocomposite concentration: for M = Au the reactivity is considerably lower and for M = Ag or Pt no catalysis is observed. Furthermore, for M = Ag or Pt H2 reduces the ˙C(CH3)2OH radicals. PMID:24947417

  3. Photo catalytic degradation of organic pollutants diluted in water using TiO2 loaded on fluoride-modified hydrophobic meso porous silica

    International Nuclear Information System (INIS)

    The synthesis of the hydrophobic meso-porous silica (denoted as HMS(F)) was performed using tetraethyl orthosilicate (TEOS), tetraethylammonium fluoride (TEAF) as the source of the fluoride and dodecyl-amine (DDA) as templates. The TiO2 loaded on the hydrophobic HMS(F) (TiO2/HMS(F)) exhibited the efficient photo-catalytic performance for the degradation of alcohols (2-propanol and 2-hexanol) diluted in water. The amount of adsorption of alcohols and the photo-catalytic reactivity for the degradation increased with increasing the content of fluoride ions in these photo-catalysts. The hydrophobic meso-porous surface is suitable as photo-catalytic reaction field for the degradation of organic compounds diluted water. (authors)

  4. Water/oil microemulsion for the preparation of robust La-hexaaluminates for methane catalytic combustion.

    Science.gov (United States)

    Jiang, Zheng; Hao, Zhengping; Su, Jixi; Xiao, Tiancun; Edwards, Peter P

    2009-06-14

    Robust and highly effective Fe-substituted and non-substituted La-Hexaaluminate methane combustion catalysts have been prepared via coprecipitation in "water-pools" of Water/Oil microemulsions with dual nonionic surfactants, followed by ethanol supercritical drying and post-annealing. PMID:19587921

  5. On the Catalytic Effect of Water in the Intramolecular Diels–Alder Reaction of Quinone Systems: A Theoretical Study

    Directory of Open Access Journals (Sweden)

    Jorge Soto-Delgado

    2012-11-01

    Full Text Available The mechanism of the intramolecular Diels–Alder (IMDA reaction of benzoquinone 1, in the absence and in the presence of three water molecules, 1w, has been studied by means of density functional theory (DFT methods, using the M05-2X and B3LYP functionals for exploration of the potential energy surface (PES. The energy and geometrical results obtained are complemented with a population analysis using the NBO method, and an analysis based on the global, local and group electrophilicity and nucleophilicity indices. Both implicit and explicit solvation emphasize the increase of the polarity of the reaction and the reduction of activation free energies associated with the transition states (TSs of this IMDA process. These results are reinforced by the analysis of the reactivity indices derived from the conceptual DFT, which show that the increase of the electrophilicity of the quinone framework by the hydrogen-bond formation correctly explains the high polar character of this intramolecular process. Large polarization at the TSs promoted by hydrogen-bonds and implicit solvation by water together with a high electrophilicity-nucleophilicity difference consistently explains the catalytic effects of water molecules.

  6. Identification of intrinsic catalytic activity for electrochemical reduction of water molecules to generate hydrogen

    KAUST Repository

    Shinagawa, Tatsuya

    2015-01-01

    Insufficient hydronium ion activities at near-neutral pH and under unbuffered conditions induce diffusion-limited currents for hydrogen evolution, followed by a reaction with water molecules to generate hydrogen at elevated potentials. The observed constant current behaviors at near neutral pH reflect the intrinsic electrocatalytic reactivity of the metal electrodes for water reduction. This journal is © the Owner Societies.

  7. A new class of photo-catalytic materials and a novel principle for efficient water splitting under infrared and visible light - MgB2 as unexpected example

    CERN Document Server

    Kravets, V G

    2015-01-01

    Water splitting is unanimously recognized as environment friendly, potentially low cost and renewable energy solution based on the future hydrogen economy. Especially appealing is photo-catalytic water splitting whereby a suitably chosen catalyst dramatically improves efficiency of the hydrogen production driven by direct sunlight and allows it to happen even at zero driving potential. Here, we suggest a new class of stable photo-catalysts and the corresponding principle for catalytic water splitting in which infrared and visible light play the main role in producing the photocurrent and hydrogen. The new class of catalysts based on ionic binary metals with layered graphite-like structures which effectively absorb visible and infrared light facilitating the reaction of water splitting, suppress the inverse reaction of ion recombination by separating ions due to internal electric fields existing near alternating layers, provide the sites for ion trapping of both polarities, and finally deliver the electrons an...

  8. Sjögren syndrome and neuromyelitis optica spectrum disorder co-exist in a common autoimmune milieu

    Directory of Open Access Journals (Sweden)

    Diogo C. Carvalho

    2014-06-01

    Full Text Available The relationship between Sjögren’s syndrome (SS and neuromyelitis optica spectrum disorder (NMOSD is not completely understood. We report two patients with both conditions and review 47 other previously reported cases meeting currently accepted diagnostic criteria, from 17 articles extracted from PubMed. Out of 44 patients whose gender was informed, 42 were females. Mean age at onset of neurological manifestation was 36.2 years (10-74. Serum anti-AQP4-IgG was positive in 32 patients, borderline in 1, and negative in 4. Our Case 1 was seronegative for AQP4-IgG and had no non-organ-specific autoantibodies other than anti-SSB antibodies. Our Case 2 had serum anti-AQP4, anti-SSA/SSB, anti-thyreoglobulin and anti-acethylcholine-receptor antibodies, as well as clinical hypothyreoidism, but no evidence of myasthenia gravis. Our Cases and others, as previously reported in literature, with similar heterogeneous autoimmune response to aquaporin-4, suggest that SS and NMO co-exist in a common autoimmune milieu which is not dependent on aquaporin-4 autoimmunity.

  9. Catalytic hydrogen production from fossil fuels via the water gas shift reaction

    International Nuclear Information System (INIS)

    Highlights: • Hydrogen is a clean alternative to hydrocarbon fuels. • Hydrogen is primarily produced with the water gas shift reaction. • Development of water gas shift catalysts is essential to the energy industry. • This work summarizes recent progress in water gas shift catalyst research. - Abstract: The production of hydrogen is a highly researched topic for many reasons. First of all, it is a clean fuel that can be used instead of hydrocarbons, which produce CO2, a greenhouse gas emission that is thought to be the reason for climate change in the world. The largest source of hydrogen is the water gas shift (WGS) reaction, where CO and water are mixed over a catalyst to produce the desired hydrogen. Many researchers have focused on development of WGS catalysts with different metals. The most notable of these metals are precious and rare earth metals which, when combined, have unique properties for the WGS reaction. Research in this area is very important to the energy industry and the future of energy around the world. However, the progress made recently has not been reviewed, and this review was designed to fill the gap

  10. The role of oxygen and water on molybdenum nanoclusters for electro catalytic ammonia production

    DEFF Research Database (Denmark)

    Howalt, Jakob Geelmuyden; Vegge, Tejs

    2014-01-01

    The presence of water often gives rise to oxygen adsorption on catalyst surfaces through decomposition of water and the adsorbed oxygen or hydroxide species often occupy important surfaces sites, resulting in a decrease or a total hindrance of other chemical reactions taking place at that site. In...... this study, we present theoretical investigations of the influence of oxygen adsorption and reduction on pure and nitrogen covered molybdenum nanocluster electro catalysts for electrochemical reduction of N2 to NH3 with the purpose of understanding oxygen and water poisoning of the catalyst. Density...... oxygen over nitrogen and hydrogen at neutral bias, but under electrochemical reaction conditions needed for nitrogen reduction, oxygen adsorption is severely weakened and the adsorption energy is comparable to hydrogen and nitrogen adsorption. The potentials required to reduce oxygen offthe surface are...

  11. Experimental studies on catalytic hydrogen recombiners for light water reactors; Experimentelle Untersuchungen zu katalytischen Wasserstoffkombinatoren fuer Leichtwasserreaktoren

    Energy Technology Data Exchange (ETDEWEB)

    Drinovac, P.

    2006-06-19

    In the course of core melt accidents in nuclear power plants a large amount of hydrogen can be produced and form an explosive or even detonative gas mixture with aerial oxygen in the reactor building. In the containment atmosphere of pressurized water reactors hydrogen combines a phlogistically with the oxygen present to form water vapor even at room temperature. In the past, experimental work conducted at various facilities has contributed little or nothing to an understanding of the operating principles of catalytic recombiners. Hence, the purpose of the present study was to conduct detailed investigations on a section of a recombiner essentially in order to deepen the understanding of reaction kinetics and heat transport processes. The results of the experiments presented in this dissertation form a large data base of measurements which provides an insight into the processes taking place in recombiners. The reaction-kinetic interpretation of the measured data confirms and deepens the diffusion theory - proposed in an earlier study. Thus it is now possible to validate detailed numeric models representing the processes in recombiners. Consequently the present study serves to broaden and corroborate competence in this significant area of reactor technology. In addition, the empirical knowledge thus gained may be used for a critical reassessment of previous numeric model calculations. (orig.)

  12. STUDY ON SYNTHESIS OF PVC SERIES OF MACROPOROUS SULFORIC RESINS AND THEIR APPLICATIONS IN CATALYTIC ESTERIFICATION AND WATER TREATMENT

    Institute of Scientific and Technical Information of China (English)

    LIYanfeng; FULiandi; 等

    1999-01-01

    The PVC serves of macroporous sulfonic cation-exchange resins were prepared by the sulfonation of a macroporous PVC bead with concentrated sulfonic acid or chlorosulfonic acid.the resulting sulfonic resin was employed in the investigation of catalytic esterification and solftening of water,The results show that the yields of esters reach 60.0-84.4% according as different fatty acids and alcohols,the refractive indexes of esters obtained resemble those reported in the references basically,meanwhile,345L softened water which holds ≤0.06mmol/L hardness would be prepared by 1 L wet sulfonic resin reusing for 4 times.The resulting sulfonic resins would have 1.6-2.0or 2.5-3.0mmol/g exchange capacity by using concentrated sulfonic acid or chlorosulfonic acid as sulfonating agent,respectively,The sulfonic resin has a macroporous structure taking the morphology with agglomerates of minutely spherical gel particles as characteristic.

  13. Catalytic Conversion of Dihydroxyacetone to Lactic Acid Using Metal Salts in Water

    NARCIS (Netherlands)

    Rasrendra, Carolus B.; Fachri, Boy A.; Makertihartha, I. Gusti B. N.; Adisasmito, Sanggono; Heeres, Hero J.

    2011-01-01

    We herein present a study on the application of homogeneous catalysts in the form of metal salts on the conversion of trioses, such as dihydroxyacetone (DHA), and glyceraldehyde (GLY) to lactic acid (LA) in water. A wide range of metal salts (26 in total) were examined. Al(III) salts were identified

  14. First-principles quantum mechanical investigations: Catalytic reactions of furfural on Pd(111) and at the water/Pd(111) interface

    Science.gov (United States)

    Xue, Wenhua

    Bio-oils have drawn more and more attention from scientists as a promising new clean, cheap energy source. One of the most interesting relevant issues is the effect of catalysts on the catalytic reactions that are used for producing bio-oils. Furfural, as a very important intermediate during these reactions, has attracted significant studies. However, the effect of catalysts, including particularly the liquid/solid interface formed by a metal catalyst and liquid water, in the catalytic reactions involving furfural still remains elusive. In this research, we performed ab initio molecular dynamics simulations and first-principles density-functional theory calculations to investigate the atomic-scale mechanisms of catalytic hydrogenation of furfural on the palladium surface and at the liquid/state interface formed by the palladium surface and liquid water. We studied all the possible mechanisms that lead to formation of furfuryl alcohol (FOL), formation of tetrahydrofurfural (THFAL), and formation of tetrahydrofurfurfuryl alcohol (THFOL). We found that liquid water plays a significant role in the hydrogenation reactions. During the reaction in the presence of water and the palladium catalyst, in particular, water directly participates in the hydrogenation of the aldehyde group of furfural and facilitates the formation of FOL by reducing the activation energy. Our calculations show that water provides hydrogen for the hydrogenation of the aldehyde group, and at the same time, a pre-existing hydrogen atom, which is resulted from dissociation of molecular hydrogen (experimentally, molecular hydrogen is always supplied for hydrogenation) on the palladium surface, is bonded to water, making the water molecule intact in structure. In the absence of water, on the other hand, formation of FOL and THFAL on the palladium surface involves almost the same energy barriers, suggesting a comparable selectivity. Overall, as water reduces the activation energy for the formation of FOL

  15. Catalytic role of tungsten electrode material in plasmachemical activity of pulsed corona discharge in water

    Czech Academy of Sciences Publication Activity Database

    Lukeš, Petr; Člupek, Martin; Babický, Václav; Tothová, I.; Janda, V.

    Gent : Universiteit Gent, 2009 - (Leys, C.; Morent, R.), s. 73-76 ISBN N. [International Congress on Cold Atmospheric Pressure Plasma: Sources and Applications CAPPSA 2009/4th./. Ghent (BE), 22.06.2009-24.06.2009] R&D Projects: GA AV ČR(CZ) IAAX00430802 Institutional research plan: CEZ:AV0Z20430508 Keywords : corona discharge * water * hydrogen peroxide * tungsten Subject RIV: BL - Plasma and Gas Discharge Physics

  16. Catalytic water dissociation by greigite Fe3S4 surfaces: density functional theory study

    OpenAIRE

    Roldan, A.; de Leeuw, N. H.

    2016-01-01

    The iron sulfide mineral greigite, Fe3S4, has shown promising capability as a hydrogenating catalyst, in particular in the reduction of carbon dioxide to produce small organic molecules under mild conditions. We employed density functional theory calculations to investigate the {001},{011} and {111} surfaces of this iron thiospinel material, as well as the production of hydrogen ad-atoms from the dissociation of water molecules on the surfaces. We systematically analysed the adsorption geomet...

  17. The role of oxygen and water on molybdenum nanoclusters for electro catalytic ammonia production

    Directory of Open Access Journals (Sweden)

    Jakob G. Howalt

    2014-01-01

    Full Text Available The presence of water often gives rise to oxygen adsorption on catalyst surfaces through decomposition of water and the adsorbed oxygen or hydroxide species often occupy important surfaces sites, resulting in a decrease or a total hindrance of other chemical reactions taking place at that site. In this study, we present theoretical investigations of the influence of oxygen adsorption and reduction on pure and nitrogen covered molybdenum nanocluster electro catalysts for electrochemical reduction of N2 to NH3 with the purpose of understanding oxygen and water poisoning of the catalyst. Density functional theory calculations are used in combination with the computational hydrogen electrode approach to calculate the free energy profile for electrochemical protonation of O and N2 species on cuboctahedral Mo13 nanoclusters. The calculations show that the molybdenum nanocluster will preferentially bind oxygen over nitrogen and hydrogen at neutral bias, but under electrochemical reaction conditions needed for nitrogen reduction, oxygen adsorption is severely weakened and the adsorption energy is comparable to hydrogen and nitrogen adsorption. The potentials required to reduce oxygen off the surface are −0.72 V or lower for all oxygen coverages studied, and it is thus possible to (reactivate (partially oxidized nanoclusters for electrochemical ammonia production, e.g., using a dry proton conductor or an aqueous electrolyte. At lower oxygen coverages, nitrogen molecules can adsorb to the surface and electrochemical ammonia production via the associative mechanism is possible at potentials as low as −0.45 V to −0.7 V.

  18. The effect of copper valence on catalytic combustion of styrene over the copper based catalysts in the absence and presence of water vapor☆

    Institute of Scientific and Technical Information of China (English)

    Hongyan Pan; Zhiyan He; Qian Lin; Fei Liu; Zhong Li

    2016-01-01

    Catalysts CuOx/γ-Al2O3-IH and CuOx/γ-Al2O3-IM were prepared, characterized, and tested for styrene combustion in the absence and presence of water vapor. The effect of copper valence of the catalysts on the catalytic activity for styrene combustion was discussed using the theory of hard soft acids and bases (HSAB). The results showed that the existence of water vapor in feed stream inhibited the catalytic activity for styrene combustion due to the competition adsorption of water molecule. HSAB theory confirmed that the local soft acidity of the catalyst CuOx/γ-Al2O3-IH was much stronger than that of the catalyst CuOx/γ-Al2O3-IM because of the higher content of soft acid Cu+on its surface, which increased the adsorption ability toward soft base of styrene and reduced the adsorption toward hard base of water vapor, and thus increased the catalytic activity for styrene combustion and weakened the negative influence of water vapor.

  19. Staphylococcus aureus SrrAB Affects Susceptibility to Hydrogen Peroxide and Co-Existence with Streptococcus sanguinis

    Science.gov (United States)

    Oogai, Yuichi; Kawada-Matsuo, Miki; Komatsuzawa, Hitoshi

    2016-01-01

    Staphylococcus aureus is a pathogen and a commensal bacterial species that is found in humans. Bacterial two-component systems (TCSs) sense and respond to environmental stresses, which include antimicrobial agents produced by other bacteria. In this study, we analyzed the relation between the TCS SrrAB and susceptibility to the hydrogen peroxide (H2O2) that is produced by Streptococcus sanguinis, which is a commensal oral streptococcus. An srrA-inactivated S. aureus mutant demonstrated low susceptibility to the H2O2 produced by S. sanguinis. We investigated the expression of anti-oxidant factors in the mutant. The expression of katA in the mutant was significantly higher than in the wild-type (WT) in the presence or absence of 0.4 mM H2O2. The expression of dps in the mutant was significantly increased compared with the WT in the presence of H2O2 but not in the absence of H2O2. A katA or a dps-inactivated mutant had high susceptibility to H2O2 compared with WT. In addition, we found that the nitric oxide detoxification protein (flavohemoglobin: Hmp), which is regulated by SrrAB, was related to H2O2 susceptibility. The hmp-inactivated mutant had slightly lower susceptibility to the H2O2 produced by S. sanguinis than did WT. When a srrA-inactivated mutant or the WT were co-cultured with S. sanguinis, the population percentage of the mutant was significantly higher than the WT. In conclusion, SrrAB regulates katA, dps and hmp expression and affects H2O2 susceptibility. Our findings suggest that SrrAB is related in vivo to the co-existence of S. aureus with S. sanguinis. PMID:27441894

  20. Effect of co-existing kaolinite and goethite on the aggregation of graphene oxide in the aquatic environment.

    Science.gov (United States)

    Huang, Guanxing; Guo, Huiyuan; Zhao, Jian; Liu, Yonghong; Xing, Baoshan

    2016-10-01

    Broad applications of graphene oxide (GO) will result in the release of GO into aquatic environments, where clay minerals and metal (hydr)oxides are commonly present. Thereby the interactions between GO and a binary system containing clay minerals and metal (hydr)oxides can occur. We investigated the aggregation of GO with kaolinite and kaolinite-goethite associations (KGAs) in aquatic systems under different pHs, ionic strengths, and GO concentrations. GO suspension was unstable at low pHs, and the aggregation of GO occurred in the presence of KGA-4% and KGA-10% until pH 5 and 6, respectively. Kaolinite decreased the critical coagulation concentration (CCC) of GO at pH 5.5 from around 50 to 20 mM NaCl due to the reduced energy barrier. Heteroaggregation of GO with KGAs was extremely sensitive to ionic strength at pH 5.5, and the CCC of GO in the presence of KGA-10% increased from less than 1 mM NaCl to 5 mM NaCl with the increase of pH from 5.5 to 9. The heteroaggregation extent of GO with KGAs was enhanced firstly, then reduced with the increase of GO concentrations at pH 5.0, which is likely because KGA plates were more efficiently wrapped by large-size GO sheets with increasing GO concentrations. These findings are useful for understanding and predicting the fate of GO in the relatively complicated aquatic and soil environments where binary minerals co-exist. PMID:27379727

  1. Catalytic subcritical water liquefaction of flax straw for high yield of furfural

    International Nuclear Information System (INIS)

    There is substantial interest in the application of biomass as a renewable fuel or for production of chemicals. Flax straw can be converted into valuable chemicals and biofuels via liquefaction in sub-critical water. In this study, the yield of furfural and the kinetics of flax straw liquefaction under sub-critical water conditions were investigated using a high-pressure autoclave reactor. The liquefaction was conducted in the temperature range of 175–325 °C, pressure of 0.1 MPa–8 MPa, retention time in the range of 0 min–120 min, and flax straw mass fraction (wF) of 5–20 %. Also, the effect of acid catalysts on furfural yield was studied. The kinetic parameters of flax straw liquefaction were determined using nonlinear regression of the experimental data, assuming second-order kinetics. The apparent activation energy was found to be 27.97 kJ mol−1 while the reaction order was 2.0. The optimum condition for furfural yield was at 250 °C, 6.0 MPa, wF of 5% and 0 retention time after reaching set conditions. An acid catalyst was found to selectively favour furfural yield with 40% flax straw conversion. - Highlights: • Flax straw liquefaction in subcritical water. • Creation of a reaction pathway that can be used to optimized furfural production. • Acid catalyst selectively favoured furfural yield with respect to other liquid products. • At the highest process temperature of 325 °C, a carbon conversion of 40% was achieved. • Activation energy and reaction order was 28 kJ/mol and 2.0 respectively

  2. Plasma power source based on a catalytic reaction of atomic hydrogen measured by water bath calorimetry

    International Nuclear Information System (INIS)

    Extreme ultraviolet (EUV) spectroscopy was recorded on microwave discharges of helium with 2% hydrogen. Novel emission lines were observed with energies of q x 13.6 eV, where q=1, 2, 3, 4, 6, 7, 8, 9, 11 or these discrete energies less 21.2 eV corresponding to inelastic scattering of these photons by helium atoms due to excitation of He (1s2) to He (1s12p1). The average hydrogen atom temperature was measured to be 180-210 eV versus ∼3 eV for pure hydrogen. The electron temperature Te for helium-hydrogen was 30,500±5% K compared to 7400±5% K for pure helium. Dominant He+ emission and an intensification of the plasma emission observed when He+ was present with atomic hydrogen demonstrated the role of He+ as a catalyst. Using water bath calorimetry, excess power was observed from the helium-hydrogen plasma compared to control krypton plasma. For example, for an input of 8.1 W, the total plasma power of the helium-hydrogen plasma measured by water bath calorimetry was 30.0 W corresponding to 21.9 W of excess power in 3 cm3. The excess power density and energy balance were high, 7.3 W/cm3 and -2.9x104 kJ/mole H2, respectively

  3. Large scale analysis of co-existing post-translational modifications in histone tails reveals global fine structure of cross-talk

    DEFF Research Database (Denmark)

    Schwämmle, Veit; Aspalter, Claudia-Maria; Sidoli, Simone;

    2014-01-01

    Mass spectrometry (MS) is a powerful analytical method for the identification and quantification of co-existing post-translational modifications in histone proteins. One of the most important challenges in current chromatin biology is to characterize the relationships between co-existing histone...... marks, the order and hierarchy of their deposition, and their distinct biological functions. We developed the database CrossTalkDB to organize observed and reported co-existing histone marks as revealed by MS experiments of histone proteins and their derived peptides. Statistical assessment revealed...... sample-specific patterns for the co-frequency of histone post-translational modifications. We implemented a new method to identify positive and negative interplay between pairs of methylation and acetylation marks in proteins. Many of the detected features were conserved between different cell types or...

  4. Micro-channel catalytic reactor integration in CAPER and research/development on highly tritiated water handling and processing

    International Nuclear Information System (INIS)

    The CAPER facility of the Tritium Laboratory Karlsruhe has demonstrated the technology for the tokamak exhaust processing. CAPER has been significantly upgraded to pursue research/development programs towards highly tritiated water (HTW) handling and processing. The preliminary tests using a metal oxide reactor producing HTW afterward de-tritiated with PERMCAT were successful. In a later stage, a micro-channel catalytic reactor was installed in view of long term research program on HTW. The integration of this new system in CAPER was carried out along with a careful safety analysis due to high risk associated with such experiments. First experiments using the μ-CCR were performed trouble free, and HTW up to 360 kCi/kg was produced at a rate of 0.5 g/h. Such HTW was collected into a platinum zeolite bed (2 g of HTW for 20 g of Pt-zeolite), and in-situ detritiation was performed via isotopic exchange with deuterium. These first experimental results with tritium confirmed the potential for the capture and exchange method to be used for HTW in ITER. (authors)

  5. 催化光度法测定水中的氟%Catalytic Spectrophotometric Determination of Fluoride in Water

    Institute of Scientific and Technical Information of China (English)

    李志英; 孙一飞

    2011-01-01

    Under neutral conditions, free fluorion ions can catalyze the discoloration reaction of acidic chrome blue K with H2O2. Based on this,a novel catalytic spectrophotometric method was proposed to determine trace F-. The results showed that the maximum absorption wavelength of the color solution was 522 nm, the linear range of the determination was 0. 4~11. 2μg/mL, and the detection limit was 9. 9×10-4 μg/mL. The method was used to determine fluoride in water with satisfactory results.%在中性溶液中,游离的F-对H2O2氧化酸性铬兰K褪色反应具有催化作用,基于此建立了测定微量F-的催化光度分析的新方法.结果表明,有色溶液的最大吸收波长为522 nm,测定的线性范围为0.4~11.2 μg/mL,检出限为9.9×10-4 μg/mL.该法用于水中微量F-的测定,结果令人满意.

  6. Solar Photo Catalytic Hydrogen Production from water using a dual bed photosystem

    Energy Technology Data Exchange (ETDEWEB)

    Florida Solar Energy Center

    2003-03-30

    A body of work was performed in which the feasibility of photocatalytically decomposing water into its constituent elements using a dual bed, or modular photosystem, under solar radiation was investigated. The system envisioned consists of two modules, each consisting of a shallow, flat, sealed container, in which microscopic photocatalytic particles are immobilized. The photocatalysts absorb light, generating free electrons and lattice vacancy holes, which are capable of performing reductive and oxidative chemistry, respectively. The photocatalysts would be chosen as to whether they specifically promote H{sub 2} or O{sub 2} evolution in their respective containers. An aqueous solution containing a redox mediator is pumped between the two chambers in order to transfer electron equivalents from one reaction to the other.

  7. Bio-electro catalytic treatment of petroleum produced water: Influence of cathode potential upliftment.

    Science.gov (United States)

    Jain, Pratiksha; Srikanth, Sandipam; Kumar, Manoj; Sarma, Priyangshu M; Singh, M P; Lal, Banwari

    2016-11-01

    Treatment of petroleum produced water (PPW) was studied using bioelectrochemical system (BES) under uplifted cathode potential. The treatment efficiency in terms of COD and hydrocarbon removal was observed at 91.25% and 76.60% respectively, along with the reduction in TDS during BES operation under 400mV of cathode potential. There was also a reduction in concentration of sulfates, however, it was not significant at, since oxidative conditions are being maintained at anode. Improved oxidation of PPW at anode also resulted in good power output (-20.47mA) and also depicted improved fuel cell behaviour. The electrochemical analysis in terms of cyclic/linear sweep voltammetry also showed well correlation with the observed treatment efficiencies. The microbial dynamics of the BES after loading real field wastewater showed the dominance of species that are reported to be effective for petroleum crude oil degradation. PMID:27544915

  8. Tandem Catalytic Depolymerization of Lignin by Water-Tolerant Lewis Acids and Rhodium Complexes.

    Science.gov (United States)

    Jastrzebski, Robin; Constant, Sandra; Lancefield, Christopher S; Westwood, Nicholas J; Weckhuysen, Bert M; Bruijnincx, Pieter C A

    2016-08-23

    Lignin is an attractive renewable feedstock for aromatic bulk and fine chemicals production, provided that suitable depolymerization procedures are developed. Here, we describe a tandem catalysis strategy for ether linkage cleavage within lignin, involving ether hydrolysis by water-tolerant Lewis acids followed by aldehyde decarbonylation by a Rh complex. In situ decarbonylation of the reactive aldehydes limits loss of monomers by recondensation, a major issue in acid-catalyzed lignin depolymerization. Rate of hydrolysis and decarbonylation were matched using lignin model compounds, allowing the method to be successfully applied to softwood, hardwood, and herbaceous dioxasolv lignins, as well as poplar sawdust, to give the anticipated decarbonylation products and, rather surprisingly, 4-(1-propenyl)phenols. Promisingly, product selectivity can be tuned by variation of the Lewis-acid strength and lignin source. PMID:27440544

  9. A non-acid-assisted and non-hydroxyl-radical-related catalytic ozonation with ceria supported copper oxide in efficient oxalate degradation in water

    KAUST Repository

    Zhang, Tao

    2012-06-01

    Oxalate is usually used as a refractory model compound that cannot be effectively removed by ozone and hydroxyl radical oxidation in water. In this study, we found that ceria supported CuO significantly improved oxalate degradation in reaction with ozone. The optimum CuO loading amount was 12%. The molar ratio of oxalate removed/ozone consumption reached 0.84. The catalytic ozonation was most effective in a neutral pH range (6.7-7.9) and became ineffective when the water solution was acidic or alkaline. Moreover, bicarbonate, a ubiquitous hydroxyl radical scavenger in natural waters, significantly improved the catalytic degradation of oxalate. Therefore, the degradation relies on neither hydroxyl radical oxidation nor acid assistance, two pathways usually proposed for catalytic ozonation. These special characters of the catalyst make it suitable to be potentially used for practical degradation of refractory hydrophilic organic matter and compounds in water and wastewater. With in situ characterization, the new surface Cu(II) formed from ozone oxidation of the trace Cu(I) of the catalyst was found to be an active site in coordination with oxalate forming multi-dentate surface complex. It is proposed that the complex can be further oxidized by molecular ozone and then decomposes through intra-molecular electron transfer. The ceria support enhanced the activity of the surface Cu(I)/Cu(II) in this process. © 2012 Elsevier B.V.

  10. Dimensional effects in the radiation-catalytic processes of water decomposition and perspectives of application of nanocatalysts

    International Nuclear Information System (INIS)

    Full text : According to the value of the coefficient of energy sources of radiation, selectivity and productivity, radiation-heterogeneous processes are one of the promising areas of radioactive processes. Interest to radiating and heterogeneous processes increased in communication by development of nuclear power systems, transformations of nuclear energy and atomic-hydrogen energy. The physical stage of radiation-heterogeneous processes comprises the steps of absorption, transformation, transport and energy transfer radiation sources. The efficiency of radioactive processes in heterogeneous systems is largely dependent on the parameters of constituent phases. In this work, the examples of the radiation-catalytic processes for hydrogen production from water presents the results of investigations of the influence of particle size of catalysts on the efficiency of energy conversion of ionizing radiation. As objects of investigation were taken oxide compounds SiO2, BeO, Al2O3, and aluminosilicates, beryllium silicates. The physical stage of radiation-heterogeneous processes was investigated by using model-calculated experiments. Calculation for well-known model of given processes of interaction of ionizing radiation with solids having the radiation-catalytic activity shows that in most experiments the energy of ionizing radiation is converted into energy imbalance of charge carriers (electrons and holes) excited states, and other defective states of the oxides. Investigated the individual and complex oxide systems containing metal oxides II-IV of the periodic table of elements. There are positions of cat ions and anions, which are the centers of localization of no equilibrium charge carriers in the ground state charged and(where 2 = 2, 4). With the capture of no equilibrium charge carriers in [3] and [4], these centers pass into the state, as a clear signs of the charges of these centers does not change. Therefore, in these oxides, the recombination of free particles

  11. How Does the Reductase Help To Regulate the Catalytic Cycle of Cytochrome P450 3A4 Using the Conserved Water Channel?

    OpenAIRE

    Fishelovitch, Dan; Shaik, Sason; Wolfson, Haim J.; Nussinov, Ruth

    2010-01-01

    Water molecules play a major role in the P450 catalytic cycle. Here, we locate the preferred water pathways and their gating mechanisms for the human cytochrome P450 3A4 (CYP3A4) and elucidate the role of the cytochrome P450 reductase (CPR) in turning on and activating these water channels. We perform explicit solvent molecular dynamic simulations of CYP3A4, unbound and bound to two substrates, and with and without the flavin mononucleotide (FMN)-binding domain of CPR. We observe in/out passa...

  12. Iridium-mediated Bond Activation and Water Oxidation as an Exemplary Case of CARISMA, A European Network for the Development of Catalytic Routines for Small Molecule Activation.

    Science.gov (United States)

    Licini, Giulia; Albrecht, Martin

    2015-01-01

    CARISMA is a currently running COST Action that pools leading European experts in computational and experimental chemistry to foster synergies for developing new catalytic processes for the transformation of abundant small molecules such as water, carbon dioxide, or ammonia into high-value chemicals and energy-relevant products. CARISMA promotes new collaborations, exchange of knowledge and skills, frontier training to young as well as established researchers, and a platform for the advancement of theoretical and experimental research in an iterative process, comprised of expertise in various connate domains including synthesis, catalysis, spectroscopy, kinetics, and computational chemistry. These interactions stimulate the discovery of new and efficient catalytic processes, illustrated in the second part of this contribution with the collaborative development of powerful iridium-based complexes for bond activation and water oxidation catalysis. PMID:26507475

  13. Catalytic activity of Ni3S2 and effects of reactor wall in hydrogen production from water with hydrogen sulphide as a reducer under hydrothermal conditions

    International Nuclear Information System (INIS)

    Catalytic activity of Ni3S2 and the effects of reactor wall in the hydrogen production from water were investigated under hydrothermal conditions using hydrogen sulphide (H2S) as a reductant. It was found that Ni3S2 catalysed the hydrogen production from water and may act as a semi-conductor catalyst. In the case of addition of Ni3S2, the time required to achieve the maximum hydrogen yield significantly decreased and the maximum hydrogen yield increased. These results suggest that the Ni3S2 formed as a corrosion product of the reactor wall when using the Hastelloy C-276 lined reactor should play a catalytic role in the hydrogen production. These results could facilitate studies for the synthesis of highly active catalysts for the production of hydrogen under mild conditions

  14. On the co-existence of chemically peculiar Bp stars, slowly pulsating B stars and constant B stars in the same part of the H-R diagram

    NARCIS (Netherlands)

    Briquet, M.; Hubrig, S.; Cat, P. de; Aerts, C.; North, P.; Schöller, M.

    2007-01-01

    Aims. In order to better model massive B-type stars, we need to understand the physical processes taking place in slowly pulsating B (SPB) stars, chemically peculiar Bp stars, and non-pulsating normal B stars co-existing in the same part of the H-R diagram. Methods: We carry out a comparative study

  15. The catalytic role of tungsten electrode material in the plasmachemical activity of a pulsed corona discharge in water

    International Nuclear Information System (INIS)

    The effects of tungsten material used as a high-voltage needle electrode on the production of hydrogen peroxide and the degradation of dimethylsulfoxide (DMSO) caused by a pulsed corona discharge in water were investigated. A reactor of needle-plate electrode geometry was used. The erosion of the tungsten electrodes by the discharge was evaluated. The yields of H2O2 production and the decomposition of DMSO by the discharge, which were obtained using the tungsten electrodes, were compared with those determined for titanium electrodes. The electrode erosion increased significantly with an increase in the solution conductivity. A large fraction (50-70%) of the eroded tungsten electrode material was released into the solution in dissolved form as tungstate WO42- ions. A correlation between the amount of eroded tungsten material released into the solution and the chemical effects induced by the discharge was determined. Lower yields of H2O2 and a higher degradation of DMSO by the discharge were obtained using the tungsten electrodes than were determined using titanium electrodes. Tungstate ions were shown to play a dominant role in the decomposition of H2O2, which was produced by the discharge using a tungsten electrode. The higher degradation of DMSO that was determined for tungsten was attributed to the tungstate-catalyzed oxidation of DMSO by H2O2, in addition to the oxidation of DMSO by OH radicals. Such a mechanism was supported by the detection of degradation by-products of DMSO (methanesulfonate, sulfate and dimethyl sulfone). The catalytic role of tungstate ions in the plasmachemical activity of the discharge generated using a tungsten electrode was also demonstrated on a pH-dependent decomposition of H2O2 and DMSO.

  16. The catalytic role of tungsten electrode material in the plasmachemical activity of a pulsed corona discharge in water

    Energy Technology Data Exchange (ETDEWEB)

    Lukes, Petr; Clupek, Martin; Babicky, Vaclav [Department of Pulse Plasma Systems, Institute of Plasma Physics, Academy of Sciences of the Czech Republic, v.v.i. Za Slovankou 3, Praha 8, 182 00 (Czech Republic); Sisrova, Irena; Janda, Vaclav, E-mail: lukes@ipp.cas.cz [Department of Water Technology and Environmental Engineering, Faculty of Environmental Technology, Institute of Chemical Technology, Technicka 5, Prague 6, 166 28 (Czech Republic)

    2011-06-15

    The effects of tungsten material used as a high-voltage needle electrode on the production of hydrogen peroxide and the degradation of dimethylsulfoxide (DMSO) caused by a pulsed corona discharge in water were investigated. A reactor of needle-plate electrode geometry was used. The erosion of the tungsten electrodes by the discharge was evaluated. The yields of H{sub 2}O{sub 2} production and the decomposition of DMSO by the discharge, which were obtained using the tungsten electrodes, were compared with those determined for titanium electrodes. The electrode erosion increased significantly with an increase in the solution conductivity. A large fraction (50-70%) of the eroded tungsten electrode material was released into the solution in dissolved form as tungstate WO{sub 4}{sup 2-} ions. A correlation between the amount of eroded tungsten material released into the solution and the chemical effects induced by the discharge was determined. Lower yields of H{sub 2}O{sub 2} and a higher degradation of DMSO by the discharge were obtained using the tungsten electrodes than were determined using titanium electrodes. Tungstate ions were shown to play a dominant role in the decomposition of H{sub 2}O{sub 2}, which was produced by the discharge using a tungsten electrode. The higher degradation of DMSO that was determined for tungsten was attributed to the tungstate-catalyzed oxidation of DMSO by H{sub 2}O{sub 2}, in addition to the oxidation of DMSO by OH radicals. Such a mechanism was supported by the detection of degradation by-products of DMSO (methanesulfonate, sulfate and dimethyl sulfone). The catalytic role of tungstate ions in the plasmachemical activity of the discharge generated using a tungsten electrode was also demonstrated on a pH-dependent decomposition of H{sub 2}O{sub 2} and DMSO.

  17. Catalytic hydrogen evolution from water by reduced forms of 12-tungstosilicic acid in the presence of heterogeneous rhodium polymeric catalysts

    International Nuclear Information System (INIS)

    Catalytic effect of heterogeneous rhodium-polymeric catalyst on the hydrogen evolution from aqueous and aqueous-alcohol solutions of slightly reduced forms of 12-tungstosilic acid has been studied. The activity of the catalyst studied under experimental conditions is limited by the reagent diffusion from the solution volume. It is found, that heteropolyacid ions, immobilized on the polymer together with fine-dispersed particles of metallic rhodium, take active part in the electron transfer from the solution volume onto metallic particles inside a polymeric carriei thus promoting the catalytic process

  18. Toward resolving the catalytic mechanism of dihydrofolate reductase using neutron and ultrahigh-resolution X-ray crystallography [Neutron and ultrahigh resolution X-ray crystallography reveals water as the proton donor in the catalytic mechanism of dihydrofolate reductase

    International Nuclear Information System (INIS)

    Dihydrofolate reductase (DHFR) catalyzes the NADPH-dependent reduction of dihydrofolate (DHF) to tetrahydrofolate (THF). An important step in the mechanism involves proton donation to the N5 atom of DHF. The inability to determine the protonation states of active site residues and substrate has led to the lack of consensus on a catalytic mechanism. To resolve this ambiguity, we conducted neutron and ultrahigh resolution X-ray crystallographic studies of the pseudo-Michaelis ternary complex of DHFR with folate and NADP+ from E. coli. The neutron data were collected to 2.0 Å resolution using a 3.6 mm3 crystal with the quasi-Laue technique, and the structure reveals that the N3 atom of folate is protonated while Asp27 is negatively charged. Previous mechanisms have proposed a keto-to-enol tautomerization of the substrate to facilitate protonation of the N5 atom. The structure supports the existence of the keto tautomer due to protonation of the N3 atom, suggesting tautomerization is unnecessary for catalysis. In the 1.05 Å resolution X-ray structure of the ternary complex, conformational disorder of the Met20 side chain is coupled to electron density for a partially occupied water within hydrogen-bonding distance of the N5 atom of folate; this suggests direct protonation of substrate by solvent. We propose a catalytic mechanism for DHFR that involves stabilization of the keto tautomer of the substrate, elevation of the pKa of the N5 atom of DHF by Asp27, and protonation of N5 by water whose access to the active site is gated by fluctuation of the Met20 side chain even though the Met-20 loop is closed

  19. EFFECTS OF FEED CONCENTRATION AND WATER VAPOR ON CATALYTIC COMBUSTION OF ETHYL ACETATE AND BENZENE IN AIR OVER CR-ZSM-5 CATALYST

    Directory of Open Access Journals (Sweden)

    Ahmad Zuhairi Abdullah

    2010-09-01

    Full Text Available Catalytic combustion of ethyl acetate (EAc and benzene (Bz over chromium exchanged ZSM-5 (Si/Al=240 is reported. An 11 mm i.d. fixed-bed catalytic reactor, operated at temperatures between 100 oC and 500 oC, and under excess oxygen condition, was used for the catalytic activity measurement. Apparent order of reaction and apparent activation energy were determined by operating the reactor differentially at a gas hourly space velocity (GHSV of 78,900 h-1 and feed concentrations between 3,500 ppm to 17,700 ppm and 3,700 to 12,400 ppm for ethyl acetate and benzene, respectively. Ethyl acetate was more reactive than benzene due to highly reactive carbonyl group in the molecule. The combustion process satisfactorily fitted pseudo first-order kinetics with respect to organic concentration and a zero-order dependence on the oxygen concentration. The presence of water vapor (9,000 ppm in the feed stream was found to weaken the reactivity of these organics which could also be demonstrated with increases in the activation energy from 23.1 kJ/mole to 37.6 kJ/mole for ethyl acetate and from 27.6 kJ/mole to 46.1 kJ/mole for benzene. Water vapor was found to play a positive role in the formation of carbon dioxide yield in ethyl acetate combustion. Deactivation of catalyst by water appeared to be only temporary and the activity reverted back to its original value once the source of water vapor was removed.

  20. Prognostic value of radical cystoprostatectomy in men with bladder cancer infiltrating prostate versus co-existing prostate cancer: a research study

    Directory of Open Access Journals (Sweden)

    Prokopowicz Grzegorz

    2010-09-01

    Full Text Available Abstract Background The aim of the following study is to evaluate the advancement of incidentally diagnosed prostate cancer in specimen after cystoprostatectomies caused by muscle-invasive bladder cancer. Secondly we assessed the survival in patients after radical cystoprostatectomy whose postoperative specimen was characterized by the presence of co-existing prostate cancer or prostate infiltration by urothelial bladder cancer. Methods Between 1993 and 2009 a total of 320 patients with muscle-invasive bladder cancer underwent cystoprostatectomy. The first analyzed group consisted of 52 patients with bladder cancer infiltrating prostate, while the second group consisted of 21 patients with co-existing prostate cancer. In all patients cancer specific survival and progression were analyzed. Average follow up was 75.2 months (range: 0 - 181. Results Cancer-specific survival was significantly shorter in group I (p = 0.03. Neoplastic progression in patients from group I was observed in 42.2% of patients, while in patients from group II in 23.6% of patients (p = 0.04. No statistical difference was observed in the percentage of positive lymph nodes between the groups (p = 0.22. The median Gleason score in patients with co-existing prostate cancer was equal to 5. The stage of prostate cancer pT2/pT3 was equal to 20 (96%/1 (4% patients. 12 (57% prostate cancers were clinically insignificant. Biochemical recurrence occurred in 2 (9% patients. Conclusions 1. Incidentally diagnosed prostate cancer in specimen after cystoprostatectomies is frequently clinically insignificant and characterized by low progression. 2. Patients with bladder cancer infiltrating prostate are characterized by higher percentage of progression and death in comparison with patients with co-existing prostate cancer.

  1. Plant co-existence patterns and High-Arctic vegetation composition in three common plant communities in north-east Greenland

    Directory of Open Access Journals (Sweden)

    Oriol Grau

    2014-09-01

    Full Text Available Arctic regions are expected to experience substantial changes in climate in the coming decades. In order to predict potential changes of Arctic vegetation, it is important to understand the distinct role of life forms of plants and of individual species in relation to plant co-existence patterns. Our aim is to investigate if three common Arctic plant patch types dominated by contrasting life forms (by the dwarf shrubs Salix arctica or Dryas octopetala×intermedia or by mosses are related (a to the co-existence of vascular plants and species richness at patch scale and (b to the floristic composition in three distinct plant communities (Salix snowbed, Dryas heath and fell-field associated with contrasting abiotic regimes. The study was conducted at Zackenberg, in north-east Greenland. Dryas patches showed a clear negative effect on small-scale plant richness and co-existence in the fell-field. Salix and moss patches showed a similar pattern in all the plant communities, although the number of individuals growing in Salix patches was lower than in moss patches. Salix and mosses in the fell-fields hosted a high number of species in spite of the much less vegetated aspect of this harsh, upper zone. The floristic composition varied between plant communities, but it did not change substantially between patch types within each community. This study provides novel background knowledge of plant co-existence patterns at patch scale and of the structure of contrasting Arctic plant communities, which will help to better assess the potential effects of varying abiotic stress regimes on Arctic vegetation.

  2. Normal Hematopoietic Stem Cells within the AML Bone Marrow Have a Distinct and Higher ALDH Activity Level than Co-Existing Leukemic Stem Cells

    OpenAIRE

    Schuurhuis, Gerrit J.; Meel, Michael H.; Wouters, Floris; Min, Lisa A.; Terwijn, Monique; de Jonge, Nick A.; Kelder, Angele; Snel, Alexander N; Zweegman, Sonja; Ossenkoppele, Gert J.; Smit, Linda

    2013-01-01

    Persistence of leukemic stem cells (LSC) after chemotherapy is thought to be responsible for relapse and prevents the curative treatment of acute myeloid leukemia (AML) patients. LSC and normal hematopoietic stem cells (HSC) share many characteristics and co-exist in the bone marrow of AML patients. For the development of successful LSC-targeted therapy, enabling eradication of LSC while sparing HSC, the identification of differences between LSC and HSC residing within the AML bone marrow is ...

  3. Basic research for nuclear energy : a study on photo-catalytic decomposition reactions of organics dissolved in water

    International Nuclear Information System (INIS)

    In an experiment on TiO2 photo-catalysis of five nitrogen-containing organic compounds, the changes of pH and total carbon contents were measured, and the dependence of their photo-catalytic characteristic upon their chemical structures were investigated. -- calculation of the effect of ionic carbon species in an aqueous solution on thermodynamic equilibrium, pH and conductivity showed a small quantity of organics could lead conductivity increase and pH reduction. -- Based on the results of photo-catalytic experiment of ethylamine, phenylhydrazine, pyridine, urea or EDTA, irradiated for 180 minutes after adsorption onto titanium dioxide for 60 minutes, relationship between nitrogen atomic charge and the first-order rate constant was as the following: R (1st - order rate constant) = δ (ε - a )1/3 + b where, ε : atomic charge of nitrogen in a molecular, δ, a and b : corrective coefficients

  4. The Impact of Co-Existing Prostate Adenocarcinoma with Bladder Carcinoma on Disease Specific Survival of The Patients in Our Radical Cystoprostatectomy Series

    Directory of Open Access Journals (Sweden)

    Özgür Ugurlu

    2010-05-01

    Full Text Available The aim of this study was to compare the patients with and without histologically proven prostate carcinoma who underwent radical cystectomy for muscle invasive bladder cancer in terms of bladder tumor properties and survival rates. Material and Methods: A total of 149 male patients who had undergone radical cystectomy and  urinary diversion between 1994-2007 in our institution were included in our study. Medical records of the patients were analyzed retrospectively. Fourteen (9.3% patients had co-existing prostate carcinoma, while remaining 135 (90.7% did not. The two groups were compared to each other with respect to the oncological properties of the bladder tumors (stage and grade and disease specific mortality rates. Results: The mean ages for the patients with and without co-existing prostate carcinoma were 64.2±8.4 and 57.7±10.8, respectively. There was a significant difference between the ages of the two groups (p=0.029. There were not any significant differences among the two groups regarding bladder cancer pathological stage (p=0.199 and grade (p=0.544. The disease specific survival rates of the two groups for three years were: 61.76% and 81.82% for the patients with and without coexisting prostate carcinoma respectively. No significant difference was observed between the disease specific survival rates of the two groups (p=0.325. Conclusion: The co-existing prostate carcinoma had no significant effect on tumor stage, grade and disease specific survival rates of patients who underwent radical cystectomy for muscle invasive bladder cancer.

  5. Governing the co-existence of GM crops : ex-ante regulation and ex-post liability under uncertainty and irreversibility

    OpenAIRE

    Beckmann, Volker; Soregaroli, Claudio; Wesseler, Justus

    2006-01-01

    "The future institutional environment for the co-existence of genetically modified (GM) crops, conventional crops and organic crops in Europe combines measures of ex-ante regulation and ex-post liability rules. Against this background we ask the following two questions: How does ex-ante regulation and ex-post liability under irreversibility and uncertainty affect the adoption of GM crops? What are the implications for regional agglomeration of GM and non-GM crops? Ex-ante regulations and ex-p...

  6. Mueller matrix analysis for all optical fiber co-existence of birefringence-polarization dependent gain-mode coupling at a single wavelength

    Institute of Scientific and Technical Information of China (English)

    Shang Chio; Wu Chong-Qing; Li Zheng-Yong; Yang Shuang-Shou; Gao Kai-Qiang; Yu Kuang-Lu; Feng Zhen

    2011-01-01

    Birefringence (polarization-related phase-shift),polarization dependent gain (PDG) and mode coupling are three factors that may synchronously influence the transmission of single-wavelength polarized light in optical fibers.This paper obtains a new Mueller matrix analysis,which can be used under conditions that all these three factors are existing and changing.According to our transmission model,the state of polarization (SOP) changes along an optical microstructure fiber with co-existence of birefringence-PDG-mode coupling were simulated. The simulated results,which show the phenomena of SOP constringency,are in good agreement with previous theoretical analyses.

  7. Resolution of Ibuprofen Ester by Catalytic Antibodies in Water-miscible Organic-solvents%水-有机溶剂混溶体系中催化抗体催化拆分布洛芳脂

    Institute of Scientific and Technical Information of China (English)

    杨根生; 应黎; 欧志敏; 姚善泾

    2009-01-01

    The asymmetric hydrolysis of racemic ibuprofen ester is one of the most important methods for chiral separation of ibuprofen. In this work, a catalytic antibody that accelerates the rate of enantioselective hydrolysis of ibuprofen methyl ester was obtained against an immunogen consisting of tetrahedral phosphonatc hapten attached to bovine serum albumin (BSA). The catalytic activity of the catalytic antibody in the water-miscible organic-solvent system composed of a buffer solution and TV, .N-dimethylformamide (DMF) was studied. With 6% DMF in the buffer solution (containing catalytic antibody 0.25 umol, 0.2 mol·L-1 phosphate buffer, pH 8) at 37℃ for 10 h, a good conversion (48.7%) and high cnantiomeric excess (>99%) could be reached. The kinetic analysis of the cata-lytic antibody-catalyzed reaction showed that the hydrolysis in the water-miscible organic-solvent system with DMF in buffer solution followed the Michaelis-Menten kinetics. The catalytic efficiency (kcat/km) was enhanced to 151.91 L·mmol-1·min-1, twice as large as that for the buffer solution only.

  8. Engineered biochar from microwave-assisted catalytic pyrolysis of switchgrass for increasing water-holding capacity and fertility of sandy soil.

    Science.gov (United States)

    Mohamed, Badr A; Ellis, Naoko; Kim, Chang Soo; Bi, Xiaotao; Emam, Ahmed El-Raie

    2016-10-01

    Engineered biochars produced from microwave-assisted catalytic pyrolysis of switchgrass have been evaluated in terms of their ability on improving water holding capacity (WHC), cation exchange capacity (CEC) and fertility of loamy sand soil. The addition of K3PO4, clinoptilolite and/or bentonite as catalysts during the pyrolysis process increased biochar surface area and plant nutrient contents. Adding biochar produced with 10wt.% K3PO4+10 wt.% clinoptilolite as catalysts to the soil at 2wt% load increased soil WHC by 98% and 57% compared to the treatments without biochar (control) and with 10wt.% clinoptilolite, respectively. Synergistic effects on increased soil WHC were manifested for biochars produced from combinations of two additives compared to single additive, which may be the result of increased biochar microporosity due to increased microwave heating rate. Biochar produced from microwave catalytic pyrolysis was more efficient in increasing the soil WHC due to its high porosity in comparison with the biochar produced from conventional pyrolysis at the same conditions. The increases in soil CEC varied widely compared to the control soil, ranging from 17 to 220% for the treatments with biochars produced with 10wt% clinoptilolite at 400°C, and 30wt% K3PO4 at 300°C, respectively. Strong positive correlations also exist among soil WHC with CEC and biochar micropore area. Biochar from microwave-assisted catalytic pyrolysis appears to be a novel approach for producing biochar with high sorption affinity and high CEC. These catalysts remaining in the biochar product would provide essential nutrients for the growth of bioenergy and food crops. PMID:27232966

  9. IN-SITU MAGIC ANGLE SPINNING NMR INVESTIGATIONS ON CATALYTIC CONVERSION OF BIOGENIC MOLECULES IN THE PRESENCE OF AQUEOUS WATER

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Mary Y.; Feng, Ju; Camaioni, Donald M.; Turcu, Romulus VF; Peden, Charles HF; Lercher, Johannes A.; Hu, Jian Z.

    2012-09-01

    The catalyzed conversion of biomass to hydrocarbon energy carriers requires a cascade of reactions that deconstruct and reduce the polymeric, highly oxofunctionalized biomass material. While lignin is the most intractable component of lignocellulose, its conversion to useful products is key in this catalytic chemistry, because the carbon in lignin is the most reduced one in lignocellulose. This chemistry faces steep challenges, as most of the reactions have to be performed in an aqueous environment under conditions that are highly corrosive towards catalysts. The anticipated scale of the transformations demands that the complex catalysts involved be highly efficient, stable, regenerable, and economically viable catalysts. Currently, none of the known heterogeneous solid catalysts meets these requirements. In order to develop new catalysts satisfying these requirements, a fundamental understanding of the active centers, reaction intermediates and reaction dynamics/kinetics associated with the multi-step conversion of biomass/biomass components, or biomass related polar molecules, i.e., the precursor molecules to fuels, on multifunctional catalytic surfaces is critically needed.

  10. Catalytic activity of hydrophobic Pt/C/PTFE catalysts of different PTFE content for hydrogen-water liquid exchange reaction

    International Nuclear Information System (INIS)

    10%Pt/C catalysts were prepared by liquid reduction method. PTFE and Pt/ C catalysts were adhered to porous metal and hydrophobic Pt/C/PTFE catalysts were prepared. The structure and size of Pt crystal particles of Pt/C catalysts were analyzed by XRD, and their mean size was 3.1 nm. The dispersion state of Pt/C and PTFE was analyzed by SEM, and they had good dispersion mostly, but PTFE membrane could be observed on local parts of Pt/C/PTFE surface. Because of low hydrophobicity, Pt/C/ PTFE catalysts have low activity when the mass ratio of PTFE and Pt/C is 0.5: 1, and their catalytic activity increases markedly when the ratio is 1:1. When the ratio increases again, more Pt active sites would be covered by PTFE and interior diffusion effect would increase, which result in the decrease of catalytic activity of Pt/C/PTFE. By PTFE pretreatment of porous metal carrier, the activity of Pt/C/PTFE catalysts decreases when the mass ratio of PTFE and Pt/C is 0.5:1, and their activity decreases when the mass ratio is 1:1. (authors)

  11. Multifunctional nanocomposites of Fe3O4-graphene-Au for repeated use in simultaneous adsorption, in situ SERS detection and catalytic reduction of 4-nitrophenol in water

    International Nuclear Information System (INIS)

    This work is directed towards the synthesis of a ternary nanocomposite of Fe3O4-graphene-Au, i.e. Fe3O4 nanoparticles (∼300 nm in size) and Au nanoparticles (∼50 nm in size) loaded on the carbon basal planes of reduced graphene oxide, aimed for repeated use in simultaneous adsorption, in situ SERS detection and catalytic reduction of 4-nitrophenol (4-NP) in water, and also for recovering the useful reduction product of 4-aminophenol (4-AP). The results indicate that the amount of 4-NP and 4-AP absorbed to the prepared Fe3O4-graphene-Au nanocomposite can reach 170 mg g−1 and 447 mg g−1, respectively. The reduction reaction of 4-NP to 4-AP by NaBH4 with the Fe3O4-graphene-Au nanocomposite as a catalyst follows first-order kinetics with a rate constant (k) of about 0.4964 min−1, remarkably superior to the 0.1199 min−1 for the reduction reaction with the bare Au nanoparticles under the same conditions. In addition, in situ SERS can also be carried out to detect 4-NP and to monitor the reduction reaction with Fe3O4-graphene-Au as the substrate. Recycling of the composite can be achieved by simply applying an external magnetic field and the results demonstrate that it can be reused at least eight times with almost unaffected catalytic efficiency. (paper)

  12. Multifunctional nanocomposites of Fe3O4-graphene-Au for repeated use in simultaneous adsorption, in situ SERS detection and catalytic reduction of 4-nitrophenol in water

    Science.gov (United States)

    Chen, Fenghua; Wang, Yongwei; Chen, Qingtao; Han, Lifeng; Chen, Zhijun; Fang, Shaoming

    2014-12-01

    This work is directed towards the synthesis of a ternary nanocomposite of Fe3O4-graphene-Au, i.e. Fe3O4 nanoparticles (˜300 nm in size) and Au nanoparticles (˜50 nm in size) loaded on the carbon basal planes of reduced graphene oxide, aimed for repeated use in simultaneous adsorption, in situ SERS detection and catalytic reduction of 4-nitrophenol (4-NP) in water, and also for recovering the useful reduction product of 4-aminophenol (4-AP). The results indicate that the amount of 4-NP and 4-AP absorbed to the prepared Fe3O4-graphene-Au nanocomposite can reach 170 mg g-1 and 447 mg g-1, respectively. The reduction reaction of 4-NP to 4-AP by NaBH4 with the Fe3O4-graphene-Au nanocomposite as a catalyst follows first-order kinetics with a rate constant (k) of about 0.4964 min-1, remarkably superior to the 0.1199 min-1 for the reduction reaction with the bare Au nanoparticles under the same conditions. In addition, in situ SERS can also be carried out to detect 4-NP and to monitor the reduction reaction with Fe3O4-graphene-Au as the substrate. Recycling of the composite can be achieved by simply applying an external magnetic field and the results demonstrate that it can be reused at least eight times with almost unaffected catalytic efficiency.

  13. Mn oxide coated catalytic membranes for a hybrid ozonation-membrane filtration: comparison of Ti, Fe and Mn oxide coated membranes for water quality.

    Science.gov (United States)

    Byun, S; Davies, S H; Alpatova, A L; Corneal, L M; Baumann, M J; Tarabara, V V; Masten, S J

    2011-01-01

    In this study the performance of catalytic membranes in a hybrid ozonation-ceramic membrane filtration system was investigated. The catalytic membranes were produced by coating commercial ceramic ultrafiltration membranes with manganese or iron oxide nanoparticles using a layer-by-layer self-assembly technique. A commercial membrane with a titanium oxide filtration layer was also evaluated. The performance of the coated and uncoated membranes was evaluated using water from a borderline eutrophic lake. The permeate flux and removal of the organic matter was found to depend on the type of the metal oxide present on the membrane surface. The performance of the manganese oxide coated membrane was superior to that of the other membranes tested, showing the fastest recovery in permeate flux when ozone was applied and the greatest reduction in the total organic carbon (TOC) in the permeate. The removal of trihalomethanes (THMs) and haloacetic acids (HAAs) precursors using the membrane coated 20 times with manganese oxide nanoparticles was significantly better than that for the membranes coated with 30 or 40 times with manganese oxide nanoparticles or 40 times with iron oxide nanoparticles. PMID:20822791

  14. Catalytic Kinetic Determination of Micro Amounts of Oxalic Acid by Second-Order Derivative Oscillopolarography

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    It was found that micro amounts of oxalate showed a very strong catalytic effect on the slow reaction between K2Cr2O7 and Orange Ⅳ in a diluted sulfuric acid medium in a water bath at 70 ℃. Orange Ⅳ exhibited a sensitive second-order derivative polarographic wave at -0.50 V(vs. SCE). This provides the basis for a sensitive and selective catalytic kinetic method for oxalate determination with second-order derivative oscillopolarography. The effects of sulphuric acid, K2Cr2O7, and orange Ⅳ concentrations, reaction temperature and reaction time were investigated. A calibration curve of oxalate in the range of 0.1—2.0 μg/mL was obtained by the fixed-time procedure. The detection limit was 0.03 μg/ mL. The possible interference from co-existing substances or ions was examined. The new method has a high sensitivity and a good selectivity compared to other existing methods for oxalic acid determination. It has been applied to the determination of micro amounts of oxalate in real urine samples with satisfactory results.

  15. An FTIR study on the catalytic effect of water molecules on the reaction of CO successive hydrogenation at 3 and 10K

    Science.gov (United States)

    Pirim, C.; Krim, L.

    2011-05-01

    The ubiquitous presence of water and the relative high abundance of H2, H and CO molecules in the interstellar medium motivated numerous studies on their potential interaction. The reaction of successive hydrogenation of CO is of large interest in astrochemistry because of its implication in the formation of formaldehyde and methanol in interstellar grains and in comets. The catalytic effect of water on the successive hydrogenation of CO has been investigated by two methods. The first is the hydrogenation of a CO/H2O surface. The second is a co-injection of (CO/H2O) mixtures and H atoms. Both methods have been performed at 3 and 10 K. When the hydrogenation of a CO surface is performed at 3 K, no products are observed. In fact, the presence of solid hydrogen screens the hydrogenation process. However, when performed at 10 K, the experiment shows that water molecules increase the concentration of the H2CO and CH3OH species. At 3 and 10K, [(CO/H2O)+H] co-depositions confirm a subtantial impact on by-products formation. We show that water molecules increase the probability of reactive to encounter H atoms either physically, or chemically, by raising the number of chemical pathways. A coordinated theoretical study of the possible chemical pathways is currently under way.

  16. Mechanism of Catalytic Water Oxidation by the Ruthenium Blue Dimer Catalyst: Comparative Study in D2O versus H2O

    Directory of Open Access Journals (Sweden)

    Yulia Pushkar

    2013-01-01

    Full Text Available Water oxidation is critically important for the development of energy solutions based on the concept of artificial photosynthesis. In order to gain deeper insight into the mechanism of water oxidation, the catalytic cycle for the first designed water oxidation catalyst, cis,cis-[(bpy2(H2ORuIIIORuIII(OH2(bpy2]4+ (bpy is 2,2-bipyridine known as the blue dimer (BD, is monitored in D2O by combined application of stopped flow UV-Vis, electron paramagnetic resonance (EPR and resonance Raman spectroscopy on freeze quenched samples. The results of these studies show that the rate of formation of BD[4,5] by Ce(IV oxidation of BD[3,4] (numbers in square bracket denote oxidation states of the ruthenium (Ru centers in 0.1 M HNO3, as well as further oxidation of BD[4,5] are slower in D2O by 2.1–2.5. Ce(IV oxidation of BD[4,5] and reaction with H2O result in formation of an intermediate, BD[3,4]′, which builds up in reaction mixtures on the minute time scale. Combined results under the conditions of these experiments at pH 1 indicate that oxidation of BD[3,4]′ is a rate limiting step in water oxidation with the BD catalyst.

  17. Improvement of catalytic activity in selective oxidation of styrene with H2O2 over spinel Mg–Cu ferrite hollow spheres in water

    International Nuclear Information System (INIS)

    Graphical abstract: Uniform spinel Mg–Cu ferrite hollow spheres were prepared using carbon spheres as templates. Solid spinel Mg0.5Cu0.5Fe2O4 ferrite nanocrystals were also prepared by sol–gel auto-combustion, hydrothermal and coprecipitation methods for comparison. The samples were found to be efficient catalysts for oxidation of styrene using hydrogen peroxide as oxidant. Especially, in the case of Mg0.5Cu0.5Fe2O4 hollow spheres, obvious improvement on catalytic activity was observed and 21.2% of styrene conversion and 75.2% of selectivity for benzaldehyde were obtained at 80 °C for 6 h reaction in water. The catalyst can be magnetically separated easily for reuse and no obvious loss of activity was observed when reused in six consecutive runs. - Highlights: • Uniform spinel ferrite hollow spheres were prepared by a simple method. • The catalyst has been proved much more efficient for styrene oxidation than the reported analogues. • The catalyst can be easily separated by external magnetic field and has exhibited excellent reusability. • The catalytic system is environmentally friendly. - Abstract: Uniform spinel Mg–Cu ferrite hollow spheres were prepared using carbon spheres as templates. For comparison, solid Mg–Cu ferrite nanocrystals were also prepared by sol–gel auto-combustion, hydrothermal and coprecipitation methods. All the samples were characterized by Fourier transform infrared spectrophotometry (FT-IR), X-ray diffractometry (XRD), transmission electron microscopy (TEM) and N2 physisorption. The samples were found to be efficient catalysts for oxidation of styrene using hydrogen peroxide as oxidant. Especially, in the case of Mg0.5Cu0.5Fe2O4 hollow spheres, obvious improvement on catalytic activity was observed, and 21.2% of styrene conversion and 75.2% of selectivity for benzaldehyde were obtained at 80 °C for 6 h reaction in water. The catalyst can be magnetically separated easily for reuse and no obvious loss of activity was

  18. Co-existence of urinary tract infection and malaria among children under five years old: A report from Benin City, Nigeria

    Directory of Open Access Journals (Sweden)

    P O Okunola

    2012-01-01

    Full Text Available Children with fever are a majority in the various emergency rooms all over the world, and especially in the tropics. Most in sub-Saharan Africa will be treated for malaria, whether confirmed or not. It therefore follows that some of the morbidities other than malaria may go undiagnosed. The comorbidities with malaria that may have similar presentation among under-fives therefore are difficult to detect, and diseases like respiratory tract infections and urinary tract infections (UTI are left to debilitate affected children. The exact burden of UTI co-existing with malaria in Nigeria remains ill defined. This study looks at the co-existence of UTI in under- fives with a primary diagnosis of malaria. Well-nourished children aged less than five years with confirmed malaria seen at the Children Emergency Room of the University of Benin Teaching Hospital were recruited into a prospective cross-sectional study between June and August 2006. The prevalence of UTI was 9% (27 of 300 children, with those aged less than 24 months comprising the majority. The uropathogens isolated included Staphylococcus aureus (55.6%, Escherichia coli (29.6% and Kleibsiella pneumonia (14.8%. The isolates demonstrated high in vitro sensitivity to clavulanic acid-potentiated amoxicillin, ciprofloxacin and gentamicin, but were resistant to other commonly used antibiotics like amoxicillin and co-trimoxazole. The study indicates that UTI is a silent comorbidity in children aged less than 5 years with malaria and there is a need to evaluate these children in order to prevent the long-term morbidity of chronic renal diseases.

  19. [State of Fungal Lipases of Rhizopus microsporus, Penicillium sp. and Oospora lactis in Border Layers Water-Solid Phase and Factors Affecting Catalytic Properties of Enzymes].

    Science.gov (United States)

    Khasanov, Kh T; Davranov, K; Rakhimov, M M

    2015-01-01

    We demonstrated that a change in the catalytic activity of fungal lipases synthesized by Rhizopus microsporus, Penicillium sp. and Oospora lactis and their ability to absorb on different sorbents depended on the nature of groups on the solid phase surface in the model systems water: lipid and water: solid phase. Thus, the stability of Penicillium sp. lipases increased 85% in the presence ofsorsilen or DEAE-cellulose, and 55% of their initial activity respectively was preserved. In the presence of silica gel and CM-cellulose, a decreased rate of lipid hydrolysis by Pseudomonas sp. enzymes was observed in water medium, and the hydrolysis rate increased by 2.4 and 1.5 times respectively in the presence of aminoaerosil and polykefamid. In an aqueous-alcohol medium, aminoaerosil and polykefamid decreased the rate of substrate hydrolysis by more than 30 times. The addition of aerosil to aqueous and aqueous-alcohol media resulted in an increase in the hydrolysis rate by 1.2-1.3 times. Sorsilen stabilized Penicillium sp. lipase activity at 40, 45, 50 and 55 degrees C. Either stabilization or inactivation of lipases was observed depending on the pH of the medium and the nature of chemical groups localized on the surface of solid phase. The synthetizing activity of lipases also changed depending on the conditions. PMID:26596088

  20. Science Letters: Structure relationship of nitrochlorobenzene catalytic degradation process in water over palladium-iron bimetallic catalyst

    Institute of Scientific and Technical Information of China (English)

    NIU Shao-feng; ZHOU Hong-yi; AO Xu-ping; XU Xin-hua; LOU Zhang-hua

    2006-01-01

    Two isomers of nitrochlorobenzene (o-, and p-NCB) were treated by a Pd/Fe catalyst in aqueous solutions through catalytic amination and dechlorination. Nitrochlorobenzenes are rapidly converted to form chloroanilines (CAN) first through an amination process, and then rapidly dechlorinated to become aniline (AN) and Cl-, without the involvement of any other intermediate reaction products. The amination and dechlorination reaction are believed to take place predominantly on the surface site of the Pd/Fe catalysts. The dechlorination rate of the reductive degradation of the two isomers of nitrochlorobenzene (o-, and p-NCB) in the presence of Pd/Fe as a catalyst was measured experimentally. In all cases, the reaction rate constants were found to increase with the decrease in the Gibbs free energy (correlation with the activation energy) of NCBs formation; the activation energy of each dechlorination reaction was measured to be 95.83 and 77.05 kJ/mol, respectively for o- and p-NCB. The results demonstrated that p-NCBs were reduced more easily than o-NCBs.

  1. Enhancement of reaction rates for catalytic benzaldehyde hydrogenation and sorbitol dehydration in water solvent by addition of carbon dioxide

    Indian Academy of Sciences (India)

    Masayuki Shirai; Osamu Sato; Norihito Hiyoshi; Aritomo Yamaguchi

    2014-03-01

    The effect of pressured carbon dioxide on heterogeneous hydrogenation of benzaldehyde and homogeneous dehydration of sorbitol in water solvent was studied. Initial hydrogenation rates of benzaldehyde over a charcoal-supported palladium catalyst in water at 313 K were enhanced by the addition of carbon dioxide. The initial rate increased with an increase in carbon dioxide pressure and became a maximum at 5 MPa. Dehydration of sorbitol proceeded in water phase at 500 K and initial dehydration rates were enhanced by addition of 30 MPa of carbon dioxide.

  2. Novel Catalytic Membrane Reactors

    Energy Technology Data Exchange (ETDEWEB)

    Stuart Nemser, PhD

    2010-10-01

    There are many industrial catalytic organic reversible reactions with amines or alcohols that have water as one of the products. Many of these reactions are homogeneously catalyzed. In all cases removal of water facilitates the reaction and produces more of the desired chemical product. By shifting the reaction to right we produce more chemical product with little or no additional capital investment. Many of these reactions can also relate to bioprocesses. Given the large number of water-organic compound separations achievable and the ability of the Compact Membrane Systems, Inc. (CMS) perfluoro membranes to withstand these harsh operating conditions, this is an ideal demonstration system for the water-of-reaction removal using a membrane reactor. Enhanced reaction synthesis is consistent with the DOE objective to lower the energy intensity of U.S. industry 25% by 2017 in accord with the Energy Policy Act of 2005 and to improve the United States manufacturing competitiveness. The objective of this program is to develop the platform technology for enhancing homogeneous catalytic chemical syntheses.

  3. Using the water signal to detect invisible exchanging protons in the catalytic triad of a serine protease

    International Nuclear Information System (INIS)

    Chemical Exchange Saturation Transfer (CEST) is an MRI approach that can indirectly detect exchange broadened protons that are invisible in traditional NMR spectra. We modified the CEST pulse sequence for use on high-resolution spectrometers and developed a quantitative approach for measuring exchange rates based upon CEST spectra. This new methodology was applied to the rapidly exchanging Hδ1 and Hε2 protons of His57 in the catalytic triad of bovine chymotrypsinogen-A (bCT-A). CEST enabled observation of Hε2 at neutral pH values, and also allowed measurement of solvent exchange rates for His57-Hδ1 and His57-Hε2 across a wide pH range (3–10). Hδ1 exchange was only dependent upon the charge state of the His57 (kex,Im+ = 470 s−1, kex,Im = 50 s−1), while Hε2 exchange was found to be catalyzed by hydroxide ion and phosphate base (k(OH)- = 1.7 × 1010 M−1 s−1, K(HPO)42- = 1.7 × 106 M−1 s−1), reflecting its greater exposure to solute catalysts. Concomitant with the disappearance of the Hε2 signal as the pH was increased above its pKa, was the appearance of a novel signal (δ = 12 ppm), which we assigned to Hγ of the nearby Ser195 nucleophile, that is hydrogen bonded to Nε2 of neutral His57. The chemical shift of Hγ is about 7 ppm downfield from a typical hydroxyl proton, suggesting a highly polarized O–Hγ bond. The significant alkoxide character of Oγ indicates that Ser195 is preactivated for nucleophilic attack before substrate binding. CEST should be generally useful for mechanistic investigations of many enzymes with labile protons involved in active site chemistry.

  4. Stopped-in-loop flow analysis system for successive determination of trace vanadium and iron in drinking water using their catalytic reactions.

    Science.gov (United States)

    Ayala Quezada, Alejandro; Ohara, Keisuke; Ratanawimarnwong, Nuanlaor; Nacapricha, Duangjai; Murakami, Hiroya; Teshima, Norio; Sakai, Tadao

    2015-11-01

    An automated stopped-in-loop flow analysis (SILFA) system is proposed for the successive catalytic determination of vanadium and iron. The determination of vanadium was based on the p-anisidine oxidation by potassium bromate in the presence of Tiron as an activator to form a reddish dye, which has an absorption maximum at 510 nm. The selectivity of the vanadium determination was greatly improved by adding diphosphate as a masking agent of iron. For the iron determination, an iron-catalyzed oxidative reaction of p-anisidine by hydrogen peroxide with 1,10-phenanthroline as an activator to produce a reddish dye (510 nm) was employed. The SILFA system consisted of two peristaltic pumps, two six-port injection valves, a four-port selection valve, a heater device, a spectrophotometric detector and a data acquisition device. One six-port injection valve was used for the isolation of a mixed solution of standard/sample and reagent to promote each catalytic reaction, and another six-port injection valve was used for switching the reagent for vanadium or iron to achieve selective determination of each analyte. The above mentioned four-port selection valve was used to select standard solutions or sample. These three valves and the two peristaltic pumps were controlled by a built-in programmable logic controller in a touchscreen controller. The obtained results showed that the proposed SILFA monitoring system constituted an effective approach for the selective determination of vanadium and iron. The limits of detection, 0.052 and 0.55 µg L(-1), were obtained for vanadium and iron, respectively. The proposed system was successfully applied to drinking water samples without any preconcentration procedures. PMID:26452899

  5. Microwave-irradiated polyol method synthesis of Pt/C catalysts and its catalytic activities for hydrogen-water liquid exchange reaction

    International Nuclear Information System (INIS)

    Pt/C catalysts with isopropanol as both dispersant and reducing agent were synthesized by microwave-irradiated polyol method. The microstructures of the catalysts were characterized by XRD and TEM. The effects of capping agents, pH and heating rate on Pt particle size were studied. Then Pt/C catalysts were loaded on foam nickel with polytetrafluoroethylene latex to obtain hydrophobic catalysts, and their catalytic activities for hydrogen-water liquid phase exchange reaction were investigated. The results show that compared to the non-capped Pt/C catalysts, the average size of Pt particles in sodium acetate, sodium glycollate and disodium hydrogen citrate capped Pt/C catalysts decreases from 4.4 nm to 2.3, 2.5, and 2.3 nm respectively, and the agglomeration of Pt particles becomes obscure. The mean size of Pt particles in Pt/C catalysts decreases evidently with the increasing of the heating rate. However, the mean sizes of Pt particles in the Pt/C catalysts prepared with different pH of the synthesis solution are similar. The activity of the hydrophobic catalysts with capping agents is high for hydro- gen-water liquid exchange reaction, and is enhanced by decreasing the average particle size, in the range of 2.3-4.4 nm. (authors)

  6. Vanadium nanobelts coated nickel foam 3D bifunctional electrode with excellent catalytic activity and stability for water electrolysis

    Science.gov (United States)

    Yu, Yu; Li, Pei; Wang, Xiaofang; Gao, Wenyu; Shen, Zongxu; Zhu, Yanan; Yang, Shuliang; Song, Weiguo; Ding, Kejian

    2016-05-01

    Pursuit of highly active, stable and low-cost electrocatalysts for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is the key point for large-scale water splitting. A vanadium nanobelts coating on a nickel foam (V/NF) is proposed as an excellent 3D bifunctional electrode for water electrolysis here, which exhibits high activities with overpotentials of 292 and 176 mV at 10 mA cm-2 for OER and HER, respectively. When employed as a bifunctional electrocatalyst in an alkaline water electrolyzer, a cell voltage of 1.80 V was required to achieve 20 mA cm-2 with a slight increase during a 24 h durability test. The existence of the appropriate amount of nitrogen and oxygen elements in the surface region of vanadium nanobelts is regarded to be responsible for the electrocatalytic activity.Pursuit of highly active, stable and low-cost electrocatalysts for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is the key point for large-scale water splitting. A vanadium nanobelts coating on a nickel foam (V/NF) is proposed as an excellent 3D bifunctional electrode for water electrolysis here, which exhibits high activities with overpotentials of 292 and 176 mV at 10 mA cm-2 for OER and HER, respectively. When employed as a bifunctional electrocatalyst in an alkaline water electrolyzer, a cell voltage of 1.80 V was required to achieve 20 mA cm-2 with a slight increase during a 24 h durability test. The existence of the appropriate amount of nitrogen and oxygen elements in the surface region of vanadium nanobelts is regarded to be responsible for the electrocatalytic activity. Electronic supplementary information (ESI) available: More SEM, TEM images, XRD patterns, LSV curves, XPS spectra. See DOI: 10.1039/c6nr02395a

  7. Bifunctional catalytic electrode

    Science.gov (United States)

    Cisar, Alan (Inventor); Murphy, Oliver J. (Inventor); Clarke, Eric (Inventor)

    2005-01-01

    The present invention relates to an oxygen electrode for a unitized regenerative hydrogen-oxygen fuel cell and the unitized regenerative fuel cell having the oxygen electrode. The oxygen electrode contains components electrocatalytically active for the evolution of oxygen from water and the reduction of oxygen to water, and has a structure that supports the flow of both water and gases between the catalytically active surface and a flow field or electrode chamber for bulk flow of the fluids. The electrode has an electrocatalyst layer and a diffusion backing layer interspersed with hydrophilic and hydrophobic regions. The diffusion backing layer consists of a metal core having gas diffusion structures bonded to the metal core.

  8. Stable solar-driven oxidation of water by semiconducting photoanodes protected by transparent catalytic nickel oxide films.

    Science.gov (United States)

    Sun, Ke; Saadi, Fadl H; Lichterman, Michael F; Hale, William G; Wang, Hsin-Ping; Zhou, Xinghao; Plymale, Noah T; Omelchenko, Stefan T; He, Jr-Hau; Papadantonakis, Kimberly M; Brunschwig, Bruce S; Lewis, Nathan S

    2015-03-24

    Reactively sputtered nickel oxide (NiOx) films provide transparent, antireflective, electrically conductive, chemically stable coatings that also are highly active electrocatalysts for the oxidation of water to O2(g). These NiOx coatings provide protective layers on a variety of technologically important semiconducting photoanodes, including textured crystalline Si passivated by amorphous silicon, crystalline n-type cadmium telluride, and hydrogenated amorphous silicon. Under anodic operation in 1.0 M aqueous potassium hydroxide (pH 14) in the presence of simulated sunlight, the NiOx films stabilized all of these self-passivating, high-efficiency semiconducting photoelectrodes for >100 h of sustained, quantitative solar-driven oxidation of water to O2(g). PMID:25762067

  9. Stable solar-driven oxidation of water by semiconducting photoanodes protected by transparent catalytic nickel oxide films

    KAUST Repository

    Sun, Ke

    2015-03-11

    Reactively sputtered nickel oxide (NiOx) films provide transparent, antireflective, electrically conductive, chemically stable coatings that also are highly active electrocatalysts for the oxidation of water to O2(g). These NiOx coatings provide protective layers on a variety of technologically important semiconducting photoanodes, including textured crystalline Si passivated by amorphous silicon, crystalline n-type cadmium telluride, and hydrogenated amorphous silicon. Under anodic operation in 1.0 M aqueous potassium hydroxide (pH 14) in the presence of simulated sunlight, the NiOx films stabilized all of these self-passivating, high-efficiency semiconducting photoelectrodes for >100 h of sustained, quantitative solar-driven oxidation of water to O2(g). © 2015, National Academy of Sciences. All rights reserved.

  10. How water molecules affect the catalytic activity of hydrolases - A XANES study of the local structures of peptide deformylase

    Science.gov (United States)

    Cui, Peixin; Wang, Yu; Chu, Wangsheng; Guo, Xiaoyun; Yang, Feifei; Yu, Meijuan; Zhao, Haifeng; Dong, Yuhui; Xie, Yaning; Gong, Weimin; Wu, Ziyu

    2014-12-01

    Peptide deformylase (PDF) is a prokaryotic enzyme that catalyzes the deformylation of nascent peptides generated during protein synthesis and water molecules play a key role in these hydrolases. Using X-ray absorption near edge spectroscopy (XANES) and ab initio calculations we accurately probe the local atomic environment of the metal ion binding in the active site of PDF at different pH values and with different metal ions. This new approach is an effective way to monitor existing correlations among functions and structural changes. We show for the first time that the enzymatic activity depends on pH values and metal ions via the bond length of the nearest coordinating water (Wat1) to the metal ion. Combining experimental and theoretical data we may claim that PDF exhibits an enhanced enzymatic activity only when the distance of the Wat1 molecule with the metal ion falls in the limited range from 2.15 to 2.55 Å.

  11. Pb, Sr and Nd isotope study of two co-existing magmas in the Nízke Tatry Mountains, Western Carpathians (Slovakia)

    Science.gov (United States)

    Poller, U.; Kohút, M.; Gaab, A. S.; Todt, W.

    2005-07-01

    Two co-existing plutonic rocks (diorite and granodiorite) were studied from an intrusion of Variscan age in the Raztocna Valley Nízke Tatry Mountains, Western Carpathians. Geochemical analyses of major and trace elements constrain a volcanic arc as emplacement environment and give the first hints of a mixture of two magmatic end-members: the so-called Prasivá granodiorite and the Raztocna diorite. The 87Sr/86Sr(0) ratios vary between 0.7075 and 0.7118, the ɛ Nd(0) values range from -1.4 to -5.0. Common Pb isotopes reveal a dominant crustal source with minor influences from a mantle and a lower crustal source. Modelling based on Sr and Nd isotope data and using three component mixing calculations indicates that mixing of 2/3 of upper mantle material with 1/3 upper crustal material can produce the isotopic composition of the Raztocna diorite. Very minor amounts of lower crust were incorporated in the diorite. For the Prasivá granodiorite, the mixing ratio of upper mantle and upper crust is similar, but a lower crustal reservoir contributed about 5 10% of the source material.

  12. Fluoride adsorption onto granular ferric hydroxide: Effects of ionic strength, pH, surface loading, and major co-existing anions

    International Nuclear Information System (INIS)

    Fluoride adsorption onto granular ferric hydroxide (GFH) was investigated using batch methods, under various ionic strength, pH, surface loading, and major co-existing anion conditions. Adsorption of fluoride on GFH included an initial fast adsorption phase followed by a slow adsorption phase. Within the pH range of 2-11, fluoride adsorption equilibrium was not affected by ionic strength, but was significantly affected by pH. Maximum adsorption was achieved in the pH range of 3-6.5. Under the same pH condition, fluoride adsorption followed the Freundlich isotherm, indicating that the GFH surface was heterogeneous. X-ray photoelectron spectroscopy (XPS) and attenuated total reflection-infrared (ATR-IR) spectroscopy data showed evidence for fluoride sorption on the GFH surface via inner-sphere complexation accompanying increased hydrogen bonding and surface hydroxylation. Major anions, including phosphate, bicarbonate, sulfate, and chloride, reduced fluoride adsorption in the following order: H2PO4- > HCO3- > SO42- > Cl-.

  13. On the co-existence of chemically peculiar Bp stars, slowly pulsating B stars and constant B stars in the same part of the H-R diagram

    CERN Document Server

    Briquet, M; De Cat, P; Aerts, C; North, P; Scholler, M; 10.1051/0004-6361:20066940

    2009-01-01

    Aims. In order to better model massive B-type stars, we need to understand the physical processes taking place in slowly pulsating B (SPB) stars, chemically peculiar Bp stars, and non-pulsating normal B stars co-existing in the same part of the H-R diagram. Methods. We carry out a comparative study between samples of confirmed and well-studied SPB stars and a sample of well-studied Bp stars with known periods and magnetic field strengths. We determine their evolutionary state using accurate HIPPARCOS parallaxes and Geneva photometry. We discuss the occurrence and strengths of magnetic fields as well as the occurrence of stellar pulsation among both groups. Further, we make a comparison of Geneva photometric variability for both kinds of stars. Results. The group of Bp stars is significantly younger than the group of SPB stars. Longitudinal magnetic fields in SPB stars are weaker than those of Bp stars, suggesting that the magnetic field strength is an important factor for B type stars to become chemically pec...

  14. The catalytic role of tungsten electrode material in the plasmachemical activity of a pulsed corona discharge in water

    Czech Academy of Sciences Publication Activity Database

    Lukeš, Petr; Člupek, Martin; Babický, Václav; Sisrová, I.; Janda, V.

    2011-01-01

    Roč. 20, č. 3 (2011), 034011-034011. ISSN 0963-0252 R&D Projects: GA AV ČR IAAX00430802; GA ČR(CZ) GD104/09/H080 Institutional research plan: CEZ:AV0Z20430508 Keywords : corona discharge * water * erosion * tungsten * hydrogen peroxide * dimethylsulfoxide Subject RIV: BL - Plasma and Gas Discharge Physics Impact factor: 2.521, year: 2011 http://www.ipp.cas.cz/Ips/public/lukes_2011a.pdf

  15. Water-soluble metal nanoparticles stabilized by plant polyphenols for improving the catalytic properties in oxidation of alcohols

    Science.gov (United States)

    Mao, H.; Liao, Y.; Ma, J.; Zhao, S. L.; Huo, F. W.

    2015-12-01

    Plant polyphenols extracted from plants are one of the most abundant biomasses in nature, which are typical water soluble natural polymers. Herein, we reported a facile approach for the synthesis of platinum nanoparticle (PtNP) aqueous colloid by utilizing black wattle tannin (BWT, a typical plant polyphenol) as amphiphilic stabilizer. The phenolic hydroxyls of BWT provide the PtNPs with enough hydrophilicity, and their reduction ability could protect the PtNPs from deactivation caused by oxygen atmosphere. Additionally, the hydrophilic nature of BWT could efficiently promote the oxidation of alcohols in water, meanwhile, the hydrophobic and rigid backbones of plant polyphenols are able to suppress the PtNPs from aggregating, thus ensuring the high dispersion of the PtNPs during reactions. Under mild aerobic conditions, the as-prepared BWT-Pt colloid catalyst exhibited high activity in a series of biphasic oxidation of aromatic alcohols and aliphatic alcohols. As for the cycling stability, the BWT-Pt catalyst showed no obvious decrease during the 7 cycles, revealing superior cycling stability as compared with the counterparts using PVP or PEG as the stabilizer.Plant polyphenols extracted from plants are one of the most abundant biomasses in nature, which are typical water soluble natural polymers. Herein, we reported a facile approach for the synthesis of platinum nanoparticle (PtNP) aqueous colloid by utilizing black wattle tannin (BWT, a typical plant polyphenol) as amphiphilic stabilizer. The phenolic hydroxyls of BWT provide the PtNPs with enough hydrophilicity, and their reduction ability could protect the PtNPs from deactivation caused by oxygen atmosphere. Additionally, the hydrophilic nature of BWT could efficiently promote the oxidation of alcohols in water, meanwhile, the hydrophobic and rigid backbones of plant polyphenols are able to suppress the PtNPs from aggregating, thus ensuring the high dispersion of the PtNPs during reactions. Under mild aerobic

  16. Water-soluble metal nanoparticles stabilized by plant polyphenols for improving the catalytic properties in oxidation of alcohols.

    Science.gov (United States)

    Mao, H; Liao, Y; Ma, J; Zhao, S L; Huo, F W

    2016-01-14

    Plant polyphenols extracted from plants are one of the most abundant biomasses in nature, which are typical water soluble natural polymers. Herein, we reported a facile approach for the synthesis of platinum nanoparticle (PtNP) aqueous colloid by utilizing black wattle tannin (BWT, a typical plant polyphenol) as amphiphilic stabilizer. The phenolic hydroxyls of BWT provide the PtNPs with enough hydrophilicity, and their reduction ability could protect the PtNPs from deactivation caused by oxygen atmosphere. Additionally, the hydrophilic nature of BWT could efficiently promote the oxidation of alcohols in water, meanwhile, the hydrophobic and rigid backbones of plant polyphenols are able to suppress the PtNPs from aggregating, thus ensuring the high dispersion of the PtNPs during reactions. Under mild aerobic conditions, the as-prepared BWT-Pt colloid catalyst exhibited high activity in a series of biphasic oxidation of aromatic alcohols and aliphatic alcohols. As for the cycling stability, the BWT-Pt catalyst showed no obvious decrease during the 7 cycles, revealing superior cycling stability as compared with the counterparts using PVP or PEG as the stabilizer. PMID:26662453

  17. SET7/9 catalytic mutants reveal the role of active site water molecules in lysine multiple methylation.

    Science.gov (United States)

    Del Rizzo, Paul A; Couture, Jean-François; Dirk, Lynnette M A; Strunk, Bethany S; Roiko, Marijo S; Brunzelle, Joseph S; Houtz, Robert L; Trievel, Raymond C

    2010-10-01

    SET domain lysine methyltransferases (KMTs) methylate specific lysine residues in histone and non-histone substrates. These enzymes also display product specificity by catalyzing distinct degrees of methylation of the lysine ε-amino group. To elucidate the molecular mechanism underlying this specificity, we have characterized the Y245A and Y305F mutants of the human KMT SET7/9 (also known as KMT7) that alter its product specificity from a monomethyltransferase to a di- and a trimethyltransferase, respectively. Crystal structures of these mutants in complex with peptides bearing unmodified, mono-, di-, and trimethylated lysines illustrate the roles of active site water molecules in aligning the lysine ε-amino group for methyl transfer with S-adenosylmethionine. Displacement or dissociation of these solvent molecules enlarges the diameter of the active site, accommodating the increasing size of the methylated ε-amino group during successive methyl transfer reactions. Together, these results furnish new insights into the roles of active site water molecules in modulating lysine multiple methylation by SET domain KMTs and provide the first molecular snapshots of the mono-, di-, and trimethyl transfer reactions catalyzed by these enzymes. PMID:20675860

  18. SET7/9 Catalytic Mutants Reveal the Role of Active Site Water Molecules in Lysine Multiple Methylation*

    Science.gov (United States)

    Del Rizzo, Paul A.; Couture, Jean-François; Dirk, Lynnette M. A.; Strunk, Bethany S.; Roiko, Marijo S.; Brunzelle, Joseph S.; Houtz, Robert L.; Trievel, Raymond C.

    2010-01-01

    SET domain lysine methyltransferases (KMTs) methylate specific lysine residues in histone and non-histone substrates. These enzymes also display product specificity by catalyzing distinct degrees of methylation of the lysine ϵ-amino group. To elucidate the molecular mechanism underlying this specificity, we have characterized the Y245A and Y305F mutants of the human KMT SET7/9 (also known as KMT7) that alter its product specificity from a monomethyltransferase to a di- and a trimethyltransferase, respectively. Crystal structures of these mutants in complex with peptides bearing unmodified, mono-, di-, and trimethylated lysines illustrate the roles of active site water molecules in aligning the lysine ϵ-amino group for methyl transfer with S-adenosylmethionine. Displacement or dissociation of these solvent molecules enlarges the diameter of the active site, accommodating the increasing size of the methylated ϵ-amino group during successive methyl transfer reactions. Together, these results furnish new insights into the roles of active site water molecules in modulating lysine multiple methylation by SET domain KMTs and provide the first molecular snapshots of the mono-, di-, and trimethyl transfer reactions catalyzed by these enzymes. PMID:20675860

  19. SET7/9 Catalytic Mutants Reveal the Role of Active Site Water Molecules in Lysine Multiple Methylation

    Energy Technology Data Exchange (ETDEWEB)

    Del Rizzo, Paul A.; Couture, Jean-François; Dirk, Lynnette M.A.; Strunk, Bethany S.; Roiko, Marijo S.; Brunzelle, Joseph S.; Houtz, Robert L.; Trievel, Raymond C. (Michigan); (NWU); (Kentucky)

    2010-11-15

    SET domain lysine methyltransferases (KMTs) methylate specific lysine residues in histone and non-histone substrates. These enzymes also display product specificity by catalyzing distinct degrees of methylation of the lysine {epsilon}-amino group. To elucidate the molecular mechanism underlying this specificity, we have characterized the Y245A and Y305F mutants of the human KMT SET7/9 (also known as KMT7) that alter its product specificity from a monomethyltransferase to a di- and a trimethyltransferase, respectively. Crystal structures of these mutants in complex with peptides bearing unmodified, mono-, di-, and trimethylated lysines illustrate the roles of active site water molecules in aligning the lysine {epsilon}-amino group for methyl transfer with S-adenosylmethionine. Displacement or dissociation of these solvent molecules enlarges the diameter of the active site, accommodating the increasing size of the methylated {epsilon}-amino group during successive methyl transfer reactions. Together, these results furnish new insights into the roles of active site water molecules in modulating lysine multiple methylation by SET domain KMTs and provide the first molecular snapshots of the mono-, di-, and trimethyl transfer reactions catalyzed by these enzymes.

  20. An efficient route for catalytic activity promotion via hybrid electro-depositional modification on commercial nickel foam for hydrogen evolution reaction in alkaline water electrolysis

    International Nuclear Information System (INIS)

    Highlights: • Mono-Cu surface modification depress the HER activity of Ni-foam. • Hybrid Ni-foam/Cu0.01/Co0.05 exhibits superior HER performance. • Layer-by-layer structure may contribute to a synergistic promoting effect. - Abstract: In this paper, the single- and hybrid-layered Cu, Ni and Co thin films were electrochemically deposited onto the three-dimensional nickel foam as composite cathode catalyst for hydrogen evolution reaction in alkaline water electrolysis. The morphology, structure and chemical composition of the electrodeposited composite catalysts were investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray analysis (EDX). Electrochemical measurement depicted that, for the case of the monometallic layered samples, the general activity for hydrogen evolution reaction followed the sequence: Ni-foam/Ni > Ni-foam/Co > bare Ni-foam > Ni-foam/Cu. It is noteworthy that, the hybrid-layered Ni-foam/Cu0.01/Co0.05 exhibited the highest catalytic activity towards hydrogen evolution reaction with the current density as high as 2.82 times that of the bare Ni-foam. Moreover, both excellent electrochemical and physical stabilities can also be acquired on the Ni-foam/Cu0.01/Co0.05, making this hybrid-layered composite structure as a promising HER electro-catalyst

  1. Phase Behaviour of 1-Ethyl-3-methylimidazolium Thiocyanate Ionic Liquid with Catalytic Deactivated Compounds and Water at Several Temperatures: Experiments and Theoretical Predictions

    Directory of Open Access Journals (Sweden)

    Ramalingam Anantharaj

    2011-01-01

    Full Text Available Density, surface tension and refractive index were determined for the binary mixture of catalytic deactivated compounds with 1-ethyl-3-methylimidazolium thiocyanate {[EMIM][SCN]} at temperature of (298.15 to 323.15 K. For all the compounds with ILs, the densities varied linearly in the entire mole fraction with increasing temperature. From the obtained data, the excess molar volume and deviation of surface tension and refractive index have been calculated. A strong interaction was found between similar (cation-thiophene or cation-pyrrole compounds. The interaction of IL with dissimilar compounds such as indoline and quinoline and other multiple ring compounds was found to strongly depend on the composition of IL at any temperatures. For the mixtures, the surface tension decreases in the order of: thiophene > quinoline > pyridine > indoline > pyrrole > water. In general from the excess volume studies, the IL-sulphur/nitrogen mixture has stronger interaction as compared to IL-IL, thiophene-thiophene or pyrrole-pyrrole interaction. The deviation of surface tension was found to be inversely proportional to deviation of refractive index. The quantum chemical based COSMO-RS was used to predict the non-ideal liquid phase activity coefficient for all mixtures. It indicated an inverse relation between activity coefficient and excess molar volumes.

  2. Catalytic Effect of Activated Carbon and Activated Carbon Fiber in Non-Equilibrium Plasma-Based Water Treatment

    International Nuclear Information System (INIS)

    Catalysis and regeneration efficiency of granular activated carbon (GAC) and activated carbon fiber (ACF) were investigated in a non-equilibrium plasma water treatment reactor with a combination of pulsed streamer discharge and GAC or ACF. The experimental results show that the degradation efficiency of methyl orange (MO) by the combined treatment can increase 22% (for GAC) and 24% (for ACF) respectively compared to pulsed discharge treatment alone, indicating that the combined treatment has a synergetic effect. The MO degradation efficiency by the combined treatment with pulsed discharge and saturated GAC or ACF can increase 12% and 17% respectively compared to pulsed discharge treatment alone. Both GAC and ACF show catalysis and the catalysis of ACF is prominent. Meanwhile, the regeneration of GAC and ACF are realized in this process. When H2O2 is introduced into the system, the utilization efficiency of ozone and ultraviolet light is improved and the regeneration efficiency of GAC and ACF is also increased.

  3. Effect of doping β-NiOOH with Co on the catalytic oxidation of water: DFT+U calculations.

    Science.gov (United States)

    Costanzo, Francesca

    2016-03-14

    Electrocatalytic water splitting using energy from sunlight represents a promising strategy for clean, low-cost, and environmentally friendly production of H2. Unfortunately, the oxygen evolution reaction (OER) at the anode is kinetically slow and represents the bottleneck of this process. Transition metal oxides are good candidates for the anode in electrochemical water splitting. Inspired by recent computational work on β-NiOOH, which is considered the active phase during the charging and discharging process in alkaline batteries, we performed density functional theory calculations with the inclusion of the Hubbard-U correction on selected surfaces of pure and Co-doped β-NiOOH to calculate the energetics of the OER. The goal of the paper is to investigate theoretically whether doping a NiOOH surface with Co might change the mechanism and lower the overpotential of the OER on a specific NiOOH surface, and to what extent the choice of the surface unit cell may affect the results. Our results indicate that the most likely reaction mechanism depends on the amount of Co doping. We find that doping the β-NiOOH surface with only 25% Co decreases the overpotential from 0.28 to 0.18 V. We also find that the theoretical overpotential, and which step is the potential limiting step, depends on the size of the surface unit cell selected in the calculations. This work highlights how optimizing the binding energies of the various intermediates (O, OH and H2O) on the Ni and Co surface sites, may be key to reducing the overpotential. PMID:26902752

  4. Co-existence of a giant splenic hemangioma and multiple hepatic hemangiomas and the potential association with the use of oral contraceptives: a case report

    Directory of Open Access Journals (Sweden)

    Chatzoulis George

    2008-05-01

    Full Text Available Abstract Introduction Hepatic and splenic hemangiomas are common benign tumors that mainly affect female patients. Giant splenic hemangiomas are extremely rare, especially when correlated with multiple hepatic hemangiomas. Pathogenetic mechanisms between hemangiomas and oral contraceptives, as well as therapeutic approaches, are analyzed in this case report, in particular for the management of synchronous splenic and hepatic hemangiomas. Case presentation We report here a 42-year-old woman with a giant splenic hemangioma, multiple hepatic hemangiomas and a history of oral estrogen intake for many years. At first it was difficult to determine the organ from which the giant hemangioma originated. Angiography proved extremely helpful in tracing its origin in the spleen. Hematomas in the giant hemangioma posed a significant threat of rupture and catastrophic hemorrhage. We left the small hepatic hemangiomas in place, and removed the spleen along with the giant splenic hemangioma. Conclusion Diagnostic pitfalls in the determination of the origin of this giant hemangioma, attribution of its origin to the spleen angiographically, the unusual co-existence of the giant splenic hemangioma with multiple hepatic ones, and the potential threat of rupture of the giant hemangioma are some of the highlights of this case report. Estrogen administration represents a pathogenic factor that has been associated with hemangiomas in solid organs of the abdominal cavity. The therapeutic dilemma between resection and embolization of giant hemangiomas is another point of discussion in this case report. Splenectomy for the giant splenic hemangioma eliminates the risk of rupture and malignant degeneration, whereas observation for the small hepatic ones (

  5. Co-existence of calcium-binding proteins and γ-aminobutyric acid or glycine in neurons of the rat medullary dorsal horn

    Institute of Scientific and Technical Information of China (English)

    王文; 武胜昔; 李云庆

    2004-01-01

    Background We investigated the co-expression of calbindin-D28k (CB), calretinin (CR) and parvalbumin (PV, a combination of the three is referred to as CaBPs) with γ-aminobutyric acid (GABA) or glycine in neurons of the rat medullary dorsal horn (MDH).Methods Immunofluorescence histochemical double-staining for CaBPs and GABA or glycine was performed on the sections from rat MDH.Results CB-, CR-, PV-, GABA- and glycine-like immunoreactive (LI) neurons were differentially observed in all layers of the MDH, but particularly in lamina Ⅱ. Neurons that exhibited immunoreactivity for both CaBPs and GABA or glycine were also observed mainly in lamina Ⅱ. A few of them were found in laminae I and III. The percentages of neurons which co-expressed CB/GABA or CB/glycine out of the total numbers of CB- and GABA-LI neurons or CB- and glycine-LI neurons were 5.3% and 12.1% or 4.1% and 10.0%, respectively. The ratios of CR/GABA or CR/glycine co-existing neurons out of the total numbers of CR- and GABA-LI neurons or CR- and glycine-LI neurons were 5.8% and 7.6% or 4.4% and 7.1%, respectively. The rates of PV/GABA or PV/glycine co-localized neurons out of the total numbers of PV- and GABA-LI neurons or PV- and glycine-LI neurons were 11.1% and 5.1% or 9.9% and 5.1%, respectively. Conclusion The results indicate that some neurons in the MDH contain both CaBPs and GABA or glycine.

  6. Modelling Niche Differentiation of Co-Existing, Elusive and Morphologically Similar Species: A Case Study of Four Macaque Species in Nakai-Nam Theun National Protected Area, Laos

    Directory of Open Access Journals (Sweden)

    Camille N. Z. Coudrat

    2013-01-01

    Full Text Available Species misidentification often occurs when dealing with co-existing and morphologically similar species such as macaques, making the study of their ecology challenging. To overcome this issue, we use reliable occurrence data from camera-trap images and transect survey data to model their respective ecological niche and potential distribution locally in Nakai-Nam Theun National Protected Area (NNT NPA, central-Eastern Laos. We investigate niche differentiation of morphologically similar species using four sympatric macaque species in NNT NPA, as our model species: rhesus Macaca mulatta (Taxonomic Serial Number, TSN 180099, Northern pig-tailed M. leonina (TSN not listed; Assamese M. assamensis (TSN 573018 and stump-tailed M. arctoides (TSN 573017. We examine the implications for their conservation. We obtained occurrence data of macaque species from systematic 2006–2011 camera-trapping surveys and 2011–2012 transect surveys and model their niche and potential distribution with MaxEnt software using 25 environmental and topographic variables. The respective suitable habitat predicted for each species reveals niche segregation between the four species with a gradual geographical distribution following an environmental gradient within the study area. Camera-trapping positioned at many locations can increase elusive-species records with a relatively reduced and more systematic sampling effort and provide reliable species occurrence data. These can be used for environmental niche modelling to study niche segregation of morphologically similar species in areas where their distribution remains uncertain. Examining unresolved species' niches and potential distributions can have crucial implications for future research and species' management and conservation even in the most remote regions and for the least-known species.

  7. Catalytic Hydrogenation of Levulinic Acid in Water into g-Valerolactone over Bulk Structure of Inexpensive Intermetallic Ni-Sn Alloy Catalysts

    Directory of Open Access Journals (Sweden)

    Rodiansono Rodiansono

    2015-07-01

    Full Text Available A bulk structure of inexpensive intermetallic nickel-tin (Ni-Sn alloys catalysts demonstrated highly selective in the hydrogenation of levulinic acid in water into g-valerolactone. The intermetallic Ni-Sn catalysts were synthesized via a very simple thermochemical method from non-organometallic precursor at low temperature followed by hydrogen treatment at 673 K for 90 min. The molar ratio of nickel salt and tin salt was varied to obtain the corresponding Ni/Sn ratio of 4.0, 3.0, 2.0, 1.5, and 0.75. The formation of Ni-Sn alloy species was mainly depended on the composition and temperature of H2 treatment. Intermetallics Ni-Sn that contain Ni3Sn, Ni3Sn2, and Ni3Sn4 alloy phases are known to be effective heterogeneous catalysts for levulinic acid hydrogenation giving very excellence g-valerolactone yield of >99% at 433 K, initial H2 pressure of 4.0 MPa within 6 h. The effective hydrogenation was obtained in H2O without the formation of by-product. Intermetallic Ni-Sn(1.5 that contains Ni3Sn2 alloy species demonstrated very stable and reusable catalyst without any significant loss of its selectivity. © 2015 BCREC UNDIP. All rights reserved. Received: 26th February 2015; Revised: 16th April 2015; Accepted: 22nd April 2015  How to Cite: Rodiansono, R., Astuti, M.D., Ghofur, A., Sembiring, K.C. (2015. Catalytic Hydrogenation of Levulinic Acid in Water into g-Valerolactone over Bulk Structure of Inexpensive Intermetallic Ni-Sn Alloy Catalysts. Bulletin of Chemical Reaction Engineering & Catalysis, 10 (2: 192-200. (doi:10.9767/bcrec.10.2.8284.192-200Permalink/DOI: http://dx.doi.org/10.9767/bcrec.10.2.8284.192-200  

  8. Catalytic supercritical water gasification of primary paper sludge using a homogeneous and heterogeneous catalyst: Experimental vs thermodynamic equilibrium results.

    Science.gov (United States)

    Louw, Jeanne; Schwarz, Cara E; Burger, Andries J

    2016-02-01

    H2, CH4, CO and CO2 yields were measured during supercritical water gasification (SCWG) of primary paper waste sludge (PWS) at 450°C. Comparing these yields with calculated thermodynamic equilibrium values offer an improved understanding of conditions required to produce near-equilibrium yields. Experiments were conducted at different catalyst loads (0-1g/gPWS) and different reaction times (15-120min) in a batch reactor, using either K2CO3 or Ni/Al2O3-SiO2 as catalyst. K2CO3 up to 1g/gPWS increased the H2 yield significantly to 7.5mol/kgPWS. However, these yields and composition were far from equilibrium values, with carbon efficiency (CE) and energy recovery (ER) of only 29% and 20%, respectively. Addition of 0.5-1g/gPWS Ni/Al2O3-SiO2 resulted in high H2 and CH4 yields (6.8 and 14.8mol/kgPWS), CE of 84-90%, ER of 83% and a gas composition relatively close to the equilibrium values (at hold times of 60-120min). PMID:26638140

  9. CATALYTIC PROPERTY OF DOUBLE LAYERED PEROVSKITES A2MM’O6 FOR RADIOLYTICAL SPLIT OF WATER

    Directory of Open Access Journals (Sweden)

    Alexandru Cecal

    2009-06-01

    Full Text Available This paper deals with a study of water splitting by gamma rays in the presence of some double perovskites A2MM’O6 and also Sr2Fe1-xTa1+xO6. The irradiation is performed using 60Co as a source with 3·104 Ci activity and 8.3 kGy/h dose rate, which simulated the radioactive wastes, resulted from reprocessing of spent nuclear fuel elements much more active: 108-109 Ci. The stable products of radiolysis, as well as the other chemical species are measured by mass spectrometry. The calculated radiation yield (GH2 generally decreases in the order: Sr2Fe1-xTa1+xO6 (x=0.5; 0.4; 0.3; 0.1 > Ca2AlTaO6 > Sr2AlTaO6 > Ba2AlTaO6, under the given experimental conditions; the yield was higher in the presence of these catalysts than in their absence.

  10. Catalytic property of double layered perovskites A2MM'O6 for radiolytic split of water

    International Nuclear Information System (INIS)

    This paper deals with a study of water splitting by gamma rays in the presence of some double perovskites A2MM'O6 and also Sr2Fe1-xTa1+xO6. The irradiation is performed using 60Co as a source with 3x104 Ci activity and 8.3 kGy/h dose rate, which simulated the radioactive wastes, resulted from reprocessing of spent nuclear fuel elements much more active: 108-109 Ci. The stable products of radiolysis, as well as the other chemical species are measured by mass spectrometry. The calculated radiation yield (GH2) generally decreases in the order: Sr2Fe1-xTa1+xO6 (x=0.5; 0.4; 0.3; 0.1) > Ca2AlTaO6 > Sr2AlTaO6 > Ba2AlTaO6, under the given experimental conditions; the yield was higher in the presence of these catalysts than in their absence. (authors)

  11. Improvement of the piezoelectric properties in (K,Na)NbO{sub 3}-based lead-free piezoelectric ceramic with two-phase co-existing state

    Energy Technology Data Exchange (ETDEWEB)

    Yamada, H., E-mail: hide-yamada@mg.ngkntk.co.jp; Matsuoka, T.; Kozuka, H.; Yamazaki, M.; Ohbayashi, K. [NGK SPARK PLUG CO., LTD., 2808 Iwasaki, Komaki, Aichi 485-8510 (Japan); Ida, T., E-mail: ida.takashi@nitech.ac.jp [Advanced Ceramics Research Center, Nagoya Institute of Technology, 10-6-29 Asahigaoka, Tajimi, Gifu 507-0071 (Japan)

    2015-06-07

    Two phases of (K,Na)NbO{sub 3} (KNN) co-exist in a KNN-based composite lead-free piezoelectric ceramic 0.910(K{sub 1−x}Na{sub x}){sub 0.86}Ca{sub 0.04}Li{sub 0.02}Nb{sub 0.85}O{sub 3−δ}–0.042K{sub 0.85}Ti{sub 0.85}Nb{sub 1.15}O{sub 5} –0.036BaZrO{sub 3}–0.0016Co{sub 3}O{sub 4}– 0.0025Fe{sub 2}O{sub 3}–0.0069ZnO system, over a wide range of Na fractions, where 0.56 ≤ x ≤ 0.75. The crystal systems of the two KNN phases are identified to tetragonal and orthorhombic by analyzing the synchrotron powder X-ray diffraction (XRD) data, high-resolution transmission electron microscopy (HR-TEM), and selected-area electron diffraction (SAD). In the range 0.33 ≤ x ≤ 0.50, the main component of the composite system is found to be single-phase KNN with a tetragonal structure. Granular nanodomains of the orthorhombic phase dispersed in the tetragonal matrix have been identified by HR-TEM and SAD for 0.56 ≤ x ≤ 0.75. Only a trace amount of the orthorhombic phase has been found in the SAD patterns at the composition x = 0.56. However, the number of orthorhombic nanodomains gradually increases with increasing Na content up to x < 0.75, as observed from the HR-TEM images. An abrupt increase and agglomeration of the nanodomains are observed at x = 0.75, where weak diffraction peaks of the orthorhombic phase have also become detectable from the XRD data. The maximum value of the electromechanical coupling coefficient, k{sub p} = 0.56, has been observed at the composition x = 0.56.

  12. Photosynthesis of co-existing Phragmites haplotypes in their non-native range: are characteristics determined by adaptations derived from their native origin?

    Science.gov (United States)

    Nguyen, Loc Xuan; Lambertini, Carla; Sorrell, Brian K.; Eller, Franziska; Achenbach, Luciana; Brix, Hans

    2013-01-01

    The Gulf Coast of North America (GC) is a ‘hot spot’ of Phragmites diversity as several lineages (defined according to the haplotypes of their chloroplast DNA) differing in origin, genetic traits and phenotype co-exist and interbreed in this area. We analysed differences in photosynthetic characteristics among and within four haplotypes to understand if differences in gas exchange can be attributed to adaptations acquired in their native ranges. We collected rhizomes of four GC haplotypes (I2, M1, M and AI; including the phenotypes ‘Land-type’, ‘Delta-type’, ‘EU-type’ and ‘Greeny-type’) and propagated them in a common controlled environment to compare photosynthesis–irradiance responses, CO2 responses, chlorophyll fluorescence, the activity of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco), specific leaf area (SLA), pigment contents, stomatal density and guard cell length. The maximum light-saturated photosynthetic rate, Amax, in the haplotype I2 (Land-type) and haplotype M1 (Delta-type) (34.3–36.1 µmol CO2 m−2 s−1) was higher than that in the invasive Eurasian haplotype M (22.4 ± 2.3 µmol CO2 m−2 s−1). The Amax of haplotype AI (Greeny3-type) was 29.1 ± 4.0 µmol CO2 m−2 s−1 and did not differ from the Amax of the other haplotypes. The carboxylation rate (Vcmax) and electron transport rate (Jmax) followed the same pattern as Amax. The haplotypes also differed in SLA (17.0–24.3 m2 kg−1 dry mass) and pigment content, whereas stomatal density and guard cell length, Rubisco activity and chlorophyll fluorescence did not differ significantly among haplotypes. The high photosynthetic activity and gas-exchange capacity of the two haplotypes originating in tropical Africa and the Mediterranean area (haplotypes I2 and M1) are apparently adaptations derived from their native ranges. Hence, the haplotypes can be regarded as ecotypes. However, it remains unclear how these differences relate to plant competitiveness and

  13. 完全性葡萄胎与胎儿共存临床研究%Clinical study of complete hydatidiform mole and co-existing fetus

    Institute of Scientific and Technical Information of China (English)

    李珠玉; 陈海天; 彭软; 王子莲; 游泽山

    2015-01-01

    Objective To explore the clinical characteristics and pregnancy outcomes of complete hy-datidiform mole and co-existing fetus (CMCF).Methods The data of six CMCF women were analyzed retro-spectively.Results Among six CMCF women,five were pregnant after in vitro fertilization and embryo trans-plantation,and one after ovulation-stimulating treatment.Five patients were diagnosed with CMCF in middle pregnancy and one in early pregnancy.Five cases had twin pregnancy with complete hydatidiform mole and one was triplet pregnanct.One case insisted on continuous pregnancy,four accepted pregnancy termination and one was forced to terminate pregnancy.All six women and one fetus survived.Conclusions The incidence of CM-CF is probably correlated with the application of assisted reproductive technology.Clinical outcomes depend on disease progression,fetal chromosome and patients’willingness.If the fetal chromosome is normal and no seri-ous maternal complications occur during pregnancy,the fetus may survive.However,the risk of continuous pregnancy remains to be evaluated.%目的:探讨完全性葡萄胎与胎儿共存(CMCF)的临床特征及妊娠结局。方法收集并分析6例 CMCF 的临床资料。结果6例中,体外受精-胚胎移植术后妊娠5例,促排卵治疗后妊娠1例;妊娠中期发现5例,妊娠早期发现1例;双胎之一完全性葡萄胎5例,三胎之一完全性葡萄胎1例;要求继续妊娠1例,要求终止妊娠4例,被迫终止妊娠1例。6例产妇均存活,胎儿存活1例。结论CMCF 的发生可能与应用辅助生殖技术相关,其结局取决于病情发展、胎儿染色体及患者意愿。若胎儿染色体正常,且妊娠期间未出现严重母体并发症,有分娩活胎可能,但其继续妊娠的风险评估仍需进一步的研究。

  14. Method of Analysis by the U.S. Geological Survey California District Sacramento Laboratory-- Determination of Dissolved Organic Carbon in Water by High Temperature Catalytic Oxidation, Method Validation, and Quality-Control Practices

    Science.gov (United States)

    Bird, Susan M.; Fram, Miranda S.; Crepeau, Kathryn L.

    2003-01-01

    An analytical method has been developed for the determination of dissolved organic carbon concentration in water samples. This method includes the results of the tests used to validate the method and the quality-control practices used for dissolved organic carbon analysis. Prior to analysis, water samples are filtered to remove suspended particulate matter. A Shimadzu TOC-5000A Total Organic Carbon Analyzer in the nonpurgeable organic carbon mode is used to analyze the samples by high temperature catalytic oxidation. The analysis usually is completed within 48 hours of sample collection. The laboratory reporting level is 0.22 milligrams per liter.

  15. Preparation of Pt/K2La2Ti3O10 and its photo-catalytic activity for hydrogen evolution from methanol water solution

    Institute of Scientific and Technical Information of China (English)

    CUI; Wenquan

    2006-01-01

    ):A new series of layered perovskites exhibiting ion exchange,Inorg.Chem.,1987,26:4299-4301.[12]Takata,T.,Shinohara,K.,Tanaka,A.,Hara,M.,Kondo,J.N.,Domen,K.,A highly active photocatalyst for overall water splitting with a hydrated layered perovskite structure,J.Photochem.Photobiol.A:Chem.,1997,106(1-3):45-49.[13]Cui,W.Q.,Feng,L.R.,Xu,C.H.,Lü,S.J.,Qiu,F.L.,Hydrogen production by photocatalytic decomposition of methanol gas on Pt/TiO2 nano-film,Catal.Comm.,2004(5):533-536.[14]Herrmann,J.M.,Disdier,J.,Pichat,P.,Photoassisted platinum deposition on TiO2 powder using various platinum complexes,J.Phys.Chem.,1986,90:6028-6034.[15]Cui,W.Q.,Feng,L.R.,Xu,C.H.,Lü,S.J.,Qiu,F.L.,Studies on the photo-catalytic decomposition of methanol vapor on Pt-loaded nano-TiO2 particles,Acta Chim.Sinica (in Chinese),2005,63(3):203-209.[16]Ikeda,S.,Hara,M.,Kondo,J.N.,Domen,K.,Preparation of K2La2Ti3O10 by polymerized complex method and photocatalytic decomposition of water,Chem.Mater.,1998,10(1):72-77.[17]Yang,X.Y.,Per,Z.F.,Bai,R.Q.,Studies on dispersion of Pt by HOT,Petrochemical Technology,1978,7(4):352.[18]Fox,M.A.,Dulay,M.Y.,Heterogeneous photocatalysis,Chem.Rev.,1993,93(1):341-357.[19]Kudo,A.,Sakata,T.,Luminescent properties of nondoped and rare earth metal ion-doped K2La2Ti3O10 with layered perovskite structures:Importance of the hole trap process,J.Phys.Chem.,1995,99:15963-15967.

  16. Mechanisms of the photo-catalytic water cleavage. Watching catalysts at their work by means of in-situ IR spectroscopy; Mechanismen der photokatalytischen Wasserspaltung. Mit in-situ IR-Spektroskopie dem Katalysator bei der Arbeit zusehen

    Energy Technology Data Exchange (ETDEWEB)

    Ludwig, Ralf [Rostock Univ. (Germany). Abt. Physikalische Chemie

    2012-11-15

    The scarcity of fossil resources and the global warming require the development of sustainable energy technologies. In this respect, the hydrogen production by means of a photo-catalytic water cleavage has a great potential. Solar energy is converted into the transportable and exploitable energy source hydrogen. The author of the contribution under consideration reports, that the in-situ infrared spectroscopy considerably contributes to the understanding of the formation, state and degradation of a catalyst. The development of an effective and environmentally friendly system of catalyst is facilitated.

  17. Diurnal and Seasonal Changes in Stem Radius Increment and Sap Flow Density Indicate Different Responses of Two Co-existing Oak Species to Drought Stress

    Directory of Open Access Journals (Sweden)

    MÉSZÁROS, Ilona

    2011-01-01

    Full Text Available Using continuous monitoring of stem radius combined with sap flow measurements weassessed the effects of environmental conditions on tree radial growth and water status of two coexistingoak species (Quercus petraea and Quercus cerris at high resolution time in growingseasons of 2008 and 2009. The forest (95–100 yr is situated in a xeric site in the transition zonebetween forested and forest-steppe regions in north-eastern Hungary, Bükk mountains (47o90’N,20o46’E, elevation 320–340 m a.s.l.. Weather conditions in the growing season of 2008 (totalrainfall 354 mm, mean daily temperature 17.0 oC was less extreme than in 2009 (total rainfall299 mm, temperature 17.9 oC. Rainfall strongly determined the course of radial growth incrementin trees. Radial growth of trees was limited in 2009 due to the drought in spring. The maximumradial increment of both species was achieved three weeks earlier (4th week of June than in 2008(4th week of July. We used dendrometer monitoring data for estimation of stem (tree waterdeficit (W by measuring water-related changes in stem radius (Zweifel et al. 2005. Themagnitude of tree water deficit variation (W was always smaller in Q. cerris than in Q. petraea.In contrast, Quercus cerris always exhibited larger daytime averages and maxima of sap flowdensity. In August of 2009 when drought became severe there were larger increases in tree waterdeficit (W (50–55 % in both species compared to July as it could be expected from the extentof decreases in sap flow density (24–28%. Our data suggested that due to the low SWC thetranspiration was supported mainly from the inner water storage of trees during prolonged droughtwhich resulted in high stem water deficit (W.

  18. A broad spectrum catalytic system for removal of toxic organics from water by deep oxidation. Annual progress report, September 15, 1996 - September 14, 1997

    International Nuclear Information System (INIS)

    'During the first year, the palladium-catalyzed deep oxidation of toxic organics by dioxygen in aqueous solution was examined in some detail. The research performed has established the viability of the catalytic system to effect the deep (and complete) oxidation of a very wide range of organic substrates under mild conditions. One significant observation was that chemical warfare agent models containing phosphorus-carbon and sulfur-carbon bonds could be eliminated by using this procedure.'

  19. Catalytic cracking process

    Science.gov (United States)

    Lokhandwala, Kaaeid A.; Baker, Richard W.

    2001-01-01

    Processes and apparatus for providing improved catalytic cracking, specifically improved recovery of olefins, LPG or hydrogen from catalytic crackers. The improvement is achieved by passing part of the wet gas stream across membranes selective in favor of light hydrocarbons over hydrogen.

  20. Catalytic distillation structure

    Science.gov (United States)

    Smith, Jr., Lawrence A.

    1984-01-01

    Catalytic distillation structure for use in reaction distillation columns, a providing reaction sites and distillation structure and consisting of a catalyst component and a resilient component intimately associated therewith. The resilient component has at least about 70 volume % open space and being present with the catalyst component in an amount such that the catalytic distillation structure consist of at least 10 volume % open space.

  1. Water-Driven Assembly of Laser Ablation-Induced Au Condensates as Mesomorphic Nano- and Micro-Tubes

    Directory of Open Access Journals (Sweden)

    Chen Shuei-Yuan

    2009-01-01

    Full Text Available Abstract Reddish Au condensates, predominant atom clusters and minor amount of multiply twinned particles and fcc nanoparticles with internal compressive stress, were produced by pulsed laser ablation on gold target in de-ionized water under a very high power density. Such condensates were self-assembled as lamellae and then nano- to micro-diameter tubes with multiple walls when aged at room temperature in water for up to 40 days. The nano- and micro-tubes have a lamellar- and relaxed fcc-type wall, respectively, both following partial epitaxial relationship with the co-existing multiply twinned nanoparticles. The entangled tubes, being mesomorphic with a large extent of bifurcation, flexibility, opaqueness, and surface-enhanced Raman scattering, may have potential encapsulated and catalytic/label applications in biomedical systems.

  2. Investigations for designing catalytic recombiners

    International Nuclear Information System (INIS)

    In case of a severe accident in pressurised water reactors (PWR) a high amount of hydrogen up to about 20,000 m3 might be generated and released into the containments. The mixture consisting of hydrogen and oxygen may either burn or detonate, if ignited. In case of detonation the generated shock wave may endanger the components of the plant or the plant itself. Consequently, effective removal of hydrogen is required. The fact that hydrogen and oxygen react exo-thermally on catalytically acting surfaces already at low temperatures generating steam and heat is made use of in catalytic recombiners. They consist of substrates coated with catalyst (mainly platinum or palladium) which are arranged inside a casing. Being passively acting measures, recombiners do not need any additional energy supply. Experimental investigations on catalytic hydrogen recombination are conducted at FZJ (Forschungszentrum Juelich) using three test facilities. The results yield insight in the development potential of contemporary recombiner systems as well as of innovative systems. Detailed investigations on a recombiner section show strong temperature gradients over the surface of a catalytically coated sample. Dependent on the flow velocity, ignition temperature may be reached at the leading edge already at an inlet hydrogen concentration of about 5 vol.-%. The thermal strain of the substrate leads to considerable detachment of catalyst particles probably causing unintended ignition of the flammable mixture. Temperature peaks can be prevented effectively by leaving the first part of the plate uncoated. In order to avoid overheating of the catalyst elements of a recombiner even at high hydrogen concentrations a modular system of porous substrates is proposed. The metallic substrates are coated with platinum at low catalyst densities thus limiting the activity of the single specimen. A modular arrangement of these elements provides high recombination rates over a large hydrogen concentration

  3. Catalytic Synthesis Lactobionic Acid

    Directory of Open Access Journals (Sweden)

    V.G. Borodina

    2014-07-01

    Full Text Available Gold nanoparticles are obtained, characterized and deposited on the carrier. Conducted catalytic synthesis of lactobionic acid from lactose. Received lactobionic acid identify on the IR spectrum.

  4. Catalytic distillation process

    Science.gov (United States)

    Smith, Jr., Lawrence A.

    1982-01-01

    A method for conducting chemical reactions and fractionation of the reaction mixture comprising feeding reactants to a distillation column reactor into a feed zone and concurrently contacting the reactants with a fixed bed catalytic packing to concurrently carry out the reaction and fractionate the reaction mixture. For example, a method for preparing methyl tertiary butyl ether in high purity from a mixed feed stream of isobutene and normal butene comprising feeding the mixed feed stream to a distillation column reactor into a feed zone at the lower end of a distillation reaction zone, and methanol into the upper end of said distillation reaction zone, which is packed with a properly supported cationic ion exchange resin, contacting the C.sub.4 feed and methanol with the catalytic distillation packing to react methanol and isobutene, and concurrently fractionating the ether from the column below the catalytic zone and removing normal butene overhead above the catalytic zone.

  5. Catalytic Coanda combustion

    Energy Technology Data Exchange (ETDEWEB)

    Coleman, J.D.; Smith, A.G.; Kopmels, M.

    1992-09-16

    A catalytic reaction is enhanced by the use of the Coanda effect to maximise contact between reactant and catalyst. A device utilising this principle comprises a Coanda surface which directs the flow of fuel from a slot to form a primary jet which entrains the surrounding ambient air and forms a combustible mixture for reaction on a catalytic surface. The Coanda surface may have an internal or external nozzle which may be axi-symmetric or two-dimensional. (author)

  6. Catalytic ignition of light hydrocarbons

    Institute of Scientific and Technical Information of China (English)

    K. L. Hohn; C.-C. Huang; C. Cao

    2009-01-01

    Catalytic ignition refers to phenomenon where sufficient energy is released from a catalytic reaction to maintain further reaction without additional extemai heating. This phenomenon is important in the development of catalytic combustion and catalytic partial oxidation processes, both of which have received extensive attention in recent years. In addition, catalytic ignition studies provide experimental data which can be used to test theoretical hydrocarbon oxidation models. For these reasons, catalytic ignition has been frequently studied. This review summarizes the experimental methods used to study catalytic ignition of light hydrocarbons and describes the experimental and theoretical results obtained related to catalytic ignition. The role of catalyst metal, fuel and fuel concentration, and catalyst state in catalytic ignition are examined, and some conclusions are drawn on the mechanism of catalytic ignition.

  7. Catalytic Decomposition of Methylene Chloride by Sulfated Titania Catalysts

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Catalytic decomposition of methylene chloride in air below 300℃ was studied.Sulfated titania was very effective in converting 959ppm methylene chloride selectively to CO,CO2 and HCl.Complete decomposition of methylene chloride was achieved at low temperature(275℃).It was found that the acidic property of catalyst was a determinant factor for the catalytic activity.The presence of water vapor in the feed stream remarkably reduced the catalytic activity,which could be due to the blockage of acidic sites on the surface of catalyst by water molecules.A bifunctional catalyst comprising copper oxide was developed to improve the selectivity of catalytic oxidation,which indicated that copper oxide can promote the deep oxidation of methylene chloride.The crystal form of TiO2 imposes an important influence upon the catalytic oxidation.

  8. Catalytic coherence transformations

    Science.gov (United States)

    Bu, Kaifeng; Singh, Uttam; Wu, Junde

    2016-04-01

    Catalytic coherence transformations allow the otherwise impossible state transformations using only incoherent operations with the aid of an auxiliary system with finite coherence that is not being consumed in any way. Here we find the necessary and sufficient conditions for the deterministic and stochastic catalytic coherence transformations between a pair of pure quantum states. In particular, we show that the simultaneous decrease of a family of Rényi entropies of the diagonal parts of the states under consideration is a necessary and sufficient condition for the deterministic catalytic coherence transformations. Similarly, for stochastic catalytic coherence transformations we find the necessary and sufficient conditions for achieving a higher optimal probability of conversion. We thus completely characterize the coherence transformations among pure quantum states under incoherent operations. We give numerous examples to elaborate our results. We also explore the possibility of the same system acting as a catalyst for itself and find that indeed self-catalysis is possible. Further, for the cases where no catalytic coherence transformation is possible we provide entanglement-assisted coherence transformations and find the necessary and sufficient conditions for such transformations.

  9. Co-existing structures in 105Ru

    CERN Document Server

    Lalkovski, S; Stefanova, E A; Korichi, A; Petkov, P; Kownacki, J; Kutsarova, T; Minkova, A; Bazzacco, D; Bergstrom, M; Gorgen, A; Herskind, B; Hubel, H; Jansen, A; Kisyov, S; Khoo, T L; Kondev, F G; Lopez-Martens, A; Podolyak, Zs; Schonwasser, G; Yordanov, O

    2014-01-01

    New positive-parity states, having a band-like structure, were observed in 105Ru. The nucleus was produced in induced fission reaction and the prompt gamma-rays, emitted from the fragments, were detected by the EUROBALL III multi-detector array. The partial scheme of excited 105Ru levels is analyzed within the Triaxial-Rotor-plus-Particle approach.

  10. Did Australopithecus and Homo co-exist

    International Nuclear Information System (INIS)

    Uranium series isotope dating of the tufas at Taung/Buxton suggests a considerably younger age for the Taung child (Australopithecus africanus) than has hitherto been accepted. If this later date is confirmed, it will necessitate a re-think of the evolutionary tree of Man and his ancestors

  11. Co-existent breast and renal cancer

    OpenAIRE

    Üreyen, Orhan; Dadalı, Emrah; Akdeniz, Fırat; Şahin, Tamer; Tekeli, Mehmet Tahsin; Eliyatkın, Nuket; Postacı, Hakan; İLHAN, Enver

    2015-01-01

    The concomitant presence of breast cancer with one or more other types of cancer such as colon, vulva, lung, larynx, liver, uterus and kidneys has been presented in the literature. However, synchronous breast and renal cancer is very uncommon. Herein we present a woman with synchronous breast and renal cancer, and review the literature. A 77-year-old post-menopausal woman was admitted to our clinic complaining of left sided breast mass. On physical examination, there was a 3 cm palpable mass ...

  12. Influence of humic substances on the removal of pentachlorophenol by a biomimetic catalytic system with a water-soluble iron(III)-porphyrin complex.

    Science.gov (United States)

    Fukushima, Masami; Sawada, Akira; Kawasaki, Mikio; Ichikawa, Hiroyasu; Morimoto, Kengo; Tatsumi, Kenji; Aoyama, Masakazu

    2003-03-01

    To investigate some basic aspects of soil remediation using biomimetic catalysts, the effects of humic substances (HSs) on the removal of xenobiotics, such as pentachlorophenol (PCP), were investigated. The use of a biomimetic catalytic system using tetra(p-sulfophenyl)porphine-iron(III) (Fe(III)-TPPS) and potassium monopersulfate (KHSO5) resulted in the disappearance of PCP, accompanied by dechlorination. In addition, this process was enhanced by the presence of several types of HSs. The degrees of enhancement (% delta(PCP)60) achieved by the presence of HSs from peat and compost soils were larger than those in the presence of other types of HSs (tropical peat, brown forest, and ando soils). In control experiments, no PCP disappearance and dechlorination were observed in the presence of only KHSO5, only Fe(III)-TPPS, or combinations of HSs and either KHSO5 or Fe(III)-TPPS. To better understand the role of added HS in enhancing or inhibiting PCP disappearance, correlations between the chemical parameters of the HSs and % delta(PCP)60 were investigated. The most effective HSs had lower carboxylic acid contents and lower degrees of unsaturation. The carboxylic acid content and degree of unsaturation increase with the extent of humification. Therefore, HSs of a lower degree of humification would be predicted to be more useful in enhancing the disappearance of PCP in an Fe(III)-TPPS/KHSO5 system. PMID:12666937

  13. Dynamics of co-existing Escherichia colilineages in situ of the infant gut and multiplex phenotypic targeted recovery of previously uncultivated bacteria from the human gut

    DEFF Research Database (Denmark)

    Gumpert, Heidi

    were selected due to an observed change in their antibiotic susceptibility profile. Via full genome sequencing, we identified that in both cases a conjugative plasmid harboring antibiotic resistance genes was transferred between co-existing E. coli lineages and is responsible for the change in...... designed conditions. Antibiotictolerance phenotypes were determined, and this mapping was used to carefully tailor antibiotic combinations to specifically select for previously uncultivated bacteria. Usingthis method, four previously uncultivated species were successfully cultured andgenome sequenced, and...... two of which had 16S rRNA identities of less than 95% topreviously cultured bacteria. We assessed the genomic coverage and abundance ofthese sequenced isolates in the gut using publicly available metagenomes....

  14. Characterization of N-acylhomoserine lactone-degrading bacteria associated with the Zingiber officinale (ginger rhizosphere: Co-existence of quorum quenching and quorum sensing in Acinetobacter and Burkholderia

    Directory of Open Access Journals (Sweden)

    Chhabra Siri

    2011-03-01

    Full Text Available Abstract Background Cell-to-cell communication (quorum sensing (QS co-ordinates bacterial behaviour at a population level. Consequently the behaviour of a natural multi-species community is likely to depend at least in part on co-existing QS and quorum quenching (QQ activities. Here we sought to discover novel N-acylhomoserine lactone (AHL-dependent QS and QQ strains by investigating a bacterial community associated with the rhizosphere of ginger (Zingiber officinale growing in the Malaysian rainforest. Results By using a basal growth medium containing N-(3-oxohexanoylhomoserine lactone (3-oxo-C6-HSL as the sole source of carbon and nitrogen, the ginger rhizosphere associated bacteria were enriched for strains with AHL-degrading capabilities. Three isolates belonging to the genera Acinetobacter (GG2, Burkholderia (GG4 and Klebsiella (Se14 were identified and selected for further study. Strains GG2 and Se14 exhibited the broadest spectrum of AHL-degrading activities via lactonolysis while GG4 reduced 3-oxo-AHLs to the corresponding 3-hydroxy compounds. In GG2 and GG4, QQ was found to co-exist with AHL-dependent QS and GG2 was shown to inactivate both self-generated and exogenously supplied AHLs. GG2, GG4 and Se14 were each able to attenuate virulence factor production in both human and plant pathogens. Conclusions Collectively our data show that ginger rhizosphere bacteria which make and degrade a wide range of AHLs are likely to play a collective role in determining the QS-dependent phenotype of a polymicrobial community.

  15. The true nature of the Di-iron(III) gamma-Keggin structure in water: catalytic aerobic oxidation and chemistry of an unsymmetrical trimer.

    Science.gov (United States)

    Botar, Bogdan; Geletii, Yurii V; Kögerler, Paul; Musaev, Djamaladdin G; Morokuma, Keiji; Weinstock, Ira A; Hill, Craig L

    2006-08-30

    The complex [gamma(1,2)-SiW(10){Fe(OH(2))}(2)O(38)](6)(-) (1) has been reported to catalyze the much sought reductant-free selective O(2)-based epoxidation of alkenes (Nishiyama, Y.; Nakagawa, Y.; Mizuno, N. Angew. Chem. Int. Ed. 2001, 40, 3639-3641) in chlorocarbon-acetonitrile solution. The challenge of reproducing catalysis by 1 led us to examine this chemistry in detail. In H(2)O, a desirable solvent for catalysis, 1, does not exist in the proposed organic-medium form in which the two iron atoms are in the binding pocket defined by the equatorial oxygens and, importantly, by two oxygens bound to the central Si heteroatom. Instead, 1 in H(2)O initially forms an unusual trimer [{Fe(2)(OH)(3)(H(2)O)(2)}(3)(gamma-SiW(10)O(36))(3)](15)(-) (2). The X-ray structure of 2 shows that the Fe-O(Si) bonds are cleaved and new bonds (mu-hydroxo bridges) form between these Fe centers and those of the neighboring [gamma(1,2)-SiW(10)Fe(2)] units. Structural, physical, and computational evidence indicate that if the bonds between the d-electron center, M (Fe in the case of 1 and 2), and the terminal ligands on M are stronger than the M-O(x)() bonds, then the out-of-pocket form is more stable and is the one observed. Significantly, 2 in H(2)O forms an intermediate that catalyzes the effective aerobic oxidation of sulfur compounds (mercaptoethanol is oxidized to the corresponding disulfide by O(2) at ambient pressure and temperature). All experimental findings are consistent with dissociation of a gamma-SiW(10) Keggin unit from the trimer, 2, to form the catalytically active species. PMID:16925446

  16. Catalytic methanol dissociation

    International Nuclear Information System (INIS)

    Results of the methanol dissociation study on copper/potassium catalyst with alumina support at various temperatures are presented. The following gaseous and liquid products at. The catalytic methanol dissociation is obtained: hydrogen, carbon monoxide, carbon dioxide, methane, and dimethyl ether. Formation rates of these products are discussed. Activation energies of corresponding reactions are calculated

  17. Catalytic Phosphination and Arsination

    Institute of Scientific and Technical Information of China (English)

    Kwong Fuk Yee; Chan Kin Shing

    2004-01-01

    The catalytic, user-friendly phosphination and arsination of aryl halides and triflates by triphenylphosphine and triphenylarsine using palladium catalysts have provided a facile synthesis of functionalized aryl phosphines and arsines in neutral media. Modification of the cynaoarisne yielded optically active N, As ligands which will be screened in various asymmetric catalysis.

  18. Monolithic catalytic igniters

    Science.gov (United States)

    La Ferla, R.; Tuffias, R. H.; Jang, Q.

    1993-01-01

    Catalytic igniters offer the potential for excellent reliability and simplicity for use with the diergolic bipropellant oxygen/hydrogen as well as with the monopropellant hydrazine. State-of-the-art catalyst beds - noble metal/granular pellet carriers - currently used in hydrazine engines are limited by carrier stability, which limits the hot-fire temperature, and by poor thermal response due to the large thermal mass. Moreover, questions remain with regard to longevity and reliability of these catalysts. In this work, Ultramet investigated the feasibility of fabricating monolithic catalyst beds that overcome the limitations of current catalytic igniters via a combination of chemical vapor deposition (CVD) iridium coatings and chemical vapor infiltration (CVI) refractory ceramic foams. It was found that under all flow conditions and O2:H2 mass ratios tested, a high surface area monolithic bed outperformed a Shell 405 bed. Additionally, it was found that monolithic catalytic igniters, specifically porous ceramic foams fabricated by CVD/CVI processing, can be fabricated whose catalytic performance is better than Shell 405 and with significantly lower flow restriction, from materials that can operate at 2000 C or higher.

  19. Rapid disinfection of E-Coliform contaminated water using WO3 semiconductor catalyst by laser-induced photo-catalytic process.

    Science.gov (United States)

    Gondal, Mohammed A; Khalil, Amjad

    2008-04-01

    Laser-induced photo-catalysis process using WO(3) semiconductor catalyst was applied for the study of disinfection effectiveness of E-coliform-contaminated water. For this purpose, wastewater polluted with E-coliform bacteria was exposed to 355 nm UV radiations generated by third harmonic of Nd: YAG laser in special glass cell with and without WO(3) catalyst. E-Coliform quantification was performed by direct plating method to obtain the efficiency of each disinfection treatment. The dependence of disinfection process on laser irradiation energy, amount of catalyst and duration of laser irradiation was also investigated. The disinfection with WO(3) was quite efficient inactivating E-coliforms. For inactivation of E-coliforms, less than 8 minutes' laser irradiation was required, so that, the treated water complies with the microbial standards for drinking water. This study opens the possibility of application of this simple method in rural areas of developing countries using solar radiation. PMID:18324535

  20. Nano sponge Mn₂O ₃ as a new adsorbent for the preconcentration of Pd(II) and Rh(III) ions in sea water, wastewater, rock, street sediment and catalytic converter samples prior to FAAS determinations.

    Science.gov (United States)

    Yavuz, Emre; Tokalıoğlu, Serife; Sahan, Halil; Patat, Saban

    2014-10-01

    In this study, a nano sponge Mn2O3 adsorbent was synthesized and was used for the first time. Various parameters affecting the recovery values of Pd(II) and Rh(III) were examined. The tolerance limits (≥ 90 %) for both Pd(II) and Rh(III) ions were found to be 75,000 mg L(-1) Na(I), 75,000 mg L(-1) K(I), 50,000 mg L(-1) Mg(II) and 50,000 mg L(-1) Ca(II). A 30s contact time was enough for both adsorption and elution. A preconcentration factor of 100 was obtained by using 100mg of the nano sponge Mn2O3. The reusability of the adsorbent was 120 times. Adsorption capacities for Pd(II) and Rh(III) were found to be 42 and 6.2 mg g(-1), respectively. The detection limits were 1.0 µg L(-1) for Pd(II) and 0.37 µg L(-1) for Rh(III) and the relative standard deviations (RSD, %) were found to be ≤ 2.5%. The method was validated by analyzing the standard reference material, SRM 2556 (Used Auto Catalyst Pellets) and spiked real samples. The optimized method was applied for the preconcentration of Pd(II) and Rh(III) ions in water (sea water and wastewater), rock, street sediment and catalytic converter samples. PMID:25059126

  1. Catalytic thermal barrier coatings

    Science.gov (United States)

    Kulkarni, Anand A.; Campbell, Christian X.; Subramanian, Ramesh

    2009-06-02

    A catalyst element (30) for high temperature applications such as a gas turbine engine. The catalyst element includes a metal substrate such as a tube (32) having a layer of ceramic thermal barrier coating material (34) disposed on the substrate for thermally insulating the metal substrate from a high temperature fuel/air mixture. The ceramic thermal barrier coating material is formed of a crystal structure populated with base elements but with selected sites of the crystal structure being populated by substitute ions selected to allow the ceramic thermal barrier coating material to catalytically react the fuel-air mixture at a higher rate than would the base compound without the ionic substitutions. Precious metal crystallites may be disposed within the crystal structure to allow the ceramic thermal barrier coating material to catalytically react the fuel-air mixture at a lower light-off temperature than would the ceramic thermal barrier coating material without the precious metal crystallites.

  2. Photo-catalytic degradation of an oil-water emulsion using the photo-Fenton treatment process : effects and statistical optimization

    OpenAIRE

    Tony, Maha A.; Purcell, Patrick J.; Zhao, Y. Q.; Tayeb, Aghareed M.; El-Sherbiny, M.F.

    2009-01-01

    The application of advanced oxidation processes (AOPs) to the treatment of an effluent contaminated with hydrocarbon oils was investigated. The AOPs conducted were Fe2+/H2O2 (Fenton’s reagent), Fe2+/H2O2/UV (Photo-Fenton’s reagent) and UV-photolysis. These technologies utilize the very strong oxidizing power of hydroxyl radicals to oxidize organic compounds to harmless end products such as CO2 and H2O. A synthetic wastewater generated by emulsifying diesel oil and water was used. This wastewa...

  3. Catalytic Hydrogenation of Levulinic Acid in Water into g-Valerolactone over Bulk Structure of Inexpensive Intermetallic Ni-Sn Alloy Catalysts

    OpenAIRE

    Rodiansono Rodiansono; Maria Dewi Astuti; Abdul Ghofur; Kiky C. Sembiring

    2015-01-01

    A bulk structure of inexpensive intermetallic nickel-tin (Ni-Sn) alloys catalysts demonstrated highly selective in the hydrogenation of levulinic acid in water into g-valerolactone. The intermetallic Ni-Sn catalysts were synthesized via a very simple thermochemical method from non-organometallic precursor at low temperature followed by hydrogen treatment at 673 K for 90 min. The molar ratio of nickel salt and tin salt was varied to obtain the corresponding Ni/Sn ratio of 4.0, 3.0, 2.0, 1.5, a...

  4. Enhanced bromate formation during chlorination of bromide-containing waters in the presence of CuO: Catalytic disproportionation of hypobromous acid

    KAUST Repository

    Liu, Chao

    2012-10-16

    Bromate (BrO3 -) in drinking water is traditionally seen as an ozonation byproduct from the oxidation of bromide (Br-), and its formation during chlorination is usually not significant. This study shows enhanced bromate formation during chlorination of bromide-containing waters in the presence of cupric oxide (CuO). CuO was effective to catalyze hypochlorous acid (HOCl) or hypobromous acid (HOBr) decay (e.g., at least 104 times enhancement for HOBr at pH 8.6 by 0.2 g L-1 CuO). Significant halate concentrations were formed from a CuO-catalyzed hypohalite disproportionation pathway. For example, the chlorate concentration was 2.7 ± 0.2 μM (225.5 ± 16.7 μg L-1) after 90 min for HOCl (Co = 37 μM, 2.6 mg L-1 Cl2) in the presence of 0.2 g L-1 CuO at pH 7.6, and the bromate concentration was 6.6 ± 0.5 μM (844.8 ± 64 μg L -1) after 180 min for HOBr (Co = 35 μM) in the presence of 0.2 g L-1 CuO at pH 8.6. The maximum halate formation was at pHs 7.6 and 8.6 for HOCl or HOBr, respectively, which are close to their corresponding pKa values. In a HOCl-Br--CuO system, BrO3 - formation increases with increasing CuO doses and initial HOCl and Br- concentrations. A molar conversion (Br - to BrO3 -) of up to (90 ± 1)% could be achieved in the HOCl-Br--CuO system because of recycling of Br - to HOBr by HOCl, whereas the maximum BrO3 - yield in HOBr-CuO is only 26%. Bromate formation is initiated by the formation of a complex between CuO and HOBr/OBr-, which then reacts with HOBr to generate bromite. Bromite is further oxidized to BrO3 - by a second CuO-catalyzed process. These novel findings may have implications for bromate formation during chlorination of bromide-containing drinking waters in copper pipes. © 2012 American Chemical Society.

  5. Microstructural and compositional change of NaOH-activated high calcium fly ash by incorporating Na-aluminate and co-existence of geopolymeric gel and C–S–H(I)

    KAUST Repository

    Oh, Jae Eun

    2012-05-01

    This study explores the reaction products of alkali-activated Class C fly ash-based aluminosilicate samples by means of high-resolution synchrotron X-ray diffraction (HSXRD), scanning electron microscope (SEM), and compressive strength tests to investigate how the readily available aluminum affects the reaction. Class C fly ash-based aluminosilicate raw materials were prepared by incorporating Na-aluminate into the original fly ashes, then alkali-activated by 10 M NaOH solution. Incorporating Na-aluminate reduced the compressive strength of samples, with the reduction magnitude relatively constant regardless of length of curing period. The HSXRD provides evidence of the co-existence of C-S-H with geopolymeric gels and strongly suggests that the C-S-H formed in the current system is C-S-H(I). The back-scattered electron images suggest that the C-S-H(I) phase exists as small grains in a finely intermixed form with geopolymeric gels. Despite providing extra source of aluminum, adding Na-aluminate to the mixes did not decrease the Si/Al ratio of the geopolymeric gel. © 2012 Elsevier Ltd.

  6. Advances in gas flow metering - end of the history, peaceful co-existence or a new beginning; Les avancees dans le mesurage des debits de gaz - fin de l'histoire, coexistence pacifique ou nouveau commencement

    Energy Technology Data Exchange (ETDEWEB)

    Studzinski, W. [NOVA Research and Technology Centre, Calgary (Canada)

    2000-07-01

    Gas flow metering plays an important role in the technical and fiscal operations of pipeline systems. Over the last hundred years, the industry has gone through several technical revolutions. The recent two decades were characterized by the introduction of flow computers in the 80's and acceptance of ultrasonic meters in the 90's. These changes, associated with measurement technology, have had a profound impact on pipeline operation, deregulation of the gas industry and gas trading. Significant advances were made, however, it is certainly not the end for progress in gas flow metering. The future development of optoelectronic and mass flow meters combined with advances in telemetry and tele-calibration may significantly reduce capital and maintenance costs. Classical flow meters will be upgraded to a new level of performance and will co-exist with the newest technologies. The uncertainty of flow measurement will be improved, mainly in terms of stability over longer periods of time. Old and new meters will be able to perform in environments other than dry natural gas. Processing of flow measurement data will evolve with the progress in flow computers and smart transmitters. The advances in gas flow metering will be driven by life cycle cost reduction as well as new business and service requirements. (author)

  7. Hydrogen production from co-gasification of coal and biomass in supercritical water by continuous flow thermal-catalytic reaction system

    Institute of Scientific and Technical Information of China (English)

    YAN Qiuhui; GUO Liejin; LIANG Xing; ZHANG Ximin

    2007-01-01

    Hydrogen is a clean energy carrier.Converting abundant coal sources and green biomass energy into hydrogen effectively and without any pollution promotes environmental protection.The co-gasification performance of coal and a model compound of biomass,carboxymethylcellulose (CMC)in supercritical water (SCW),were investigated experimentally.The influences of temperature,pressure and concentration on hydrogen production from co-gasification of coal and CMC in SCW under the given conditions (20-25 MPa,650℃,15-30 s) are discussed in detail.The experimental results show that H2,CO2 and CH4 are the main gas products,and the molar fraction of hydrogen reaches in excess of 60%.The higher pressure and higher CMC content facilitate hydrogen production;production is decreased remarkably given a longer residence time.

  8. Treatment of reverse osmosis concentrated water by ClO2 three-phase catalytic oxidation%二氧化氯三相催化氧化法处理反渗透浓水试验研究

    Institute of Scientific and Technical Information of China (English)

    李常青; 杨岳; 刘发强; 刘光利; 江岩; 巫树峰

    2011-01-01

    In view of the fact that the reverse osmosis concentrated water from wastewater reuse device of Petrochemical Corporation is hard to be biodegraded for its high CODcr. And salt concentration, C1O2 three-phase catalytic oxidation process was used to treat the said kind of wastewater. The results of the test showed that: with the aid of catalyst under the condition that the optimal active components of the catalyst was CuO/NiO/La2O3/ CeO2, the optimal mole ratio of these metal oxides was 3 : 1 : 2 : 2; when the input flow of the reverse osmosis concentrated water was 50 L/h, the mass concentration of CODcr was 95 - 230 mg/L, the optimal pH value was 6.0 - 7.0, the C1O2 dosage was 90 - 120 mg/L, the air input was 0.6 - 0.9 mVh, the reaction time was 30 min, the removal rate of CODcr. Reached above 85%, the treated reverse osmosis concentrated water quality was stable and could meet the discharge standard. Thus it could draw a conclusion that, C1O2 three-phase catalytic oxidation is a feasible and competitive technology for reverse osmosis concentrated water treatment.%针对炼化企业污水回用装置反渗透单元浓水CODCr浓度高、难生化降解以及含盐量高等特点,利用ClO2三相催化氧化法处理反渗透浓水.试验结果表明:在催化剂存在条件下,催化剂的最佳活性组成为CuO/NiO/La2O3/CeO2,活性组分的最佳物质的量之比为3∶1∶2∶2;在反渗透浓水进水量为50 L/h、进水CODCr的质量浓度为95 ~ 230 mg/L时,最佳反应pH值为6.0~7.0,ClO2投加量为90~120 mg/L,空气进气量为0.6 ~ 0.9 m3/h,反应时间为30 min,CODCr去除率大于85%,处理后的反渗透浓水可以实现稳定达标排放.C1O2三相催化氧化处理反渗透浓水是一项具有良好实用性和很强竞争力的处理方法.

  9. Preparation and High-Temperature Water-Gas Shift Catalytic Features of La1-xCexFeO3 Perovskite

    Institute of Scientific and Technical Information of China (English)

    马红钦; 朱慧铭; 谭欣; 张继炎; 张鎏

    2004-01-01

    Based on water-gas shift reaction mechanism and perovskite compounds characteristics, La1-xCexFeO3 (.K) perovskite were designed and prepared as shift catalysts. DTA and XRD results reveal that La1-xCexFeO3 can be formed at 730~760 ℃ by mechanic-mix thermal decomposition method. Activity and heat-resisting tests show that La1-xCexFeO3 (.K) possess high thermal stability if x is less than or equals to 0.5. But when x is greater than 0.5, La1-xCexFeO3 (.K) will be converted into ceria and magnetite partially or completely under shift reaction conditions. In the case of x=0.5, the conversion of CO is about 68% at 530 ℃. Potassium can greatly improve the low temperature activity, but slightly reduces the high temperature activity, and has little impact on the thermal stability. La0.5Ce0.5FeO3 (.K) is a promising chromium-free high temperature shift catalyst.

  10. Catalytic reforming process

    Energy Technology Data Exchange (ETDEWEB)

    Absil, R.P.; Huss, A. Jr.; McHale, W.D.; Partridge, R.D.

    1989-06-13

    This patent describes a catalytic reforming process which comprises contacting a naphtha range feed with a low acidity extrudate comprising an intermediate and/or a large pore acidic zeolite bound with a low acidity refractory oxide under reforming conditions to provide a reaction product of increased aromatic content, the extrudate having been prepared with at least an extrusion-facilitating amount of a low acidity refractory oxide in colloidal form and containing at least one metal species selected from the platinum group metals.

  11. Modeling the Complete Catalytic Cycle of Aspartoacylase.

    Science.gov (United States)

    Kots, Ekaterina D; Khrenova, Maria G; Lushchekina, Sofya V; Varfolomeev, Sergei D; Grigorenko, Bella L; Nemukhin, Alexander V

    2016-05-12

    The complete catalytic cycle of aspartoacylase (ASPA), a zinc-dependent enzyme responsible for cleavage of N-acetyl-l-aspartate, is characterized by the methods of molecular modeling. The reaction energy profile connecting the enzyme-substrate (ES) and the enzyme-product (EP) complexes is constructed by the quantum mechanics/molecular mechanics (QM/MM) method assisted by the molecular dynamics (MD) simulations with the QM/MM potentials. Starting from the crystal structure of ASPA complexed with the intermediate analogue, the minimum-energy geometry configurations and the corresponding transition states are located. The stages of substrate binding to the enzyme active site and release of the products are modeled by MD calculations with the replica-exchange umbrella sampling technique. It is shown that the first reaction steps, nucleophilic attack of a zinc-bound nucleophilic water molecule at the carbonyl carbon and the amide bond cleavage, are consistent with the glutamate-assisted mechanism hypothesized for the zinc-dependent hydrolases. The stages of formation of the products, acetate and l-aspartate, and regeneration of the enzyme are characterized for the first time. The constructed free energy diagram from the reactants to the products suggests that the enzyme regeneration, but not the nucleophilic attack of the catalytic water molecule, corresponds to the rate-determining stage of the full catalytic cycle of ASPA. PMID:27089954

  12. Improved catalytic activity of laser generated bimetallic and trimetallic nanoparticles.

    Science.gov (United States)

    Singh, Rina; Soni, R K

    2014-09-01

    We report synthesis of silver nanoparticles, bimetallic (Al2O3@Ag) nanoparticles and trimetallic (Al2O3@AgAu) nanoparticles by nanosecond pulse laser ablation (PLA) in deionized water. Two-step laser ablation methodologies were adopted for the synthesis of bi- and tri-metallic nanoparticles. In this method a silver or gold target was ablated in colloidal solution of γ-alumina nanoparticles prepared by PLA. The TEM image analysis of bimetallic and trimetallic particles reveals deposition of fine silver particles and Ag-Au alloy particles, respectively, on large alumina particles. The laser generated nanoparticles were tested for catalytic reduction of 4-nitrophenol to 4-aminophenol and showed excellent catalytic behaviour. The catalytic rate was greatly improved by incorporation of additional metal in silver nanoparticles. The catalytic efficiency of trimetallic Al2O3@AgAu for reduction of 4-nitrophenol to 4-aminophenol was remarkably enhanced and the catalytic reaction was completed in just 5 sec. Even at very low concentration, both Al2O3@Ag nanoparticles and Al2O3@AgAu nanoparticles showed improved rate of catalytic reduction than monometallic silver nanoparticles. Our results demonstrate that alumina particles in the solution not only provide the active sites for particle dispersion but also improve the catalytic activity. PMID:25924343

  13. Numerical Study of Passive Catalytic Recombiner for Hydrogen Mitigation

    Directory of Open Access Journals (Sweden)

    Pavan K Sharma

    2010-10-01

    Full Text Available A significant amount of hydrogen is expected to be released within the containment of a water cooled power reactor after a severe accident. To reduce the risk of deflagration/detonation various means for hydrogen control have been adopted all over the world. Passive catalytic recombiner with vertical flat catalytic plate is one of such hydrogen mitigating device. Passive catalytic recombiners are designed for the removal of hydrogen generated in order to limit the impact of possible hydrogen combustion. Inside a passive catalytic recombiner, numerous thin steel sheets coated with catalyst material are vertically arranged at the bottom opening of a sheet metal housing forming parallel flow channels for the surrounding gas atmosphere. Already below conventional flammability limits, hydrogen and oxygen react exothermally on the catalytic surfaces forming harmless steam. Detailed numerical simulations and experiments are required for an in-depth knowledge of such plate type catalytic recombiners. Specific finite volume based in-house CFD code has been developed to model and analyse the working of these recombiner. The code has been used to simulate the recombiner device used in the Gx-test series of Battelle-Model Containment (B-MC experiments. The present paper briefly describes the working principle of such passive catalytic recombiner and salient feature of the CFD model developed at Bhabha Atomic Research Centre (BARC. Finally results of the calculations and comparison with existing data are discussed.

  14. Detection of protozoans Babesia microti and [i]Toxoplasma gondii[/i] and their co-existence in ticks (Acari: Ixodida collected in Tarnogórski district (Upper Silesia, Poland

    Directory of Open Access Journals (Sweden)

    Marek Asman

    2015-02-01

    Full Text Available [b]Introduction[/b]. Ticks (Acari: Ixodida are vectors of many pathogens i. a: [i]Babesia microti [/i][Bm] and [i]Toxoplasma gondii[/i] [Tg]. In Poland, Ixodes ricinus [Ir] is the main vector of both pathogens. This tick species and pathogens transmitted by them are a significant threat to human and animal health. objectives of the study. Detection of the protozoans Bm and Tg in ticks collected in the Tarnogórski district area. [b]Material and methods[/b]. The ticks were collected from vegetation and pets in the spring period of their activity on the territory of the Tarnogórski district. The parasites were preserved in 70% ethanol. DNA was isolated by ammonia method. Bm was detected by nested-PCR using specific primers for the 18S rRNA sequence. To detect the Tg a commercial kit was used. The PCR products were separated on 2% ethidium bromide stained agarose gels and visualised under UV light. [b]Results[/b]. It was showed that all collected ticks belonged to the species Ir. Bm was detected in 50.87% and Tg in 64.91% of all examined ticks. Co-existence of these both protozoans in 36.84% of total examined ticks was noted. [b]Conclusions[/b]. The study showed a high risk of exposure to Bm and Tg in the studied area. Ticks Ir play an important role in the transmission of Bm in this region. Demonstrating a high percentage of ticks collected from animals infected with Tg may indicate their important role in the transmission of this pathogen, but it requires a further studies.

  15. Evolution of random catalytic networks

    Energy Technology Data Exchange (ETDEWEB)

    Fraser, S.M. [Santa Fe Inst., NM (United States); Reidys, C.M. [Santa Fe Inst., NM (United States)]|[Los Alamos National Lab., NM (United States)

    1997-06-01

    In this paper the authors investigate the evolution of populations of sequences on a random catalytic network. Sequences are mapped into structures, between which are catalytic interactions that determine their instantaneous fitness. The catalytic network is constructed as a random directed graph. They prove that at certain parameter values, the probability of some relevant subgraphs of this graph, for example cycles without outgoing edges, is maximized. Populations evolving under point mutations realize a comparatively small induced subgraph of the complete catalytic network. They present results which show that populations reliably discover and persist on directed cycles in the catalytic graph, though these may be lost because of stochastic effects, and study the effect of population size on this behavior.

  16. Catalytic Combustion of Gasified Waste

    Energy Technology Data Exchange (ETDEWEB)

    Kusar, Henrik

    2003-09-01

    This thesis concerns catalytic combustion for gas turbine application using a low heating-value (LHV) gas, derived from gasified waste. The main research in catalytic combustion focuses on methane as fuel, but an increasing interest is directed towards catalytic combustion of LHV fuels. This thesis shows that it is possible to catalytically combust a LHV gas and to oxidize fuel-bound nitrogen (NH{sub 3}) directly into N{sub 2} without forming NO{sub x} The first part of the thesis gives a background to the system. It defines waste, shortly describes gasification and more thoroughly catalytic combustion. The second part of the present thesis, paper I, concerns the development and testing of potential catalysts for catalytic combustion of LHV gases. The objective of this work was to investigate the possibility to use a stable metal oxide instead of noble metals as ignition catalyst and at the same time reduce the formation of NO{sub x} In paper II pilot-scale tests were carried out to prove the potential of catalytic combustion using real gasified waste and to compare with the results obtained in laboratory scale using a synthetic gas simulating gasified waste. In paper III, selective catalytic oxidation for decreasing the NO{sub x} formation from fuel-bound nitrogen was examined using two different approaches: fuel-lean and fuel-rich conditions. Finally, the last part of the thesis deals with deactivation of catalysts. The various deactivation processes which may affect high-temperature catalytic combustion are reviewed in paper IV. In paper V the poisoning effect of low amounts of sulfur was studied; various metal oxides as well as supported palladium and platinum catalysts were used as catalysts for combustion of a synthetic gas. In conclusion, with the results obtained in this thesis it would be possible to compose a working catalytic system for gas turbine application using a LHV gas.

  17. Hydrophobic catalysts for liquid phase catalytic exchange: a review of preparation methods and influencing factors of catalytic activities

    International Nuclear Information System (INIS)

    Liquid phase catalytic exchange (LPCE) between liquid water and gaseous hydro- gen has been developed for various applications, such as tritium recovery, water upgrade and heavy-water production. Good wetproofing properties of the hydrophobic catalysts can make the reaction to proceed smoothly. In this article, the preparation methods of the hydrophobic catalysts and the factors affecting the catalytic activities are reviewed. In particular, progress on the hydrophobic Pt/C/inert carrier catalysts is introduced, including the selection of inert carrier and active metal carrier, and the preparation methods of carbon- supported Pt based catalysts. Basic research activities on controllable fabrication of hydro- phobic catalysts are discussed, including the LPCE reaction mechanism, and the relation between the microstructure of active metal and the catalytic activity, etc. Finally, questions remaining to be answered and future directions in the field of hydrophobic catalysts are discussed. (authors)

  18. Unsteady catalytic processes and sorption-catalytic technologies

    International Nuclear Information System (INIS)

    Catalytic processes that occur under conditions of the targeted unsteady state of the catalyst are considered. The highest efficiency of catalytic processes was found to be ensured by a controlled combination of thermal non-stationarity and unsteady composition of the catalyst surface. The processes based on this principle are analysed, in particular, catalytic selective reduction of nitrogen oxides, deep oxidation of volatile organic impurities, production of sulfur by the Claus process and by hydrogen sulfide decomposition, oxidation of sulfur dioxide, methane steam reforming and anaerobic combustion, selective oxidation of hydrocarbons, etc.

  19. Water

    Science.gov (United States)

    ... www.girlshealth.gov/ Home Nutrition Nutrition basics Water Water Did you know that water makes up more ... to drink more water Other drinks How much water do you need? top Water is very important, ...

  20. Catalytic pyrolysis of olive mill wastewater sludge

    Science.gov (United States)

    Abdellaoui, Hamza

    From 2008 to 2013, an average of 2,821.4 kilotons/year of olive oil were produced around the world. The waste product of the olive mill industry consists of solid residue (pomace) and wastewater (OMW). Annually, around 30 million m3 of OMW are produced in the Mediterranean area, 700,000 m3 year?1 in Tunisia alone. OMW is an aqueous effluent characterized by an offensive smell and high organic matter content, including high molecular weight phenolic compounds and long-chain fatty acids. These compounds are highly toxic to micro-organisms and plants, which makes the OMW a serious threat to the environment if not managed properly. The OMW is disposed of in open air evaporation ponds. After evaporation of most of the water, OMWS is left in the bottom of the ponds. In this thesis, the effort has been made to evaluate the catalytic pyrolysis process as a technology to valorize the OMWS. The first section of this research showed that 41.12 wt. % of the OMWS is mostly lipids, which are a good source of energy. The second section proved that catalytic pyrolysis of the OMWS over red mud and HZSM-5 can produce green diesel, and 450 °C is the optimal reaction temperature to maximize the organic yields. The last section revealed that the HSF was behind the good fuel-like properties of the OMWS catalytic oils, whereas the SR hindered the bio-oil yields and quality.

  1. Electrochemical catalytic treatment of phenol wastewater

    International Nuclear Information System (INIS)

    The slurry bed catalytic treatment of contaminated water appears to be a promising alternative for the oxidation of aqueous organic pollutants. In this paper, the electrochemical oxidation of phenol in synthetic wastewater catalyzed by ferric sulfate and potassium permanganate adsorbed onto active bentonite in slurry bed electrolytic reactor with graphite electrode has been investigated. In order to determine the optimum operating condition, the orthogonal experiments were devised and the results revealed that the system of ferric sulfate, potassium permanganate and active bentonite showed a high catalytic efficiency on the process of electrochemical oxidation phenol in initial pH 5. When the initial concentration of phenol was 0.52 g/L (the initial COD 1214 mg/L), up to 99% chemical oxygen demand (COD) removal was obtained in 40 min. According to the experimental results, a possible mechanism of catalytic degradation of phenol was proposed. Environmental estimation was also done and the results showed that the treated wastewater have little impact on plant growth and could totally be applied to irrigation.

  2. Catalytic production of biodiesel

    Energy Technology Data Exchange (ETDEWEB)

    Theilgaard Madsen, A.

    2011-07-01

    The focus of this thesis is the catalytic production of diesel from biomass, especially emphasising catalytic conversion of waste vegetable oils and fats. In chapter 1 an introduction to biofuels and a review on different catalytic methods for diesel production from biomass is given. Two of these methods have been used industrially for a number of years already, namely the transesterification (and esterification) of oils and fats with methanol to form fatty acid methyl esters (FAME), and the hydrodeoxygenation (HDO) of fats and oils to form straight-chain alkanes. Other possible routes to diesel include upgrading and deoxygenation of pyrolysis oils or aqueous sludge wastes, condensations and reductions of sugars in aqueous phase (aqueous-phase reforming, APR) for monofunctional hydrocarbons, and gasification of any type of biomass followed by Fischer-Tropsch-synthesis for alkane biofuels. These methods have not yet been industrialised, but may be more promising due to the larger abundance of their potential feedstocks, especially waste feedstocks. Chapter 2 deals with formation of FAME from waste fats and oils. A range of acidic catalysts were tested in a model fat mixture of methanol, lauric acid and trioctanoin. Sulphonic acid-functionalised ionic liquids showed extremely fast convertion of lauric acid to methyl laurate, and trioctanoate was converted to methyl octanoate within 24 h. A catalyst based on a sulphonated carbon-matrix made by pyrolysing (or carbonising) carbohydrates, so-called sulphonated pyrolysed sucrose (SPS), was optimised further. No systematic dependency on pyrolysis and sulphonation conditions could be obtained, however, with respect to esterification activity, but high activity was obtained in the model fat mixture. SPS impregnated on opel-cell Al{sub 2}O{sub 3} and microporous SiO{sub 2} (ISPS) was much less active in the esterification than the original SPS powder due to low loading and thereby low number of strongly acidic sites on the

  3. Catalytic performance of Fe3O4-CoO/Al2O3 catalyst in ozonation of 2-(2,4-dichlorophenoxy) propionic acid,nitrobenzene and oxalic acid in water

    Institute of Scientific and Technical Information of China (English)

    Shaoping Tong; Rui Shi; Hua Zhang; Chunan Ma

    2010-01-01

    the precursors,and its catalytic performance was investigated in ozonation of 2-(2,4-dichlorophenoxy) propionic acid (2,4-DP),nitrobenzene and oxalic acid.The experimental results indicated that Fe3O4-CoO/Al2O3 catalyst enabled an interesting improvement of ozonation efficiency during the degradation of each organic pollutant,and the Fe3O4-CoO/Al2O3 catalytic ozonation system followed a radical-type mechanism.The kinetics of ozonation alone and Fe3O4-CoO/Al2O3 catalytic ozonation of three organic pollutants in aqueous solution were discussed under the mere consideration of direct ozone reaction and OH radical reaction to well investigate its performance.In the catalytic ozonation of 2,4-DP,the apparent reaction rate constants (k) were determined to be 1.456×10-2 min-1 for ozonation alone and 4.740×10-2 min-1 for O3/Fe3O4-CoO/Al2O3.And O3/Fe3O4-CoO/Al2O3 had a larger Rct (6.614×10-9) calculated by the relative method than O3 did (1.800×10-9),showing O3/Fe3O4-CoO/Al2O3 generated more hydroxyl radical.Similar results were also obtained in the catalytic ozonation of nitrobenzene and oxalic acid.The above results demonstrated that the catalytic performance of Fe3O4-CoO/Al2O3 in ozonation of studied organic substance was universal to a certain degree.

  4. Qualification of a passive catalytic module for hydrogen mitigation

    International Nuclear Information System (INIS)

    The advantage of passive catalytic modules for hydrogen mitigation during core-melt accidents, as compared with active devices like forced-flow recombiners or ignitors, is given by the high reliability of operation and the elimination of potentially violent combustion events. An important step in the qualification of a passive catalytic module system is the determination of the total required capacity and its distribution at various locations in the containment. Experiments and analytic modeling work were performed to qualify the installation of a system of catalytic modules for a large dry pressurized water reactor (PWR) containment. The operational capacity of a prototype catalytic module was determined experimentally, and a corresponding model correlation was developed and integrated into the GOTHIC containment code. This modified code was validated against experimental data. As an application, predictions of the effects, resulting from backfitting a large, dry PWR containment with 50 catalytic modules, were done using the modified code. The catalytic modules keep the hydrogen concentrations below a level of 10% where violent deflagrations could be expected. Local higher concentrations near the release location are inert due to associated low oxygen and high steam concentrations. A proper distribution of the modules in the containment guarantees full mixing of the atmosphere due to natural convective currents

  5. Catalytic Pyrolysis of Olive Mill Wastewater Sludge

    OpenAIRE

    Abdellaoui, Hamza

    2015-01-01

    Olive mill wastewater sludge (OMWS) is the solid residue that remains in the evaporation ponds after evaporation of the majority of water in the olive mill wastewater (OMW). OMWS is a major environmental pollutant in the olive oil producing regions. Approximately 41.16 wt. % of the OMWS was soluble in hexanes (HSF). The fatty acids in this fraction consist mainly of oleic and palmitic acid. Catalytic pyrolysis of the OMWS over red mud and HZSM-5 has been demonstrated to be an effective techno...

  6. Immigration process in catalytic medium

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The longtime behavior of the immigration process associated with a catalytic super-Brownian motion is studied. A large number law is proved in dimension d≤3 and a central limit theorem is proved for dimension d=3.

  7. Catalytic Kinetic Determination of Bicarbonate and Carbonate in Leather Water by FIA%FIA-催化动力学法在线测定制革用水HCO3-和CO32-

    Institute of Scientific and Technical Information of China (English)

    俞凌云; 尚永昌; 安胜波; 卢艳青; 张新申

    2011-01-01

    A flow injection catalytic kinetic spectrophotometic method was developed for the rapid determination of bicarbonate and carbonate in water. The chromogenic reaction of trivalent chromium and xylenol orange is catalysed by bicarbonate and carbonate under heating condition. The optimum analysis conditions are as follows: detection wavelength is 550nm, temperature is 75 ℃;the length of the reaction coil is 3.9m; the volume of the sampling loop is 250μL; the concentration of chromogenic reagent R1 ( xylenol orange) is 0.004g/L and the concentration of chromogenic reagent R2 ( Chromium Nitrate) is 0.04mol/L. When the concentration of bicarbonate and carbonate was between 10mg/L and 220mg/L, the peak height was proportional was to the content of bicarbonate; the linear correlation coefficient is 0. 998 7; the relative standard deviation is 0. 609% measuring 10 times repeatedly. And the method is used to determine the content of bicarbonate in several samples, and it shows its good reproducibility and accuracy, with the recoveries of standard addition between 97.88% and 99.47%.%根据三价铬与二甲酚橙在碳酸氢根或碳酸根的催化作用下发生的显色反应,建立了流动注射催化动力学分光光度法,对水中的碳酸氢根和碳酸根浓度进行了检测.通过对各种影响因素进行优化,确定最佳分析条件为:波长550nm,温度75℃,反应圈3.9m,进样环体积250μL,R1显色液二甲酚橙的浓度为0.004g/L,R2显色液硝酸铬的浓度为0.04mol/L.HCO3-和CO32-含量在10~220mg/L范围内峰高与浓度成正比,线性相关系数为R2=0.9987,精密度RSD=0.609%(n=10).用该法检测实际水样中的碳酸氢根时,加标回收率为97.88%~99.47%,具有良好的重现性和准确性.

  8. Catalytic DNA with phosphatase activity

    OpenAIRE

    Chandrasekar, Jagadeeswaran; Silverman, Scott K.

    2013-01-01

    Catalytic DNA sequences (deoxyribozymes, DNA enzymes, or DNAzymes) have been identified by in vitro selection for various catalytic activities. Expanding the limits of DNA catalysis is an important fundamental objective and may facilitate practical utility of catalysts that can be obtained from entirely unbiased (random) sequence populations. In this study, we show that DNA can catalyze Zn2+-dependent phosphomonoester hydrolysis of tyrosine and serine side chains (i.e., exhibit phosphatase ac...

  9. Post-treatment of refinery wastewater effluent using a combination of AOPs (H2O2 photolysis and catalytic wet peroxide oxidation) for possible water reuse. Comparison of low and medium pressure lamp performance.

    Science.gov (United States)

    Rueda-Márquez, J J; Levchuk, I; Salcedo, I; Acevedo-Merino, A; Manzano, M A

    2016-03-15

    The main aim of this work was to study the feasibility of multi-barrier treatment (MBT) consisting of filtration, hydrogen peroxide photolysis (H2O2/UVC) and catalytic wet peroxide oxidation (CWPO) for post-treatment of petroleum refinery effluent. Also the possibility of water reuse or safe discharge was considered. The performance of MBT using medium (MP) and low (LP) pressure lamps was compared as well as operation and maintenance (O&M) cost. Decomposition of organic compounds was followed by means of gas chromatography-mass spectrometry (GC-MS), total organic carbon (TOC) and chemical oxygen demand (COD) analysis. After filtration step (25 μm) turbidity and concentration of suspended solids decreased by 92% and 80%, respectively. During H2O2/UVC process with LP lamp at optimal conditions (H2O2:TOC ratio 8 and UVC dose received by water 5.28 WUVC s cm(-2)) removal of phenolic compounds, TOC and COD was 100%, 52.3% and 84.3%, respectively. Complete elimination of phenolic compounds, 47.6% of TOC and 91% of COD was achieved during H2O2/UVC process with MP lamp at optimal conditions (H2O2:TOC ratio 5, UVC dose received by water 6.57 WUVC s cm(-2)). In order to compare performance of H2O2/UVC treatment with different experimental set up, the UVC dose required for removal of mg L(-1) of COD was suggested as a parameter and successfully applied. The hydrophilicity of H2O2/UVC effluent significantly increased which in turn enhanced the oxidation of organic compounds during CWPO step. After H2O2/UVC treatment with LP and MP lamps residual H2O2 concentration was 160 mg L(-1) and 96.5 mg L(-1), respectively. Remaining H2O2 was fully consumed during subsequent CWPO step (6 and 3.5 min of contact time for LP and MP, respectively). Total TOC and COD removal after MBT was 94.7% and 92.2% (using LP lamp) and 89.6% and 95%, (using MP lamp), respectively. The O&M cost for MBT with LP lamp was estimated to be 0.44 € m(-3) while with MP lamp it was nearly five

  10. Changes of Serotonin (5-HT), 5-HT2A Receptor, and 5-HT Transporter in the Sprague-Dawley Rats of Depression,Myocardial Infarction and Myocardial Infarction Co-exist with Depression

    Institute of Scientific and Technical Information of China (English)

    Mei-Yan Liu; Yah-Ping Ren; Wan-Lin Wei; Guo-Xiang Tian; Guo Li

    2015-01-01

    Background:To evaluate whether serotonin (5-HT),5-HT2A receptor (5-HT2AR),and 5-HT transporter (serotonin transporter [SERT]) are associated with different disease states of depression,myocardial infarction (MI) and MI co-exist with depression in Sprague-Dawley rats.Methods:After established the animal model of four groups include control,depression,MI and MI with depression,we measured 5-HT,5-HT2AR and SERT from serum and platelet lysate.Results:The serum concentration of 5-HT in depression rats decreased significantly compared with the control group (303.25 ± 9.99 vs.352.98 ± 13.73;P =0.000),while that in MI group increased (381.78 ± 14.17 vs.352.98 ± 13.73;P =0.000).However,the depression + MI group had no change compared with control group (360.62 ± 11.40 vs.352.98 ± 13.73;P =0.036).The changes of the platelet concentration of 5-HT in the depression,MI,and depression + MI group were different from that of serum.The levels of 5-HT in above three groups were lower than that in the control group (380.40 ± 17.90,387.75 ± 22.28,246.40 ± 18.99 vs.500.29 ± 20.91;P =0.000).The platelet lysate concentration of 5-HT2AR increased in depression group,MI group,and depression + MI group compared with the control group (370.75 ± 14.75,393.47 ± 15.73,446.66 ± 18.86 vs.273.66 ± 16.90;P =0.000).The serum and platelet concentration of SERT in the depression group,MI group and depression + MI group were all increased compared with the control group (527.51 ± 28.32,602.02 ± 23.32,734.76 ± 29.59 vs.490.56 ± 16.90;P =0.047,P =0.000,P =0.000 in each and 906.38 ± 51.84,897.33 ± 60.34,1030.17 ± 58.73 vs.708.62 ± 51.15;P =0.000 in each).Conclusions:The concentration of 5-HT2AR in platelet lysate and SERT in serum and platelet may be involved in the pathway of MI with depression.Further studies should examine whether elevated 5-HT2AR and SERT may contribute to the biomarker in MI patients with depression.

  11. Preparation of Pt-Ru hydrophobic catalysts and catalytic activities for liquid phase catalytic exchange reaction

    International Nuclear Information System (INIS)

    Pt/C and Pt-Ru/C catalysts with different ratios of Pt to Ru were synthesized, using ethylene glycol as both the dispersant and reducing agent at 1-2 MPa by microwave-assisted method. The catalysts were characterized by XRD, TEM and XPS. The mean particle sizes of the Pt/C and Pt-Ru/C catalysts were 1.9-2.0 nm. Pt and Ru existed as Pt(0), Pt(II), Pt(IV), Ru(0) and Ru(IV) for Pt-Ru/C catalysts, respectively. The face-centered cubic structure of the active mental particles would be changed upon the addition of Ru gradually. Then polytetrafluoroethylene and carbon-supported Pt and Pt-Ru catalysts were supported on foamed nickel to obtain hydrophobic catalysts. The catalytic activity was increased for liquid phase catalytic exchange (LPCE) when uniform Pt based hydrophobic catalysts was mixed into appropriate Ru. Hydrogen isotope exchange reaction occurs between hydration layer(H2O)nH+(ads)(n≥2) and D atoms due to intact water molecules being on Pt surface for LPCE. Water molecules have a tendency to dissociate to OH(ads) and H(ads) on metal Ru surface, and there is the other reaction path for Pt-Ru binary catalysts, which is probably the main reason of the increase of the catalytic activity of the hydrophobic Pt-Ru catalyst. (authors)

  12. Reduction of nitrate from groundwater: powder catalysts and catalytic membrane

    Institute of Scientific and Technical Information of China (English)

    CHEN Ying-xu; ZHANG Yan; LIU Hong-yuan

    2003-01-01

    The reduction of nitrate contaminant in groundwater has gained renewed and intensive attention due to the environmental problems and health risks. Catalytic denetrification presents one of the most promising approaches for the removal of nitrate from water. Catalytic nitrate reduction from water by powder catalysts and catalytic membrane in a batch reactor was studied. And the effects of the initial concentration, the amounts of catalyst, and the flux H2 on the nitrate reduction were also discussed. The results demonstrated that nitrate reduction activity and the selectivity to nitrogen gas were mainly controlled by diffusion limitations and the mass transfer of the reactants. The selectivity can improved while retaining a high catalytic activity under controlled diffusion condition or the intensification of the mass transfer, and a good reaction condition. The total nitrogen removal efficiency reached above 80%. Moreover, catalytic membrane can create a high effective gas/liquid/solid interface, and show a good selectivity to nitrogen in comparative with the powder catalyst, the selectivity to nitrogen was improved from 73.4% to 89.4%.

  13. 油包水微乳液中抗体酶催化布洛芬酯选择性水解的酶学特性%Enzymological Characteristics of Catalytic Antibody-catalyzed enantioselective Hydrolysis of Ibuprofen Ester in Water-in-oil microemulsion

    Institute of Scientific and Technical Information of China (English)

    杨根生; 戚映丹; 欧志敏; 姚善泾

    2009-01-01

    The asymmetric hydrolyzation of racemic ibuprofen ester is one of the most important methods for chiral separation of ibuprofen. A catalytic antibody that accelerates the rate of enantioselective hydrolysis of ibuprofen methyl ester was successfully elicited against an immunogen consisting of tetrahedral sulfate hapten attached to bovine serum albumin (BSA). The rate constant enhancement factor Kcat/Kuncat was about 1.6x104. The catalytic activity of the catalytic antibody in a reverse micelle reaction system based on sodium b/s (2-ethylhexyl) sodium sulfosuccinate (AOT) in isooctane was studied. Kinetic analysis of the catalytic antibody-catalyzed reaction was found to be possible in this system. Kinetic studies showed that hydrolysis in the microemulsion system follow Michaelis-Menten kinetics. The catalytic antibody can also accelerate catalysis of S-ibuprofen methyl ester in the microemulsion system. Temperature effects, the pH profile, Km,app and Kcat were determined. The dependence of the catalytic antibody hydrolytic activity on the Wo (molar ratio of water to surfactant) showed a bell-shaped curve, presenting a maximum at about wo = 21.%根据过渡态理论设计和合成了能诱导产生催化选择性水解布洛芬甲酯的催化抗体的四面体硫酸盐半抗原,并与牛血清白蛋白(BSA)偶联制备成免疫源,通过免疫手段成功筛选出具有加速选择性水解生成S-布洛芬的特异性催化抗体.其Kcat,app/Kuncat,app达1.6x104.进一步地将催化抗体运用到W/O微乳体系(反胶束)中进行布洛芬酯的选择性水解研究,其动力学研究证明其催化过程同样遵循Michaelis.Menten方程.考察了pH值和温度对催化初速度影响,Wo(体系中水和琥珀酸二辛酯磺酸钠(AOT)的摩尔比)对催化初速度影响呈现为钟罩型,最适的Wo.为21.

  14. Clay Minerals as Solid Acids and Their Catalytic Properties.

    Science.gov (United States)

    Helsen, J.

    1982-01-01

    Discusses catalytic properties of clays, attributed to acidity of the clay surface. The formation of carbonium ions on montmorillonite is used as a demonstration of the presence of surface acidity, the enhanced dissociation of water molecules when polarized by cations, and the way the surface can interact with organic substances. (Author/JN)

  15. The tritium labelling of butibufen by herterogeneous catalytic exchange

    International Nuclear Information System (INIS)

    The labelling of a new non-steroidal antiinflammatory agent, butibufen (2-(4-isobutylphenyl) butyric acid) was studied. The method used was heterogeneous catalytic exchange between butibufen and tritiated water, obtained ''in situ''. Purification was accomplished through thin layer chromatography. Concentration, purity and specific activity of the labeled drug were determined by ultraviolet and liquid scintillation techniques. (author)

  16. The tritium labeling of Butibufen by heterogeneous catalytic exchange

    International Nuclear Information System (INIS)

    The labeling of a new non-steroidal antiinflammatory agent, Butibufen (2-(4-isobutylphenyl) butyric acid) was studied. The method used was heterogeneous catalytic exchange between Butibufen and tritiated water, obtained in situ. Purification was accomplished through thin layer chromatography. Concentration, purity and specific activity of the labeled drug were determined by ultraviolet and liquid scintillation techniques. (Author) 7 refs

  17. 多重抗神经元抗体阳性的自身免疫性脑炎临床分析%Clinical analysis of autoimmune encephalitis with co-existence of multiple anti-neuronal antibodies

    Institute of Scientific and Technical Information of China (English)

    任海涛; 杨洵哲; 关鸿志; 高鑫雅; 彭斌; 朱以诚; 崔丽英

    2016-01-01

    antibodies to neuronal cell-surface or synaptic receptors (including N-methyl-D-aspartate receptor (NMDAR),contactin-associated protein-like 2 (CASPR2),α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR),leucine-rich glioma inactivated protein 1 (LGI1),and gamma-aminobutyric acid beta receptor (GABABR)).In those patients with positive antibodies,antibodies against intracellular neuronal antigens associated with paraneoplastic neurological symptoms were tested.Anti-aquaporin protein-4 (AQP4) antibody was tested depending on patients' clinical manifestations.Results Ten patients were detected combined with additional autoantibodies in 531 patients with positive antibodies related to autoimmune encephalitis.AntiHu antibody was positive in 5 patients with anti-GABABR encephalitis,in 1 of whom anti-NMDAR antibody was also identified;anti-AQP4 antibody was positive in 1 patient with relapsing anti-NMDAR encephalitis;anti-CASPR2 and anti-Yo antibodies were respectively positive in 2 patients with anti-LGI1 encephalitis;anti-CV2 and anti-Hu antibodies were respectively positive in 2 patients with anti-AMPAR encephalitis.Clinical presentation of all cases was consistent with typical encephalitis or limbic encephalitis.Brain stem was involved in 3 patients.Peripheral sensory neuropathy was present in 1 patient,while myalgia and fasciculation were present in 1 patient.Seven patients responded well to the immunotherapy.Tumors were pathologically or radiologically confirmed in 7 cases,including lung cancer in 5 cases,suspected thymoma in 1 case and highly suspected mediastinal tumor without pathological identification in 1 case.Conclusions Due to the pathological mechanism,co-existence of multiple autoantibodies affects clinical manifestations of patients and results in variation and overlap of them.The additional positivity of onconeuronal antibodies directs the search for occult tumor.

  18. Production of furfural from xylose, water-insoluble hemicelluloses and water-soluble fraction of corncob via a tin-loaded montmorillonite solid acid catalyst.

    Science.gov (United States)

    Li, Huiling; Ren, Junli; Zhong, Linjie; Sun, Runcang; Liang, Lei

    2015-01-01

    The conversion of xylose, water-insoluble hemicelluloses (WIH) and water-soluble fraction (WSF) of corncob to furfural was performed using montmorillonite with tin ions (Sn-MMT) containing double acid sites as a solid acid catalyst. The co-existence of Lewis acids and Brønsted acids in Sn-MMT was shown to improve the furfural yield and selectivity. 76.79% furfural yield and 82.45% furfural selectivity were obtained from xylose using Sn-MMT as a catalyst in a biphasic system with 2-s-butylphenol (SBP) as the organic extracting layer and dimethyl sulfoxide (DMSO) as the co-solvent in contact with an aqueous phase saturated with NaCl (SBP/NaCl-DMSO) at 180°C for 30min. Furthermore, Sn-MMT also demonstrated the excellent catalytic performance in the conversion of pentose-rich materials of corncob and 39.56% and 54.15% furfural yields can be directly obtained from WIH and WSF in the SBP/NaCl-DMSO system, respectively. PMID:25461009

  19. Catalytic activity of Au nanoparticles

    DEFF Research Database (Denmark)

    Larsen, Britt Hvolbæk; Janssens, Ton V.W.; Clausen, Bjerne;

    2007-01-01

    Au is usually viewed as an inert metal, but surprisingly it has been found that Au nanoparticles less than 3–5 nm in diameter are catalytically active for several chemical reactions. We discuss the origin of this effect, focusing on the way in which the chemical activity of Au may change with par......Au is usually viewed as an inert metal, but surprisingly it has been found that Au nanoparticles less than 3–5 nm in diameter are catalytically active for several chemical reactions. We discuss the origin of this effect, focusing on the way in which the chemical activity of Au may change...... with particle size. We find that the fraction of low-coordinated Au atoms scales approximately with the catalytic activity, suggesting that atoms on the corners and edges of Au nanoparticles are the active sites. This effect is explained using density functional calculations....

  20. Engineering reactors for catalytic reactions

    Indian Academy of Sciences (India)

    Vivek V Ranade

    2014-03-01

    Catalytic reactions are ubiquitous in chemical and allied industries. A homogeneous or heterogeneous catalyst which provides an alternative route of reaction with lower activation energy and better control on selectivity can make substantial impact on process viability and economics. Extensive studies have been conducted to establish sound basis for design and engineering of reactors for practising such catalytic reactions and for realizing improvements in reactor performance. In this article, application of recent (and not so recent) developments in engineering reactors for catalytic reactions is discussed. Some examples where performance enhancement was realized by catalyst design, appropriate choice of reactor, better injection and dispersion strategies and recent advances in process intensification/ multifunctional reactors are discussed to illustrate the approach.

  1. Catalytic Hydrothermal Gasification

    Energy Technology Data Exchange (ETDEWEB)

    Elliott, Douglas C.

    2015-05-31

    The term “hydrothermal” used here refers to the processing of biomass in water slurries at elevated temperature and pressure to facilitate the chemical conversion of the organic structures in biomass into useful fuels. The process is meant to provide a means for treating wet biomass materials without drying and to access ionic reaction conditions by maintaining a liquid water processing medium. Typical hydrothermal processing conditions are 523-647K of temperature and operating pressures from 4-22 MPa of pressure. The temperature is sufficient to initiate pyrolytic mechanisms in the biopolymers while the pressure is sufficient to maintain a liquid water processing phase. Hydrothermal gasification is accomplished at the upper end of the process temperature range. It can be considered an extension of the hydrothermal liquefaction mechanisms that begin at the lowest hydrothermal conditions with subsequent decomposition of biopolymer fragments formed in liquefaction to smaller molecules and eventually to gas. Typically, hydrothermal gasification requires an active catalyst to accomplish reasonable rates of gas formation from biomass.

  2. Fluid catalytic cracking of biomass pyrolysis vapors

    Energy Technology Data Exchange (ETDEWEB)

    Mante, Ofei Daku [Virginia Polytechnic Institute and State University, Biological Systems Engineering, Blacksburg, VA (United States); Agblevor, Foster A. [Utah State University, Biological Engineering, Logan, UT (United States); McClung, Ron [BASF Inc, Florham, NJ (United States)

    2011-12-15

    Catalytic cracking of pyrolysis oils/vapors offers the opportunity of producing bio-oils which can potentially be coprocessed with petroleum feedstocks in today's oil refinery to produce transportation fuel and chemicals. Catalyst properties and process conditions are critical in producing and maximizing desired product. In our studies, catalyst matrix (kaolin) and two commercial fluid catalytic cracking (FCC) catalysts, FCC-H and FCC-L, with different Y-zeolite contents were investigated. The catalytic cracking of hybrid poplar wood was conducted in a 50-mm bench-scale bubbling fluidized-bed pyrolysis reactor at 465 C with a weight hourly space velocity of 1.5 h{sup -1}. The results showed that the yields and quality of the bio-oils was a function of the Y-zeolite content of the catalyst. The char/coke yield was highest for the higher Y-zeolite catalyst. The organic liquid yields decreased inversely with increase in zeolite content of the catalyst whereas the water and gas yields increased. Analysis of the oils by both Fourier-transform infrared and {sup 13}C-nuclear magnetic resonance indicated that the catalyst with higher zeolite content (FCC-H) was efficient in the removal of compounds like levoglucosan, carboxylic acids and the conversion of methoxylated phenols to substituted phenols and benzenediols. The cracking of pyrolysis products by kaolin suggests that the activity of the FCC catalyst on biomass pyrolysis vapors can be attributed to both Y-zeolite and matrix. The FCC-H catalyst produced much more improved oil. The oil was low in oxygen (22.67 wt.%), high in energy (29.79 MJ/kg) and relatively stable over a 12-month storage period. (orig.)

  3. Study of catalytic phenomena in radiation chemistry

    International Nuclear Information System (INIS)

    Two phenomena have been studied: the action of γ rays from radio-cobalt on the adsorption and catalytic properties of ZnO and NiO in. relationship with the heterogeneous oxidation of CO, and the homogeneous catalysis by OsO4 of the oxidation of various aqueous phase solutes by the same radiation. The prior irradiation of ZnO and of NiO does not modify their catalytic activity but generally increases the adsorption energy of -the gases CO and O2. The influence of the radiations appears to be connected with the presence of traces of water on ZnO and of an excess of oxygen on NiO. Osmium tetroxide which is not degraded by irradiation in acid solution, accelerates the radiolytic oxidation of certain compounds (TeIV, Pt11, As111) in the presence of oxygen, as a result of its sensitizing effect on the oxidation by H2O2. In the case of phosphites on the other hand, OsO4 has a protecting action under certain conditions of acidity and may suppress entirely the chain reaction which characterizes the oxidation of this solute byγ rays. A general mechanism is proposed for these phenomena. The rate constant for the OsO4 + HO2 reaction is calculated to be 5.7 x 105 l.mol-1. sec-1. (author)

  4. Numerical and experimental investigations on catalytic recombiners

    International Nuclear Information System (INIS)

    Numerous containments of European light water reactors (LWR) are equipped with passive auto-catalytic recombiners (PAR). These devices are designed for the removal of hydrogen generated during a severe accident in order to avoid serious damage caused by a detonation. PARs make use of the fact that hydrogen and oxygen react exothermally on catalytic surfaces generating steam and heat even below conventional ignition concentrations and temperatures. Activities at ISR aim at overcoming existing limitations of today's systems. These are e.g. limited conversion capacity or unintended ignition of the gaseous mixture due to overheating of the catalyst elements caused by strong reaction heat generation. Experiments at the REKO facilities are conducted in order to achieve a profound understanding of the processes inside a recombiner, such as reaction kinetics or heat and mass transfer. Innovative PAR designs which may overcome existing limitations can be developed based on the knowledge obtained from these experiments. For the analysis of the processes inside a PAR the numerical code REKO-DIREKT is being developed. The code calculates the local catalyst temperatures and the concentration regression along the catalyst plates. For the validation of the model numerous experiments have been performed with different types of coating and different plate arrangements. The first calculations fit well with the experimental results indicating a proper understanding of the fundamental processes. The paper describes the experiments as well as the numerical model and presents model calculations in comparison with experimental results. (authors)

  5. Catalytic properties of niobium compounds

    International Nuclear Information System (INIS)

    The catalytic activity and selectivity of niobium compounds including oxides, salts, organometallic compounds and others are outlined. The application of these compounds as catalysts to diversified reactions is reported. The nature and action of niobium catalysts are characteristic and sometimes anomalous, suggesting the necessity of basic research and the potential use as catalysts for important processes in the chemical industry. (Author)

  6. Catalytic upgrading of biomass pyrolysis vapours using faujasite zeolite catalysts

    International Nuclear Information System (INIS)

    Bio-oil produced via fast pyrolysis of biomass has the potential to be processed in a FCC (fluid catalytic cracking) unit to generate liquid fuel. However, this oil requires a significant upgrade to become an acceptable feedstock for refinery plants due to its high oxygen content. One promising route to improve the quality of bio-oil is to pyrolyse the parent biomass in the presence of a catalyst. This work investigates the influence of faujasite catalysts on the pyrolysis of pinewood. Pyrolysis process with Na-faujasite, Na0.2H0.8-faujasite, and H-faujasite (Na-FAU, Na0.2H0.8-FAU, and H-FAU) were carried out in a fixed-bed reactor at 500 °C. It is shown that, in the same condition, catalytic upgrading of pyrolysis vapour is superior to in-situ catalytic pyrolysis of biomass when it comes to quality of bio-oil. The yields of coke, gas and water increase while that of organic phase decreases proportional with the concentration of protons in catalysts. Compared to the other two catalysts, Na0.2H0.8-FAU removes the most oxygen from bio-oil, reduces amount of acids and aldehydes/ketones which result in a higher energy-contained and more stable oil with less corrosive property. However, the biggest contribution to the oxygen removal is via the formation of reaction water, which is not an optimum path. This leaves space for future development. -- Highlights: ► Upgrading of biomass pyrolysis vapours was carried out using faujasite catalysts. ► Catalytic upgrading of pyrolysis vapours is superior to in-situ catalytic pyrolysis of biomass. ► Optimization of the amount of Na+ and H+ in faujasites is important. ► Losing high-energy hydrogen via the formation of reaction water is a drawback

  7. Catalytic Polymer Multilayer Shell Motors for Separation of Organics.

    Science.gov (United States)

    Lin, Zhihua; Wu, Zhiguang; Lin, Xiankun; He, Qiang

    2016-01-26

    A catalytic polymer multilayer shell motor has been developed, which effects fast motion-based separation of charged organics in water. The shell motors are fabricated by sputtering platinum onto the exposed surface of silica templates embedded in Parafilm, followed by layer-by-layer assembly of polyelectrolyte multilayers to the templates. The catalytic shell motors display high bubble propulsion with speeds of up to 260 μm s(-1) (13 body lengths per second). Moreover, the polyelectrolyte multilayers assembled at high pH (pH>9.0) adsorb approximately 89% of dye molecules from water, owing to the electrostatic interaction between the positively charged polymers and the anionic dye molecules, and subsequently release them at neutral pH in a microfluidic device. The efficient propulsion coupled with the effective adsorption behavior of the catalytic shell motors in a microfluidic device results in accelerated separation of organics in water and thus holds considerable promise for water analysis. PMID:26632275

  8. Experimental catalytic isotopic exchange column control

    International Nuclear Information System (INIS)

    Full text: In this paper we present a method for monitoring and control of the experimental catalytic isotopic exchange column which is part of ETRF (experimental tritium removal facility) of the ICIT Rm. Valcea. The initial data acquisition system based on analogue instruments is now upgraded to a fully digital system. Therefore we chose to use Compact Field Point which is a programmable automation controller (PAC) and LabVIEW software. To operate the catalytic isotopic exchange column there are some control loops that need to be operated simultaneously, namely: the heavy water column feed temperature and flow rate; the hydrogen gas column feed temperature; the flow rate and pressure at the top of the column; the water vapor flow rate; the hydrogen gas temperature at the condenser output. The human machine interface (HMI) realized with LabVIEW software is very friendly. The use of the PAC graphics interface makes isotopic exchange process operation easier for operators and researchers. The HMI has the functions to provide visualization of process parameters, to enable interaction with the process and also to provide alarms and event notification to operators about any abnormal situation in the plant. To interact with the process, detailed displays which contain specific control functions to operate the column, can be used. Usually, the faceplate display shows the controlled process variable and the output of the control loop. Furthermore, the set point and the operating mode of the control loop can be changed. Additionally, detailed information is available related to the parameters of PID controller and the different alarms that can be authorized in this control loop with its corresponding values of activation. (authors)

  9. Water

    International Nuclear Information System (INIS)

    An up-date overview of the situation of the Austrian waters is given by analyzing the status of the water quality (groundwater, surface waters) and water protection measures. Maps containing information of nitrate and atrazine in groundwaters (analyses at monitoring stations), nitrate contents and biological water quality of running waters are included. Finally, pollutants (nitrate, orthophosphate, ammonium, nitrite, atrazine etc.) trends in annual mean values and median values for the whole country for the years 1992-1999 are presented in tables. Figs. 5. (nevyjel)

  10. Catalytic Fast Pyrolysis: A Review

    Directory of Open Access Journals (Sweden)

    Theodore Dickerson

    2013-01-01

    Full Text Available Catalytic pyrolysis is a promising thermochemical conversion route for lignocellulosic biomass that produces chemicals and fuels compatible with current, petrochemical infrastructure. Catalytic modifications to pyrolysis bio-oils are geared towards the elimination and substitution of oxygen and oxygen-containing functionalities in addition to increasing the hydrogen to carbon ratio of the final products. Recent progress has focused on both hydrodeoxygenation and hydrogenation of bio-oil using a variety of metal catalysts and the production of aromatics from bio-oil using cracking zeolites. Research is currently focused on developing multi-functional catalysts used in situ that benefit from the advantages of both hydrodeoxygenation and zeolite cracking. Development of robust, highly selective catalysts will help achieve the goal of producing drop-in fuels and petrochemical commodities from wood and other lignocellulosic biomass streams. The current paper will examine these developments by means of a review of existing literature.

  11. Combined catalytic converter and afterburner

    Energy Technology Data Exchange (ETDEWEB)

    Ma, T.T.-H.

    1994-11-30

    This patent describes the combined use of a catalytic converter and afterburner. An afterburner chamber and a catalyst matrix are disposed in series within a casing. A combustible premixed charge is ignited in the afterburner chamber before it enters the catalyst matrix. This invention overcomes the problem encountered in previous designs of some of the premixed charge passing unreacted through the device unless a very long afterburner chamber is used. (UK)

  12. Catalytic combustion in gas stoves - Phase II

    Energy Technology Data Exchange (ETDEWEB)

    Hjelm, Anna-Karin [CATATOR AB, Lund (Sweden)

    2003-06-01

    . To overcome the latter, improved aeration of the system is needed, e.g. modification of nozzle-size and/or flame port plate. The effects of installing a retro-fit catalytic design onto the burner in the gas oven were also examined. Similar to the burners of the cooking plates, the emitted NO{sub x} was greatly reduced, i.e. up to 90 %. Other on-going projects using similar catalyst concepts as in this study have shown that the life-time of the catalyst, i.e. the mechanical stability and the catalytic activity, is extremely good (> 1000 h). To examine if this durability of the catalyst is limited in this specific application by deactivation caused by possible food spillage, a number of commonly used food ingredients were painted onto the catalysts and the activity of the catalyst prior to and after the 'deactivation' was investigated. The results show that no ingredients of organic type (fat, milk, egg, sugar) have any significant impact on the catalytic activity. Salt however was seen to block active reaction sites of the catalyst, but the tests showed that the catalyst could in this case be easily re-activated by simply washing it in water. The design modifications are very modest and the amount of catalyst is small, costing about 6-10 SEK (0.80-1.2 USD) per cooking plate.

  13. 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.

  14. Atomic Scale Analysis of the Enhanced Electro- and Photo-Catalytic Activity in High-Index Faceted Porous NiO Nanowires

    OpenAIRE

    Meng Shen; Ali Han; Xijun Wang; Yun Goo Ro; Alireza Kargar; Yue Lin; Hua Guo; Pingwu Du; Jun Jiang; Jingyu Zhang; Dayeh, Shadi A.; Bin Xiang

    2015-01-01

    Catalysts play a significant role in clean renewable hydrogen fuel generation through water splitting reaction as the surface of most semiconductors proper for water splitting has poor performance for hydrogen gas evolution. The catalytic performance strongly depends on the atomic arrangement at the surface, which necessitates the correlation of the surface structure to the catalytic activity in well-controlled catalyst surfaces. Herein, we report a novel catalytic performance of simple-synth...

  15. The tritium labelling of ibuprofen by heterogeneous catalytic exchange

    International Nuclear Information System (INIS)

    The tritium labelling of 2-(4-isobutylphenyl) propionic acid (ibuprofen) was performed. The method employed was heterogeneous catalytic exchange between ibuprofen and tritiated water. Prior to labelling, thermic stability of ibuprofen was studied. Purification was accomplished through thin layer chromatography (TLC) and high performance liquid chromatography (HPLC). Concentration, purity and specific activity of the labelled compound were determined by ultraviolet, HPLC and liquid scintillation techniques. (author)

  16. Catalytic Partial Oxidation of Biomass/Oil Mixture

    OpenAIRE

    Veselý, V; Hanika, J. (Jiří); Tukač, V.; LEDERER, J.; Kovač, D.

    2013-01-01

    Investigation was focussed to application of waste POX (partial oxidation), e.g., meal rape in form of suspension in high boiling hydrocarbons from crude oil distillation. There is an opportunity for utilization of biomass waste resulted from fuels bio-components production. A decrease of oxygen and water steam demand in feed for POX process was observed in this variant. Catalytic effect of iron nanoparticles or nickel nitrate as catalysts in improvement of the pilot plant biomass/oil partial...

  17. Catalytic pyrolysis of Pubescens to phenols over Ni/C catalyst

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    The pyrolysis of Pubescens over Ni/C catalyst was studied at 350°C in H2 flow.The presence of Ni/C catalyst efficiently improved the degradation of raw materials,and produced bio-oil with high content of phenols but low contents of acetic acid,furfural and water.In the reaction,Ni/C catalyst plays the role of catalytic decomposition and catalytic hydrogenation.The existence of the carbon carrier favors the formation of active Ni in small sizes with more defects,which results in high catalytic activity of Ni in biomass decomposition and selective production of phenols.

  18. Performance of a Novel Hydrophobic Mesoporous Material for High Temperature Catalytic Oxidation of Naphthalene

    Directory of Open Access Journals (Sweden)

    Guotao Zhao

    2014-01-01

    Full Text Available A high surface area, hydrophobic mesoporous material, MFS, has been successfully synthesized by a hydrothermal synthesis method using a perfluorinated surfactant, SURFLON S-386, as the single template. N2 adsorption and TEM were employed to characterize the pore structure and morphology of MFS. Static water adsorption test indicates that the hydrophobicity of MFS is significantly higher than that of MCM-41. XPS and Py-GC/MS analysis confirmed the existence of perfluoroalkyl groups in MFS which led to its high hydrophobicity. MFS was used as a support for CuO in experiments of catalytic combustion of naphthalene, where it showed a significant advantage over MCM-41 and ZSM-5. SEM was helpful in understanding why CuO-MFS performed so well in the catalytic combustion of naphthalene. Experimental results indicated that MFS was a suitable support for catalytic combustion of large molecular organic compounds, especially for some high temperature catalytic reactions when water vapor was present.

  19. Kinetics of heterogeneous catalytic reactions

    CERN Document Server

    Boudart, Michel

    2014-01-01

    This book is a critical account of the principles of the kinetics of heterogeneous catalytic reactions in the light of recent developments in surface science and catalysis science. Originally published in 1984. The Princeton Legacy Library uses the latest print-on-demand technology to again make available previously out-of-print books from the distinguished backlist of Princeton University Press. These paperback editions preserve the original texts of these important books while presenting them in durable paperback editions. The goal of the Princeton Legacy Library is to vastly increase acc

  20. Molecular catalytic coal liquid conversion

    Energy Technology Data Exchange (ETDEWEB)

    Stock, L.M.; Yang, Shiyong [Univ. of Chicago, IL (United States)

    1995-12-31

    This research, which is relevant to the development of new catalytic systems for the improvement of the quality of coal liquids by the addition of dihydrogen, is divided into two tasks. Task 1 centers on the activation of dihydrogen by molecular basic reagents such as hydroxide ion to convert it into a reactive adduct (OH{center_dot}H{sub 2}){sup {minus}} that can reduce organic molecules. Such species should be robust withstanding severe conditions and chemical poisons. Task 2 is focused on an entirely different approach that exploits molecular catalysts, derived from organometallic compounds that are capable of reducing monocyclic aromatic compounds under very mild conditions. Accomplishments and conclusions are discussed.

  1. Studies of Catalytic Model Systems

    DEFF Research Database (Denmark)

    Holse, Christian

    the Cu/ZnO nanoparticles is highly relevant to industrial methanol synthesis for which the direct interaction of Cu and ZnO nanocrystals synergistically boost the catalytic activity. The dynamical behavior of the nanoparticles under reducing and oxidizing environments were studied by means of ex situ...... observed by XPS as the nanoparticles are reduced. The Cu/ZnO nanoparticles are tested on a  µ-reactor platform and prove to be active towards methanol synthesis, making it an excellent model system for further investigations into activity depended morphology changes....

  2. Catalytic Spectrophotometric Determination of Chromium

    OpenAIRE

    STOYANOVA, Angelina Miltcheva

    2005-01-01

    The catalytic effect of chromium(III) and chromium(VI) on the oxidation of sulfanilic acid by hydrogen peroxide was studied. The reaction was followed spectrophotometrically by measuring the absorbance of the reaction product at 360 nm. Under the optimum conditions 2 calibration graphs (for chromium(III) up to 100 ng mL-1, and for chromium(VI) up to 200 ng mL-1) were obtained, using the ``fixed time'' method with detection limits of 4.9 ng mL-1 and 3.8 ng mL-1, respectively...

  3. Catalytic Combustion of Ethyl Acetate

    OpenAIRE

    ÖZÇELİK, Tuğba GÜRMEN; ATALAY, Süheyda; ALPAY, Erden

    2007-01-01

    The catalytic combustion of ethyl acetate over prepared metal oxide catalysts was investigated. CeO, Co2O3, Mn2O3, Cr2O3, and CeO-Co2O3 catalysts were prepared on monolith supports and they were tested. Before conducting the catalyst experiments, we searched for the homogeneous gas phase combustion reaction of ethyl acetate. According to the homogeneous phase experimental results, 45% of ethyl acetate was converted at the maximum reactor temperature tested (350 °C). All the prepare...

  4. Estimating the temperature of a catalytic converter

    Energy Technology Data Exchange (ETDEWEB)

    Ma, T.T.-H.

    1994-11-02

    A method is described for estimating the temperature in a catalytic converter used in the exhaust system of an internal combustion engine. Pressure sensors monitor the flow resistance across the catalytic converter to provide an indication of the temperature inside. This feedback system allows heating devices to be switched off and thus avoid overheating, while maintaining the catalytic converter's efficiency by assuring that it does not operate below its light off temperature. (UK)

  5. Estimating the temperature of a catalytic converter

    Energy Technology Data Exchange (ETDEWEB)

    Ma, T.T.-H.

    1994-11-02

    A method of estimating the temperature of a catalytic converter used in the exhaust system of an internal combustion engine is described. Heated exhaust gas oxygen (HEGO) sensors are placed upstream and downstream of the catalytic converter. The temperature of the catalytic converter shortly after start-up is measured by monitoring the resistance of the HEGO sensor's heating element. The downstream sensor is used for mixture control and to double check results of the upstream sensor. (UK)

  6. Bacterial Cellulose Supported Gold Nanoparticles with Excellent Catalytic Properties.

    Science.gov (United States)

    Chen, Meiyan; Kang, Hongliang; Gong, Yumei; Guo, Jing; Zhang, Hong; Liu, Ruigang

    2015-10-01

    Amidoxime surface functionalized bacterial cellulose (AOBC) has been successfully prepared by a simple two-step method without obviously changing the morphology of bacterial cellulose. AOBC has been used as the reducing agent and carrier for the synthesis of gold nanoparticles (AuNPs) that distributed homogeneously on bacterial cellulose surface. Higher content in amidoxime groups in AOBC is beneficial for the synthesis of AuNPs with smaller and more uniform size. The AuNPs/AOBC nanohybrids have excellent catalytic activity for reduction of 4-nitrophenol (4-NP) by using NaBH4. It was found that catalytic activity of AuNPs/AOBC first increases with increasing NaBH4 concentration and temperature, and then leveled off at NaBH4 concentration above 238 mM and temperature above 50 °C. Moreover, AuNPs with smaller size have higher catalytic activity. The highest apparent turnover frequency of AuNPs/AOBC is 1190 h(-1). The high catalytic activity is due to the high affinity of 4-NP with AuNPs/AOBC and the reduced product 4-aminophenol has good solubility in water in the presence of AuNPs/AOBC. The catalytic stability of the AuNPs/AOBC was estimated by filling a fluid column contained AuNPs/AOBC and used for continuously catalysis of the reduction of 4-NP by using NaBH4. The column works well without detection of 4-NP in the eluent after running for more than two months, and it is still running. This work provides an excellent catalyst based on bacterial cellulose stabilized AuNPs and has promising applications in industry. PMID:26357993

  7. Nanostructured Catalytic Reactors for Air Purification Project

    Data.gov (United States)

    National Aeronautics and Space Administration — This SBIR Phase II project proposes the development of lightweight compact nanostructured catalytic reactors for air purification from toxic gaseous organic...

  8. Nanostructured Catalytic Reactors for Air Purification Project

    Data.gov (United States)

    National Aeronautics and Space Administration — This SBIR Phase I project proposes the development of lightweight compact nanostructured catalytic reactors for air purification from toxic gaseous organic...

  9. Fabrication of MgAl2Si2O8 : M0.01 (M = Ni2+, Cu2+, Pd2+, Pt2+ and Ru3+): catalytic effects for the reduction of 2- or 4-nitroanilines in water

    Indian Academy of Sciences (India)

    Serkan Dayan; Sevgi Öztürk; Nilgün Kayaci; Nilgun Kalaycioglu Ozpozan; Esra Öztürk

    2015-10-01

    Five new MgAl2Si2O8 : M0.01 (M = Ni2+, Cu2+, Pd2+, Pt2+ and Ru3+) materials were developed for the reduction of nitroarenes as catalysts by conventional solid state reaction at 1300°C. The prepared materials were characterized by thermal analysis, Fourier transform infrared spectroscopy, X-ray powder diffraction analysis, scanning electron microscopy, energy-dispersive X-ray analysis and nitrogen adsorption–desorption analysis. The catalytic activities of the prepared catalysts were tested in the reduction of 2- or 4-nitroanilines in aqueous media at ambient temperature in the presence of NaBH4 by UV–vis spectrophotometer. Furthermore, the MgAl2Si2O8 : M0.01 catalysts can be recovered by filtration and reused for five cycles for the reduction of 2-nitroaniline. These results show that the MgAl2Si2O8 : M0.01 catalysts can be used in practical applications in the reduction of nitroanilines.

  10. Supercritical water

    CERN Document Server

    Marcus, Yizhak

    2012-01-01

    Discover the many new and emerging applications of supercritical water as a green solvent Drawing from thousands of original research articles, this book reviews and summarizes what is currently known about the properties and uses of supercritical water. In particular, it focuses on new and emerging applications of supercritical water as a green solvent, including the catalytic conversion of biomass into fuels and the oxidation of hazardous materials. Supercritical Water begins with an introduction that defines supercritical fluids in general. It then defines supercritical wa

  11. Catalytic conversion of light alkanes

    Energy Technology Data Exchange (ETDEWEB)

    Lyons, J.E.

    1992-06-30

    The second Quarterly Report of 1992 on the Catalytic Conversion of Light Alkanes reviews the work done between April 1, 1992 and June 31, 1992 on the Cooperative Agreement. The mission of this work is to devise a new catalyst which can be used in a simple economic process to convert the light alkanes in natural gas to oxygenate products that can either be used as clean-burning, high octane liquid fuels, as fuel components or as precursors to liquid hydrocarbon uwspomdon fuel. During the past quarter we have continued to design, prepare, characterize and test novel catalysts for the mild selective reaction of light hydrocarbons with air or oxygen to produce alcohols directly. These catalysts are designed to form active metal oxo (MO) species and to be uniquely active for the homolytic cleavage of the carbon-hydrogen bonds in light alkanes producing intermediates which can form alcohols. We continue to investigate three molecular environments for the active catalytic species that we are trying to generate: electron-deficient macrocycles (PHASE I), polyoxometallates (PHASE II), and regular oxidic lattices including zeolites and related structures as well as other molecular surface structures having metal oxo groups (PHASE I).

  12. Catalytic converters in the fireplace

    International Nuclear Information System (INIS)

    In addition to selecting the appropriate means of heating and using dry fuel, the amount of harmful emissions contained by flue gases produced by fireplaces can be reduced by technical means. One such option is to use an oxidising catalytic converter. Tests at TTS Institute's Heating Studies Experimental Station have focused on two such converters (dense and coarse) mounted in light-weight iron heating stoves. The ability of the dense catalytic converter to oxidise carbon monoxide gases proved to be good. The concentration of carbon monoxide in the flue gases was reduced by as much as 90 %. Measurements conducted by VTT (Technical Research Centre of Finland) showed that the conversion of other gases, e.g. of methane, was good. The exhaust resistance caused by the dense converter was so great as to necessitate the mounting of a fluegas evacuation fan in the chimney for the purpose of creating sufficient draught. When relying on natural draught, the dense converter requires a chimney of at least 7 metres and a by-pass connection while the fire is being lit. In addition, the converter will have to be constructed to be less dense and this will mean that it's capability to oxidise non-combusted gases will be reduced. The coarse converter did not impair the draught but it's oxidising property was insufficient. With the tests over, the converter was not observed to have become blocked up by impurities

  13. Catalytic reforming feed characterisation technique

    Energy Technology Data Exchange (ETDEWEB)

    Larraz Mora, R.; Arvelo Alvarez, R. [Univ. of La Laguna, Chemical Engineering Dept., La Laguna (Spain)

    2002-09-01

    The catalytic reforming of naphtha is one of the major refinery processes, designed to increase the octane number of naphtha or to produce aromatics. The naphtha used as catalytic reformer feedstock usually contains a mixture of paraffins, naphthenes, and aromatics in the carbon number range C{sub 6} to C{sub 10}. The detailed chemical composition of the feed is necessary to predict the aromatics and hydrogen production as well as the operation severity. The analysis of feed naphtha is usually reported in terms of its ASTM distillation curve and API or specific gravity. Since reforming reactions are described in terms of lumped chemical species (paraffins, naphthenes and aromatics), a feed characterisation technique should be useful in order to predict reforming operating conditions and detect feed quality changes. Unfortunately online analyzer applications as cromatography or recently introduced naphtha NMR [1] are scarce in most of refineries. This work proposes an algorithmic characterisation method focusing on its main steps description. The method could help on the subjects previously described, finally a calculation example is shown. (orig.)

  14. Catalytic hot gas cleaning of gasification gas

    Energy Technology Data Exchange (ETDEWEB)

    Simell, P. [VTT Energy, Espoo (Finland). Energy Production Technologies

    1997-12-31

    The aim of this work was to study the catalytic cleaning of gasification gas from tars and ammonia. In addition, factors influencing catalytic activity in industrial applications were studied, as well as the effects of different operation conditions and limits. Also the catalytic reactions of tar and ammonia with gasification gas components were studied. The activities of different catalyst materials were measured with laboratory-scale reactors fed by slip streams taken from updraft and fluid bed gasifiers. Carbonate rocks and nickel catalysts proved to be active tar decomposing catalysts. Ammonia decomposition was in turn facilitated by nickel catalysts and iron materials like iron sinter and iron dolomite. Temperatures over 850 deg C were required at 2000{sup -1} space velocity at ambient pressure to achieve almost complete conversions. During catalytic reactions H{sub 2} and CO were formed and H{sub 2}O was consumed in addition to decomposing hydrocarbons and ammonia. Equilibrium gas composition was almost achieved with nickel catalysts at 900 deg C. No deactivation by H{sub 2}S or carbon took place in these conditions. Catalyst blocking by particulates was avoided by using a monolith type of catalyst. The apparent first order kinetic parameters were determined for the most active materials. The activities of dolomite, nickel catalyst and reference materials were measured in different gas atmospheres using laboratory apparatus. This consisted of nitrogen carrier, toluene as tar model compound, ammonia and one of the components H{sub 2}, H{sub 2}O, CO, CO{sub 2}, CO{sub 2}+H{sub 2}O or CO+CO{sub 2}. Also synthetic gasification gas was used. With the dolomite and nickel catalyst the highest toluene decomposition rates were measured with CO{sub 2} and H{sub 2}O. In gasification gas, however, the rate was retarded due to inhibition by reaction products (CO, H{sub 2}, CO{sub 2}). Tar decomposition over dolomite was modelled by benzene reactions with CO{sub 2}, H

  15. Catalytic Conversion of Cellulose to Levulinic Acid by Metal Chlorides

    Directory of Open Access Journals (Sweden)

    Beixiao Zhang

    2010-08-01

    Full Text Available The catalytic performance of various metal chlorides in the conversion of cellulose to levulinic acid in liquid water at high temperatures was investigated. The effects of reaction parameters on the yield of levulinic acid were also explored. The results showed that alkali and alkaline earth metal chlorides were not effective in conversion of cellulose, while transition metal chlorides, especially CrCl3, FeCl3 and CuCl2 and a group IIIA metal chloride (AlCl3, exhibited high catalytic activity. The catalytic performance was correlated with the acidity of the reaction system due to the addition of the metal chlorides, but more dependent on the type of metal chloride. Among those metal chlorides, chromium chloride was found to be exceptionally effective for the conversion of cellulose to levulinic acid, affording an optimum yield of 67 mol % after a reaction time of 180 min, at 200 °C, with a catalyst dosage of 0.02 M and substrate concentration of 50 wt %. Chromium metal, most of which was present in its oxide form in the solid sample and only a small part in solution as Cr3+ ion, can be easily separated from the resulting product mixture and recycled. Finally, a plausible reaction scheme for the chromium chloride catalyzed conversion of cellulose in water was proposed.

  16. Catalytic combustion of actual low and medium heating value gases

    Science.gov (United States)

    Bulzan, D. L.

    1982-01-01

    Catalytic combustion of both low and medium heating value gases using actual coal derived gases obtained from operating gasifiers was demonstrated. A fixed bed gasifier with a complete product gas cleanup system was operated in an air blown mode to produce low heating value gas. A fluidized bed gasifier with a water quench product gas cleanup system was operated in both an air enriched and an oxygen blown mode to produce low and medium, heating value gas. Noble metal catalytic reactors were evaluated in 12 cm flow diameter test rigs on both low and medium heating value gases. Combustion efficiencies greater than 99.5% were obtained with all coal derived gaseous fuels. The NOx emissions ranged from 0.2 to 4 g NO2 kg fuel.

  17. Heterogeneous Photo catalytic Degradation of Hazardous Waste in Aqueous Suspension

    International Nuclear Information System (INIS)

    The photo catalytic degradation of hazardous waste like chlorinated paraffin compound (1,12-Dichlorodoecane Ded) was investigated in different aquatic media using GC-MSD. The direct photolysis of Ded in HPLC water was considered to be negligible (k = 0.0020+-0.0007h-1). An acceleration of the photodegradation rate was occurred in presence of different TiO2 catalyst systems. Molecular oxygen was found to play a vital role in the degradation process. Anatase TiO2 was proved to be the most efficient one (k=0.7670+-0.0876h-1), while the rate constant of the rutile TiO2 was calculated to be 0.2780+-0.0342h-1. Improvement of photo catalytic efficiency of rutile TiO2 was achieved by addition of Fe+2 giving a rate constant =0.6710+-0.0786h-1

  18. Process design for wastewater treatment: catalytic ozonation of organic pollutants.

    Science.gov (United States)

    Derrouiche, S; Bourdin, D; Roche, P; Houssais, B; Machinal, C; Coste, M; Restivo, J; Orfão, J J M; Pereira, M F R; Marco, Y; Garcia-Bordeje, E

    2013-01-01

    Emerging micropollutants have been recently the target of interest for their potential harmful effects in the environment and their resistance to conventional water treatments. Catalytic ozonation is an advanced oxidation process consisting of the formation of highly reactive radicals from the decomposition of ozone promoted by a catalyst. Nanocarbon materials have been shown to be effective catalysts for this process, either in powder form or grown on the surface of a monolithic structure. In this work, carbon nanofibers grown on the surface of a cordierite honeycomb monolith are tested as catalyst for the ozonation of five selected micropollutants: atrazine (ATZ), bezafibrate, erythromycin, metolachlor, and nonylphenol. The process is tested both in laboratorial and real conditions. Later on, ATZ was selected as a target pollutant to further investigate the role of the catalytic material. It is shown that the inclusion of a catalyst improves the mineralization degree compared to single ozonation. PMID:24056437

  19. Pherotypes of pneumococcal strains co-existing in healthy children.

    Science.gov (United States)

    Vestrheim, Didrik F; Gaustad, Peter; Aaberge, Ingeborg S; Caugant, Dominique A

    2011-10-01

    Genetic diversity in the species Streptococcus pneumoniae is mainly driven by horizontal gene transfer. S. pneumoniae is naturally competent for transformation. Competence is induced by a pheromone termed competence stimulating peptide (CSP) by a quorum-sensing mechanism. Two CSP pherotypes predominate amongst clinical isolates of S. pneumoniae, CSP-1 and CSP-2, with ability to trigger competence in bacteria of the homologue pherotype. Opposing theories on the effect of pherotypes on speciation have been proposed, either as a barrier for intra-pherotype gene transfer, or as a mechanism for fratricide resulting in lysis of non-competent bacterial cells. The aim of the present study was to determine pherotype distribution in strains of S. pneumococci isolated from the nasopharynges of healthy children. We sequenced the locus encoding CSP, comC, in sets of strains obtained from children colonised by multiple pneumococcal strains simultaneously. The impact of pherotype on co-colonisation was determined by comparing the observed distribution of pherotypes in co-colonising strains with the estimated pair-wise probability based on the overall pherotype distribution in the sample set. Five distinct comC alleles were identified, encoding CSP belonging to the two dominating pherotypes, CSP-1 (62.7%) and CSP-2 (37.3%). The observed distribution of pherotypes in sets of co-colonising pneumococcal strains did not differ from the probability estimate. Thus, co-colonisation of S. pneumoniae in healthy children is not restricted by pherotype. PMID:21763465

  20. Waste management and quality assurance: Reasonable co-existence?

    Energy Technology Data Exchange (ETDEWEB)

    Bresson, J.F.

    1989-11-01

    Implementing Chapter 3, Low-Level Waste Management, of DOE Order 5820-2, ``Radioactive Waste Management`` has created a major change in the operating philosophy of DOE`s prime contractors. So has the decision of May 1, 1987, when it was made clear that EPA has regulatory authority over DOE`s mixed waste. Suddenly two additional items became clear. First, DOE and its contractors were going to learn more about composition of low-level and low-level mixed waste than ever before. Second, low-level waste management was about to become a more focused, formal program, complete with needs for: (1) waste form identification, (2) program documentation; and (3) assurance that DOE`s waste does in fact comply with applicable requirements. The importance of the above items is clearly emphasized by the inclusion of Data Quality Objectives in the Waste Acceptance Criteria section of DOE 5820-2 Chapter 3 guidance called Data Quality Objectives, (DQO). Simply put, the purpose of the DQO is to identify the quality (and quantity) of information necessary to convince a regulator or decision maker that enough is known about DOE`s low-level and low-level mixed waste to allow safe disposal. The main objectives of the DOE and EPA shallow land burial requirements are to: (1) generate, with documented evidence, waste forms which are chemically inert and immobile, such that the waste will not tend to move about in the disposal medium; (2) select a disposal medium which would not let the wastes move about anyway; and (3) build some barriers around the wastes as emplaced in burial grounds, to provide additional assurance that buried wastes will stay in place. Compliance with these requirements must be demonstrated by quality data which describes the entire series of compliance activities.

  1. The Co-existence of Innovation and Platforms

    DEFF Research Database (Denmark)

    Hansen, Poul H. Kyvsgård; Gertsen, Frank; Bessant, John

    2006-01-01

    This paper present explorative results from an initial effort to explore the current state and the actual requirements to combine the challenges in meeting the need for efficient platforms and the need for effectiveness in terms of a sufficient high degree of newness to the customer. Empirical ob...

  2. Co-existence of hepatitis A and adult Reye's syndrome.

    OpenAIRE

    Duerksen, D R; Jewell, L.D.; Mason, A L; Bain, V. G.

    1997-01-01

    Reye's syndrome is most frequently seen in children but has also been described in adults. This syndrome is usually associated with ingestion of 5-aminosalicylates (ASA) or infection with influenza A, influenza B, or varicella virus. A case of Reye's syndrome in a 47 year old, previously healthy woman precipitated by ingestion of ASA and acute hepatitis A virus infection is described. Reye's syndrome was diagnosed on the basis of her clinical course, and the presence of hepatic microvesicular...

  3. Tobacco or healthy children: the two cannot co-exist.

    Science.gov (United States)

    Pattemore, Philip Keith

    2013-01-01

    Tobacco exposure increases mortality and morbidity of the fetus, the child, the adolescent, and their children in turn. Nearly half the children in the world are exposed. Smoking is not merely personal choice or personal responsibility; those subtle phrases undermine those who have no choice in the matter. Tobacco control must take a multi-pronged attack. Smoking cessation by adults in childbearing years must take center stage of these efforts, because it is the only way to ensure a smoke-free environment for children. Smoke-free parents provide a role model for smoke-free young people, and erode the image of smoking as a desirable adult behavior to emulate. Pediatricians and pediatric pulmonologists have a key role to play here. This goal will reduce morbidity and mortality among adults and children. Legislation regarding taxation, environments, tobacco constituents, product placement and display, packaging, and media education are all key to this core goal. Smoke-free policy must be protected from attack based on trade agreements. Research is needed into more effective ways to attract and help people give up smoking, and into educating and re-deploying tobacco industry workers in emerging and developed countries. PMID:24400266

  4. Birds and wind turbines: can they co-exist?

    International Nuclear Information System (INIS)

    The wind farm is situated along an exposed pier at Blyth Harbour and has now been designated as part of a SSI and part of a proposed RAMSAR site. The bird activity within the harbour is high and is also the wintering home of the Purple Sandpiper. An offshore wind farm is proposed for the area, one kilometre from the pier. Two turbines will be erected with the support of the European Commission THERMIE Programme. The bird study at Blyth has been funded by Border Wind, Blyth Harbour Wind Farm Company and the DTI as part of an ETSU funded study. (UK)

  5. Added value, co-existence and the environment

    International Nuclear Information System (INIS)

    Based on interviews and data from various studies of the Northern Norway, it is concluded that establishing oil industry in Northern Norway will have a positive co-localisation effect on other industries in the region. The analysis is based on models from economic geography affirming that the establishment or termination of an enterprise creates positive or negative effects for the availability and input factor cost for other companies in the same place (ml)

  6. Dams and river dolphins: Can they co-exist?

    International Nuclear Information System (INIS)

    Dam construction is one of many ways that humans have modified river-dolphin habitats. It is suggested that physiographic and hydrologic complexity plays an important role in making rivers suitable for dolphins. If this hypothesis is true, then it can be assumed that dams and other artificial obstructions degrade dolphin habitat insofar as they reduce such complexity. This paper identifies some of the impacts that dams, barrages, and dikes might have on dolphins. Research is needed at project sites, both before and after construction, to document impacts. Specially designed ''swimways'' may allow upstream and downstream passage by dolphins and thus mitigate at least one of the adverse effects of dam projects, namely population fragmentation, but such measures aimed at benefiting single species are no substitute for protecting ecosystems. 30 refs

  7. Electrical signaling and photosynthesis: Can they co-exist together?

    OpenAIRE

    Pavlovič, Andrej; Mancuso, Stefano

    2011-01-01

    Mechanical irritation of trigger hairs and subsequent generation of action potentials have significant impact on photosynthesis and respiration in carnivorous Venus flytrap (Dionaea muscipula). Action potential-mediated inhibition of photosynthesis and stimulation of respiration is confined only to the trap and was not recorded in adjacent photosynthetic lamina. We showed that the main primary target of electrical signals on assimilation is in the dark enzymatic reaction of photosynthesis. Wi...

  8. Tobacco or healthy children: the two cannot co-exist

    Directory of Open Access Journals (Sweden)

    Philip Keith Pattemore

    2013-08-01

    Full Text Available Tobacco exposure increases mortality and morbidity of the fetus, the child, the adolescent, and their children in turn. Nearly half the children in the world are exposed. Smoking is not merely personal choice or personal responsibility; those subtle phrases undermine those who have no choice in the matter.Tobacco control must take a multi-pronged attack. Smoking cessation by adults in childbearing years must take centre stage of these efforts, because it is the only way to ensure a smoke-free environment for children. Smoke-free parents provide a role model for smoke-free young people, and erode the image of smoking as a desirable adult behaviour to emulate. Pediatricians and pediatric pulmonologists have a key role to play here. This goal will reduce morbidity and mortality among adults and children. Legislation regarding taxation, environments, tobacco constituents, product placement and display, packaging, and media education are all key to this core goal. Smokefree policy must be protected from attack based on trade agreements.Research is needed into more effective ways to attract and help people give up smoking, and into educating and re-deploying tobacco industry workers in emerging and developed countries.

  9. Molar Pregnancy with a Co-Existing Viable Fetus

    OpenAIRE

    Ruya Deveer

    2014-01-01

        The aim of this study was to report the clinical features, management, and outcome of a case of molar pregnancy with a coexisting viable fetus and to review the literature. In this article, we report a case of pregnancy with diffuse placental molar change and a normal fetus which presented with hyperemesis gravidarum and hyperthyroidism. Genetic amniocentesis showed normal fetal karyotype. A healthy full-term live male infant was delivered by cesarean section. In molar preg...

  10. Newspaper and internet display advertising - co-existence or substitution?

    OpenAIRE

    Lindstädt, Nadine; Budzinski, Oliver

    2012-01-01

    Newspapers have been experiencing declining circulation figures and diminishing advertising revenues for several years – both effects might pose a threat to the continuing existence of (print) newspapers. In an earlier paper, Lindstädt & Budzinski (2011) argued from a theoretical viewpoint that industry-specific patterns exist that determine substitution or complementation effects between internet and newspaper advertising. It was argued that retail advertising, in particular, may offer a nic...

  11. Aconitase: its source of catalytic protons

    International Nuclear Information System (INIS)

    An ordinary isotope partition experiment was performed to determine the rate of dissociation of the proton from the donor site for the hydration of cis-aconitate. Aconitase in [3H] water was efficiently diluted into well-mixed solutions of cis-aconitate. Citrate and isocitrate that were formed within 2 s were more heavily labeled than could be explained by consideration of an isotope effect in the processing of one proton per enzyme equivalent. Control experiments indicate that mixing was much more rapid than catalytic turnover, ruling out incompletely diluted [3H] water as a significant isotope source. Therefore, it appears that significantly more than one enzyme-bound tritium atom (protons) must have been used in the course of the multiple turnover of the enzyme after the dilution was complete. Isotope incorporation reached values in excess of four proton equivalent as a limit with simple Michaelis dependence on cis-aconitate. From the half-saturation concentration value for trapping, 0.15 mM, the t/sub 1/2/ for exchange of each of these protons with solvent appears to be ∼0.1 s at 00C. The large number of protons trapped seems to suggest the existence of a structurally stabilized pool of protons, or water, that communicates between the active site base and the medium in the hydration of cis-aconitate. The proton abstracted in the dehydration of [3H] citrate is transferred directly to undissociated cis-aconitate to form isocitrate without dilution, or cis-aconitate having dissociated, the tritium passes to the medium, presumably through the pool of bound protons indicated above. All of the citrate-derived protons can be found in isocitrate if cis-aconitate is added in sufficient concentration. Therefore, the abstracted proton dissociates slowly, if at all, from the enzyme in all intermediates except those from which cis-aconitate has dissociated

  12. Acoustics of automotive catalytic converter assemblies

    Science.gov (United States)

    Dickey, Nolan S.; Selamet, Ahmet; Parks, Steve J.; Tallio, Kevin V.; Miazgowicz, Keith D.; Radavich, Paul M.

    2003-10-01

    In an automotive exhaust system, the purpose of the catalytic converter is to reduce pollutant emissions. However, catalytic converters also affect the engine and exhaust system breathing characteristics; they increase backpressure, affect exhaust system acoustic characteristics, and contribute to exhaust manifold tuning. Thus, radiated sound models should include catalytic converters since they can affect both the source characteristics and the exhaust system acoustic behavior. A typical catalytic converter assembly employs a ceramic substrate to carry the catalytically active noble metals. The substrate has numerous parallel tubes and is mounted in a housing with swelling mat or wire mesh around its periphery. Seals at the ends of the substrate can be used to help force flow through the substrate and/or protect the mat material. Typically, catalytic converter studies only consider sound propagation in the small capillary tubes of the substrate. Investigations of the acoustic characteristics of entire catalytic converter assemblies (housing, substrate, seals, and mat) do not appear to be available. This work experimentally investigates the acoustic behavior of catalytic converter assemblies and the contributions of the separate components to sound attenuation. Experimental findings are interpreted with respect to available techniques for modeling sound propagation in ceramic substrates.

  13. Understanding catalytic biomass conversion through data mining

    NARCIS (Netherlands)

    E.J. Ras; B. McKay; G. Rothenberg

    2010-01-01

    Catalytic conversion of biomass is a key challenge that we chemists face in the twenty-first century. Worldwide, research is conducted into obtaining bulk chemicals, polymers and fuels. Our project centres on glucose valorisation via furfural derivatives using catalytic hydrogenation. We present her

  14. Catalytic poly(vinyl alcohol) functionalized membranes obtained by gamma irradiation

    Science.gov (United States)

    Casimiro, M. H.; Silva, A. G.; Pinto, J. V.; Ramos, A. M.; Vital, J.; Ferreira, L. M.

    2012-09-01

    Polymeric catalytic membranes bearing sulfonic acid functions have been prepared by mutual gamma irradiation at a 60Co source, of poly(vinyl alcohol) (PVA) membranes and methanesulfonic acid. The effect of various synthesis conditions on membranes' physical-chemical properties and catalytic activity in the esterification reaction between acetic acid and isoamyl alcohol to obtain isoamyl acetate (banana flavor), was evaluated. The membranes were characterized by ATR-FTIR, TPP, AFM and SEM. Water contact angle determinations were also performed. The obtained results showed that within the range of conditions studied the increase in sulfonic acid groups' content is accompanied by an enhancement in the membranes catalytic activity, while the increase in absorbed dose leads to a decrease in catalytic activity.

  15. Esterification of glycerol from biodiesel production to glycerol carbonate in non-catalytic supercritical dimethyl carbonate.

    Science.gov (United States)

    Ilham, Zul; Saka, Shiro

    2016-01-01

    Conversion of glycerol from biodiesel production to glycerol carbonate was studied by esterification with dimethyl carbonate in a non-catalytic supercritical condition. It was found that in a non-catalytic supercritical condition, glycerol at higher purity gave higher yield of glycerol carbonate at 98 wt% after reaction at 300 °C/20-40 MPa/15 min. The yield of glycerol carbonate was observed to increase with molar ratio, temperature, pressure and time until a certain equilibrium limit. The existence of impurities such as water and remnants of alkaline catalyst in crude glycerol will direct the reaction to produce glycidol. Although impurities might not be desirable, the non-catalytic supercritical dimethyl carbonate could be an alternative method for conversion of glycerol from biodiesel production to value-added glycerol carbonate.Graphical abstractPlausible reaction scheme for conversion of glycerol to glycerol carbonate in non-catalytic supercritical dimethyl carbonate. PMID:27386367

  16. Effect of plant cultivation,phosphorus fertilization and co-existing polycyclic aromatic hydrocarbons (PAHs) on biodegradation of PAHs%植物、施磷量及多环芳烃共存对多环芳烃生物降解影响

    Institute of Scientific and Technical Information of China (English)

    周笑白; 周集体; 项学敏

    2012-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are persistent organic pollutants with toxic, mutagenic and carcingenic properties. Pot experiment and microplate experiments are conducted to investigate the impact of plant cultivation, phosphorus fertilization and PAHs co-existence on the removal rate of phenanthracene (PHE), pyrene (PYR) and dihenzo [a, hi anthracene (DBA). Results show that the dissipation and degraders of PHE are significantly higher than those of PYR and DBA in both pot and microplate experiments. In pot experiment, plants and higher quantity of phosphorus fertilizer increase DBA dissipation. Different interactions are obtained among the co- existing PAHs. The results show that co-existence of different PAH compounds can lead to synergistic co-metabolism (PHE enhanced DBA degradation), no co-metabolism (PYR and DBA) and inhibition of PAH degradation (PYR inhibited PHE+DBA degradation). The positive effect of PHE on DBA dissipation decreases with time course, which is probably due to the decrease of PHE concentration or the toxicity and accumulation of DBA degradation products in the substrate.%多环芳烃(PAHs)是具有“三致”效应的持久性有机污染物.通过盆栽及微生物培养实验,考察了植物、施磷量及PAHs共存对菲(PHE)、芘(PYR)和二苯并葸(DBA)去除率的影响,发现PHE的降解率和降解菌量均高于PYR和DBA.盆栽实验中,植物种植和给植物施加高磷浓度的营养液可促进DBA的降解;微生物培养实验表明共存的PAHs之间存在相互作用,而这种作用随PAHs种类不同可表现为促进降解作用(如PHE促进DBA降解)、无作用(如PYR和DBA)或抑制作用(如PYR抑制PHE+DBA降解).PHE对DBA降解的促进作用随时间的增加而减弱,这可能与PHE浓度降低和DBA中间产物的毒性及其积累有关.

  17. Selective catalytic oxidation of ammonia

    Energy Technology Data Exchange (ETDEWEB)

    Leppaelahti, J.; Koljonen, T. [VTT Energy, Espoo (Finland)

    1996-12-31

    In the combustion of fossil fuels, the principal source of nitrogen oxides is nitrogen bound in the fuel structure. In gasification, a large part of fuel nitrogen forms NH{sub 3}, which may form nitrogen oxides during gas combustion. If NH{sub 3} and other nitrogen species could be removed from hot gas, the NO emission could be considerably reduced. However, relatively little attention has been paid to finding new means of removing nitrogen compounds from the hot gasification gas. The possibility of selectively oxidizing NH{sub 3} to N{sub 2} in the hot gasification has been studied at VTT Energy. The largest NH{sub 3} reductions have been achieved by catalytic oxidation on aluminium oxides. (author) (4 refs.)

  18. Catalytic hydrogenation of carbon monoxide

    International Nuclear Information System (INIS)

    Focus of this project is on developing new approaches for hydrogenation of carbon monoxide to produce organic oxygenates at mild conditions. The strategies to accomplish CO reduction are based on favorable thermodynamics manifested by rhodium macrocycles for producing a series of intermediates implicated in the catalytic hydrogenation of CO. Metalloformyl complexes from reactions of H2 and CO, and CO reductive coupling to form metallo α-diketone species provide alternate routes to organic oxygenates that utilize these species as intermediates. Thermodynamic and kinetic-mechanistic studies are used in guiding the design of new metallospecies to improve the thermodynamic and kinetic factors for individual steps in the overall process. Electronic and steric effects associated with the ligand arrays along with the influences of the reaction medium provide the chemical tools for tuning these factors. Non-macrocyclic ligand complexes that emulate the favorable thermodynamic features associated with rhodium macrocycles, but that also manifest improved reaction kinetics are promising candidates for future development

  19. Catalytic Graphitization of Phenolic Resin

    Institute of Scientific and Technical Information of China (English)

    Mu Zhao; Huaihe Song

    2011-01-01

    The catalytic graphitization of thermal plastic phenolic-formaldehyde resin with the aid of ferric nitrate (FN) was studied in detail. The morphologies and structural features of the products including onion-like carbon nanoparticles and bamboo-shaped carbon nanotubes were investigated by transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), X-ray diffraction and Raman spectroscopy measurements. It was found that with the changes of loading content of FN and residence time at 1000℃, the products exhibited various morphologies. The TEM images showed that bamboo-shaped carbon nanotube consisted of tens of bamboo sticks and onion-like carbon nanoparticle was made up of quasi-spherically concentrically closed carbon nanocages.

  20. Reducing catalytic converter pressure loss

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-06-01

    This article examines why approximately 30--40% of total exhaust-system pressure loss occurs in the catalytic converter and what can be done to reduce pressure loss. High exhaust-system backpressure is of concern in the design of power trains for passenger cars and trucks because it penalizes fuel economy and limits peak power. Pressure losses occur due to fluid shear and turning during turbulent flow in the converter headers and in entry separation and developing laminar-flow boundary layers within the substrate flow passages. Some of the loss mechanisms are coupled. For example, losses in the inlet header are influenced by the presence of the flow resistance of a downstream substrate. Conversely, the flow maldistribution and pressure loss of the substrate(s) depend on the design of the inlet header.

  1. Non-catalytic recuperative reformer

    Energy Technology Data Exchange (ETDEWEB)

    Khinkis, Mark J.; Kozlov, Aleksandr P.; Kurek, Harry

    2015-12-22

    A non-catalytic recuperative reformer has a flue gas flow path for conducting hot flue gas from a thermal process and a reforming mixture flow path for conducting a reforming mixture. At least a portion of the reforming mixture flow path is embedded in the flue gas flow path to permit heat transfer from the hot flue gas to the reforming mixture. The reforming mixture flow path contains substantially no material commonly used as a catalyst for reforming hydrocarbon fuel (e.g., nickel oxide, platinum group elements or rhenium), but instead the reforming mixture is reformed into a higher calorific fuel via reactions due to the heat transfer and residence time. In a preferred embodiment, extended surfaces of metal material such as stainless steel or metal alloy that are high in nickel content are included within at least a portion of the reforming mixture flow path.

  2. Fluctuations in catalytic surface reactions

    CERN Document Server

    Imbihl, R

    2003-01-01

    The internal reaction-induced fluctuations which occur in catalytic CO oxidation on a Pt field emitter tip have been studied using field electron microscopy (FEM) as a spatially resolving method. The structurally heterogeneous Pt tip consists of facets of different orientations with nanoscale dimensions. The FEM resolution of roughly 2 nm corresponds to a few hundred reacting adsorbed particles whose variations in the density are imaged as brightness fluctuations. In the bistable range of the reaction one finds fluctuation-induced transitions between the two stable branches of the reaction kinetics. The fluctuations exhibit a behaviour similar to that of an equilibrium phase transition, i.e. the amplitude diverges upon approaching the bifurcation point terminating the bistable range of the reaction. Simulations with a hybrid Monte Carlo/mean-field model reproduce the experimental observations. Fluctuations on different facets are typically uncorrelated but within a single facet a high degree of spatial cohere...

  3. Catalytic, enantioselective, vinylogous aldol reactions.

    Science.gov (United States)

    Denmark, Scott E; Heemstra, John R; Beutner, Gregory L

    2005-07-25

    In 1935, R. C. Fuson formulated the principle of vinylogy to explain how the influence of a functional group may be felt at a distant point in the molecule when this position is connected by conjugated double-bond linkages to the group. In polar reactions, this concept allows the extension of the electrophilic or nucleophilic character of a functional group through the pi system of a carbon-carbon double bond. This vinylogous extension has been applied to the aldol reaction by employing "extended" dienol ethers derived from gamma-enolizable alpha,beta-unsaturated carbonyl compounds. Since 1994, several methods for the catalytic, enantioselective, vinylogous aldol reaction have appeared, with which varying degrees of regio- (site), enantio-, and diastereoselectivity can be attained. In this Review, the current scope and limitations of this transformation, as well as its application in natural product synthesis, are discussed. PMID:15940727

  4. Electrochemical promotion of catalytic reactions

    Science.gov (United States)

    Imbihl, R.

    2010-05-01

    The electrochemical promotion of heterogeneously catalyzed reactions (EPOC) became feasible through the use of porous metal electrodes interfaced to a solid electrolyte. With the O 2- conducting yttrium stabilized zirconia (YSZ), the Na + conducting β″-Al 2O 3 (β-alumina), and several other types of solid electrolytes the EPOC effect has been demonstrated for about 100 reaction systems in studies conducted mainly in the mbar range. Surface science investigations showed that the physical basis for the EPOC effect lies in the electrochemically induced spillover of oxygen and alkali metal, respectively, onto the surface of the metal electrodes. For the catalytic promotion effect general concepts and mechanistic schemes were proposed but these concepts and schemes are largely speculative. Applying surface analytical tools to EPOC systems the proposed mechanistic schemes can be verified or invalidated. This report summarizes the progress which has been achieved in the mechanistic understanding of the EPOC effect.

  5. Catalytic converter with thermoelectric generator

    Energy Technology Data Exchange (ETDEWEB)

    Parise, R.J.

    1998-07-01

    The unique design of an electrically heated catalyst (EHC) and the inclusion of an ECO valve in the exhaust of an internal combustion engine will meet the strict new emission requirements, especially at vehicle cold start, adopted by several states in this country as well as in Europe and Japan. The catalytic converter (CC) has been a most useful tool in pollution abatement for the automobile. But the emission requirements are becoming more stringent and, along with other improvements, the CC must be improved to meet these new standards. Coupled with the ECO valve, the EHC can meet these new emission limits. In an internal combustion engine vehicle (ICEV), approximately 80% of the energy consumed leaves the vehicle as waste heat: out the tail pipe, through the radiator, or convected/radiated off the engine. Included with the waste heat out the tail pipe are the products of combustion which must meet strict emission requirements. The design of a new CC is presented here. This is an automobile CC that has the capability of producing electrical power and reducing the quantity of emissions at vehicle cold start, the Thermoelectric Catalytic Power Generator. The CC utilizes the energy of the exothermic reactions that take place in the catalysis substrate to produce electrical energy with a thermoelectric generator. On vehicle cold start, the thermoelectric generator is used as a heat pump to heat the catalyst substrate to reduce the time to catalyst light-off. Thus an electrically heated catalyst (EHC) will be used to augment the abatement of tail pipe emissions. Included with the EHC in the exhaust stream of the automobile is the ECO valve. This valve restricts the flow of pollutants out the tail pipe of the vehicle for a specified amount of time until the EHC comes up to operating temperature. Then the ECO valve opens and allows the full exhaust, now treated by the EHC, to leave the vehicle.

  6. The evolution of catalytic function

    Science.gov (United States)

    Maurel, Marie-Christine; Ricard, Jacques

    2006-03-01

    It is very likely that the main driving force of enzyme evolution is the requirement to improve catalytic and regulatory efficiency which results from the intrinsic performance as well as from the spatial and functional organization of enzymes in living cells. Kinetic co-operativity may occur in simple monomeric proteins if they display “slow” conformational transitions, at the cost of catalytic efficiency. Oligomeric enzymes on the other hand can be both efficient and co-operative. We speculate that the main reason for the emergence of co-operative oligomeric enzymes is the need for catalysts that are both cooperative and efficient. As it is not useful for an enzyme to respond to a change of substrate concentration in a complex kinetic way, the emergence of symmetry has its probable origin in a requirement for “functional simplicity”. In a living cell, enzyme are associated with other macromolecules and membranes. The fine tuning of their activity may also be reached through mutations of the microenvironment. Our hypothesis is that these mutations are related to the vectorial transport of molecules, to achieve the hysteresis loops of enzyme reactions generated by the coupling of reaction and diffusion, through the co-operativity brought about by electric interactions between a charged substrate and a membrane, and last but not least, through oscillations. As the physical origins of these effects are very simple and do not require complex molecular devices, it is very likely that the functional advantage generated by the spatial and functional organization of enzyme molecules within the cell have appeared in prebiotic catalysis or very early during the primeval stages of biological evolution. We shall began this paper by presenting the nature of the probable earliest catalysts in the RNA world.

  7. Catalytic pyrolysis using UZM-39 aluminosilicate zeolite

    Science.gov (United States)

    Nicholas, Christpher P; Boldingh, Edwin P

    2013-12-17

    A new family of coherently grown composites of TUN and IMF zeotypes has been synthesized and show to be effective catalysts for catalytic pyrolysis of biomass. These zeolites are represented by the empirical formula. Na.sub.nM.sub.m.sup.n+R.sub.rQ.sub.qAl.sub1-xE.sub.xSi.sub.yO.s- ub.z where M represents zinc or a metal or metals from Group 1, Group 2, Group 3 or the lanthanide series of the periodic table, R is an A,.OMEGA.-dihalosubstituted paraffin such as 1,4-dibromobutane, Q is a neutral amine containing 5 or fewer carbon atoms such as 1-methylpyrrolidine and E is a framework element such as gallium. The process involves contacting a carbonaceous biomass feedstock with UZM-39 at pyrolysis conditions to produce pyrolysis gases comprising hydrocarbons. The catalyst catalyzes a deoxygenation reaction converting oxygenated hyrdocarbons into hydrocarbons removing the oxygen as carbon oxides and water. A portion of the pyrolysis gases is condensed to produce low oxygen biomass-derived pyrolysis oil.

  8. Catalytic glycerol steam reforming for hydrogen production

    International Nuclear Information System (INIS)

    Hydrogen production from glycerol by steam reforming combine two major advantages: (i) using glycerol as raw material add value to this by product of bio-diesel production which is obtained in large quantities around the world and have a very limited utilization now, and (ii) by implication of water molecules in the reaction the efficiency of hydrogen generation is increased as each mol of glycerol produces 7 mol of H2. In this work we present the results obtained in the process of steam reforming of glycerol on Ni/Al2O3. The catalyst was prepared by wet impregnation method and characterized through different methods: N2 adsorption-desorption, XRD, TPR. The catalytic study was performed in a stainless steel tubular reactor at atmospheric pressure by varying the reaction conditions: steam/carbon ratio (1-9), gas flow (35 ml/min -133 ml/min), temperature (450-650°C). The gaseous fraction of the reaction products contain: H2, CH4, CO, CO2. The optimum reaction conditions as resulted from this study are: temperature 550°C, Gly:H2O ratio 9:1 and Ar flow 133 ml/min. In these conditions the glycerol conversion to gaseous products was 43% and the hydrogen yield was 30%

  9. Catalytic pyrolysis using UZM-39 aluminosilicate zeolite

    Energy Technology Data Exchange (ETDEWEB)

    Nicholas, Christopher P; Boldingh, Edwin P

    2014-10-07

    A new family of coherently grown composites of TUN and IMF zeotypes has been synthesized and shown to be effective catalysts for catalytic pyrolysis of biomass. These zeolites are represented by the empirical formula. Na.sub.nM.sub.m.sup.n+R.sub.rQ.sub.qAl.sub.1-xE.sub.xSi.sub.yO.s- ub.z where M represents zinc or a metal or metals from Group 1, Group 2, Group 3 or the lanthanide series of the periodic table, R is an A,.OMEGA.-dihalosubstituted paraffin such as 1,4-dibromobutane, Q is a neutral amine containing 5 or fewer carbon atoms such as 1-methylpyrrolidine and E is a framework element such as gallium. The process involves contacting a carbonaceous biomass feedstock with UZM-39 at pyrolysis conditions to produce pyrolysis gases comprising hydrocarbons. The catalyst catalyzes a deoxygenation reaction converting oxygenated hydrocarbons into hydrocarbons and removing the oxygen as carbon oxides and water. A portion of the pyrolysis gases is condensed to produce low oxygen biomass-derived pyrolysis oil.

  10. Catalytic glycerol steam reforming for hydrogen production

    Energy Technology Data Exchange (ETDEWEB)

    Dan, Monica, E-mail: monica.dan@itim-cj.ro; Mihet, Maria, E-mail: maria.mihet@itim-cj.ro; Lazar, Mihaela D., E-mail: diana.lazar@itim-cj.ro [National Institute for Research and Development of Isotopic and Molecular Technologies, 67-103 Donat Street, 400293 Cluj Napoca (Romania)

    2015-12-23

    Hydrogen production from glycerol by steam reforming combine two major advantages: (i) using glycerol as raw material add value to this by product of bio-diesel production which is obtained in large quantities around the world and have a very limited utilization now, and (ii) by implication of water molecules in the reaction the efficiency of hydrogen generation is increased as each mol of glycerol produces 7 mol of H{sub 2}. In this work we present the results obtained in the process of steam reforming of glycerol on Ni/Al{sub 2}O{sub 3}. The catalyst was prepared by wet impregnation method and characterized through different methods: N{sub 2} adsorption-desorption, XRD, TPR. The catalytic study was performed in a stainless steel tubular reactor at atmospheric pressure by varying the reaction conditions: steam/carbon ratio (1-9), gas flow (35 ml/min -133 ml/min), temperature (450-650°C). The gaseous fraction of the reaction products contain: H{sub 2}, CH{sub 4}, CO, CO{sub 2}. The optimum reaction conditions as resulted from this study are: temperature 550°C, Gly:H{sub 2}O ratio 9:1 and Ar flow 133 ml/min. In these conditions the glycerol conversion to gaseous products was 43% and the hydrogen yield was 30%.

  11. Catalytic glycerol steam reforming for hydrogen production

    Science.gov (United States)

    Dan, Monica; Mihet, Maria; Lazar, Mihaela D.

    2015-12-01

    Hydrogen production from glycerol by steam reforming combine two major advantages: (i) using glycerol as raw material add value to this by product of bio-diesel production which is obtained in large quantities around the world and have a very limited utilization now, and (ii) by implication of water molecules in the reaction the efficiency of hydrogen generation is increased as each mol of glycerol produces 7 mol of H2. In this work we present the results obtained in the process of steam reforming of glycerol on Ni/Al2O3. The catalyst was prepared by wet impregnation method and characterized through different methods: N2 adsorption-desorption, XRD, TPR. The catalytic study was performed in a stainless steel tubular reactor at atmospheric pressure by varying the reaction conditions: steam/carbon ratio (1-9), gas flow (35 ml/min -133 ml/min), temperature (450-650°C). The gaseous fraction of the reaction products contain: H2, CH4, CO, CO2. The optimum reaction conditions as resulted from this study are: temperature 550°C, Gly:H2O ratio 9:1 and Ar flow 133 ml/min. In these conditions the glycerol conversion to gaseous products was 43% and the hydrogen yield was 30%.

  12. Revolutionary systems for catalytic combustion and diesel catalytic particulate traps.

    Energy Technology Data Exchange (ETDEWEB)

    Stuecker, John Nicholas; Witze, Peter O.; Ferrizz, Robert Matthew; Cesarano, Joseph, III; Miller, James Edward

    2004-12-01

    This report is a summary of an LDRD project completed for the development of materials and structures conducive to advancing the state of the art for catalyst supports and diesel particulate traps. An ancillary development for bio-medical bone scaffolding was also realized. Traditionally, a low-pressure drop catalyst support, such as a ceramic honeycomb monolith, is used for catalytic reactions that require high flow rates of gases at high-temperatures. A drawback to the traditional honeycomb monoliths under these operating conditions is poor mass transfer to the catalyst surface in the straight-through channels. ''Robocasting'' is a unique process developed at Sandia National Laboratories that can be used to manufacture ceramic monoliths with alternative 3-dimensional geometries, providing tortuous pathways to increase mass transfer while maintaining low-pressure drops. These alternative 3-dimensional geometries may also provide a foundation for the development of self-regenerating supports capable of trapping and combusting soot particles from a diesel engine exhaust stream. This report describes the structures developed and characterizes the improved catalytic performance that can result. The results show that, relative to honeycomb monolith supports, considerable improvement in mass transfer efficiency is observed for robocast samples synthesized using an FCC-like geometry of alternating rods. Also, there is clearly a trade-off between enhanced mass transfer and increased pressure drop, which can be optimized depending on the particular demands of a given application. Practical applications include the combustion of natural gas for power generation, production of syngas, and hydrogen reforming reactions. The robocast lattice structures also show practicality for diesel particulate trapping. Preliminary results for trapping efficiency are reported as well as the development of electrically resistive lattices that can regenerate the structure

  13. Synthesis, catalytic properties and biological activity of new water soluble ruthenium cyclopentadienyl PTA complexes [(C5R5)RuCl(PTA)2] (R = H, Me; PTA = 1,3,5-triaza-7-phosphaadamantane).

    Science.gov (United States)

    Akbayeva, Dina N; Gonsalvi, Luca; Oberhauser, Werner; Peruzzini, Maurizio; Vizza, Francesco; Brüggeller, Peter; Romerosa, Antonio; Sava, Gianni; Bergamo, Alberta

    2003-01-21

    The new water soluble ruthenium complexes [(C5R5)RuCl(PTA)2] (R = H, Me; PTA = 1,3,5-triaza-7-phosphaadamantane) were synthesised and characterised. Their evaluation as regioselective catalysts for hydrogenation of unsaturated ketones in aqueous biphasic conditions and as cytotoxic agents towards the TS/A adenocarcinoma cell line is briefly presented. PMID:12585422

  14. Water Purification

    Science.gov (United States)

    1994-01-01

    The Vision Catalyst Purifier employs the basic technology developed by NASA to purify water aboard the Apollo spacecraft. However, it also uses an "erosion" technique. The purifier kills bacteria, viruses, and algae by "catalytic corrosion." A cartridge contains a silver-impregnated alumina bed with a large surface area. The catalyst bed converts oxygen in a pool of water to its most oxidative state, killing over 99 percent of the bacteria within five seconds. The cartridge also releases into the pool low levels of ionic silver and copper through a controlled process of erosion. Because the water becomes electrochemically active, no electricity is required.

  15. Catalytic electrolytic extraction of long-lived fission products

    International Nuclear Information System (INIS)

    An electrolytic extraction method has been studied to separate fission products (Ru, Rh, Pd, Tc, Se, Te, etc) from the nuclear spent fuel. Yet they are rare metal fission products (RMFP), most are long-lived (LLFP; Pd, Tc, Se, Te). In the applied electrochemical separation process, Pd2+ cation itself would not only be easily deposited from various nitric acid solutions, but also enhances the other deposition of RuNO3+ and ReO4 by acting catalyst as Pdadatom. The same role also applies to the case of TcO4 deposition (i.e., CEE: Catalytic Electrolytic Extraction). One of the promising utilizations will be hydrogen production by alkaline or sea water electrolysis as FP-catalyst. The deposits of quaternary alloy consisting of Ru, Rh, Pd and Re show the highest catalytic reactivity, even superior to that of the smooth Pt electrode. Current interests are focused on the separability and catalytic reactivity of Re and Tc. (author)

  16. New Catalytic DNA Biosensors for Radionuclides and Metal ions

    International Nuclear Information System (INIS)

    The goals of the project are to develop new catalytic DNA biosensors for simultaneous detection and quantification of bioavailable radionuclides and metal ions, and apply the sensors for on-site, real-time assessment of concentration, speciation and stability of the individual contaminants during and after bioremediation. A negative selection strategy was tested and validated. In vitro selection was shown to yield highly active and specific transition metal ion-dependent catalytic DNA/RNA. A fluorescence resonance energy transfer (FRET) study of in vitro selected DNA demonstrated that the trifluorophore labeled system is a simple and powerful tool in studying complex biomolecules structure and dynamics, and is capable of revealing new sophisticated structural changes. New fluorophore/quenchers in a single fluorosensor yielded improved signal to noise ratio in detection, identification and quantification of metal contaminants. Catalytic DNA fluorescent and colorimetric sensors were shown useful in sensing lead in lake water and in leaded paint. Project results were described in two papers and two patents, and won an international prize

  17. Modelling of procecces in catalytic recombiners

    International Nuclear Information System (INIS)

    In order to achieve a high degree of safety in nuclear power plants and prevent possible accident scenarios, their consequences are calculated and analysed with numeric codes. One of the most important part of nuclear safety research of hazardous incidents are development and validation of these numeric models, which are implemented into accident codes. The severe hydrogen release during a core meltdown is one of the considered scenario of performed accident analyses. One of the most important measure for the elimination of the hydrogen is catalytic recombiners. Converting the hydrogen with the atmospheric oxygen to water vapor in an exothermic reaction will prevent possible detonation of the hydrogen/air atmosphere. Within the dissertation the recombiner simulation REKO-DIREKT was developed and validated by an extensive experimental database. The performance of recombiners with regard to the conversion of the hydrogen and the temperature development is modelled. The REKO-DIREKT program is unique and has made significant revolution in research of hydrogen safety. For the first time it has been possible to show the performance of the recombiner so great in detail by using REKO-DIREKT. In the future engineers of nuclear power plants will have opportunity to have precise forecasts about the process of the possible accidents with hydrogen release. Also with presence of water vapor or with oxygen depletion which are included in the model. The major discussion of the hydrogen ignition at hot catalyst steel plates can be evaluated in the future with REKO-DIREKT more reliably than the existing used models. (orig.)

  18. Structure-based identification of catalytic residues.

    Science.gov (United States)

    Yahalom, Ran; Reshef, Dan; Wiener, Ayana; Frankel, Sagiv; Kalisman, Nir; Lerner, Boaz; Keasar, Chen

    2011-06-01

    The identification of catalytic residues is an essential step in functional characterization of enzymes. We present a purely structural approach to this problem, which is motivated by the difficulty of evolution-based methods to annotate structural genomics targets that have few or no homologs in the databases. Our approach combines a state-of-the-art support vector machine (SVM) classifier with novel structural features that augment structural clues by spatial averaging and Z scoring. Special attention is paid to the class imbalance problem that stems from the overwhelming number of non-catalytic residues in enzymes compared to catalytic residues. This problem is tackled by: (1) optimizing the classifier to maximize a performance criterion that considers both Type I and Type II errors in the classification of catalytic and non-catalytic residues; (2) under-sampling non-catalytic residues before SVM training; and (3) during SVM training, penalizing errors in learning catalytic residues more than errors in learning non-catalytic residues. Tested on four enzyme datasets, one specifically designed by us to mimic the structural genomics scenario and three previously evaluated datasets, our structure-based classifier is never inferior to similar structure-based classifiers and comparable to classifiers that use both structural and evolutionary features. In addition to the evaluation of the performance of catalytic residue identification, we also present detailed case studies on three proteins. This analysis suggests that many false positive predictions may correspond to binding sites and other functional residues. A web server that implements the method, our own-designed database, and the source code of the programs are publicly available at http://www.cs.bgu.ac.il/∼meshi/functionPrediction. PMID:21491495

  19. Catalytic partial oxidation of pyrolysis oils

    Science.gov (United States)

    Rennard, David Carl

    2009-12-01

    details the catalytic partial oxidation of glycerol without preheat: droplets of glycerol are sprayed directly onto the top of the catalyst bed, where they react autothermally with contact times on the order of tau ≈ 30 ms. The reactive flash volatilization of glycerol results in equilibrium syngas production over Rh-Ce catalysts. In addition, water can be added to the liquid glycerol, resulting in true autothermal reforming. This highly efficient process can increase H2 yields and alter the H2 to CO ratio, allowing for flexibility in syngas quality depending on the purpose. Chapter 5 details the results of a time on stream experiment, in which optimal syngas conditions are chosen. Although conversion is 100% for 450 hours, these experiments demonstrate the deactivation of the catalyst over time. Deactivation is exhibited by decreases in H2 and CO 2 production accompanied by a steady increase in CO and temperature. These results are explained as a loss of water-gas shift equilibration. SEM images suggest catalyst sintering may play a role; EDS indicates the presence of impurities on the catalyst. In addition, the instability of quartz in the reactor is demonstrated by etching, resulting in a hole in the reactor tube at the end of the experiment. These results suggest prevaporization may be desirable in this application, and that quartz is not a suitable material for the reactive flash volatilization of oxygenated fuels. In Chapter 6, pyrolysis oil samples from three sources - poplar, pine, and hardwoods - are explored in the context of catalytic partial oxidation. Lessons derived from the tests with model compounds are applied to reactor design, resulting in the reactive flash vaporization of bio oils. Syngas is successfully produced, though deactivation due to coke and ash deposition keeps H2 below equlibrium. Coke formation is observed on the reactor walls, but is avoided between the fuel injection site and catalyst by increasing the proximity of these in the reactor

  20. Development of Catalytic Cooking Plates

    Energy Technology Data Exchange (ETDEWEB)

    Hjelm, Anna-Karin; Silversand, Fredrik [CATATOR AB, Lund (Sweden); Tena, Emmanuel; Berger, Marc [Gaz de France (France)

    2004-04-01

    Gas catalytic combustion for gas stoves or cooking plates (closed catalytic burner system with ceramic plates) is a very promising technique in terms of ease of cleaning, power modulation and emissions. Previous investigations show that wire mesh catalysts, prepared and supplied by Catator AB (CAT), seem to be very well suited for such applications. Beside significantly reducing the NOx-emissions, these catalysts offer important advantages such as good design flexibility, low pressure drop and high heat transfer capacity, where the latter leads to a quick thermal response. Prior to this project, Gaz de France (GdF) made a series of measurements with CAT's wire mesh catalysts in their gas cooking plates and compared the measured performance with similar results obtained with theirs cordierite monolith catalysts. Compared to the monolith catalyst, the wire mesh catalyst was found to enable very promising results with respect to both emission levels (<10 mg NO{sub x} /kWh, <5 mg CO/kWh) and life-time (>8000 h vs. 700 h at 200 kW/m{sup 2}). It was however established that the radiation and hence, the thermal efficiency of the cooking plate, was significantly less than is usually measured in combination with the monolith (15 % vs. 32 %). It was believed that the latter could be improved by developing new burner designs based on CAT's wire mesh concept. As a consequence, a collaboration project between GdF, CAT and the Swedish Gas Technology AB was created. This study reports on the design, the construction and the evaluation of new catalytic burners, based on CAT's wire mesh catalysts, used for the combustion of natural gas in gas cooking stoves. The evaluation of the burners was performed with respect to key factors such as thermal efficiency, emission quality and pressure drop, etc, by the use of theoretical simulations and experimental tests. Impacts of parameters such as the the wire mesh number, the wire mesh structure (planar or folded), the

  1. Catalytic reaction in confined flow channel

    Energy Technology Data Exchange (ETDEWEB)

    Van Hassel, Bart A.

    2016-03-29

    A chemical reactor comprises a flow channel, a source, and a destination. The flow channel is configured to house at least one catalytic reaction converting at least a portion of a first nanofluid entering the channel into a second nanofluid exiting the channel. The flow channel includes at least one turbulating flow channel element disposed axially along at least a portion of the flow channel. A plurality of catalytic nanoparticles is dispersed in the first nanofluid and configured to catalytically react the at least one first chemical reactant into the at least one second chemical reaction product in the flow channel.

  2. Catalytic hydrogen currents in solutions of some transition metal complexes with 8-mercaptoquinoline

    International Nuclear Information System (INIS)

    Electrochemical behaviour of complexes with general formula ML2 where L-8-mercaptoquinoline, M-V(4)(VO2+) was studied. Investigations were carried out by classical and voltampere oscillographic polarography in water alcohol media. Measurements were performed at 25 deg C. It was found that chelate V(4) gives in classical polarogrammes the wave as a peak at 1.5-1.7 v depending on pH and the nature of the central ion; during electrolysis of the investigated solutions the release of gas bubbles was observed. Waves observed in the potential region 1.5-1.7 v are the catalytic waves of hydrogen. Results obtained on the catalytic activity of structurally related complexes of transitional metals with mercaptoquinoline indicate a definite influence of the central atom nature on the catalytic effect. Intermediate particles with central atom in the lower degree of oxidation formed at catalytic wave may be responsible for the catalytic effect. The rate of their formation on the electrode and the rate of their protonization determine the catalytic wave height

  3. Catalytic pyrolysis of microalgae to high-quality liquid bio-fuels

    International Nuclear Information System (INIS)

    The pyrolytic conversion of chlorella algae to liquid fuel precursor in presence of a catalyst (Na2CO3) has been studied. Thermal decomposition studies of the algae samples were performed using TGA coupled with MS. Liquid oil samples were collected from pyrolysis experiments in a fixed-bed reactor and characterized for water content and heating value. The oil composition was analyzed by GC-MS. Pretreatment of chlorella with Na2CO3 influences the primary conversion of chlorella by shifting the decomposition temperature to a lower value. In the presence of Na2CO3, gas yield increased and liquid yield decreased when compared with non-catalytic pyrolysis at the same temperatures. However, pyrolysis oil from catalytic runs carries higher heating value and lower acidity. Lower content of acids in the bio-oil, higher aromatics, combined with higher heating value show promise for production of high-quality bio-oil from algae via catalytic pyrolysis, resulting in energy recovery in bio-oil of 40%. -- Highlights: → The pyrolytic catalytic conversion of chlorella algae to liquid fuel precursor. → Na2CO3 as a catalyst for the primary conversion of chlorella. → Pyrolysis oil from catalytic runs carries higher heating value and lower acidity. → High-quality bio-oil from algae via catalytic pyrolysis with energy recovery in bio-oil of 40%.

  4. A review of liquid-phase catalytic hydrodechlorination

    Directory of Open Access Journals (Sweden)

    Alba Nelly Ardila Arias

    2010-04-01

    Full Text Available This survey was aimed at introducing the effect of light organochlorinated compound emissions on the envi-ronment, particularly on water, air, soil, biota and human beings. The characteristics and advantages of liquid phase catalytic hydrodechlorination as a technology for degrading these chlorinated compounds is also outlined and the main catalysts used in the hydrodechlorination process are described. Special emphasis is placed on palladium catalysts, their activity, the nature of active species and deactivation. The effect of several parameters is introduced, such as HCl, solvent, base addition and type of reducing agent used. The main results of kinetic studies, reactors used and the most important survey conclusions are presented.

  5. The tritium labelling of organic molecules by heterogeneous catalytic exchange

    International Nuclear Information System (INIS)

    The influence of the temperature at 65 degree centigree and 120 degree centigree on the labelling of three organic molecules with tritium was studied. The compounds were: benzoic acid, de phenyl glyoxal and 2,3-tetramethylene-4-pantothenyl-7-oxo diacetin.The method employed was the heterogeneous catalytic exchange between tritiated water and the organic compound. The purification was made by thin-layer chromatography and the concentration, purity and specific activity of the products were determined by counting and ultraviolet techniques. The thermal stability and the radiolytic effects on labelled benzoic acid were also considered. (Author) 9 refs

  6. Catalytic Chemistry on Oxide Nanostructures

    Energy Technology Data Exchange (ETDEWEB)

    Asthagiri, Aravind; Dixon, David A.; Dohnalek, Zdenek; Kay, Bruce D.; Rodriquez, Jose A.; Rousseau, Roger J.; Stacchiola, Dario; Weaver, Jason F.

    2016-05-29

    Metal oxides represent one of the most important and widely employed materials in catalysis. Extreme variability of their chemistry provides a unique opportunity to tune their properties and to utilize them for the design of highly active and selective catalysts. For bulk oxides, this can be achieved by varying their stoichiometry, phase, exposed surface facets, defect, dopant densities and numerous other ways. Further, distinct properties from those of bulk oxides can be attained by restricting the oxide dimensionality and preparing them in the form of ultrathin films and nanoclusters as discussed throughout this book. In this chapter we focus on demonstrating such unique catalytic properties brought by the oxide nanoscaling. In the highlighted studies planar models are carefully designed to achieve minimal dispersion of structural motifs and to attain detailed mechanistic understanding of targeted chemical transformations. Detailed level of morphological and structural characterization necessary to achieve this goal is accomplished by employing both high-resolution imaging via scanning probe methods and ensemble-averaged surface sensitive spectroscopic methods. Three prototypical examples illustrating different properties of nanoscaled oxides in different classes of reactions are selected.

  7. Halogen Chemistry on Catalytic Surfaces.

    Science.gov (United States)

    Moser, Maximilian; Pérez-Ramírez, Javier

    2016-01-01

    Halogens are key building blocks for the manufacture of high-value products such as chemicals, plastics, and pharmaceuticals. The catalytic oxidation of HCl and HBr is an attractive route to recover chlorine and bromine in order to ensure the sustainability of the production processes. Very few materials withstand the high corrosiveness and the strong exothermicity of the reactions and among them RuO2 and CeO2-based catalysts have been successfully applied in HCl oxidation. The search for efficient systems for HBr oxidation was initiated by extrapolating the results of HCl oxidation based on the chemical similarity of these reactions. Interestingly, despite its inactivity in HCl oxidation, TiO2 was found to be an outstanding HBr oxidation catalyst, which highlighted that the latter reaction is more complex than previously assumed. Herein, we discuss the results of recent comparative studies of HCl and HBr oxidation on both rutile-type (RuO2, IrO2, and TiO2) and ceria-based catalysts using a combination of advanced experimental and theoretical methods to provide deeper molecular-level understanding of the reactions. This knowledge aids the design of the next-generation catalysts for halogen recycling. PMID:27131113

  8. Vacuum-insulated catalytic converter

    Energy Technology Data Exchange (ETDEWEB)

    Benson, David K. (Golden, CO)

    2001-01-01

    A catalytic converter has an inner canister that contains catalyst-coated substrates and an outer canister that encloses an annular, variable vacuum insulation chamber surrounding the inner canister. An annular tank containing phase-change material for heat storage and release is positioned in the variable vacuum insulation chamber a distance spaced part from the inner canister. A reversible hydrogen getter in the variable vacuum insulation chamber, preferably on a surface of the heat storage tank, releases hydrogen into the variable vacuum insulation chamber to conduct heat when the phase-change material is hot and absorbs the hydrogen to limit heat transfer to radiation when the phase-change material is cool. A porous zeolite trap in the inner canister absorbs and retains hydrocarbons from the exhaust gases when the catalyst-coated substrates and zeolite trap are cold and releases the hydrocarbons for reaction on the catalyst-coated substrate when the zeolite trap and catalyst-coated substrate get hot.

  9. Synthesis of water-dispersed magnetic nanoparticles (H2O-DMNPs) of β-cyclodextrin modified Fe3O4 and its catalytic application in Kabachnik-Fields multicomponent reaction

    Science.gov (United States)

    Rostamnia, Sadegh; Doustkhah, Esmail

    2015-07-01

    Water-dispersed magnetic nanoparticles (H2O-DMNPs) of β-cyclodextrin modified Fe3O4 were successfully synthesized. β-Cyclodextrin acts as stabilizer and structure directing agent of Fe3O4. Subsequently, the dispersion of Fe3O4@β-CD was applied for the Kabachnik-Fields multicomponent reaction through three-component synthesis of an amine, aldehyde, and dimethylphosphonate. β-CD had also a drastic effect in accelerating the catalysis of phosphonate synthesis. By this protocol, phosphonate derivatives were synthesized in high yields and the catalyst was recycled for 10 successful runs.

  10. Catalytic models developed through social work

    DEFF Research Database (Denmark)

    Jensen, Mogens

    2015-01-01

    The article develops the concept of catalytic processes in relation to social work with adolescents in an attempt to both reach a more nuanced understanding of social work and at the same time to develop the concept of catalytic processes in psychology. The social work is pedagogical treatment of...... adolescents placed in out-of-home care and is characterised using three situated cases as empirical data. Afterwards the concept of catalytic processes is briefly presented and then applied in an analysis of pedagogical treatment in the three cases. The result is a different conceptualisation of the social...... work with new possibilities of development of the work, but also suggestions for development of the concept of catalytic processes....

  11. Catalytic converters as a source of platinum

    Directory of Open Access Journals (Sweden)

    A. Fornalczyk

    2011-10-01

    Full Text Available The increase of Platinum Group Metals demand in automotive industry is connected with growing amount of cars equipped with the catalytic converters. The paper presents the review of available technologies during recycling process. The possibility of removing platinum from the used catalytic converters applying pyrometallurgical and hyrdometallurgical methods were also investigated. Metals such as Cu, Pb, Ca, Mg, Cd were used in the pyrometallurgical research (catalytic converter was melted with Cu, Pb and Ca or Mg and Cd vapours were blown through the whole carrier. In hydrometallurgical research catalytic converters was dissolved in aqua regia. Analysis of Pt contents in the carrier before and after the process was performed by means of atomic absorption spectroscopy. Obtained result were discussed.

  12. Kinetic catalytic studies of scorpion's hemocyanin

    International Nuclear Information System (INIS)

    Hemocyanins are copper proteins which function as oxygen carriers in the haemolymph of Molluscs and Arthropods. They possess enzymatic properties: peroxidatic and catalatic activities, although they have neither iron nor porphyrin ring at the active site. The kinetics of the catalytic reaction is described. The reaction of superoxide anion with hemocyanin has been studied using pulse radiolysis at pH 9. The catalytic rate constant is 3.5 X 107 mol-1.l.s-1

  13. Characterization of Aqueous Peroxomolybdates with Catalytic Applicability

    OpenAIRE

    Taube, Fabian

    2003-01-01

    Abstract This thesis is a summary of five papers, containing equilibrium and structure studies of aqueous molybdate and peroxomolybdate species. Some of the peroxomolybdate species have also been studied in terms of their dynamic and catalytic properties. The primary objective was to characterize species with potential catalytic activity, with emphasis on thebleach process of kraft pulp. For this, potentiometry, EXAFS and 17O, 31P, 1H and 95 Mo NMR have been used. The molybdate speciation in ...

  14. MOBILE COMPLEX FOR CATALYTIC THERMAL WASTE TREATMENT

    OpenAIRE

    Vedi V.E.; Rovenskii A.I.

    2012-01-01

    The design and purpose of the basic units of the mobile waste processing complex “MPK” are described. Experimental data of catalytic purification of exhaust gases are presented. Experimental data on catalytic clearing of final gases of a designed mobile incinerator plant are shown. It is defined, that concentrating of parasitic bridging in waste gases of the complex are considerably smaller, rather than allowed by normative documents.

  15. MOBILE COMPLEX FOR CATALYTIC THERMAL WASTE TREATMENT

    Directory of Open Access Journals (Sweden)

    Vedi V.E.

    2012-12-01

    Full Text Available The design and purpose of the basic units of the mobile waste processing complex “MPK” are described. Experimental data of catalytic purification of exhaust gases are presented. Experimental data on catalytic clearing of final gases of a designed mobile incinerator plant are shown. It is defined, that concentrating of parasitic bridging in waste gases of the complex are considerably smaller, rather than allowed by normative documents.

  16. Temperature Modulation of a Catalytic Gas Sensor

    OpenAIRE

    Eike Brauns; Eva Morsbach; Sebastian Kunz; Marcus Baeumer; Walter Lang

    2014-01-01

    The use of catalytic gas sensors usually offers low selectivity, only based on their different sensitivities for various gases due to their different heats of reaction. Furthermore, the identification of the gas present is not possible, which leads to possible misinterpretation of the sensor signals. The use of micro-machined catalytic gas sensors offers great advantages regarding the response time, which allows advanced analysis of the sensor response. By using temperature modulation, additi...

  17. Catalytic ammonia oxidation to nitrogen (I) oxide

    OpenAIRE

    MASALITINA NATALIYA YUREVNA; SAVENKOV ANATOLIY SERGEEVICH

    2015-01-01

    The process of synthesis of nitrous oxide by low-temperature catalytical oxidation of NH has been investigated for organic synthesis. The investigation has been carried out by the stage separation approach with NH oxidation occurring in several reaction zones, which characterized by different catalytic conditions. The selectivity for N₂O was 92–92,5 % at the ammonia conversion of 98–99.5 % in the optimal temperature range.

  18. Preparation and Catalytic Oxidation Activity on 2-mercaptoethanol of a Novel Catalytic Cellulose Fibres

    Institute of Scientific and Technical Information of China (English)

    YAO Yu-yuan; LI Ying-jie; CHEN Wen-xing; Lü Wang-yang; Lü Su-fang; XU Min-hong; LIU Fan

    2007-01-01

    Cobalt tetra(N-carbonylacylic) aminophthalocyanine was supported on cellulose fibres by graft reaction to obtain a novel polymer catalyst, catalytic cellulose fibres (CCF),and the optimal supporting conditions were pH = 6, 80℃,t = 120 min. The catalytic oxidation activity of CCF towards oxidation of 2-mereaptoethanol (MEA) in aqueous solution was investigated. The experimental results demonstrated that CCF had good catalytic oxidation activity on MEA at room temperature, causing no secondary pollution and remaining efficient for the repetitive tests with no obvious decrease of catalytic activity.

  19. Low efficiency deasphalting and catalytic cracking

    International Nuclear Information System (INIS)

    This patent describes a process for converting an asphaltene and metals containing heavy hydrocarbon feed to lighter, more valuable products the metals comprising Ni and V. It comprises: demetallizing the feed by deasphalting the feed in a solvent deasphalting means operating at solvent deasphalting conditions including a solvent: feed volume ratio of about 1:1 to 4:1, using a solvent selected from the group of C4 to 400 degrees F. hydrocarbons and mixtures thereof; recovering from the solvent rich fraction a demetallized oil intermediate product, having a boiling range and containing at least 10 wt.% of the asphaltenes, and 5 to 30% of the Ni and V, and at least 10 wt.% of the solvent present in the solvent rich phase produced in the deasphalting means; catalytically cracking the demetallized oil intermediate product in a catalytic cracking means operating at catalytic cracking conditions to produce a catalytically cracked product vapor fraction having a lower boiling range than the boiling range of the demetallized oil intermediate product; and fractionating the catalytically cracked product in a fractionation means to produce catalytically cracked product fractions

  20. Synthesis of water-dispersed magnetic nanoparticles (H2O-DMNPs) of β-cyclodextrin modified Fe3O4 and its catalytic application in Kabachnik–Fields multicomponent reaction

    International Nuclear Information System (INIS)

    Water-dispersed magnetic nanoparticles (H2O-DMNPs) of β-cyclodextrin modified Fe3O4 were successfully synthesized. β-Cyclodextrin acts as stabilizer and structure directing agent of Fe3O4. Subsequently, the dispersion of Fe3O4@β-CD was applied for the Kabachnik–Fields multicomponent reaction through three-component synthesis of an amine, aldehyde, and dimethylphosphonate. β-CD had also a drastic effect in accelerating the catalysis of phosphonate synthesis. By this protocol, phosphonate derivatives were synthesized in high yields and the catalyst was recycled for 10 successful runs. - Highlights: • Fe3O4@β-CD as a nanomagnetically catalyst. • A reusable magnetic nanocatalyst synthesis using commercially available compounds. • Represents advantages, operational simplicity, no waste, higher yield and with easy workup

  1. Synthesis of water-dispersed magnetic nanoparticles (H{sub 2}O-DMNPs) of β-cyclodextrin modified Fe{sub 3}O{sub 4} and its catalytic application in Kabachnik–Fields multicomponent reaction

    Energy Technology Data Exchange (ETDEWEB)

    Rostamnia, Sadegh, E-mail: srostamnia@gmail.com [Organic and Nano Group (ONG), Department of Chemistry, Faculty of Science, University of Maragheh, P.O. Box. 55181-83111, Maragheh (Iran, Islamic Republic of); Doustkhah, Esmail [Organic and Nano Group (ONG), Department of Chemistry, Faculty of Science, University of Maragheh, P.O. Box. 55181-83111, Maragheh (Iran, Islamic Republic of); Young Researchers and Elite Club, Maragheh Branch, Islamic Azad University, Maragheh (Iran, Islamic Republic of)

    2015-07-15

    Water-dispersed magnetic nanoparticles (H{sub 2}O-DMNPs) of β-cyclodextrin modified Fe{sub 3}O{sub 4} were successfully synthesized. β-Cyclodextrin acts as stabilizer and structure directing agent of Fe{sub 3}O{sub 4}. Subsequently, the dispersion of Fe{sub 3}O{sub 4}@β-CD was applied for the Kabachnik–Fields multicomponent reaction through three-component synthesis of an amine, aldehyde, and dimethylphosphonate. β-CD had also a drastic effect in accelerating the catalysis of phosphonate synthesis. By this protocol, phosphonate derivatives were synthesized in high yields and the catalyst was recycled for 10 successful runs. - Highlights: • Fe{sub 3}O{sub 4}@β-CD as a nanomagnetically catalyst. • A reusable magnetic nanocatalyst synthesis using commercially available compounds. • Represents advantages, operational simplicity, no waste, higher yield and with easy workup.

  2. Catalytic and surface oxidation processes on transition metal surfaces

    OpenAIRE

    Jaatinen, Sampsa

    2007-01-01

    Transition metals are technologically important catalytic materials. The transition metal catalysts are used for example in petroleum and fertilizer industry. In the car industry the catalytic materials are used in the catalytic converters. Because of the industrial importance the catalytic metals have been widely studied throughout the past decades. Nonetheless, the oxidation mechanisms of small molecules and the effect of alloying to catalytic properties of metals are not fully understood. ...

  3. On the Structural Context and Identification of Enzyme Catalytic Residues

    OpenAIRE

    Yu-Tung Chien; Shao-Wei Huang

    2013-01-01

    Enzymes play important roles in most of the biological processes. Although only a small fraction of residues are directly involved in catalytic reactions, these catalytic residues are the most crucial parts in enzymes. The study of the fundamental and unique features of catalytic residues benefits the understanding of enzyme functions and catalytic mechanisms. In this work, we analyze the structural context of catalytic residues based on theoretical and experimental structure flexibility. The...

  4. Determination of Trace Mercury by Catalytic Solid Substrate-room Temperature Phosphorimetry

    Institute of Scientific and Technical Information of China (English)

    Jia Ming LIU; Yun Xiong WU; Shao Xian LIN; Fei Ming LI; Xiu Mei SHI; Zhong Bin SHI; Guo Hui ZHU; Zhi Ming LI; Xiao Mei HUANG

    2006-01-01

    A new highly sensitive method (detection limit: 4.1 ag spot-1, sample volume: 0.4 μL spot-1) for the determination of trace Hg2+ by catalytic solid substrate-room temperature phosphorimetry has been established in this paper. This method has been successfully applied to determine trace Hg2+ in water.

  5. Ozone catalytic oxidation of benzene over AgMn/HZSM-5 catalysts at room temperature:Effects of Mn loading and water content%AgMn/HZSM-5催化剂上室温O3氧化脱除空气中的苯:Mn含量和水含量的影响

    Institute of Scientific and Technical Information of China (English)

    刘阳; 李小松; 刘景林; 石川; 朱爱民

    2014-01-01

    考察了Mn含量和水含量对AgMn/HZSM-5(AgMn/HZ)催化剂上室温O3氧化(OZCO)脱除空气中苯的影响.研究发现, Mn含量为2.4 wt%的AgMn/HZ催化剂(AgMn/HZ(2.4))具有大的比表面积和高的MnOx分散度, OZCO活性和稳定性最高.反应后的程序升温脱附结果表明,2.4 wt%的Mn含量能有效抑制苯和甲酸在催化剂上的残留.当Mn含量≤2.4 wt%时,催化剂分解O3的活性在苯氧化过程中占主导;当Mn含量>2.4 wt%时,苯的活化起主要作用.基于AgMn/HZ(2.4)催化剂优越的反应活性和稳定性,进一步研究了湿气流中该催化剂上苯的氧化.与干气流相比,水汽的加入能显著提高催化剂的反应活性和稳定性,且以0.1-0.2 vol%水含量时最优.%The effects of Mn loading and water content on AgMn/HZSM-5 (AgMn/HZ) catalysts were investi-gated in the ozone catalytic oxidation (OZCO) of benzene in a continuous air flow at room tempera-ture. The catalytic activity is closely related to the Mn loading, and the AgMn/HZ catalyst with 2.4 wt%Mn (AgMn/HZ(2.4)) had the highest activity and stability in benzene oxidation as a result of its large surface area and high MnOx dispersion. Temperature-programmed desorption of the used catalysts demonstrated that 2.4 wt%was also the optimal Mn loading for suppressing the accumu-lation of benzene and HCOOH over the catalyst surface after benzene oxidation. For AgMn/HZ cata-lysts with Mn loadings≤2.4 wt%, O3 decomposition to active oxygen species (O*) plays the most important role in benzene oxidation;however, benzene activation is the crucial step for benzene oxidation by O3 over AgMn/HZ catalysts with Mn loadings>2.4 wt%. The AgMn/HZ(2.4) catalyst was then used to perform OZCO of benzene in a humid stream. Compared with dry gas, water vapor greatly enhanced the activity and stability of the AgMn/HZ(2.4) catalyst, and 0.1-0.2 vol%was the optimal water content for benzene oxidation.

  6. Biodiesel from waste cooking oil via base-catalytic and supercritical methanol transesterification

    Energy Technology Data Exchange (ETDEWEB)

    Demirbas, Ayhan [Sila Science, Trabzon 61040 (Turkey)

    2009-04-15

    In this study, waste cooking oil has subjected to transesterification reaction by potassium hydroxide (KOH) catalytic and supercritical methanol methods obtaining for biodiesel. In catalyzed methods, the presence of water has negative effects on the yields of methyl esters. In the catalytic transesterification free fatty acids and water always produce negative effects since the presence of free fatty acids and water causes soap formation, consumes catalyst, and reduces catalyst effectiveness. Free fatty acids in the waste cooking oil are transesterified simultaneously in supercritical methanol method. Since waste cooking oil contains water and free fatty acids, supercritical transesterification offers great advantage to eliminate the pre-treatment and operating costs. The effects of methanol/waste cooking oils ratio, potassium hydroxide concentration and temperature on the biodiesel conversion were investigated. (author)

  7. Biodiesel from waste cooking oil via base-catalytic and supercritical methanol transesterification

    International Nuclear Information System (INIS)

    In this study, waste cooking oil has subjected to transesterification reaction by potassium hydroxide (KOH) catalytic and supercritical methanol methods obtaining for biodiesel. In catalyzed methods, the presence of water has negative effects on the yields of methyl esters. In the catalytic transesterification free fatty acids and water always produce negative effects since the presence of free fatty acids and water causes soap formation, consumes catalyst, and reduces catalyst effectiveness. Free fatty acids in the waste cooking oil are transesterified simultaneously in supercritical methanol method. Since waste cooking oil contains water and free fatty acids, supercritical transesterification offers great advantage to eliminate the pre-treatment and operating costs. The effects of methanol/waste cooking oils ratio, potassium hydroxide concentration and temperature on the biodiesel conversion were investigated

  8. Azomethine Ylides from Nitrones: Using Catalytic nBuLi for the Totally Stereoselective Synthesis of trans-2-Alkyl-3-oxazolines.

    Science.gov (United States)

    Juste-Navarro, Veronica; Delso, Ignacio; Tejero, Tomás; Merino, Pedro

    2016-08-01

    The cycloaddition of azomethine ylide N-oxides (nitrone ylides) with aldehydes provides 3-oxazolines in a completely stereoselective manner in the presence of a catalytic amount of n-butyllithium. The process involves an initial nucleophilic attack on the aldehyde, followed by intramolecular oxygen addition to the nitrone moiety and lithium-assisted elimination of water, regenerating the catalytic species. Various Li-based catalytic systems are possible and the in situ generated water is required for continuing the catalytic cycle. The best results are observed with 20 mol % of n-butyllithium, whereas the use of stoichiometric amounts inhibit the rate of catalysis. Experimental, spectroscopic, and computational mechanistic studies have provided evidence of lithium-ion catalysis and rationalized several competing catalytic pathways. PMID:27258625

  9. A theoretical study on the catalytic effect of nanoparticle confined in carbon nanotube

    Science.gov (United States)

    Qin, Wu; Li, Xin

    2011-01-01

    We investigated the catalytic effect of CuO nanoparticles confined in carbon nanotubes using molecular dynamics simulations and density functional theory calculations. Ozone decomposition and hydroxyl radical generation were used as the probe reactions to investigate the catalytic behavior of catalyst. The effects of the confined environment of carbon nanotubes induced more reactants into the channel. Interface interactions between reactants and CuO nanoparticles in the channel and charge transfer accelerated the decomposition of ozone into oxygen molecule and atomic oxygen species. The atomic oxygen species then interacted to water molecule to generate hydroxyl radicals, which were truly identified by electron paramagnetic resonance (EPR) technique.

  10. A novel liquid system of catalytic hydrogenation

    Institute of Scientific and Technical Information of China (English)

    LI; XiaoNian; XIANG; YiZhi

    2007-01-01

    On the basis that endothermic aqueous-phase reforming of oxygenated hydrocarbons for H2 production and exothermic liquid phase hydrogenation of organic compounds are carried out under extremely close conditions of temperature and pressure over the same type of catalyst, a novel liquid system of catalytic hydrogenation has been proposed, in which hydrogen produced from aqueous-phase reforming of oxygenated hydrocarbons is in situ used for liquid phase hydrogenation of organic compounds. The usage of active hydrogen generated from aqueous-phase reforming of oxygenated hydrocarbons for liquid catalytic hydrogenation of organic compounds could lead to increasing the selectivity to H2 in the aqueous-phase reforming due to the prompt removal of hydrogen on the active centers of the catalyst. Meanwhile, this novel liquid system of catalytic hydrogenation might be a potential method to improve the selectivity to the desired product in liquid phase catalytic hydrogenation of organic compounds. On the other hand, for this novel liquid system of catalytic hydrogenation, some special facilities for H2 generation, storage and transportation in traditional liquid phase hydrogenation industry process are yet not needed. Thus, it would simplify the working process of liquid phase hydrogenation and increase the energy usage and hydrogen productivity.

  11. Catalytic oxidations by vanadium complexes

    OpenAIRE

    Ligtenbarg, A.G J; Hage, R.; Feringa, B. L.

    2003-01-01

    Vanadium haloperoxidases catalyse the oxidation of halides leading to halogenation of substrates or, in the absence of suitable substrates, to oxidation of hydrogen peroxide into singlet oxygen and water. Furthermore, V-haloperoxidases are capable to give enantioselective sulfoxidation under the appropriate conditions. The most interesting model compounds that have been synthesised and studied as bromination catalysts, and catalysts for, i.e. epoxidation, hydroxylation, sulfoxidation and alco...

  12. Highly Dense Isolated Metal Atom Catalytic Sites

    DEFF Research Database (Denmark)

    Chen, Yaxin; Kasama, Takeshi; Huang, Zhiwei; Hu, Pingping; Chen, Jianmin; Liu, Xi; Tang, Xingfu

    2015-01-01

    Atomically dispersed noble-metal catalysts with highly dense active sites are promising materials with which to maximise metal efficiency and to enhance catalytic performance; however, their fabrication remains challenging because metal atoms are prone to sintering, especially at a high metal...... loading. A dynamic process of formation of isolated metal atom catalytic sites on the surface of the support, which was achieved starting from silver nanoparticles by using a thermal surface-mediated diffusion method, was observed directly by using in situ electron microscopy and in situ synchrotron X......-ray diffraction. A combination of electron microscopy images with X-ray absorption spectra demonstrated that the silver atoms were anchored on five-fold oxygen-terminated cavities on the surface of the support to form highly dense isolated metal active sites, leading to excellent reactivity in catalytic oxidation...

  13. ADAR proteins: structure and catalytic mechanism.

    Science.gov (United States)

    Goodman, Rena A; Macbeth, Mark R; Beal, Peter A

    2012-01-01

    Since the discovery of the adenosine deaminase (ADA) acting on RNA (ADAR) family of proteins in 1988 (Bass and Weintraub, Cell 55:1089-1098, 1988) (Wagner et al. Proc Natl Acad Sci U S A 86:2647-2651, 1989), we have learned much about their structure and catalytic mechanism. However, much about these enzymes is still unknown, particularly regarding the selective recognition and processing of specific adenosines within substrate RNAs. While a crystal structure of the catalytic domain of human ADAR2 has been solved, we still lack structural data for an ADAR catalytic domain bound to RNA, and we lack any structural data for other ADARs. However, by analyzing the structural data that is available along with similarities to other deaminases, mutagenesis and other biochemical experiments, we have been able to advance the understanding of how these fascinating enzymes function. PMID:21769729

  14. Catalytic microreactors for portable power generation

    Energy Technology Data Exchange (ETDEWEB)

    Karagiannidis, Symeon [Paul Scherer Institute, Villigen (Switzerland)

    2011-07-01

    ''Catalytic Microreactors for Portable Power Generation'' addresses a problem of high relevance and increased complexity in energy technology. This thesis outlines an investigation into catalytic and gas-phase combustion characteristics in channel-flow, platinum-coated microreactors. The emphasis of the study is on microreactor/microturbine concepts for portable power generation and the fuels of interest are methane and propane. The author carefully describes numerical and experimental techniques, providing a new insight into the complex interactions between chemical kinetics and molecular transport processes, as well as giving the first detailed report of hetero-/homogeneous chemical reaction mechanisms for catalytic propane combustion. The outcome of this work will be widely applied to the industrial design of micro- and mesoscale combustors. (orig.)

  15. Catalytic nanoarchitectonics for environmentally compatible energy generation

    Directory of Open Access Journals (Sweden)

    Hideki Abe

    2016-01-01

    Full Text Available Environmentally compatible energy management is one of the biggest challenges of the 21st century. Low-temperature conversion of chemical to electrical energy is of particular importance to minimize the impact to the environment while sustaining the consumptive economy. In this review, we shed light on one of the most versatile energy-conversion technologies: heterogeneous catalysts. We establish the integrity of structural tailoring in heterogeneous catalysts at different scales in the context of an emerging paradigm in materials science: catalytic nanoarchitectonics. Fundamental backgrounds of energy-conversion catalysis are first provided together with a perspective through state-of-the-art energy-conversion catalysis including catalytic exhaust remediation, fuel-cell electrocatalysis and photosynthesis of solar fuels. Finally, the future evolution of catalytic nanoarchitectonics is overviewed: possible combinations of heterogeneous catalysts, organic molecules and even enzymes to realize reaction-selective, highly efficient and long-life energy conversion technologies which will meet the challenge we face.

  16. Use catalytic combustion for LHV gases

    Energy Technology Data Exchange (ETDEWEB)

    Tucci, E.R.

    1982-03-01

    This paper shows how low heating value (LHV) waste gases can be combusted to recover energy even when the gases won't burn in a normal manner. Significant energy and economic savings can result by adopting this process. Catalytic combustion is a heterogeneous surface-catalyzed air oxidation of fuel, gaseous or liquid, to generate thermal energy in a flameless mode. The catalytic combustion process is quite complex since it involves numerous catalytic surface and gas-phase chemical reactions. During low temperature surface-catalyzed combustion, as in start-up, the combustion stage is under kinetically controlled conditions. The discussion covers the following topics - combustor substrates; combustor washcoating and catalyzing; combustor operational modes (turbine or tabular modes); applications in coal gasification and in-situ gasification; waste process gases. 16 refs.

  17. Xylan-Degrading Catalytic Flagellar Nanorods.

    Science.gov (United States)

    Klein, Ágnes; Szabó, Veronika; Kovács, Mátyás; Patkó, Dániel; Tóth, Balázs; Vonderviszt, Ferenc

    2015-09-01

    Flagellin, the main component of flagellar filaments, is a protein possessing polymerization ability. In this work, a novel fusion construct of xylanase A from B. subtilis and Salmonella flagellin was created which is applicable to build xylan-degrading catalytic nanorods of high stability. The FliC-XynA chimera when overexpressed in a flagellin deficient Salmonella host strain was secreted into the culture medium by the flagellum-specific export machinery allowing easy purification. Filamentous assemblies displaying high surface density of catalytic sites were produced by ammonium sulfate-induced polymerization. FliC-XynA nanorods were resistant to proteolytic degradation and preserved their enzymatic activity for a long period of time. Furnishing enzymes with self-assembling ability to build catalytic nanorods offers a promising alternative approach to enzyme immobilization onto nanostructured synthetic scaffolds. PMID:25966869

  18. Flow parameters of IC engine catalytic converters

    Energy Technology Data Exchange (ETDEWEB)

    Zmudka, Z.; Postrzednik, S. [Silesian Univ. of Tech., Gliwice (Poland)

    2007-07-01

    Conversion rate of harmful substances is the principal parameter of catalyst work in respect of ecology. However, resistance of exhaust gas flow through the catalytic converter is also essential problem, apart from its chemical efficiency because fitting the catalyst in exhaust system alters flow characteristic of this system significantly. Catalytic converter can be treated as local or linear resistance element of exhaust system. The first model, in which flow resistance generated by a catalyst is treated as local resistance, is more simplified. Resistance number of the converter was calculated using Darcy model. In the second case, exhaust gas flow resistance through catalyst is treated as linear resistance with energy dissipation (linear frictional resistance) distributed linearly along way of exhaust gas flow. Friction number for the tested converter was calculated and analysed. The problem has been illustrated by results of experimental researches of three-way catalytic converter installed in exhaust system of spark ignition engine and its basic analysis. (orig.)

  19. Electro Catalytic Oxidation (ECO) Operation

    Energy Technology Data Exchange (ETDEWEB)

    Morgan Jones

    2011-03-31

    The power industry in the United States is faced with meeting many new regulations to reduce a number of air pollutants including sulfur dioxide, nitrogen oxides, fine particulate matter, and mercury. With over 1,000 power plants in the US, this is a daunting task. In some cases, traditional pollution control technologies such as wet scrubbers and SCRs are not feasible. Powerspan's Electro-Catalytic Oxidation, or ECO{reg_sign} process combines four pollution control devices into a single integrated system that can be installed after a power plant's particulate control device. Besides achieving major reductions in emissions of sulfur dioxide (SO{sub 2}), nitrogen oxides (NOx), fine particulate matter (PM2.5) and mercury (Hg), ECO produces a highly marketable fertilizer, which can help offset the operating costs of the process system. Powerspan has been operating a 50-MW ECO commercial demonstration unit (CDU) at FirstEnergy Corp.'s R.E. Burger Plant near Shadyside, Ohio, since February 2004. In addition to the CDU, a test loop has been constructed beside the CDU to demonstrate higher NOx removal rates and test various scrubber packing types and wet ESP configurations. Furthermore, Powerspan has developed the ECO{reg_sign}{sub 2} technology, a regenerative process that uses a proprietary solvent to capture CO{sub 2} from flue gas. The CO{sub 2} capture takes place after the capture of NOx, SO{sub 2}, mercury, and fine particulate matter. Once the CO{sub 2} is captured, the proprietary solution is regenerated to release CO{sub 2} in a form that is ready for geological storage or beneficial use. Pilot scale testing of ECO{sub 2} began in early 2009 at FirstEnergy's Burger Plant. The ECO{sub 2} pilot unit is designed to process a 1-MW flue gas stream and produce 20 tons of CO{sub 2} per day, achieving a 90% CO{sub 2} capture rate. The ECO{sub 2} pilot program provided the opportunity to confirm process design and cost estimates, and prepare for large

  20. Polyethersulfone hollow fiber modified with poly(styrenesulfonate) and Pd nanoparticles for catalytic reaction

    Science.gov (United States)

    Emin, C.; Gu, Y.; Remigy, J.-C.; Lahitte, J.-F.

    2015-07-01

    The aim of this work is the synthesis of polymer-stabilized Pd nanoparticles (PdNP) inside a functionalized polymeric porous membrane in order to develop hybrid catalytic membrane reactors and to test them in model metal-catalyzed organic reactions. For this goal, a polymeric membrane support (Polyethersulfone hollow fiber-shaped) was firstly functionalized with an ionogenic polymer (i.e. poly(styrenesulfonate) capable to retain PdNP precursors using an UV photo-grafting method. PdNP were then generated inside the polymeric matrix by chemical reduction of precursor salts (intermatrix synthesis). The catalytic performance of the PdNP catalytic membranes was evaluated using reduction of nitrophenol by sodium borohydride (NaBH4) in water.

  1. A catalytic surface for amyloid fibril formation

    Energy Technology Data Exchange (ETDEWEB)

    Hammarstroem, P; Ali, M M; Mishra, R; Tengvall, P; Lundstroem, I [Department of Physics, Biology and Chemistry, Linkoeping University, SE-581 83 Linkoeping (Sweden); Svensson, S [Astra Zeneca R and D, SE-151 85 Soedertaelje (Sweden)], E-mail: ingemar@ifm.liu.se

    2008-03-15

    A hydrophobic surface incubated in a solution of protein molecules (insulin monomers) was made into a catalytic surface for amyloid fibril formation by repeatedly incubate, rinse and dry the surface. The present contribution describes how this unexpected transformation occurred and its relation to rapid fibrillation of insulin solutions in contact with the surface. A tentative model of the properties of the catalytic surface is given, corroborated by ellipsometric measurements of the thickness of the organic layer on the surface and by atomic force microscopy. The surfaces used were spontaneously oxidized silicon made hydrophobic through treatment in dichlorodimethylsilane.

  2. Thermal and catalytic pyrolysis of plastic waste

    Directory of Open Access Journals (Sweden)

    Débora Almeida

    2016-02-01

    Full Text Available Abstract The amount of plastic waste is growing every year and with that comes an environmental concern regarding this problem. Pyrolysis as a tertiary recycling process is presented as a solution. Pyrolysis can be thermal or catalytical and can be performed under different experimental conditions. These conditions affect the type and amount of product obtained. With the pyrolysis process, products can be obtained with high added value, such as fuel oils and feedstock for new products. Zeolites can be used as catalysts in catalytic pyrolysis and influence the final products obtained.

  3. Catalytic Enantioselective Functionalization of Unactivated Terminal Alkenes.

    Science.gov (United States)

    Coombs, John R; Morken, James P

    2016-02-01

    Terminal alkenes are readily available functional groups which appear in α-olefins produced by the chemical industry, and they appear in the products of many contemporary synthetic reactions. While the organic transformations that apply to alkenes are amongst the most studied reactions in all of chemical synthesis, the number of reactions that apply to nonactivated terminal alkenes in a catalytic enantioselective fashion is small in number. This Minireview highlights the cases where stereocontrol in catalytic reactions of 1-alkenes is high enough to be useful for asymmetric synthesis. PMID:26764019

  4. Catalytic gasification of oil-shales

    Energy Technology Data Exchange (ETDEWEB)

    Lapidus, A.; Avakyan, T. [I.M. Gubkin Russian State Univ. of Oil and Gas, Moscow (Russian Federation); Strizhakova, Yu. [Samara State Univ. (Russian Federation)

    2012-07-01

    Nowadays, the problem of complex usage of solid fossil fuels as raw materials for obtaining of motor fuels and chemical products is becoming increasingly important. A one of possible solutions of the problem is their gasification with further processing of gaseous and liquid products. In this work we have investigated the process of thermal and catalytic gasification of Baltic and Kashpir oil-shales. We have shown that, as compared with non-catalytic process, using of nickel catalyst in the reaction increases the yield of gas, as well as hydrogen content in it, and decreases the amount of liquid products. (orig.)

  5. Heterogeneous Catalytic Ozonization of Sulfosalicylic Acid

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    This paper describes the potential of heterogeneous catalytic ozonization of sulfo-salicylic acid (SSal). It was found that catalytic ozonization in the presence of Mn-Zr-O (a modified manganese dioxide supported on silica gel) had significantly enhanced the removal rate (72%) of total organic carbon (TOC) compared with that of ozonization alone (19%). The efficient removal rate of TOC was probably due to increasing the adsorption ability of catalyst and accelerating decomposition of ozone to produce more powerful oxidants than ozone.

  6. Synthesis of silver nanoparticles: Effects of anionic ligands on formation and catalytic activity

    International Nuclear Information System (INIS)

    We report a facile method to synthesize water soluble Ag nanoparticles (NPs) using various anionic complexing ligands as reducing as well as stabilizing agents. The formation of the particles depends on the initial molar ratio of ligands to silver nitrate. Also, the alkaline condition of preparative solution is found to be necessary for the formation of Ag NPs. It has been important to mention here that the temperature of the reaction mixture plays an important factor on the rate of formation of the particles. The particles were characterized by UV–vis spectroscopy, transmission electron microscopy, dynamic light scattering and X-ray diffraction techniques. The formed particles were found to be stable for more than a month. Zeta potential measurements suggest that the negative potential created by the adsorbed complexing ligands contribute to the stability of the Ag NPs suspensions. The effect of the ligands on the formation, stability and catalytic activity of the Ag NPs was evaluated. The obtained Ag NPs exhibit a good catalytic activity toward reduction of o-nitroaniline. The results reveal that the presence of more coordination sites in the ligands affects the catalytic activity of the particles. - Highlights: • Formation of Ag nanoparticles using anionic ligands as reducing agents and stabilizers. • Number of –COOH groups in the ligands affect the formation of particles. • The formed nanoparticles show good catalytic activity. • Number of –COOH groups in the ligands affect the catalytic activity of the particles

  7. Degradation of paracetamol by catalytic wet air oxidation and sequential adsorption – Catalytic wet air oxidation on activated carbons

    International Nuclear Information System (INIS)

    Highlights: ► Three activated carbons (AC) compared as adsorbents and oxidation catalysts. ► Similar evolution for catalytic and adsorptive properties of AC over reuses. ► Acidic and mesoporous AC to be preferred, despite lower initial efficiency. ► Oxidative degradation of paracetamol improves biodegradability. ► Convenient hybrid adsorption–regenerative oxidation process for continuous treatment. - Abstract: The concern about the fate of pharmaceutical products has raised owing to the increasing contamination of rivers, lakes and groundwater. The aim of this paper is to evaluate two different processes for paracetamol removal. The catalytic wet air oxidation (CWAO) of paracetamol on activated carbon was investigated both as a water treatment technique using an autoclave reactor and as a regenerative treatment of the carbon after adsorption in a sequential fixed bed process. Three activated carbons (ACs) from different source materials were used as catalysts: two microporous basic ACs (S23 and C1) and a meso- and micro-porous acidic one (L27). During the first CWAO experiment the adsorption capacity and catalytic performance of fresh S23 and C1 were higher than those of fresh L27 despite its higher surface area. This situation changed after AC reuse, as finally L27 gave the best results after five CWAO cycles. Respirometry tests with activated sludge revealed that in the studied conditions the use of CWAO enhanced the aerobic biodegradability of the effluent. In the ADOX process L27 also showed better oxidation performances and regeneration efficiency. This different ageing was examined through AC physico-chemical properties.

  8. Degradation of paracetamol by catalytic wet air oxidation and sequential adsorption - Catalytic wet air oxidation on activated carbons

    Energy Technology Data Exchange (ETDEWEB)

    Quesada-Penate, I. [Universite de Toulouse, INPT, UPS, Laboratoire de Genie Chimique, 4, Allee Emile Monso, F-31432 Toulouse (France); CNRS, Laboratoire de Genie Chimique, F-31432 Toulouse (France); Julcour-Lebigue, C., E-mail: carine.julcour@ensiacet.fr [Universite de Toulouse, INPT, UPS, Laboratoire de Genie Chimique, 4, Allee Emile Monso, F-31432 Toulouse (France); CNRS, Laboratoire de Genie Chimique, F-31432 Toulouse (France); Jauregui-Haza, U.J. [Instituto Superior de Tecnologias y Ciencias Aplicadas, Ave. Salvador Allende y Luaces, Habana (Cuba); Wilhelm, A.M.; Delmas, H. [Universite de Toulouse, INPT, UPS, Laboratoire de Genie Chimique, 4, Allee Emile Monso, F-31432 Toulouse (France); CNRS, Laboratoire de Genie Chimique, F-31432 Toulouse (France)

    2012-06-30

    Highlights: Black-Right-Pointing-Pointer Three activated carbons (AC) compared as adsorbents and oxidation catalysts. Black-Right-Pointing-Pointer Similar evolution for catalytic and adsorptive properties of AC over reuses. Black-Right-Pointing-Pointer Acidic and mesoporous AC to be preferred, despite lower initial efficiency. Black-Right-Pointing-Pointer Oxidative degradation of paracetamol improves biodegradability. Black-Right-Pointing-Pointer Convenient hybrid adsorption-regenerative oxidation process for continuous treatment. - Abstract: The concern about the fate of pharmaceutical products has raised owing to the increasing contamination of rivers, lakes and groundwater. The aim of this paper is to evaluate two different processes for paracetamol removal. The catalytic wet air oxidation (CWAO) of paracetamol on activated carbon was investigated both as a water treatment technique using an autoclave reactor and as a regenerative treatment of the carbon after adsorption in a sequential fixed bed process. Three activated carbons (ACs) from different source materials were used as catalysts: two microporous basic ACs (S23 and C1) and a meso- and micro-porous acidic one (L27). During the first CWAO experiment the adsorption capacity and catalytic performance of fresh S23 and C1 were higher than those of fresh L27 despite its higher surface area. This situation changed after AC reuse, as finally L27 gave the best results after five CWAO cycles. Respirometry tests with activated sludge revealed that in the studied conditions the use of CWAO enhanced the aerobic biodegradability of the effluent. In the ADOX process L27 also showed better oxidation performances and regeneration efficiency. This different ageing was examined through AC physico-chemical properties.

  9. Photothermally enhanced catalytic activity of partially aggregated gold nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Jun-Hyun, E-mail: jkim5@ilstu.edu; Lavin, Brian W.; Boote, Brett W.; Pham, Julie A. [Illinois State University, Department of Chemistry (United States)

    2012-07-15

    This report describes the catalytic reduction of 4-nitrophenol (4-NP) using gold nanoparticles (GNPs) in aqueous solution upon exposure to a solar-simulated light. As monodispersed GNPs possess a strong but narrow absorption band in the visible areas, anisotropic/partially aggregated GNPs are designed to have a strong and wide absorption band across visible to near-infrared wavelengths of light. Given their strong and broad absorption properties, these partially aggregated GNPs exhibited slightly superior photothermally induced heating of the reaction medium (i.e., water) when compared to the monodispersed GNPs upon exposure to a solar-simulated light. Subsequently, the catalytic reduction of 4-NP to 4-aminophenol was examined in the presence of various GNPs with and without the irradiation of light. While the monodispersed GNPs exhibited a moderate increase in the reaction rates of 4-NP with the light irradiation, the partially aggregated GNPs afforded the notable enhancement of the reaction rate, presumably due to their higher photon-to-heat conversion efficiency.

  10. Photothermally enhanced catalytic activity of partially aggregated gold nanoparticles

    International Nuclear Information System (INIS)

    This report describes the catalytic reduction of 4-nitrophenol (4-NP) using gold nanoparticles (GNPs) in aqueous solution upon exposure to a solar-simulated light. As monodispersed GNPs possess a strong but narrow absorption band in the visible areas, anisotropic/partially aggregated GNPs are designed to have a strong and wide absorption band across visible to near-infrared wavelengths of light. Given their strong and broad absorption properties, these partially aggregated GNPs exhibited slightly superior photothermally induced heating of the reaction medium (i.e., water) when compared to the monodispersed GNPs upon exposure to a solar-simulated light. Subsequently, the catalytic reduction of 4-NP to 4-aminophenol was examined in the presence of various GNPs with and without the irradiation of light. While the monodispersed GNPs exhibited a moderate increase in the reaction rates of 4-NP with the light irradiation, the partially aggregated GNPs afforded the notable enhancement of the reaction rate, presumably due to their higher photon-to-heat conversion efficiency.

  11. Diesel NO{sub x} catalytic converter development: A review

    Energy Technology Data Exchange (ETDEWEB)

    Heimrich, M.J. [Southwest Research Inst., San Antonio, TX (United States)

    1996-07-01

    This paper summarizes the findings of several technical articles on diesel NO{sub x} catalytic converter technology. Simplified theoretical reactions for NO{sub x} removal are discussed. Currently, development of catalytic NO{sub x} control technology for diesel engines is focused on systems that incorporate fuel hydrocarbons as the chemical reducing agent. Copper- and zeolite-based catalysts have been the predominant systems studied to date, but now catalysts containing precious metals are being investigated. Observed NO{sub x} reduction efficiencies typically ranged from 10 to 30 percent on actual engine exhaust systems when exhaust hydrocarbon enrichment strategies were used. Effects of carbon monoxide, sulfur dioxide, and water on NO{sub x} reduction efficiencies are reviewed. Recommendations for future research include attempts to broaden the temperature range of efficient NO{sub x} reduction, improving hydrocarbon selectivity toward the NO{sub x} reduction reaction, and the development of a supplementary reductant delivery system suitable for transient diesel engine operation.

  12. Copper on activated carbon for catalytic wet air oxidation

    Directory of Open Access Journals (Sweden)

    Nora Dolores Martínez

    2009-03-01

    Full Text Available Textile industry is an important source of water contamination. Some of the organic contaminants cannot be eliminated by nature in a reasonable period. Heterogeneous catalytic wet air oxidation is one of the most effective methods to purify wastewater with organic contaminants. In this work, catalysts based on copper supported on activated carbon were synthesized. The activated carbons were obtained from industrial wastes (apricot core and grape stalk of San Juan, Argentina. These were impregnated with a copper salt and thermically treated in an inert atmosphere. Analysis of specific surface, pore volume, p zc, acidity, basicity and XRD patterns were made in order to characterize the catalysts. The catalytic activity was tested in the oxidation of methylene blue (MB and polyvinyl alcohol (PVA in aqueous phase with pure oxygen. Reaction tests were carried out in a Parr batch reactor at different temperatures, with a 0.2 MPa partial pressure of oxygen. The amount of unconverted organics was measured by spectrophotometry. Higher temperatures were necessary for the degradation of PVA compared to those for methylene blue.

  13. Catalytic conversion of biomass to bio-syncrude oil

    Energy Technology Data Exchange (ETDEWEB)

    Mante, Ofei Daku [Virginia Polytechnic Institute and State University, Biological Systems Engineering, Blacksburg, VA (United States); Agblevor, Foster A. [Utah State University, Biological Engineering, Logan, UT (United States)

    2011-12-15

    The conversion of biomass to transportation fuels and chemicals has been of immense interest in recent years. In this study, the production of high quality bio-oil (bio-syncrude oil) was achieved by catalytically cracking pyrolysis vapors from hybrid poplar in a dual-fluidized bed reactor. The catalytic deoxygenation of the primary pyrolysis vapors was achieved with a commercial HZSM-5 at 425-450 C. The organic, water, char, coke, and gas yields were 11.9, 20.9, 16.5, 3.8, and 46.8 wt.%, respectively. This work demonstrated that the use of a fluidized bed reactor for the catalytic upgrading reduces coke formation and increases catalyst lifetime. The concentration of the permanent gases was in the order of CO > CO{sub 2}> C{sub 3}H{sub 6}> CH{sub 4}> H{sub 2}> other C{sub 2}-C{sub 4}. The light bio-syncrude (LBS) oil collected from the condenser was predominately aromatic hydrocarbons. The heavy bio-syncrude (HBS) oil collected from the electrostatic precipitator consisted of mainly phenols, methyl-substituted phenols, naphthalenes, benzenediols, and naphthalenol. The bio-syncrude oils were low in oxygen, less viscous, less acidic, stable, and high in energy density. The higher heating value of the light and heavy bio-syncrude oil was 36.89 and 33.98 MJ/kg, respectively. The distillate yields from the atmospheric distillation showed that 91 wt.% of the LBS oil distills up to 220 C and 76 wt.% of the HBS oil distills up to 440 C. Accelerated stability test of the oils at 90 C for 24 h and storage of the oils at room temperature for 10 months showed that the bio-syncrude oils were stable. The catalytic deoxygenation of the pyrolysis vapors resulted in the removal of undesirable oxygenates such as levoglucosan, carboxylic acids, aldehydes, and ketones. The bio-syncrude oil can be considered as a suitable feed for use in a petroleum refinery for the production of transportation fuels and chemicals. (orig.)

  14. Toward a catalytic site in DNA

    DEFF Research Database (Denmark)

    Jakobsen, Ulla; Rohr, Katja; Vogel, Stefan

    2007-01-01

    A number of functionalized polyaza crown ether building blocks have been incorporated into DNA-conjugates as catalytic Cu(2+) binding sites. The effect of the DNA-conjugate catalyst on the stereochemical outcome of a Cu(2+)-catalyzed Diels-Alder reaction will be presented....

  15. SELECTIVE CATALYTIC REDUCTION MERCURY FIELD SAMPLING PROJECT

    Science.gov (United States)

    A lack of data still exists as to the effect of selective catalytic reduction (SCR), selective noncatalytic reduction (SNCR), and flue gas conditioning on the speciation and removal of mercury (Hg) at power plants. This project investigates the impact that SCR, SNCR, and flue gas...

  16. Toward Facilitative Mentoring and Catalytic Interventions

    Science.gov (United States)

    Smith, Melissa K.; Lewis, Marilyn

    2015-01-01

    In TESOL teacher mentoring, giving advice can be conceptualized as a continuum, ranging from directive to facilitative feedback. The goal, over time, is to lead toward the facilitative end of the continuum and specifically to catalytic interventions that encourage self-reflection and autonomous learning. This study begins by examining research on…

  17. Catalytic reaction dynamics in inhomogeneous networks.

    Science.gov (United States)

    Watanabe, Akitomo; Yakubo, Kousuke

    2014-05-01

    Biochemical reactions in a cell can be modeled by a catalytic reaction network (CRN). It has been reported that catalytic chain reactions occur intermittently in the CRN with a homogeneous random-graph topology and its avalanche-size distribution obeys a power law with the exponent 4/3 [A. Awazu and K. Kaneko, Phys. Rev. E 80, 010902(R) (2009)]. This fact indicates that the catalytic reaction dynamics in homogeneous CRNs exhibits self-organized criticality (SOC). Structures of actual CRNs are, however, known to be highly inhomogeneous. We study the influence of various types of inhomogeneities found in real-world metabolic networks on the universality class of SOC. Our numerical results clarify that SOC keeps its universality class even for networks possessing structural inhomogeneities such as the scale-free property, community structures, and degree correlations. In contrast, if the CRN has inhomogeneous catalytic functionality, the universality class of SOC depends on how widely distributed the number of reaction paths catalyzed by a single chemical species is. PMID:25353843

  18. Novel Metal Nanomaterials and Their Catalytic Applications.

    Science.gov (United States)

    Wang, Jiaqing; Gu, Hongwei

    2015-01-01

    In the rapidly developing areas of nanotechnology, nano-scale materials as heterogeneous catalysts in the synthesis of organic molecules have gotten more and more attention. In this review, we will summarize the synthesis of several new types of noble metal nanostructures (FePt@Cu nanowires, Pt@Fe₂O₃ nanowires and bimetallic Pt@Ir nanocomplexes; Pt-Au heterostructures, Au-Pt bimetallic nanocomplexes and Pt/Pd bimetallic nanodendrites; Au nanowires, CuO@Ag nanowires and a series of Pd nanocatalysts) and their new catalytic applications in our group, to establish heterogeneous catalytic system in "green" environments. Further study shows that these materials have a higher catalytic activity and selectivity than previously reported nanocrystal catalysts in organic reactions, or show a superior electro-catalytic activity for the oxidation of methanol. The whole process might have a great impact to resolve the energy crisis and the environmental crisis that were caused by traditional chemical engineering. Furthermore, we hope that this article will provide a reference point for the noble metal nanomaterials' development that leads to new opportunities in nanocatalysis. PMID:26393550

  19. Catalytic dehydrogenations of ethylbenzene to styrene

    NARCIS (Netherlands)

    Nederlof, C.

    2012-01-01

    This research work on the catalytic dehydrogenation of ethylbenzene (EB) to styrene (ST) had a primary goal of developing improved catalysts for dehydrogenation processes both in CO2 as well as with O2 that can compete with the conventional dehydrogenation process in steam. In order to achieve this

  20. Electrochemical Promotion of Catalytic Reactions Using

    DEFF Research Database (Denmark)

    Petrushina, Irina; Bjerrum, Niels; Cleemann, Lars Nilausen;

    2007-01-01

    This paper presents the results of a study on electrochemical promotion (EP) of catalytic reactions using Pt/C/polybenzimidazole(H3PO4)/Pt/C fuel cell performed by the Energy and Materials Science Group (Technical University of Denmark) during the last 6 years[1-4]. The development of our...

  1. Shungite carbon catalytic effect on coal treatment

    Energy Technology Data Exchange (ETDEWEB)

    Grigorieva, E.N.; Rozhkova, N.N. [Russian Academy of Sciences, Moscow (Russian Federation). Institute for High Temperature

    1999-07-01

    The catalytic ability of shungite carbon in reactions of coal organic matter models appeared to be due to its fullerene structure only. Transition metal sulphides present in shungite carbon are not active in the conditions of coal treatment. Shungite carbon was shown to exhibit an acceleration of thermolysis of coal and organic matter models, mainly dehydrogenation. 5 refs., 1 tabs.

  2. Catalytic oxidation of industrial organic solvent vapors.

    Science.gov (United States)

    Tzortzatou, Katerina; Grigoropoulou, Eleni

    2010-01-01

    In the present study the catalytic oxidation of an industrial organic solvent consisting predominantly of C-9 to C-10 paraffins and napthtenics and derived from low aromatic white spirit on CuO and Pt catalysts was investigated at ambient pressure and temperatures between 330 and 770 K. Catalysts were prepared in the laboratory and compared to commercial ones. Characterization was based on x-ray diffraction (XRD) analysis, x-ray fluorescence (XRF) analysis, scanning electron microscope (SEM) analysis and nitrogen adsorption data. The commercial platinum catalyst was proved highly efficient in the oxidation of the commercial solvent, necessitating lower temperatures for total oxidation. Catalyst loading in active component is clearly not of primordial importance, since its dispersion and crystallinity as well as the presence of other metallic compounds influence also the catalytic activity. In the case of copper catalysts studied, the different support (alumina) characteristics also would contribute to the difference in catalytic activity. Finally, the power law kinetics may successfully be used in order to explain the catalytic oxidation data of the organic solvent, where its constituents are modeled as a single carbon-containing compound. PMID:20390900

  3. Catalytic Converters Maintain Air Quality in Mines

    Science.gov (United States)

    2014-01-01

    At Langley Research Center, engineers developed a tin-oxide based washcoat to prevent oxygen buildup in carbon dioxide lasers used to detect wind shears. Airflow Catalyst Systems Inc. of Rochester, New York, licensed the technology and then adapted the washcoat for use as a catalytic converter to treat the exhaust from diesel mining equipment.

  4. Novel Metal Nanomaterials and Their Catalytic Applications

    Directory of Open Access Journals (Sweden)

    Jiaqing Wang

    2015-09-01

    Full Text Available In the rapidly developing areas of nanotechnology, nano-scale materials as heterogeneous catalysts in the synthesis of organic molecules have gotten more and more attention. In this review, we will summarize the synthesis of several new types of noble metal nanostructures (FePt@Cu nanowires, Pt@Fe2O3 nanowires and bimetallic Pt@Ir nanocomplexes; Pt-Au heterostructures, Au-Pt bimetallic nanocomplexes and Pt/Pd bimetallic nanodendrites; Au nanowires, CuO@Ag nanowires and a series of Pd nanocatalysts and their new catalytic applications in our group, to establish heterogeneous catalytic system in “green” environments. Further study shows that these materials have a higher catalytic activity and selectivity than previously reported nanocrystal catalysts in organic reactions, or show a superior electro-catalytic activity for the oxidation of methanol. The whole process might have a great impact to resolve the energy crisis and the environmental crisis that were caused by traditional chemical engineering. Furthermore, we hope that this article will provide a reference point for the noble metal nanomaterials’ development that leads to new opportunities in nanocatalysis.

  5. Performance characterization of a hydrogen catalytic heater.

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, Terry Alan; Kanouff, Michael P.

    2010-04-01

    This report describes the performance of a high efficiency, compact heater that uses the catalytic oxidation of hydrogen to provide heat to the GM Hydrogen Storage Demonstration System. The heater was designed to transfer up to 30 kW of heat from the catalytic reaction to a circulating heat transfer fluid. The fluid then transfers the heat to one or more of the four hydrogen storage modules that make up the Demonstration System to drive off the chemically bound hydrogen. The heater consists of three main parts: (1) the reactor, (2) the gas heat recuperator, and (3) oil and gas flow distribution manifolds. The reactor and recuperator are integrated, compact, finned-plate heat exchangers to maximize heat transfer efficiency and minimize mass and volume. Detailed, three-dimensional, multi-physics computational models were used to design and optimize the system. At full power the heater was able to catalytically combust a 10% hydrogen/air mixture flowing at over 80 cubic feet per minute and transfer 30 kW of heat to a 30 gallon per minute flow of oil over a temperature range from 100 C to 220 C. The total efficiency of the catalytic heater, defined as the heat transferred to the oil divided by the inlet hydrogen chemical energy, was characterized and methods for improvement were investigated.

  6. Exact Results for Kinetics of Catalytic Reactions

    OpenAIRE

    Frachebourg, L.; Krapivsky, P. L.

    1995-01-01

    The kinetics of an irreversible catalytic reaction on substrate of arbitrary dimension is examined. In the limit of infinitesimal reaction rate (reaction-controlled limit), we solve the dimer-dimer surface reaction model (or voter model) exactly in arbitrary dimension $D$. The density of reactive interfaces is found to exhibit a power law decay for $D

  7. Catalytic asymmetric synthesis of mycocerosic acid

    NARCIS (Netherlands)

    ter Horst, B.; Feringa, B.L.; J. Minnaard, A.

    2007-01-01

    The first catalytic asymmetric total synthesis of mycocerosic acid was achieved via the application of iterative enantioselective 1,4-addition reactions and allows for the efficient construction of 1,3-polymethyl arrays with full stereocontrol; further exemplified by the synthesis of tetramethyl-dec

  8. Electrochemical promotion of sulfur dioxide catalytic oxidation

    DEFF Research Database (Denmark)

    Petrushina, Irina; Bandur, Viktor; Cappeln, Frederik Vilhelm;

    2000-01-01

    The effect of electrochemical polarization on the catalytic SO2 oxidation in the molten V2O5-K2S2O7 system has been studied using a gold working electrode in the temperature range 400-460 degrees C. A similar experiment has been performed with the industrial catalyst VK-58. The aim of the present...

  9. Catalytic site interactions in yeast OMP synthase

    DEFF Research Database (Denmark)

    Hansen, Michael Riis; Barr, Eric W.; Jensen, Kaj Frank; Willemoës, Martin; Grubmeyer, Charles; Winther, Jakob R.

    2014-01-01

    45 (2006) 5330-5342]. This behavior was investigated in the yeast enzyme by mutations in the conserved catalytic loop and 5-phosphoribosyl-1-diphosphate (PRPP) binding motif. Although the reaction is mechanistically sequential, the wild-type (WT) enzyme shows parallel lines in double reciprocal...

  10. Catalytic treatment of diesel engines, NOx emissions

    International Nuclear Information System (INIS)

    Some aspects of the operation of diesel engines are revised together with the pollutant emissions they produce, as well as the available catalytic technologies for the treatment of diesel emissions. Furthermore the performance of a catalyst developed in the environmental catalysis group for NOx reduction using synthetic gas mixtures simulating the emissions from diesel engines is presented

  11. Plasma catalytic reforming of methane

    Energy Technology Data Exchange (ETDEWEB)

    Bromberg, L.; Cohn, D.R.; Rabinovich, A. [Massachusetts Inst. of Technology, Cambridge, MA (United States). Plasma Science and Fusion Center; Alexeev, N. [Russian Academy of Sciences, Moscow (Russian Federation). Baikov Inst. of Metallurgy

    1998-08-01

    Thermal plasma technology can be efficiently used in the production of hydrogen and hydrogen-rich gases from methane and a variety of fuels. This paper describes progress in plasma reforming experiments and calculations of high temperature conversion of methane using heterogeneous processes. The thermal plasma is a highly energetic state of matter that is characterized by extremely high temperatures (several thousand degrees Celsius) and high degree of dissociation and substantial degree of ionization. The high temperatures accelerate the reactions involved in the reforming process. Hydrogen-rich gas (50% H{sub 2}, 17% CO and 33% N{sub 2}, for partial oxidation/water shifting) can be efficiently made in compact plasma reformers. Experiments have been carried out in a small device (2--3 kW) and without the use of efficient heat regeneration. For partial oxidation/water shifting, it was determined that the specific energy consumption in the plasma reforming processes is 16 MJ/kg H{sub 2} with high conversion efficiencies. Larger plasmatrons, better reactor thermal insulation, efficient heat regeneration and improved plasma catalysis could also play a major role in specific energy consumption reduction and increasing the methane conversion. A system has been demonstrated for hydrogen production with low CO content ({approximately} 1.5%) with power densities of {approximately} 30 kW (H{sub 2} HHV)/liter of reactor, or {approximately} 10 m{sup 3}/hr H{sub 2} per liter of reactor. Power density should further increase with increased power and improved design.

  12. 碳质材料催化臭氧氧化去除水中溶解性有机物的研究进展%Catalytic ozonation based on carbon materials for removing dissolved organic compounds from water:A review

    Institute of Scientific and Technical Information of China (English)

    钱飞跃; 王翻翻; 刘小朋; 李月寒; 王建芳

    2015-01-01

    Catalytic ozonation based on carbon materials labeled as CMs/O3 was well characterized by superior organics removal,high ozone utilization and without metal leaching;however,most of them were still at the stage of laboratory research,since a stable catalytic property of CMs could not be expected after a long running. In this paper,the main reaction mechanisms in CMs/O3 system for removing dissolved organics from water,both surface catalytic oxidation and hydroxyl radicals (HO·)oxidation in bulk solution were discussed and the influences of critical factors in heterogeneous reaction pathways and organics removal efficiency were elaborated. It was pointed out that the consumption of basic active sites and the accumulation of acid oxygen-containing groups on the surface were considered to cause a partial deactivation of CMs in cyclic experiments. In addition,using mesoporous catalyst,optimizing pH and normalized ozone dosage,could help in reducing internal mass transfer resistances,thus enhance target organics removal. This paper reviewed the recent advances of CMs/O3 applied in model organic pollutants removal and industrial wastewater treatment. Multi-walled carbon nanotube ( MWCNT ) and the innovative loading technology could improve CMs/O3 performances in deep purification of micro-polluted water body. Coupling mature treatment methods and CMs/O3 in an efficient and low-cost process was proposed as the important direction of further study.%碳质材料催化臭氧氧化(CMs/O3)体系具有除污性能强、臭氧利用率高和无金属溶出的特点,但受制于CMs催化性能的易失性,该方法目前仍处于实验室研发阶段。本文系统阐述了CMs/O3体系的反应原理,并认为表面催化氧化与均相羟自由基(HO·)反应是去除水中溶解性有机物的主要途径;详细分析了影响非均相反应机理与体系处理效能的关键因素,并指出在反应过程中,碳表面碱性活性点位的消耗与酸性

  13. High-pressure catalytic reactions over single-crystal metal surfaces

    Science.gov (United States)

    Rodriguez, JoséA.; Wayne Goodman, D.

    1991-11-01

    Studies dealing with high-pressure catalytic reactions over single-crystal surfaces are reviewed. The coupling of an apparatus for the measurement of reaction kinetics at elevated pressures with an ultrahigh vacuum system for surface analysis allows detailed study of structure sensitivity, the effects of promoters and inhibitors on catalytic activity, and, in certain cases, identification of reaction intermediates by post-reaction surface analysis. Examples are provided which demonstrate the relevance of single-crystal studies for modeling the behaviour of high-surface-area supported catalysts. Studies of CO methanation and CO oxidation over single-crystal surfaces provide convincing evidence that these reactions are structure insensitive. For structure-sensitive reactions (ammonia synthesis, alkane hydrogenolysis, alkane isomerization, water-gas shift reaction, etc.) model single-crystal studies allow correlations to be established between surface structure and catalytic activity. The effects of both electronegative (S and P) and electropositive (alkali metals) impurities upon the catalytic activity of metal single crystals for ammonia synthesis, CO methanation, alkane hydrogenolysis, ethylene epoxidation and water-gas shift are discussed. The roles of "ensemble" and "ligand" effects in bimetallic catalysts are examined in light of data obtained using surfaces prepared by vapor-depositing one metal onto a crystal face of a dissimilar metal.

  14. Asymmetric Catalytic Reactions Catalyzed by Chiral Titanium Complexes

    Institute of Scientific and Technical Information of China (English)

    FENG; XiaoMing

    2001-01-01

    Chiral titanium complexes is very importance catalyst to asymmetric catalytic reactions. A series of catalytic systems based on titanium-chiral ligands complexes has been reported. This presentation will discuss some of our recent progress on asymmetric catalytic reactions catalyzed by chiral titanium complexes.  ……

  15. Asymmetric Catalytic Reactions Catalyzed by Chiral Titanium Complexes

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    @@ Chiral titanium complexes is very importance catalyst to asymmetric catalytic reactions. A series of catalytic systems based on titanium-chiral ligands complexes has been reported. This presentation will discuss some of our recent progress on asymmetric catalytic reactions catalyzed by chiral titanium complexes.

  16. Liquid-Phase Catalytic Hydrogenation of Furfural in Variable Solvent Media

    Institute of Scientific and Technical Information of China (English)

    夏淑倩; 李阳; 商巧燕; 张成武; 马沛生

    2016-01-01

    Water is the most abundant compound inherently existing in bio-oils. Thus understanding the role of water within bio-oils upgrading process is essential for future engineering scale-up design. In this study, furfural was chosen as bio-oils model compound, and the catalytic hydrogenation of furfural over commercial 5%, Ru/C catalyst was firstly investigated in a series of gradient variable water/ethanol mixture solvents. Water had a signifi-cant effect on the distribution of product yields. The dominant reaction pathways varied with the water contents in the water/ethanol mixture solvents. Typically, when ethanol was used as the solvent, the main products were ob-tained by the hydrogenation of carbonyl group or furan ring. When pure water was used as the solvent, the rear-rangement reaction of furfural to cyclopentanone should be selectively promoted theoretically. However, serious polymerization and resinification were observed herein in catalytic hydrogenation system of pure water. The cata-lyst surface was modified by the water-insoluble polymers, and consequently, a relative low yield of cyclopenta-none was obtained. A plausible multiple competitive reaction mechanism between polymerization reaction and the hydrogenation of furfural was suggested in this study. Characterizations(TG,FT-IR,SEM)were employed to analyze and explain our experiments.

  17. Catalytic aerobic oxidation of bio-renewable chemicals

    DEFF Research Database (Denmark)

    Gorbanev, Yury

    This thesis covers the investigation of new catalytic systems for the aerobic oxidation of chemicals derived from bio-renewable sources. The effects of different factors and conditions on the reactions were examined. The employed catalysts were characterized by physisorption measurements, SEM, TEM......, EDS, XRF and other methods. Supported gold and ruthenium hydroxide catalyst systems were explored for the aerobic oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDA), a potential polymer building block for the plastic industry, or its dimethyl ester (FDMC). High product...... selectivities and yields were obtained under optimized conditions. Heterogeneous catalysts consisting of Au nanoparticles on different supports were shown to efficiently oxidize HMF to FDA or FDMC in water or methanol, respectively. Additionally, the reaction conditions were shown to be adjustable...

  18. Catalytic Oxygen Evolution by Cobalt Oxido Thin Films.

    Science.gov (United States)

    Bediako, D Kwabena; Ullman, Andrew M; Nocera, Daniel G

    2016-01-01

    The contemporary demand to generate fuels from solar energy has stimulated intense effort to develop water splitting catalysts that can be coupled to light-absorbing materials. Cobalt oxido catalyst (Co-OECs) films deposited from buffered Co(II) solutions have emerged as arguably the most studied class of heterogeneous oxygen evolution catalysts. The interest in these materials stems from their formation by self-assembly, their self-healing properties, and their promising catalytic activity under a variety of conditions. The structure and function of these catalysts are reviewed here together with studies of molecular Co-O cluster compounds, which have proven invaluable in elucidating the chemistry of the Co-OECs. PMID:26245626

  19. Advances in solid-catalytic and non-catalytic technologies for biodiesel production

    International Nuclear Information System (INIS)

    Highlights: • The recent technologies for promoting biodiesel synthesis were elucidated. • The design of catalyst consideration of biodiesel production was proposed. • The recent advances and remaining difficulties in biodiesel synthesis were outlined. • The future research trend in biodiesel synthesis was highlighted. - Abstract: The insecure supply of fossil fuel coerces the scientific society to keep a vision to boost investments in the renewable energy sector. Among the many renewable fuels currently available around the world, biodiesel offers an immediate impact in our energy. In fact, a huge interest in related research indicates a promising future for the biodiesel technology. Heterogeneous catalyzed production of biodiesel has emerged as a preferred route as it is environmentally benign needs no water washing and product separation is much easier. The number of well-defined catalyst complexes that are able to catalyze transesterification reactions efficiently has been significantly expanded in recent years. The activity of catalysts, specifically in application to solid acid/base catalyst in transesterification reaction depends on their structure, strength of basicity/acidity, surface area as well as the stability of catalyst. There are various process intensification technologies based on the use of alternate energy sources such as ultrasound and microwave. The latest advances in research and development related to biodiesel production is represented by non-catalytic supercritical method and focussed exclusively on these processes as forthcoming transesterification processes. The latest developments in this field featuring highly active catalyst complexes are outlined in this review. The knowledge of more extensive research on advances in biofuels will allow a deeper insight into the mechanism of these technologies toward meeting the critical energy challenges in future

  20. ZEOLITES: EFFECTIVE WATER PURIFIERS

    Science.gov (United States)

    Zeolites are known for their adsorption, ion exchange and catalytic properties. Various natural zeolites are used as odor and moisture adsorbents and water softeners. Due to their acidic nature, synthetic zeolites are commonly employed as solid acid catalysts in petrochemical ind...

  1. Reforming of methane in tubes with a catalytic active wall

    International Nuclear Information System (INIS)

    The heterogeneous steam reforming process in tubes with catalytic active inner surface is studied. The purpose of this ivestigation is to find a method of predicting the reaction rate of the catalytic conversion of methane by steam. The dependency of the reaction rate upon the temperature, pressure, gas composition, Reynolds number, geometrical sizes of tubes and catalytic behaviour of the catalytic active inner wall of these tubes has been examined. It was found that the reaction rate mainly depends on the temperature. The reaction rate is limited by the catalytic behaviour and the heat resisting properties of the materials used. (author)

  2. Analysis of hapten binding and catalytic determinants in a family of catalytic antibodies.

    Science.gov (United States)

    Ulrich, H D; Schultz, P G

    1998-01-01

    We report here the cloning and kinetic analysis of a family of catalytic antibodies raised against a common transition state (TS) analog hapten, which accelerate a unimolecular oxy-Cope rearrangement. Sequence analysis revealed close homologies among the heavy chains of the catalytically active members of this set of antibodies, which derive mainly from a single germline gene, whereas the light chains can be traced back to several different, but related germline genes. The requirements for hapten binding and catalytic activity were determined by the construction of hybrid antibodies. Characterization of the latter antibodies again indicates a strong conservation of binding site structure among the catalytically active clones. The heavy chain was found to be the determining factor for catalytic efficiency, while the light chain exerted a smaller modulating effect that depended on light chain gene usage and somatic mutations. Within the heavy chain, the catalytic activity of a clone, but not hapten binding affinity, depended on the sequence of the third complementarity determining region (CDR). No correlation between high affinity for the hapten and high rate enhancement was found in the oxy-Cope system, a result that stands in contrast to the expectations from transition state theory. A mechanistic explanation for this observation is provided based on the three-dimensional crystal structure of the most active antibody, AZ-28, in complex with the hapten. This study demonstrates the utility of catalytic antibodies in examining the relationship between binding energy and catalysis in the evolution of biological catalysis, as well as expanding our understanding of the molecular basis of an immune response. PMID:9451442

  3. Janus droplet as a catalytic micromotor

    CERN Document Server

    Shklyaev, Sergey

    2015-01-01

    Self-propulsion of a Janus droplet in a solution of surfactant, which reacts on a half of a drop surface, is studied theoretically. The droplet acts as a catalytic motor creating a concentration gradient, which generates its surface-tension-driven motion; the self-propulsion speed is rather high, $60\\; {\\rm \\mu m/s}$ and more. This catalytic motor has several advantages over other micromotors: simple manufacturing, easily attained neutral buoyancy. In contrast to a single-fluid droplet, which demonstrates a self-propulsion as a result of symmetry breaking instability, for Janus one no stability threshold exists; hence, the droplet radius can be scaled down to micrometers. The paper was finalized and submitted by Denis S. Goldobin after Sergey Sklyaev had sadly passed away on June 2, 2014.

  4. From Catalytic Reaction Networks to Protocells

    Science.gov (United States)

    Kaneko, Kunihiko

    2013-12-01

    In spite of recent advances, there still remains a large gape between a set of chemical reactions and a biological cell. Here we discuss several theoretical efforts to fill in the gap. The topics cover (i) slow relaxation to equilibrium due to glassy behavior in catalytic reaction networks (ii) consistency between molecule replication and cell growth, as well as energy metabolism (iii) control of a system by minority molecules in mutually catalytic system, which work as a carrier of genetic information, and leading to evolvability (iv) generation of a compartmentalized structure as a cluster of molecules centered around the minority molecule, and division of the cluster accompanied by the replication of minority molecule (v) sequential, logical process over several states from concurrent reaction dynamics, by taking advantage of discreteness in molecule number.

  5. Analysis of the Staphylococcus aureus DgkB Structure Reveals a Common Catalytic Mechanism for the Soluble Diacylglycerol Kinases

    Energy Technology Data Exchange (ETDEWEB)

    Miller, Darcie J.; Jerga, Agoston; Rock, Charles O.; White, Stephen W. (SJCH)

    2008-08-11

    Soluble diacylglycerol (DAG) kinases function as regulators of diacylglycerol metabolism in cell signaling and intermediary metabolism. We report the structure of a DAG kinase, DgkB from Staphylococcus aureus, both as the free enzyme and in complex with ADP. The molecule is a tight homodimer, and each monomer comprises two domains with the catalytic center located within the interdomain cleft. Two distinctive features of DkgB are a structural Mg{sup 2+} site and an associated Asp{center_dot}water{center_dot}Mg{sup 2+} network that extends toward the active site locale. Site-directed mutagenesis revealed that these features play important roles in the catalytic mechanism. The key active site residues and the components of the Asp{center_dot}water{center_dot}Mg{sup 2+} network are conserved in the catalytic cores of the mammalian signaling DAG kinases, indicating that these enzymes use the same mechanism and have similar structures as DgkB.

  6. Analysis of the Staphylococcus aureus DgkB structure reveals a common catalytic mechanism for the soluble diacylglycerol kinases.

    Science.gov (United States)

    Miller, Darcie J; Jerga, Agoston; Rock, Charles O; White, Stephen W

    2008-07-01

    Soluble diacylglycerol (DAG) kinases function as regulators of diacylglycerol metabolism in cell signaling and intermediary metabolism. We report the structure of a DAG kinase, DgkB from Staphylococcus aureus, both as the free enzyme and in complex with ADP. The molecule is a tight homodimer, and each monomer comprises two domains with the catalytic center located within the interdomain cleft. Two distinctive features of DkgB are a structural Mg2+ site and an associated Asp*water*Mg2+ network that extends toward the active site locale. Site-directed mutagenesis revealed that these features play important roles in the catalytic mechanism. The key active site residues and the components of the Asp*water*Mg2+ network are conserved in the catalytic cores of the mammalian signaling DAG kinases, indicating that these enzymes use the same mechanism and have similar structures as DgkB. PMID:18611377

  7. Catalytic extraction processing of contaminated scrap metal

    International Nuclear Information System (INIS)

    Molten Metal Technology was awarded a contract to demonstrate the applicability of the Catalytic Extraction Process, a proprietary process that could be applied to US DOE's inventory of low level mixed waste. This paper is a description of that technology, and included within this document are discussions of: (1) Program objectives, (2) Overall technology review, (3) Organic feed conversion to synthetic gas, (4) Metal, halogen, and transuranic recovery, (5) Demonstrations, (6) Design of the prototype facility, and (7) Results

  8. Thermal and catalytic pyrolysis of plastic waste

    OpenAIRE

    Débora Almeida; Maria de Fátima Marques

    2016-01-01

    Abstract The amount of plastic waste is growing every year and with that comes an environmental concern regarding this problem. Pyrolysis as a tertiary recycling process is presented as a solution. Pyrolysis can be thermal or catalytical and can be performed under different experimental conditions. These conditions affect the type and amount of product obtained. With the pyrolysis process, products can be obtained with high added value, such as fuel oils and feedstock for new products. Zeolit...

  9. Materials for High-Temperature Catalytic Combustion

    Energy Technology Data Exchange (ETDEWEB)

    Ersson, Anders

    2003-04-01

    Catalytic combustion is an environmentally friendly technique to combust fuels in e.g. gas turbines. Introducing a catalyst into the combustion chamber of a gas turbine allows combustion outside the normal flammability limits. Hence, the adiabatic flame temperature may be lowered below the threshold temperature for thermal NO{sub X} formation while maintaining a stable combustion. However, several challenges are connected to the application of catalytic combustion in gas turbines. The first part of this thesis reviews the use of catalytic combustion in gas turbines. The influence of the fuel has been studied and compared over different catalyst materials. The material section is divided into two parts. The first concerns bimetallic palladium catalysts. These catalysts showed a more stable activity compared to their pure palladium counterparts for methane combustion. This was verified both by using an annular reactor at ambient pressure and a pilot-scale reactor at elevated pressures and flows closely resembling the ones found in a gas turbine combustor. The second part concerns high-temperature materials, which may be used either as active or washcoat materials. A novel group of materials for catalysis, i.e. garnets, has been synthesised and tested in combustion of methane, a low-heating value gas and diesel fuel. The garnets showed some interesting abilities especially for combustion of low-heating value, LHV, gas. Two other materials were also studied, i.e. spinels and hexa aluminates, both showed very promising thermal stability and the substituted hexa aluminates also showed a good catalytic activity. Finally, deactivation of the catalyst materials was studied. In this part the sulphur poisoning of palladium, platinum and the above-mentioned complex metal oxides has been studied for combustion of a LHV gas. Platinum and surprisingly the garnet were least deactivated. Palladium was severely affected for methane combustion while the other washcoat materials were

  10. Materials for High-Temperature Catalytic Combustion

    OpenAIRE

    Ersson, Anders

    2003-01-01

    Catalytic combustion is an environmentally friendlytechnique to combust fuels in e.g. gas turbines. Introducing acatalyst into the combustion chamber of a gas turbine allowscombustion outside the normal flammability limits. Hence, theadiabatic flame temperature may be lowered below the thresholdtemperature for thermal NOXformation while maintaining a stable combustion.However, several challenges are connected to the application ofcatalytic combustion in gas turbines. The first part of thisthe...

  11. Catalytic fast pyrolysis of lignocellulosic biomass

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Changjun; Wang, Huamin; Karim, Ayman M.; Sun, Junming; Wang, Yong

    2014-11-21

    Increasing energy demand, especially in the transportation sector, and soaring CO2 emissions necessitate the exploitation of renewable sources of energy. Despite the large variety of new energy Q3 carriers, liquid hydrocarbon still appears to be the most attractive and feasible form of transportation fuel taking into account the energy density, stability and existing infrastructure. Biomass is an abundant, renewable source of energy; however, utilizing it in a cost-effective way is still a substantial challenge. Lignocellulose is composed of three major biopolymers, namely cellulose, hemicellulose and lignin. Fast pyrolysis of biomass is recognized as an efficient and feasible process to selectively convert lignocellulose into a liquid fuel—bio-oil. However bio-oil from fast pyrolysis contains a large amount of oxygen, distributed in hundreds of oxygenates. These oxygenates are the cause of many negative properties, such as low heating values, high corrosiveness, high viscosity, and instability; they also greatly Q4 limit the application of bio-oil particularly as transportation fuel. Hydrocarbons derived from biomass are most attractive because of their high energy density and compatibility with the existing infrastructure. Thus, converting lignocellulose into transportation fuels via catalytic fast pyrolysis has attracted much attention. Many studies related to catalytic fast pyrolysis of biomass have been published. The main challenge of this process is the development of active and stable catalysts that can deal with a large variety of decomposition intermediates from lignocellulose. This review starts with the current understanding of the chemistry in fast pyrolysis of lignocellulose and focuses on the development of catalysts in catalytic fast pyrolysis. Recent progress in the experimental studies on catalytic fast pyrolysis of biomass is also summarized with the emphasis on bio-oil yields and quality.

  12. Computer Aided Enzyme Design and Catalytic Concepts

    OpenAIRE

    Frushicheva, Maria P.; Mills, Matthew J. L.; Schopf, Patrick; Singh, Manoj K.; Warshel, Arieh

    2014-01-01

    Gaining a deeper understanding of enzyme catalysis is of great practical and fundamental importance. Over the years it has become clear that despite advances made in experimental mutational studies, a quantitative understanding of enzyme catalysis will not be possible without the use of computer modeling approaches. While we believe that electrostatic preorganization is by far the most important catalytic factor, convincing the wider scientific community of this may require the demonstration ...

  13. Ubiquitous "glassy" relaxation in catalytic reaction networks

    OpenAIRE

    Awazu, Akinori; Kaneko, Kunihiko

    2009-01-01

    Study of reversible catalytic reaction networks is important not only as an issue for chemical thermodynamics but also for protocells. From extensive numerical simulations and theoretical analysis, slow relaxation dynamics to sustain nonequlibrium states are commonly observed. These dynamics show two types of salient behaviors that are reminiscent of glassy behavior: slow relaxation along with the logarithmic time dependence of the correlation function and the emergence of plateaus in the rel...

  14. Physico-chemical and catalytic properties of poly-oxo-metalate surfactants

    International Nuclear Information System (INIS)

    Hydrophilic poly-oxo-metalates (POM) are made surface active by coupling them to cationic amphiphilic moieties to form catalytic surfactants (catasurfs). In controlled conditions this procedure results in the formation of water and organic solvent insoluble nanoparticles that show the ability to stabilize water-in-oil emulsions, the so-called Pickering emulsions. Formation of monomolecular catasurf films, and their deposition on solid substrate by the Langmuir-Blodgett technique, is also investigated. It is shown that the catalytic activity of POM is maintained in the solid state, i.e. as nanoparticle or 2D nano-crystallite in the deposited film. The supramolecular structure of catasurfs is explored by means of physical characterisation techniques such as small angle X-ray/neutron/light scattering, electron diffraction and X-ray reflectivity. (authors)

  15. Incorporation of catalytic dehydrogenation into fischer-tropsch synthesis to significantly reduce carbon dioxide emissions

    Energy Technology Data Exchange (ETDEWEB)

    Huffman, Gerald P.

    2012-11-13

    A new method of producing liquid transportation fuels from coal and other hydrocarbons that significantly reduces carbon dioxide emissions by combining Fischer-Tropsch synthesis with catalytic dehydrogenation is claimed. Catalytic dehydrogenation (CDH) of the gaseous products (C1-C4) of Fischer-Tropsch synthesis (FTS) can produce large quantities of hydrogen while converting the carbon to multi-walled carbon nanotubes (MWCNT). Incorporation of CDH into a FTS-CDH plant converting coal to liquid fuels can eliminate all or most of the CO.sub.2 emissions from the water-gas shift (WGS) reaction that is currently used to elevate the H.sub.2 level of coal-derived syngas for FTS. Additionally, the FTS-CDH process saves large amounts of water used by the WGS reaction and produces a valuable by-product, MWCNT.

  16. Probing catalytic rate enhancement during intramembrane proteolysis.

    Science.gov (United States)

    Arutyunova, Elena; Smithers, Cameron C; Corradi, Valentina; Espiritu, Adam C; Young, Howard S; Tieleman, D Peter; Lemieux, M Joanne

    2016-09-01

    Rhomboids are ubiquitous intramembrane serine proteases involved in various signaling pathways. While the high-resolution structures of the Escherichia coli rhomboid GlpG with various inhibitors revealed an active site comprised of a serine-histidine dyad and an extensive oxyanion hole, the molecular details of rhomboid catalysis were unclear because substrates are unknown for most of the family members. Here we used the only known physiological pair of AarA rhomboid with its psTatA substrate to decipher the contribution of catalytically important residues to the reaction rate enhancement. An MD-refined homology model of AarA was used to identify residues important for catalysis. We demonstrated that the AarA active site geometry is strict and intolerant to alterations. We probed the roles of H83 and N87 oxyanion hole residues and determined that substitution of H83 either abolished AarA activity or reduced the transition state stabilization energy (ΔΔG‡) by 3.1 kcal/mol; substitution of N87 decreased ΔΔG‡ by 1.6-3.9 kcal/mol. Substitution M154, a residue conserved in most rhomboids that stabilizes the catalytic general base, to tyrosine, provided insight into the mechanism of nucleophile generation for the catalytic dyad. This study provides a quantitative evaluation of the role of several residues important for hydrolytic efficiency and oxyanion stabilization during intramembrane proteolysis. PMID:27071148

  17. Catalytic applications of bio-inspired nanomaterials

    Science.gov (United States)

    Pacardo, Dennis Kien Balaong

    The biomimetic synthesis of Pd nanoparticles was presented using the Pd4 peptide, TSNAVHPTLRHL, isolated from combinatorial phage display library. Using this approach, nearly monodisperse and spherical Pd nanoparticles were generated with an average diameter of 1.9 +/- 0.4 nm. The peptide-based nanocatalyst were employed in the Stille coupling reaction under energy-efficient and environmentally friendly reaction conditions of aqueous solvent, room temperature and very low catalyst loading. To this end, the Pd nanocatalyst generated high turnover frequency (TOF) value and quantitative yields using ≥ 0.005 mol% Pd as well as catalytic activities with different aryl halides containing electron-withdrawing and electron-donating groups. The Pd4-capped Pd nanoparticles followed the atom-leaching mechanism and were found to be selective with respect to substrate identity. On the other hand, the naturally-occurring R5 peptide (SSKKSGSYSGSKGSKRRIL) was employed in the synthesis of biotemplated Pd nanomaterials which showed morphological changes as a function of Pd:peptide ratio. TOF analysis for hydrogenation of olefinic alcohols showed similar catalytic activity regardless of nanomorphology. Determination of catalytic properties of these bio-inspired nanomaterials are important as they serve as model system for alternative green catalyst with applications in industrially important transformations.

  18. Catalytic hydrogen recombination for nuclear containments

    International Nuclear Information System (INIS)

    Catalytic recombiners appear to be a credible option for hydrogen mitigation in nuclear containments. The passive operation, versatility and ease of back fitting are appealing for existing stations and new designs. Recently, a generation of wet-proofed catalyst materials have been developed at AECL which are highly specific to H2-O2, are active at ambient temperatures and are being evaluated for containment applications. Two types of catalytic recombiners were evaluated for hydrogen removal in containments based on the AECL catalyst. The first is a catalytic combustor for application in existing air streams such as provided by fans or ventilation systems. The second is an autocatalytic recombiner which uses the enthalpy of reaction to produce natural convective flow over the catalyst elements. Intermediate-scale results obtained in 6 m3 and 10 m3 spherical and cylindrical vessels are given to demonstrate self-starting limits, operating limits, removal capacity, scaling parameters, flow resistance, mixing behaviour in the vicinity of an operating recombiner and sensitivity to poisoning, fouling and radiation. (author). 13 refs., 10 figs

  19. IFP solutions for revamping catalytic reforming units

    Energy Technology Data Exchange (ETDEWEB)

    Gendler, J.L. [HRI, Inc., Princeton, NJ (United States); Domergue, B.; Mank, L. [Inst. Francais du Petrole, Rueil Malmaison (France)

    1996-12-01

    The decision-making process for the refiner considering a revamp of a catalytic reforming unit comprises many factors. These may be grouped in two broad areas: technical and economic. This paper presents the results of a study performed by IFP that illustrates catalytic reforming unit revamp options. Three IFP processes are described and operating conditions, expected yields, and economic data are presented. The following options are discussed: base case Conventional, fixed-bed, semi-regenerative catalytic reformer; Case 1--revamp using IFP Dualforming technology; Case 2--revamp using IFP Dualforming Plus technology; and Case 3--revamp to IFP Octanizing technology. The study illustrates various options for the refiner to balance unit performance improvements with equipment, site, and economic constraints. The study was performed assuming design feedrate of 98.2 tons/hour (20,000 BPSD) in all cases. Because of the increased need for octane in many refineries, the study assumed that operating severity was set at a design value of 100 research octane number clear (RON). In all of the cases in this study, it was assumed that the existing recycle compressor was reused. Operating pressure differences between the cases is discussed separately. Also, in all cases, a booster compressor was included in order to return export hydrogen pressure to that of the conventional unit.

  20. Fuzzy logic for burner, solar boiler and catalytic converter; Brander, zonneboiler en katalysator vaag geregeld

    Energy Technology Data Exchange (ETDEWEB)

    Voorter, P.H.C.

    1995-05-01

    The application of fuzzy logic in the process control of a cement furnace at a Dutch cement industry (Enci in Maastricht) proved to be successful: the production increased by 4% and the energy consumption was reduced by 3% per ton product. Fuzzy logic can also be used in smaller energy equipment. Applications in a burner of a central heating boiler, a solar water heater and a catalytic converter in a motorcycle are discussed. 5 figs., 1 tab., 2 refs.

  1. Modeling the Catalysis of Anti-Cocaine Catalytic Antibody: Competing Reaction Pathways and Free Energy Barriers

    OpenAIRE

    Pan, Yongmei; Gao, Daquan; Zhan, Chang-Guo

    2008-01-01

    The competing reaction pathways and the corresponding free energy barriers for cocaine hydrolysis catalyzed by an anti-cocaine catalytic antibody, mAb 15A10, were studied by using a novel computational strategy based on the binding free energy calculations on the antibody binding with cocaine and transition states. The calculated binding free energies were used to evaluate the free energy barrier shift from the cocaine hydrolysis in water to the antibody-catalyzed cocaine hydrolysis for each ...

  2. The influence of carbon material properties on the efficiency of catalytic wet peroxide oxidation processes

    OpenAIRE

    Gomes, Helder; R. Ribeiro; Silva, Adrián; Figueiredo, José; Faria, Joaquim

    2015-01-01

    Carbon materiais are well known catalysts for activatin§ H^O^ into hydroxyl radicais (HO'), which are efficient oxidizin § agents. By making use of highly reactive HO" radicais, the elimination of organic compounds can be accomplished by catalytic wet peroxide oxidation (CWPO), a water treatment technology operating under mild conditions of pressure and temperature that hás gained importance due to the decreasing cost of H;0; and its increasing use in wastewater treatm...

  3. Magnetic carbon xerogels for the catalytic wet peroxide oxidation of 4-nitrophenol solutions

    OpenAIRE

    Ribeiro, R; Silva, Adrián; Faria, Joaquim; Gomes, Helder

    2015-01-01

    Catalytic wet peroxide oxidation (CWPO) is a well-known advanced oxidation process for the removal of organic pollutants from industrial process waters and wastewater. Specifically, CWPO employs hydrogen peroxide (H2O2) as oxidation source and a suitable catalyst to promote its decomposition via formation of hydroxyl radicals (HO•), which exhibit high oxidizing potential and serve as effective species in the destruction of a huge range of organic pollutants

  4. Catalytic dechlorination of diclofenac by biogenic palladium in a microbial electrolysis cell

    OpenAIRE

    De Gusseme, Bart; Soetaert, Maarten; Hennebel, Tom; Vanhaecke, Lynn; Boon, Nico; Verstraete, Willy

    2012-01-01

    Summary Diclofenac is one of the most commonly detected pharmaceuticals in wastewater treatment plant (WWTP) effluents and the receiving water bodies. In this study, biogenic Pd nanoparticles (‘bio‐Pd’) were successfully applied in a microbial electrolysis cell (MEC) for the catalytic reduction of diclofenac. Hydrogen gas was produced in the cathodic compartment, and consumed as a hydrogen donor by the bio‐Pd on the graphite electrodes. In this way, complete dechlorination of 1 mg diclofenac ...

  5. A selective hydrogen peroxide sensor based on chemiresistive polyaniline nanowires modified with silver catalytic nanoparticles

    International Nuclear Information System (INIS)

    This paper presents a novel method to selectively detect hydrogen peroxide using a chemiresistive polyaniline nanowire network. The polyaniline nanowires modified with silver catalytic nanoparticles were demonstrated to give selective responses to hydrogen peroxide by changing the conductivity of the polyaniline. The proposed mechanism for the selectivity in the H2O2 sensing is based on a catalytic reaction between the silver nanoparticles and the hydrogen peroxide which generates hydroxide ions and water to influence the conductivity of polyaniline. The catalytic effect of the silver nanoparticles was confirmed by characterizing the relationship between the amount of catalysts and the current response. The results indicate that the rate of the catalytic reaction is proportional to the number of silver nanoparticles attached on the surfaces of polyaniline. By observing the conductance change, the developed chemiresistive sensor was able to selectively detect H2O2 while exhibiting minimal response to other chemical species. The objective of this paper is to address the selectivity issue of a chemiresistor by suggesting a catalyst-based selective detection of an analyte for a polyaniline-based chemiresistive sensor. This technology may have potential applications in microscale or microfluidic chemical and biological sensors requiring a selective detection of hydrogen peroxide concentrations. (paper)

  6. 一种水溶性氢氧根钌配合物的合成及其对乙腈的催化水化作用%Synthesis of a Water-Soluble Ruthenium Hydroxide Complex and Its Role in Catalytic Hydration of Acetonitrile

    Institute of Scientific and Technical Information of China (English)

    尹传奇; 刘珺; 柏正武

    2011-01-01

    以RuCl3·3H2O为原料合成了水溶性钌配合物[(bipy)2Ru(H2O)2](OTf)2(bipy=2,2'-bipyridine,Otf-=triflate),利用DBU(1,8-Diazabicyclo[5.4.0]undec-7-ene)脱质子化合成了水溶性氢氧根配合物[(bipy)2Ru(H2O)(OH)](OTf).研究了[(bipy)2Ru(H2O)(OH)](OTf)催化水化乙腈生成乙酰胺的反应.机理研究表明,催化循环的关键中间体为氧配位的酰亚胺配合物[(bipy)2Ru(CH3CN)(OCMe=NH)]+,经过生成[(bipy)2Ru(κ2-N,O-NH=CMeN=CMeO)]+、水亲核进攻开环生成{(bipy)2Ru[NH=C(OH)Me](OCMe=NH)}+、乙腈取代其NH=C(OH)Me配体产生乙酰胺,同时再生成[(bipy)2Ru-(CH3CN)(OCMe=NH)]+完成催化循环.%In the presence of DBU(1,8-Diazabicycloundec-7-ene),a novel water-soluble hydroxide ruthenium complex [(bipy)2Ru(H2O)(OH)](OTf) was synthesized by deprotonation of [(bipy)2Ru(H2O)2]-(OTf)2(bipy=2,2'-bipyridine,Otf-=triflate),which was prepared using RuCl3·3H2O as starting material.The hydration of acetonitrile to form acetamide catalyzed by [(bipy)2Ru(H2O)(OH)](OTf) was studied.O-bonded imido complex [(bipy)2Ru(N≡CCH3)(OCMe=NH)]+ is postulated to be the key intermediate,which then undergoes nucleophilic attack at the carbon atom of nitrile ligand to form [(bipy)2Ru(k2-N,ONH=CMeN=CMeO)]+.Ring-opening nucleophilic attack of [(bipy)2Ru(k2-N,O-NH=CMeN=CMeO)]+by water produces {(bipy)2Ru[NH=C(OH)Me](OCMe=NH)}+.The displacement of NH=C(OH)Me ligand in the latter complex by acetonitrile forms acetamide,and regenerates [(bipy)2Ru(N≡CCH3)-(OCMe=NH)]+ to fulfill catalytic cycle.

  7. Development of a water detritiation facility for JET

    Energy Technology Data Exchange (ETDEWEB)

    Perevezentsev, A.N. E-mail: alex.perevezentsev@jet.uk; Bell, A.C.; Brennan, P.D.; Hemmerich, J.L

    2002-11-01

    A water detritiation facility, based on a world-wide adopted combined electrolysis catalytic exchange (CECE) process, for the JET active gas handling plant is described. A research and development programme is presented. The programme includes the testing of structured inert packing with an incorporated hydrophobic catalyst for increased throughput of a liquid phase catalytic exchange (LPCE) column, a vapour phase catalytic exchange (VPCE) process for reduction of tritium inventory in the alkali electrolyser and a column of high effectiveness for alkali retention.

  8. Development of a water detritiation facility for JET

    International Nuclear Information System (INIS)

    A water detritiation facility, based on a world-wide adopted combined electrolysis catalytic exchange (CECE) process, for the JET active gas handling plant is described. A research and development programme is presented. The programme includes the testing of structured inert packing with an incorporated hydrophobic catalyst for increased throughput of a liquid phase catalytic exchange (LPCE) column, a vapour phase catalytic exchange (VPCE) process for reduction of tritium inventory in the alkali electrolyser and a column of high effectiveness for alkali retention

  9. Effects of Reduced Sulfur Compounds on Pd-catalytic Hydrodechlorination of TCE in Groundwater by Cathodic H2 under Electrochemically-induced Oxidizing Conditions

    OpenAIRE

    Yuan, Songhu; Chen, Mingjie; Mao, Xuhui; Alshawabkeh, Akram N.

    2013-01-01

    Reduced sulfur compounds (RSCs) poison Pd catalysts for catalytic hydrodechlorination of contaminants in anoxic groundwater. This study investigates the effects of RSCs on Pd-catalytic hydrodechlorination of trichloroethylene (TCE) in oxic groundwater. Water electrolysis in an undivided electrolytic cell is used to produce H2 for TCE hydrodechlorination under oxidizing conditions. TCE is efficiently hydrodechlorinated to ethane, with significant accumulation of H2O2 under acidic conditions. P...

  10. The tritium labeling of Butibufen by heterogeneous catalytic exchange; Marcado del Butibufen con Tritio por inter- cambio catalitico en disolucion

    Energy Technology Data Exchange (ETDEWEB)

    Santamaria, J.; Rebollo, D.

    1986-07-01

    The labeling of a new non-steroidal antiinflammatory agent, Butibufen (2-(4-isobutylphenyl) butyric acid) was studied. The method used was heterogeneous catalytic exchange between Butibufen and tritiated water, obtained in situ. Purification was accomplished through thin layer chromatography. Concentration, purity and specific activity of the labeled drug were determined by ultraviolet and liquid scintillation techniques. (Author) 7 refs.

  11. Heterogeneous catalytic materials solid state chemistry, surface chemistry and catalytic behaviour

    CERN Document Server

    Busca, Guido

    2014-01-01

    Heterogeneous Catalytic Materials discusses experimental methods and the latest developments in three areas of research: heterogeneous catalysis; surface chemistry; and the chemistry of catalysts. Catalytic materials are those solids that allow the chemical reaction to occur efficiently and cost-effectively. This book provides you with all necessary information to synthesize, characterize, and relate the properties of a catalyst to its behavior, enabling you to select the appropriate catalyst for the process and reactor system. Oxides (used both as catalysts and as supports for cata

  12. Catalytic oxidation of tritium in air at ambient temperature

    International Nuclear Information System (INIS)

    Tritium/air oxidation kinetic data are derived from ambient-temperature measurements carried out with three precious-metal catalysts. Each catalyst consists of a high-surface-area substrate in pelletized form, onto which precious metal has been dispersed. The metal/substrate combinations investigated are platinum/alumina, palladium/kaolin, and palladium/zeolite. Electron-microprobe scans reveal that the dispersed metal is deposited in each case near the outer surface of the pellet, with metal concentration decreasing exponentially from the pellet surface. Kinetic oxidation measurements are made in a unique apparatus consisting of a large Lucite enclosure with an air atmosphere processed by a recirculating cleanup system. Dual-ionization chambers with an intermediate adsorption bed permit measurement of tritium gas and tritiated water vapor. Rate coefficients are determined from concentration decay following a spike injection of tritium into the enclosure. The catalytic reaction is first-order in tritium concentration in the range 10 to 105 μCi/m3. Addition of hydrogen carrier gas is unnecessary. Each of the dispersed-metal catalysts is extremely active in promoting tritium oxidation in comparison with self-catalyzed atmospheric conversion; equivalent first-order rate constants are higher by roughly 9 orders of magnitude. The platinum-based catalyst is more effective than the palladium catalysts on a surface-area basis by about a factor of 3. Catalytic activity for all three catalysts declines with time of exposure to air after activation, following a power-law decay with an exponent of -1/2. A model for optimization of the catalyst reactivation cycle is proposed, revealing that the optimum catalyst volume scales with flow rate to the 2/3 power. Ambient-temperature tritium oxidation is cost-effective for small- to intermediate-scale cleanup systems. A heated catalyst is desirable for large-scale systems

  13. Engineering Metallic Nanoparticles for Enhancing and Probing Catalytic Reactions.

    Science.gov (United States)

    Collins, Gillian; Holmes, Justin D

    2016-07-01

    Recent developments in tailoring the structural and chemical properties of colloidal metal nanoparticles (NPs) have led to significant enhancements in catalyst performance. Controllable colloidal synthesis has also allowed tailor-made NPs to serve as mechanistic probes for catalytic processes. The innovative use of colloidal NPs to gain fundamental insights into catalytic function will be highlighted across a variety of catalytic and electrocatalytic applications. The engineering of future heterogenous catalysts is also moving beyond size, shape and composition considerations. Advancements in understanding structure-property relationships have enabled incorporation of complex features such as tuning surface strain to influence the behavior of catalytic NPs. Exploiting plasmonic properties and altering colloidal surface chemistry through functionalization are also emerging as important areas for rational design of catalytic NPs. This news article will highlight the key developments and challenges to the future design of catalytic NPs. PMID:26823380

  14. Catalytic bioscavengers in nerve agent poisoning: A promising approach?

    Science.gov (United States)

    Worek, Franz; Thiermann, Horst; Wille, Timo

    2016-02-26

    The repeated use of the nerve agent sarin against civilians in Syria in 2013 emphasizes the continuing threat by chemical warfare agents. Multiple studies demonstrated a limited efficacy of standard atropine-oxime treatment in nerve agent poisoning and called for the development of alternative and more effective treatment strategies. A novel approach is the use of stoichiometric or catalytic bioscavengers for detoxification of nerve agents in the systemic circulation prior to distribution into target tissues. Recent progress in the design of enzyme mutants with reversed stereo selectivity resulting in improved catalytic activity and their use in in vivo studies supports the concept of catalytic bioscavengers. Yet, further research is necessary to improve the catalytic activity, substrate spectrum and in vivo biological stability of enzyme mutants. The pros and cons of catalytic bioscavengers will be discussed in detail and future requirements for the development of catalytic bioscavengers will be proposed. PMID:26200600

  15. Conventional and catalytic pyrolysis of pinyon juniper biomass

    Science.gov (United States)

    Yathavan, Bhuvanesh Kumar

    Pinyon and juniper are invasive woody species in Western United States that occupy over 47 million acres of land. The US Bureau of Land Management (BLM) has embarked on harvesting these woody species to make room for range grasses for grazing. The major application of harvested pinyon-juniper (PJ) is low value firewood. Thus, there is a need to develop new high value products from this woody biomass to reduce the cost of harvesting. In this research PJ biomass was processed through pyrolysis technology to produce value added products. The first part of the thesis demonstrates the effect of PJ wood, bark and mixture biomass and temperature on the product yield and on the quality of the bio-oil produced. The second part focuses on the optimization of process parameters for maximum yield and the third part focuses on upgrading the bio-oil with an industrial catalyst (HZSM5) and an industrial waste product (red mud). The results obtained from the first part showed that PJ wood produced maximum bio-oil yield, followed by PJ mixture and bark. The bio-oil yield from PJ wood had low viscosity when compared to PJ mixture and PJ bark. The second part focused on studying the effect of process parameters (temperature, feed rate and the gas flow rate) on the total liquid, organic, water, char and gas yield. The results show that each response is affected by different factor level combinations, and maximum yield for each response was obtained at different factors level. The third part focused on catalytic pyrolysis of PJ biomass using both HZSM-5 catalyst and red mud. The mechanisms of catalysis by the two catalysts were quite different. Whereas the HZSM-5 rejected oxygen mostly as carbon monoxide and water and produced lower amounts of carbon dioxide, on the contrary the red mud produced more carbon dioxide and water and less carbon monoxide. The higher heating value of the red mud catalyzed oil (29.46 MJ/kg) was slightly higher than that catalyzed by HZSM-5 (28.55 MJ/kg). Thus

  16. Catalytic Mechanism of Human Alpha-galactosidase

    Energy Technology Data Exchange (ETDEWEB)

    Guce, A.; Clark, N; Salgado, E; Ivanen, D; Kulinskaya, A; Brumer, H; Garman, S

    2010-01-01

    The enzyme {alpha}-galactosidase ({alpha}-GAL, also known as {alpha}-GAL A; E.C. 3.2.1.22) is responsible for the breakdown of {alpha}-galactosides in the lysosome. Defects in human {alpha}-GAL lead to the development of Fabry disease, a lysosomal storage disorder characterized by the buildup of {alpha}-galactosylated substrates in the tissues. {alpha}-GAL is an active target of clinical research: there are currently two treatment options for Fabry disease, recombinant enzyme replacement therapy (approved in the United States in 2003) and pharmacological chaperone therapy (currently in clinical trials). Previously, we have reported the structure of human {alpha}-GAL, which revealed the overall structure of the enzyme and established the locations of hundreds of mutations that lead to the development of Fabry disease. Here, we describe the catalytic mechanism of the enzyme derived from x-ray crystal structures of each of the four stages of the double displacement reaction mechanism. Use of a difluoro-{alpha}-galactopyranoside allowed trapping of a covalent intermediate. The ensemble of structures reveals distortion of the ligand into a {sup 1}S{sub 3} skew (or twist) boat conformation in the middle of the reaction cycle. The high resolution structures of each step in the catalytic cycle will allow for improved drug design efforts on {alpha}-GAL and other glycoside hydrolase family 27 enzymes by developing ligands that specifically target different states of the catalytic cycle. Additionally, the structures revealed a second ligand-binding site suitable for targeting by novel pharmacological chaperones.

  17. De novo design of catalytic proteins

    OpenAIRE

    Kaplan, J; DeGrado, W. F.

    2004-01-01

    The de novo design of catalytic proteins provides a stringent test of our understanding of enzyme function, while simultaneously laying the groundwork for the design of novel catalysts. Here we describe the design of an O2-dependent phenol oxidase whose structure, sequence, and activity are designed from first principles. The protein catalyzes the two-electron oxidation of 4-aminophenol (kcat/KM = 1,500 M·1·min·1) to the corresponding quinone monoimine by using a diiron cofactor. The catalyti...

  18. Transport in a Microfluidic Catalytic Reactor

    Energy Technology Data Exchange (ETDEWEB)

    Park, H G; Chung, J; Grigoropoulos, C P; Greif, R; Havstad, M; Morse, J D

    2003-04-30

    A study of the heat and mass transfer, flow, and thermodynamics of the reacting flow in a catalytic microreactor is presented. Methanol reforming is utilized in the fuel processing system driving a micro-scale proton exchange membrane fuel cell. Understanding the flow and thermal transport phenomena as well as the reaction mechanisms is essential for improving the efficiency of the reforming process as well as the quality of the processed fuel. Numerical studies have been carried out to characterize the transport in a silicon microfabricated reactor system. On the basis of these results, optimized conditions for fuel processing are determined.

  19. Asymmetric catalytic aziridination of cyclic enones.

    Science.gov (United States)

    De Vincentiis, Francesco; Bencivenni, Giorgio; Pesciaioli, Fabio; Mazzanti, Andrea; Bartoli, Giuseppe; Galzerano, Patrizia; Melchiorre, Paolo

    2010-07-01

    The first catalytic method for the asymmetric aziridination of cyclic enones is described. The presented organocatalytic strategy is based on the use of an easily available organocatalyst that is able to convert a wide range of cyclic enones into the desired aziridines with very high enantiomeric purity and good chemical yield. Such a method may very well open up new opportunities to stereoselectively prepare complex chiral molecules that possess an indane moiety, a framework that is found in a large number of bioactive and pharmaceutically important molecules. PMID:20512797

  20. Electrospun Catalytic Support Prepared by Electrospinning Technique

    Czech Academy of Sciences Publication Activity Database

    Soukup, Karel; Topka, Pavel; Petráš, D.; Klusoň, Petr; Šolcová, Olga

    Praha : Orgit, 2012, C4.1. ISBN 978-80-905035-1-9. [International Congress of Chemical and Process Engineering CHISA 2012 and 15th Conference PRES 2012 /20./. Prague (CZ), 25.08.2012-29.08.2012] R&D Projects: GA ČR GPP106/11/P459; GA ČR(CZ) GAP204/11/1206 Institutional support: RVO:67985858 Keywords : catalytic tests * electrospun * gas transport properties Subject RIV: CI - Industrial Chemistry, Chemical Engineering www.chisa.cz/2012