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Sample records for tolerant zeolite supported

  1. Sulfur tolerant zeolite supported platinum catalysts for aromatics hydrogenation

    Science.gov (United States)

    1997-04-01

    An experimental study of sulfur tolerant zeolite platinum catalysts for aormatics hydrogenation. Platinum catalysts supported on Y-zeolite have been prepared and characterized in various ways, including the hydrogenation of toluene in a high pressure...

  2. Sulfur tolerant zeolite supported platinum catalysts for aromatics hydrogenation

    Energy Technology Data Exchange (ETDEWEB)

    Bergem, Haakon

    1997-12-31

    The increased demand for transportation fuels at the expence of heavier fuel oil has forced the refinery industry to expand their conversion capacity with hydrotreating as one of the key processes. A shift towards more diesel powered vehicles along with tightening fuel regulations demanding cleaner fuels has lead to increasing interest in catalytic processes for the manufacturing of such environmentally acceptable fuels. This provides the motivation for this thesis. Its main objective was to study possible catalysts active for desulfurization, hydrogenation, and ring-opening of aromatics all in the presence of sulfur. A close examination of the physical properties and kinetical behaviour of the chosen catalysts has been performed. A high pressure reactor setup was designed and built for activity measurements. Zeolite supported platinum catalysts were prepared and both the metal and acid functions were characterized utilizing various experimental techniques. Hydrogenation of toluene was used as a model reaction and the effect of sulfur adsorption on the activity and kinetic behaviour of the catalysts was investigated. The catalyst samples showed hydrogenation activities comparable to a commercial Pt/Al2O3 catalyst. There were no clear differences in the effect of the various sulfur compounds studied. Platinum supported on zeolite Y gave considerably more sulfur tolerant catalysts compared to Al2O3 as support. 155 refs., 58 figs., 36 tabs.

  3. Magnetically supported zeolite adsorbents for effluent treatment

    International Nuclear Information System (INIS)

    Gaydardjiev, S.

    1998-01-01

    An attempt was made to remove heavy metal ions from metallurgical effluents by means of magnetically supported fluidized bed column employing zeolite-magnetite complexes as adsorbents. The natural sorptive properties of acid modified clinoptilolite were used instead of synthetic beads. X-ray diffraction and DTA studies on the raw material confirmed that the main zeolite mineral was clinoptilolite. (author)

  4. Polypropylene obtained through zeolite supported catalysts

    Directory of Open Access Journals (Sweden)

    Queli C. Bastos

    2004-01-01

    Full Text Available Propylene polymerizations were carried out with f2C(Flu(CpZrCl2 and SiMe2(Ind2ZrCl2 catalysts supported on silica, zeolite sodic mordenite (NaM and acid mordenite (HM. The polymerizations were performed at different temperatures and varying aluminium/zirconium molar ratios ([Al]/[Zr]. The effect of these reaction parameters on the catalyst activity was investigated using a proposed statistical experimental planning. In the case of f2C(Flu(CpZrCl2, SiO2 and NaM were used as support and the catalyst performance evaluated using toluene and pentane as polymerization solvent. The molecular weight, molecular weight distribution, melting point and crystallinity of the polymers were examined. The results indicate very high activities for the syndiospecific heterogeneous system. Also, the polymers obtained had superior Mw and stereoregularity.

  5. Performance Evaluations of Ion Exchanged Zeolite Membranes on Alumina Supports

    Energy Technology Data Exchange (ETDEWEB)

    Bhave, Ramesh R. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Jubin, Robert Thomas [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Spencer, Barry B. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Nair, Sankar [Georgia Inst. of Technology, Atlanta, GA (United States)

    2017-08-27

    This report describes the synthesis and evaluation of molecular sieve zeolite membranes to separate and concentrate tritiated water (HTO) from dilute HTO-bearing aqueous streams. In the first phase of this effort, several monovalent and divalent cation-exchanged silico alumino phosphate (SAPO-34) molecular sieve zeolite membranes were synthesized on disk supports and characterized with gas and vapor permeation measurements. In the second phase, Linde Type A (LTA) zeolite membranes were synthesized in disk and tubular supports. The pervaporation process performance was evaluated for the separation and concentration of tritiated water.

  6. Crystallization and melting behavior of isotactic polypropylene composites filled by zeolite supported {beta}-nucleator

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, Juan [Materials Science Institute, School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 510275 (China); Key Laboratory of Polymeric Composites and Functional Materials, the Ministry of Education, Key Laboratory of Designed Synthesis and Application of Polymer Material of Guangdong Province, Guangzhou 510275 (China); Li, Gu, E-mail: ceslg@mail.sysu.edu.cn [Key Laboratory of Polymeric Composites and Functional Materials, the Ministry of Education, Key Laboratory of Designed Synthesis and Application of Polymer Material of Guangdong Province, Guangzhou 510275 (China); Tan, Nanshu [Key Laboratory of Polymeric Composites and Functional Materials, the Ministry of Education, Key Laboratory of Designed Synthesis and Application of Polymer Material of Guangdong Province, Guangzhou 510275 (China); Ding, Qian [Materials Science Institute, School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 510275 (China); Key Laboratory of Polymeric Composites and Functional Materials, the Ministry of Education, Key Laboratory of Designed Synthesis and Application of Polymer Material of Guangdong Province, Guangzhou 510275 (China); Mai, Kancheng, E-mail: cesmkc@mail.sysu.edu.cn [Materials Science Institute, School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 510275 (China); Key Laboratory of Polymeric Composites and Functional Materials, the Ministry of Education, Key Laboratory of Designed Synthesis and Application of Polymer Material of Guangdong Province, Guangzhou 510275 (China)

    2012-10-20

    Highlights: Black-Right-Pointing-Pointer The supported calcium pimelate {beta}-zeolite was prepared. Black-Right-Pointing-Pointer The {beta}-nucleation of zeolite was enhanced dramatically through reaction. Black-Right-Pointing-Pointer High {beta}-phase content iPP composites were obtained by introducing the {beta}-zeolite into iPP. - Abstract: In order to prepare the zeolite filled {beta}-iPP composites, the calcium pimelate as {beta}-nucleator supported on the surface of zeolite ({beta}-zeolite) was prepared by the interaction between calcified zeolite and pimelic acid. The {beta}-nucleation, crystallization behavior and melting characteristic of zeolite, calcified zeolite and {beta}-zeolite filled iPP composites were investigated by differential scanning calorimetry and wide-angle X-ray diffractometer. The results indicated that addition of the zeolite and calcified zeolite as well as {beta}-zeolite increased the crystallization temperature of iPP. The zeolite and calcified zeolite filled iPP composites mainly crystallized in the {alpha}-crystal form and the strong {beta}-heterogeneous nucleation of {beta}-zeolite results in the formation of only {beta}-crystal in {beta}-zeolite filled iPP composites. The zeolite filled {beta}-iPP composites with high {beta}-crystal contents (above 0.90) can be easily obtained by adding {beta}-zeolite into iPP matrix.

  7. Vanadia supported on zeolites for SCR of NO by ammonia

    DEFF Research Database (Denmark)

    Putluru, Siva Sankar Reddy; Riisager, Anders; Fehrmann, Rasmus

    2010-01-01

    , acidity and micropore structure of the support. Apparently the support hosted the potassium oxide on the acid sites, thereby protecting the active vanadium species from poisoning. Zeolite based catalysts might therefore prove useful for SCR of NO in alkali-containing flue gases from, e.g. biomass fired...

  8. Zeolite

    Indian Academy of Sciences (India)

    49

    The unit cell volume change and the shift in XRD reflection positions. 18 showed a positive correlation with .... Molar ratios of the components in the gel with other conditions maintained during. 79 the synthesis of the MFI zeolite .... The reaction mixtures were analyzed by Gas Chromatography. 116. In the present study, the ...

  9. PHENOL OXIDATION USING NATURAL ZEOLITE SUPPORTED METAL ION CATALYST

    Directory of Open Access Journals (Sweden)

    Sri Wardhani

    2010-06-01

    Full Text Available Phenol which contained in waste water has to be reduced and it could be done by oxygen oxidation.  In order to increase the rate of reaction it was needed a catalyst. In this research the capability of various catalysts, namely zeolite-Zn(II, zeolite-Cu(II and zeolite-Co(IIin oxidation of phenol has been investigated. The aim of this research was to study the type of metal ion catalyst towards the percentage of oxidated phenol. The oxidation process were carried out in an aqueous phenol of 100 ppm with oxygen flow rate of 200 mL/min. in the presence of catalysts with 0.2M of initial impregnation concentration. The capabilities of catalysts were performed by calculating the activation energy and it was done at two different temperatures, i.e. 70 and 90 oC. The percentage of oxidated phenol was determinated by measuring its concentration using UV-VIS spectrophotometer. In addition, the impregnated metal was calculated by measuring the ion concentration remains in the filtrate solution and it was determined using Atomic Absorption Spectrophotometer. The results showed that metal ion types affected the catalytic activity. The order of phenol oxidationactivity decreased as Co(II > Cu(II > Zn(II. The surface characteristics of catalysts were supported by pore volume and pore diameter i.e 0.009 cm3/g and 16.59 Å for Zn(II whereas specific surface area was 10.32 m2/g for Zn(II, 0.004 cm3/g and 24.37 Å for Cu(II whereas specific surface area was 3.57 m2/g for Cu(II, 0.001 cm3/g and 19.63 Å for Co(II whereas specific surface area was 10.26m2/g for Co(II.   Keywords: phenol,natural zeolite, catalyst, oxidation

  10. Fabrication of zeolite/polymer multilayer composite membranes for carbon dioxide capture: Deposition of zeolite particles on polymer supports.

    Science.gov (United States)

    Ramasubramanian, Kartik; Severance, Michael A; Dutta, Prabir K; Ho, W S Winston

    2015-08-15

    Membranes, due to their smaller footprint and potentially lower energy consumption than the amine process, offer a promising route for post-combustion CO2 capture. Zeolite Y based inorganic selective layers offer a favorable combination of CO2 permeance and CO2/N2 selectivity, membrane properties crucial to the economics. For economic viability on large scale, we propose to use flexible and scalable polymer supports for inorganic selective layers. The work described in this paper developed a detailed protocol for depositing thin zeolite Y seed layers on polymer supports, the first step in the synthesis of a polycrystalline zeolite Y membrane. We also studied the effects of support surface morphology (pore size and surface porosity) on the quality of deposition and identified favorable supports for the deposition. Two different zeolite Y particles with nominal sizes of 200 nm and 40 nm were investigated. To obtain a complete coverage of zeolite particles on the support surface with minimum defects and in a reproducible manner, a vacuum-assisted dip-coating technique was developed. Images obtained using both digital camera and optical microscope showed the presence of color patterns on the deposited surface which suggested that the coverage was complete. Electron microscopy revealed that the particle packing was dense with some drying cracks. Layer thickness with the larger zeolite Y particles was close to 1 μm while that with the smaller particles was reduced to less than 0.5 μm. In order to reduce drying cracks for layers with smaller zeolite Y particles, thickness was reduced by lowering the dispersion concentration. Transport measurement was used as an additional technique to characterize these layers. Copyright © 2015 Elsevier Inc. All rights reserved.

  11. Fly ash zeolite catalyst support for Fischer-Tropsch synthesis

    Science.gov (United States)

    Campen, Adam

    This dissertation research aimed at evaluating a fly ash zeolite (FAZ) catalyst support for use in heterogeneous catalytic processes. Gas phase Fischer-Tropsch Synthesis (FTS) over a fixed-bed of the prepared catalyst/FAZ support was identified as an appropriate process for evaluation, by comparison with commercial catalyst supports (silica, alumina, and 13X). Fly ash, obtained from the Wabash River Generating Station, was first characterized using XRD, SEM/EDS, particle size, and nitrogen sorption techniques. Then, a parametric study of a two-step alkali fusion/hydrothermal treatment process for converting fly ash to zeolite frameworks was performed by varying the alkali fusion agent, agent:flyash ratio, fusion temperature, fused ash/water solution, aging time, and crystallization time. The optimal conditions for each were determined to be NaOH, 1.4 g NaOH: 1 g fly ash, 550 °C, 200 g/L, 12 hours, and 48 hours. This robust process was applied to the fly ash to obtain a faujasitic zeolite structure with increased crystallinity (40 %) and surface area (434 m2/g). Following the modification of fly ash to FAZ, ion exchange of H+ for Na+ and cobalt incipient wetness impregnation were used to prepare a FTS catalyst. FTS was performed on the catalysts at 250--300 °C, 300 psi, and with a syngas ratio H2:CO = 2. The HFAZ catalyst support loaded with 11 wt% cobalt resulted in a 75 % carbon selectivity for C5 -- C18 hydrocarbons, while methane and carbon dioxide were limited to 13 and 1 %, respectively. Catalyst characterization was performed by XRD, N2 sorption, TPR, and oxygen pulse titration to provide insight to the behavior of each catalyst. Overall, the HFAZ compared well with silica and 13X supports, and far exceeded the performance of the alumina support under the tested conditions. The successful completion of this research could add value to an underutilized waste product of coal combustion, in the form of catalyst supports in heterogeneous catalytic processes.

  12. Novel zeolite-supported rhodium catalysts for ethanol steam reforming

    Energy Technology Data Exchange (ETDEWEB)

    Campos-Skrobot, Fabiana C.; Cantao, Mauricio P. [LACTEC, Instituto de Tecnologia para o Desenvolvimento, C.P. 19067, 81531-980 Curitiba, PR (Brazil); Rizzo-Domingues, Roberta C.P.; Fernandes-Machado, Nadia R.C. [UEM, Universidade Estadual de Maringa, Departamento de Engenharia Quimica, Av. Colombo, 5790 Bloco D-90, 87020-900 Maringa, PR (Brazil)

    2008-09-01

    Renewable bioethanol is an interesting hydrogen source for fuel cells through steam reforming, but its C-C bond promotes parallel reactions, mainly coke and by-products formation. In this way, good ethanol reforming catalysts are still needed, which explains current research and development efforts around the world. Most catalysts proposed for ethanol reforming are based on oxide-supported noble metals with surface area below 100 m{sup 2} g{sup -1} and reaction temperatures above 500 C. Novel Rh and Rh-K catalysts supported on NaY zeolite with surface area above 440 m{sup 2} g{sup -1} are presented in this work. Reaction temperature was fixed at 300 C and H{sub 2}O/EtOH molar ratio and reagent flow were varied. Ethanol conversion varied from 50 to 99%, with average increase of 50% due to K promoter, and hydrogen production yield achieved 68%. (author)

  13. Fabrication of hydrophobic zeolites using triethoxyfluorosilane and their application as supports for TiO(2) photocatalysts.

    Science.gov (United States)

    Kuwahara, Yasutaka; Kamegawa, Takashi; Mori, Kohsuke; Yamashita, Hiromi

    2008-10-21

    Hydrophobically modified Y-zeolites were prepared by simple modification with triethoxyfluorosilane (TEFS). These zeolites, used as supports, enhanced the efficiency of deposited TiO(2) for the photocatalytic degradation of organics diluted in water.

  14. Electrochemical water splitting using nano-zeolite Y supported tungsten oxide electrocatalysts

    Science.gov (United States)

    Anis, Shaheen Fatima; Hashaikeh, Raed

    2018-02-01

    Zeolites are often used as supports for metals and metal oxides because of their well-defined microporous structure and high surface area. In this study, nano-zeolite Y (50-150 nm range) and micro-zeolite Y (500-800 nm range) were loaded with WO3, by impregnating the zeolite support with ammonium metatungstate and thermally decomposing the salt thereafter. Two different loadings of WO3 were studied, 3 wt.% and 5 wt.% with respect to the overall catalyst. The prepared catalysts were characterized for their morphology, structure, and surface areas through scanning electron microscope (SEM), XRD, and BET. They were further compared for their electrocatalytic activity for hydrogen evolution reaction (HER) in 0.5 M H2SO4. On comparing the bare micro-zeolite particles with the nano-form, the nano-zeolite Y showed higher currents with comparable overpotentials and lower Tafel slope of 62.36 mV/dec. WO3 loading brought about a change in the electrocatalytic properties of the catalyst. The overpotentials and Tafel slopes were observed to decrease with zeolite-3 wt.% WO3. The smallest overpotential of 60 mV and Tafel slope of 31.9 mV/dec was registered for nano-zeolite with 3 wt.% WO3, while the micro-zeolite gave an overpotential of 370 mV and a Tafel slope of 98.1 mV/dec. It was concluded that even with the same metal oxide loading, nano-zeolite showed superior performance, which is attributed to its size and hence easier escape of hydrogen bubbles from the catalyst.

  15. Supported Zeolite Beta Layers via an Organic Template-Free Preparation Route

    Directory of Open Access Journals (Sweden)

    Stephanie Reuss

    2018-01-01

    Full Text Available Layers of high silica zeolites, synthesized with an organic structure directing agent (OSDA and grown onto porous support structures, frequently suffer from the thermal stress during the removal of OSDA via the calcination process. The different thermal expansion coefficients of the zeolite and the support material, especially when stainless steel is used as a support, causes enormous tension resulting in defect formation in the zeolite layer. However, the calcination is an easy procedure to decompose the OSDA in the pore system of the zeolite. Recently, methods to synthesize zeolite beta without the use of an organic structure directing agent have been described. In the present study, a seed-directed synthesis is used to prepare OSDA-free zeolite beta layers on stainless steel supports via an in situ preparation route. For the application as membrane, a porous stainless steel support has been chosen. The beta/stainless steel composites are characterized by X-ray diffraction (XRD and scanning electron microscopy (SEM. To prove its possible application as a membrane, the beta/stainless steel composites were also tested by single gas permeances of H2, He, CO2, N2, and CH4.

  16. Supported Zeolite Beta Layers via an Organic Template-Free Preparation Route.

    Science.gov (United States)

    Reuss, Stephanie; Sanwald, Dirk; Schülein, Marion; Schwieger, Wilhelm; Al-Thabaiti, Shaeel A; Mokhtar, Mohamed; Basahel, Sulaiman N

    2018-01-21

    Layers of high silica zeolites, synthesized with an organic structure directing agent (OSDA) and grown onto porous support structures, frequently suffer from the thermal stress during the removal of OSDA via the calcination process. The different thermal expansion coefficients of the zeolite and the support material, especially when stainless steel is used as a support, causes enormous tension resulting in defect formation in the zeolite layer. However, the calcination is an easy procedure to decompose the OSDA in the pore system of the zeolite. Recently, methods to synthesize zeolite beta without the use of an organic structure directing agent have been described. In the present study, a seed-directed synthesis is used to prepare OSDA-free zeolite beta layers on stainless steel supports via an in situ preparation route. For the application as membrane, a porous stainless steel support has been chosen. The beta/stainless steel composites are characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). To prove its possible application as a membrane, the beta/stainless steel composites were also tested by single gas permeances of H₂, He, CO₂, N₂, and CH₄.

  17. XAFS study of Ru(II)-Sn(II) cluster supported on NaY zeolite

    International Nuclear Information System (INIS)

    Udagawa, Y.; Hatanaka, H.; Yang Lichang; Shinoda, S.

    1995-01-01

    Complexes having Ru(II)-Sn(II) bond(s) are very effective for acetic acid synthesis from methanol alone. In particular the catalyst shows a very long life if supported on Y-type zeolite, suggesting that the Ru-Sn cluster species are encapsuled in zeolite supercages. Local structures around Ru were studied by XAFS at several stages of the catalyst preparation procedure, and it has been clearly shown that Ru are coordinated by Sn atoms in the catalyst. ((orig.))

  18. Synthesis and characterization of alumina application in support of zeolite membrane

    International Nuclear Information System (INIS)

    Barbosa, A.S.; Rodrigues, M.G.F.

    2012-01-01

    Much interest has been aroused in process applications using zeolite membrane. The physicochemical properties of the support have a strong effect on the quality of zeolite membrane. This work is to synthesize and characterize alumina for use as a support for zeolite membrane. In this work was synthesized α-alumina: 40% alumina, 0.2% for PABA, 0.5% oleic acid and 59.3% ethyl alcohol. The mixture was ground in ball mill and placed in an oven for 24 hours at 60 °C, allowed to stand for 24h. The pressing was performed with 4 tons. The pressed material was subjected to sintering at 1400 °C/hour. The samples were characterized by EDX, XRD and SEM. The results for the media by XRD showed that they are crystalline and pure. By EDX was observed that the supports consist essentially of alumina. (author)

  19. Palladium Catalyst Supported on Zeolite for Cross-coupling Reactions: An Overview of Recent Advances.

    Science.gov (United States)

    Kumbhar, Arjun

    2017-02-01

    Over the last 30-40 years, Pd-catalyzed C-C bond-forming reactions have gained immense importance for their use in synthesis of biologically and pharmaceutically important organic fragments. Heterogeneous Pd catalysts supported on porous materials, especially zeolites, have many advantages as they have high surface area with tunable acidity and basicity, hydrophobic and hydrophilic character, shape and size selectivity, as well as chemical and thermal stability. They also offer very easy recovery and reusability. This review covers the literature published on the synthesis and characterization of Pd catalysts supported on zeolites and their applications in various organic transformations.

  20. Enhanced photocatalytic activity of supported TiO{sub 2} by selective surface modification of zeolite Y

    Energy Technology Data Exchange (ETDEWEB)

    Guesh, Kiros [Chemistry-Department, Addis Ababa University, P.O. Box 1176, Addis Ababa (Ethiopia); Mizan-Tepi University, P.O. Box 260, Mizan-Teferi (Ethiopia); Márquez-Álvarez, Carlos [Instituto de Catálisis y Petroleoquímica, CSIC, c/Marie Curie 2, 28049 Madrid (Spain); Chebude, Yonas [Chemistry-Department, Addis Ababa University, P.O. Box 1176, Addis Ababa (Ethiopia); Díaz, Isabel, E-mail: idiaz@icp.csic.es [Chemistry-Department, Addis Ababa University, P.O. Box 1176, Addis Ababa (Ethiopia); Instituto de Catálisis y Petroleoquímica, CSIC, c/Marie Curie 2, 28049 Madrid (Spain)

    2016-08-15

    Highlights: • XPS analysis confirmed that 50% of the Al was removed from the surface of zeolite Y. • Loaded TiO{sub 2} on the treated zeolites showed 12 times higher TORm than the parent zeolite. • Supported TiO{sub 2} showed very low leaching of TiO{sub 2} nanoparticles than non supported. - Abstract: Zeolite Y was treated using ammonium acetate and ammonium fluoride sequentially. As a consequence the aluminum from the surface was selectively removed. Then, loading with TiO{sub 2} (20 wt%) led to a final photocatalyst. The samples were characterized by X-ray diffraction (XRD), elemental analysis (ICP-OES), N{sub 2} adsorption, diffuse reflectance UV–vis spectroscopy (DRS), photoluminescence spectroscopy (PL), and X-ray photoelectron spectroscopy (XPS). It was found that 50% of the Al atoms were removed from the surface of the zeolite without affecting the framework structure. The TiO{sub 2}/treated zeolite sample yielded 92% photocatalytic degradation of 10 ppm methyl orange (MO), a model pollutant, while the TiO{sub 2}/parent zeolite converted only 7.6%. The mass normalized turnover rate (TOR{sub m}) of the treated zeolite loaded with TiO{sub 2} was about 12 times higher than that of the parent zeolite loaded with the same amount of TiO{sub 2} precursor. This higher photocatalytic activity of the TiO{sub 2} supported on treated zeolite can be attributed to a more efficient interaction of the TiO{sub 2} with the zeolite leading to higher adsorption capacity. Reusability of the photocatalysts was assessed by performing three consecutive reaction cycles that showed no significant loss of photocatalytic activity.

  1. Hydrodeoxygenation of Methyl Laurate over Ni Catalysts Supported on Hierarchical HZSM-5 Zeolite

    Directory of Open Access Journals (Sweden)

    Nana Li

    2017-12-01

    Full Text Available The hierarchical HZSM-5 zeolite was prepared successfully by a simple NaOH treatment method. The concentration of NaOH solution was carefully tuned to optimal the zeolite acidity and pore structure. Under NaOH treatment conditions, a large number of mesopores, which interconnected with the retained micropores, were created to facilitate mass transfer performance. There are very good correlations between the decline of the relative zeolite crystallinity and the loss of micropores volume. The Ni nanoclusters were uniformly confined in the mesopores of hierarchical HZSM-5 by the excessive impregnation method. The direct deoxygenation in N2 and hydrodeoxygenation in H2 of the methyl laurate were compared respectively over the Ni/HZSM-5 catalysts. In the N2 atmosphere, the deoxygenation rate of the methyl laurate on the Ni/HZSM-5 catalyst is relatively slow. In the presence of H2, the synergistic effect between the hydrogenation function of the metal and the acid function of the zeolite supports can make the deoxygenation level more obvious. The yield of hydrocarbon products gradually reached the maximum with the appropriate treatment concentration of 1M NaOH, which could be attributed to the improved mass transfer in the hierarchical HZSM-5 supports.

  2. Evaluation of photocatalytic activities of supported catalysts on NaX zeolite or activated charcoal.

    Science.gov (United States)

    de Brites-Nóbrega, Fernanda F; Polo, Aldino N B; Benedetti, Angélica M; Leão, Mônica M D; Slusarski-Santana, Veronice; Fernandes-Machado, Nádia R C

    2013-12-15

    This study aimed to evaluate the photocatalytic activity of ZnO and Nb2O5 catalysts, both supported on NaX zeolite and activated charcoal (AC). The synergistic effect between oxide and support and the influence of solution pH (3, 7 and 9) on photocatalytic degradation of reactive blue 5G (C.I. 222) were analyzed. The catalysts Nb2O5/NaX, Nb2O5/AC and ZnO/NaX, ZnO/AC with 5 and 10% (wt%) were prepared by wet impregnation. The results showed that the catalysts exhibit quite different structural and textural properties. The synergic effect between ZnO and NaX support was higher than that with the activated charcoal, showing that these catalysts were more efficient. The most photoactive catalyst was 10% ZnO/NaX which showed 100% discoloration of the dye solution at pH 3, 7 and 9 after 0.5, 5 and 2h of irradiation, respectively. The hydrolytic nature of zeolite favored the formation of surface hydroxyl radicals, which increased the activity of the photocatalyst. Thus, catalysts supported on NaX zeolite are promising for use in photocatalysis. Copyright © 2013 Elsevier B.V. All rights reserved.

  3. Zeolite supported palladium catalysts for hydroalkylation of phenolic model compounds

    Czech Academy of Sciences Publication Activity Database

    Akhmetzyanova, U.; Opanasenko, Maksym; Horáček, J.; Montanari, E.; Čejka, Jiří; Kikhtyanin, O.

    2017-01-01

    Roč. 252, NOV 2017 (2017), s. 116-124 ISSN 1387-1811 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : Phenol hydroalkylation * Cyclohexylcyclohexane * MWW Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry Impact factor: 3.615, year: 2016

  4. Synthesis and characterization of 12-phosphotungstic acid supported on BEA zeolite

    Energy Technology Data Exchange (ETDEWEB)

    Jović, A.; Bajuk-Bogdanović, D.; Nedić Vasiljević, B. [Faculty of Physical Chemistry, University of Belgrade, Studentski trg 12-16, 11000 Belgrade (Serbia); Milojević-Rakić, M., E-mail: maja@ffh.bg.ac.rs [Faculty of Physical Chemistry, University of Belgrade, Studentski trg 12-16, 11000 Belgrade (Serbia); Krajišnik, D. [Department of Pharmaceutical Technology and Cosmetology, University of Belgrade-Faculty of Pharmacy, Vojvode Stepe 450, 11000 Belgrade (Serbia); Dondur, V. [Faculty of Physical Chemistry, University of Belgrade, Studentski trg 12-16, 11000 Belgrade (Serbia); Popa, A. [Institute of Chemistry Timisoara, Bl. Mihai Viteazul 24, 300223 Timisoara (Romania); Uskoković-Marković, S. [Department of Analytical Chemistry, University of Belgrade-Faculty of Pharmacy, Vojvode Stepe 450, 11000 Belgrade (Serbia); Holclajtner-Antunović, I. [Faculty of Physical Chemistry, University of Belgrade, Studentski trg 12-16, 11000 Belgrade (Serbia)

    2017-01-15

    An optimized synthetic route for obtaining heteropoly acid (HPA) species supported on BEA zeolite was applied, and different samples, comprising 20 to 50 wt% of 12-phosphotungstic acid (HPW) were prepared. The as-synthesized supported HPW were subjected to different post-synthesis routes, which involved calcination and ultrasound treatment. Characterization of these materials was performed by means of Scanning Electron Microscopy, zeta potential measurements, Infrared Spectroscopy and X-ray Powder Diffraction analysis. Results suggest strong interaction of HPW with the support and revealed that ultrasound treatment resulted in better dispersion of active phase and thus homogeneous morphology of the samples. The zeta potential was found to be dependent on the preparation procedure and HPW content in these materials, while higher HPW loadings induced its agglomeration. Catalytic activity of the synthesized materials was investigated in an ethanol dehydration reaction, where lower HPW loadings induced higher ethanol conversion. Acid sites distribution and accessibility for ethanol molecules were found to be more essential for catalytic activity than HPW loadings, i.e., amount of active sites present in these hybrid materials. - Highlights: • An optimized route for supporting heteropoly acid on beta zeolite is applied. • Ultrasound treatment of the composites gives dispersed morphology. • Lower heteropoly acid amount induces higher conversion in ethanol dehydration. • Acid sites distribution and accessibility for ethanol are essential for catalytic activity.

  5. Catalytic upgrading of oleic acid into biofuel using Mo modified zeolite supported Ni oxalate catalyst functionalized with fluoride ion

    International Nuclear Information System (INIS)

    Ayodele, O.B.; Abbas, Hazzim F.; Daud, Wan Mohd Ashri Wan

    2014-01-01

    Highlights: • Modification of zeolite with freshly prepared molybdenum oxalate. • Functionalization of Ni oxalate with HF and incorporation into Mo modified zeolite. • Characterization of synthesized Mo modified zeolite supported Ni oxalate catalyst. • Deoxygenation of oleic acid with the synthesized zeolite supported catalyst. • Reusability study on the synthesized zeolite supported catalyst. - Abstract: In this study, fluoride ion functionalized nickel oxalate supported on molybdenum modified zeolite (NiMoFOx/Zeol) catalyst was synthesized, characterized and tested on the hydrodeoxygenation (HDO) of oleic acid (OA) into paraffinic fuel. The NiMoFOx/Zeol characterization results confirmed the presence of both Ni and Mo as well as the formation of NiMoO 4 which is a highly HDO reactive specie at 2θ value of 43.6° according to the XRD result. NiMoFOx/Zeol also showed loss in crystallinity and reduction in the average particle size leading to increase in the pore volume and specific surface area due to the combined effects of fluoride ion presence, oxalic acid functionalization and calcination. The effect of temperature, pressure and NiMoFOx/Zeol loading studied showed that initial increase in their values increased the yield of the target fractions until some points where reduction was observed. The best observed experimental conditions to hydrodeoxygenate 40 g (∼45 mL) of OA into 75% n-C 18 and 23% i-C 18 were 360 °C, 30 mg NiMoFOx/Zeol loading and 20 bar using 100 mL H 2 /min. The presence of i-C 18 was due to the functionalization of the catalyst with fluoride ion. The catalyst reusability result displayed excellent qualities with marginal loss of only 2% in activity after third reuse due to the improved synthesis protocol that employed organometallic precursor. The results are strongly encouraging for further studies toward industrialization of HDO process

  6. Rheology-sensitive response of zeolite-supported anti-inflammatory drug systems.

    Science.gov (United States)

    Pasquino, R; Di Domenico, M; Izzo, F; Gaudino, D; Vanzanella, V; Grizzuti, N; de Gennaro, B

    2016-10-01

    Drug release from inorganic supports is a challenge for the scientific community for various reasons, related to the low costs of the systems and the possibility of easily regulating the drug release. In the present work, surface-modified zeolite particles are used as carriers for non steroidal antiflammatory drugs (NSAIDs). The release of the drug has been studied in a solution that simulates the intestinal fluid as well as in a gel-like system, based on a surfactant and a binding salt. In the solution case, the quantity of drug released has been tracked via spectrophotometric assay. Release in the gel has been monitored by rheological methods. The molecular conformation of the NSAIDs is fundamental for the interaction with the zeolite surface, whose modified surface has a strong binding energy. It has been proven that the main mechanism for the drug release is anion exchange. It has been found that the NSAIDs, used in their sodic form, can act as binding salts by themselves in the gel-like system, thus changing the viscoelastic response of the overall solution. Drug release kinetics in the solution compare quantitatively well with the released drug in the gel-like fluid, as measured by rheometry. Copyright © 2016 Elsevier B.V. All rights reserved.

  7. Light alkane (mixed feed selective dehydrogenation using bi-metallic zeolite supported catalyst

    Directory of Open Access Journals (Sweden)

    Zeeshan Nawaz

    2009-12-01

    Full Text Available Light alkanes are the important intermediates of many refinery processes and their catalytic dehydrogenation gives corresponding alkenes. The aim behind this experimentation is to investigate reaction behavior of mixed alkanes during direct catalytic dehydrogenation and emphasis has been given to enhance propene. Bi-metallic zeolite supported catalyst Pt-Sn/ZSM-5 was prepared by sequentional impregnation method and characterized by BET, EDS and XRD. Direct dehydrogenation reaction is highly endothermic and its conversion is thermodynamically limited. Results showed that the increase in temperature increases the conversion to some extent but there is no overall effect on selectivity of propene. Increase in time-on-stream (TOS remarkably improves propene selectivity at the expense of lower conversion. The performances of bi-metallic zeolite based catalyst largely affected by coke deposition. The presence of butane and ethane adversely affected propane conversion. Optimum propene selectivity is about 48 %, obtained at 600 oC and time-on-stream 10 h.

  8. Obtaining of supports macro and micro nutrients with base in zeolites mexicans

    International Nuclear Information System (INIS)

    Cordova H, A.; Islas M, M.; Bascunan S, C.; Martines G, M.; Nikolaev N, S.

    2001-01-01

    Study the effect of application of the zeolites modified by the ionico interchange with fertilizers (NPK), N-p in the production of tomatos. The cultive of tomatos was made in lands of the Benemerita Autonoma Universidad de Puebla, Mexico, taking equal quadrants with the following ground treatments: 1) zeolite interchanged with fertilizers, 2) zeolite interchanged with a solution that contained only N-p, 3) natural zeolite without ionica modification and a quadrant witness represented by the ground without treatment. The collected data show an increase in the harvest of tomatos, as well as the retention of the decomposition of the harvested tomatos. In addition, it determinated that the optimal concentrations in the case of the zeolite dealt with 3% of fertilizer NPK are: 0,91% of potassium and 0.61% of nitrogen. These results allow to suggest the use of zeolites modified by ionico interchange in agriculture to elevate the level of the harvests of the tomato [es

  9. Templating mesoporous zeolites

    DEFF Research Database (Denmark)

    Egeblad, Kresten; Christensen, Christina Hviid; Kustova, Marina

    2008-01-01

    The application of templating methods to produce zeolite materials with hierarchical bi- or trimodal pore size distributions is reviewed with emphasis on mesoporous materials. Hierarchical zeolite materials are categorized into three distinctly different types of materials: hierarchical zeolite...... originates almost exclusively from the support material. The methods for introducing mesopores into zeolite materials are discussed and categorized. In general, mesopores can be templated in zeolite materials by use of solid templating, supramolecular templating, or indirect templating....... In this categorization of templating methods, the nature of the interface between the zeolite crystal and the mesopore exactly when the mesopore starts to form is emphasized. In solid templating, the zeolite crystal is in intimate contact with a solid material that is being removed to produce the mesoporosity. Similarly...

  10. Ultraviolet Raman spectroscopy of catalysts: Adsorption and coke formation in zeolites and vibrational spectra of supported metal oxides

    Science.gov (United States)

    Chua, Yek Tann

    2001-10-01

    The primary goal of this dissertation is to study the physicochemical and catalytic properties of zeolites and supported metal oxide catalysts using UV Raman spectroscopy. In order to reduce the thermal degradation and possible photodecomposition of adsorbates by UV radiation, we have developed a novel fluidized bed method for measuring the UV Raman spectra of catalysts and adsorbates. The UV Raman spectra of various organic compounds adsorbed in zeolites H-USY and H-ZSM-5 are recorded. When measurements are performed on stationary and spinning samples, the Raman spectra show the presence of coke, a typical end product of heat and photochemistry. In contrast, the Raman peaks of the unreacted adsorbates dominate the spectra measured using the fluidized bed method. These results indicate that the fluidized bed technique is a good method for measuring UV Raman spectra of catalysts and adsorbates. The formation of coke in the methanol-to-gasoline conversion over zeolite H-ZSM-5 causes deactivation of the catalyst. To gain insight into the formation of coke, we have studied this reaction using UV Raman spectroscopy. The Raman spectral changes suggest coke is produced from conjugated olefins via cyclopentadiene intermediates. Aromatic compounds in gasoline may also be produced from cyclopentadienes. The adsorbate-induced structural changes of zeolites may alter the molecular sieving characteristics of these materials which ultimately affect their performance as catalysts and adsorbents. We have quantified the adsorbate-induced structural changes of zeolite H-RHO using UV Raman spectroscopy. The Raman spectra of the zeolite after the adsorption of water, methanol or acetonitrile are consistent with an increase in the average T-O-T angle of the zeolite of 5-8°. The adsorption of ammonia, on the other hand, decreases the average T-O-T angle by 5°. Because of certain advantages of UV Raman spectroscopy over visible Raman spectroscopy, recently there is a strong interest in

  11. Synthesis of Fatty Alcohols from Oil Palm Using a Catalyst of Ni-Cu Supported onto Zeolite

    OpenAIRE

    L. Giraldo; G. Camargo; J. Tirano; J. C. Moreno-Piraján

    2010-01-01

    A series of Ni-Cu supported onto zeolite type ZSM-5 has been synthesized by direct hydrothermal method without template agent and characterized using XRD, FT-IR, NRM mass, SEM, CG and N2 adsorption techniques. The catalytic performance of the obtained materials was evaluated and utilized for the hydrogenation of palm oil at 453 K and 40 atmospheres of pressure. The results show that the samples exhibited typical hexagonal arrangement of mesoporous structure with high surface area and the hete...

  12. Hydrogenation of Anthracene in Supercritical Carbon Dioxide Solvent Using Ni Supported on Hβ-Zeolite Catalyst

    Directory of Open Access Journals (Sweden)

    Ashraf Aly Hassan

    2012-01-01

    Full Text Available Catalytic hydrogenation of anthracene was studied over Ni supported on Hβ-zeolite catalyst under supercritical carbon dioxide (sc-CO2 solvent. Hydrogenation of anthracene in sc-CO2 yielded 100% conversion at 100 °C, which is attributed to the reduced mass transfer limitations, and increased solubility of H2 and substrate in the reaction medium. The total pressure of 7 MPa was found to be optimum for high selectivity of octahydroanthracene (OHA. The conversion and selectivity for OHA increased with an increase in H2 partial pressure, which is attributed to higher concentration of hydrogen atoms at higher H2 pressures. The selectivity reduced the pressure below 7 MPa because of enhanced desorption of the tetrahydro-molecules and intermediates from Ni active sites, due to higher solubility of the surface species in sc-CO2. The selectivity of OHA increased with the increase in catalyst weight and reaction time. The rate of hydrogenation of anthracene was compared with that found for napthalene and phenanthrene. The use of acetonitrile as co-solvent or expanded liquid with CO2 decreased the catalytic activity.

  13. Catalytic Performance of Zeolite-Supported Vanadia in the Aerobic Oxidation of 5-hydroxymethylfurfural to 2,5- diformylfuran

    DEFF Research Database (Denmark)

    Sádaba, Irantzu; Gorbanev, Yury; Kegnæs, Søren

    2013-01-01

    /Vis spectrophotometry. The H-beta zeolite catalysts were found to contain highly dispersed vanadium oxide species at all loadings, and provided the highest reaction selectivity towards DFF and the lowest metal leaching of the examined systems. In particular, 1 wt % V2O5/H-beta was found to be a stable, recyclable......The catalytic performance of zeolite-supported vanadia catalysts was examined for the aerobic oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-diformylfuran (DFF) in organic solvents such as N,N-dimethylformamide (DMF), methyl isobutyl ketone, toluene, trifluorotoluene and DMSO. Catalysts based......, and non-leaching catalyst for the production of DFF under mild conditions in DMF as solvent, although with low DFF yield. To increase the yield, oxidation of HMF at elevated pressures was also investigated with this catalyst. Under optimized conditions, a reaction selectivity towards DFF of >99 % at 84...

  14. Synthesis of Zeolite-X Supported On Glasswool for CO2 Capture Material: Variation of Immersion Time and NaOH Concentration at Glasswool Activation

    Directory of Open Access Journals (Sweden)

    Anggita R.K. Wardani

    2016-03-01

    Full Text Available Zeolite X supported on fiber material (glasswool was successfully synthesized using a simple hydrothermal method. Variation of immersion time and NaOH concentration were used for glasswool activation. Activation process of glasswool has effects toward crystallinity and growth of zeolite X on glasswool surface. The results of characterization using XRD, SEM and AFM showed that zeolite X crystal grew on glasswool surface with high crystallinity using NaOH concentration 4M for 24 h. BET surface area and pore characteristics were analyzed by N2 isothermal adsorption. Carbon dioxide adsorption measurement using gravimetric method showed that zeolite X supported on glasswool has capability to capture carbon dioxide at room temperature up to 2.83 weight %.

  15. Ni catalysts with different promoters supported on zeolite for dry reforming of methane

    KAUST Repository

    Alotaibi, Raja

    2015-07-08

    Dry reforming of methane (DRM) is considered a high endothermic reaction with operating temperatures between 700 and 1000 °C to achieve high equilibrium conversion of CH4 and CO2 to the syngas (H2 and CO). The conventional catalysts used for DRM are Ni-based catalysts. However, many of these catalysts suffer from the short longevity due to carbon deposition. This study aims to evaluate the effect of La and Ca as promoters for Ni-based catalysts supported on two different zeolite supports, ZL (A) (BET surface area = 925 m2/g, SiO2/Al2O3 mol ratio = 5.1), and ZL (B) (BET surface area = 730 m2/g, SiO2/Al2O3 mol ratio = 12), for DRM. The physicochemical properties of the prepared catalysts were characterized with XRD, BET, TEM and TGA. These catalysts were tested for DRM in a microtubular reactor at reaction conditions of 700 °C. The catalyst activity results show that the catalysts Ni/ZL (B) and Ca-Ni/ZL (B) give the highest methane conversion (60 %) with less time on stream stability compared with promoted Ni on ZL (A). In contrast, La-containing catalysts, La-Ni/ZL (B), show more time on stream stability with minimum carbon content for the spent catalyst indicating the enhancement of the promoters to the Ni/ZL (A) and (B), but with less catalytic activity performance in terms of methane and carbon dioxide conversions due to rapid catalyst deactivation.

  16. Method for producing zeolites and zeotypes

    DEFF Research Database (Denmark)

    2015-01-01

    The invention relates to a method for producing zeolite, zeolite-like or zeotype particles comprising the steps of: 1 ) Adding one or more metal precursors to a silica or alumina source; 2) Reducing the one or more metal precursors to form metal nanoparticles on the surface of the silica or alumina...... source; 3) Passing a gaseous hydrocarbon, alkyl alcohol or alkyl ether over the silica or alumina supported metal nanoparticle to form a carbon template coated zeolite, zeolite-like or zeotype precursor composition; 4a) Adding a structure directing agent to the carbon template coated zeolite, zeolite......-like or zeotype precursor composition thereby creating a zeolite, zeolite-like or zeotype gel composition; 4b) Crystallising the zeolite, zeolite-like or zeotype gel composition by subjecting said composition to a hydrothermal treatment; 5) Removing the carbon template and structure directing agent and isolating...

  17. Method of producing zeolite encapsulated nanoparticles

    DEFF Research Database (Denmark)

    2015-01-01

    The invention therefore relates to a method for producing zeolite, zeolite-like or zeotype encapsulated metal nanoparticles, the method comprises the steps of: 1) Adding one or more metal precursors to a silica or alumina source; 2) Reducing the one or more metal precursors to form metal...... nanoparticles on the surface of the silica or alumina source; 3) Passing a gaseous hydrocarbon, alkyl alcohol or alkyl ether over the silica or alumina supported metal nanoparticles to form a carbon template coated zeolite, zeolite-like or zeotype precursor composition; 4a) Adding a structure directing agent...... to the carbon template coated zeolite, zeolite-like or zeotype precursor composition thereby creating a zeolite, zeolite-like or zeotype gel composition; 4b) Crystallising the zeolite, zeolite-like or zeotype gel composition by subjecting said composition to a hydrothermal treatment; 5) Removing the carbon...

  18. Noble-metal-based catalysts supported on zeolites and macro-mesoporous metal oxide supports for the total oxidation of volatile organic compounds.

    Science.gov (United States)

    Barakat, Tarek; Rooke, Joanna C; Tidahy, Haingomalala Lucette; Hosseini, Mahsa; Cousin, Renaud; Lamonier, Jean-François; Giraudon, Jean-Marc; De Weireld, Guy; Su, Bao-Lian; Siffert, Stéphane

    2011-10-17

    The use of porous materials to eliminate volatile organic compounds (VOCs) has proven very effective towards achieving sustainability and environmental protection goals. The activity of zeolites and macro-mesoporous metal-oxide supports in the total oxidation of VOCs has been investigated, with and without noble-metal deposition, to develop highly active catalyst systems where the formation of by-products was minimal. The first catalysts employed were zeolites, which offered a good activity in the oxidation of VOCs, but were rapidly deactivated by coke deposition. The effects of the acido-basicity and ionic exchange of these zeolites showed that a higher basicity was related to exchanged ions with lower electronegativities, resulting in better catalytic performances in the elimination of VOCs. Following on from this work, noble metals were deposited onto macro-mesoporous metal-oxide supports to form mono and bimetallic catalysts. These were then tested in the oxidation of toluene to study their catalytic performance and their deactivation process. PdAu/TiO(2) and PdAu/TiO(2) -ZrO(2) 80/20 catalysts demonstrated the best activity and life span in the oxidation of toluene and propene and offered the lowest temperatures for a 50 % conversion of VOCs and the lowest coke content after catalytic testing. Different characterization techniques were employed to explain the changes occurring in catalyst structure during the oxidation of toluene and propene. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  19. Clouds: A support architecture for fault tolerant, distributed systems

    Science.gov (United States)

    Dasgupta, P.; Leblanco, R. J., Jr.

    1986-01-01

    Clouds is a distributed operating system providing support for fault tolerance, location independence, reconfiguration, and transactions. The implementation paradigm uses objects and nested actions as building blocks. Subsystems and applications that can be supported by Clouds to further enhance the performance and utility of the system are also discussed.

  20. Isomerization of hexane on PtAu nanoparticles supported on zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Fraissard, Jacques [P. and M. Curie University, 4 Place Jussieu, 75252 Paris Cedex 05 (France); Laboratoire de Physique Quantique, 10 rue Vauquelin, ESPCI, 75231 Paris Cedex 05 (France); Gerda, Vasilyi [Taras Shevchenko National University, 64 Volodymyrskaya str., 01033 Kiev (Ukraine); Patrylak, Kazymyr I.; Voloshyna, Yu.G. [Institute of Biorganic Chemistry and Petrochemistry, Academy of Science, 02660 Kiev (Ukraine)

    2007-04-30

    When lead-based anti-knock additives were withdrawn, petrol was enriched with benzene and benzene derivatives in order to maintain an excellent octane number. However, because of their toxicity, it is planned to eliminate these also and to replace them by methylated alkanes, whence the importance of n-alkane isomerization. Some PtAu-zeolite catalysts tested for n-hexane isomerization reveal that the addition of gold to platinum generally changes the activity and/or the selectivity for methylpentane to the detriment of cracking. The influence of the zeolite structure is also important. At 275 C, the activity and selectivity of PtAu-HZSM5 are about 75%, showing that this catalyst can be useful for such a reaction. (author)

  1. Synthesis of Fatty Alcohols from Oil Palm Using a Catalyst of Ni-Cu Supported onto Zeolite

    Directory of Open Access Journals (Sweden)

    L. Giraldo

    2010-01-01

    Full Text Available A series of Ni-Cu supported onto zeolite type ZSM-5 has been synthesized by direct hydrothermal method without template agent and characterized using XRD, FT-IR, NRM mass, SEM, CG and N2 adsorption techniques. The catalytic performance of the obtained materials was evaluated and utilized for the hydrogenation of palm oil at 453 K and 40 atmospheres of pressure. The results show that the samples exhibited typical hexagonal arrangement of mesoporous structure with high surface area and the heteroatoms were probably incorporated into the framework of ZSM-5. Catalytic tests show that the bimetallic incorporated materials were effective as catalysts in the hydrogenation of oil palm producing fatty alcohols typical.

  2. Fault-Tolerant Onboard Monitoring and Decision Support Systems

    DEFF Research Database (Denmark)

    Lajic, Zoran

    The purpose of this research project is to improve current onboard decision support systems. Special focus is on the onboard prediction of the instantaneous sea state. In this project a new approach to increasing the overall reliability of a monitoring and decision support system has been...... advice regarding speed and course changes to decrease the wave-induced loads. The SeaSense system is based on the combined use of a mathematical model and measurements from a set of sensors. The overall dependability of a shipboard monitoring and decision support system such as the SeaSense system can...... of a fault. A supervisory function determines the severity of the fault once its origin has been isolated and its magnitude estimated. Fault-tolerant Sensor Fusion means that the monitoring and decision support system can accommodate faults so that the overall system continues to satisfy its goal...

  3. Selective production of chemicals from biomass pyrolysis over metal chlorides supported on zeolite.

    Science.gov (United States)

    Leng, Shuai; Wang, Xinde; Cai, Qiuxia; Ma, Fengyun; Liu, Yue'e; Wang, Jianguo

    2013-12-01

    Direct biomass conversion into chemicals remains a great challenge because of the complexity of the compounds; hence, this process has attracted less attention than conversion into fuel. In this study, we propose a simple one-step method for converting bagasse into furfural (FF) and acetic acid (AC). In this method, bagasse pyrolysis over ZnCl2/HZSM-5 achieved a high FF and AC yield (58.10%) and a 1.01 FF/AC ratio, but a very low yield of medium-boiling point components. However, bagasse pyrolysis using HZSM-5 alone or ZnCl2 alone still remained large amounts of medium-boiling point components or high-boiling point components. The synergistic effect of HZSM-5 and ZnCl2, which combines pyrolysis, zeolite cracking, and Lewis acid-selective catalysis results in highly efficient bagasse conversion into FF and AC. Therefore, our study provides a novel, simple method for directly converting biomass into high-yield useful chemical. Copyright © 2013 Elsevier Ltd. All rights reserved.

  4. The fabrication of porous 4A-zeolite-supported Ag nanoparticles catalysts and its catalytic activity for styrene epoxidation

    Directory of Open Access Journals (Sweden)

    Youkui Wu

    Full Text Available Binderless hierarchically porous 4A-zeolite has been successful produced through hydrothermal crystallization, in which silicon-aluminum sol binded to the carbon nanofibers (CNFs, that is to say, where the CNFs powder was coated during the crystallization 4A-zeolite. The mixing of silica-alumina sol and CNFs was only a simple physical mixing process. The samples of micropores-macroporous hierarchical 4A-zeolite (P-4A-zeolite was analyzed by a series of characterization techniques, such as field emission scanning electron microscope (FESEM, transmission electron microscopy (TEM, simultaneous thermal analysis (STA and CO2 adsorption-desorption (BET and BJH, and so on. In addition, the adsorption test of silver nanoparticles was carried out. The characterization results indicated the presence of micropores and the formation of macroporous. At the same time, silver adsorption test proved that the prepared P-4A-zeolite had good adsorption performance and the catalytic performance of Ag/P-4A-zeolite was further investigated through the epoxidation of styrene. Keywords: Carbon nanofibers, Porous 4A-zeolite, Silver nanoparticles, Styrene epoxidation

  5. I. Synthesis, characterization, and base catalysis of novel zeolite supported super-basic materials II. Oxidative dehydrogenation of ethane over reduced heteropolyanion catalysts

    Science.gov (United States)

    Galownia, Jonathan M.

    This thesis is composed of two separate and unrelated projects. The first part of this thesis outlines an investigation into the synthesis and characterization of a novel zeolite supported super-base capable of carbon-carbon olefin addition to alkyl aromatics. A zeolite supported basic material capable of such reactions would benefit many fine chemical syntheses, as well as vastly improve the economics associated with production of the high performance thermoplastic polyester polyethylene naphthalate. The thermal decomposition of alkali---metal azides impregnated in zeolite X is investigated as a novel route to the synthesis of a zeolite supported super-base. Impregnation of the alkali---metal azide precursor is shown to result in azide species occluded within the pores of the zeolite support by using high speed, solid-state 23Na MAS and 2D MQMAS NMR, FTIR, and TGA characterization methods. Addition of alkali---metal azides to the zeolite results in redistribution of the extra-lattice cations in the zeolite framework. Thermal decomposition of impregnated azide species produces further cation redistribution, but no neutral metallic clusters are detected by high speed, solid-state 23Na MAS NMR following thermal activation of the materials. Instead, it is possible that inactive ionic clusters are formed. The thermally activated materials do not promote base catalysis for the isomerization of 1-butene, the ethylation of toluene and o-xylene, and the alkenylation of o-xylene with 1,3-butadiene to produce 5-ortho-tolyl-pent-2-ene (5-OTP). The lack of catalytic activity in the materials is attributed to failure of the materials to form neutral metallic clusters during thermal treatment, possibly due to preferential formation of NMR silent ionic clusters. The formation of neutral metallic clusters is found to be insensitive to synthesis technique and activation procedure. It is concluded that the impregnation of alkali---metal azides in zeolite X does not provide a

  6. Les zéolithes: supports des complexes des métaux de transition Using Zeolites As Supports for Transition-Metal Complexes

    Directory of Open Access Journals (Sweden)

    Le Van Mao R.

    2006-11-01

    Full Text Available On met en évidence dans cet article les principales caractéristiques structurales et superficielles des zéolithes qui peuvent être avantageusement utilisées comme catalyseurs acides ou bifonctionnels et comme supports présentant une grande dispersion de métal de transition et d'intéressants effets sélectifs. Les résultats plutôt encourageants, obtenus dans l'hétérogénéisation de certains complexes des métaux de transition sur des polymères organiques ou sur la silice, ont servi à mesurer les progrès réalisés dans le domaine de leur introduction dans les zéolithes : l'intérêt scientifique et pratique d'une telle opération augmenterait considérablement si l'on pouvait « encager s directement ces complexes dans les cavités - de dimensions moléculaires - des zéolithes ou des silicates récemment synthétisés et dont la cristallisation est caractérisée par une cinétique très lente. This article describes the leading structural and superficial properties of zeolites which can be advantageously used as acid or bifunctional catalysts and as supports offering a considerable capacity for dispersing transition metal as well as interesting selective effects.The rather encouraging results obtained in heterogenizing various transition-metal complexes on org anic polymers or on silica have been used to measure the advances made in the field of incorporating them in zeolites. The scientific and pratical impor-tance of such an operation would be considerably enhanced if such complexes could be « encaged » in molecular-size cavities in zeolites or in recently-synthetized silicates whose crystallization is characterized by very slow kinetics.

  7. Synthesis of ceramic hollow fiber supported zeolitic imidazolate framework-8 (ZIF-8) membranes with high hydrogen permeability

    KAUST Repository

    Pan, Yichang

    2012-12-01

    Purification and recovery of hydrogen from hydrocarbons in refinery streams in the petrochemical industry is an emerging research field in the study of membrane gas separation. Hollow fiber membrane modules can be easily implemented into separation processes at the industrial scale. In this report, hollow yttria-stabilized zirconia (YSZ) fiber-supported zeolitic imidazole framework-8 (ZIF-8) membranes were successfully prepared using a mild and environmentally friendly seeded growth method. Our single-component permeation studies demonstrated that the membrane had a very high hydrogen permeance (~15×10 -7mol/m 2sPa) and an ideal selectivity of H 2/C 3H 8 of more than 1000 at room temperature. This high membrane permeability and selectivity caused serious concentration polarization in the separation of H 2/C 3H 8 mixtures, which led to almost 50% drop in both the H 2 permeance and the separation factor. Enhanced mixing on the feed side could reduce the effect of the concentration polarization. Our experimental data also indicated that the membranes had excellent reproducibility and long-term stability, indicating that the hollow fiber-supported ZIF-8 membranes developed in this study have great potential in industry-scale separation of hydrogen. © 2012 Elsevier B.V.

  8. RuO2 supported NaY zeolite catalysts: Effect of preparation methods on catalytic performance during aerobic oxidation of benzyl alcohol

    Science.gov (United States)

    Jung, Dasom; Lee, Sunwoo; Na, Kyungsu

    2017-10-01

    The effects of preparation method for RuO2 supported zeolite catalysts on the catalytic consequences during the aerobic oxidation of benzyl alcohol to benzaldehyde were investigated. Three preparation methods, i.e., (i) simultaneous crystallization of the zeolite framework in the presence of RuCl3 (Ru(SC)/NaY), (ii) post ion-exchange with RuCl3 on the zeolite framework (Ru(IE)/NaY), and (iii) post support of preformed Ru metal nanoparticles on the zeolite surface (Ru(PS)/NaY), were used to construct three different RuO2 supported NaY zeolite catalysts. The catalyst performance was investigated as functions of the reaction time and temperature, in correlation with the structural changes of the catalysts, as analyzed by X-ray diffraction (XRD). The results revealed that the catalytic consequences were dramatically affected by the preparation methods. Although similar conversion was achieved with all three catalysts, the turnover frequency (TOF) differed. The Ru(PS)/NaY catalyst exhibited the highest TOF (33-48 h-1), whereas the other catalysts produced much lower TOFs (9-12 h-1). The Ru(PS)/NaY catalyst also had the highest activation energy (Ea) of 48.39 kJ mol-1, whereas the Ru(SC)/NaY and Ru(IE)/NaY catalysts had Ea values of 18.58 and 24.11 kJ mol-1, respectively. Notably, the Ru(PS)/NaY catalyst yielded a significantly higher pre-exponential factor of 5.22 × 105 h-1, which is about 5 orders of magnitude larger than that of the Ru(SC)/NaY catalyst (7.15 × 100 h-1). This suggests that collision between benzyl alcohol and molecular oxygen was very intensive on the Ru(PS)/NaY catalyst, which explains the higher TOF of the Ru(PS)/NaY catalyst relative to the others in spite of the higher Ea value of the former. In terms of recyclability, the pristine crystallinity of the zeolite framework was maintained in the Ru(SC)/NaY catalyst and the RuO2 phase exhibited an insignificant loss of the initial activity up to three catalytic cycles, whereas Ru(PS)/NaY showed slight

  9. for zeolite coating

    Directory of Open Access Journals (Sweden)

    Carlos Renato Rambo

    2006-01-01

    Full Text Available Biotemplating is the processing of microcellular ceramics by reproduction of natural morphologies, where the microstructural features of the biotemplate are maintained in the biomorphic ceramic. Different biotemplates with distinct pore anatomies were used to produce biomorphic supports for the zeolite coating: wood, cardboard, sea-sponge and sisal. The biomorphic ceramics were produced by distinguished processing routes: Al-gas infiltration-reaction, liquid-metal infiltration, dip-coating and sol-gel synthesis, in order to produce nitrides, carbides and oxides, depending on the processing conditions. The zeolite coating was performed by hydrothermal growth of MFI-type (Silicalite-1 and ZSM-5 zeolite crystals onto the internal pore walls of the biomorphic templates. The final biomorphic ceramic-zeolite composites were physically characterized, evaluated in terms of their gas adsorption capabilities and correlated to their microstructure and specific pore anatomy. The combination of the properties of the biomorphic ceramics with the adsorption properties of zeolites results in materials with distinct properties as potential candidates for adsorption and catalytic applications due to their characteristic porosity, molecular sieving capabilities and high thermo-mechanical strength.

  10. Modular, Fault-Tolerant Electronics Supporting Space Exploration, Phase II

    Data.gov (United States)

    National Aeronautics and Space Administration — Modern electronic systems tolerate only as many point failures as there are redundant system copies, using mere macro-scale redundancy. Fault Tolerant Electronics...

  11. A comprehensive study on photocatalytic activity of supported Ni/Pb sulfide and oxide systems onto natural zeolite nanoparticles

    International Nuclear Information System (INIS)

    Babaahamdi-Milani, Majid; Nezamzadeh-Ejhieh, Alireza

    2016-01-01

    Highlights: • Increase in photocatalytic activity of hybridized/supported PbO/NiO and PbS/NiS systems with respect to semiconductors alone. • Higher efficiency of PbO/NiO than PbS/NiS. • Positive role of p-n junction for enhancement of photocatalytic activity of the used semiconductors. - Abstract: The Ni(II)-Pb(II) exchanged clinoptilolite nanoparticles (NCP) were transformed to corresponding oxides and sulfides via calcination and sulfiding processes, respectively. The obtained catalysts were characterized by XRD, FT-IR, TEM and DRS and used in photodegradation of p-nitrophenol (4-NP) aqueous solution under Hg-lamp irradiation. Results showed considerable increase in activity of the coupled semiconductors with respect to monocomponent one. In NiO-PbO-NCP system, conduction band (CB) of NiO is enough negative for easily migration of photogenerated electrons to CB-PbO level, while such phenomena take place from more negative CB-PbS level to CB-NiS level in NiS-PbS-NCP. These phenomena significantly prevented from electron-hole recombination which increased photocatalytic activity of the coupled semiconductors. Best photodegradation activities obtained by NiO 1.3% –PbO 14.7% -NCP and NiS 2.1% –PbS 10.0% -NCP, confirming semiconductors' mass-ratio dependence of the photocatalytic process. The supported coupled semiconductors showed blue shifts in band gap energies with respect to the bulk semiconductors which confirm formation of semiconductors nanoparticles inside the zeolite framework. The highest degradation percentage of 4-NP was obtained at: 0.5 g L −1 photocatalysts, 15 mg L −1 4-NP at pH 7.5.

  12. Removal of ethylene from air stream by adsorption and plasma-catalytic oxidation using silver-based bimetallic catalysts supported on zeolite.

    Science.gov (United States)

    Trinh, Quang Hung; Lee, Sang Baek; Mok, Young Sun

    2015-03-21

    Dynamic adsorption of ethylene on 13X zeolite-supported Ag and Ag-M(x)O(y) (M: Co, Cu, Mn, and Fe), and plasma-catalytic oxidation of the adsorbed ethylene were investigated. The experimental results showed that the incorporation of Ag into zeolite afforded a marked enhancement in the adsorptivity for ethylene. The addition of transition metal oxides was found to have a positive influence on the ethylene adsorption, except Fe(x)O(y). The presence of the additional metal oxides, however, appeared to somewhat interrupt the diffusion of ozone into the zeolite micro-pores, leading to a decrease in the plasma-catalytic oxidation efficiency of the ethylene adsorbed there. Among the second additional metal oxides, Fe(x)O(y) was able to reduce the emission of ozone during the plasma-catalytic oxidation stage while keeping a high effectiveness for the oxidative removal of the adsorbed ethylene. The periodical treatment consisting of adsorption followed by plasma-catalytic oxidation may be a promising energy-efficient ethylene abatement method. Copyright © 2014 Elsevier B.V. All rights reserved.

  13. HYDROGENATION OF POLYCYCLIC AROMATIC COMPOUNDS USING NI SUPPORT ON H-BETA ZEOLITE IN SUPERCRITICAL CARBON DIOXIDE

    Science.gov (United States)

    The primary rationale for use of supercritical carbon dioxide as a solvent in hydrogenation is the elimination of mass transfer limitations, through enhancement of the solubility of hydrogen at the reaction locus. Hydrogenation of anthracene was performed using NiHB-zeolite catal...

  14. Synthesis and testing of nanosized zeolite Y

    Science.gov (United States)

    Karami, Davood

    kept constant. The extent to which the nanosized zeolite Y was formed depended on the types and amount of the organic templates as well as the ageing duration. The activity testing of four FCC catalysts prepared by using CREY (Calcined Rare Earth ion-exchanged) zeolites with different particle sizes was carried out in a fluidized bench-scale batch riser simulator reactor. The starting zeolites NaY of different particle sizes were subjected to two cycles of ion exchange treatment. The particle size of the supported zeolites was varied between 150 and 1800 nm. The preparation of FCC catalysts was conducted by mixing the CREY zeolite with silica-alumina matrix and silica sol binder. Each catalyst contained 25% zeolite. The results of catalytic cracking demonstrated the significant effect of size reduction of the starting zeolite Y on catalytic performance of FCC catalyst. Keywords. Zeolite NaY, Faujasite, Nanosized particles, Nanozeolite, Nanotechnology, Synthesis, Crystallization, Seeding, Ageing, Precipitated silica, Sylopol silica, Fumed silica, Silica sol, Soluble silicates, Alumina, SAR or SiO2/Al2O3 Ratios, Sodium hydroxide, Sodium aluminate, Organic templates, TMAOH, Surfactant (CTAB), Ammonium Sulfate, BET surface area, BJH Pore Size Distribution, Zetasizer Particle Size Distribution, Powder XRD, 27Al Solid-State NMR, Catalytic Impregnation, CREY Zeolite, Silica-Alumina Matrix, Ion Exchange, FCC Catalyst, Catalytic cracking, Riser SimulatorRTM, Steaming, Zeolite HY, Utrastable Zeolite Y (USY)

  15. Reductive deconstruction of organosolv lignin catalyzed by zeolite supported nickel nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Kasakov, Stanislav; Shi, Hui; Camaioni, Donald M.; Zhao, Chen; Barath, Eszter; Jentys, Andreas; Lercher, Johannes A.

    2015-11-01

    Mechanistic aspects of deconstruction and hydrodeoxygenation of organosolv lignin using supported Ni catalysts with (Ni/HZSM-5 and Ni/HBEA) and without Brønsted acid sites (Ni/SiO2) are reported. Lignin was deconstructed and converted to saturated cyclic hydrocarbons ranging from C5 to C14. In the one-stage reaction, full conversion with total yield of 70 ± 5 wt.% saturated hydrocarbons was achieved at 593 K and 20 bar H2. The organosolv lignin used consists of seven to eight monolignol subunits and has an average molecular weight of ca. 1200 g mol-1. The monolignols were mainly guaiacyl, syringyl and phenylcoumaran, randomly interconnected through β-O-4, 4-O-5, β-1, 5-5’ and β-β ether bonds. In situ IR spectroscopy was used to follow the changes in lignin constituents during reaction. The proposed reaction pathways for the catalytic transformation of this organosolv lignin to alkanes start with the hydrogenolysis of aryl alkyl ether bonds, followed by hydrogenation of the aromatic compounds on Ni to cyclic alcohols. Oxygen is removed from the alcohols via dehydration on Brønsted acid sites to yield cyclic alkenes that are further hydrogenated to alkanes. Formation of condensation products may occur via intermolecular recombination of aromatic monomers or alkylation of aromatic compounds by alkenes. The financial support from TUM-PNNL cooperation project “Development of new methods for in situ characterization in liquid phase reactions” (CN-177939) is highly appreciated. The work by S.K., H.S., and J.A.L was partially supported by the US Department of Energy, Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences.

  16. Carbon monoxide and carbon dioxide hydrogenation catalyzed by supported ruthenium carbonyl clusters: a novel procedure for encapsulating Ru3(Co)12 within the pores of Na-Y zeolite. Technical report No. 1, 1986-1987

    Energy Technology Data Exchange (ETDEWEB)

    Hastings, W.R.; Cameron, C.J.; Thomas, M.J.; Baird, M.C.

    1988-01-01

    Zeolite-supported ruthenium catalysts for the hydrogenation of carbon monoxide and carbon dioxide were prepared by sorbing Ru(CO)5 (molecular diameter 6.3 A) onto Na-Y zeolite and Linde 5A molecular sieve. Although the metal carbonyl is not absorbed into the pores of the molecular sieve (diameter 4.2 A), it is readily absorbed into the pores (diameter 7.4 A) and supercages (diameter 13 A) of the Na-Y zeolite. The Ru(CO)5 in Na-Y coverts in the absence of carbon monoxide to the much larger Ru3(CO)12 (diameter 9.2 A), which remains on the surface of the molecular sieve but is trapped within the supercages of the Na-Y zeolite because it cannot pass through the smaller pores. Slow, temperature-programmed heating of the Ru3(CO)12 in Na-Y to 350 C under a flow of hydrogen results in decarbonylation and formation of a CO hydrogenation catalyst that produces a very atypical (for ruthenium) hydrocarbon distribution truncated at about C10. The unusual product distribution presumably arises because the catalyst sites are situated within the zeolite supercages. Thus the metal is highly dispersed and or the growing hydrocarbon chains are subject to geometrical limitations on their growth. Consistent with this prothesis, ruthenium carbonyl clusters immobilized on the external surfaces of Na-Y zeolite, Linde 5A molecular sieve, and gamma alumina all exhibit typical, nonselective hydrocarbon-product distributions.

  17. {gamma} alumina- and HY zeolite-supported molybdenum catalysts: characterisation of the oxidic and sulfided phases; Catalyseurs a base de molybdene supporte sur alumine {gamma} et zeolithe HY: caracterisation des phases oxydes et sulfures

    Energy Technology Data Exchange (ETDEWEB)

    Plazenet, G.

    2001-10-01

    Oxidic precursors of hydro-treatment catalysts (Co)Mo/alumina or zeolite were characterised by Raman spectroscopy, NMR and EXAFS at the Mo and Co K-edges. The formation of an Anderson-type alumino-molybdate compound upon impregnation of the support with an ammonium hepta-molybdate solution was confirmed for alumina, and also observed for the HY zeolitic support, with consumption of the amorphous alumina of the zeolite. In absence of the latter, ammonium hepta-molybdate precipitates. The species are conserved upon drying; upon calcination, the alumino-molybdate evolves into a surface aluminium molybdate type phase, whereas the hepta-molybdate transforms into MoO{sub 3}. The species formed upon impregnation are located in the inter-granular porosity whereas MoO{sub 3} vapor-condensation leads to formation of dimers located inside the zeolitic structure. The study of the cobalt-promoted precursors showed that the evolution of the molybdenum is the same in the case of co-impregnation preparation. Impregnation with cobalt-molybdate prevents the formation of the alumino-molybdate anion and thus enables the preservation of the Mo-Co interaction but, whatever the precursor, the leveling effect of the calcination-re-hydration steps was demonstrated. An EXAFS study at different sulfur coverages of the MoS{sub 2} platelets in the alumina-supported sulfided catalysts showed the limitations of EXAFS for size determination of MoS{sub 2} crystallites, a parameter that can be reached by AWAXS, which also conveys information about sheet-stacking. The EXAFS study of sulfided (Co)Mo/HY systems revealed incomplete sulfidation of the samples and the very high dispersion of the active phase. The absence of an observable Mo-Co interaction whatever the preparation of the promoted catalysts is consistent with the absence of promoting effect in toluene hydrogenation. (author)

  18. Gallium Modified HUSY Zeolite as an Effective Co-support for NiMo Hydrodesulfurization Catalyst and the Catalyst's High Isomerization Selectivity.

    Science.gov (United States)

    Zhou, Wenwu; Zhou, Yasong; Wei, Qiang; Du, Lin; Ding, Sijia; Jiang, Shujiao; Zhang, Yanan; Zhang, Qing

    2017-07-12

    The effects of metal-modified acidic co-supports on the hydrodesulfurization (HDS) activity and isomerization selectivity of highly refractory organosulfur compounds such as 4,6-dimethyldibenzothiophene have been investigated. Y zeolite crystals with high Si/Al ratios and small crystallite sizes were successfully synthesized by a new hydrothermal synthesis approach. The synthesized Y zeolite crystals were ion-exchanged and stabilized. The prepared samples were then modified with different gallium contents using an impregnation method to adjust their acidity properties, and these modified samples were used as co-supports for NiMo sulfide HDS catalysts. The catalyst containing 10 wt.% zeolite Y modified by 2 wt.% gallium (NiMo/2GaY-ASA-A) exhibited the highest HDS activity, with 4,6-dimethyldibenzothiophene (4,6-DMDBT) conversion nearly double the rate of the catalyst without zeolite at 563 K, 4.0 MPa and liquid hourly space velocity (LHSV) of 40 h -1 . NiMo/2GaY-ASA-A also exhibited superior isomerization ability, with 3,4'-DMBP, 4,4'DMBP, and 3,6-DMDBT as the main products, indicating that the isomerization pathway was the main reaction route over NiMo/2GaY-ASA-A. The superior catalytic performance is related to the synergistic effect of the proper amount of medium and strong Brønsted acid sites. The compounds 3,6-DMDBT and 3,7-DMDBT (isomers of 4,6-DMDBT) and 3,4,6-TMDBT and tetra-methyl-DBT (transmethyl products) were detected simultaneously in the HDS product of 4,6-DMDBT for the first time over NiMo/GaY-ASA-A catalysts. Finally, a new reaction network over NiMo/2GaY-ASA-A was proposed. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  19. Tolerance

    DEFF Research Database (Denmark)

    Tønder, Lars

    Tolerance: A Sensorial Orientation to Politics is an experiment in re-orientation. The book is based on the wager that tolerance exceeds the more prevalent images of self-restraint and repressive benevolence because neither precludes the possibility of a more “active tolerance” motivated...... by the desire to experiment and to become otherwise. The objective is to discuss what gets lost, conceptually as well as politically, when we neglect the subsistence of active tolerance within other practices of tolerance, and to develop a theory of active tolerance in which tolerance's mobilizing character...... the current models of restraint and benevolence, other ways of understanding the politics of democratic pluralism might be developed, which will enable us to conceive of tolerance's future in terms different than those currently on offer. Tolerance: A Sensorial Orientation to Politics develops...

  20. Factors supporting cysteine tolerance and sulfite production in Candida albicans.

    Science.gov (United States)

    Hennicke, Florian; Grumbt, Maria; Lermann, Ulrich; Ueberschaar, Nico; Palige, Katja; Böttcher, Bettina; Jacobsen, Ilse D; Staib, Claudia; Morschhäuser, Joachim; Monod, Michel; Hube, Bernhard; Hertweck, Christian; Staib, Peter

    2013-04-01

    The amino acid cysteine has long been known to be toxic at elevated levels for bacteria, fungi, and humans. However, mechanisms of cysteine tolerance in microbes remain largely obscure. Here we show that the human pathogenic yeast Candida albicans excretes sulfite when confronted with increasing cysteine concentrations. Mutant construction and phenotypic analysis revealed that sulfite formation from cysteine in C. albicans relies on cysteine dioxygenase Cdg1, an enzyme with similar functions in humans. Environmental cysteine induced not only the expression of the CDG1 gene in C. albicans, but also the expression of SSU1, encoding a putative sulfite efflux pump. Accordingly, the deletion of SSU1 resulted in enhanced sensitivity of the fungal cells to both cysteine and sulfite. To study the regulation of sulfite/cysteine tolerance in more detail, we screened a C. albicans library of transcription factor mutants in the presence of sulfite. This approach and subsequent independent mutant analysis identified the zinc cluster transcription factor Zcf2 to govern sulfite/cysteine tolerance, as well as cysteine-inducible SSU1 and CDG1 gene expression. cdg1Δ and ssu1Δ mutants displayed reduced hypha formation in the presence of cysteine, indicating a possible role of the newly proposed mechanisms of cysteine tolerance and sulfite secretion in the pathogenicity of C. albicans. Moreover, cdg1Δ mutants induced delayed mortality in a mouse model of disseminated infection. Since sulfite is toxic and a potent reducing agent, its production by C. albicans suggests diverse roles during host adaptation and pathogenicity.

  1. Factors Supporting Cysteine Tolerance and Sulfite Production in Candida albicans

    OpenAIRE

    Hennicke, Florian; Grumbt, Maria; Lermann, Ulrich; Ueberschaar, Nico; Palige, Katja; Böttcher, Bettina; Jacobsen, Ilse D.; Staib, Claudia; Morschhäuser, Joachim; Monod, Michel; Hube, Bernhard; Hertweck, Christian; Staib, Peter

    2013-01-01

    The amino acid cysteine has long been known to be toxic at elevated levels for bacteria, fungi, and humans. However, mechanisms of cysteine tolerance in microbes remain largely obscure. Here we show that the human pathogenic yeast Candida albicans excretes sulfite when confronted with increasing cysteine concentrations. Mutant construction and phenotypic analysis revealed that sulfite formation from cysteine in C. albicans relies on cysteine dioxygenase Cdg1, an enzyme with similar functions ...

  2. Zeolitic materials with hierarchical porous structures.

    Science.gov (United States)

    Lopez-Orozco, Sofia; Inayat, Amer; Schwab, Andreas; Selvam, Thangaraj; Schwieger, Wilhelm

    2011-06-17

    During the past several years, different kinds of hierarchical structured zeolitic materials have been synthesized due to their highly attractive properties, such as superior mass/heat transfer characteristics, lower restriction of the diffusion of reactants in the mesopores, and low pressure drop. Our contribution provides general information regarding types and preparation methods of hierarchical zeolitic materials and their relative advantages and disadvantages. Thereafter, recent advances in the preparation and characterization of hierarchical zeolitic structures within the crystallites by post-synthetic treatment methods, such as dealumination or desilication; and structured devices by in situ and ex situ zeolite coatings on open-cellular ceramic foams as (non-reactive as well as reactive) supports are highlighted. Specific advantages of using hierarchical zeolitic catalysts/structures in selected catalytic reactions, such as benzene to phenol (BTOP) and methanol to olefins (MTO) are presented. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  3. Zeolite and swine inoculum effect on poultry manure biomethanation

    DEFF Research Database (Denmark)

    Kougias, Panagiotis; Fotidis, Ioannis; Zaganas, I.D.

    2013-01-01

    Poultry manure is an ammonia-rich substrate that inhibits methanogenesis, causing severe problems to the anaerobic digestion process. In this study, the effect of different natural zeolite concentrations on the mesophilic anaerobic digestion of poultry waste inoculated with well-digested swine...... manure was investigated. A significant increase in methane production was observed in treatments where zeolite was added, compared to the treatment without zeolite.Methane production in the treatment with 10 g dm-3 of natural zeolite was found to be 109.75% higher compared to the treatment without...... zeolite addition. The results appear to be influenced by the addition of zeolite, which reduces ammonia toxicity in anaerobic digestion and by the ammonia-tolerant swine inoculum....

  4. Theoretical investigation of layered zeolite frameworks: Surface properties of 2D zeolites

    Czech Academy of Sciences Publication Activity Database

    Hermann, Jan; Trachta, Michal; Nachtigall, P.; Bludský, Ota

    2014-01-01

    Roč. 227, May 15 (2014), s. 2-8 ISSN 0920-5861 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388963 Keywords : layered zeolite frameworks * surface properties * 2D zeolites Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.893, year: 2014

  5. Tolerance to uncertainty in the context of social support:gender specificity in the youth environment

    Directory of Open Access Journals (Sweden)

    Dmitry V. Lifintsev

    2017-06-01

    Full Text Available The paper presents the results of a study of social support for young males and females, and also its relationship with tolerance of uncertainty. A series of psychodiagnostic tools were used to study gender determinants of social support, tolerance of uncertainty and interpersonal intolerance in young people with different levels of emotional and instrumental support. Young males and females aged 18–22 years with a high level of tolerance of uncertainty are susceptible to various forms of social support. The ability to accept uncertainty, to function in the system of unclear interpersonal communication and to act in the face of changing circumstances determine the level of satisfaction with social support in the participants. The research (N=165 confirmed the assumption that first and foremost social support as a communicative phenomenon has differences in the perception of emotional forms in young males and females. Secondly, the specific features of person functioning in the social supporting act system are interrelated, including the level of tolerance of uncertainty. Thirdly, social support can reduce human state of uncertainty and eventually neutralize the negative impact of stressful events. The human ability to «see and discover» the social support, be sensitive and attentive to the supporting acts of social environment has a close relationship with the ability to accept uncertainty and maintain stability in a state of discomfort if any.

  6. Performance evaluation of an anaerobic fluidized bed reactor with natural zeolite as support material when treating high-strength distillery wastewater

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez, N. [Renewable Energy Technology Center (CETER), ' ' Jose Antonio Echeverria' ' Polytechnical University, Calle 127 s/n, CP 19390, Apdo. 6028, Habana 6 Marianao, Ciudad de La Habana (Cuba); Montalvo, S. [Department of Chemical Engineering, Santiago de Chile University, Ave. Lib. Bernardo O' Higgins 3363, Santiago de Chile (Chile); Borja, R.; Travieso, L.; Raposo, F. [Instituto de la Grasa (CSIC), Avenida Padre Garcia Tejero 4, 41012 Sevilla (Spain); Guerrero, L. [Department of Chemical, Biotechnological and Environmental Processes, Federico Santa Maria Technical University, Casilla 110-V, Valparaiso (Chile); Sanchez, E.; Colmenarejo, M.F. [Centro de Ciencias Medioambientales (CSIC), C/Serrano, 115-Duplicado, 28006 Madrid (Spain); Cortes, I. [Environment Nacional Center, Chile University, Ave. Larrain 9975, La Reina, Santiago de Chile (Chile)

    2008-11-15

    The performance of two laboratory-scale fluidized bed reactors with natural zeolite as support material when treating high-strength distillery wastewater was assessed. Two sets of experiments were carried out. In the first experimental set, the influences of the organic loading rate (OLR), the fluidization level (FL) and the particle diameter of the natural zeolite (D{sub P}) were evaluated. This experimental set was carried out at an OLR from 2 to 5 g COD (chemical oxygen demand)/l d, at FL 20% and 40% and with D{sub P} in the range of 0.2-0.5 mm (reactor 1) and of 0.5-0.8 mm (reactor 2). It was demonstrated that OLR and FL had a slight influence on COD removal, whereas they had a strong influence on the methane production rate. The COD removal was slightly higher for the highest particle diameter used. The second experimental set was carried out at an OLR from 3 to 20 g COD/l d with 25% of fluidization and D{sub P} in the above-mentioned ranges for reactors 1 and 2. The performance of the two reactors was similar; no significant differences were found. The COD removal efficiency correlated with the OLR based on a straight line. COD removal efficiencies higher than 80% were achieved in both reactors without significant differences. In addition, a straight line equation with a slope of 1.74 d{sup -1} and an intercept on the y-axis equal to zero described satisfactorily the effect of the influent COD on the COD removal rate. It was also observed that both COD removal rate and methane production (Q{sub M}) increased linearly with the OLR, independently of the D{sub P} used. (author)

  7. Nanoscale zero valent supported by Zeolite and Montmorillonite: Template effect of the removal of lead ion from an aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Arancibia-Miranda, Nicolás, E-mail: nicolas.arancibia@usach.cl [Facultad de Química y Biología, CEDENNA, Universidad de Santiago de Chile, USACH, Casilla 40, Santiago C.P. 33 (Chile); Baltazar, Samuel E. [Departamento de Física, CEDENNA, Universidad de Santiago de Chile, USACH, Av. Ecuador 3493, Santiago 9170124 (Chile); García, Alejandra [CIMAV, S.C. Alianza Norte 202, Carretera Monterrey-Aeropuerto Km 10, C.P. 66600, Apodaca Nuevo León (Mexico); University of Texas at San Antonio, Physics and Astronomy Department, One UTSA circle 78249, San Antonio, Texas (United States); Muñoz-Lira, Daniela [Facultad de Química y Biología, CEDENNA, Universidad de Santiago de Chile, USACH, Casilla 40, Santiago C.P. 33 (Chile); Facultad de Ciencias, Universidad de Chile, UCH, Las Palmeras 3425, Santiago 7800024 (Chile); Sepúlveda, Pamela; Rubio, María A. [Facultad de Química y Biología, CEDENNA, Universidad de Santiago de Chile, USACH, Casilla 40, Santiago C.P. 33 (Chile); Altbir, Dora [Departamento de Física, CEDENNA, Universidad de Santiago de Chile, USACH, Av. Ecuador 3493, Santiago 9170124 (Chile)

    2016-01-15

    Highlights: • The Z–nZVI and Mt–nZVI composites showed a high efficiency in the removal of Pb{sup 2+} present in aqueous solutions. • The fastest removal of Pb{sup 2+} was obtained with Mt–nZVI. • The adsorption intensity increased 300 times in the composites, respect to the pristine materials. • The magnetic behavior of the composites reveals a high presence of nZVI particles. • These composites have potential industrial and environmental applications. - Abstract: In this work, we have studied the Pb{sup 2+} sorption capacity of Zeolite (Z) and Montmorillonite (Mt) functionalized with nanoscale zero-valent iron (nZVI), at 50% w/w, obtained by means of an impregnating process with a solvent excess. The composites were characterized by several techniques including X-ray diffraction; scanning electron microscopy (SEM); BET area; isoelectric point (IEP); and, finally a magnetic response. Comparatively significant differences in terms of electrophoretic and magnetic characteristics were found between the pristine materials and the composites. Both structures show a high efficiency and velocity in the removal of Pb{sup 2+} up to 99.0% (200.0 ppm) after 40 min of reaction time. The removal kinetics of Pb{sup 2+} is adequately described by the pseudo second-order kinetic model, and the maximum adsorbed amounts (q{sub e}) of this analyte are in close accordance with the experimental results. The intraparticle diffusion model shows that this is not the only rate-limiting step, this being the Langmuir model which was well adjusted to our experimental data. Therefore, maximum sorption capacities were found to be 115.1 ± 11.0, 105.5 ± 9.0, 68.3 ± 1.3, 54.2 ± 1.3, and 50.3 ± 4.2 mg g{sup −1}, for Mt–nZVI, Z–nZVI, Zeolite, Mt, and nZVI, respectively. The higher sorption capacities can be attributed to the synergetic behavior between the clay and iron nanoparticles, as a consequence of the clay coating process with nZVI. These results suggest that both

  8. Comparative study of activated carbon, natural zeolite, and green sand supports for CuOX and ZnO sites as ozone decomposition catalyst

    Science.gov (United States)

    Azhariyah, A. S.; Pradyasti, A.; Dianty, A. G.; Bismo, S.

    2018-03-01

    This research was based on ozone decomposition in industrial environment. Ozone is harmful to human. Therefore, catalysts were made as a mask filter to decompose ozone. Comparison studies of catalyst supports were done using Granular Activated Carbon (GAC), Natural Zeolite (NZ), and Green Sand (GS). GAC showed the highest catalytic activity compared to other supports with conversion of 98%. Meanwhile, the conversion using NZ was only 77% and GS had been just 27%. GAC had the highest catalytic activity because it had the largest pore volume, which is 0.478 cm3/g. So GAC was used as catalyst supports. To have a higher conversion in ozone decomposition, GAC was impregnated with metal oxide as the active site of the catalyst. Active site comparison was made using CuOX and ZnO as the active site. Morphology, composition, and crystal phase were analyzed using SEM-EDX, XRF, and XRD methods. Mask filter, which contained catalysts for ozone decomposition, was tested using a fixed bed reactor at room temperature and atmospheric pressure. The result of conversion was analyzed using iodometric method. CuOX/GAC and ZnO/GAC 2%-w showed the highest catalytic activity and conversion reached 100%. From the durability test, CuOX/GAC 2%-w was better than ZnO/GAC 2%-w because the conversion of ozone to oxygen reached 100% with the lowest conversion was 70% for over eight hours.

  9. Wireless Avionics Packet to Support Fault Tolerance for Flight Applications

    Science.gov (United States)

    Block, Gary L.; Whitaker, William D.; Dillon, James W.; Lux, James P.; Ahmad, Mohammad

    2009-01-01

    In this protocol and packet format, data traffic is monitored by all network interfaces to determine the health of transmitter and subsystems. When failures are detected, the network inter face applies its recover y policies to provide continued service despite the presence of faults. The protocol, packet format, and inter face are independent of the data link technology used. The current demonstration system supports both commercial off-the-shelf wireless connections and wired Ethernet connections. Other technologies such as 1553 or serial data links can be used for the network backbone. The Wireless Avionics packet is divided into three parts: a header, a data payload, and a checksum. The header has the following components: magic number, version, quality of service, time to live, sending transceiver, function code, payload length, source Application Data Interface (ADI) address, destination ADI address, sending node address, target node address, and a sequence number. The magic number is used to identify WAV packets, and allows the packet format to be updated in the future. The quality of service field allows routing decisions to be made based on this value and can be used to route critical management data over a dedicated channel. The time to live value is used to discard misrouted packets while the source transceiver is updated at each hop. This information is used to monitor the health of each transceiver in the network. To identify the packet type, the function code is used. Besides having a regular data packet, the system supports diagnostic packets for fault detection and isolation. The payload length specifies the number of data bytes in the payload, and this supports variable-length packets in the network. The source ADI is the address of the originating interface. This can be used by the destination application to identify the originating source of the packet where the address consists of a subnet, subsystem class within the subnet, a subsystem unit

  10. Towards fault-tolerant decision support systems for ship operator guidance

    DEFF Research Database (Denmark)

    Nielsen, Ulrik Dam; Lajic, Zoran; Jensen, Jørgen Juncher

    2012-01-01

    Fault detection and isolation are very important elements in the design of fault-tolerant decision support systems for ship operator guidance. This study outlines remedies that can be applied for fault diagnosis, when the ship responses are assumed to be linear in the wave excitation. A novel num...

  11. Influence of Levulinic Acid Hydrogenation on Aluminum Coordination in Zeolite-Supported Ruthenium Catalysts: A 27Al 3QMAS Nuclear Magnetic Resonance Study.

    Science.gov (United States)

    Luo, Wenhao; van Eck, Ernst R H; Bruijnincx, Pieter C A; Weckhuysen, Bert M

    2018-02-19

    The influence of a highly oxygenated, polar protic reaction medium, that is, levulinic acid in 2-ethylhexanoic acid, on the dealumination of two zeolite-supported ruthenium catalysts, namely Ru/H-β and Ru/H-ZSM-5, has been investigated by 27 Al triple-quantum magic-angle spinning nuclear magnetic resonance spectroscopy (3QMAS NMR). Upon use of these catalysts in the hydrogenation of levulinic acid, the heterogeneity in aluminum speciation is found to increase for both Ru/H-ZSM-5 and Ru/H-β. For Ru/H-ZSM-5, the symmetric, tetrahedral framework aluminum species (FAL) were found to be mainly converted into distorted tetrahedral FAL species, with limited loss of aluminum to the solution by leaching. A severe loss of both FAL and extra-framework aluminum (EFAL) species into the liquid phase was observed for Ru/H-β instead. The large decrease in tetrahedral FAL species, in particular, results in a significant decrease in strong acid sites, as corroborated by Fourier transform infrared spectroscopy (FT-IR). This decrease in acidity, evidence of the inferior stability of the strongly acidic sites in Ru/H-β relative to Ru/H-ZSM-5 under the applied conditions, is considered as the main reason for differences seen in catalyst performance. ©2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.

  12. Separation of BSA through FAU-type zeolite ceramic composite membrane formed on tubular ceramic support: Optimization of process parameters by hybrid response surface methodology and biobjective genetic algorithm.

    Science.gov (United States)

    Vinoth Kumar, R; Ganesh Moorthy, I; Pugazhenthi, G

    2017-08-09

    In this study, Faujasite (FAU) zeolite was coated on low-cost tubular ceramic support as a separating layer through hydrothermal route. The mixture of silicate and aluminate solutions was used to create a zeolitic separation layer on the support. The prepared zeolite ceramic composite membrane was characterized using X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), particle size distribution (PSD), field emission scanning electron microscopy (FESEM), and zeta potential measurements. The porosity of ceramic support (53%) was reduced by the deposition of FAU (43%) zeolite layer. The pore size and water permeability of the membrane were evaluated as 0.179 µm and 1.62 × 10 -7  m 3 /m 2  s kPa, respectively, which are lower than that of the support (pore size of 0.309 µm and water permeability of 5.93 × 10 -7  m 3 /m 2  s kPa). The permeate flux and rejection potential of the prepared membrane were evaluated by microfiltration of bovine serum albumin (BSA). To study the influences of three independent variables such as operating pressure (68.94-275.79 kPa), concentration of BSA (100-500 ppm), and solution pH (2-4) on permeate flux and percentage of rejection, the response surface methodology (RSM) was used. The predicted models for permeate flux and rejection were further subjected to biobjective genetic algorithm (GA). The hybrid RSM-GA approach resulted in a maximum permeate flux of 2.66 × 10 -5  m 3 /m 2  s and BSA rejection of 88.02%, at which the optimum conditions were attained as 100 ppm BSA concentration, 2 pH solution, and 275.79 kPa applied pressure. In addition, the separation efficiency was compared with other membranes applied for BSA separation to know the potential of the fabricated FAU zeolite ceramic composite membrane.

  13. Deuterium exchange with the surface hydrogen of zeolite catalysts. 7. Nickel-containing zeolites

    International Nuclear Information System (INIS)

    Minachev, Kh.M.; Dmitriev, R.V.; Penchev, V.; Kanazirev, V.; Minchev, Kh.; Kasimov, Ch.K.

    1982-01-01

    An in-depth study of heteromolecular isotopic hydrogen exchange (HIHE) in Ni zeolites was undertaken with a view to measuring surface OH group concentrations and determining effectiveness of Ni, on the one hand, and Pd and Pt, on the other, in promoting chemical reactions. Here the degree of metal dispersion in the Ni zeolite was characterized through H 2 chemisorption and thermosorption data. A study was made of the action of these zeolites in catalyzing the disproportionation of toluene. The data obtained here have given an understanding of the effect of the metal, the OH-group concentration, and the mutual arrangement of OH groups and Ni atoms on catalyzed toluene reactions. Results indicated that HIHE occurs on reduced nickel-containing zeolite catalysts at temperatures in excess of 100 0 C, and is limited by the rate of transport of activated hydrogen from the metal particles on the support surface. High-temperature oxidation-reduction of the nickel-containing zeolite-leads to the formation of coarse nickel crystals on the external zeolite crystal faces. Also, the reduced NiCaNaY zeolites show high catalytic activity in the toluene disproportionation only when the nickel has been introduced through ion exchange. Both isotopic exchange and toluene disproportionation are promoted when the nickel particles and OH groups are in close proximity

  14. Catalysis with hierarchical zeolites

    DEFF Research Database (Denmark)

    Holm, Martin Spangsberg; Taarning, Esben; Egeblad, Kresten

    2011-01-01

    zeolites that have been reported hitherto. Prototypical examples from some of the different categories of catalytic reactions that have been studied using hierarchical zeolite catalysts are highlighted. This clearly illustrates the different ways that improved performance can be achieved with this family...

  15. Wild Vervet Monkeys Trade Tolerance and Specific Coalitionary Support for Grooming in Experimentally Induced Conflicts.

    Science.gov (United States)

    Borgeaud, Christèle; Bshary, Redouan

    2015-11-16

    Grooming is a key social behavior in many primate species. Research has focused on three important aspects: the short- and long-term trading patterns of grooming for itself and/or for other commodities like tolerance or coalitionary support, the issue of whether exchanges are a convincing example for reciprocity, and what decision rules underlie trading. These issues remain largely unresolved due to the correlative nature of observational studies and the rarity of experimental studies. Here, we present a new experimental paradigm to address these questions in wild vervet monkeys (Chlorocebus pygerythrus). Adult females were first trained to approach a personal box, identifiable by unique color patterns, to access high-quality food. During the experiments, two boxes were placed next to each other to induce conflict through forced proximity. We found that while dominants were generally more tolerant toward bonded individuals, recent grooming increased tolerance independently of relationship quality. The latter result shows that vervet monkeys traded grooming for short-term tolerance, where dominants used a direct-reciprocity decision rule. In contrast, females invariably supported the higher-ranking opponent in a conflict, independently of who was the recent grooming partner. Nevertheless, recent grooming increased the probability that a female supported the partner during conflicts with a low-ranking third party. Thus, females' decisions about coalitionary support seem to integrate information about the current social hierarchy with recent grooming events. In conclusion, decision rules underlying trading of grooming for other commodities involve a variety of timescales and factors. Copyright © 2015 Elsevier Ltd. All rights reserved.

  16. Preparation of Zeolitic Imidazolate Framework-8 (ZIF-8) Membrane on Porous Polymeric Support via Contra-Diffusion Method

    KAUST Repository

    Tan, Xiaoyu

    2016-05-18

    In the last decade, many attempts were made to put metal organic frameworks (MOFs) in industrial applications, but most of these efforts weren’t successfully. As one of the few MOFs produced on industrial scale, ZIF-8 has interesting pore size, huge internal surface area and great thermal and chemical stability. Therefore, ZIF-8 might become the first MOF, which will be applied in industrial separation processes. In this thesis, a synthesis study is presented, which leads to a cheap and convenient way to
fabricate defect-free and thin ZIF-8 membranes on porous polymeric supports showing high selectivity and high gas permeance. The ZIF-8 layers were produced via a contra-diffusion method. Several polymeric membranes were employed as support in this study, such as PAN, PEI, PSU, PA and PTSC. We studied the influence of the polymeric support properties for the ZIF-8 membrane preparation and optimized the ZIF-8 preparation conditions. The ZIF-8 membranes were characterized via scanning electron microscopy (SEM) and X-ray diffraction (XRD). For gas permeation test, we chose a Wicke-Kallenbach apparatus to measure membrane’s gas permeance and selectivity. One of the best ZIF-8 membranes exhibited a hydrogen permeance of 3.45 × 10-8 mol m-2 s-1 Pa-1 and
an ideal selectivity of hydrogen over propane of about 500.

  17. Supported zirconium sulfate on carbon nanotubes as water-tolerant solid acid catalyst

    International Nuclear Information System (INIS)

    Juan, Joon Ching; Jiang Yajie; Meng Xiujuan; Cao Weiliang; Yarmo, Mohd Ambar; Zhang Jingchang

    2007-01-01

    A new solid acid of zirconium sulfate (CZ) was successfully supported on carbon nanotube (CNT) for esterification reaction. Preparation conditions of the supported CZ have been investigated, to obtain highest catalytic activity for esterification reaction. XRD, TEM, BET, X-ray photoelectron spectra (XPS) and in situ FTIR analysis has also been carried out to understand the characteristics of the catalyst. In the esterification of acrylic acid with n-octanol, the supported CZ exhibited high catalytic activity and stability. The catalytic activity was nearly unchanged during four times of reuse. XRD and TEM analysis indicated that CZ was finely dispersed on CNT. XPS analysis shows that the CZ species was preserved and the chemical environment of the CZ has changed after loaded on CNT. This finding show that CNT as CZ support is an efficient water-tolerant solid acid

  18. Flexibility of zeolite frameworks

    Science.gov (United States)

    Kapko, Vitaliy; Treacy, Michael; Thorpe, Michael

    2009-03-01

    Zeolites are an important class of industrial catalysts because of their large internal surfaces and molecular-sieving properties. Recent geometric simulations (1) show that almost all of the known zeolites can exist without distortion of their tetrahedra within some range of densities, which we call the flexibility window. Within this window, the framework accommodates density changes by rotations about the shared tetrahedral corners. We argue that the presence of a flexibility window can be used as a topological criterion to select potential candidates for synthesis from millions of hypothetical structures. We also investigate the exceptions to the rule, as well as the shape of the flexibility window and the symmetric properties of zeolites inside it. (1) A. Sartbaeva, S.A. Wells, M.M.J. Treacy and M.F. Thorpe The flexibility window in zeolites, Nature Materials 5, 962-965 (2006); I. Rivin, commentary 931-932.

  19. Use of Natural Zeolite to Upgrade Activated Sludge Process

    Directory of Open Access Journals (Sweden)

    Hanife Büyükgüngör

    2003-01-01

    Full Text Available The objective of this study was to achieve better efficiency of phosphorus removal in an enhanced biological phosphorus removal process by upgrading the system with different amounts of natural zeolite addition. The system performance for synthetic wastewater containing different carbon sources applied at different initial concentrations of phosphorus, as well as for municipal wastewater, was investigated. Natural zeolite addition in the aerobic phase of the anaerobic/aerobic bioaugmented activated sludge system contributed to a significant improvement of phosphorus removal in systems with synthetic wastewater and fresh municipal wastewater. Improvement of phosphorus removal with regard to the control reactors was higher with the addition of 15 than with 5 g/L of natural zeolite. In reactors with natural zeolite addition with regard to the control reactors significantly decreased chemical oxygen demand, ammonium and nitrate, while higher increment and better-activated sludge settling were achieved, without changes in the pH-values of the medium. It was shown that the natural zeolite particles are suitable support material for the phosphate-accumulating bacteria Acinetobacter calcoaceticus (DSM 1532, which were adsorbed on the particle surface, resulting in increased biological activity of the system. The process of phosphorus removal in a system with bioaugmented activated sludge and natural zeolite addition consisted of: metabolic activity of activated sludge, phosphorus uptake by phosphate-accumulating bacteria adsorbed on the natural zeolite particles and suspended in solution, and phosphorus adsorption on the natural zeolite particles.

  20. UTL zeolite and the way beyond

    Czech Academy of Sciences Publication Activity Database

    Shvets, O. V.; Nachtigall, P.; Roth, Wieslaw Jerzy; Čejka, Jiří

    2013-01-01

    Roč. 182, DEC 2013 (2013), s. 229-238 ISSN 1387-1811 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : zeolite UTL * synthesis * hydrolysis Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.209, year: 2013

  1. Dispersion enhanced metal/zeolite catalysts

    Science.gov (United States)

    Sachtler, Wolfgang M. H.; Tzou, Ming-Shin; Jiang, Hui-Jong

    1987-01-01

    Dispersion stabilized zeolite supported metal catalysts are provided as bimetallic catalyst combinations. The catalyst metal is in a reduced zero valent form while the dispersion stabilizer metal is in an unreduced ionic form. Representative catalysts are prepared from platinum or nickel as the catalyst metal and iron or chromium dispersion stabilizer.

  2. Functional diversity supports the physiological tolerance hypothesis for plant species richness along climatic gradients

    Science.gov (United States)

    Spasojevic, Marko J.; Grace, James B.; Harrison, Susan; Damschen, Ellen Ingman

    2013-01-01

    1. The physiological tolerance hypothesis proposes that plant species richness is highest in warm and/or wet climates because a wider range of functional strategies can persist under such conditions. Functional diversity metrics, combined with statistical modeling, offer new ways to test whether diversity-environment relationships are consistent with this hypothesis. 2. In a classic study by R. H. Whittaker (1960), herb species richness declined from mesic (cool, moist, northerly) slopes to xeric (hot, dry, southerly) slopes. Building on this dataset, we measured four plant functional traits (plant height, specific leaf area, leaf water content and foliar C:N) and used them to calculate three functional diversity metrics (functional richness, evenness, and dispersion). We then used a structural equation model to ask if ‘functional diversity’ (modeled as the joint responses of richness, evenness, and dispersion) could explain the observed relationship of topographic climate gradients to species richness. We then repeated our model examining the functional diversity of each of the four traits individually. 3. Consistent with the physiological tolerance hypothesis, we found that functional diversity was higher in more favorable climatic conditions (mesic slopes), and that multivariate functional diversity mediated the relationship of the topographic climate gradient to plant species richness. We found similar patterns for models focusing on individual trait functional diversity of leaf water content and foliar C:N. 4. Synthesis. Our results provide trait-based support for the physiological tolerance hypothesis, suggesting that benign climates support more species because they allow for a wider range of functional strategies.

  3. Preparation of functionalized zeolitic frameworks

    Science.gov (United States)

    Yaghi, Omar M; Hayashi, Hideki; Banerjee, Rahul; Park, Kyo Sung; Wang, Bo; Cote, Adrien P

    2012-11-20

    The disclosure provides zeolitic frameworks for gas separation, gas storage, catalysis and sensors. More particularly the disclosure provides zeolitic frameworks (ZIFs). The ZIF of the disclosure comprises any number of transition metals or a homogenous transition metal composition.

  4. Preparation of functionalized zeolitic frameworks

    Science.gov (United States)

    Yaghi, Omar M; Furukawa, Hiroyasu; Wang, Bo

    2013-07-09

    The disclosure provides zeolitic frameworks for gas separation, gas storage, catalysis and sensors. More particularly the disclosure provides zeolitic frameworks (ZIFs). The ZIF of the disclosure comprises any number of transition metals or a homogenous transition metal composition.

  5. Rapid synthesis of beta zeolites

    Science.gov (United States)

    Fan, Wei; Chang, Chun -Chih; Dornath, Paul; Wang, Zhuopeng

    2015-08-18

    The invention provides methods for rapidly synthesizing heteroatom containing zeolites including Sn-Beta, Si-Beta, Ti-Beta, Zr-Beta and Fe-Beta. The methods for synthesizing heteroatom zeolites include using well-crystalline zeolite crystals as seeds and using a fluoride-free, caustic medium in a seeded dry-gel conversion method. The Beta zeolite catalysts made by the methods of the invention catalyze both isomerization and dehydration reactions.

  6. The support for smoke free policy and how it is influenced by tolerance to smoking - experience of a developing country.

    Science.gov (United States)

    Rashid, Abdul; Manan, Azizah Ab; Yahya, Noorlia; Ibrahim, Lailanor

    2014-01-01

    This cross sectional survey was conducted to determine the support in making Penang UNESCO World Heritage Site (GTWHS) smoke free and to determine the influence of tolerance towards smoking on this support. This is the first phase in making Penang, Malaysia a smoke free state. A multistage sampling process was done to select a sample of respondents to represent the population of GTWHS. Attitude towards smoking was assessed using tolerance as a proxy. A total of 3,268 members of the community participated in the survey. A big majority (n = 2969; 90.9%) of the respondents supported the initiative. Support was lowest among the owners and residents/tenants, higher age groups, the Chinese, men, respondents who had poor knowledge of the places gazetted as smoke free, and respondents with poor knowledge of the health effects on smokers and on passive smokers. The odds (both adjusted and unadjusted) of not supporting the initiative was high among those tolerant to smoking in public areas. Tolerance towards smoking was associated with 80.3% risk of non-support in the respondents who were tolerant to smoking and a 57.2% risk in the population. Health promotion and education concerning the harm of tobacco smoke in Malaysia, which has mainly targeted smokers, must change. Health education concerning the risks of second hand smoke must also be given to non-smokers and efforts should be made to denormalize smoking.

  7. The support for smoke free policy and how it is influenced by tolerance to smoking - experience of a developing country.

    Directory of Open Access Journals (Sweden)

    Abdul Rashid

    Full Text Available This cross sectional survey was conducted to determine the support in making Penang UNESCO World Heritage Site (GTWHS smoke free and to determine the influence of tolerance towards smoking on this support. This is the first phase in making Penang, Malaysia a smoke free state. A multistage sampling process was done to select a sample of respondents to represent the population of GTWHS. Attitude towards smoking was assessed using tolerance as a proxy. A total of 3,268 members of the community participated in the survey. A big majority (n = 2969; 90.9% of the respondents supported the initiative. Support was lowest among the owners and residents/tenants, higher age groups, the Chinese, men, respondents who had poor knowledge of the places gazetted as smoke free, and respondents with poor knowledge of the health effects on smokers and on passive smokers. The odds (both adjusted and unadjusted of not supporting the initiative was high among those tolerant to smoking in public areas. Tolerance towards smoking was associated with 80.3% risk of non-support in the respondents who were tolerant to smoking and a 57.2% risk in the population. Health promotion and education concerning the harm of tobacco smoke in Malaysia, which has mainly targeted smokers, must change. Health education concerning the risks of second hand smoke must also be given to non-smokers and efforts should be made to denormalize smoking.

  8. Performance Factors and Sulfur Tolerance of Metal Supported Solid Oxide Fuel Cells with Nanostructured Ni:GDC Infiltrated Anodes

    DEFF Research Database (Denmark)

    Nielsen, Jimmi; Sudireddy, Bhaskar Reddy; Hagen, Anke

    2016-01-01

    Two metal supported solid oxide fuel cells (active area 16 cm2) with nanostructured Ni:GDC infiltrated anodes, possessing different anode and support microstructures were studied in respect to sulfur tolerance at an operating temperature of 650°C. The studied MS-SOFCs are based on ferretic...

  9. Performance Factors and Sulfur Tolerance of Metal Supported Solid Oxide Fuel Cells with Nanostructured Ni:GDC Infiltrated Anodes

    DEFF Research Database (Denmark)

    Nielsen, Jimmi; Sudireddy, Bhaskar Reddy; Hagen, Anke

    2015-01-01

    Two metal supported solid oxide fuel cells (active area 16 cm2) with nanostructured Ni:GDC infiltrated anodes, but different anode and support microstructures were studied in respect to sulfur tolerance at the aimed operating temperature of 650ºC. The studied MS-SOFCs are based on ferretic...

  10. Protection of Proprietary Data Rights for Data Used to Support Tolerance Exemptions for Inert Ingredients

    Science.gov (United States)

    The FFDCA provides both exclusive use and data compensation protections for data that inert ingredient manufacturers submit to EPA to establish or maintain tolerances or tolerance exemptions for these ingredients. Find information about these protections.

  11. Distribution of metal and adsorbed guest species in zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Chmelka, B.F.

    1989-12-01

    Because of their high internal surface areas and molecular-size cavity dimensions, zeolites are used widely as catalysts, shape- selective supports, or adsorbents in a variety of important chemical processes. For metal-catalyzed reactions, active metal species must be dispersed to sites within the zeolite pores that are accessible to diffusing reactant molecules. The distribution of the metal, together with transport and adsorption of reactant molecules in zeolite powders, are crucial to ultimate catalyst performance. The nature of the metal or adsorbed guest distribution is known, however, to be dramatically dependent upon preparatory conditions. Our objective is to understand, at the molecular level, how preparatory treatments influence the distribution of guest species in zeolites, in order that macroscopic adsorption and reaction properties of these materials may be better understood. The sensitivity of xenon to its adsorption environment makes {sup 129}Xe NMR spectroscopy an important diagnostic probe of metal clustering and adsorbate distribution processes in zeolites. The utility of {sup 129}Xe NMR depends on the mobility of the xenon atoms within the zeolite-guest system, together with the length scale of the sample heterogeneity being studied. In large pore zeolites containing dispersed guest species, such as Pt--NaY, {sup 129}Xe NMR is insensitive to fine structural details at room temperature.

  12. Positron annihilation in modified zeolites LTA and 13X

    Energy Technology Data Exchange (ETDEWEB)

    Cabral-Prieto, A.; Garcia-Sosa, I.; Jimenez-Becerril, J. [Departamento de Quimica, Instituto Nacional de Investigaciones Nucleares, Apartado Postal 18-1027, Col. Escandon, Del. M. Hidalgo, Mexico D. F., c. p. 11801 (Mexico); Lopez-Castanares, R.; Olea-Cardoso, O. [Facultad de Quimica, Universidad Autonoma del Estado de Mexico, Paseo Tollocan esquina paseo Tollocan, esquina paseo Colon, Toluca, c. p. 50120, Estado de Mexico (Mexico)

    2007-07-01

    The pick-off annihilation lifetimes of o -Ps, {tau}{sub po}, in dehydrated Co{sup 2+} and Mn{sup 2+} exchanged zeolites LTA, in dehydrated Co{sup 2+} exchanged zeolite 13X, and in dehydrated Na{sup +} zeolites LTA and 13X, are estimated. Although {tau}{sub po} can be estimated from the lifetime spectra of the cation exchanged zeolites LTA and 13X, this lifetime can not be estimated from those spectra of Na{sup +} zeolite LTA unambiguously. The estimated pick-off lifetimes due to the annihilation of o-Ps in the internal walls of the zeolites are systematically lower than the average lifetime of p-Ps and o-Ps in vacuum {tau}{sub a}=0.5 ns. Since the pick-off process of o-Ps occurs particularly on the internal cavity walls of dehydrated zeolites, the replacement of {tau}{sub a} by {tau}{sub po} within the classical model of Tao-Eldrup to calculate cavity radius should provide more realistic cavity radii of these porous materials than when using {l_brace}{tau}{sub a}{r_brace}. This suggestion is supported by previous and present results. (copyright 2007 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  13. Distribution of metal and adsorbed guest species in zeolites

    International Nuclear Information System (INIS)

    Chmelka, B.F.

    1989-12-01

    Because of their high internal surface areas and molecular-size cavity dimensions, zeolites are used widely as catalysts, shape- selective supports, or adsorbents in a variety of important chemical processes. For metal-catalyzed reactions, active metal species must be dispersed to sites within the zeolite pores that are accessible to diffusing reactant molecules. The distribution of the metal, together with transport and adsorption of reactant molecules in zeolite powders, are crucial to ultimate catalyst performance. The nature of the metal or adsorbed guest distribution is known, however, to be dramatically dependent upon preparatory conditions. Our objective is to understand, at the molecular level, how preparatory treatments influence the distribution of guest species in zeolites, in order that macroscopic adsorption and reaction properties of these materials may be better understood. The sensitivity of xenon to its adsorption environment makes 129 Xe NMR spectroscopy an important diagnostic probe of metal clustering and adsorbate distribution processes in zeolites. The utility of 129 Xe NMR depends on the mobility of the xenon atoms within the zeolite-guest system, together with the length scale of the sample heterogeneity being studied. In large pore zeolites containing dispersed guest species, such as Pt--NaY, 129 Xe NMR is insensitive to fine structural details at room temperature

  14. One-Pot Process for Hydrodeoxygenation of Lignin to Alkanes Using Ru-Based Bimetallic and Bifunctional Catalysts Supported on Zeolite Y

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Hongliang [Department of Biological Systems Engineering, Washington State University, Richland WA 99354 USA; Ruan, Hao [Department of Biological Systems Engineering, Washington State University, Richland WA 99354 USA; Feng, Maoqi [Chemistry & Chemical Engineering Division, Southwest Research Institute, San Antonio TX 78238 USA; Qin, Yuling [Department of Biological Systems Engineering, Washington State University, Richland WA 99354 USA; Job, Heather [Pacific Northwest National Laboratory, 902 Battelle Blvd Richland WA 99354 USA; Luo, Langli [Environmental Molecular Sciences Laboratory, 3335 Q Ave Richland WA 99354 USA; Wang, Chongmin [Environmental Molecular Sciences Laboratory, 3335 Q Ave Richland WA 99354 USA; Engelhard, Mark H. [Environmental Molecular Sciences Laboratory, 3335 Q Ave Richland WA 99354 USA; Kuhn, Erik [National Bioenergy Center, National Renewable Energy Laboratory, 15013 Denver West Parkway Golden CO. 80401 USA; Chen, Xiaowen [National Bioenergy Center, National Renewable Energy Laboratory, 15013 Denver West Parkway Golden CO. 80401 USA; Tucker, Melvin P. [National Bioenergy Center, National Renewable Energy Laboratory, 15013 Denver West Parkway Golden CO. 80401 USA; Yang, Bin [Department of Biological Systems Engineering, Washington State University, Richland WA 99354 USA

    2017-03-16

    The synthesis of high-efficiency and low-cost multifunctional catalysts for hydrodeoxygenation (HDO) of waste lignin into advanced biofuels is crucial for enhancing current biorefinery processes. Inexpensive transition metals, including Fe, Ni, Cu, Zn, were severally co-loaded with Ru on HY zeolite to form bimetallic and bifunctional catalysts. These catalysts were subsequently tested for HDO conversion of softwood lignin and several lignin model compounds. Results indicated that the inexpensive earth abundant metals could modulate the hydrogenolysis activity of Ru and decrease the yield of low molecular weight gaseous side-products. Among all the prepared catalysts, Ru-Cu/HY showed the best HDO performance, giving the highest selectivity to hydrocarbon products. The improved catalytic performance of Ru-Cu/HY was probably due to the following three factors: (1) high total and strong acid sites, (2) good dispersion of metal species and limited segregation, (3) high adsorption capacity for polar fractions, including hydroxyl groups and ether bonds. Moreover, all the bifunctional catalysts were proven to be superior over the combination catalysts of Ru/Al2O3 and HY zeolite, and this could be attributed to the “intimacy criterion”. The practical use of the designed catalysts would be promising in lignin valorization.

  15. One-Pot Process for Hydrodeoxygenation of Lignin to Alkanes Using Ru-Based Bimetallic and Bifunctional Catalysts Supported on Zeolite Y.

    Science.gov (United States)

    Wang, Hongliang; Ruan, Hao; Feng, Maoqi; Qin, Yuling; Job, Heather; Luo, Langli; Wang, Chongmin; Engelhard, Mark H; Kuhn, Erik; Chen, Xiaowen; Tucker, Melvin P; Yang, Bin

    2017-04-22

    The synthesis of high-efficiency and low-cost catalysts for hydrodeoxygenation (HDO) of waste lignin to advanced biofuels is crucial for enhancing current biorefinery processes. Inexpensive transition metals, including Fe, Ni, Cu, and Zn, were severally co-loaded with Ru on HY zeolite to form bimetallic and bifunctional catalysts. These catalysts were subsequently tested for HDO conversion of softwood lignin and several lignin model compounds. Results indicated that the inexpensive earth-abundant metals could modulate the hydrogenolysis activity of Ru and decrease the yield of low-molecular-weight gaseous products. Among these catalysts, Ru-Cu/HY showed the best HDO performance, affording the highest selectivity to hydrocarbon products. The improved catalytic performance of Ru-Cu/HY was probably a result of the following three factors: (1) high total and strong acid sites, (2) good dispersion of metal species and limited segregation, and (3) high adsorption capacity for polar fractions, including hydroxyl groups and ether bonds. Moreover, all bifunctional catalysts proved to be superior over the combination catalysts of Ru/Al 2 O 3 and HY zeolite. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. Removal of Cr(VI) from aqueous solutions by a bacterial biofilm supported on zeolite: optimisation of the operational conditions and Scale-Up of the bioreactor

    Energy Technology Data Exchange (ETDEWEB)

    Pazos, M. [IBB - Instituto de Biotecnologia e Bioengenharia, Centro de Engenharia Biologica, Universidade do Minho, Braga (Portugal); Departamento de Ingenieria Quimica, Universidade de Vigo, Vigo (Spain); Branco, M.; Tavares, T. [IBB - Instituto de Biotecnologia e Bioengenharia, Centro de Engenharia Biologica, Universidade do Minho, Braga (Portugal); Neves, I.C. [Departamento de Quimica, Centro de Quimica, Universidade do Minho, Braga (Portugal); Sanroman, M.A. [Departamento de Ingenieria Quimica, Universidade de Vigo, Vigo (Spain)

    2010-12-15

    The aim of this study was to investigate the feasibility of a bioreactor system and its scale-up to remove Cr(VI) from solution. The bioreactor is based on an innovative process that combines bioreduction of Cr(VI) to Cr(III) by the bacterium Arthrobacter viscosus and Cr(III) sorption by a specific zeolite. Batch studies were conducted in a laboratory-scale bioreactor, taking into account different operating conditions. Several variables, such as biomass concentration, pH and zeolite pre-treatment, were evaluated to increase removal efficiency. The obtained results suggest that the Cr removal efficiency is improved when the initial biomass concentration is approximately 5 g L{sup -1} and the pH in the system is maintained at an acidic level. Under the optimised conditions, approximately 100 % of the Cr(VI) was removed. The scale-up of the developed biofilm process operating under the optimised conditions was satisfactorily tested in a 150-L bioreactor. (Copyright copyright 2010 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  17. Hierarchical zeolites: progress on synthesis and characterization of mesoporous zeolite single crystal catalysts

    DEFF Research Database (Denmark)

    Kustova, Marina; Egeblad, Kresten; Christensen, Claus H.

    2007-01-01

    in a hierarchical pore size distribution. In this work, the preparation of mesoporous ZSM-12 single crystal catalysts using a new improved procedure for directly introducing carbon in the reaction mixture is reported. The microwave heating technique is also applied for the synthesis of mesoporous silicalite-1...... measurements. Additionally, the results of diffusion of n-hexadecane in conventional and mesoporous zeolites are presented. Isomerization and cracking of n-hexadecane was chosen as model test reaction for these materials. All results support that mesoporous zeolites are superior catalysts due to improved mass...

  18. Isobutane/2-butene alkylation with zeolite Y without BrÆnsted acidity

    OpenAIRE

    Rosenbach Jr,Nilton; Mota,Claudio J. A.

    2005-01-01

    Alkylation of isobutane with 2-butene was performed on metal-exchanged Y zeolites, using an alkylchloride as carbocation initiator. The results indicated that, compared with a protonic zeolite, the deactivation was significantly slower and the production of trimethylpentanes was higher on the metal-exchanged zeolites. The metal cations act as Lewis acids, interacting with the chloride initiating the carbocationic reactions. The results also support the view that protonic sites on the catalyst...

  19. Theoretical investigation of layered zeolite frameworks: Interaction between IPC-1P layers derived from zeolite UTL

    Czech Academy of Sciences Publication Activity Database

    Grajciar, L.; Bludský, Ota; Roth, Wieslaw Jerzy; Nachtigall, P.

    2013-01-01

    Roč. 204, Apr 15 (2013), s. 15-21 ISSN 0920-5861 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388963 ; RVO:61388955 Keywords : layered zeolites * density functional theory * hydrogen bonding * structure Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.309, year: 2013

  20. Adsorption of CO2 in FAU zeolites: Effect of zeolite composition

    Czech Academy of Sciences Publication Activity Database

    Thang, H. V.; Grajciar, L.; Nachtigall, P.; Bludský, Ota; Areán, C. O.; Frýdová, E.; Bulánek, R.

    2014-01-01

    Roč. 227, May 15 (2014), s. 50-56 ISSN 0920-5861 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388963 Keywords : DFT/CC * CO2 * carbon capture and storage * zeolite * adsorption calorimetry Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.893, year: 2014

  1. Hierarchical zeolites from class F coal fly ash

    Science.gov (United States)

    Chitta, Pallavi

    Fly ash, a coal combustion byproduct is classified as types class C and class F. Class C fly ash is traditionally recycled for concrete applications and Class F fly ash often disposed in landfills. Class F poses an environmental hazard due to disposal and leaching of heavy metals into ground water and is important to be recycled in order to mitigate the environmental challenges. A major recycling option is to reuse the fly ash as a low-cost raw material for the production of crystalline zeolites, which serve as catalysts, detergents and adsorbents in the chemical industry. Most of the prior literature of fly ash conversion to zeolites does not focus on creating high zeolite surface area zeolites specifically with hierarchical pore structure, which are very important properties in developing a heterogeneous catalyst for catalysis applications. This research work aids in the development of an economical process for the synthesis of high surface area hierarchical zeolites from class F coal fly ash. In this work, synthesis of zeolites from fly ash using classic hydrothermal treatment approach and fusion pretreatment approach were examined. The fusion pretreatment method led to higher extent of dissolution of silica from quartz and mullite phases, which in turn led to higher surface area and pore size of the zeolite. A qualitative kinetic model developed here attributes the difference in silica content to Si/Al ratio of the beginning fraction of fly ash. At near ambient crystallization temperatures and longer crystallization times, the zeolite formed is a hierarchical faujasite with high surface area of at least 360 m2/g. This work enables the large scale recycling of class F coal fly ash to produce zeolites and mitigate environmental concerns. Design of experiments was used to predict surface area and pore sizes of zeolites - thus obviating the need for intense experimentation. The hierarchical zeolite catalyst supports tested for CO2 conversion, yielded hydrocarbons

  2. Dispersible Exfoliated Zeolite Nanosheets and Their Application as a Selective Membrane

    Science.gov (United States)

    Varoon, Kumar; Zhang, Xueyi; Elyassi, Bahman; Brewer, Damien D.; Gettel, Melissa; Kumar, Sandeep; Lee, J. Alex; Maheshwari, Sudeep; Mittal, Anudha; Sung, Chun-Yi; Cococcioni, Matteo; Francis, Lorraine F.; McCormick, Alon V.; Mkhoyan, K. Andre; Tsapatsis, Michael

    2011-10-01

    Thin zeolite films are attractive for a wide range of applications, including molecular sieve membranes, catalytic membrane reactors, permeation barriers, and low-dielectric-constant materials. Synthesis of thin zeolite films using high-aspect-ratio zeolite nanosheets is desirable because of the packing and processing advantages of the nanosheets over isotropic zeolite nanoparticles. Attempts to obtain a dispersed suspension of zeolite nanosheets via exfoliation of their lamellar precursors have been hampered because of their structure deterioration and morphological damage (fragmentation, curling, and aggregation). We demonstrated the synthesis and structure determination of highly crystalline nanosheets of zeolite frameworks MWW and MFI. The purity and morphological integrity of these nanosheets allow them to pack well on porous supports, facilitating the fabrication of molecular sieve membranes.

  3. Virtual-view PSNR prediction based on a depth distortion tolerance model and support vector machine.

    Science.gov (United States)

    Chen, Fen; Chen, Jiali; Peng, Zongju; Jiang, Gangyi; Yu, Mei; Chen, Hua; Jiao, Renzhi

    2017-10-20

    Quality prediction of virtual-views is important for free viewpoint video systems, and can be used as feedback to improve the performance of depth video coding and virtual-view rendering. In this paper, an efficient virtual-view peak signal to noise ratio (PSNR) prediction method is proposed. First, the effect of depth distortion on virtual-view quality is analyzed in detail, and a depth distortion tolerance (DDT) model that determines the DDT range is presented. Next, the DDT model is used to predict the virtual-view quality. Finally, a support vector machine (SVM) is utilized to train and obtain the virtual-view quality prediction model. Experimental results show that the Spearman's rank correlation coefficient and root mean square error between the actual PSNR and the predicted PSNR by DDT model are 0.8750 and 0.6137 on average, and by the SVM prediction model are 0.9109 and 0.5831. The computational complexity of the SVM method is lower than the DDT model and the state-of-the-art methods.

  4. Biodiesel synthesis via transesterification of lipid Chlorophyta cultivated in walne rich carbon medium using KOH/Zeolite catalyst

    Science.gov (United States)

    Dianursanti, Hayati, Siti Zahrotul; Putri, Dwini Normayulisa

    2017-11-01

    Microalgae from the Chlorophyta division such as Nannochloropsis oculata and Chlorella vulgaris are highly potential to be developed as biodiesel feedstocks because they have a high oil content up to 58%. Biodiesel is produced by transesterification of triglycerides and alcohols with the aid of homogeneous catalysts such as KOH. However, the use of KOH catalysts produces soaps in the biodiesel synthesis. Heterogeneous catalysts are known to solve this problem. One of them is natural zeolite. Zeolite can be used as a catalyst and as a support catalyst. Loading KOH on the zeolite surface is expected to increase alkalinity in KOH/Zeolite catalysts so as to increase the activity of KOH/Zeolite catalyst in transesterification of triglyceride with methanol. In this experimental lipid of microalgae will be used for produced biodiesel via transesterification reaction with methanol and KOH/Zeolite as a catalyst heterogeneous at 60 °C for 3h and utilized catalyst modificated KOH/Zeolite with variation 0.5 M, 1 M and 1.5 M KOH. The modified zeolite was then analyzed by XRF, XRD and BET. The result showed that the yield of biodiesel from lipid N.oculata was 81,09% by 0.5KOH/Zeolite catalyst, 86,53% by 1KOH/Zeolite catalyst, 1,5KOH/Zeolite and 88,13% by 1.5KOH/Zeolit, while the biodiesel produced from lipid C.vulgaris was 59.29% by 0.5KOH/Zeolite, 82.27% by 1KOH/Zeolite and 83.72% by 1.5KOH/Zeolite.

  5. Investigation of Supported Pd-Based Electrocatalysts for the Oxygen Reduction Reaction: Performance, Durability and Methanol Tolerance.

    Science.gov (United States)

    Lo Vecchio, Carmelo; Alegre, Cinthia; Sebastián, David; Stassi, Alessandro; Aricò, Antonino S; Baglio, Vincenzo

    2015-11-25

    Next generation cathode catalysts for direct methanol fuel cells (DMFCs) must have high catalytic activity for the oxygen reduction reaction (ORR), a lower cost than benchmark Pt catalysts, and high stability and high tolerance to permeated methanol. In this study, palladium catalysts supported on titanium suboxides (Pd/Ti n O 2 n -1 ) were prepared by the sulphite complex route. The aim was to improve methanol tolerance and lower the cost associated with the noble metal while enhancing the stability through the use of titanium-based support; 30% Pd/Ketjenblack (Pd/KB) and 30% Pd/Vulcan (Pd/Vul) were also synthesized for comparison, using the same methodology. The catalysts were ex-situ characterized by physico-chemical analysis and investigated for the ORR to evaluate their activity, stability, and methanol tolerance properties. The Pd/KB catalyst showed the highest activity towards the ORR in perchloric acid solution. All Pd-based catalysts showed suitable tolerance to methanol poisoning, leading to higher ORR activity than a benchmark Pt/C catalyst in the presence of low methanol concentration. Among them, the Pd/Ti n O 2 n -1 catalyst showed a very promising stability compared to carbon-supported Pd samples in an accelerated degradation test of 1000 potential cycles. These results indicate good perspectives for the application of Pd/Ti n O 2 n -1 catalysts in DMFC cathodes.

  6. Investigation of Supported Pd-Based Electrocatalysts for the Oxygen Reduction Reaction: Performance, Durability and Methanol Tolerance

    Directory of Open Access Journals (Sweden)

    Carmelo Lo Vecchio

    2015-11-01

    Full Text Available Next generation cathode catalysts for direct methanol fuel cells (DMFCs must have high catalytic activity for the oxygen reduction reaction (ORR, a lower cost than benchmark Pt catalysts, and high stability and high tolerance to permeated methanol. In this study, palladium catalysts supported on titanium suboxides (Pd/TinO2n–1 were prepared by the sulphite complex route. The aim was to improve methanol tolerance and lower the cost associated with the noble metal while enhancing the stability through the use of titanium-based support; 30% Pd/Ketjenblack (Pd/KB and 30% Pd/Vulcan (Pd/Vul were also synthesized for comparison, using the same methodology. The catalysts were ex-situ characterized by physico-chemical analysis and investigated for the ORR to evaluate their activity, stability, and methanol tolerance properties. The Pd/KB catalyst showed the highest activity towards the ORR in perchloric acid solution. All Pd-based catalysts showed suitable tolerance to methanol poisoning, leading to higher ORR activity than a benchmark Pt/C catalyst in the presence of low methanol concentration. Among them, the Pd/TinO2n–1 catalyst showed a very promising stability compared to carbon-supported Pd samples in an accelerated degradation test of 1000 potential cycles. These results indicate good perspectives for the application of Pd/TinO2n–1 catalysts in DMFC cathodes.

  7. Applications of natural zeolites on agriculture and food production.

    Science.gov (United States)

    Eroglu, Nazife; Emekci, Mevlut; Athanassiou, Christos G

    2017-08-01

    Zeolites are crystalline hydrated aluminosilicates with remarkable physical and chemical properties, which include losing and receiving water in a reverse way, adsorbing molecules that act as molecular sieves, and replacing their constituent cations without structural change. The commercial production of natural zeolites has accelerated during the last 50 years. The Structure Commission of the International Zeolite Association recorded more than 200 zeolites, which currently include more than 40 naturally occurring zeolites. Recent findings have supported their role in stored-pest management as inert dust applications, pesticide and fertilizer carriers, soil amendments, animal feed additives, mycotoxin binders and food packaging materials. There are many advantages of inert dust application, including low cost, non-neurotoxic action, low mammalian toxicity and safety for human consumption. The latest consumer trends and government protocols have shifted toward organic origin materials to replace synthetic chemical products. In the present review, we summarize most of the main uses of zeolites in food and agruculture, along with the with specific paradigms that illustrate their important role. © 2017 Society of Chemical Industry. © 2017 Society of Chemical Industry.

  8. Remarkable catalytic properties of hierarchical zeolite-Beta in epoxide rearrangement reactions

    Czech Academy of Sciences Publication Activity Database

    García-Munoz, J.L.; Serrano, D. P.; Vicente, G.; Linares, M.; Vitvarová, Dana; Čejka, Jiří

    2015-01-01

    Roč. 243, APR 2015 (2015), s. 141-152 ISSN 0920-5861 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : hierarchical zeolites * zeolite beta * hybridzeolitic - mesostructured materials Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.312, year: 2015

  9. Mesoporous MFI Zeolite Nanosponge as a High-Performance Catalyst in the Pechmann Condensation Reaction

    Czech Academy of Sciences Publication Activity Database

    Kim, J. Ch.; Ryoo, R.; Opanasenko, Maksym; Shamzhy, Mariya; Čejka, Jiří

    2015-01-01

    Roč. 5, č. 4 (2015), s. 2596-2604 ISSN 2155-5435 R&D Projects: GA ČR(CZ) GAP106/12/0189 Institutional support: RVO:61388955 Keywords : nanomorphic zeolite * MFI * hierarchical zeolite Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 9.307, year: 2015

  10. Synthesis of zeolite NaA membrane from fused fly ash extract

    CSIR Research Space (South Africa)

    Ameh, AE

    2016-01-01

    Full Text Available Zeolite-NaA membranes were synthesized from an extract of fused South African fly ash on a porous titanium support by a secondary growth method. The influence of the synthesis molar regime on the formation of zeolite NaA membrane layer...

  11. Spontaneous dispersion of PdO onto acid sites of zeolites studied by in situ DXAFS

    CERN Document Server

    Okumura, K; Niwa, M; Yokota, S; Kato, K; Tanida, H; Uruga, T

    2003-01-01

    The generation of highly dispersed PdO over zeolite supports was studied using in situ energy-dispersive XAFS (DXAFS) technique. From the comparison with the Na-ZSM-5, it was found that the oxidation as well as the spontaneous dispersion of Pd was promoted through the interaction between PdO and acid sites of H-form zeolites. (author)

  12. Thermal behavior of natural zeolites

    International Nuclear Information System (INIS)

    Bish, D.L.

    1993-01-01

    Thermal behavior of natural zeolites impacts their application and identification and varies significantly from zeolite to zeolite. Zeolites evolve H 2 0 upon heating, but recent data show that distinct ''types'' of water (e.g., loosely bound or tightly bound zeolitic water) do not exist. Rather water is bound primarily to extra-framework cations with a continuum of energies, giving rise to pseudocontinuous loss of water accompanied by a dynamic interaction between remaining H 2 0 molecules and extra-framework cations. These interactions in the channels of zeolites give rise to dehydration dependent on the extra-framework cation, in addition to temperature and water vapor pressure. The dehydration reaction and the extra-framework cation also affect the thermal expansion/contraction. Most zeolites undergo dehydration-induced contractions that may be anisotropic, although minor thermal expansion can be seen with some zeolites. Such contractions can be partially or completely irreversible if they involve modifications of the tetrahedral framework and/or if rehydration is sluggish. Thermally induced structural modifications are also driven initially by dehydration and the concomitant contraction and migration of extra-framework cations. Contraction is accommodated by rotations of structural units and tetrahedral cation-oxygen linkages may break. Thermal reactions that involve breaking of tetrahedral cation-oxygen bonds markedly irreversible and may be kinetically limited, producing large differences between short- and long-term heating

  13. Mesoporous zeolites obtained by desilication

    NARCIS (Netherlands)

    Groen, J.C.

    2007-01-01

    Zeolites are crystalline microporous materials consisting of silicon, aluminium and oxygen atoms. A unique combination of properties such as high surface area, high (hydro)thermal stability, and strong acidity, makes that zeolites are frequently used as catalysts in various (petro)chemical

  14. Trait-based model development to support breeding programs. A case study for salt tolerance and rice.

    Science.gov (United States)

    Paleari, Livia; Movedi, Ermes; Confalonieri, Roberto

    2017-06-28

    Eco-physiological models are increasingly used to analyze G × E × M interactions to support breeding programs via the design of ideotypes for specific contexts. However, available crop models are only partly suitable for this purpose, since they often lack clear relationships between parameters and traits breeders are working on. Taking salt stress tolerance and rice as a case study, we propose a paradigm shift towards the building of ideotyping-specific models explicitly around traits involved in breeding programs. Salt tolerance is a complex trait relying on different physiological processes that can be alternatively selected to improve the overall crop tolerance. We developed a new model explicitly accounting for these traits and we evaluated its performance using data from growth chamber experiments (e.g., R 2 ranged from 0.74 to 0.94 for the biomass of different plant organs). Using the model, we were able to show how an increase in the overall tolerance can derive from completely different physiological mechanisms according to soil/water salinity dynamics. The study demonstrated that a trait-based approach can increase the usefulness of mathematical models for supporting breeding programs.

  15. The role of natural zeolite and of zeolite modified with ammnonium ions to reduce the uptake of lead, zinc, copper and iron ions in Hieracium aurantium and Rumex acetosella grown on tailing ponds

    Directory of Open Access Journals (Sweden)

    Anca PETER

    2011-11-01

    Full Text Available The objective of this research is to determine if zeolite modified with ammonium ions has a higher capacity than natural zeolite to protect Hieracium aurantium and Rumex acetosella growing on tailing ponds, by reducing the quantity of metal ions these plants would accumulate in their roots and leaves. The influence of the amount of zeolite in the substrate (5% and 10% mass percentage was also studied. The experiments were carried out in laboratory and the concentration of the ions of heavy metal in roots and leaves, after 38 days of growth was established by Flame Atomic Adsorption Spectroscopy. The pH, conductivity and redox potential for each of the substrate considered were measured. The results were statistically processed using the one-way analysis of variance (one-way ANOVA. FTIR analyses were performed to establish the structural differences between the natural and modified zeolite. Hieracium aurantium and Rumex acetosella accumulate a smaller quantity of metal ions in roots and leaves in the presence of zeolite modified with ammonium ions than in the presence of natural zeolite. Laboratory tests showed that Hieracium aurantium is more tolerant to ions of heavy metals than Rumex acetosella, as demonstrated by their translocation factors.In terms of reducing the uptake of ions of heavy metals, only the zeolite modified with ammonium has a significant protective effecton Hieracium aurantium, while both natural zeolite and zeolite modified demonstrate a significant role for Rumex acetosella, asrevealed by statistical tests.

  16. Bendable Zeolite Membranes: Synthesis and Improved Gas Separation Performance.

    Science.gov (United States)

    Wang, Bo; Ho, W S Winston; Figueroa, Jose D; Dutta, Prabir K

    2015-06-23

    Separation and sequestration of CO2 emitted from fossil energy fueled electric generating units and industrial facilities will help in reducing anthropogenic CO2, thereby mitigating its adverse climate change effects. Membrane-based gas separation has the potential to meet the technical challenges of CO2 separation if high selectivity and permeance with low costs for large-scale manufacture are realized. Inorganic zeolite membranes in principle can have selectivity and permeance considerably higher than polymers. This paper presents a strategy for zeolite growth within the pores of a polymer support, with crystallization time of an hour. With a thin coating of 200-300 nm polydimethylsiloxane (PDMS) on the zeolite-polymer composite, transport data for CO2/N2 separation indicate separation factors of 35-45, with CO2 permeance between 1600 and 2200 GPU (1 GPU = 3.35 × 10(-10) mol/(m(2) s Pa)) using dry synthetic mixtures of CO2 and N2 at 25 °C. The synthesis process results in membranes that are highly reproducible toward transport measurements and exhibit long-term stability (3 days). Most importantly, these membranes because of the zeolite growth within the polymer support, as contrasted to conventional zeolite growth on top of a support, are mechanically flexible.

  17. INTERKALASI XILENOL ORANGE PADA ZEOLIT ALAM LAMPUNG SEBAGAI ELEKTRODA ZEOLIT TERMODIFIKASI

    Directory of Open Access Journals (Sweden)

    Fitriyah Fitriyah

    2016-07-01

    Full Text Available Zeolit terbagi menjadi zeolit alam dan zeolit sintesis, kapasitas adsorpsi zeolit alam umumnya lebih rendah daripada zeolit sintesis, sehingga untuk meningkatkan kapasitas adsorpsinya, karakter permukaan zeolit alam perlu diubah dengan melakukan proses modifikasi permukaan melalui berbagai metode, salah satunya dengan metode interkalasi. Tujuan penelitian ini yaitu menginterkalasi zat warna xilenol orange ke dalam zeolit alam Lampung dan mengaplikasikannya sebagai elektroda zeolit termodifikasi. Melalui proses interkalasi diharapkan dapat meningkatkan kegunaan dan nilai tambah dari zeolit. Data hasil penelitian menunjukkan bahwa xilenol orange (XO dapat diinterkalasikan ke dalam zeolit, hal ini dapat dilihat dari pita spektrum FTIR yang memiliki serapan pada bilangan gelombang 1383 cm-1, yaitu menunjukkan serapan dari S=O simetris dan asimetris pada gugus –SO3H,hal ini diduga karena XO memiliki gugus SO3 sehingga menyebabkan adanya serangan pada proton zeolit. Berdasarkan penelitian dapat disarikan bahwa xilanol orange dapat terinterkalasi pada zeolit alam Lampung dan dapat dimanfaatkan sebagai elektroda pendeteksi logam.

  18. Preparation and Characterization of Zeolite Membrane for Bioethanol Purification

    Directory of Open Access Journals (Sweden)

    Aprilina Purbasari

    2013-06-01

    Full Text Available The use of bioethanol as an alternative fuel with a purity of more than 99.5% wt has prompted research on bioethanol purification. One of the promising methods used for bioethanol purification is pervaporation membrane. This research is aimed to prepare and characterize zeolite membranes for pervaporation membrane. The membrane preparation consisted of two stages, namely support preparation and zeolite deposition on the support. In support preparation, α- alumina and kaolin with specific composition (50:30; 40:40; 50:30 was mixed with additives and water. After pugging and aging process, the mixture became paste and extruded into tubular shape. The tube was then calcined at temperature of 1250 °C for 3 hours. After that, zeolite 4A was deposited on the tubes using clear solution made of 10 %wt zeolite and 90 %wt water and heated at temperature of 80 °C for 3 hours. Furthermore, the resulting zeolite membranes was washed with deionized water for 5 minutes and dried in oven at temperature of 100 °C for 24 hours. Characterization of zeolite membranes included mechanical strength test, XRD, and SEM. In the mechanical strength test, the membrane sample with α- alumina:kaolin = 50:30 (membrane A has the highest mechanical strength of 46.65 N/mm2. Result of XRD analysis for the membrane A indicated that mullite and corundum phases were formed, which mullite phase was more dominant. Meanwhile the result of SEM analysis shows that zeolite crystals have been formed and covered the pores support, but the deposition of zeolite has not been optimal yet. The performance examination for bioethanol purification showed that the membrane could increase the purity of bioethanol from 95% to 98.5% wt. © 2013 BCREC UNDIP. All rights reservedReceived: 23rd October 2012; Revised: 15th February 2013; Accepted: 16th February 2013[How to Cite: Purbasari, A., Istirokhatun, T., Devi, A.M., Mahsunnah, L. , Susanto, H. (2013. Preparation and Characterization of Zeolite

  19. The flexibility window in zeolites.

    Science.gov (United States)

    Sartbaeva, Asel; Wells, Stephen A; Treacy, M M J; Thorpe, M F

    2006-12-01

    Today synthetic zeolites are the most important catalysts in petrochemical refineries because of their high internal surface areas and molecular-sieving properties. There have been considerable efforts to synthesize new zeolites with specific pore geometries, to add to the 167 available at present. Millions of hypothetical structures have been generated on the basis of energy minimization, and there is an ongoing search for criteria capable of predicting new zeolite structures. Here we show, by geometric simulation, that all realizable zeolite framework structures show a flexibility window over a range of densities. We conjecture that this flexibility window is a necessary structural feature that enables zeolite synthesis, and therefore provides a valuable selection criterion when evaluating hypothetical zeolite framework structures as potential synthetic targets. We show that it is a general feature that experimental densities of silica zeolites lie at the low-density edge of this window--as the pores are driven to their maximum volume by Coulomb inflation. This is in contrast to most solids, which have the highest density consistent with the local chemical and geometrical constraints.

  20. Zeolitization at uranium ore manifestation

    International Nuclear Information System (INIS)

    Petrosyan, R.V.; Buntikova, A.F.

    1981-01-01

    The process of zeolitization at uranium ore manifestation is studied. A specific type of low-temperature wall endogenous alteration of rocks due to the effect of primary acid solution with low content of carbonic acid is established. Leaching of calcium from enclosing rocks and its deposition in ore-accompanying calcium zeolites is a characteristic feature of wall-metasomatosis. Formation of desmin- calcite-laumontite and quartz-fluoroapatite of vein associations, including ore minerals (uranophane and metaotenite), is genetically connected with calcium metasomatosis. On the basis of the connection of ore minerals with endogeneous process of zeolitization a conclusion can be made on endogenous origin of uranophane and metaotenite [ru

  1. Isobutane/2-butene alkylation with zeolite Y without BrÆnsted acidity

    OpenAIRE

    Rosenbach Jr, Nilton; Mota, Claudio J. A.

    2005-01-01

    Alkylation of isobutane with 2-butene was performed on metal-exchanged Y zeolites, using an alkylchloride as carbocation initiator. The results indicated that, compared with a protonic zeolite, the deactivation was significantly slower and the production of trimethylpentanes was higher on the metal-exchanged zeolites. The metal cations act as Lewis acids, interacting with the chloride initiating the carbocationic reactions. The results also support the view that protonic sites on the catalyst...

  2. Natural zeolite bitumen cracking

    Energy Technology Data Exchange (ETDEWEB)

    Kuznicki, S.M.; McCaffrey, W.C.; Bian, J.; Wangen, E.; Koenig, A. [Alberta Univ., Edmonton, AB (Canada). Dept. of Chemical and Materials Engineering

    2006-07-01

    A study was conducted to demonstrate how low cost heavy oil upgrading in the field could reduce the need for diluents while lowering the cost for pipelining. Low cost field upgrading could also contribute to lowering contaminant levels. The performance of visbreaking processes could be improved by using disposable cracking agents. In turn, the economics of field upgrading of in-situ derived bitumen would be improved. However, in order to be viable, such agents would have to be far less expensive than current commercial cracking catalysts. A platy natural zeolite was selected for modification and testing due to its unique chemical and morphological properties. A catalyst-bearing oil sand was then heat-treated for 1 hour at 400 degrees C in a sealed microreactor. Under these mild cracking conditions, the catalyst-bearing oil sand produced extractable products of much lower viscosity. The products also contained considerably more gas oil and middle distillates than raw oil sand processed under the same conditions as thermal cracking alone. According to model cracking studies using hexadecane, these modified mineral zeolites may be more active cracking agents than undiluted premium commercial FCC catalyst. These materials hold promise for partial upgrading schemes to reduce solvent requirements in the field. tabs., figs.

  3. Hydrolyzed caseinomacropeptide conjugated galactooligosaccharides support the growth and enhance the bile tolerance in Lactobacillus strains.

    Science.gov (United States)

    Muthaiyan, Arunachalam; Hernandez-Hernandez, Oswaldo; Moreno, F Javier; Sanz, Maria Luz; Ricke, Steven C

    2012-07-11

    In this study bioactive caseinomacropeptide was conjugated with prebiotic galactooligosaccharides (hCMP:GOS) by Maillard reaction to synthesize value added prebiotic compounds to Lactobacillus strains. Growth study showed the ability of hCMP:GOS to serve as a sole carbon source for Lactobacillus strains. A significant amount of acetate and lactate was detected in cell free culture supernatant by HPLC. It demonstrated the ability of Lactobacillus strains to ferment the hCMP:GOS as a carbon source. In addition, hCMP:GOS grown Lactobacillus cells exhibited enhanced bile tolerance and retained 90% viability. Overall results of this study indicate that the hCMP conjugated GOS can be potential multipurpose prebiotic substrates to enhance the growth and bile tolerance in Lactobacillus strains and serve as a fermentable substrate to produce beneficial metabolites in the host.

  4. Pillared MFI zeolite nanosheets of a single-unit-cell thickness.

    Science.gov (United States)

    Na, Kyungsu; Choi, Minkee; Park, Woojin; Sakamoto, Yasuhiro; Terasaki, Osamu; Ryoo, Ryong

    2010-03-31

    Zeolite MFI nanosheets of 2-nm thickness have been hydrothermally synthesized via cooperative assembly between silica and an organic surfactant, which is functionalized with a diquaternary ammonium group. The zeolite nanosheets have been further assembled into their ordered multilamellar mesostructure through hydrophobic interactions between the surfactant tails located outside the zeolite nanosheet. This assembly process involves successive transformations from an initially hexagonal mesophase to a multilamellar mesophase without crystallinity and then to a lamellar mesophase with a crystalline zeolite framework. The mesopore volume in the interlamellar space could be retained by supporting the zeolite nanosheets with silica pillars, as in pillared clays, even after surfactant removal by calcination. The mesopore diameters could be controlled according to the surfactant tail lengths. Due to the interlamellar structural coherence, the hierarchically mesoporous/microporous zeolite could exhibit small-angle X-ray diffraction peaks up to the fourth-order reflections corresponding to the interlayer distance. In addition, an Ar adsorption analysis and transmission electron microscopic investigation indicated that the pillars were highly likely to be built with an MFI structure. The present approach using a zeolite structure-directing functional group contained in a surfactant would be suitable for the synthesis of other related nanomorphous zeolites in the future.

  5. π-π interaction of aromatic groups in amphiphilic molecules directing for single-crystalline mesostructured zeolite nanosheets

    Science.gov (United States)

    Xu, Dongdong; Ma, Yanhang; Jing, Zhifeng; Han, Lu; Singh, Bhupendra; Feng, Ji; Shen, Xuefeng; Cao, Fenglei; Oleynikov, Peter; Sun, Huai; Terasaki, Osamu; Che, Shunai

    2014-06-01

    One of the challenges in material science has been to prepare macro- or mesoporous zeolite. Although examples of their synthesis exist, there is a need for a facile yet versatile approach to such hierarchical structures. Here we report a concept for designing a single quaternary ammonium head amphiphilic template with strong ordered self-assembling ability through π-π stacking in hydrophobic side, which stabilizes the mesostructure to form single-crystalline mesostructured zeolite nanosheets. The concept is demonstrated for the formation of a new type of MFI (zeolite framework code by International Zeolite Association) nanosheets joined with a 90° rotational boundary, which results in a mesoporous zeolite with highly specific surface area even after calcination. Low binding energies for this self-assembling system are supported by a theoretical analysis. A geometrical matching between the arrangement of aromatic groups and the zeolitic framework is speculated for the formation of single-crystalline MFI nanosheets.

  6. Mesoporous Zeolite Single Crystals for Catalytic Hydrocarbon Conversion

    DEFF Research Database (Denmark)

    Schmidt, I.; Christensen, Claus H.; Kustova, Marina

    2005-01-01

    Recently, mesoporous zeolite single crystals were discovered. They constitute a novel family of materials that features a combined micropore and mesopore architecture within each individual crystal. Here, we briefly summarize recent catalytic results from cracking and isomerization of alkalies......, alkylation of aromatics and present new results on isomerization of aromatics. Specifically, the shape-selective isomerization of meta-xylenc into para-xylene and ortho-xylene is studied. In all these reactions, rnesoporous zeolite single crystals prove to be unique catalysts since they provide easy...... transport to and from active sites and at the same time maintain the shape-selectivity required. Thus, all these results support the idea that the beneficial effect of the mesopores system in the mesoporous zeolite single crystals call be solely attributed to enhanced mass transport....

  7. Zeolite-zeolite composite composed of Y zeolite and single-crystal-like ZSM-5 zeolite: Fabricated by a process like “big fish swallowing little one”

    Energy Technology Data Exchange (ETDEWEB)

    Pan, Meng; Li, Peng [Research Centre of Energy Chemical & Catalytic Technology, Taiyuan University of Technology, Taiyuan 030024 (China); Zheng, Jiajun, E-mail: zhengjiajun@tyut.edu.cn [Research Centre of Energy Chemical & Catalytic Technology, Taiyuan University of Technology, Taiyuan 030024 (China); Liu, Yujian [SINOPEC Research Institute of Petroleum Processing, Beijing, 100083 (China); Kong, Qinglan [Research Centre of Energy Chemical & Catalytic Technology, Taiyuan University of Technology, Taiyuan 030024 (China); Tian, Huiping [SINOPEC Research Institute of Petroleum Processing, Beijing, 100083 (China); Li, Ruifeng, E-mail: rfli@tyut.edu.cn [Research Centre of Energy Chemical & Catalytic Technology, Taiyuan University of Technology, Taiyuan 030024 (China)

    2017-06-15

    Zeolite-zeolite composite composed of Y and ZSM-5 zeolite was prepared using depolymerized Y as partial nutrients for the growth of ZSM-5. The as-synthesized samples were characterized by X-ray powder diffraction (XRD), FT-IR, scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), transmission electron microscopy (TEM), N{sub 2} adsorption-desorption measurement and Thermogravimetric analysis (TG). Chemical equilibrium at the solution-crystal interface was changed because of the partially depolymerized Y zeolite, the conditions necessary for the growth of ZSM-5 were therefore obtained. ZSM-5 zeolite crystals nucleated and grew on the interface, and Y zeolite crystals were then gradually swallowed by the growing single-crystal-like ZSM-5. - Graphical abstract: Y zeolite crystals in the hydrothermal system were partially depolymerized and an ambience in favor of the formation of ZSM-5 was formed, and ZSM-5 zeolite crystals nucleated and grew up on the external surfaces of Y zeolite crystals. As a consequence, Y zeolite crystals were swallowed by single-crystal-like ZSM-5. - Highlights: • Zeolite composite is composed by Y zeolite and single-crystal-like ZSM-5. • A composite material formed by a process like “big fish swallowing little one”. • Ratio of two zeolites in the as-synthesized sample can be adjusted.

  8. Performance Factors and Sulfur Tolerance of Metal Supported Solid Oxide Fuel Cells with Nanostructured Ni:GDC Infiltrated Anodes

    DEFF Research Database (Denmark)

    Nielsen, Jimmi; Persson, Åsa Helen; Sudireddy, Bhaskar Reddy

    2015-01-01

    cells (active area 16 cm2) have initial area specific resistances (ASR) at 650ºC of 0.35 Ωcm2 and 0.7 Ωcm2 respectively. It was found that the porosity of the support and the AFL seems to have a pronounced effect on the resulting performance. The MS-SOFCs were subjected to technologically relevant H2S......In recent years, there has been a growing interest in developing metal supported solid oxide fuel cells (MS-SOFCs). MS-SOFCs are interesting as they potentially offer some advantages compared to conventional electrode and electrolyte supported SOFCs, such as low materials cost, better thermal......’s commercially available and relevant SOFC fuels such as natural gas and diesel etc. contain trace amounts of sulfur. Thus, tolerance towards sulfur poisoning is desirable. Ceria and gadolinium doped ceria (GDC) have been reported in the literature to have a beneficial effect on the tolerance towards sulfur...

  9. An Analysis of Failure Handling in Chameleon, A Framework for Supporting Cost-Effective Fault Tolerant Services

    Science.gov (United States)

    Haakensen, Erik Edward

    1998-01-01

    The desire for low-cost reliable computing is increasing. Most current fault tolerant computing solutions are not very flexible, i.e., they cannot adapt to reliability requirements of newly emerging applications in business, commerce, and manufacturing. It is important that users have a flexible, reliable platform to support both critical and noncritical applications. Chameleon, under development at the Center for Reliable and High-Performance Computing at the University of Illinois, is a software framework. for supporting cost-effective adaptable networked fault tolerant service. This thesis details a simulation of fault injection, detection, and recovery in Chameleon. The simulation was written in C++ using the DEPEND simulation library. The results obtained from the simulation included the amount of overhead incurred by the fault detection and recovery mechanisms supported by Chameleon. In addition, information about fault scenarios from which Chameleon cannot recover was gained. The results of the simulation showed that both critical and noncritical applications can be executed in the Chameleon environment with a fairly small amount of overhead. No single point of failure from which Chameleon could not recover was found. Chameleon was also found to be capable of recovering from several multiple failure scenarios.

  10. The ADOR synthesis of new zeolites: In silico investigation

    Czech Academy of Sciences Publication Activity Database

    Trachta, Michal; Nachtigal, P.; Bludský, Ota

    2015-01-01

    Roč. 243, Apr (2015), s. 32-38 ISSN 0920-5861 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388963 Keywords : ADOR * DFT calculations * zeolites * synthesis Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.312, year: 2015

  11. Aldol condensation of furfural and acetone on zeolites

    Czech Academy of Sciences Publication Activity Database

    Kikhtyanin, O.; Kelbichová, V.; Vitvarová, Dana; Kubů, Martin; Kubička, D.

    2014-01-01

    Roč. 227, MAY 2014 (2014), s. 154-162 ISSN 0920-5861 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : aldol condensation * oligomerization * zeolites Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.893, year: 2014

  12. Intercalation chemistry of layered zeolite precursor IPC-1P

    Czech Academy of Sciences Publication Activity Database

    Mazur, Michal; Eliášová, Pavla; Roth, Wieslaw Jerzy; Čejka, Jiří

    2014-01-01

    Roč. 227, MAY 2014 (2014), s. 37-44 ISSN 0920-5861 R&D Projects: GA ČR(CZ) GAP106/12/0189 Institutional support: RVO:61388955 Keywords : UTL germanosilicate * IPC-1P layered precursor * Two-dimensional zeolites Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.893, year: 2014

  13. Zeolite-derived hybrid materials with adjustable organic pillars

    Czech Academy of Sciences Publication Activity Database

    Opanasenko, Maksym; Shamzhy, Mariya; Yu, F.; Zhou, W.; Morris, R. E.; Čejka, Jiří

    2016-01-01

    Roč. 7, č. 6 (2016), s. 3589-3601 ISSN 2041-6520 R&D Projects: GA ČR GP13-17593P; GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : zeolites * inorganic aluminosilicate * nanoporous materials Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 8.668, year: 2016

  14. Microwave heating and the fast ADOR process for preparing zeolites

    Czech Academy of Sciences Publication Activity Database

    Navarro, M.; Morris, S. A.; Mayoral, A.; Čejka, Jiří; Morris, R. E.

    2017-01-01

    Roč. 5, č. 17 (2017), s. 8037-8043 ISSN 2050-7488 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : membranes * zeolites * microwave heating Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry Impact factor: 8.867, year: 2016

  15. Silicalite-1 zeolite membranes on unmodified and modified surfaces

    Indian Academy of Sciences (India)

    Silicalite-1 zeolite membranes were prepared hydrothermally on the porous ceramic supports, both unmodified and modified with 3-aminopropyl triethoxysilane (APTES) as a coupling agent following ex situ (secondary) crystal growth process. The microstructure of the membranes was examined by scanning electron ...

  16. Two component permeation through thin zeolite MFI membranes

    NARCIS (Netherlands)

    Keizer, K.; Burggraaf, A.J.; Vroon, Z.A.E.P.; Verweij, H.

    1998-01-01

    Two component permeation measurements have been performed by the Wicke-Kallenbach method on a thin (3 μm) zeolite MFI (Silicalite-1) membrane with molecules of different kinetic diameters, d(k). The membrane was supported by a flat porous α-Al2O3 substrate. The results obtained could be classified

  17. Two-Dimensional Zeolites: Current Status and Perspectives

    Czech Academy of Sciences Publication Activity Database

    Roth, Wieslaw Jerzy; Nachtigall, P.; Morris, R. E.; Čejka, Jiří

    2014-01-01

    Roč. 114, č. 9 (2014), s. 4807-4837 ISSN 0009-2665 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : zeolites * mesoporous molecular sieves * Fischer-Tropsch synthesis Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 46.568, year: 2014

  18. Hydrocracking activity of NiMo-USY zeolite hydrotreating catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Egia, B.; Cambra, J.F.; Gueemez, B.; Arias, P.L. [Departamento de Ingeniera Quimica y del Medio Ambiente. Escuela de Ingenieros, Bilbao (Spain); Pawelec, B.; Fierro, J.L.G. [Instituto de Catalisis y Petroleoquimica, Madrid (Spain)

    1997-07-01

    In previous works the hydrodesulfurization and hydrodenitrogenation activities of Ni, Mo and MoNi zeolite supported catalysts were studied, and a remarkable initial deactivation by cocking was detected. In the present work the hydrocracking activity of these catalysts in the sulfided state has been studied. 21 refs.

  19. Neutral molecular markers support common origin of aluminium tolerance in three congeneric grass species growing in acidic soils.

    Science.gov (United States)

    Contreras, Roberto; Figueiras, Ana M; Gallego, F Javier; Benavente, Elena; Manzaneda, Antonio J; Benito, César

    2017-11-01

    Aluminium (Al) toxicity is the main abiotic stress limiting plant productivity in acidic soils that are widely distributed among arable lands. Plant species differ in the level of Al resistance showing intraspecific and interspecific variation in many crop species. However, the origin of Al-tolerance is not well known. Three annual species, difficult to distinguish phenotypically and that were until recently misinterpreted as a single complex species under Brachypodium distachyon , have been recently separated into three distinct species: the diploids B. distachyon (2 n = 10) and B. stacei (2 n = 20), and B. hybridum (2 n = 30), the allotetraploid derived from the two diploid species. The aims of this work were to know the origin of Al-tolerance in acidic soil conditions within these three Brachypodium species and to develop new DNA markers for species discrimination. Two multiplex SSR-PCRs allowed to genotype a group of 94 accessions for 17 pentanucleotide microsatellite (SSRs) loci. The variability for 139 inter-microsatellite (ISSRs) markers was also examined. The genetic relationships obtained using those neutral molecular markers (SSRs and ISSRs) support that all Al-tolerant allotetraploid accessions of B. hybridum have a common origin that is related with both geographic location and acidic soils. The possibility that the adaptation to acidic soils caused the isolation of the tolerant B. hybridum populations from the others is discussed. We finally describe a new, easy, DNA barcoding method based in the upstream-intron 1 region of the ALMT1 gene, a tool that is 100 % effective to distinguish among these three Brachypodium species.

  20. Critical evaluation of the role of the distribution of Al atoms in the framework for the activity of metallo-zeolites in redox N2O/NOx reactions

    Czech Academy of Sciences Publication Activity Database

    Sobalík, Zdeněk; Sazama, Petr; Dědeček, Jiří; Wichterlová, Blanka

    2014-01-01

    Roč. 474, MAR 2014 (2014), s. 178-185 ISSN 0926-860X R&D Projects: GA ČR GAP106/11/0624 Institutional support: RVO:61388955 Keywords : Cu-zeolite * Co-zeolite * Fe-zeolite Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.942, year: 2014

  1. Synthesis of LTA zeolite on corundum supports: Preliminary assessment for heavy metal removal from waste water; Sintesis de zeolita LTA sobre soportes de corindon: Evaluacion preliminar para la eliminacion de metales pesados de efluentes acuosos

    Energy Technology Data Exchange (ETDEWEB)

    Jacas, A.; Ortega, P.; Velasco, M. J.; Camblor, M. A.; Rodriguez, M. A.

    2012-11-01

    The effectiveness of materials based on LTA Zeolite as active phase, for their incorporation into systems aimed at the removal of heavy metals on waste water is evaluated in a preliminary way. This type of Zeolite with the main channel of a minimum free diameter of 0,41 nm and a low SiO{sub 2}/Al{sub 2}O{sub 3} ratio is an interesting molecular sieve, which in turn display a high ion exchange capacity. From this point of view, LTA Zeolite crystals were obtained in situ by hydrothermal synthesis and characterized by x ray diffraction (XRD) and scanning electron microscopy (SEM). We have studied the effect of hydrothermal synthesis time at 378 K. Likewise, the removal capacity of heavy metal from the active phase was evaluated in as a first step on diluted solutions of cooper salts at slightly acidic pH ({approx} 4,7). (Author) 28 refs.

  2. Reciprocation and interchange of grooming, agonistic support, feeding tolerance, and aggression in semi-free-ranging Barbary macaques.

    Science.gov (United States)

    Carne, Charlotte; Wiper, Sue; Semple, Stuart

    2011-11-01

    Evidence from a range of primate species indicates that grooming can be exchanged either for itself or for other rank-related "commodities," such as agonistic support, feeding tolerance, or reduced aggression. Patterns of exchange behavior have been found to vary considerably between species, and understanding the causes of this variation is central to the study of the evolution of primate social systems. It is, therefore, essential that exchange behavior is examined in a wide range of species and settings. This article is the first to explore the reciprocation and interchange of grooming in the Barbary macaque (Macaca sylvanus). We collected focal data on semi-free-ranging adult female Barbary macaques at Trentham Monkey Forest, England, and analyzed dyadic data using Generalized Linear Mixed Models. We found evidence for the reciprocal exchange of grooming and for the interchange of grooming for agonistic support and tolerance while feeding. There was no evidence that grooming was traded for a reduction in aggression; indeed, we found a positive relationship between aggression given and grooming received. This may reflect the "extortion" of grooming from subordinates by dominant animals. These results will facilitate comparative analyses of exchange behavior by adding to the current database a new species, characterized by a different social style from those macaque species previously investigated. © 2011 Wiley Periodicals, Inc.

  3. Metal immobilization in soils using synthetic zeolites

    NARCIS (Netherlands)

    Osté, L.A.; Lexmond, T.M.; Riemsdijk, van W.H.

    2002-01-01

    In situ immobilization of heavy metals in contaminated soils is a technique to improve soil quality. Synthetic zeolites are potentially useful additives to bind heavy metals. This study selected the most effective zeolite in cadmium and zinc binding out of six synthetic zeolites (mordenite-type,

  4. Zeolite from fly ash: synthesis and characterization

    Indian Academy of Sciences (India)

    ... area of the product was found to be 383 m2/g with high purity. The crystallinity of the prepared zeolite was found to change with fusion temperature and a maximum value was obtained at 823 K. The cost of synthesized zeolite was estimated to be almost one-fifth of that of commercial 13X zeolite available in the market.

  5. Surfactant-directed mesoporous zeolites with enhanced catalytic activity in tetrahydropyranylation of alcohols: Effect of framework type and morphology

    Czech Academy of Sciences Publication Activity Database

    Shin, H. S.; Opanasenko, Maksym; Cabello, C. P.; Ryoo, R.; Čejka, Jiří

    2017-01-01

    Roč. 537, MAY 2017 (2017), s. 24-32 ISSN 0926-860X R&D Projects: GA ČR(CZ) GAP106/12/0189 Institutional support: RVO:61388955 Keywords : Nanosponge zeolite * Hierarchical zeolite * Tetrahydropyranylation Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry Impact factor: 4.339, year: 2016

  6. Characterization of Mexican zeolite minerals

    International Nuclear Information System (INIS)

    Jimenez C, M.J.

    2005-01-01

    50% of the Mexican territory is formed by volcanic sequences of the Pliocene type, which appear extensively in the northwest states (Sonora, Sinaloa, Chihuahua, Durango) and west of Mexico (Jalisco and Nayarit), in central Mexico (Zacatecas, Guanajuato, San Luis Potosi, Queretaro, Hidalgo) and south of Mexico (Guerrero, Oaxaca); therefore, it is to be expected that in our country big locations of natural zeolites exist in its majority of the clinoptilolite type. The present study was focused toward the characterization of two Mexican natural zeolite rocks presumably of the clinoptilolite and filipsite types, one of them comes from the state of Chihuahua and the other of a trader company of non metallic minerals, due that these materials are not characterized, its are not known their properties completely and therefore, the uses that can be given to these materials. In this investigation work it was carried out the characterization of two Mexican zeolite rocks, one coming from the Arroyo zone, municipality of La Haciendita, in the state of Chihuahua; and the other one was bought to a trader company of non metallic minerals. The two zeolites so much in their natural form as conditioned with sodium; they were characterized by means of X-ray diffraction, scanning electron microscopy of high vacuum and elementary microanalysis (EDS), surface area analysis (BET), thermal gravimetric analysis. To differentiate the heulandite crystalline phase of the other clinoptilolite rock, its were carried out thermal treatments. The quantification of Al, Na, Ca, K, Mg, Fe was carried out in solution, by means of atomic absorption spectroscopy and the quantity of Si was determined by gravimetry. The zeolite rocks presented for the major part the crystalline heulandite and clinoptilolite phases for the most part, and it was found that the zeolite coming from the state of Chihuahua possesses a bigger content of heulandite and the denominated filipsite it is really a zeolite

  7. The Metal-Support Interaction in Pt/Y Zeolite: Evidence for a Shift in Energy of Metal d-Valence Orbitals by Pt-H Shape Resonance and Atomic XAFS spectroscopy

    NARCIS (Netherlands)

    Koningsberger, D.C.; Graaf, J. de; Mojet, B.L.; Ramaker, D.E.; Miller, J.T.

    2000-01-01

    The turnover frequency (TOF) for conversion of neo-pentane was determined for Pt in Y zeolite with different numbers of protons and La}+{}3{ ions, different Si/Al ratios and with non-framework Al being present. Comparing Pt/NaY to Pt/H-NaY and Pt/K-USY with Pt/H-USY, respectively, shows an increase

  8. Tolerance of chufa (Cyperus esculentus) as a vegetation unit's representative of bioregenerative life support systems to elevated temperatures

    Science.gov (United States)

    Shklavtsova, Ekaterina; Ushakova, Sofya; Shikhov, Valentin; Kudenko, Yurii

    Plants inclusion in the photosynthesizing unit of bioregenerative life support systems (BLSS) expects knowledge of both production characteristics of plants cultivated under optimal condi-tions and their tolerance to stress-factors' effect caused by contingency origination in a system. The work was aimed at investigation of chufa (Cyperus esculentus) tolerance to the effect of super optimal air temperature of 44 subject to PAR intensity and exposure duration. Chufa was grown in light culture conditions by hydroponics method on expanded clay aggregate. The Knop solution was used as nutrition medium. Up to 30 days the plants were cultivated at the intensity of 690 micromole*m-2*s*-1 and air temperature of 25. Heat shock was employed at the age of 30 days under the air temperature of 44 during 7, 20 and 44 hours at two different PAR intensities of 690 and 1150 micromole*m-2*s*-1. Chufa heat tolerance was estimated by intensity of external 2 gas exchange and by state of leaves' photosynthetic apparatus (PSA). Effect of disturbing temperature during 44 hours at PAR intensity of 690 micromole*m-2*s*-1 resulted in frozen-in damage of PSA-leaves' die-off. Chufa plants exposed to heat stress at PAR intensity of 690 micromole*m-2*s*-1 during both 7 and 20-hours demonstrated respiration dominance over photosynthesis; and 2 emission was observed by light. Functional activity of photosynthetic apparatus estimated with respect to parameters of pulse-amplitude-modulated chlorophyll fluorescence of photosystem 2 (PS 2) decreased on 40

  9. Characterization of natural zeolite clinoptilolite for sorption of contaminants

    Energy Technology Data Exchange (ETDEWEB)

    Xingu-Contreras, E., E-mail: nyleve-18@hotmail.com; García-Rosales, G., E-mail: gegaromx@yahoo.com.mx [Instituto Tecnológico de Toluca (Mexico); García-Sosa, I., E-mail: irma.garcia@inin.gob.mx; Cabral-Prieto, A., E-mail: agustin.cabral@inin.gob.mx; Solache-Ríos, M., E-mail: marcos.solache@inin.gob.mx [Instituto Nacional de Investigaciones Nucleares, Departamento de Química (Mexico)

    2015-06-15

    The nanoparticles technology has received considerable attention for its potential applications in groundwater treatment for the removal of various pollutants as Cadmium. In this work, iron boride nanoparticles were synthesized in pure form and in presence of homo-ionized zeolite clinoptilolite, as support material. These materials were used for removing Cd (II) from aqueous solutions containing 10, 50, 100, 150, 200, 250, 300 and 400 mg/L. The characterization of these materials was made by using X-ray Diffraction, Scanning Electron Microscopy and Mössbauer Spectroscopy. Pure iron boride particles show a broad X-ray diffraction peak centered at 45{sup ∘} (2θ), inferring the presence of nanocrystals of Fe{sub 2}B as identified from Mössbauer Spectroscopy. The size of these Fe{sub 2}B particles was within the range of 50 and 120 nm. The maximum sorption capacities for Cd (II) of iron boride particles and supported iron boride particles in homo-ionized zeolitic material were nearly 100 %. For homo-ionized zeolite and homo-ionized zeolite plus sodium borohydride was ≥ 95 %.

  10. The Support for Smoke Free Policy and How It Is Influenced by Tolerance to Smoking – Experience of a Developing Country

    Science.gov (United States)

    Rashid, Abdul; Manan, Azizah Ab; Yahya, Noorlia; Ibrahim, Lailanor

    2014-01-01

    This cross sectional survey was conducted to determine the support in making Penang UNESCO World Heritage Site (GTWHS) smoke free and to determine the influence of tolerance towards smoking on this support. This is the first phase in making Penang, Malaysia a smoke free state. A multistage sampling process was done to select a sample of respondents to represent the population of GTWHS. Attitude towards smoking was assessed using tolerance as a proxy. A total of 3,268 members of the community participated in the survey. A big majority (n = 2969; 90.9%) of the respondents supported the initiative. Support was lowest among the owners and residents/tenants, higher age groups, the Chinese, men, respondents who had poor knowledge of the places gazetted as smoke free, and respondents with poor knowledge of the health effects on smokers and on passive smokers. The odds (both adjusted and unadjusted) of not supporting the initiative was high among those tolerant to smoking in public areas. Tolerance towards smoking was associated with 80.3% risk of non-support in the respondents who were tolerant to smoking and a 57.2% risk in the population. Health promotion and education concerning the harm of tobacco smoke in Malaysia, which has mainly targeted smokers, must change. Health education concerning the risks of second hand smoke must also be given to non-smokers and efforts should be made to denormalize smoking. PMID:25338116

  11. High permeability and salt rejection reverse osmosis by a zeolite nano-membrane.

    Science.gov (United States)

    Liu, Yilun; Chen, Xi

    2013-05-14

    The possibility of employing a zeolite nano-membrane for seawater desalination is studied using comprehensive molecular dynamics simulations. Two types of zeolite with different wetting properties, the hydrophilic FAU and hydrophobic MFI, are used as the reverse osmosis (RO) membrane. Both can reach nearly 100% rejection of salt ions, and when the membrane thickness is smaller than 3.5 nm, the permeability is about 2 × 10(-9) m Pa(-1) s(-1), which is two orders of magnitude higher than that of the commercial state-of-the-art RO membrane. The relation between the permeability and thickness of the zeolite membrane is studied through the pressure drop-flux dependence. The pressure drop is linearly dependent on the thickness of the zeolite membrane. As the thickness approaches nanoscale, the end effect of water molecules entering the zeolite membrane has apparent influence on the pressure drop. For the FAU membrane the hydrophilicity can assist the water molecules entering the nanopore with reduced pressure drop, while for the hydrophobic MFI zeolite additional pressure drop arises from the capillary resistance. In order to sustain the pressure drop during desalination, the nanoscale zeolite membrane should be placed on a porous substrate and the ratio of the thickness of the nano-membrane to the radius of the supporting pore in the substrate should be properly optimized.

  12. Regioselective nitration of aromatic substrates in zeolite cages

    Indian Academy of Sciences (India)

    Unknown

    meet market demand, Choudary et al have achieved a zeolite-based methodology for the nitration of aromatic compounds.13 They have carried out nitration of toluene with various zeolite catalysts and zeolite beta of different Si/Al ratios. Zeolite beta has proved to be the best catalyst among the zeolites used in terms of ...

  13. The effect of pore size dimensions in isoreticular zeolites on carbon dioxide adsorption heats

    Czech Academy of Sciences Publication Activity Database

    Zukal, Arnošt; Shamzhy, Mariya; Kubů, Martin; Čejka, Jiří

    Roč. 24, MAR2018 ( 2018 ), s. 157-163 ISSN 2212-9820 R&D Projects: GA ČR GBP106/12/G015 EU Projects: European Commission(XE) 640979 - ShaleXenvironmenT Institutional support: RVO:61388955 Keywords : UTL zeolite * IPC-n zeolites * Carbon dioxide adsorption Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry Impact factor: 4.292, year: 2016

  14. The effect of pore size dimensions in isoreticular zeolites on carbon dioxide adsorption heats

    Czech Academy of Sciences Publication Activity Database

    Zukal, Arnošt; Shamzhy, Mariya; Kubů, Martin; Čejka, Jiří

    2018-01-01

    Roč. 24, MAR2018 (2018), s. 157-163 ISSN 2212-9820 R&D Projects: GA ČR GBP106/12/G015 EU Projects: European Commission(XE) 640979 - ShaleXenvironmenT Institutional support: RVO:61388955 Keywords : UTL zeolite * IPC-n zeolites * Carbon dioxide adsorption Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry Impact factor: 4.292, year: 2016

  15. Zeolite Membrane Reactor for Water Gas Shift Reaction for Hydrogen Production

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Jerry Y.S. [Arizona State Univ., Mesa, AZ (United States)

    2013-01-29

    Gasification of biomass or heavy feedstock to produce hydrogen fuel gas using current technology is costly and energy-intensive. The technology includes water gas shift reaction in two or more reactor stages with inter-cooling to maximize conversion for a given catalyst volume. This project is focused on developing a membrane reactor for efficient conversion of water gas shift reaction to produce a hydrogen stream as a fuel and a carbon dioxide stream suitable for sequestration. The project was focused on synthesizing stable, hydrogen perm-selective MFI zeolite membranes for high temperature hydrogen separation; fabricating tubular MFI zeolite membrane reactor and stable water gas shift catalyst for membrane reactor applications, and identifying experimental conditions for water gas shift reaction in the zeolite membrane reactor that will produce a high purity hydrogen stream. The project has improved understanding of zeolite membrane synthesis, high temperature gas diffusion and separation mechanisms for zeolite membranes, synthesis and properties of sulfur resistant catalysts, fabrication and structure optimization of membrane supports, and fundamentals of coupling reaction with separation in zeolite membrane reactor for water gas shift reaction. Through the fundamental study, the research teams have developed MFI zeolite membranes with good perm-selectivity for hydrogen over carbon dioxide, carbon monoxide and water vapor, and high stability for operation in syngas mixture containing 500 part per million hydrogen sulfide at high temperatures around 500°C. The research teams also developed a sulfur resistant catalyst for water gas shift reaction. Modeling and experimental studies on the zeolite membrane reactor for water gas shift reaction have demonstrated the effective use of the zeolite membrane reactor for production of high purity hydrogen stream.

  16. Synergistic effect of p-n heterojunction, supporting and zeolite nanoparticles in enhanced photocatalytic activity of NiO and SnO2.

    Science.gov (United States)

    Derikvandi, Hadis; Nezamzadeh-Ejhieh, Alireza

    2017-03-15

    Increased photocatalytic activity of NiO and SnO 2 was achieved by coupling and supporting of them onto clinoptilolite nanoparticles (NC) via calcination of Ni(II)-Sn(IV) - exchanged NC in photocatalytic degradation of metronidazole (MZ) aqueous solution. XRD, XRF, FTIR, SEM, X-ray mapping, DRS, TEM, BET Cyclic voltammetry and electrochemical impedance spectroscopy techniques (EIS) were used for characterization of samples. Red shift occurred in bang gap energies of the coupled semiconductors with respect to monocomponent one. This p-n hetero-junction forms a depletion layer in the semiconductors interface with negative and positive charges, causing considerable enhancement in the photocatalytic activity. The calcined catalyst at 600°C for 4h showed the best photocatalytic activity and charge transfer efficiency (in EIS results). The mole ratio of SnO 2 /NiO affects the degradation activity of the catalysts and the best activity were was obtained for the NiO 1.1 -SnO 2(6.7) /NC (NS 5 -NC) catalyst at pH 3, 1.2gL - 1 of the catalyst and 2mgL - 1 of MZ. SnO 2 played electron sink role and the photogenerated electrons migrate from more negative C b -NiO (E=-3.0V) to C b -SnO 2 (E=-0.3V vs SHE). Initial pH of MZ solution was changed from 6.20 to 4.73 during 180min that confirms formation of Oxalic acid and Maleic acid. Copyright © 2016 Elsevier Inc. All rights reserved.

  17. Hydrodesulfurization over PdMo/HY zeolite catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Pawelec, B.; Navarro, R.; Fierro, J.L.G.; Cambra, J.F.; Zugazaga, F.; Guemez, M.B.; Arias, P.L. [Instituto de Catalisis y Petroleoquimica, Madrid (Spain)

    1997-01-01

    A series of palladium-promoted Mo catalysts was prepared by a two-step impregnation procedure using an ultrastable HY zeolite carrier. The mutual effect of Pd and Mo phases and zeolitic support was investigated in hydrodesulfurization (HDS) of dibenzothiophene (DBT) and diesel oil (1.1. wt% S), Pd/HY was more active than its binary PdMo/HY counterparts, suggesting an inhibitory effect of Mo on Pd. The incorporation of Pd probably prevented deactivation of PdMo catalysts in HDS of DBT. The initial sulfur conversion in HDS of gas oil over Pd/HY was similar to that on a commercial CoMo/Al{sub 2}O{sub 3} catalysts; however, both Pd/HY catalyst and the blank HY zeolite deactivated very fast at short times on-stream. On the basis of catalyst characterization by X-ray photoelectron spectroscopy, Fourier transform i.r. spectroscopy of adsorbed CO and pyridine, and temperature-programmed reduction, it is concluded that formation of hydride-like species in PdMo zeolites are probably responsible for the inhibitory effect on HDS activity. 38 refs., 8 figs., 3 tabs.

  18. Direct activation of microcrystalline zeolites

    NARCIS (Netherlands)

    Ortiz-Iniesta, Maria Jesus; Heeres, Hero Jan; Melian-Cabrera, Ignacio

    2013-01-01

    In this work a direct activation route of zeolites is assessed. It consists of NH4-exchanging the as-synthesized solids before removing the organic template. Calcination afterwards serves to combust the organic template and creates the Bronsted sites directly; thus applying merely a single thermal

  19. Fixing noble gas in zeolites

    International Nuclear Information System (INIS)

    Rocha Dorea, A.L. da.

    1980-09-01

    In order to increase safety during the long-term storage of Kr-85 it has been proposed to encaosulate this gas in zeolite 5A. Due to the decay heat of Kr-85 it is expected, however, that the inorganic matrix will be at an increased temperature over several decades. Below 600 0 C only very small Kr-desorption rates are observed when a linear temperature gradient is applied to a loaded 5A zeolite sample. If heating is interrupted and the temperature kept konstant at a certain value (>600 0 C), it is observed that the desorption rate either decreased below the detection limit or stayed constant at some measurable value. The overall activation energy in the temperature range 570 0 C-745 0 C is found to be 250 kJ/mol. At temperature above 790 0 C the total encapsulated gas is rapidly liberated. No significant leakage was apparent from zeolite 5A samples containing between 19 and 57 cm 3 STP Kr/g kept at 200 0 C for up to 2500 h and 400 0 C for up to 3500 h. From these studies it is found that type 5A zeolites are particularly suitable as a matrix for the inmobilization of Kr-85. (Author) [pt

  20. Hydrogen Selective Exfoliated Zeolite Membranes

    Energy Technology Data Exchange (ETDEWEB)

    Tsapatsis, Michael [Univ. of Minnesota, Minneapolis, MN (United States). Department of Chemical Engineering and Materials Science; Daoutidis, Prodromos [Univ. of Minnesota, Minneapolis, MN (United States). Department of Chemical Engineering and Materials Science; Elyassi, Bahman [Univ. of Minnesota, Minneapolis, MN (United States). Department of Chemical Engineering and Materials Science; Lima, Fernando [Univ. of Minnesota, Minneapolis, MN (United States). Department of Chemical Engineering and Materials Science; Iyer, Aparna [Univ. of Minnesota, Minneapolis, MN (United States). Department of Chemical Engineering and Materials Science; Agrawal, Kumar [Univ. of Minnesota, Minneapolis, MN (United States). Department of Chemical Engineering and Materials Science; Sabnis, Sanket [Univ. of Minnesota, Minneapolis, MN (United States). Department of Chemical Engineering and Materials Science

    2015-04-06

    The objective of this project was to develop and evaluate an innovative membrane technology at process conditions that would be representative of Integrated Gasification Combined Cycle (IGCC) advanced power generation with pre-combustion capture of carbon dioxide (CO2). This research focused on hydrogen (H2)-selective zeolite membranes that could be utilized to separate conditioned syngas into H2-rich and CO2-rich components. Both experiments and process design and optimization calculations were performed to evaluate the concept of ultra-thin membranes made from zeolites nanosheets. In this work, efforts in the laboratory were made to tackle two fundamental challenges in application of zeolite membranes in harsh industrial environments, namely, membrane thickness and membrane stability. Conventional zeolite membranes have thicknesses in the micron range, limiting their performance. In this research, we developed a method for fabrication of ultimately thin zeolite membranes based on zeolite nanosheets. A range of layered zeolites (MWW, RWR, NSI structure types) suitable for hydrogen separation was successfully exfoliated to their constituent nanosheets. Further, membranes were made from one of these zeolites, MWW, to demonstrate the potential of this group of materials. Moreover, long-term steam stability of these zeolites (up to 6 months) was investigated in high concentrations of steam (35 mol% and 95 mole%), high pressure (10 barg), and high temperatures (350 °C and 600 °C) relevant to conditions of water-gas-shift and steam methane reforming reactions. It was found that certain nanosheets are stable, and that stability depends on the concentration of structural defects. Additionally, models that represent a water-gas-shift (WGS) membrane reactor equipped with the zeolite membrane were developed for systems studies. These studies had the aim of analyzing the effect of the membrane reactor integration into IGCC plants

  1. Pure zeolite exchange to synthetic zeolite characterized by XRD to produce cation exchange materials

    International Nuclear Information System (INIS)

    Zainab Ramli; Dewi Jamaliah Kamsiar; Hasidah Mohd Arsat

    2008-01-01

    In this study, natural mordenite was modified to other zeolites phases having low Si/ Al in order to increase the cation exchange capacity of the material. Modification was carried out hydrothermally at 100 degree Celsius in time range between 0 to 24 hours. The samples obtained were characterized by XRD and infrared spectroscopy. Results showed that a mixture of zeolite X and P were formed zeolite X was the dominant zeolite at 6 hrs heating time while zeolite P were dominant after 6 hrs. Ion Exchange capacity of natural mordenite, samples at 6 hr and 24 hrs heating, performed using Ca 2+ cation gave cation exchange in the decreasing order of 83.57 % , 72.50 %, 69.45 % for sample 24 hrs, 6 hrs and natural mordenite respectively. It indicates that sample having zeolite P phase is the best cation exchange capacity with 21 mg Ca 2+ / g zeolite with an increased of 23 % capacity compared to natural zeolite. (author)

  2. Is carbon-supported Pt-WOx composite a CO-tolerant material?

    International Nuclear Information System (INIS)

    Maillard, F.; Peyrelade, E.; Soldo-Olivier, Y.; Chatenet, M.; Chainet, E.; Faure, R.

    2007-01-01

    Pt-WO x /C composite materials elaborated via a two-step impregnation/electrochemical reduction method have been characterized and tested for the electrooxidation of CO/H 2 mixtures. TEM and EDS measurements revealed that WO x covered imperfectly the C particles. Nanometer-sized or agglomerated Pt particles were found on the WO x /C surface. XRD measurements revealed the absence of diffraction peaks characteristic of crystalline WO x and could indicate that this material is amorphous. No evidence of alloying between the Pt and W was observed. A significant improvement toward the electrooxidation of a CO ads monolayer was observed for the composite material compared to pure Pt/C electrocatalyst, which is evidenced by a new electrooxidation peak at 0.55V versus RHE (v=0.02Vs -1 ). As the electrical charge below this electrooxidation peak is sweep rate dependant, it is probably associated to the electrooxidation of CO ads on Pt sites at the interface with the WO x /C support. The performance of the Pt-WO x /C material for the electrooxidation of CO/H 2 mixtures was tested by polarization curves under steady-state conditions (0.001Vs -1 ) or potentiostatic measurements under fuel cell relevant conditions and compared with that of commercial 20wt% Pt/C and Pt-Ru/C materials

  3. THE EFFECT OF TYPE ZEOLITE ON THE GAS TRANSPORT PROPERTIES OF POLYIMIDE-BASED MIXED MATRIX MEMBRANES

    Directory of Open Access Journals (Sweden)

    Tutuk Djoko Kusworo

    2012-01-01

    Full Text Available The permeation rates of O2, N2, CO2 and CH4 has been studied for polyimide-polyethersulfone (PI/PES blends-zeolite mixed matrix membranes synthesized in our laboratory. The study investigated the effect of zeolite loading and different zeolite type on the gas separation performance of these mixed matrix membranes. Frequency shifts and absorption intensity changes in the FTIR spectra of the PI/PES blends as compared with those of the pure polymers indicate that there is a mixing of polymer blends at the molecular level. Differential scanning calorimetry measurements of pure and PI/PES blends membranes have showed one unique glass transition temperature that supports the miscible character of the PI/PES mixture. The PI/PES-zeolite 4A mixed matrix membrane with 25 wt % zeolite loading produced the highest O2/N2 and CO2/CH4 selectivity of around 7.45 and 46.05, respectively.

  4. Synthesis of mesoporous zeolite catalysts by in situ formation of carbon template over nickel nanoparticles

    DEFF Research Database (Denmark)

    Abildstrøm, Jacob Oskar; Kegnæs, Marina; Hytoft, Glen

    2016-01-01

    A novel synthesis procedure for the preparation of the hierarchical zeolite materials with MFI structure based on the carbon templating method with in situ generated carbon template is presented in this study. Through chemical vapour deposition of coke on nickel nanoparticles supported on silica...... oxide, a carbon-silica composite is obtained and exploited as a combined carbon template/silica source for zeolite synthesis. This approach has several advantages in comparison with conventional carbon templating methods, where relatively complicated preparative strategies involving multistep...... impregnation procedures and rather expensive chemicals are used. Removal of the carbon template by combustion results in zeolite single crystals with intracrystalline pore volumes between 0.28 and 0.48 cm3/g. The prepared zeolites are characterized by XRD, SEM, TEM and physisorption analysis. The isomerization...

  5. Tailoring Silica-alumina Supported Pt-Pd As Poison Tolerant Catalyst For Aromatics Hydrogenation

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Yanzhe; Gutierrez, Oliver Y.; Haller, Gary L.; Colby, Robert J.; Kabius, Bernd C.; Rob van Veen, J. A.; Jentys, Andreas; Lercher, Johannes A.

    2013-08-01

    The tailoring of the physicochemical and catalytic properties of mono- and bimetallic Pt-Pd catalysts supported on amorphous silica-alumina is studied. Electron energy loss spectroscopy and extended X-ray absorption fine structure analyses indicated that bimetallic Pt-Pd and relatively large monometallic Pd particles were formed, whereas the X-ray absorption near edge structure provided direct evidence for the electronic deficiency of the Pt atoms. The heterogeneous distribution of metal particles was also shown by high resolution transmission electron microscopy. The average structure of the bimetallic particles (Pt-rich core and Pd-rich shell) and the presence of Pd particles led to surface Pd enrichment, which was independently shown by IR spectra of adsorbed CO. The specific metal distribution, average size, and surface composition of the Pt-Pd particles depend to a large extent on the metal precursors. In the presence of NH3 ligands, Pt-Pd particles with a fairly homogeneous bulk and surface metal distribution were formed. Also high Lewis acid site concentration of the carrier leads to more homogeneous bimetallic particles. All catalysts were active for the hydrogenation of tetralin in the absence and presence of quinoline and dibenzothiophene (DBT). Monometallic Pt catalysts had the highest hydrogenation activity in poison-free and quinoline-containing feed. When DBT was present, bimetallic Pt-Pd catalysts with the most homogenous metal distribution showed the highest activity. The higher resistance of bimetallic catalysts towards sulfur poisoning compared to their monometallic Pt counterparts results from the weakened metal-sulfur bond on the electron deficient Pt atoms. Thus, increasing the fraction of electron deficient Pt on the surface of the bimetallic particles increases the efficiency of the catalyst in the presence of sulfur.

  6. Selective catalytic reduction of nitric oxide by ammonia over Cu-exchanged Cuban natural zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Moreno-Tost, Ramon; Santamaria-Gonzalez, Jose; Rodriguez-Castellon, Enrique; Jimenez-Lopez, Antonio [Departamento de Quimica Inorganica, Cristalografia y Mineralogia, Facultad de Ciencias, Unidad Asociada del Instituto de Catalisis y Petroleoquimica, CSIC, Universidad de Malaga, Campus de Teatinos, 29071 Malaga (Spain); Autie, Miguel A.; Glacial, Marisol Carreras [Centro Nacional de Investigaciones Cientificas, Ciudad de la Habana, La Habana (Cuba); Gonzalez, Edel [Instituto Superior Pedagogico ' Enrique Jose Varona' , La Habana (Cuba); Pozas, Carlos De las [Centro de Gerencia de Programas y Proyectos Priorizados, La Habana (Cuba)

    2004-07-15

    The catalytic selective reduction of NO over Cu-exchanged natural zeolites (mordenite (MP) and clinoptilolite (HC)) from Cuba using NH{sub 3} as reducing agent and in the presence of excess oxygen was studied. Cu(II)-exchanged zeolites are very active catalysts, with conversions of NO of 95%, a high selectivity to N{sub 2} at low temperatures, and exhibiting good water tolerance. The chemical state of the Cu(II) in exchanged zeolites was characterized by H{sub 2}-TPR and XPS. Cu(II)-exchanged clinoptilolite underwent a severe deactivation in the presence of SO{sub 2}. However, Cu(II)-exchanged mordenite not only maintained its catalytic activity, but even showed a slight improvement after 20h of reaction in the presence of 100ppm of SO{sub 2}.

  7. Selective catalytic reduction of nitric oxide by ammonia over Cu-exchanged Cuban natural zeolites

    International Nuclear Information System (INIS)

    Moreno-Tost, Ramon; Santamaria-Gonzalez, Jose; Rodriguez-Castellon, Enrique; Jimenez-Lopez, Antonio; Autie, Miguel A.; Glacial, Marisol Carreras; Gonzalez, Edel; Pozas, Carlos De las

    2004-01-01

    The catalytic selective reduction of NO over Cu-exchanged natural zeolites (mordenite (MP) and clinoptilolite (HC)) from Cuba using NH 3 as reducing agent and in the presence of excess oxygen was studied. Cu(II)-exchanged zeolites are very active catalysts, with conversions of NO of 95%, a high selectivity to N 2 at low temperatures, and exhibiting good water tolerance. The chemical state of the Cu(II) in exchanged zeolites was characterized by H 2 -TPR and XPS. Cu(II)-exchanged clinoptilolite underwent a severe deactivation in the presence of SO 2 . However, Cu(II)-exchanged mordenite not only maintained its catalytic activity, but even showed a slight improvement after 20h of reaction in the presence of 100ppm of SO 2

  8. Spin probes of chemistry in zeolites

    International Nuclear Information System (INIS)

    Werst, D.W.; Trifunac, A.D.

    1997-09-01

    Electron spin resonance (EPR) studies in zeolites are reviewed in which radiolysis was used to ionize the zeolite lattice, create reactive intermediates, spin label reaction products and to provide a window onto chemistry and transport of adsorbates and matrix control of chemistry. The review examines reactions of radical cations and the influence of the geometry constraints inside the zeolite, explores how zeolite model systems can be used to learn about energy and charge transfer in solids and illustrates the use of radiolysis and EPR for in situ spectroscopic studies of solid-acid catalysis. The various spin probes created inside the zeolite pores report on properties of the zeolites as well as shed light on radiolytic processes

  9. Synthesis, Characterization and Application of Hydrophobic Zeolites

    OpenAIRE

    Heidari, Rulis

    2016-01-01

    The aim of the thesis was to design and synthesize a type of zeolite with the characteristics of hydrophobicity, high porosity, and proper pore size, which can be used for high-performance adsorption of ethanol from aqueous solution. In addition, the aim was to synthesize hydrophobic microporous zeolites including theoretic and experimental content. The experiment was carried out using hydroxide basic system and hydrogen fluoride neutral based on hydrothermal methods. Pure silica zeolites...

  10. 85Kr storage by zeolite encapsulation

    International Nuclear Information System (INIS)

    Brown, R.A.; Hoza, M.; Knecht, D.A.

    1976-01-01

    The technology of 85 Kr storage by zeolite encapsulation is described. The prcess of encapsulation takes place at high temperatures and pressures, and involves the activated diffusion of krypton into zeolite cages. Experimental results for krypton encapsulation in various zeolites are reviewed and discussed. Activated diffusion parameters determined by measuring krypton leakage rates from zeolites at high temperatures and low pressures are used to estimate leakage rates of 85 Kr during long-term storage. The potential safety benefits are determined for krypton-85 storage by encapsulation in sodalite. Requirements for pilot-scale and process-scale development are discussed briefly

  11. Increased thermal conductivity monolithic zeolite structures

    Science.gov (United States)

    Klett, James; Klett, Lynn; Kaufman, Jonathan

    2008-11-25

    A monolith comprises a zeolite, a thermally conductive carbon, and a binder. The zeolite is included in the form of beads, pellets, powders and mixtures thereof. The thermally conductive carbon can be carbon nano-fibers, diamond or graphite which provide thermal conductivities in excess of about 100 W/mK to more than 1,000 W/mK. A method of preparing a zeolite monolith includes the steps of mixing a zeolite dispersion in an aqueous colloidal silica binder with a dispersion of carbon nano-fibers in water followed by dehydration and curing of the binder is given.

  12. The ADOR mechanism for the synthesis of new zeolites

    Czech Academy of Sciences Publication Activity Database

    Eliášová, Pavla; Opanasenko, Maksym; Wheatley, P. S.; Shamzhy, Mariya; Mazur, Michal; Nachtigall, P.; Roth, Wieslaw Jerzy; Morris, R. E.; Čejka, Jiří

    2015-01-01

    Roč. 44, č. 20 (2015), s. 7177-7206 ISSN 0306-0012 R&D Projects: GA ČR GBP106/12/G015; GA ČR(CZ) GP14-30898P Institutional support: RVO:61388955 Keywords : STRUCTURE -DIRECTING AGENTS * LARGE-PORE ZEOLITES * PILLARED MOLECULAR-SIEVE Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 34.090, year: 2015

  13. Mesoporous zeolite single crystal catalysts: Diffusion and catalysis in hierarchical zeolites

    DEFF Research Database (Denmark)

    Christensen, Christina Hviid; Johannsen, Kim; Toernqvist, Eric

    2007-01-01

    in the zeolite micropores. Here, we briefly discuss the most important ways of introducing mesopores into zeolites and, for the first time, we show experimentally that the presence of mesopores dramatically increases the rate of diffusion in zeolite catalysts. This is done by studying the elution of iso-butane...... from packed beds of conventional and mesoporous zeolite catalysts. Moreover, we discuss in detail the recent observation of improved activity and selectivity in the alkylation of benzene with ethene using mesoporous zeolite single crystal catalysts. For this reaction, we show by calculation...

  14. Electrochemically reduced graphene-oxide supported bimetallic nanoparticles highly efficient for oxygen reduction reaction with excellent methanol tolerance

    Science.gov (United States)

    Yasmin, Sabina; Cho, Sung; Jeon, Seungwon

    2018-03-01

    We report a simple and facile method for the fabrication of bimetallic nanoparticles on electrochemically reduced graphene oxide (ErGO) for electrocatalytic oxygen reduction reaction (ORR) in alkaline media. First, reduced graphene oxide supported palladium and manganese oxide nanoparticle (rGO/Pd-Mn2O3) catalyst was synthesized via a simple chemical method at room temperature; then, it was electrochemically reduced for oxidation reduction reaction (ORR) in alkaline media. The chemical composition and morphological properties of ErGO/Pd-Mn2O3 was characterized by X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and energy-dispersive X-ray spectroscopy (EDS). The TEM images reveals that, nano-sized Pd and Mn2O3 particles were disperse on the ErGO sheet without aggregation. The as-prepared ErGO/Pd-Mn2O3 was employed for ORR in alkaline media which shows higher ORR activity with more positive onset and half-wave potential, respectively. Remarkably, ErGO/Pd-Mn2O3 reduced oxygen via four-electron transfer pathway with negligible amount of intermediate peroxide species (HO2-). Furthermore, the higher stability and excellent methanol tolerance of the ErGO/Pd-Mn2O3 compared to commercial Pt/C (20 wt%) catalyst, indicating its suitability for fuel cells.

  15. Analysis and Support Initiative for Structural Technology (ASIST) Delivery Order 0016: USAF Damage Tolerant Design Handbook: Guidelines For the Analysis and Design of Damage Tolerant Aircraft Structures

    Science.gov (United States)

    2002-11-01

    Catastrophic Failure of Thin Metal Sheet”. AIAA paper, pp. 71-113. D.A. Skinn, J.P. Gallagher, A.P. Berens, P.D. Huber , and J. Smith (1994). Damage...1973). Fracture Toughness Evaluation by R-Curve Method. ASTM STP 527. American Society for Testing and Materials. W.T. Fujimoto (1976, May 4-7...Prospects of Fracture Mechanics, Noordhoff, pp. 237-250. D.A. Skinn, J.P. Gallagher, A.P. Berens, P.D. Huber , and J. Smith (1994). Damage Tolerant

  16. Transition metals-incorporated zeolites as environmental catalysts for indoor air ozone decomposition.

    Science.gov (United States)

    Mohamed, E F; Awad, G; Zaitan, H; Andriantsiferana, C; Manero, M-H

    2018-04-01

    The present study aimed to prepare catalysts of Fe- and Cu-loaded zeolite via ion-exchange technique using dilute solutions of metal nitrate precursors followed by calcination at 600°C in the air for 4 h. Commercial zeolite ZSM-5 with specific surface area of 400 m 2 /g and diameter particle of 1.2-2 mm was used as a parent support. The prepared catalysts were characterized by Fourier transform infrared spectroscopy analysis. The IR absorbed bands of Cu-ZSM-5 and Fe-ZSM-5 revealed a shift in the frequency and a reduction in the intensity framework. This indicates that both catalysts have a significant change in the number of the zeolite structure bonds. The catalytic activity of the prepared materials compared to the parent zeolite was evaluated for the catalytic ozone decomposition. The ozone stream of the initial concentration (13 g/m 3 ) with air flow rate (Q) of 0.18 m 3 /h was passed through a glass jacket column reactor filled with a fixed bed of 40 g zeolites. It was showed that the ozone removal efficiency by Cu-ZSM-5 and Fe-ZSM-5 was obviously higher than that found with the parent ZSM-5. In terms of O 3 removal efficiency, zeolite samples could be ranked as follows: Fe-ZSM-5 > Cu-ZSM-5> parent ZSM-5. The results revealed about 90% O 3 removal efficiency for Fe-ZSM-5 and 70% for Cu-ZSM-5 as compared to nearly 40% for the parent zeolite. Consequently, the incorporation of Fe and Cu metals onto the zeolite surface plays a key role for enhancing the gaseous ozone elimination.

  17. Synthesis, structure, and optical activity of HPM-1, a pure silica chiral zeolite.

    Science.gov (United States)

    Rojas, Alex; Arteaga, Oriol; Kahr, Bart; Camblor, Miguel A

    2013-08-14

    2-Ethyl-1,3,4-trimethylimidazolium is a poor organic structure-directing agent in the synthesis of pure silica zeolites using fluoride as a mineralizer at 150 °C. Under these conditions only ill-crystallized solids are obtained after long hydrothermal treatments (several weeks). It disappoints despite its relatively large size, conformational rigidity, and intermediate hydrophilic/hydrophobic character, attributes which would qualify it as a promising structure-directing agent, according to prior investigations. By raising the crystallization temperature to 175 °C under otherwise identical conditions, crystallization is dramatically accelerated. Depending on the water/silica ratio and crystallization time, two different materials are obtained: the recently reported pure silica polymorph of the chiral STW-type zeolite, HPM-1, and the new layered organosilicate, HPM-2. Prolonged heating transforms these phases into the small-pore ITW-type zeolite, while no signs of the SOF-type zeolite (formally built from the same layers as STW) was found. A complete physicochemical and structural characterization of the as-made chiral HPM-1 zeolite is provided, and the proposed stabilization of this zeolite by polarization of the Si-O bond is supported by the observed deviation from tetrahedrality. HPM-1 is optically active, and a study of several crystallites by Mueller matrix microscopy shows that their optical activity can be individually measured and that this technique could be useful for the assessment of the enantiomeric purity of a microcrystalline powder.

  18. Selective adsorption of bacterial cells onto zeolites.

    Science.gov (United States)

    Kubota, Munehiro; Nakabayashi, Tadashi; Matsumoto, Yuki; Shiomi, Tohru; Yamada, Yusuke; Ino, Keita; Yamanokuchi, Hiroyuki; Matsui, Masayoshi; Tsunoda, Tatsuo; Mizukami, Fujio; Sakaguchi, Kengo

    2008-06-15

    Zeolites adsorb microbial cells on their surfaces and selective adsorption for specific microorganisms was seen with certain zeolites. Tests for the adsorption ability of zeolites were conducted using various established microbial cell lines. Specific cell lines were shown to selectively absorb to certain zeolites, species to species. In order to understand the selectivity of adsorption, we tested adsorption under various pH conditions and determined the zeta-potentials of zeolites and cells. The adsorption of some cell lines depended on the pH, and some microorganisms were preferentially adsorbed at acidic pH. The values of zeta-potentials were used for calculating the electric double layer interaction energy between zeolites and microbial cells. There was a correlation between the experimental adsorption results and the interaction energy. Moreover, we evaluated the surface hydrophobicity of bacterial cells by using the microbial adherence to hydrocarbon (MATH) assay. In addition, we also applied this method for zeolites to quantify relative surface hydrophobicity. As a result, we found a correlation between the adsorption results and the hydrophobicity of bacterial cells and zeolites. These results suggested that adsorption could be explained mainly by electric double layer interactions and hydrophobic interactions. Finally, by using the zeolites Na-BEA and H-Y, we succeeded in clearly separating three representative microbes from a mixture of Escherichia coli, Bacillus subtilis and Staphylococcus aureus. Zeolites could adsorb each of the bacterial cell species with high selectivity even from a mixed suspension. Zeolites can therefore be used as effective carrier materials to provide an easy, rapid and accurate method for cell separation.

  19. Measuring the Bronsted acid strength of zeolites - does it correlate with the O-H frequency shift probed by a weak base?

    Czech Academy of Sciences Publication Activity Database

    Arean, C. O.; Delgado, M. R.; Nachtigall, P.; Thang, H. V.; Rubeš, M.; Bulánek, R.; Eliášová, Pavla

    2014-01-01

    Roč. 16, č. 21 (2014), s. 10129-10141 ISSN 1463-9076 R&D Projects: GA ČR GBP106/12/G015 Grant - others:GA MŠk(CZ) LM2010005 Institutional support: RVO:61388955 Keywords : zeolites * catalysis * H-MSM+22 zeolites Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.493, year: 2014

  20. Incorporation of metals (Pt-Ni-Ru) in the zeolite ZSM-5 through ion exchange competitive: synthesis and characterization

    International Nuclear Information System (INIS)

    Barbosa, A.S.; Rodrigues, M.G.F.

    2012-01-01

    Zeolites are very important materials due to their high specific surface area. Moreover, they are suitable for use as catalyst support. Noble metals supported on zeolites have been widely used as catalysts in the petrochemical industry. This paper was prepared and characterized, a powder aiming its use in heterogeneous catalysis. Support was used as ZSM-5 and the method of incorporation of the metals (Ru-PtNi) was competitive ion exchange. The materials (ZSM-5 and Pt-Ni-Ru/ZSM-5) were characterized by spectrophotometry Energy Dispersive X-ray (EDX), X-Ray Diffraction (XRD) and nitrogen physisorption (BET method). Based on the results of X-ray diffraction, it is possible to demonstrate the preservation of the structure of zeolite ZSM-5 after the competitive ion Exchange with metals (Ru-Pt-Ni) and calcination. The dispersion of metals on ZSM-5 did not change the textural characteristics of the zeolite. (author)

  1. Zeolite from fly ash: synthesis and characterization

    Indian Academy of Sciences (India)

    Coal fly ash was used to synthesize X-type zeolite by alkali fusion followed by hydrothermal treatment. The synthesized zeolite was characterized using various techniques such as X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, BET method for surface area measurement etc.

  2. Geopolymer materials based on natural zeolite

    NARCIS (Netherlands)

    Nikolov, A.; Rostovsky, Ivan; Nugteren, H.W.

    2017-01-01

    One of the potential raw materials for preparation of geopolymers is the natural zeolite. In the present report, the used natural zeolite (clinoptilolite) is from huge deposit near Beli Plast, Bulgaria. Geopolymer pastes and mortars are prepared by using three different alkaline activators—sodium

  3. ETHIOPIAN NATURAL ZEOLITES FOR PHOTOCATALYSIS Kiros ...

    African Journals Online (AJOL)

    B. S. Chandravanshi

    This sample, called ET4, contains other non-zeolitic phases like celadonite and ilmenite, which may synergize the potential application of this high Ti- containingsample for photocatalysis. EXPERIMENTAL. Sample preparation. Three different approaches were carried out: i) simple calcination of raw zeolite ET4 sample: 1.

  4. Zeolite from fly ash: synthesis and characterization

    Indian Academy of Sciences (India)

    Unknown

    disposal or to minimize the environmental impact. One of the approaches is the conversion of fly ash to zeolites, which have wide applications in ion exchange, as mole- cular sieves, catalysts, and adsorbents (Breck 1974). The present study is concerned with the synthesis of zeolite from coal fly ash and its characterization ...

  5. Synthesis of LTA zeolite for bacterial adhesion

    Directory of Open Access Journals (Sweden)

    Raja Belaabed

    2016-07-01

    X-ray diffraction, environmental scanning electron microscope and attenuated total reflection-Fourier transform infrared spectroscopy were used to characterize the synthesized zeolite. To evaluate the bacterial adhesion to zeolite LTA the hydrophobicity and surface properties are examined using contact angle measurement.

  6. Exfoliation of two-dimensional zeolites in liquid polybutadienes

    KAUST Repository

    Sabnis, Sanket

    2017-06-16

    Layered zeolite precursors were successfully exfoliated by brief shearing or sonication with the assistance of commercially available telechelic liquid polybutadienes at room temperature. The exfoliated zeolite nanosheets can form a stable suspension in an organic solvent, providing exciting potential for the fabrication of zeolite membranes, composite materials and hierarchical zeolites.

  7. Mesoporous MEL, BEA, and FAU zeolite crystals obtained by in situ formation of carbon template over metal nanoparticles

    DEFF Research Database (Denmark)

    Abildstrøm, Jacob Oskar; Ali, Zahra Nasrudin; Mentzel, Uffe Vie

    2016-01-01

    Here, we report the synthesis and characterization of hierarchical zeolite materials with MEL, BEA and FAU structures. The synthesis is based on the carbon templating method with an in situ-generated carbon template. Through the decomposition of methane and deposition of coke over nickel...... nanoparticles supported on silica, a carbon–silica composite is obtained and exploited as a combined carbon template/silica source for the zeolite synthesis. The mesoporous zeolite materials were all prepared by hydrothermal crystallization in alkaline media followed by removal of the carbon template...

  8. Nuclear waste treatment using Iranian natural zeolites

    International Nuclear Information System (INIS)

    Kazemian, H.; Ghannadi Maraghe, M.

    2001-01-01

    Full text: The zeolite researches in Iran is a relatively new subject which has started about 10 years ago. The motivation for this scientific and interesting field was provided after discovery of significant deposits of natural zeolites in different regions of Iran as well as further developments of research institutions and the national concern to environmental protection especially the wastewater clean-up in point of view of recycling of such waste water to compensate some needs to water in other utilizations. This paper intends to review and describes scientific researches which have done on using zeolites in the field of nuclear waste treatment in Iran to introduce the potential resources to the world in more details. Zeolite tuffs are widely distributed in huge deposits in different regions of Iran. So far, the clinoptilolite tuffs are the most abundant natural zeolite which exist with zeolite content of 65%- 95%. Nowadays several different types of Iranian natural zeolites are characterized in point of view of chemical composition, type of structure, chemical, thermal, and radiation resistance using different instrumental and classical methods such as; X-ray diffraction (XRD), X-ray fluoresce (XRF), thermal methods of analysis (TA), scanning electron microscopy (SEM), analytical chemistry and radioanalytical methods as well as different ion-exchange techniques (e.g.3-7). The ability of Iranian natural clinoptilolite for removal of some fission products from nuclear wastewaters have been investigated. The selectivity of all investigated zeolites toward radiocesium and radiostrontium have been promising (e.g. 8-10). The successful synthesize of P zeolite from Iranian clinoptilolite-reach tuffs under different conditions were performed. The compatibility of zeolites with glass and cement matrices, for final disposal of radwaste, as well as their selectivity toward most dangerous heat generating radionuclides (e.g. 137 Cs and 90 Sr) is very important in using

  9. Synthesis and evaluation of Pt-alloys supported on MWCNTS as ethylene glycol-tolerant ORR cathodes

    Energy Technology Data Exchange (ETDEWEB)

    Morales-Acosta, D.; Arriaga, L.G. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica, Pedro Escobedo, Queretaro (Mexico); Alvarez-Contreras, L. [Centro de Investigacion en Materiales Avanzados S. C., Chihuahua, Chihuahua (Mexico); Fraire Luna, S.; Rodriguez Varela, F.J. [Cinvestav, Unidad Saltillo, Ramos Arizpe, Coahuila (Mexico)]. E-mail: javier.varela@cinvestav.edu.mx

    2009-09-15

    In this work, a Pt-Co/MWCNT alloy (atomic ratio 70:30) was synthesized and evaluated as oxygen reduction reaction (ORR) cathode for Direct Ethylene Glycol Fuel Cells (DEGFC) applications. The alloy showed good performance for the ORR in acid medium, while in the presence of 0.125M EG (C{sub 2}H{sub 6}O{sub 2}) the MWCNTs-supported electrocatalyst showed a very high selectivity for the cathodic reaction and a high degree of tolerance to the organic fuel, i.e., a very small shift in the onset potential for the ORR, Eonset, and no peak current densities associated to the oxidation of EG, a detrimental effect of organic fuels normally observed in the case of Pt-alone electrocatalysts. [Spanish] En este trabajo, se sintetizo y evaluo una aleacion Pt-Co/NTCMP (razon atomica 70/30) como catodo de reaccion de reduccion de oxigeno (RRO) para aplicaciones de celdas de combustible de glicol de etileno directo (CCGED). La aleacion mostro buen desempeno para la RRO en medio acido, en tanto que la presencia de 0.125M de GE (C{sub 2}H{sub 6}O{sub 2}) del electrocatalizador soportado por NTCMP mostro una muy alta selectividad para la reaccion catodica y un alto grado de tolerancia al combustible organico, es decir, un corrimiento muy pequeno del potencial de inicio para la RRO, Einicio, y no densidades de corriente asociadas a la oxidacion del GE, efecto perjudicial de los combustibles organicos que se observa en el caso del electrocatalizadores solo de Pt.

  10. Proton Adsorption Selectivity of Zeolites in Aqueous Media: Effect of Si/Al Ratio of Zeolites

    Directory of Open Access Journals (Sweden)

    Moses Wazingwa Munthali

    2014-12-01

    Full Text Available In addition to their well-known uses as catalysts, zeolites are utilized to adsorb and remove various cations from aqueous system. The adsorption of the cations is ascribed to the negative charge of zeolites derived from isomorphous substitution of Si by Al. The amount of Na+ adsorption on 4A, X, Y, Na-P1 and mordenite type zeolites were determined in aqueous media, in a two-cation (Na+ and H+ system. Although each zeolite has a constant amount of negative charge, the amount of Na+ adsorption of each zeolite decreased drastically at low pH−pNa values, where pH−pNa is equal to log{(Na+/(H+}. By using the plot of the amount of Na+ adsorption versus pH−pNa, an index of the H+ selectivity, which is similar to the pKa of acids, of each zeolite was estimated, and the index tended to increase with decreasing Si/Al ratio of zeolites. These indicate that zeolites with lower Si/Al and higher negative charge density have higher H+ adsorption selectivity, and in fact, such a zeolite species (4A and X adsorbed considerable amount of H+ even at weakly alkaline pH region. The adsorption of H+ results in the decrease of cation adsorption ability, and may lead to the dissolution of zeolites in aqueous media.

  11. Effect of Ge/Si substitutions on the local geometry of Si framework sites in zeolites: A combined high resolutionsup29/supSi MAS NMR and DFT/MM study on zeolite Beta polymorph C (BEC)

    Czech Academy of Sciences Publication Activity Database

    Whittleton, Sarah R.; Vicente, A.; Fernandez, C.; Rastegar, Somayeh F.; Fishchuk, Anna V.; Sklenák, Štěpán

    2018-01-01

    Roč. 267, SEP 2018 (2018), s. 124-133 ISSN 1387-1811 R&D Projects: GA ČR(CZ) GA15-14007S Grant - others:Ga MŠk(CZ) LM2015070 Institutional support: RVO:61388955 Keywords : 29 Si MAS NMR * bec * Ge-zeolites * Germanoaluminosilicates * Zeolite Beta polymorph C Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry Impact factor: 3.615, year: 2016

  12. Epitaxially Grown Layered MFI–Bulk MFI Hybrid Zeolitic Materials

    KAUST Repository

    Kim, Wun-gwi

    2012-11-27

    The synthesis of hybrid zeolitic materials with complex micropore-mesopore structures and morphologies is an expanding area of recent interest for a number of applications. Here we report a new type of hybrid zeolite material, composed of a layered zeolite material grown epitaxially on the surface of a bulk zeolite material. Specifically, layered (2-D) MFI sheets were grown on the surface of bulk MFI crystals of different sizes (300 nm and 10 μm), thereby resulting in a hybrid material containing a unique morphology of interconnected micropores (∼0.55 nm) and mesopores (∼3 nm). The structure and morphology of this material, referred to as a "bulk MFI-layered MFI" (BMLM) material, was elucidated by a combination of XRD, TEM, HRTEM, SEM, TGA, and N2 physisorption techniques. It is conclusively shown that epitaxial growth of the 2-D layered MFI sheets occurs in at least two principal crystallographic directions of the bulk MFI crystal and possibly in the third direction as well. The BMLM material combines the properties of bulk MFI (micropore network and mechanical support) and 2-D layered MFI (large surface roughness, external surface area, and mesoporosity). As an example of the uses of the BMLM material, it was incorporated into a polyimide and fabricated into a composite membrane with enhanced permeability for CO2 and good CO2/CH4 selectivity for gas separations. SEM-EDX imaging and composition analysis showed that the polyimide and the BMLM interpenetrate into each other, thereby forming a well-adhered polymer/particle microstructure, in contrast with the defective interfacial microstructure obtained using bare MFI particles. Analysis of the gas permeation data with the modified Maxwell model also allows the estimation of the effective volume of the BMLM particles, as well as the CO2 and CH4 gas permeabilities of the interpenetrated layer at the BMLM/polyimide interface. © 2012 American Chemical Society.

  13. Water nanodroplets confined in zeolite pores.

    Science.gov (United States)

    Coudert, François-Xavier; Cailliez, Fabien; Vuilleumier, Rodolphe; Fuchs, Alain H; Boutin, Anne

    2009-01-01

    We provide a comprehensive depiction of the behaviour of a nanodroplet of approximately equal to 20 water molecules confined in the pores of a series of 3D-connected isostructural zeolites with varying acidity, by means of molecular simulations. Both grand canonical Monte Carlo simulations using classical interatomic forcefields and first-principles Car-Parrinello molecular dynamics were used in order to characterise the behaviour of confined water by computing a range of properties, from thermodynamic quantities to electronic properties such as dipole moment, including structural and dynamical information. From the thermodynamic point of view, we have identified the all-silica zeolite as hydrophobic, and the cationic zeolites as hydrophilic; the condensation transition in the first case was demonstrated to be of first order. Furthermore, in-depth analysis of the dynamical and electronic properties of water showed that water in the hydrophobic zeolite behaves as a nanodroplet trying to close its hydrogen-bond network onto itself, with a few short-lived dangling OH groups, while water in hydrophilic zeolites "opens up" to form weak hydrogen bonds with the zeolite oxygen atoms. Finally, the dipole moment of confined water is studied and the contributions of water self-polarisation and the zeolite electric field are discussed.

  14. The role of zeolite in the Fischer–Tropsch synthesis over cobalt–zeolite catalysts

    International Nuclear Information System (INIS)

    Sineva, L V; Mordkovich, V Z; Asalieva, E Yu

    2015-01-01

    The review deals with the specifics of the Fischer–Tropsch synthesis for the one-stage syncrude production from CO and H 2 in the presence of cobalt–zeolite catalytic systems. Different types of bifunctional catalysts (hybrid, composite) combining a Fischer–Tropsch catalyst and zeolite are reviewed. Special attention focuses on the mechanisms of transformations of hydrocarbons produced in the Fischer–Tropsch process on zeolite acid sites under the synthesis conditions. The bibliography includes 142 references

  15. A general method to incorporate metal nanoparticles in zeolites and zeotypes

    DEFF Research Database (Denmark)

    2015-01-01

    Disclosed herein is a method for producing a zeolite, zeolite-like or zeotype structure with selective formation of metal, metal oxide or metal sulphide nanoparticles and/or clusters inside the zeolite, zeolite-like or zeotype structure.......Disclosed herein is a method for producing a zeolite, zeolite-like or zeotype structure with selective formation of metal, metal oxide or metal sulphide nanoparticles and/or clusters inside the zeolite, zeolite-like or zeotype structure....

  16. Tolerating Zero Tolerance?

    Science.gov (United States)

    Moore, Brian N.

    2010-01-01

    The concept of zero tolerance dates back to the mid-1990s when New Jersey was creating laws to address nuisance crimes in communities. The main goal of these neighborhood crime policies was to have zero tolerance for petty crime such as graffiti or littering so as to keep more serious crimes from occurring. Next came the war on drugs. In federal…

  17. Nanoporosity of MCM-41 Materials and Y-Zeolites Created by Deposition of Tournefortia hirsutissima L. Plant Extract

    Directory of Open Access Journals (Sweden)

    Miguel Angel Hernández

    2017-01-01

    Full Text Available Hybrid materials based on MCM-41 silica and Y-zeolites with a variable Si/Al ratio and an appropriate countercationic composition were prepared by impregnating inorganic substrates with an organic extract. The organic phase was previously characterized by GC-MS and IRTF, while XRD, SEM, TEM, N2-physisorption, and TPD of NH3 were used to analyze the selected inorganic supports. The effect of size- and shape-selectivity was manifested in MCM-41 and Y-zeolites. Texture results confirm that the extract containing relatively large branched organic molecules is deposited in the internal voids of MCM-41 material and on the outer area of Y-zeolites. In the case of Y-zeolites, the results demonstrate the effect of the SiO2/Al2O3 molar ratio and countercations on the textural properties of the samples.

  18. Synthesis of K2O/Zeolite catalysts by KOH impregnation for biodiesel production from waste frying oil

    Science.gov (United States)

    Fitriana, N.; Husin, H.; Yanti, D.; Pontas, K.; Alam, P. N.; Ridho, M.; Iskandar

    2018-03-01

    K2O/Zeolite compounds were successfully synthesized using KOH as starting material and natural zeolite as support. The catalysts were calcined at 500°C for 3 h and then characterized by X-Ray Diffractometer (XRD) and Scanning Electron Microscopy (SEM). The SEM images reveal that the zeolite and K2O/zeolite particles are irregular in shape (100 to 400 nm). The independent variables were impregnated amounts of KOH (15 - 25%), catalyst to oil ratios of 1.0 - 6.0 wt.%, and reaction time of 2 h. The highest biodiesel yield of 95% was produced from the reaction with 2.1 wt.% catalyst of 25% KOH impregnated. The properties of produced biodiesel complied with SNI. The catalytic stability test showed that the 25% KOH impregnated catalyst was stable.

  19. Preparation and characterization of new zeolite membranes. Application to gaseous separation; Preparation et caracterisation de nouvelles membranes de zeolithe application a la separation gazeuse

    Energy Technology Data Exchange (ETDEWEB)

    Anstett, M.

    1996-11-25

    Zeolites are interesting for the preparation of inorganic membranes which could be used for the continuous separation of gas and liquids by gas permeation and pervaporation. Zeolites membranes are obtained by hydrothermal synthesis and are characterized by XRD, SEM, TDA, IR, chemical analysis, EPMA, NMR, MAS NMR and gas permeation. After some tests of preparation of zeolite CHA and MFI self supporting membranes, the work is turned towards the preparation of zeolite MFI membranes supported by porous disks or {alpha} alumina, glass and tubes of carbon covered with a thin layer or zirconium dioxide. It is shown that the characteristics of the support (reactivity, pores dimensions, ...) strongly influence the quality of the prepared membrane. Two originals preparation processes are finalized. For the alumina disks, a gel precursor of zeolite is firs formed at the surface of the support by immersing successively that support in two non miscible liquids before the crystallisation. The gel is then converted into the zeolite by contact with water vapor. The zeolite layer obtained is localized at the surface of the support and present not only at the outside but also at the inside of the support. The characteristics of the zeolite layer can be controlled and the method can be adapted to various porous supports. The membrane obtained is interesting for hydrocarbons separations, for example the separation of methane and isobutane. In the case of Vycor glass disks, the reactivity of the support is first enhanced by contact with saturated water vapour. The temperature of the synthesis is then chosen relatively low in order to limit the attack of the support. With that method, a basic solution can be used without degradation of the support.The basicity leads to the formation of little crystals whose assembling is compact and homogeneous. The membrane obtained is interesting for example for the separation of normal butane and isobutane. (author) 71 refs.

  20. Analysis Of Natural Zeolites For Technical Nuclear

    International Nuclear Information System (INIS)

    Sarria, P.; Desdin, L.; Dominguez, O.

    1999-01-01

    In this article a methodology of elementary analysis of natural zeolites is reported using different technical nuclear (AANR, FRX, MRN and EG). Determines the elementary composition of ours of two Cuban locations. (Author) [es

  1. Enriched natural zeolites – mineral fertilizer

    Directory of Open Access Journals (Sweden)

    Rybárová Lucia

    2001-12-01

    Full Text Available Clinoptilolit belongs to the big group of minerals called zeolites. Chemically they are alumosilicates and have a very difficult crystal structure. Nature zeolites are used as sorbents, molecular sieves and catalyzators. Their application is also in agriculture and horticulture. Endeavour of all agricurtural subjects from the plant area is to reach a maximum efficiency and production.Charges for the fertilization are 14 – 40% of all charges depending on the structure of product, intensity of production and share of nutrition in soil. For the elimination of the loss in the nutrition matter, it is possible to use a „porter“, which secures a regular and inteligent supply of nutrition to plants.Regarding the physical and chemical properties is good to use natural zeolites as a „porter“.The experiments were made with enriched zeolites, and their influences an vegetables and flowers roots was reserched. Results were positive.

  2. Diagenetic Quartz Morphologies and Zeolite formation

    DEFF Research Database (Denmark)

    Kazerouni, Afsoon Moatari; Hansen, Rikke Weibel; Friis, Henrik

    sands in these wells all contain authigenic silica/quartz of various morphologies identified with a combination of traditional optical microscopy and scanning electron microscopy. Late Paleocene–early Eocene volcanic ash layers are recognized throughout most of the North Sea and also recorded from......, the precipitation of zeolite may later facilitate further quartz cementation, which might otherwise be retarded by the presence of disordered microquartz. The silica activity of pore fluids can influence zeolite precipitation.  Although zeolite formation is clearly related to volcanic ash, zeolite has also formed...... are abundant in some of associated shales; and 2) volcanic ash. The dissolution of biogenic silica may result in a rapid release of silica thereby promoting the formation of diagenetic opal/microquartz, but there may be a limited release of Al. A limited release of Al may result in precipitation of Si...

  3. The thermal dehydration of natural zeolites

    NARCIS (Netherlands)

    Reeuwijk, van L.P.

    1974-01-01

    The zeolites constitute a group of minerals of much interest from geological, mineralogical and technological points of view. Structurally, they are tectosilicates with an 'open' framework containing channels and cavities which accommodate cations and water molecules. Generally, these

  4. Synthesis of LTA zeolite for bacterial adhesion

    Energy Technology Data Exchange (ETDEWEB)

    Belaabed, R.; Eabed, S.; Addaou, A.; Laajab, A.; Rodriguez, M.A.; Lahsini, A.

    2016-07-01

    High affinity and adhesion capacity for Gram-positive bacteria on minerals has been widely studied. In this work the adhesion of bacteria on synthesized zeolite has been studied. The Zeolite Linde Type A (LTA) has been synthesized using hydrothermal route using processing parameters to obtain low cost materials. For adhesion studies Staphylococcus aureus and Bacillus subtilis were used as Gram-positive bacteria, Escherichia coli and Pseudomonas aeruginosa are used as Gram-negative bacteria. X-ray diffraction, environmental scanning electron microscope and attenuated total reflection-Fourier transform infrared spectroscopy were used to characterize the synthesized zeolite. To evaluate the bacterial adhesion to zeolite LTA the hydrophobicity and surface properties are examined using contact angle measurement. (Author)

  5. Mixing of zeolite powders and molten salt

    International Nuclear Information System (INIS)

    Pereira, C.; Zyryanov, V.N.; Lewis, M.A.; Ackerman, J.P.

    1996-01-01

    Transuranics and fission products in a molten salt can be incorporated into zeolite A by an ion exchange process and by a batch mixing or blending process. The zeolite is then mixed with glass and consolidated into a monolithic waste form for geologic disposal. Both processes require mixing of zeolite powders with molten salt at elevated temperatures (>700 K). Complete occlusion of salt and a uniform distribution of chloride and fission products are desired for incorporation of the powders into the final waste form. The relative effectiveness of the blending process was studied over a series of temperature, time, and composition profiles. The major criteria for determining the effectiveness of the mixing operations were the level and uniformity of residual free salt in the mixtures. High operating temperatures (>775 K) improved salt occlusion. Reducing the chloride levels in the mixture to below 80% of the full salt capacity of the zeolite significantly reduced the free salt level in the final product

  6. Alkali resistant Fe-zeolite catalysts for SCR of NO with NH3 in flue gases

    DEFF Research Database (Denmark)

    Putluru, Siva Sankar Reddy; Jensen, Anker Degn; Riisager, Anders

    2011-01-01

    Fe-zeolite catalysts were prepared by ionexchange and characterized by nitrogen physisorption, electron paramagnetic resonance (EPR) spectroscopy, NH3-temperature programmed desorption (TPD), H2-temperature programmed reduction (TPR) and Energy dispersive X-ray spectroscopy (EDX) methods. The eff......Fe-zeolite catalysts were prepared by ionexchange and characterized by nitrogen physisorption, electron paramagnetic resonance (EPR) spectroscopy, NH3-temperature programmed desorption (TPD), H2-temperature programmed reduction (TPR) and Energy dispersive X-ray spectroscopy (EDX) methods....... The effect of potassium doping on the acidic and redox properties of the Fe-zeolite catalysts were studied. The prepared catalysts showed high surface area and surface acidity. This is essential for increased alkali resistivity in comparison with conventional metal oxide supports like, e.g. TiO2 and ZrO2......, towards e.g. potassium salts in flue gases from biomass fired power plants. These properties allowed both undoped and potassium doped Fe-zeolite catalysts to posses high activity during the selective catalytic reduction (SCR) of NO with NH3. The extent of deactivation of the Fe-zeolite catalysts...

  7. Discovery of optimal zeolites for challenging separations and chemical conversions through predictive materials modeling

    Science.gov (United States)

    Siepmann, J. Ilja; Bai, Peng; Tsapatsis, Michael; Knight, Chris; Deem, Michael W.

    2015-03-01

    Zeolites play numerous important roles in modern petroleum refineries and have the potential to advance the production of fuels and chemical feedstocks from renewable resources. The performance of a zeolite as separation medium and catalyst depends on its framework structure and the type or location of active sites. To date, 213 framework types have been synthesized and >330000 thermodynamically accessible zeolite structures have been predicted. Hence, identification of optimal zeolites for a given application from the large pool of candidate structures is attractive for accelerating the pace of materials discovery. Here we identify, through a large-scale, multi-step computational screening process, promising zeolite structures for two energy-related applications: the purification of ethanol beyond the ethanol/water azeotropic concentration in a single separation step from fermentation broths and the hydroisomerization of alkanes with 18-30 carbon atoms encountered in petroleum refining. These results demonstrate that predictive modeling and data-driven science can now be applied to solve some of the most challenging separation problems involving highly non-ideal mixtures and highly articulated compounds. Financial support from the Department of Energy Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences and Biosciences under Award DE-FG02-12ER16362 is gratefully acknowledged.

  8. Kinetic Adsorption Study of Silver Nanoparticles on Natural Zeolite: Experimental and Theoretical Models

    Directory of Open Access Journals (Sweden)

    Alvaro Ruíz-Baltazar

    2015-12-01

    Full Text Available In this research, the adsorption capacity of Ag nanoparticles on natural zeolite from Oaxaca is presented. In order to describe the adsorption mechanism of silver nanoparticles on zeolite, experimental adsorption models for Ag ions and Ag nanoparticles were carried out. These experimental data obtained by the atomic absorption spectrophotometry technique were compared with theoretical models such as Lagergren first-order, pseudo-second-order, Elovich, and intraparticle diffusion. Correlation factors R2 of the order of 0.99 were observed. Analysis by transmission electron microscopy describes the distribution of the silver nanoparticles on the zeolite outer surface. Additionally, a chemical characterization of the material was carried out through a dilution process with lithium metaborate. An average value of 9.3 in the Si/Al ratio was observed. Factors such as the adsorption behavior of the silver ions and the Si/Al ratio of the zeolite are very important to support the theoretical models and establish the adsorption mechanism of Ag nanoparticles on natural zeolite.

  9. Zeolite membranes for efficient synthesis of biofuels

    OpenAIRE

    Sandström, Linda

    2009-01-01

    The greenhouse effect and the limited fossil oil resources have increased the demand of renewable fuels. Zeolite membranes have potential applications in numerous separation processes, and could be useful in the development of efficient processes for renewable fuel production. Methanol synthesis from synthesis gas is equilibrium limited, and continuous removal of products in a zeolite membrane reactor could improve the productivity of a conventional methanol synthesis process. In this work, m...

  10. Zeolitic catalytic conversion of alcohols to hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Narula, Chaitanya K.; Davison, Brian H.; Keller, Martin

    2018-04-10

    A method for converting an alcohol to a hydrocarbon, the method comprising contacting said alcohol with a metal-loaded zeolite catalyst at a temperature of at least 100.degree. C. and up to 550.degree. C., wherein said alcohol can be produced by a fermentation process, said metal is a positively-charged metal ion, and said metal-loaded zeolite catalyst is catalytically active for converting said alcohol to said hydrocarbon.

  11. Zeolitic catalytic conversion of alochols to hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Narula, Chaitanya K.; Davison, Brian H.; Keller, Martin

    2017-01-03

    A method for converting an alcohol to a hydrocarbon, the method comprising contacting said alcohol with a metal-loaded zeolite catalyst at a temperature of at least 100.degree. C. and up to 550.degree. C., wherein said alcohol can be produced by a fermentation process, said metal is a positively-charged metal ion, and said metal-loaded zeolite catalyst is catalytically active for converting said alcohol to said hydrocarbon.

  12. Synthesis and characterization of zeolite L

    International Nuclear Information System (INIS)

    Ko, Yong Sig; Ahn, Wha Seung

    1999-01-01

    Substantial reduction in synthesis time was achieved for zeolite L crystallization by attempting a hydrothermal synthesis at elevated temperature of 443K in a Na + /K+ mixed alkali system. Pure zeolite L could be obtained from a gel with the molar composition 5.4K 2 O-5.7Na 2 O-Al 2 O 3 -30SiO 2 -500H 2 O after 24h. Zeolite L could be obtained in high purity at the optimum Na 2 O/(K 2 O+Na 2 O) ratio of around 0.5, while zeolite W was formed when the Na 2 O/(K 2 O+Na 2 O) ratio was more than 0.66. The crystalline zeolite L samples obtained were characterized by means of elemental chemical analysis, XRD, SEM, FTi.r. spectroscopy, and particle size analyzer. In addition, two probe reaction studies were conducted. In toluene alkylation, H-L catalyst showed high catalytic activity at the beginning, but was deactivated quickly probably due to one-dimensional pore structure being blocked by the coke formed. High amounts of trimethylbenzene or diethylbenzene were observed due to the large 12-membered ring pore structure of zeolite L. Pt/NaKL catalyst prepared showed a high conversion of n-hexane and high selectivity to benzene in n-hexane aromatization reaction

  13. Thermal Properties of Zeolite-Containing Composites.

    Science.gov (United States)

    Shimonosono, Taro; Hirata, Yoshihiro; Nishikawa, Kyohei; Sameshima, Soichiro; Sodeyama, Kenichi; Masunaga, Takuro; Yoshimura, Yukio

    2018-03-13

    A zeolite (mordenite)-pore-phenol resin composite and a zeolite-pore-shirasu glass composite were fabricated by hot-pressing. Their thermal conductivities were measured by a laser flash method to determine the thermal conductivity of the monolithic zeolite with the proposed mixing rule. The analysis using composites is useful for a zeolite powder with no sinterability to clarify its thermal properties. At a low porosity thermal conductivity of the composite was in excellent agreement with the calculated value for the structure with phenol resin or shirasu glass continuous phase. At a higher porosity above 40%, the measured value approached the calculated value for the structure with pore continuous phase. The thermal conductivity of the monolithic mordenite was evaluated to be 3.63 W/mK and 1.70-2.07 W/mK at room temperature for the zeolite-pore-phenol resin composite and the zeolite-pore-shirasu glass composite, respectively. The analyzed thermal conductivities of monolithic mordenite showed a minimum value of 1.23 W/mK at 400 °C and increased to 2.51 W/mK at 800 °C.

  14. Properties of glass-bonded zeolite monoliths

    International Nuclear Information System (INIS)

    Lewis, M.A.; Fischer, D.F.; Murphy, C.D.

    1994-01-01

    It has been shown that mineral waste forms can be used to immobilize waste salt generated during the pyrochemical processing of spent fuel from the Integral Fast Reactor (IFR). Solid, leach resistant monoliths were formed by hot-pressing mixtures of salt-occluded zeolite A powders and glass frit at 990 K and 28 MPa. Additional samples have now been fabricated and tested. Normalized release rates for all elements, including iodide and chloride, were less than 1 g/m 2 d in 28-day tests in deionized water and in brine at 363 K (90 degrees C). Preliminary results indicate that these rates fall with time with both leachants and that the zeolite phase in the glass-bonded zeolite does not function as an ion exchanger. Some material properties were measured. The Poisson ratio and Young's modulus were slightly smaller in glass-bonded zeolite than in borosilicate glass. Density depended on zeolite fraction. The glass-bonded zeolite represents a promising mineral waste form for IFR salt

  15. Powder Diffraction in Zeolite Science

    Science.gov (United States)

    Burton, Allen W.

    This tutorial discusses the fundamental principles of X-ray diffraction and its applications in zeolite science. The early sections review the physics of diffraction, crystal symmetry, and reciprocal space. We discuss how the intensity of diffracted radiation is affected both by geometric effects involving detection (the Lorentz-polarization factor) and by the arrangement of atoms within the crystal (the structure factor). The differences between powder diffraction and single-crystal diffraction are then described, and differences between X-ray and neutron diffraction are also discussed. Later sections describe the effects of symmetry, lattice substitution, crystallite size, residual strain, preferred orientation, and X-ray absorption. Special emphasis is placed on the proper application of the Scherrer analysis in reporting crystalize size. The principles of structure solution from direct methods and Patterson methods are then introduced, and a description of Rietveld analysis is given. Finally the effects of stacking disorder on a powder diffraction pattern are presented.

  16. Salt-occluded zeolite waste forms: Crystal structures and transformability

    International Nuclear Information System (INIS)

    Richardson, J.W. Jr.

    1996-01-01

    Neutron diffraction studies of salt-occluded zeolite and zeolite/glass composite samples, simulating nuclear waste forms loaded with fission products, have revealed complex structures, with cations assuming the dual roles of charge compensation and occlusion (cluster formation). These clusters roughly fill the 6--8 angstrom diameter pores of the zeolites. Samples are prepared by equilibrating zeolite-A with complex molten Li, K, Cs, Sr, Ba, Y chloride salts, with compositions representative of anticipated waste systems. Samples prepared using zeolite 4A (which contains exclusively sodium cations) as starting material are observed to transform to sodalite, a denser aluminosilicate framework structure, while those prepared using zeolite 5A (sodium and calcium ions) more readily retain the zeolite-A structure. Because the sodalite framework pores are much smaller than those of zeolite-A, clusters are smaller and more rigorously confined, with a correspondingly lower capacity for waste containment. Details of the sodalite structures resulting from transformation of zeolite-A depend upon the precise composition of the original mixture. The enhanced resistance of salt-occluded zeolites prepared from zeolite 5A to sodalite transformation is thought to be related to differences in the complex chloride clusters present in these zeolite mixtures. Data relating processing conditions to resulting zeolite composition and structure can be used in the selection of processing parameters which lead to optimal waste forms

  17. Germanosilicate UTL and its rich chemistry of solid-statetransformations towards IPC-2 (OKO) zeolite

    Czech Academy of Sciences Publication Activity Database

    Mazur, Michal; Kubů, Martin; Wheatley, P. S.; Eliášová, Pavla

    2015-01-01

    Roč. 243, APR 2015 (2015), s. 23-31 ISSN 0920-5861 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : ADOR * zeolite UTL * IPC-2 Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.312, year: 2015

  18. Modification of textural and acidic properties of -SVR zeolite by desilication

    Czech Academy of Sciences Publication Activity Database

    Kubů, Martin; Opanasenko, Maksym; Shamzhy, Mariya

    2014-01-01

    Roč. 227, MAY 2014 (2014), s. 26-32 ISSN 0920-5861 R&D Projects: GA ČR GP13-17593P Institutional support: RVO:61388955 Keywords : -SVR zeolite * desilication * hierarchical materials Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.893, year: 2014

  19. Transformation of aromatic hydrocarbons over isomorphously substituted UTL: Comparison with large and medium pore zeolites

    Czech Academy of Sciences Publication Activity Database

    Žilková, Naděžda; Shamzhy, Mariya; Shvets, O. V.; Čejka, Jiří

    2013-01-01

    Roč. 204, APR 2013 (2013), s. 22-29 ISSN 0920-5861 R&D Projects: GA ČR(CZ) GAP106/12/0189 Institutional support: RVO:61388955 Keywords : UTL zeolite * Isomorphous substitution * Toluene alkylation with isopropyl alcohol Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.309, year: 2013

  20. Assembly-Disassembly-Organization-Reassembly Synthesis of Zeolites Based on cfi-Type Layers

    Czech Academy of Sciences Publication Activity Database

    Firth, D. S.; Morris, S. A.; Wheatley, P. S.; Russell, S. E.; Slawin, A. M. Z.; Dawson, D. M.; Mayoral, A.; Opanasenko, Maksym; Položij, M.; Čejka, Jiří; Nachtigall, P.; Morris, R. E.

    2017-01-01

    Roč. 29, č. 13 (2017), s. 5605-5611 ISSN 0897-4756 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : large-pore zeolite * hydrothermal synthesis * preferential location Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry Impact factor: 9.466, year: 2016

  1. From Double-Four-Ring Germanosilicates to New Zeolites: In Silico Investigation

    Czech Academy of Sciences Publication Activity Database

    Trachta, Michal; Bludský, Ota; Čejka, Jiří; Morris, R. E.; Nachtigall, P.

    2014-01-01

    Roč. 15, č. 14 (2014), s. 2972-2976 ISSN 1439-4235 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388963 ; RVO:61388955 Keywords : density functional calculations * in silico studies * structure * synthesis * zeolites Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.419, year: 2014

  2. Combined PDF and Rietveld studies of ADORable zeolites and the disordered intermediate IPC-1P

    Czech Academy of Sciences Publication Activity Database

    Morris, S. A.; Wheatley, P. S.; Položij, M.; Nachtigall, P.; Eliášová, Pavla; Čejka, Jiří; Lucas, T. C.; Hriljac, J. A.; Pinar, A. B.; Morris, R. E.

    2016-01-01

    Roč. 45, č. 36 (2016), s. 14124-14130 ISSN 1477-9226 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : Distribution functions * Rietveld refinement * Zeolites Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.029, year: 2016

  3. Desilication of SSZ-33 zeolite – Post-synthesis modification of textural and acidic properties

    Czech Academy of Sciences Publication Activity Database

    Kubů, Martin; Opanasenko, Maksym; Vitvarová, Dana

    2015-01-01

    Roč. 243, APR 2015 (2015), s. 46-52 ISSN 0920-5861 R&D Projects: GA ČR GP13-17593P Institutional support: RVO:61388955 Keywords : SSZ-33 zeolite * desilication * hierarchical materials Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.312, year: 2015

  4. High-resolution adsorption analysis of pillared zeolites IPC-3PI and MCM-36

    Czech Academy of Sciences Publication Activity Database

    Zukal, Arnošt; Kubů, Martin

    2014-01-01

    Roč. 43, č. 27 (2014), s. 10558-10565 ISSN 1477-9226 R&D Projects: GA ČR GP13-17593P Institutional support: RVO:61388955 Keywords : zeolites * adsorption * microporosity Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.197, year: 2014

  5. Adsorption of Carbon Dioxide on Sodium and Potassium Forms of STI Zeolite

    Czech Academy of Sciences Publication Activity Database

    Zukal, Arnošt; Zones, S. I.; Kubů, Martin; Davis, T. M.; Čejka, Jiří

    2012-01-01

    Roč. 77, č. 8 (2012), s. 675-681 ISSN 2192-6506 R&D Projects: GA ČR GA203/08/0604 Institutional support: RVO:61388955 Keywords : adsorption * carbon dioxide * zeolites Subject RIV: CF - Physical ; Theoretical Chemistry

  6. Aldol condensation of furfural with acetone over ion-exchanged and impregnated potassium BEA zeolites

    Czech Academy of Sciences Publication Activity Database

    Kikhtyanin, O.; Bulánek, R.; Frolich, K.; Čejka, Jiří; Kubička, D.

    2016-01-01

    Roč. 424, DEC 2016 (2016), s. 358-368 ISSN 1381-1169 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : activated hydrotalcites * carbon-monoxide * cyclic-ketones * Acetone * Furfural * Condensation * Potassium-BEA * Zeolite Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.211, year: 2016

  7. The effect of UTL layer connectivity in isoreticular zeolites on the catalytic performance in toluene alkylation

    Czech Academy of Sciences Publication Activity Database

    Žilková, Naděžda; Eliášová, Pavla; Al-Khattaf, S.; Morris, R. E.; Mazur, Michal; Čejka, Jiří

    2016-01-01

    Roč. 277, č. 1 (2016), s. 55-60 ISSN 0920-5861 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : UTL * ADOR zeolites * PCR Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.636, year: 2016

  8. Ru complexes of Hoveyda–Grubbs type immobilized on lamellar zeolites: activity in olefin metathesis reactions

    Czech Academy of Sciences Publication Activity Database

    Balcar, Hynek; Žilková, Naděžda; Kubů, Martin; Mazur, Michal; Bastl, Zdeněk; Čejka, Jiří

    2015-01-01

    Roč. 11, NOV 2015 (2015), s. 2087-2096 ISSN 1860-5397 Institutional support: RVO:61388955 Keywords : Hoveyda-Grubbs type catalyst * hybrid catalysts * lamellar zeolites Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.697, year: 2015

  9. Transformation of analcime into IMF structure during the synthesis of IMF zeolite

    Czech Academy of Sciences Publication Activity Database

    Kubů, Martin; Přech, Jan

    2015-01-01

    Roč. 206, APR 2015 (2015), s. 121-126 ISSN 1387-1811 R&D Projects: GA ČR GP13-17593P Institutional support: RVO:61388955 Keywords : IMF zeolite * analcime * crystallization Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.349, year: 2015

  10. Transformation of analcime into IMF structure during the synthesis of IMF zeolite

    Czech Academy of Sciences Publication Activity Database

    Kubů, Martin; Přech, Jan

    2015-01-01

    Roč. 206, C (2015), s. 121-126 ISSN 1387-1811 R&D Projects: GA ČR GP13-17593P Institutional support: RVO:61388955 Keywords : Analcime * Crystallization * IMF zeolite Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.349, year: 2015

  11. Mechanism of Framework Oxygen Exchange in Fe-Zeolites: A Combined DFT and Mass Spectrometry Study

    Czech Academy of Sciences Publication Activity Database

    Andrikopoulos, Prokopis C.; Sobalík, Zdeněk; Nováková, Jana; Sazama, Petr; Sklenák, Štěpán

    2013-01-01

    Roč. 14, č. 3 (2013), s. 520-531 ISSN 1439-4235 R&D Projects: GA AV ČR IAA400400812; GA ČR GA203/09/1627 Institutional support: RVO:61388955 Keywords : density functional theory * iron * zeolites Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.360, year: 2013

  12. Synthesis of Zeolites Using the ADOR (Assembly-Disassembly-Organization-Reassembly) Route

    Czech Academy of Sciences Publication Activity Database

    Wheatley, P. S.; Čejka, Jiří; Morris, R. E.

    2016-01-01

    Roč. 2016, č. 110 (2016), č. článku e53463. ISSN 1940 -087X R&D Projects: GA ČR GBP106/12/G015 EU Projects: European Commission(XE) 604307 - CASCATBEL Institutional support: RVO:61388955 Keywords : Chemistry * zeolites * synthesis * ADOR mechanism Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 1.232, year: 2016

  13. Synthesis and catalytic properties of titanium containing extra-large pore zeolite CIT-5

    Czech Academy of Sciences Publication Activity Database

    Přech, Jan; Kubů, Martin; Čejka, Jiří

    2014-01-01

    Roč. 227, MAY 2014 (2014), s. 80-86 ISSN 0920-5861 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : zeolite CIT-5 * titanosilicate * epoxidation Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.893, year: 2014

  14. Three-dimensional 10-ring zeolites: The activities in toluene alkylation and disproportionation

    Czech Academy of Sciences Publication Activity Database

    Kubů, Martin; Žilková, Naděžda; Zones, S. I.; Chen, C.-Y.; Al-Khattaf, S.; Čejka, Jiří

    2016-01-01

    Roč. 259, JAN 2016 (2016), s. 97-106 ISSN 0920-5861 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : 10-ring zeolites * TUN * IMF Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.636, year: 2016

  15. Catalytic behavior of metal-organic frameworks and zeolites: Rationalization and comparative analysis

    Czech Academy of Sciences Publication Activity Database

    Opanasenko, Maksym

    2015-01-01

    Roč. 243, APR 2015 (2015), s. 2-9 ISSN 0920-5861 R&D Projects: GA ČR GA14-07101S Institutional support: RVO:61388955 Keywords : Metal - organic frameworks * Zeolites * heterogeneous catalysis Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.312, year: 2015

  16. Selective synthesis of linear alkylbenzene by alkylation of benzene with 1-dodecene over desilicated zeolites

    Czech Academy of Sciences Publication Activity Database

    Aslam, W.; Siddiqui, M. A. B.; Jermy, B. R.; Aitani, A.; Čejka, Jiří; Al-Khattaf, S.

    2014-01-01

    Roč. 227, MAY 2014 (2014), s. 187-197 ISSN 0920-5861 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : zeolites * benzene alkylation * long-chain olefin Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.893, year: 2014

  17. Methylene blue removal from contaminated waters using O3, natural zeolite, and O3/zeolite.

    Science.gov (United States)

    Valdés, H; Tardón, R F; Zaror, C A

    2009-01-01

    This paper compares experimental results on methylene blue (MB) removal systems based on ozone oxidation, zeolite adsorption, and simultaneous adsorption-oxidation using ozone in the presence of natural zeolite. The effect of pH (2-8), and the presence of radical scavengers (sodium acetate) on process rates and removal efficiencies are assessed at laboratory scale. The experimental system consisted of a 1 L differential circular flow reactor and an ozone generator rated at 5 g O3/h. Results show that ozone oxidation combined with zeolite adsorption increases the overall MB oxidation rate with respect to ozonation process and zeolite adsorption. In presence of free radical scavenger, only a 25% of reduction on MB removal rate are observed in the simultaneous treatment, as compared with 70% when ozonation treatment is used, suggesting that MB oxidation reactions take mainly place on the zeolite surface.

  18. Limestone and Zeolite as Alternative Media in Horizontal Subsurface Flow Constructed Wetlands: Laboratory-Scale Studies

    Science.gov (United States)

    Lizama, K.; Jaque, I.; Ayala, J.

    2016-12-01

    Arsenic is well known for its chronic toxicity. Millions of people around the world are currently at risk, drinking water with As concentrations above 10 ppb, the WHO drinking water guideline. Although different treatment options exist, they are often limited by elevated costs and maintenance requirements. Constructed wetlands are a natural water treatment system, capable to remove metals and metalloids -including As- via different physical, chemical and biological processes. The use of alternative supporting media to enhance As removal in subsurface flow wetlands has been recommended, but not sufficiently studied. Limestone and zeolite have been identified as effective supporting media in subsurface flow wetlands aiming As removal. However, there are still key aspects to be addressed, such as the implications of using these media, the speciation in the solid phase, the role of vegetation, etc. This study investigated the performance of limestone and zeolite in three types of experiments: batch, column and as main supporting media in a bench scale horizontal subsurface flow wetland system. Synthetic water resembling a contaminated river in Chile (As concentration=3 mg/L, Fe concentration= 100 mg/L, pH=2) was used in all experiments. In the batch experiments, the As concentration, the mass of media and the contact time were varied. The column system consisted of three limestone columns and three zeolite columns, operated under a hydraulic loading of 20 mm/d. The wetland system consisted of twelve PVC cells: six filled with zeolite and six with limestone. Phragmites australis were planted in three cells of each media type, as control cells. From the batch experiments, maximum As sorption capacities as indicated by Langmuir model were 1.3 mg/g for limestone and 0.17 mg/g for zeolite, at 18 h contact time and 6.3 g/L medium concentration. EDS and XPS analyses revealed that As and Fe were retained in zeolite at the end of the batch experiments. Zeolite and limestone

  19. Nanocrystalline zeolite beta and zeolite Y as catalysts in used palm oil cracking for the production of biofuel

    Science.gov (United States)

    Taufiqurrahmi, Niken; Mohamed, Abdul Rahman; Bhatia, Subhash

    2011-08-01

    Nanocrystalline zeolites with crystal size smaller than 100 nm are potential replacement for conventional zeolite catalysts due to their unique characteristics and advantages. In this study, the synthesis of nanocrystalline zeolite Y (FAU) and nanocrystalline zeolite beta (BEA) under hydrothermal conditions is reported. The effect of crystal size on the physico-chemical characteristics of the zeolite, Y (FAU), and beta (BEA) is reported. The properties of nanocrystalline zeolites Y and Beta with crystal size around 50 nm are compared with the microcrystalline zeolite Y and microcrystalline zeolite beta, respectively. The performance of the nanocrystalline zeolite as a catalyst was investigated in the cracking of used palm oil for the production of biofuel. The nanocrystalline zeolite catalytic activity was compared with the activity of microcrystalline zeolite in order to study the effect of crystal size on the catalytic activity. Both nanocrystalline zeolites gave better performance in terms of conversion of used palm oil as well as selectivity for the formation of gasoline fraction. The increase in surface area and improved accessibility of the reactant in nanocrystalline zeolites enhanced the cracking activity as well as the desired product selectivity.

  20. Cultivation of Chlorella vulgaris and Arthrospira platensis with Recovered Phosphorus from Wastewater by Means of Zeolite Sorption

    Directory of Open Access Journals (Sweden)

    Giorgos Markou

    2015-02-01

    Full Text Available In this study, zeolite was employed for the separation and recovery of P from synthetic wastewater and its use as phosphorus (P source for the cultivation of the green microalga Chlorella vulgaris and the cyanobacterium Arthrospira (Spirulina platensis. At P-loaded zeolite concentration of 0.15–1 g/L, in which P was limited, the two species displayed quite different behavior regarding their growth and biomass composition. C. vulgaris preferred to increase the intracellular P and did not synthesize biomass, while A. platensis synthesized biomass keeping the intracellular P as low as possible. In addition under P limitation, C. vulgaris did display some little alteration of the biomass composition, while A. platensis did it significantly, accumulating carbohydrates around 70% from about 15%–20% (control. Both species could desorb P from zeolite biologically. A. platensis could recover over 65% and C. vulgaris 25% of the P bounded onto zeolite. When P-loaded zeolite concentration increased to 5 g/L, P was adequate to support growth for both species. Especially in the case of C. vulgaris, growth was stimulated from the presence of P-loaded zeolite and produced more biomass compared to the control.

  1. Cultivation of Chlorella vulgaris and Arthrospira platensis with Recovered Phosphorus from Wastewater by Means of Zeolite Sorption

    Science.gov (United States)

    Markou, Giorgos; Depraetere, Orily; Vandamme, Dries; Muylaert, Koenraad

    2015-01-01

    In this study, zeolite was employed for the separation and recovery of P from synthetic wastewater and its use as phosphorus (P) source for the cultivation of the green microalga Chlorella vulgaris and the cyanobacterium Arthrospira (Spirulina) platensis. At P-loaded zeolite concentration of 0.15–1 g/L, in which P was limited, the two species displayed quite different behavior regarding their growth and biomass composition. C. vulgaris preferred to increase the intracellular P and did not synthesize biomass, while A. platensis synthesized biomass keeping the intracellular P as low as possible. In addition under P limitation, C. vulgaris did display some little alteration of the biomass composition, while A. platensis did it significantly, accumulating carbohydrates around 70% from about 15%–20% (control). Both species could desorb P from zeolite biologically. A. platensis could recover over 65% and C. vulgaris 25% of the P bounded onto zeolite. When P-loaded zeolite concentration increased to 5 g/L, P was adequate to support growth for both species. Especially in the case of C. vulgaris, growth was stimulated from the presence of P-loaded zeolite and produced more biomass compared to the control. PMID:25690037

  2. Zeolite Membranes: Ozone Detemplation, Modeling, and Performance Characterization

    OpenAIRE

    Kuhn, J.

    2009-01-01

    Membrane technology plays an increasingly important role in developing a more sustainable process industry. Zeolites are a novel class of membrane materials with unique properties enabling molecular sieving and affinity based separations. This thesis proposes some new concepts in zeolite membrane synthesis, application, and modeling. The influence of zeolite polarity is assessed and the use of a hydrophobic zeolite membrane for water separation is explored. Ozonication, a novel method for zeo...

  3. Polyphosphates substitution for zeolite to in detergents

    International Nuclear Information System (INIS)

    Restrepo V, Gloria M.; Ocampo G, Aquiles; Saldarriaga M, Carlos

    1996-01-01

    The detergents, as well as the cleaning products, contain active ingredients that are good to increase their efficiency and some of them, as the sodium Tripoli-phosphate (TPF), they have turned out to be noxious for the environment. The zeolites use in the formulation of detergents has grown substantially since they fulfill the same function of the TPF and they have been recommended ecologically as substitutes from these when not being polluting. The objective of this work is to obtain a zeolite with appropriate characteristics for its use in the formulation of detergents, reproducing those of the zeolites used industrially. The zeolite synthesis is studied 4A starting from hydro-gels of different composition, varying the operation conditions and using two raw materials: (sodium meta-silicate, commercial degree and metallic aluminum) and clay type kaolin like silica source and aluminum It is looked for to get a product of beveled cubic morphology, or spherical, with glass size between 1 and 3 microns and that it possesses good capacity of conical exchange. Since the capacity and speed of ionic exchange is influenced by the particle size, time of contact and temperature, experimentation conditions settle down to measure the exchange of ions calcium and magnesium in watery solutions that they simulate the real situation of a laundry process in the country. This way the ability of the zeolite 4A obtained to diminish the concentration of these ions in the laundry waters is evaluated and its possibilities like component in the formulation of detergents non-phosphatates. Of the synthesized zeolites, the best in agreement is chosen with chemical properties as ionic and physical exchange capacity as crystalline, particle size and color, to prepare a detergent in which the polyphosphates is substituted partial and totally for the synthesized zeolite

  4. Molecular Simulation of Adsorption in Zeolites

    Science.gov (United States)

    Bai, Peng

    Zeolites are a class of crystalline nanoporous materials that are widely used as catalysts, sorbents, and ion-exchangers. Zeolites have revolutionized the petroleum industry and have fueled the 20th-century automobile culture, by enabling numerous highly-efficient transformations and separations in oil refineries. They are also posed to play an important role in many processes of biomass conversion. One of the fundamental principles in the field of zeolites involves the understanding and tuning of the selectivity for different guest molecules that results from the wide variety of pore architectures. The primary goal of my dissertation research is to gain such understanding via computer simulations and eventually to reach the level of predictive modeling. The dissertation starts with a brief introduction of the applications of zeolites and computer modeling techniques useful for the study of zeolitic systems. Chapter 2 then describes an effort to improve simulation efficiency, which is essential for many challenging adsorption systems. Chapter 3 studies a model system to demonstrate the applicability and capability of the method used for the majority of this work, configurational-bias Monte Carlo simulations in the Gibbs ensemble (CBMC-GE). After these methodological developments, Chapter 4 and 5 report a systematic parametrization of a new transferable force field for all-silica zeolites, TraPPE-zeo, and a subsequent, relatively ad-hoc extension to cation-exchanged aluminosilicates. The CBMC-GE method and the TraPPE-zeo force field are then combined to investigate some complex adsorption systems, such as linear and branched C6-C 9 alkanes in a hierarchical microporous/mesoporous material (Chapter 6), the multi-component adsorption of aqueous alcohol solutions (Chapter 7) and glucose solutions (Chapter 8). Finally, Chapter 9 describes an endeavor to screen a large number of zeolites with the purpose of finding better materials for two energy-related applications

  5. Selective methane chlorination to methyl chloride by zeolite Y-based catalysts

    Science.gov (United States)

    Joo, Hyeonho; Kim, Daeho; Lim, Kwang Soo; Choi, Yong Nam; Na, Kyungsu

    2018-03-01

    The CH4 chlorination over Y zeolites was investigated to produce CH3Cl in a high yield. Three different catalytic systems based on Y zeolite were tested for enhancement of CH4 conversion and CH3Cl selectivity: (i) HY zeolites in H+-form having various Si/Al ratios, (ii) Pt/HY zeolites supporting Pt metal nanoparticles, (iii) Pt/NaY zeolites in Na+-form supporting Pt metal nanoparticles. The reaction was carried out using the gas mixture of CH4 and Cl2 with the respective flow rates of 15 and 10 mL min-1 at 300-350 °C using a fixed-bed reactor under a continuous gas flow condition (gas hourly space velocity = 3000 mL g-1 h-1). Above the reaction temperature of 300 °C, the CH4 chlorination is spontaneous even in the absence of catalyst, achieving 23.6% of CH4 conversion with 73.4% of CH3Cl selectivity. Under sufficient supplement of thermal energy, Cl2 molecules can be dissociated to two chlorine radicals, which triggered the C-H bond activation of CH4 molecule and thereby various chlorinated methane products (i.e., CH3Cl, CH2Cl2, CHCl3, CCl4) could be produced. When the catalysts were used under the same reaction condition, enhancement in the CH4 conversion was observed. The Pt-free HY zeolite series with varied Si/Al ratios gave around 27% of CH4 conversion, but there was a slight decrease in CH3Cl selectivity with about 64%. Despite the difference in acidity of HY zeolites having different Si/Al ratios, no prominent effect of the Si/Al ratios on the catalytic performance was observed. This suggests that the catalytic contribution of HY zeolites under the present reaction condition is not strong enough to overcome the spontaneous CH4 chlorination. When the Pt/HY zeolite catalysts were used, the CH4 conversion reached further up to 30% but the CH3Cl selectivity decreased to 60%. Such an enhancement of CH4 conversion could be attributed to the strong catalytic activity of HY and Pt/HY zeolite catalysts. However, both catalysts induced the radical cleavage of Cl2

  6. Effect of micronized zeolite addition to lamb concentrate feeds on ...

    African Journals Online (AJOL)

    OEM

    2016-09-21

    Sep 21, 2016 ... Natural zeolites are utilized in a number of industries such as pollution control ... the impact of zeolites on milk quality, an addition of 2.5% of clinoptilolite (zeolite) to goat feeds was demonstrated to ... triglyceride, calcium and phosphorus was carried out with spectrophotometry, and the tests for sodium,.

  7. Zeolites and Zeotypes for Oil and Gas Conversion

    NARCIS (Netherlands)

    Vogt, Eelco T C; Whiting, Gareth T.; Dutta Chowdhury, Abhishek; Weckhuysen, Bert M.

    2015-01-01

    Zeolite-based catalyst materials are widely used in chemical industry. In this chapter, the applications of zeolites and zeotypes in the catalytic conversion of oil and gas are reviewed. After a general introduction to zeolite science and technology, we discuss refinery applications, such as fluid

  8. defluorination of drinking water using surfactant modified zeolites

    African Journals Online (AJOL)

    PUBLICATIONS1

    The unmodified zeolite NaLSX was incapable of adsorbing fluoride ions but the surfactant modified zeolite adsorbed fluoride. The fluoride adsorption capacity of the modified zeolite was. pH dependent and peaked at pH 6.0 – 7.0. INTRODUCTION. Groundwater is often presumed to be fairly safe for consumption compared ...

  9. Influencing the selectivity of zeolite Y for triglycine adsorption

    NARCIS (Netherlands)

    Wijntje, R.; Bosch, H.; Haan, A.B. de; Bussmann, P.J.T.

    2007-01-01

    In prior work we studied the adsorption of triglycine on zeolite Y under reference conditions. This study aims to solve the question of which adsorbent properties and process conditions influence the adsorption triglycine from an aqueous solution by zeolite Y. Relevant zeolite parameters to study

  10. Antimicrobial and mechanical properties of acrylic resins with incorporated silver-zinc zeolite - part I.

    Science.gov (United States)

    Casemiro, Luciana Assirati; Gomes Martins, Carlos Henrique; Pires-de-Souza, Fernanda de Carvalho Panzeri; Panzeri, Heitor

    2008-09-01

    The purpose of this in vitro study was to evaluate the antimicrobial activity of acrylic resins containing different percentages of silver and zinc zeolite, and to assess whether the addition of zeolite alters the flexural and impact strength of the resins. The characteristics of acrylic resins support microorganism development that can threaten the health of the dentures user. A microwave-polymerised (Onda-Cryl) and two heat-polymerised (QC20 and Lucitone 550) acrylic resins were used. The materials were handled according to the manufacturers' instructions. Fifty rectangular-shaped specimens (8 x 10 x 4mm) were fabricated from each resin and assigned to 5 groups (n = 10) according to their percentage of Irgaguard B5000 silver-zinc zeolite (0%- control, 2.5%, 5.0%, 7.5% and 10%). Flexural strength and Izod impact strength were evaluated. The antimicrobial activity against two strains of Candida albicans and two strains of Streptococcus mutans was assessed by agar diffusion method. Data were analysed statistically by one-way anova and Tukey's test at 5% significance level. The addition of 2.5% of Irgaguard B5000 to the materials resulted in antimicrobial activity against all strains. Flexural strength decreased significantly with the addition of 2.5% (QC20 and Lucitone 550) and 5.0% (Onda-Cryl) of Irgaguard B5000. The impact strength decreased significantly with the addition of 2.5% (Lucitone 550) and 5.0% (QC20 and Onda-Cryl) of zeolite. The addition of silver-zinc zeolite to acrylic resins yields antimicrobial activity, but may affect negatively the mechanical properties, depending on the percentage of zeolite.

  11. Molecular simulations and experimental studies of zeolites

    Science.gov (United States)

    Moloy, Eric C.

    Zeolites are microporous aluminosilicate tetrahedral framework materials that have symmetric cages and channels with open-diameters between 0.2 and 2.0 nm. Zeolites are used extensively in the petrochemical industries for both their microporosity and their catalytic properties. The role of water is paramount to the formation, structure, and stability of these materials. Zeolites frequently have extra-framework cations, and as a result, are important ion-exchange materials. Zeolites also play important roles as molecular sieves and catalysts. For all that is known about zeolites, much remains a mystery. How, for example, can the well established metastability of these structures be explained? What is the role of water with respect to the formation, stabilization, and dynamical properties? This dissertation addresses these questions mainly from a modeling perspective, but also with some experimental work as well. The first discussion addresses a special class of zeolites: pure-silica zeolites. Experimental enthalpy of formation data are combined with molecular modeling to address zeolitic metastability. Molecular modeling is used to calculate internal surface areas, and a linear relationship between formation enthalpy and internal surface areas is clearly established, producing an internal surface energy of approximately 93 mJ/m2. Nitrate bearing sodalite and cancrinite have formed under the caustic chemical conditions of some nuclear waste processing centers in the United States. These phases have fouled expensive process equipment, and are the primary constituents of the resilient heels in the bottom of storage tanks. Molecular modeling, including molecular mechanics, molecular dynamics, and density functional theory, is used to simulate these materials with respect to structure and dynamical properties. Some new, very interesting results are extracted from the simulation of anhydrous Na6[Si6Al 6O24] sodalite---most importantly, the identification of two distinct

  12. Characterization of Zeolite in Zeolite-Geopolymer Hybrid Bulk Materials Derived from Kaolinitic Clays.

    Science.gov (United States)

    Takeda, Hayami; Hashimoto, Shinobu; Yokoyama, Hiroaki; Honda, Sawao; Iwamoto, Yuji

    2013-05-06

    Zeolite-geopolymer hybrid materials have been formed when kaolin was used as a starting material. Their characteristics are of interest because they can have a wide pore size distribution with micro- and meso-pores due to the zeolite and geopolymer, respectively. In this study, Zeolite-geopolymer hybrid bulk materials were fabricated using four kinds of kaolinitic clays (a halloysite and three kinds of kaolinite). The kaolinitic clays were first calcined at 700 °C for 3 h to transform into the amorphous aluminosilicate phases. Alkali-activation treatment of the metakaolin yielded bulk materials with different amounts and types of zeolite and different compressive strength. This study investigated the effects of the initial kaolinitic clays on the amount and types of zeolite in the resultant geopolymers as well as the strength of the bulk materials. The kaolinitic clays and their metakaolin were characterized by XRD analysis, chemical composition, crystallite size, 29 Si and 27 Al MAS NMR analysis, and specific surface area measurements. The correlation between the amount of zeolite formed and the compressive strength of the resultant hybrid bulk materials, previously reported by other researchers was not positively observed. In the studied systems, the effects of Si/Al and crystalline size were observed. When the atomic ratio of Si/Al in the starting kaolinitic clays increased, the compressive strength of the hybrid bulk materials increased. The crystallite size of the zeolite in the hybrid bulk materials increased with decreasing compressive strength of the hybrid bulk materials.

  13. Effect of zeolites on chitosan/zeolite hybrid membranes for direct methanol fuel cell

    Science.gov (United States)

    Wang, Jingtao; Zheng, Xiaohong; Wu, Hong; Zheng, Bin; Jiang, Zhongyi; Hao, Xiaopeng; Wang, Baoyi

    Zeolites including 3A, 4A, 5A, 13X, mordenite, and HZSM-5 were incorporated into chitosan (CS) matrix to fabricate the hybrid membranes for direct methanol fuel cell (DMFC). Due to the presence of hydrogen bonds between CS and zeolite, the hybrid membranes displayed desirable thermal and mechanical stabilities. Through free volume characteristics analysis by positron annihilation lifetime spectroscopy (PALS) technique, it was found that incorporation of hydrophilic zeolites would increase the free volume cavity size whereas incorporation of hydrophobic zeolites would decrease the free volume cavity size. Through the investigations on water/methanol uptake, swelling, and methanol permeability, it was found that the membrane performance was highly dependent on the zeolite particle and pore size, content, and hydrophilic/hydrophobic nature. Based on the solution-diffusion mechanism, it was found that incorporation of hydrophobic zeolites increased the diffusion resistance of methanol and consequently decreased the methanol permeability, whereas incorporation of hydrophilic zeolites decreased the diffusion resistance of methanol and consequently increased the methanol permeability. Moreover, under the identical conditions, all the as-prepared membranes exhibited much lower methanol permeability than Nafion ® 117 while the proton conductivity of the membranes remained high enough for DMFC applications.

  14. Environmental application of modified natural zeolites

    International Nuclear Information System (INIS)

    Nikashina, V.A.; Myasoedov, B.F.

    1998-01-01

    The following techniques were used for the chemical modification of the natural zeolites: (1) treatment of natural zeolites with organic substances. Examples of applications of these sorbents to the decontamination and disinfection of solutions of different composition and surface waters are presented. (2) Treatment of the natural zeolites with a inorganic substances. (2.1) The clinoptilolite-rich tuffs were treated with a hot suspensions of freshly precipitated magnetite. This leads to the preparation of sorbents possessing magnetic properties. The radionuclides and heavy metals recovery from soils and silts was investigated using different soil and ferromagnetic zeolite weights ratios and contact times. Different soils and sorbent of varying capacities were used for these investigations. As example, the recovery 137 Cs and 85 Sr from soils of different nature is presented. (2.2) Treatment of natural zeolites with Fe-containing solutions of Fe-containing natural waters. The filtration of these solutions through clinoptilolite-rich tuffs makes leads to preparation of materials possessing high selectivity to PO 4 3- ions. The properties of these sorbents can be utilized for the PO 4 3+ decontamination of waters (e.g. waste waters) and for the subsequent use of these materials in agriculture as fertilizers.(author)

  15. Synthesis and Characterization of Zeolite Na−Y and Its Conversion to the Solid Acid Zeolite H−Y

    DEFF Research Database (Denmark)

    Warner, Terence Edwin; Galsgaard Klokker, Mads; Nielsen, Ulla Gro

    2017-01-01

    various preparative strategies with the students, such as the three-stage procedure described here. Stage I concerns the hydrothermal synthesis of zeolite Na−Y, followed by ion-exchange with an ammonium acetate solution to form zeolite NH4−Y, and the latter is subsequently converted to zeolite H...

  16. Modificação de zeólitas para uso em catálise Modifying zeolites for use in catalysis

    Directory of Open Access Journals (Sweden)

    Fernando J. Luna

    2001-12-01

    Full Text Available The use of zeolites and other molecular sieves as catalysts is discussed at an introductory level. The text includes a brief historic background on the use of zeolites in catalysis, and a discussion of some chemical and physical properties of silicalite, aluminosilicate, and aluminophosphate molecular sieves. The strategies currently used to chemically modify zeolites and related materials to produce catalysts with increased activity and selectivity are discussed, including the use of redox molecular sieves for hydrocarbon oxidation and the leaching of the active metals from the support.

  17. Treating Coalbed Natural Gas Produced Water for Beneficial Use By MFI Zeolite Membranes

    Energy Technology Data Exchange (ETDEWEB)

    Robert Lee; Liangxiong Li

    2008-03-31

    the membranes and optimize operating conditions to enhance water flux and ion rejection, and (3) to perform long-term RO operation on tubular membranes to study membrane stability and to collect experimental data necessary for reliable evaluations of technical and economic feasibilities. Our completed research has resulted in deep understanding of the ion and organic separation mechanism by zeolite membranes. A two-step hydrothermal crystallization process resulted in a highly efficient membrane with good reproducibility. The zeolite membranes synthesized therein has an overall surface area of {approx}0.3 m{sup 2}. Multichannel vessels were designed and machined for holding the tubular zeolite membrane for water purification. A zeolite membrane RO demonstration with zeolite membranes fabricated on commercial alpha-alumina support was established in the laboratory. Good test results were obtained for both actual produced water samples and simulated samples. An overall 96.9% ion rejection and 2.23 kg/m{sup 2}.h water flux was achieved in the demonstration. In addition, a post-synthesis modification method using Al{sup 3+}-oligomers was developed for repairing the undesirable nano-scale intercrystalline pores. Considerable enhancement in ion rejection was achieved. This new method of zeolite membrane modification is particularly useful for enhancing the efficiency of ion separation from aqueous solutions because the modification does not need high temperature operation and may be carried out online during the RO operation. A long-term separation test for actual CBM produced water has indicated that the zeolite membranes show excellent ion separation and extraordinary stability at high pressure and produced water environment.

  18. Natural zeolite polypropylene composite film preparation and characterization

    OpenAIRE

    Özmıhçı, Filiz; Balköse, Devrim; Ülkü, Semra

    2001-01-01

    In this research, the preparation and characterization of polypropylene (PP) and natural zeolite composites were studied. Natural zeolite mined in Gördes, Turkey was used as an alternative filler to CaCO3. Films were prepared by the extrusion of PP, and surface-modified zeolite was made by polyethylene glycol 4000 with 2-4% zeolite. Zeolite-filled composites had densities between 0.73 and 0.83 g/cm3 and had void fractions of 0.07-0.20. Although the permeability of water vapour through 2% zeol...

  19. Reorientational dynamics of water confined in zeolites.

    Science.gov (United States)

    Fogarty, Aoife C; Coudert, François-Xavier; Boutin, Anne; Laage, Damien

    2014-02-24

    We present a detailed molecular-dynamics study of water reorientation and hydrogen-bond dynamics in a strong confinement situation, within the narrow pores of an all-silica Linde type A (LTA) zeolite. Two water loadings of the zeolite are compared with the bulk case. Water dynamics are retarded in this extreme hydrophobic confinement and the slowdown is more pronounced at higher water loading. We show that water reorientation proceeds mainly by large-amplitude angular jumps, whose mechanism is similar to that determined in the bulk. The slowdown upon hydrophobic confinement arises predominantly from an excluded-volume effect on the large fraction of water molecules lying at the interface with the zeolite matrix, with an additional minor contribution coming from a structuring effect induced by the confinement. Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  20. Cupric natural zeolites as microbic ides

    International Nuclear Information System (INIS)

    Contreras A, D.; Olguin G, M. T.; Alcantara D, D.; Burrola A, C.

    2009-01-01

    The Escherichia coli and the Candida albicans are considered contamination indicators for what these organisms reflect the water quality. The natural zeolites by their characteristics and properties, they could incorporate to a waters treatment system, as ion exchange, adsorbents and/or microbiocid agents, representing an alternative method of low cost. Inside this investigation work was found that depending on the microorganism type, it varies the quantity of cupric zeolite that is required to carry out the water disinfection, being great for the case of yeasts than the bacteria s. In addition to that marked differences are presented in the required time to reach this process. The characterization of the natural zeolite material, sodium and cupric, was realized by means of scanning electron microscopy, determining the elementary composition (Energy Dispersive Spectroscopy) of each one of them, and by X-ray diffraction. (Author)

  1. Methanol-Tolerant Platinum-Palladium Catalyst Supported on Nitrogen-Doped Carbon Nanofiber for High Concentration Direct Methanol Fuel Cells

    Science.gov (United States)

    Kim, Jiyoung; Jang, Jin-Sung; Peck, Dong-Hyun; Lee, Byungrok; Yoon, Seong-Ho; Jung, Doo-Hwan

    2016-01-01

    Pt-Pd catalyst supported on nitrogen-doped carbon nanofiber (N-CNF) was prepared and evaluated as a cathode electrode of the direct methanol fuel cell (DMFC). The N-CNF, which was directly synthesized by the catalytic chemical vapor deposition from acetonitrile at 640 °C, was verified as having a change of electrochemical surface properties such as oxygen reduction reaction (ORR) activities and the electrochemical double layer compared with common carbon black (CB). To attain the competitive oxygen reduction reaction activity with methanol tolerance, the Pt and Pd metals were supported on the CB or the N-CNF. The physical and electrochemical characteristics of the N-CNF–supported Pt-Pd catalyst were examined and compared with catalyst supported on the CB. In addition, DMFC single cells using these catalysts as the cathode electrode were applied to obtain I-V polarization curves and constant current operating performances with high-concentration methanol as the fuel. Pt-Pd catalysts had obvious ORR activity even in the presence of methanol. The higher power density was obtained at all the methanol concentrations when it applied to the membrane electrode assembly (MEA) of the DMFC. When the N-CNF is used as the catalyst support material, a better performance with high-concentration methanol is expected. PMID:28335275

  2. Methanol-Tolerant Platinum-Palladium Catalyst Supported on Nitrogen-Doped Carbon Nanofiber for High Concentration Direct Methanol Fuel Cells.

    Science.gov (United States)

    Kim, Jiyoung; Jang, Jin-Sung; Peck, Dong-Hyun; Lee, Byungrok; Yoon, Seong-Ho; Jung, Doo-Hwan

    2016-08-15

    Pt-Pd catalyst supported on nitrogen-doped carbon nanofiber (N-CNF) was prepared and evaluated as a cathode electrode of the direct methanol fuel cell (DMFC). The N-CNF, which was directly synthesized by the catalytic chemical vapor deposition from acetonitrile at 640 °C, was verified as having a change of electrochemical surface properties such as oxygen reduction reaction (ORR) activities and the electrochemical double layer compared with common carbon black (CB). To attain the competitive oxygen reduction reaction activity with methanol tolerance, the Pt and Pd metals were supported on the CB or the N-CNF. The physical and electrochemical characteristics of the N-CNF-supported Pt-Pd catalyst were examined and compared with catalyst supported on the CB. In addition, DMFC single cells using these catalysts as the cathode electrode were applied to obtain I-V polarization curves and constant current operating performances with high-concentration methanol as the fuel. Pt-Pd catalysts had obvious ORR activity even in the presence of methanol. The higher power density was obtained at all the methanol concentrations when it applied to the membrane electrode assembly (MEA) of the DMFC. When the N-CNF is used as the catalyst support material, a better performance with high-concentration methanol is expected.

  3. Methanol-Tolerant Platinum-Palladium Catalyst Supported on Nitrogen-Doped Carbon Nanofiber for High Concentration Direct Methanol Fuel Cells

    Directory of Open Access Journals (Sweden)

    Jiyoung Kim

    2016-08-01

    Full Text Available Pt-Pd catalyst supported on nitrogen-doped carbon nanofiber (N-CNF was prepared and evaluated as a cathode electrode of the direct methanol fuel cell (DMFC. The N-CNF, which was directly synthesized by the catalytic chemical vapor deposition from acetonitrile at 640 °C, was verified as having a change of electrochemical surface properties such as oxygen reduction reaction (ORR activities and the electrochemical double layer compared with common carbon black (CB. To attain the competitive oxygen reduction reaction activity with methanol tolerance, the Pt and Pd metals were supported on the CB or the N-CNF. The physical and electrochemical characteristics of the N-CNF–supported Pt-Pd catalyst were examined and compared with catalyst supported on the CB. In addition, DMFC single cells using these catalysts as the cathode electrode were applied to obtain I-V polarization curves and constant current operating performances with high-concentration methanol as the fuel. Pt-Pd catalysts had obvious ORR activity even in the presence of methanol. The higher power density was obtained at all the methanol concentrations when it applied to the membrane electrode assembly (MEA of the DMFC. When the N-CNF is used as the catalyst support material, a better performance with high-concentration methanol is expected.

  4. Characterization and antibacterial activity of silver exchanged regenerated NaY zeolite from surfactant-modified NaY zeolite

    Energy Technology Data Exchange (ETDEWEB)

    Salim, Mashitah Mad; Malek, Nik Ahmad Nizam Nik, E-mail: niknizam@fbb.utm.my

    2016-02-01

    The antibacterial activity of regenerated NaY zeolite (thermal treatment from cetyltrimethyl ammonium bromide (CTAB)-modified NaY zeolite and pretreatment with Na ions) loaded with silver ions were examined using the broth dilution minimum inhibitory concentration (MIC) method against Escherichia coli (E. coli ATCC 11229) and Staphylococcus aureus (S. aureus ATCC 6538). X-ray diffraction (XRD), attenuated total reflectance–Fourier transform infrared (ATR–FTIR) spectroscopy, field emission scanning electron microscopy (FESEM), energy dispersive X-ray (EDX) and chemical elemental analyses were used to characterize the regenerated NaY and AgY zeolites. The XRD patterns indicated that the calcination and addition of silver ions on regenerated NaY zeolite did not affect the structure of the regenerated NaY zeolite as the characteristic peaks of the NaY zeolite were retained, and no new peaks were observed. The regenerated AgY zeolite showed good antibacterial activity against both bacteria strains in distilled water, and the antibacterial activity of the samples increased with increasing Ag loaded on the regenerated AgY zeolite; the regenerated AgY zeolite was more effective against E. coli than S. aureus. However, the antibacterial activity of the regenerated AgY was not effective in saline solution for both bacteria. The study showed that CTAB-modified NaY zeolite materials could be regenerated to NaY zeolite using thermal treatment (550 °C, 5 h) and this material has excellent performance as an antibacterial agent after silver ions loading. - Highlights: • Thermal treatment was used to regenerate surfactant modified zeolite. • The regenerated NaY zeolite formed was added with different silver loadings. • Regenerated AgY zeolite was tested for antibacterial activity on E. coli and S. aureus. • The antibacterial activity increased with increased of the amount of silver loadings. • The zeolite structure did not change with thermal and modification

  5. Effects of aeration and natural zeolite on ammonium removal during the treatment of sewage by mesocosm-scale constructed wetlands.

    Science.gov (United States)

    Araya, F; Vera, I; Sáez, K; Vidal, G

    2016-01-01

    The objective was to evaluate the effects of intermittent artificial aeration cycles and natural zeolite as a support medium, in addition to the contribution of plants (Schoenoplectus californicus) on NH4(+)-N removal during sewage treatment by Constructed Wetlands (CW). Two lines of Mesocosm Constructed Wetland (MCW) were installed: (a) gravel line (i.e. G-Line) and (b) zeolite line (i.e. Z-Line). Aeration increased the NH4(+)-N removal efficiency by 20-45% in the G-Line. Natural zeolite increased the NH4(+)-N removal efficiency by up to 60% in the Z-Line. Plants contributed 15-30% of the NH4(+)-N removal efficiency and no difference between the G-Line and the Z-Line. Conversely, the NH4(+)-N removal rate was shown to only increase with the use of natural zeolite. However, the MCW with natural zeolite, the NH4(+)-N removal rate showed a direct relationship only with the NH4(+)-N influent concentration. Additionally, relationship between the oxygen, energy and area regarding the NH4(+)-N removal efficiency was established for 2.5-12.5 gO2/(kWh-m(2)) in the G-Line and 0.1-2.6 gO2/(kWh-m(2)) in the Z-Line. Finally, it was established that a combination of natural zeolite as a support medium and the aeration strategy in a single CW could regenerate the zeolite's adsorption sites and maintain a given NH4(+)-N removal efficiency over time.

  6. Adsorption Cooling System Using Metal-Impregnated Zeolite-4A

    Directory of Open Access Journals (Sweden)

    Somsuk Trisupakitti

    2016-01-01

    Full Text Available The adsorption cooling systems have been developed to replace vapor compression due to their benefits of being environmentally friendly and energy saving. We prepared zeolite-4A and experimental cooling performance test of zeolite-water adsorption system. The adsorption cooling test-rig includes adsorber, evaporator, and condenser which perform in vacuum atmosphere. The maximum and minimum water adsorption capacity of different zeolites and COP were used to assess the performance of the adsorption cooling system. We found that loading zeolite-4A with higher levels of silver and copper increased COP. The Cu6%/zeolite-4A had the highest COP at 0.56 while COP of zeolite-4A alone was 0.38. Calculating the acceleration rate of zeolite-4A when adding 6% of copper would accelerate the COP at 46%.

  7. AKTIVASI ZEOLIT ALAM SEBAGAI ADSORBEN PADA ALAT PENGERING BERSUHU RENDAH

    Directory of Open Access Journals (Sweden)

    Laeli Kurniasari

    2012-04-01

    Full Text Available ACTIVATION OF NATURAL ZEOLITE AS AN ADSORBENT FOR LOW TEMPERATURE DRYING SYSTEM. Drying is one process which is used in many industries, especially in food product. The process usually still has low energy efficiency and can make food deterioration because of the usage of high temperature. One alternative in drying technology is the use of zeolite as a water vapor adsorbent. This kind of drying method make it possible to operate in lower temperature, hence it will be suitable for heat sensitive product. Natural zeolit can be one promising adsorbent since it is spreadly abundant in Indonesia. Natural zeolite must be activated first before used, in order to get zeolite with high adsorption capacity. Activation process in natural zeolite will change the Si/Al ratio, polarity, and affinity of zeolite toward water vapor and also increase the porosity. Activation of natural zeolite can be done with two methods, chemical activation use NaOH and physical activation use heat. In the activation using NaOH, natural zeolite is immersed with NaOH solution 0.5-2N in 2 hour with temperature range 60-900C. The process is continued with the drying of zeolite in oven with 1100C for 4 hours. While in heat treatment, zeolit is heated into 200-5000C in furnace for 2-5 hours. SEM analysis is used to compare the change in zeolite morphology before and after each treatment, while to know the adsorption capacity of zeolite, the analyses were done in many temperature and relative humidity. Result gives the best condition in NaOH activation is NaOH 1N and temperature 700C, with water vapor loading is 0.171 gr/gr adsorbent. In heat treatment, the best condition is 3000C and 3 hours with loading 0.137 gr water vapor/gr adsorbent.  Pengeringan merupakan salah satu proses yang banyak digunakan pada produk pangan. Proses ini umumnya menyebabkan kerusakan pada bahan pangan, disamping masih rendahnya efisiensi energi. Salah satu alternatif pada proses pengeringan yaitu

  8. Neuromuscular electrical stimulation improves exercise tolerance in patients with advanced heart failure on continuous intravenous inotropic support use-randomized controlled trial.

    Science.gov (United States)

    Forestieri, Patrícia; Bolzan, Douglas W; Santos, Vinícius B; Moreira, Rita Simone Lopes; de Almeida, Dirceu Rodrigues; Trimer, Renata; de Souza Brito, Flávio; Borghi-Silva, Audrey; de Camargo Carvalho, Antonio Carlos; Arena, Ross; Gomes, Walter J; Guizilini, Solange

    2018-01-01

    To evaluate the impact of a short-term neuromuscular electrical stimulation program on exercise tolerance in hospitalized patients with advanced heart failure who have suffered an acute decompensation and are under continuous intravenous inotropic support. A randomized controlled study. Initially, 195 patients hospitalized for decompensated heart failure were recruited, but 70 were randomized. Patients were randomized into two groups: control group subject to the usual care ( n = 35); neuromuscular electrical stimulation group ( n = 35) received daily training sessions to both lower extremities for around two weeks. The baseline 6-minute walk test to determine functional capacity was performed 24 hours after hospital admission, and intravenous inotropic support dose was daily checked in all patients. The outcomes were measured in two weeks or at the discharge if the patients were sent back home earlier than two weeks. After losses of follow-up, a total of 49 patients were included and considered for final analysis (control group, n = 25 and neuromuscular electrical stimulation group, n = 24). The neuromuscular electrical stimulation group presented with a higher 6-minute walk test distance compared to the control group after the study protocol (293 ± 34.78 m vs. 265.8 ± 48.53 m, P Neuromuscular electrical stimulation group also demonstrated a significantly higher dose reduction of dobutamine compared to control group after the study protocol (2.72 ± 1.72 µg/kg/min vs. 3.86 ± 1.61 µg/kg/min, P = 0.001, respectively). A short-term inpatient neuromuscular electrical stimulation rehabilitation protocol improved exercise tolerance and reduced intravenous inotropic support necessity in patients with advanced heart failure suffering a decompensation episode.

  9. Effect of an Sb-Doped SnO2 Support on the CO-Tolerance of Pt2Ru3 Nanocatalysts for Residential Fuel Cells

    Directory of Open Access Journals (Sweden)

    Yoshiyuki Ogihara

    2016-09-01

    Full Text Available We prepared monodisperse Pt2Ru3 nanoparticles supported on carbon black and Sb-doped SnO2 (denoted as Pt2Ru3/CB and Pt2Ru3/Sb-SnO2 with identical alloy composition and particle size distribution by the nanocapsule method. The activities for the hydrogen oxidation reaction (HOR of these anode catalysts were examined in H2-saturated 0.1 M HClO4 solution in both the presence and absence of carbon monoxide by use of a channel flow electrode at 70 °C. It was found that the CO-tolerant HOR mass activity at 0.02 V versus a reversible hydrogen electrode (RHE on the Pt2Ru3/Sb-SnO2 electrode was higher than that at the Pt2Ru3/CB electrode in 0.1 M HClO4 solution saturated with 1000 ppm CO (H2-balance. The CO tolerance mechanism of these catalysts was investigated by in situ attenuated total reflection Fourier transform infrared reflection-adsorption spectroscopy (ATR-FTIRAS in 1% CO/H2-saturated 0.1 M HClO4 solution at 60 °C. It was found, for the Pt2Ru3/Sb-SnO2 catalyst, that the band intensity of CO linearly adsorbed (COL at step/edge sites was suppressed, together with a blueshift of the COL peak at terrace sites. On this surface, the HOR active sites were concluded to be more available than those on the CB-supported catalyst surface. The observed changes in the adsorption states of CO can be ascribed to an electronic modification effect by the Sb-SnO2 support.

  10. Development of spent salt treatment technology by zeolite column system. Performance evaluation of zeolite column

    International Nuclear Information System (INIS)

    Miura, Hidenori; Uozumi, Koichi

    2009-01-01

    At electrorefining process, fission products(FPs) accumulate in molten salt. To avoid influence on heating control by decay heat and enlargement of FP amount in the recovered fuel, FP elements must be removed from the spent salt of the electrorefining process. For the removal of the FPs from the spent salt, we are investigating the availability of zeolite column system. For obtaining the basic data of the column system, such as flow property and ion-exchange performance while high temperature molten salt is passing through the column, and experimental apparatus equipped with fraction collector was developed. By using this apparatus, following results were obtained. 1) We cleared up the flow parameter of column system with zeolite powder, such as flow rate control by argon pressure. 2) Zeolite 4A in the column can absorb cesium that is one of the FP elements in molten salt. From these results, we got perspective on availability of the zeolite column system. (author)

  11. TITANIUM OXIDE DISPERSED ON NATURAL ZEOLITE (TiO2/ZEOLITE AND ITS APPLICATION FOR CONGO RED PHOTODEGRADATION

    Directory of Open Access Journals (Sweden)

    Is Fatimah

    2010-06-01

    Full Text Available The utilization of TiO2 dispersed on natural zeolite (TiO2/Zeolite for degradation of Congo Red photocatlytically has been performed. The TiO2/Zeolite was prepared by mechanically mixing of 100 g of natural zeolite, which it has been heated at 400oC, with TiO2 powder, the final weight ratio of the mixture was 5% (w/w. The mixture was then calcined at 400oC for 6 hours. The calcined product was characterized using x-ray diffractometry, x-ray fluorescence analysis and gas sorption analysis methods to determine its physicochemical properties changes caused by mixing and calcination. Investigation of Congo Red photodegradation using TiO2/Zeolite was carried out by mixing 25 mL 10-4 M solution of Congo Red with 25 mg of TiO2/Zeolite and irradiating the suspention with UV-light of 350 nm for 10, 20, 30, 40, 50 and 60 minutes, respectively. The characterization results showed that dispertion of TiO2 on zeolite resulted in the increasing of titanium concentration on TiO2/Zeolite. The concentration of Ti on natural zeolite was found to be 0.15%(w/w, meanwhile on TiO2/Zeolite was 2.29% (w/w. From X-ray diffractometry analysis result no information was found that TiO2 was dipersed on natural zeolite. It was caused by overlapping of the reflections of zeolite with reflections of TiO2. On the otherhand, the gas sorption analysis result exhibited that the dispersion of TiO2 on zeolite resulted in the decreasing of total pore volume as well as specific surface area of the natural zeolite. The specific surface areas of natural zeolite and TiO2/Zeolite were 21.98 and 16.74 m2/g, respectively, meanwhile the total pore volumes of natural zeolite and TiO2/Zeolite were 20.10x10-3 and 13.47x10-3 mL/g. The simple kinetic of photodegradation of Congo Red exhibited that the rate of degradation followed a first order kinetic and the reaction rate constant was 0.0017 minute-1.   Keywords: natural zeolite, TiO2, photodegradation, Congo Red

  12. Nano Sized Ni/TiO2 @ NaX Zeolite with Enhanced Photocatalytic Activity

    Directory of Open Access Journals (Sweden)

    Leila Torkian

    2016-10-01

    Full Text Available Nickel doped TiO2nano particles (1% w/w were prepared and immobilized on NaX zeolite and after characterization by X-ray diffraction and scanning electron microscopy used as photo catalyts for degradation of orange G. The X-ray diffraction patterns show that the supported TiO2 are crystallized in anatase form and the intensity of the zeolite peaks decreases with the increase of TiO2loading. Scanning electron micrographs of synthesized samples show that nano size titanium dioxide particles are accumulated on the surface of the zeolite. These materials are applied as photo catalysts for the degradation of orange G in aqueous solution by means of ultraviolet light irradiation at room temperature. The effect of solution pH, ultraviolet irradiation time and catalyst in degradation of orange G was investigated. The results show that nickel doped TiO2/NaX zeolite as a photo catalyst in degradation of orange G in acidic solution is superior to the Ni/TiO2 nano composite and also undoped nano size titanium dioxide particles.

  13. Two-dimensional zeolites: dream or reality?

    Czech Academy of Sciences Publication Activity Database

    Roth, W. J.; Čejka, Jiří

    2011-01-01

    Roč. 1, č. 1 (2011), s. 43-53 ISSN 2044-4753 R&D Projects: GA AV ČR KAN100400701; GA ČR GA104/09/0561; GA ČR GA203/08/0604 Institutional research plan: CEZ:AV0Z40400503 Keywords : catalysis * physical chemistry * zeolites Subject RIV: CF - Physical ; Theoretical Chemistry

  14. Zeolite from fly ash: synthesis and characterization

    Indian Academy of Sciences (India)

    Unknown

    brought the success in obtaining Na–A zeolite also. Lin and Hsi (1995) extensively investigated effects of ... the reaction parameters to obtain best quality product. They carried out experiments in open as well as in .... and data files compiled in the book by Szostak (1976). The diffractograms show that the original crystalline ...

  15. Extreme Flexibility in a Zeolitic Imidazolate Framework

    DEFF Research Database (Denmark)

    Wharmby, M.T.; Henke, S.; Bennett, T.D.

    2015-01-01

    Desolvated zeolitic imidazolate framework ZIF-4(Zn) undergoes a discontinuous porous to dense phase transition on cooling through 140 K, with a 23% contraction in unit cell volume. The structure of the non-porous, low temperature phase was determined from synchrotron X-ray powder diffraction data...

  16. Ultrasound-assisted dealumination of zeolite Y

    Indian Academy of Sciences (India)

    We demonstrate a new procedure for dealumination of zeolite Y. The method employs a 28 KHz ultrasound bath and an ethanolic acetylacetone solution. Acetylacetone was used as chelating agent and ultrasound irradiation was used as extraction intensifier. Four types of samples, as-synthesized, ammoniumexchanged, ...

  17. Zeolites Promoting Quinoline Synthesis via Friedlander Reaction

    Czech Academy of Sciences Publication Activity Database

    López-Sanz, J.; Pérez-Mayoral, E.; Vitvarová, Dana; Martín-Aranda, R. M.; López-Peinado, A. J.

    2010-01-01

    Roč. 53, 19-20 (2010), s. 1430-1437 ISSN 1022-5528 R&D Projects: GA ČR GD203/08/H032 Institutional research plan: CEZ:AV0Z40400503 Keywords : heterogeneous catalysis * zeolites * quinolines Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.359, year: 2010

  18. Ultrasound-assisted dealumination of zeolite Y

    Indian Academy of Sciences (India)

    Higher dealumination was observed for those samples subjected to both ultrasound irradiation and acetylacetone extraction. Keywords. Microporous; zeolite Y; dealumination; ultrasound irradiation; extraction. 1. ..... ture has also been claimed while ultrasound waves were used for the extraction of contaminants in food and.

  19. Selective synthesis of FAU-type zeolites

    Science.gov (United States)

    Garcia, Gustavo; Cabrera, Saúl; Hedlund, Jonas; Mouzon, Johanne

    2018-05-01

    In the present work, parameters influencing the selectivity of the synthesis of FAU-zeolites from diatomite were studied. The final products after varying synthesis time were characterized by scanning electron microscopy, energy dispersive spectroscopy, X-ray diffraction and gas adsorption. It was found that high concentrations of NaCl could completely inhibit the formation of zeolite P, which otherwise usually forms as soon as maximum FAU crystallinity is reached. In the presence of NaCl, the FAU crystals were stable for extended time after completed crystallization of FAU before formation of sodalite. It was also found that addition of NaCl barely changed the crystallization kinetics of FAU zeolite and only reduced the final FAU particle size and SiO2/Al2O3 ratio slightly. Other salts containing either Na or Cl were also investigated. Our results suggest that there is a synergistic effect between Na+ and Cl-. This is attributed to the formation of (Na4Cl)3+ clusters that stabilize the sodalite cages. This new finding may be used to increase the selectivity of syntheses leading to FAU-zeolites and avoid the formation of undesirable by-products, especially if impure natural sources of aluminosilica are used.

  20. Multicomponent liquid ion exchange with chabazite zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Robinson, S.M.; Arnold, W.D. Jr.; Byers, C.W.

    1993-10-01

    In spite of the increasing commercial use of zeolites for binary and multicomponent sorption, the understanding of the basic mass-transfer processes associated with multicomponent zeolite ion-exchange systems is quite limited. This study was undertaken to evaluate Na-Ca-Mg-Cs-Sr ion exchange from an aqueous solution using a chabazite zeolite. Mass-transfer coefficients and equilibrium equations were determined from experimental batch-reactor data for single and multicomponent systems. The Langmuir isotherm was used to represent the equilibrium relationship for binary systems, and a modified Dubinin-Polyani model was used for the multicomponent systems. The experimental data indicate that diffusion through the microporous zeolite crystals is the primary diffusional resistance. Macropore diffusion also significantly contributes to the mass-transfer resistance. Various mass-transfer models were compared to the experimental data to determine mass-transfer coefficients. Effective diffusivities were obtained which accurately predicted experimental data using a variety of models. Only the model which accounts for micropore and macropore diffusion occurring in series accurately predicted multicomponent data using single-component diffusivities. Liquid and surface diffusion both contribute to macropore diffusion. Surface and micropore diffusivities were determined to be concentration dependent.

  1. Utilization of Zeolites in environmentally protection

    Energy Technology Data Exchange (ETDEWEB)

    Kallo, D. [Hungarian Academy of Sciences, Chemical Research Center, Institute of Chemistry, Budapest (Hungary)

    2000-07-01

    It has been attempted to present the most important fields of natural zeolite applications in environmental protection. Realized and approved utilizations were demonstrated inciting the reader to take these materials into consideration for solution of similar problems. The outlined properties can be used for other purposes not discussed in this review. They can be applied, e.g., in fish farming, transportation of living fishes when simultaneous ammonium and carbon dioxide removals is required: ammonium is exchanged for calcium present in the zeolite and CO{sub 2} is then precipitated in the form of CaCO{sub 3}; in treatment of diluted manure when undesired organics can be fixed and bactericide effects can be attained. Natural zeolites are used, therefore, as deodorant of litter of dogs or cats. Small amounts of metal cations, e.g., Cu{sup 2+}, Ag{sup +} or Zn{sup 2+}, introduced by ion exchange may disinfect contacting water. Due to water adsorption and desorption capability natural zeolite as construction materials exert some conditioning effect without any mechanical accessory. It seems likely the human ingenuity will continue to discover new applications in the future.

  2. Synthesis of Diphenylamine Catalyzed by Zeolites

    Czech Academy of Sciences Publication Activity Database

    Hronec, M.; Cvengrošová, Z.; Čejka, Jiří

    2003-01-01

    Roč. 255, - (2003), s. 197-202 ISSN 0926-860X Institutional research plan: CEZ:AV0Z4040901 Keywords : zeolites beta * bentonite * Bronsted site Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.825, year: 2003

  3. Detergents - Zeolites and Enzymes Excel Cleaning Power

    Indian Academy of Sciences (India)

    Presently used detergent formulations generally consist of surfactants, builder and cobuilder, bleaching agents, addi- tives for secondary benefits and enzymes. Zeolites are basically hydrated crystalline aluminium silicates which function as ion exchangers and make the water soft by removing calcium, magnesium and ...

  4. Ultrasound-assisted dealumination of zeolite Y

    Indian Academy of Sciences (India)

    Higher dealumination was observed for those samples subjected to both ultrasound irradiation and acetylacetone extraction ... lite was prepared upon conventional ion-exchange treat- ment using an aqueous solution of 0.4 M NH4Cl at 25. ◦. C ... form of the zeolite to acidic one, it was heated in a muf- fle furnace at rate of 10.

  5. Factors affecting drug adsorption on beta zeolites.

    Science.gov (United States)

    Pasti, Luisa; Sarti, Elena; Cavazzini, Alberto; Marchetti, Nicola; Dondi, Francesco; Martucci, Annalisa

    2013-05-01

    The adsorption behaviour of three commonly used drugs, namely ketoprofen, hydrochlorothiazide and atenolol, from diluted aqueous solutions on beta zeolites with different SiO2/Al2O3 ratio (i.e. 25, 38 and 360) was investigated by changing the ionic strength and the pH, before and after thermal treatment of the adsorbents. The selective adsorption of drugs was confirmed by thermogravimetry and X-ray diffraction. The adsorption capacity of beta zeolites was strongly dependent on both the solution pH and the alumina content of the adsorbent. Such a remarkable difference was interpreted as a function of the interactions between drug molecules and zeolite surface functional groups. Atenolol was readily adsorbed on the less hydrophobic zeolite, under pH conditions in which electrostatic interactions were predominant. On the other hand, ketoprofen adsorption was mainly driven by hydrophobic interactions. For undissociated molecules the adsorption capability increased with the increase of hydrophobicity. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  6. Transport through zeolite filled polymeric membranes

    NARCIS (Netherlands)

    Boom, J.P.; Boom, J.P.; Punt, Ineke G.M.; Zwijnenberg, Harmen Jan; Bargeman, D.; de Boer, R.; Smolders, C.A.; Bargeman, D.; Strathmann, H.; Smolders, C.A.

    1998-01-01

    In this paper the effect of zeolite particles incorporated in rubbery polymers on the pervaporation properties of membranes made from these polymers is discussed. Pervaporation of methanol/toluene mixtures was carried out with membranes prepared from the toluene selective polymer EPDM and the

  7. MERCURY SEPARATION FROM POLLUTANT WATER USING ZEOLITES

    Science.gov (United States)

    Arsenic is known to be a hazardous contaminant in drinking water that causes arsenical dermatitis and skin cancer. In the present work, the potential use of a variety of synthetic zeolites for removal of arsenic from water has been examined at room temperature. Experiments have...

  8. Environmental application of russian natural zeolites

    International Nuclear Information System (INIS)

    Fursenko, B.

    1998-01-01

    There are more than 70 deposits and localities of zeolite-containing rocks (ZCR) in Russia. Total resources of relatively rich (more than 40% of zeolites) rocks are estimated as 3.8 billion tons. The main Russian deposits are located in Siberia and Far East. A number of traditional ways of ZCR utilization for environmental protection have been developed in Russia during last two decades, when a few governmental scientific programs were in operation. These were: (1) waste water treatment (galvanic waste, oil-product pollution, municipal waste water, radioactive pollution); (2) drinking water preparation (municipal and individual filters, coagulation method, lemonade production); (3) gas drying and purification (natural gas drying, stack-gas cleanup, oxygen enriched air production). Growing interest was attracted to zeolites due to their potential utilization in the nuclear waste treatment, re-cultivation of technically polluted territories and especially after they were used for localization of the radioactive accidents on the atomic power stations (Three Mile Island, U.S.A. in 1981 and Chernobyl, USSR in 1986). Structure, ion-exchange capacity and phase transformations of the zeolites are discussed

  9. Ru complexes of Hoveyda-Grubbs type immobilized on lamellar zeolites: activity in olefin metathesis reactions.

    Science.gov (United States)

    Balcar, Hynek; Žilková, Naděžda; Kubů, Martin; Mazur, Michal; Bastl, Zdeněk; Čejka, Jiří

    2015-01-01

    Hoveyda-Grubbs type catalysts with cationic tags on NHC ligands were linker-free immobilized on the surface of lamellar zeolitic supports (MCM-22, MCM-56, MCM-36) and on mesoporous molecular sieves SBA-15. The activity of prepared hybrid catalysts was tested in olefin metathesis reactions: the activity in ring-closing metathesis of citronellene and N,N-diallyltrifluoroacetamide decreased in the order of support MCM-22 ≈ MCM-56 > SBA-15 > MCM-36; the hybrid catalyst based on SBA-15 was found the most active in self-metathesis of methyl oleate. All catalysts were reusable and exhibited low Ru leaching (<1% of Ru content). XPS analysis revealed that during immobilization ion exchange between Hoveyda-Grubbs type catalyst and zeolitic support occurred in the case of Cl(-) counter anion; in contrast, PF6 (-) counter anion underwent partial decomposition.

  10. Temperature-dependence of hydrogen oxidation reaction rates and CO-tolerance at carbon-supported Pt, Pt-Co, and Pt-Ru catalysts.

    Science.gov (United States)

    Uchida, Hiroyuki; Izumi, Kenji; Aoki, Koichi; Watanabe, Masahiro

    2009-03-21

    The temperature-dependence of the hydrogen oxidation reaction (HOR) rate was examined at commercial Pt, Pt3Co, PtRu, and PtRu(1.5) nano-sized catalysts (diameter, d = ca. 3 nm) supported on carbon black in 0.1 M HClO4 solution in the presence and absence of carbon monoxide by use of a channel flow electrode at temperatures from 30 to 90 degrees C. It was found that the values of the apparent rate constant k(app) (per real Pt active surface area) for the HOR at these supported catalysts agreed beautifully with those of the corresponding bulk electrodes in the whole temperature range. The dependence of the kinetically controlled current density (jk) on CO coverage at each supported catalyst was also identical to that of the bulk. Hence, no particle size effect was observed on the HOR activity and the CO tolerance, at least, was brought down to d = 3 nm.

  11. Preparation of Bimetallic Pd-Co Nanoparticles on Graphene Support for Use as Methanol Tolerant Oxygen Reduction Electrocatalysts

    Directory of Open Access Journals (Sweden)

    R. N. Singh

    2012-12-01

    Full Text Available Graphene-supported (40-x wt% Pd x wt% Co (0≤x≤13.33 alloys/composites have been prepared by a microwave-assisted polyol reduction method and been investigated for their structural and electrocatalytic properties for the oxygen reduction reaction (ORR in 0.5 M H2SO4 at 298 K. The study demonstrated that the bimetallic Pd-Co composite nanoparticles are, in fact, alloy nanoparticles with fcc crystalline structure. Partial substitution of Pd by Co (from 3.64 to 13.33 wt% in 40 wt% Pd/graphene decreases the lattice parameter as well as the crystallite size and increases the apparent catalytic activity, the latter, however, being the greatest with 8 wt% Co. The ORR activity of the active 32 wt% Pd 8wt% Co is found to be considerably low when it was deposited on the support multiwall carbon nanotubes under similar conditions. The rotating disk electrode study indicated that the ORR on 32 wt% Pd 8 wt% Co/GNS in 0.5 M H2SO4 follows approximately the four-electron pathway.

  12. Metallocene supported core@LDH catalysts for slurry phase ethylene polymerisation.

    Science.gov (United States)

    Buffet, Jean-Charles; Byles, Coral F H; Felton, Ryan; Chen, Chunping; O'Hare, Dermot

    2016-03-14

    We report the synthesis of solid catalysts based on a zirconocene supported on either silica@AMO-LDH or zeolite@AMO-LDH for the slurry phase polymerisation of ethylene. The hybrid catalysts demonstrate synergistic effects in which the polymerisation activity is up to three times higher than the zirconocene supported on analogous single phase silica or zeolite supports.

  13. Synthesis strategies in the search for hierarchical zeolites.

    Science.gov (United States)

    Serrano, D P; Escola, J M; Pizarro, P

    2013-05-07

    Great interest has arisen in the past years in the development of hierarchical zeolites, having at least two levels of porosities. Hierarchical zeolites show an enhanced accessibility, leading to improved catalytic activity in reactions suffering from steric and/or diffusional limitations. Moreover, the secondary porosity offers an ideal space for the deposition of additional active phases and for functionalization with organic moieties. However, the secondary surface represents a discontinuity of the crystalline framework, with a low connectivity and a high concentration of silanols. Consequently, hierarchical zeolites exhibit a less "zeolitic behaviour" than conventional ones in terms of acidity, hydrophobic/hydrophilic character, confinement effects, shape-selectivity and hydrothermal stability. Nevertheless, this secondary surface is far from being amorphous, which provides hierarchical zeolites with a set of novel features. A wide variety of innovative strategies have been developed for generating a secondary porosity in zeolites. In the present review, the different synthetic routes leading to hierarchical zeolites have been classified into five categories: removal of framework atoms, surfactant-assisted procedures, hard-templating, zeolitization of preformed solids and organosilane-based methods. Significant advances have been achieved recently in several of these alternatives. These include desilication, due to its versatility, dual templating with polyquaternary ammonium surfactants and framework reorganization by treatment with surfactant-containing basic solutions. In the last two cases, the materials so prepared show both mesoscopic ordering and zeolitic lattice planes. Likewise, interesting results have been obtained with the incorporation of different types of organosilanes into the zeolite crystallization gels, taking advantage of their high affinity for silicate and aluminosilicate species. Crystallization of organofunctionalized species favours the

  14. Chromium (VI Ion Adsorption Features of Chitosan Film and Its Chitosan/Zeolite Conjugate 13X Film

    Directory of Open Access Journals (Sweden)

    Maria Teresa Tavares

    2011-04-01

    Full Text Available This research evaluated the importance of the adsorption properties of chitosan a chitosan/zeolite conjugate film for the removal of Cr(VI ions from solutions in the 5–260 mg/L concentration range, when the pH was adjusted to 4.0 and 6.0. The uptake capacities of the films formed by chitosan and by the chitosan/zeolite conjugate were calculated by mass balance. The equilibrium isotherms were fitted to the Langmuir, Freundlich and Redlich-Peterson models. The chitosan film seems to be a good sorbent for Cr(VI at pH 4, but its physical instability suggests the need for a more resilient support. Due to this fact zeolite was added to the chitosan matrix in solution and a chitosan/zeolite (CS/Zeo film was thus formed. The solubility of the film and the characterization of the different matrices by FTIR, TGA and X-Ray showed that a cross-linked structure was formed between the chitosan and zeolite and the solubility of the film increased. In this study, the low manufacturing cost of the CS/Zeo matrix, the good uptake of Cr(VI at acidic pH (17.28 mg/g and the non desorption of Cr(VI from the film in water suggests this combination should be tested in industrial environment.

  15. Zeolites as candidate materials for aqueous tritiated waste storage

    International Nuclear Information System (INIS)

    Todorovic, M.; Radak-Jovanovic, Z.; Gal, I.J.; Brucher, H.

    1987-01-01

    Zeolites have been considered as storage materials for aqueous tritiated waste, owing to their relatively high water contents, low diffusion coefficient of water in their pores and their accessibility. The diffusion coefficient of tritiated water in the solid particles seems to be the most important factor in the selection of zeolites for tritiated water storage. This work summarizes investigations done in The Boris Kidric Institute and Juelich Nuclear Research Center on zeolites as storage materials for tritiated water. Modified 4A zeolites as CsA, ZnA, CoA, Fe(III)A, as well as synthetic and natural analcime, have been investigated. Self-diffusion coefficients of THO in zeolites have been calculated using the Boyd-Reichenberg model of diffusion. The results obtained are discussed from the point of view of using zeolites as storage materials for tritiated waste water. In this respect, natural and synthetic analcime seem to be promising

  16. Treatments of reverse osmosis concentrate using natural zeolites

    OpenAIRE

    Taherifar Hossein; Rezvantalab Sima; Bahadori Fatemeh; Khoei Omid Sadrzadeh

    2015-01-01

    The purpose of the current study is to experimentally investigate the reduction of sodium adsorption ratio (SAR) from a concentrated stream of reversed osmosis (RO) using natural zeolites. In order to reduce the salinity of solution, experiments were carried out using zeolites of varying concentration, pretreatment of adsorbents, and the addition of Ethylenediaminetetraacetic acid (EDTA). The results show that both zeolites can be used in an RO brine treatment; however, Rhyolitic tuff is more...

  17. Large zeolites - Why and how to grow in space

    Science.gov (United States)

    Sacco, Albert, Jr.

    1991-01-01

    The growth of zeolite crystals which are considered to be the most valuable catalytic and adsorbent materials of the chemical processing industry are discussed. It is proposed to use triethanolamine as a nucleation control agent to control the time release of Al in a zeolite A solution and to increase the average and maximum crystal size by 25-50 times. Large zeolites could be utilized to make membranes for reactors/separators which will substantially increase their efficiency.

  18. Multi-elemental characterization of Cuban natural zeolites

    International Nuclear Information System (INIS)

    Diaz Rizo, O.; Herrera Peraza, E.F.

    1996-01-01

    Concentrations of 38 elements in samples from four important Cuban zeolite bed have beam obtained by Instrumental Neutron Activation (INAA) and X-Ray Fluorescence Analysis (XRFA). In comparison with other analytical techniques good agreement was achieved. The concentration values of minor element Ba, Sr, Zn, and Mn, and 25 trace element (including 9 REE) are at the first time reported in Cuban zeolite. It is important for the zeolite evaluation in different industrial uses

  19. Influence of zeolite nanofillers on properties of polymeric materials

    OpenAIRE

    Kopcová, M.; Ondrušová, D.; Krmela, J.; Průša, P.; Pajtášová, M.; Jankurová, Z.

    2012-01-01

    The present work deals with the preparation and study of modified polymeric materials with the replacement of carbon black by nanofillers on the basis of zeolite that is environmentally friendly. Natural zeolites from a group of aluminosilicate nanoporous materials have wide range of possibilities for applications that are environmentally friendly. Zeolites can be used in the role of fillers into the polymer materials too [1]. The given work deals with the preparation and study of modif...

  20. Aqueous interactions of zeolitic material in acidic and basic solutions

    OpenAIRE

    Polatoğlu, İlker; Çakıcıoğlu Özkan, Seher Fehime

    2010-01-01

    Aqueous interactions of natural zeolitic material in as-received and modified forms were studied. The zeolitic materials was interacted with acidic (hydrochloric acid, lactic acid, acetic acid) and basic (sodium hydroxide) solutions. Ion exchange, adsorption, complex formation, precipitation and cation hydrolysis were possible interaction mechanisms affected by the amount and cation content of zeolite and pH. The dominant mechanisms seemed to be ion exchange and adsorption in HCl solution whe...

  1. Platinum incorporation in the Na Y zeolite through impregnation method, and characterization by XRD, FTIR and nitrogen adsorption

    International Nuclear Information System (INIS)

    Araujo, A.S.; Sousa, B.V.; Andrade, A.C.C.; Rodrigues, M.G.F.; Rangel, M.C.

    2007-01-01

    Supported metal catalysts are widely used in petroleum refining, chemical and petroleum industries. These catalysts are important in ammonia synthesis, conversion of hydrocarbons with water vapor to synthesis gas, reforming, hydrocracking, ... Platinum has long been used in cracking, hydrogenation and dehydrogenation processes. The aim of this project is the Na Y zeolitic sample preparation through impregnation for incipient humidity, with 0,5% concentration of platinum, aiming its use as a catalyst in the steam reforming reaction. The characterization techniques used were: X Rays Diffraction (XRD), Fourier Transform Infrared spectroscopy (FTIR) and Nitrogen Adsorption (BET Method). From the obtained results through the techniques mentioned previously it is possible to evidence that the platinum impregnation process did not change the Na Y zeolite structure. Through the superficial specific area (BET) it was possible to observe that the platinum impregnation process caused a decrease in the specific area due to the reduction to the accessibility to the micropores of the zeolitic structure. (author)

  2. ZEOLITIZATION OF SEWAGE SLUDGE ASH WITH A FUSION METHOD

    Directory of Open Access Journals (Sweden)

    Jolanta Latosińska

    2016-11-01

    Full Text Available The study shows the results of zeolitization of municipal sewage sludge ash with the indirect fusion method followed by a hydrothermal method. The zeolitization of sewage sludge ash was conducted at the melting temperature of 550°C and the melting time of 60 minutes, crystallization temperatures of 60°C and 90°C, crystallization time of 6 hours and the SSA:NaOH ratio of 1:1.8; 1:1.4. The research of modified sewage sludge ashes included the observation of changes of ash particles surface and the identification of crystalized phases. The zeolitization of sewage sludge ash at the ratio of SSA:NaOH 1.0:1.4 did not cause the formation of zeolite phases. On the other hand, the zeolitization at the ratio of SSA:NaOH 1.0:1.8 resulted in the formation of desired zeolite phases such as zeolite Y (faujasite and hydroxysodalite. The presented method of sewage sludge ash zeolitization allows to obtain highly usable material. Synthesized zeolites may be used as adsorbents and ion exchangers. They can be potentially used to remove heavy metals as well as ammonia from water and wastewater.

  3. Aluminum-rich mesoporous MFI - type zeolite single crystals

    DEFF Research Database (Denmark)

    Kustova, Marina; Kustov, Arkadii; Christensen, Christina Hviid

    2005-01-01

    are characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), ammonia temperature programmed desorption (NH3-TPD), and N-2 adsorption measurements. The obtained zeolites combine the high crystallinity and the characteristic micropores of zeolites with an intracrystalline mesopore system....... With this technique, only zeolites with relatively low Al contents were reported (Si/Al ratio about 100). In this work, the preparation of aluminum-rich mesoporous MFI-type zeolite single crystals (Si/Al similar to 16-50) using aluminum isopropoxide as the aluminum Source is reported for the first time. All samples...

  4. Human bile sorption by cancrinite-type zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Linares, Carlos F. [Laboratorio de Catalisis y Metales de Transicion, Facultad de Ciencias y Tecnologia, Departamento de Quimica, Universidad de Carabobo, Valencia. Edo. Carabobo, Apartado Postal 3336 (Venezuela, Bolivarian Republic of)], E-mail: clinares@uc.edu.ve; Colmenares, Maryi; Ocanto, Freddy [Laboratorio de Catalisis y Metales de Transicion, Facultad de Ciencias y Tecnologia, Departamento de Quimica, Universidad de Carabobo, Valencia. Edo. Carabobo, Apartado Postal 3336 (Venezuela, Bolivarian Republic of); Valbuena, Oscar [Facultad de Ciencias y Tecnologia, Departamento de Biologia, Universidad de Carabobo, Valencia. Edo. Carabobo, Apartado Postal 3336 (Venezuela, Bolivarian Republic of)], E-mail: ovalbuena@uc.edu.ve

    2009-01-01

    A nitrated cancrinite-type zeolite was synthesized from zeolite X, NaOH and NaNO{sub 3} solutions under autogeneous pressure at 80 deg. C for 48 h. This zeolite was characterized by X-ray diffraction (XRD), FT-IR-spectroscopy, scanning electron microscopy (SEM) and BET surface area. XRD, SEM and FT-IR confirmed the presence of nitrated cancrinite-type zeolite without other collateral phases as sodalite. Then, this sodium zeolite was exchanged with potassium and calcium cations and finally, these modified zeolites were reacted with biliar solutions from human gallbladder. Several factors such as: mass of used cancrinite, nature of the exchanged cation and reaction time of the cancrinite-bile solution interactions were studied. The composition of bile solutions (bile acids, phospholipids and bilirubin) was analyzed before and after the cancrinite-bile solution reaction. Results showed that the components of the bile were notably reduced after the contact with solids. Ca-cancrinite, 120 min of reaction time and 500 mg of solids were the best conditions determined for the bile acid reduction in human bile. When the modified zeolites were compared with the commercial cholestyramine, it was found that zeolites were more active than the latter. These zeolites may be an alternative choice to diminish cholesterol levels in hypercholesterolemic patients.

  5. Hydrothermal synthesis of free-template zeolite T from kaolin

    Science.gov (United States)

    Arshad, Sazmal E.; Yusslee, Eddy F.; Rahman, Md. Lutfor; Sarkar, Shaheen M.; Patuwan, Siti Z.

    2017-12-01

    Free-template zeolite T crystals were synthesized via hydrothermal synthesis by utilizing the activated kaolin as silica and alumina source, with the molar composition of 1 SiO2: 0.04 Al2O3: 0.26 Na2O: 0.09 K2O: 14 H2O. Observation of the formation of free-template zeolite crystals were done at temperature 90°C, 100 °C and 110 °C respectively. It was therefore determined that during the 120 h of the synthesis at 90 °C, zeolite T nucleated and formed a first competitive phase with zeolite L. As temperature increases to 100 °C, zeolite T presented itself as a major phase in the system at time 168 h. Subsequently, development of Zeolite T with second competitive phase of zeolite W was observed at temperature 110 °C. In this study, XRD and SEM instruments were used to monitor the behavior of zeolite T crystals with respect of temperature and time. By using natural resource of kaolin clay as a starting material, this paper hence aims to provide new findings in synthesis of zeolite T using low energy consumption and low production cost.

  6. Progress on Zeolite-membrane-aided Organic Acid Esterification

    Science.gov (United States)

    Makertiharta, I. G. B. N.; Dharmawijaya, P. T.

    2017-07-01

    Esterification is a common route to produce carboxylic acid esters as important intermediates in chemical and pharmaceutical industries. However, the reaction is equilibrium limited and needs to be driven forward by selective removal one of the products. There have been some efforts to selectively remove water from reaction mixture via several separation processes (such as pervaporation and reactive distillation). Integrated pervaporation and esterification has gained increasing attention towards. Inorganic zeolite is the most popular material for pervaporation due to its high chemical resistant and separation performance towards water. Zeolite also has proven to be an effective material in removing water from organic compound. Zeolite can act not only as selective layer but also simultaneously act as a catalyst on promoting the reaction. Hence, there are many configurations in integrating zeolite membrane for esterification reaction. As a selective layer to remove water from reaction mixture, high Si/Al zeolite is preferred to enhance its hydrophilicity. However, low Si/Al zeolite is unstable in acid condition due to dealumination thus eliminate its advantages. As a catalyst, acid zeolites (e.g. H-ZSM-5) provide protons for autoprotolysis of the carboxylic acid similar to other catalyst for esterification (e.g. inorganic acid, and ion exchange resins). There are many studies related to zeolite membrane aided esterification. This paper will give brief information related to zeolite membrane role in esterification and also research trend towards it.

  7. Influencing the selectivity of zeolite Y for triglycine adsorption.

    Science.gov (United States)

    Wijntje, R; Bosch, H; de Haan, A B; Bussmann, P J T

    2007-02-16

    In prior work we studied the adsorption of triglycine on zeolite Y under reference conditions. This study aims to solve the question of which adsorbent properties and process conditions influence the adsorption triglycine from an aqueous solution by zeolite Y. Relevant zeolite parameters to study are: the amount of acidic sites (Si/Al(2) ratio), counter ion, micropore structure. Process conditions that may influence triglycine adsorption are pH, other components such as sugars, amino acids and salts, and temperature. Adsorption of triglycine on zeolite HY is dominated by ionic interaction. The capacity and selectivity of zeolite HY for triglycine can be changed by choosing different Si/Al(2) ratios or changing the counter ion. The presence of cations and basic anions in solutions reduces triglycine adsorption. Fructose and glycine have no significant influence on triglycine adsorption. Temperature only has a slight influence. The pore structure of zeolite Y is not a critical factor for triglycine adsorption, provided pores are accessible to triglycine and in the micropore range (<2 nm). While this allows other zeolites than zeolite Y to be applied, the presence of the supercage structure of zeolite Y is beneficial to obtain better adsorption of triglycine in its neutral form.

  8. Regeneration of zeolite catalysts of isobutane alkylation with butenes

    Energy Technology Data Exchange (ETDEWEB)

    Manza, I.A.; Tsupryk, I.N.; Bartyshevskii, V.A.; Gaponenko, O.I.; Petrilyak, K.I.

    1986-12-10

    The industrial adoption of alkylation of isoalkanes with alkenes is held back by the rapid and irreversible deactivation of the zeolite catalysts appropriate to the process. This paper is aimed specifically at the restoration of the catalytic activity and increase in the service life of zeolite alkylation catalysts. The catalyst chosen for the investigation was HLaCaNaX zeolite both unmodified and modified with various multivalence cations. The thermochemical and oxidative regeneration process as well as the equipment utilized are described. Both the advantages and the drawbacks of the method are given; explanations for the possibly irreversible losses of the catalytic properties in the regenerated zeolites are also put forward.

  9. Performance of zeolite scavenge column in Xe monitoring system

    International Nuclear Information System (INIS)

    Wang Qian; Wang Hongxia; Li Wei; Bian Zhishang

    2010-01-01

    In order to improve the performance of zeolite scavenge column, its ability of removal of humidity and carbon dioxide was studied by both static and dynamic approaches. The experimental results show that various factors, including the column length and diameter, the mass of zeolite, the content of water in air, the temperature rise during adsorption, and the activation effectiveness all effect the performance of zeolite column in scavenging humanity and carbon dioxide. Based on these results and previous experience, an optimized design of the zeolite column is made for use in xenon monitoring system. (authors)

  10. Direct incorporation of B, Al, and Ga into medium-pore ITH zeolite: Synthesis, acidic, and catalytic properties

    Czech Academy of Sciences Publication Activity Database

    Shamzhy, Mariya; Ochoa-Hernández, C.; Kasneryk, Valeryia I.; Opanasenko, Maksym; Mazur, Michal

    2016-01-01

    Roč. 277, č. 1 (2016), s. 37-47 ISSN 0920-5861 R&D Projects: GA ČR(CZ) GP14-30898P Institutional support: RVO:61388955 Keywords : germanosilicate zeolites * ITH * isomorphous substitution Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.636, year: 2016

  11. Two-dimensional zeolites: Adsorption of carbon dioxide on pristine materials and on materials modified by magnesium oxide

    Czech Academy of Sciences Publication Activity Database

    Zukal, Arnošt; Kubů, Martin; Pastva, Jakub

    2017-01-01

    Roč. 21, OCT 2017 (2017), s. 9-16 ISSN 2212-9820 R&D Projects: GA ČR(CZ) GAP106/12/0189 Institutional support: RVO:61388955 Keywords : Carbon dioxide adsorption * Two-dimensional zeolites * Magnesium oxide incorporation Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry Impact factor: 4.292, year: 2016

  12. Self-templating synthesis of hollow spheres of zeolite ZSM-5 from spray-dried aluminosilicate precursor

    Czech Academy of Sciences Publication Activity Database

    Pashková, Veronika; Tokarová, V.; Brabec, Libor; Dědeček, Jiří

    2016-01-01

    Roč. 228, JUL 2016 (2016), s. 59-63 ISSN 1387-1811 R&D Projects: GA ČR GA15-13876S; GA MŠk LM2015073 Institutional support: RVO:61388955 Keywords : MFI * zeolite shells * template free synthesis Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.615, year: 2016

  13. Tuning of acidic and catalytic properties of IWR zeolite by post-synthesis incorporation of three-valent elements

    Czech Academy of Sciences Publication Activity Database

    Shamzhy, Mariya; de O. Ramos, F. S.

    2015-01-01

    Roč. 243, APR 2015 (2015), s. 76-84 ISSN 0920-5861 R&D Projects: GA ČR(CZ) GP14-30898P Institutional support: RVO:61388955 Keywords : germanosilicate zeolites * IWR * alumination Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.312, year: 2015

  14. H-ZSM-5 Zeolite Model Crystals: Structure-Diffusion-Activity Relationship in Methanol-to-Olefins Catalysis.

    Czech Academy of Sciences Publication Activity Database

    Losch, P.; Pinar, A.B.; Willinger, M.G.; Soukup, Karel; Chavan, S.; Vincent, B.; Pale, P.; Louis, B.

    2017-01-01

    Roč. 345, JAN 1 (2017), s. 11-23 ISSN 0021-9517 Grant - others:NRFL(LU) 5898454 Institutional support: RVO:67985858 Keywords : zeolite * methanol -to-olefins (MTO) * model catalyst Subject RIV: CI - Industrial Chemistry, Chemical Engineering OBOR OECD: Chemical process engineering Impact factor: 6.844, year: 2016

  15. Catalytic cracking of Arabian Light VGO over novel zeolites as FCC catalyst additives for maximizing propylene yield

    Czech Academy of Sciences Publication Activity Database

    Hussain, A. I.; Aitani, A.; Kubů, Martin; Čejka, Jiří; Al-Khattaf, S.

    2016-01-01

    Roč. 167, MAR 2016 (2016), s. 226-239 ISSN 0016-2361 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : catalytic cracking * FCC additives * 10-ring zeolites Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.601, year: 2016

  16. Biomass catalytic fast pyrolysis over hierarchical ZSM-5 and Beta zeolites modified with Mg and Zn oxides

    Czech Academy of Sciences Publication Activity Database

    Hernando, H.; Moreno, I.; Fermoso, J.; Ochoa-Hernández, Cristina; Pizarro, P.; Coronado, J. M.; Čejka, Jiří; Serrano, D. P.

    2017-01-01

    Roč. 7, č. 3 (2017), s. 289-304 ISSN 2190-6815 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : catalytic fast pyrolysis * hierarchial zeolite * bio -oil upgrading Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry

  17. Biomass catalytic fast pyrolysis over hierarchical ZSM-5 and Beta zeolites modified with Mg and Zn oxides

    Czech Academy of Sciences Publication Activity Database

    Hernando, H.; Moreno, I.; Fermoso, J.; Ochoa-Hernández, Cristina; Pizarro, P.; Coronado, J. M.; Čejka, Jiří; Serrano, D. P.

    2017-01-01

    Roč. 7, č. 3 (2017), s. 289-304 ISSN 2190-6815 R&D Projects: GA ČR GBP106/12/G015 Institutional support: RVO:61388955 Keywords : catalytic fast pyrolysis * hierarchial zeolite * bio-oil upgrading Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry

  18. Zeolite MCM-22 Modified with Au and Cu for Catalytic Total Oxidation of Methanol and Carbon Monoxide

    Czech Academy of Sciences Publication Activity Database

    Kaminski, P.; Sobczak, I.; Decyk, P.; Ziolek, M.; Roth, Wieslaw Jerzy; Campo, B.; Daturi, M.

    2013-01-01

    Roč. 117, č. 5 (2013), s. 2147-2159 ISSN 1932-7447 R&D Projects: GA ČR(CZ) GAP106/12/0189 Institutional support: RVO:61388955 Keywords : adsorption * carbon dioxide * MCM-22 zeolites Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.835, year: 2013

  19. Unprecedented propane–SCR-NOx activity over template-free synthesized Al-rich Co-BEA* zeolite

    Czech Academy of Sciences Publication Activity Database

    Sazama, Petr; Mokrzycki, Lukasz; Wichterlová, Blanka; Vondrová, Alena; Pilař, Radim; Dědeček, Jiří; Sklenák, Štěpán; Tabor, Edyta

    2015-01-01

    Roč. 332, DEC 2015 (2015), s. 201-211 ISSN 0021-9517 R&D Projects: GA TA ČR(CZ) TH01021259; GA ČR GA15-13876S Institutional support: RVO:61388955 Keywords : beta zeolite * Al-rich BEA* * OSDA-free synthesis Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 7.354, year: 2015

  20. The Effect of Synthesis Conditions and Nature of Heteroelement on Acidic Properties of Isomorphously Substituted UTL Zeolites

    Czech Academy of Sciences Publication Activity Database

    Shamzhy, Mariya; Shvets, O. V.; Opanasenko, Maksym; Vitvarová, Dana; Nachtigall, P.; Čejka, Jiří

    2013-01-01

    Roč. 1, č. 1 (2013), s. 103-113 ISSN 2327-3941 R&D Projects: GA ČR GBP106/12/G015; GA ČR GAP106/11/0819 Institutional support: RVO:61388955 Keywords : Extra-Large Pore Zeolite * Isomorphous Substitution * Brønsted and Lewis Acidity Subject RIV: CF - Physical ; Theoretical Chemistry

  1. H-ZSM-5 Zeolite Model Crystals: Structure-Diffusion-Activity Relationship in Methanol-to-Olefins Catalysis.

    Czech Academy of Sciences Publication Activity Database

    Losch, P.; Pinar, A.B.; Willinger, M.G.; Soukup, Karel; Chavan, S.; Vincent, B.; Pale, P.; Louis, B.

    2017-01-01

    Roč. 345, JAN 1 (2017), s. 11-23 ISSN 0021-9517 Grant - others:NRFL(LU) 5898454 Institutional support: RVO:67985858 Keywords : zeolite * methanol-to-olefins (MTO) * model catalyst Subject RIV: CI - Industrial Chemistry, Chemical Engineering OBOR OECD: Chemical process engineering Impact factor: 6.844, year: 2016

  2. Synthesis of beta zeolite with mesopores from a milk containing precursor and its performance in naphthalene isopropylation

    Czech Academy of Sciences Publication Activity Database

    Tokarová, V.; Šťávová, G.; Nováková, J.; Stiborová, S.; Kašpárek, A.; Zukal, Arnošt

    2017-01-01

    Roč. 222, č. 1 (2017), s. 343-356 ISSN 1878-5190 Institutional support: RVO:61388955 Keywords : Beta zeolite * Mesopores * Naphthalene isopropylation Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry Impact factor: 1.264, year: 2016

  3. REMOVAL OF DIQUATERNARY AMMONIUM CATIONS FROM AS-SYNTHESIZED SSZ-16 ZEOLITE

    Czech Academy of Sciences Publication Activity Database

    Supiňková, Taťána; Jirka, Ivan; Drahokoupil, Jan; Langmaier, Jan; Fíla, V.; Brabec, Libor; Kočiřík, Milan

    2017-01-01

    Roč. 9, č. 2017 (2017), s. 26-31 E-ISSN 2336-5382 R&D Projects: GA ČR(CZ) GA16-02681S Institutional support: RVO:61388955 ; RVO:68378271 Keywords : zeolite * hydrothermal synthesis * SSZ-16 Subject RIV: CF - Physical ; Theoretical Chemistry; BM - Solid Matter Physics ; Magnetism (FZU-D) OBOR OECD: Physical chemistry; Condensed matter physics (including formerly solid state physics, supercond.) (FZU-D)

  4. Consecutive interlayer disassembly-reassembly during alumination of UOV zeolites: insight into the mechanism

    Czech Academy of Sciences Publication Activity Database

    Kasneryk, Valeryia I.; Opanasenko, Maksym; Shamzhy, Mariya; Musilová, Zuzana; Avadhut, Y. S.; Hartmann, M.; Čejka, Jiří

    2017-01-01

    Roč. 5, č. 43 (2017), s. 22576-22587 ISSN 2050-7488 R&D Projects: GA ČR GA17-01440S Institutional support: RVO:61388955 Keywords : post-synthesis incorporation * structure directing agents * large-pore zeolites * isomorphous substitution * preferential location * catalytic-properties Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry Impact factor: 8.867, year: 2016

  5. TNU-9 Zeolite: Aluminum Distribution and Extra-Framework Sites of Divalent Cations

    Czech Academy of Sciences Publication Activity Database

    Karcz, R.; Dědeček, Jiří; Supronowicz, B.; Thomas, Haunani M.; Klein, Petr; Tabor, Edyta; Sazama, Petr; Pashková, Veronika; Sklenák, Štěpán

    2017-01-01

    Roč. 23, JUL 2017 (2017), s. 8857-8870 ISSN 1521-3765 R&D Projects: GA ČR(CZ) GA15-14007S; GA MŠk(CZ) LM2015073 Grant - others:Ga MŠk(CZ) LM2015070 Institutional support: RVO:61388955 Keywords : Aluminum * Cobalt * Density functional calculations * Structure elucidation * Zeolites Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry

  6. TNU-9 Zeolite: Aluminum Distribution and Extra-Framework Sites of Divalent Cations

    Czech Academy of Sciences Publication Activity Database

    Karcz, R.; Dědeček, Jiří; Supronowicz, B.; Thomas, Haunani M.; Klein, Petr; Tabor, Edyta; Sazama, Petr; Pashková, Veronika; Sklenák, Štěpán

    Roč. 23, JUL 2017 (2017), s. 8857-8870 ISSN 1521-3765 R&D Projects: GA ČR(CZ) GA15-14007S; GA MŠk(CZ) LM2015073 Grant - others:Ga MŠk(CZ) LM2015070 Institutional support: RVO:61388955 Keywords : Aluminum * Cobalt * Density functional calculations * Structure elucidation * Zeolites Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry

  7. Reduction of Nitrogen Oxides using zeolite catalysts exchanged with cobalt

    International Nuclear Information System (INIS)

    Garcia M, E.A.; Bustamante L, F.; Montes de C, C.

    1999-01-01

    The Selective Catalytic Reduction (SCR) of NOx by methane in excess oxygen was studied over several zeolite catalysts; namely cobalt loaded mordenite, ferrierite, SM-5 and the corresponding acid forms. When NO2 predominated n the NOx mixture the acid forms showed the highest N2 formation rates under dry conditions. Mordenite supported catalysts were the most active ones followed by ferrierite and ZSM-5. The most active Co-Mordenite catalyst was tested using a NOx mixture, containing mostly NO, under dry conditions and in the presence of water and SO2. The addition of 8 % water to the reaction mixture lead to a reversible deactivation, mainly at low temperatures. When the reaction mixture contained 60 ppm SO2, the N2 formation rate decreased about a half likely due to SO2 poisoning

  8. Zeolites as possible biofortifiers in Maitake cultivation

    Directory of Open Access Journals (Sweden)

    Vunduk Jovana

    2014-01-01

    Full Text Available The levels of Ni, Cu and Mg in Grifola frondosa (also known as Maitake mushroom fruit body produced on zeolite Minazel Plus (MG-supplemented substrate were measured with inductively coupled plasma optical emission spectrometry (ICP-OES. Two different concentrations of MG were added to the substrate for mushroom cultivation. Levels of selected metals were measured in cultivated dry carpophores. The content of Ni increased in fruit bodies produced on supplemented substrate, while in case of Cu, a pronounced decrease was observed. When two different concentrations of MG were implemented, the Mg level showed both positive and negative trend, depending on the applied concentration of zeolite. MG in a concentration of 1% showed the strongest influence on the observed elements in the cultivated fruiting body of Maitake mushroom. [Projekat Ministarstva nauke Republike Srbije, br. 46010

  9. Zeolite membranes for effective production of biofuels

    OpenAIRE

    Sjöberg, Erik

    2012-01-01

    To deal with the increasing demand of renewable fuels, more efficient processes for the production of biofuels are needed. Zeolite membranes have the potential to improve many existing processes that could be used for production of biofuels. Methanol is a potential biofuel that may be produced from synthesis gas in an equilibrium limited reaction. The production of methanol from synthesis gas could be improved by use of a membrane reactor, which could increase the conversion of synthesis gas ...

  10. Acylation Reactions over Zeolites and Mesoporous Catalysts

    Czech Academy of Sciences Publication Activity Database

    Voláková, Martina; Vitvarová, Dana; Čejka, Jiří

    2009-01-01

    Roč. 2, č. 6 (2009), s. 486-499 ISSN 1864-5631 R&D Projects: GA ČR GA104/07/0383; GA ČR GD203/08/H032; GA MPO FT-TA5/005 Institutional research plan: CEZ:AV0Z40400503 Keywords : acylation * ketones * mesoporous materials * shape-selectivity * zeolites Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 4.767, year: 2009

  11. Transformations of aromatic hydrocarbons over zeolites

    Czech Academy of Sciences Publication Activity Database

    Voláková, Martina; Žilková, Naděžda; Čejka, Jiří

    2008-01-01

    Roč. 34, 5-7 (2008), s. 439-454 ISSN 0922-6168 R&D Projects: GA ČR GA203/05/0197; GA AV ČR 1QS400400560; GA AV ČR KJB4040402 Institutional research plan: CEZ:AV0Z40400503 Keywords : aromatic hydrocarbons * zeolites * alkylation Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 0.514, year: 2008

  12. Characterization of active sites in zeolite catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Eckert, J. [Los Alamos National Lab., NM (United States); Bug, A. [Swarthmore Coll., PA (United States); Nicol, J.M. [MOLTECH (United States)] [and others

    1997-11-01

    This is the final report of a three-year, Laboratory Directed Research and Development (LDRD) project at the Los Alamos National Laboratory (LANL). Atomic-level details of the interaction of adsorbed molecules with active sites in catalysts are urgently needed to facilitate development of more effective and/or environmentally benign catalysts. To this end the authors have carried out neutron scattering studies combined with theoretical calculations of the dynamics of small molecules inside the cavities of zeolite catalysts. The authors have developed the use of H{sub 2} as a probe of adsorption sites by observing the hindered rotations of the adsorbed H{sub 2} molecule, and they were able to show that an area near the four-rings is the most likely adsorption site for H{sub 2} in zeolite A while adsorption of H{sub 2} near cations located on six-ring sites decreases in strength as Ni {approximately} Co > Ca > Zn {approximately} Na. Vibrational and rotational motions of ethylene and cyclopropane adsorption complexes were used as a measure for zeolite-adsorbate interactions. Preliminary studies of the binding of water, ammonia, and methylamines were carried out in a number of related guest-host materials.

  13. Periodic modeling of zeolite Ti-LTA.

    Science.gov (United States)

    Hernandez-Tamargo, Carlos E; Roldan, Alberto; Ngoepe, Phuti E; de Leeuw, Nora H

    2017-08-21

    We have proposed a combination of density functional theory calculations and interatomic potential-based simulations to study the structural, electronic, and mechanical properties of pure-silica zeolite Linde Type A (LTA), as well as two titanium-doped compositions. The energetics of the titanium distribution within the zeolite framework suggest that the inclusion of a second titanium atom with configurations Ti-(Si) 0 -Ti, Ti-(Si) 1 -Ti, and Ti-(Si) 2 -Ti is more energetically favorable than the mono-substitution. Infra-red spectra have been simulated for the pure-silica LTA, the single titanium substitution, and the configurations Ti-(Si) 0 -Ti and Ti-(Si) 2 -Ti, comparing against experimental benchmarks where available. The energetics of the direct dissociation of water on these Lewis acid sites indicate that this process is only favored when two titanium atoms form a two-membered ring (2MR) sharing two hydroxy groups, Ti-(OH) 2 -Ti, which suggests that the presence of water may tune the distribution of titanium atoms within the framework of zeolite LTA. The electronic analysis indicates charge transfer from H 2 O to the Lewis acid site and hybridization of their electronic states.

  14. Isotopic exchange of deuterium in zeolites

    International Nuclear Information System (INIS)

    Novakova, J.; Kubelkova, L.; Jiru, P.

    1981-01-01

    The information obtainable from the study of deuterium isotope exchange in zeolites by i.r. and m.s. methods is discussed. The conditions necessary for high sensitivity determination of OH groups by gas-phase analysis are mentioned together with a determination of the hydroxyl number in the 3 types of OH groups found in HNaY zeolite by solid-phase analysis. The advantage of the i.r. method in the study of hydroxyl heterogeneity in isotopic exchange is compared with the limited success of the m.s. method. The evaluation of the rates of homo- and hetero-exchange and their dependences on cationic exchange, stabilization and the pretreatment of Msup(n+)HY zeolites are shown. The activation of hydrogen molecules seems to be the slowest step in the exchange which proceeds by a single-step mechanism. The OH groups alone do not activate hydrogen molecules as opposed to Lewis sites formed by dehydroxylation and cations and/or metal particles in suitable concentrations at suitable locations. (author)

  15. Adsorption of ions onto treated natural zeolite

    Directory of Open Access Journals (Sweden)

    Cristiane da Rosa Oliveira

    2007-12-01

    Full Text Available This work presents studies of modification of a natural zeolite by activation with Na+ cations and functionalisation with Ba+2 and/or Cu2+ ions (FZ. The zeolite was characterized, modified and applied in adsorption studies of sulphate and isopropilxanthate ions as flocculated and powdered forms. The reuse of SO4Ba-FZ was investigated by adsorption-removal of either Ba2+ or sulphate ions in stages. Equilibrium data showed that the FZ, flocculated or as powder, provide considerable removal of sulphate ions (q mLangmuir: 1.15 and 1.35 meq.g-1, respectively and isopropilxanthate (q mLangmuir: 0.35 and 0.93 meq.g-1, respectively. The reuse of the SO4-FZ, either powdered or flocculated also uptake significant amount of Ba2+ or sulphate ions (q mLangmuir: 1.15 meq.g-1, providing a new alternative for the exhausted adsorbent. Thus the activated and functionalised zeolites create new options on the materials engineering area with applications in environmental applied adsorption processes.

  16. Hydrophilic and hydrophobic adsorption on Y zeolites

    Science.gov (United States)

    Halasz, Istvan; Kim, Song; Marcus, Bonnie

    The uniform large micropores of hydrothermally stable Y zeolites are used widely to confine both polar and non-polar molecules. This paper compares the physisorption of water, methanol, cyclohexane, benzene and other adsorbates over various Y zeolites. These adsorbents are commercial products with reproducibly controllable physical and chemical characteristics. Results indicate that the type I isotherms typical for micropore adsorption can turn into type II or type III isotherms depending on either or both the hydrophobicity of the adsorbent and the polarity of the adsorbate. Methanol produced a rare type V isotherm not reported over zeolites before. Canonical and grand canonical Monte Carlo molecular simulations with Metropolis importance sampling reproduced the experimental isotherms and showed characteristic geometric patterns for molecules confined in Na-X, Na-Y, dealuminated Y, and ZSM5 structures. Adsorbate-adsorbate interactions seem to determine the micropore condensation of both polar and non-polar molecules. Exchanged ions and lattice defects play a secondary role in shaping the adsorption isotherms. The force field of hydrophobic Y appears to exert an as yet unexplored sieving effect on adsorbates having different dipole moments and partial charge distributions. This mechanism is apparently different from both the monolayer formation controlled adsorption on hydrophobic mesopores and macropores and the polarizability and small-pore opening controlled micropore confinement in hydrophobic ZSM5.

  17. Zeolite thin films: from computer chips to space stations.

    Science.gov (United States)

    Lew, Christopher M; Cai, Rui; Yan, Yushan

    2010-02-16

    Zeolites are a class of crystalline oxides that have uniform and molecular-sized pores (3-12 A in diameter). Although natural zeolites were first discovered in 1756, significant commercial development did not begin until the 1950s when synthetic zeolites with high purity and controlled chemical composition became available. Since then, major commercial applications of zeolites have been limited to catalysis, adsorption, and ion exchange, all using zeolites in powder form. Although researchers have widely investigated zeolite thin films within the last 15 years, most of these studies were motivated by the potential application of these materials as separation membranes and membrane reactors. In the last decade, we have recognized and demonstrated that zeolite thin films can have new, diverse, and economically significant applications that others had not previously considered. In this Account, we highlight our work on the development of zeolite thin films as low-dielectric constant (low-k) insulators for future generation computer chips, environmentally benign corrosion-resistant coatings for aerospace alloys, and hydrophilic and microbiocidal coatings for gravity-independent water separation in space stations. Although these three applications might not seem directly related, they all rely on the ability to fine-tune important macroscopic properties of zeolites by changing their ratio of silicon to aluminum. For example, pure-silica zeolites (PSZs, Si/Al = infinity) are hydrophobic, acid stable, and have no ion exchange capacity, while low-silica zeolites (LSZs, Si/Al zeolites that have not been exploited before, such as a higher elastic modulus, hardness, and heat conductivity than those of amorphous porous silicas, and microbiocidal capabilities derived from their ion exchange capacities. Finally, we briefly discuss our more recent work on polycrystalline zeolite thin films as promising biocompatible coatings and environmentally benign wear-resistant and

  18. New antiaxillary odour deodorant made with antimicrobial Ag-zeolite (silver-exchanged zeolite).

    Science.gov (United States)

    Nakane, T; Gomyo, H; Sasaki, I; Kimoto, Y; Hanzawa, N; Teshima, Y; Namba, T

    2006-08-01

    The causative substances for axillary osmidrosis, which are often found in apocrine sweat, are the decomposed/denatured products of short-chain fatty acid and other biological metabolite compounds produced by axillary-resident bacteria. Conventional underarm deodorants suppress the process of odour production mostly by the following mechanism: (1) suppression of perspiration, (2) reduction in numbers of resident bacteria, (3) deodorization and (4) masking. The most important and effective method to reduce odour is to suppress the growth of resident bacteria with antimicrobials, which have several drawbacks, especially in their safety aspect. To solve these problems, we focused on Ag-zeolite (silver-exchanged zeolite) that hold stable Ag, an inorganic bactericidal agent, in its structure, and therefore, poses less risk in safety. Its bactericidal effect on skin-resident bacteria was found to be excellent and comparable with that of triclosan, a most frequently used organic antimicrobial in this product category. The dose-response study of Ag-zeolite powder spray (0-40 w/w%) using 39 volunteers revealed that 5-40 w/w% Ag-zeolite could show a sufficient antimicrobial effect against skin-resident bacteria. The comparison study using 0.2 w/w% triclosan as the control and 10 w/w% Ag-zeolite indicated that: (1) one application of the powder spray containing 10 w/w% Ag-zeolite could show a sufficient antimicrobial effect against the resident bacteria and its effect continued for 24 h, (2) a powder spray containing 0.2 w/w% triclosan was unable to show a sufficient antimicrobial effect, and (3) no adverse event was observed. These studies show that Ag-zeolite has a superior antimicrobial ability that is rarely found in conventional antimicrobials used in deodorant products and a strong antiaxillary odour deodorant ability because of its long-lasting effect. During clinical study, patch tests with humans and other clinical studies of this product showed no adverse events

  19. Design and characterization of chitosan/zeolite composite films — Effect of zeolite type and zeolite dose on the film properties

    Energy Technology Data Exchange (ETDEWEB)

    Barbosa, Gustavo P.; Debone, Henrique S. [Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Universidade Federal de São Paulo, Diadema (Brazil); Severino, Patrícia [Universidade Tiradentes, Instituto de Tecnologia e Pesquisa, Aracaju (Brazil); Souto, Eliana B. [Department of Pharmaceutical Technology, Faculty of Pharmacy, University of Coimbra (FFUC), Pólo das Ciências da Saúde, Azinhaga de Santa Comba, 3000-548, Coimbra (Portugal); Center for Neuroscience and Cell Biology & Institute for Biomedical Imaging and Life Sciences (CNC-IBILI), University of Coimbra, Pólo das Ciências da Saúde, Azinhaga de Santa Comba, 3000-548, Coimbra (Portugal); Silva, Classius F. da, E-mail: cfsilva@unifesp.br [Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Universidade Federal de São Paulo, Diadema (Brazil)

    2016-03-01

    Chitosan films can be used as wound dressings for the treatment of chronic wounds and severe burns. The antimicrobial properties of these films may be enhanced by the addition of silver. Despite the antimicrobial activity of silver, several studies have reported the cytotoxicity as a factor limiting its biomedical applications. This problem may, however, be circumvented by the provision of sustained release of silver. Silver zeolites can be used as drug delivery platforms to extend the release of silver. The objective of this study was to evaluate the addition of clinoptilolite and A-type zeolites in chitosan films. Sodium zeolites were initially subjected to ion-exchange in a batch reactor. Films were prepared by casting technique using a 2% w/w chitosan solution and two zeolite doses (0.1 or 0.2% w/w). Films were characterized by thermal analysis, color analysis, scanning electron microscopy, X-ray diffraction, and water vapor permeation. The results showed that films present potential for application as dressing. The water vapor permeability is one of the main properties in wound dressings, the best results were obtained for A-type zeolite/chitosan films, which presented a brief reduction of this property in relation to zeolite-free chitosan film. On the other hand, the films containing clinoptilolite showed lower water vapor permeation, which may be also explained by the best distribution of the particles into the polymer which also promoted greater thermal resistance. - Highlights: • Zeolite/chitosan composite films were prepared by casting technique. • Micrographs showed slight difference according to the content and A-type zeolite. • The barrier properties of the films were suitable to the dressing application. • Film characterization suggested that zeolites interacted with the chitosan chain.

  20. Comparison of the defluoridation capacity of zeolites from Ethiopia ...

    African Journals Online (AJOL)

    Fluorosis, either dental or skeleton, is often due to the high fluoride content of well waters. In this work, using solutions which contain different amounts of fluoride, natural zeolites from Ethiopia and Mexico were tested. It is shown that, although zeolites are known to be cationic exchangers, their extra-framework aluminum ...

  1. Rotational dynamics of propylene inside Na-Y zeolite cages

    Indian Academy of Sciences (India)

    of propylene molecules (r ~ 1.91 Å), shape (asymmetry of propylene molecules) and higher concentration of propylene molecules in Na-Y zeolite (~5 molecules per supercage). References. [1] G Tomlinson, Modern zeolites, structure and function in detergents and petrochemicals. (Traw Tech Publications Ltd., Switzerland, ...

  2. Zeolite H-BEA catalysed multicomponent reaction: One-pot ...

    Indian Academy of Sciences (India)

    lent thermal stability which make them economically and environmentally feasible.2 The use of zeolites as a ... of zeolite H-BEA was added. The mixture was stirred under thermal solvent-free condition at 120. ◦. C in oil bath for 5–7min and the reaction was followed by. TLC. After completion of reaction, mass was cooled to.

  3. Inelastic neutron scattering from non-framework species within zeolites

    International Nuclear Information System (INIS)

    Newsam, J.M.; Brun, T.O.; Trouw, F.; Iton, L.E.; Curtiss, L.A.

    1990-01-01

    Inelastic and quasielastic neutron scattering have special advantages for studying certain of the motional properties of protonated or organic species within zeolites and related microporous materials. In this paper these advantages and various experimental methods are outlined, and illustrated by measurements of torsional vibrations and rotational diffusion of tetramethylammonium (TMA) cations occluded within zeolites TMA-sodalite, omega, ZK-4 and SAPO-20

  4. Structure modification of natural zeolite for waste removal application

    Science.gov (United States)

    Widayatno, W. B.

    2018-03-01

    Tremendous industrialization in the last century has led to the generation of huge amount of waste. One of the recent hot research topics is utilizing any advance materials and methods for waste removal. Natural zeolite as an inexpensive porous material with a high abundance holds a key for efficient waste removal owing to its high surface area. However, the microporous structure of natural zeolite hinders the adsorption of waste with a bigger molecular size. In addition, the recovery of natural zeolite after waste adsorption into its pores should also be considered for continuous utilization of this material. In this study, the porosity of natural zeolite from Tasikmalaya, Indonesia, was hydrothermally-modified in a Teflon-lined autoclave filled with certain pore directing agent such as distilled water, KOH, and NH4OH to obtain hierarchical pore structure. After proper drying process, the as-treated natural zeolite is impregnated with iron cation and heat-treated at specified temperature to get Fe-embedded zeolite structure. XRD observation is carried out to ensure the formation of magnetic phase within the zeolite pores. The analysis results show the formation of maghemite phase (γ-Fe2O3) within the zeolite pore structure.

  5. Nonionic emulsion-mediated synthesis of zeolite beta

    Indian Academy of Sciences (India)

    Zeolite beta synthesis was first carried out in a newly developed emulsion system containing nonionic polyoxyethylated alkylphenol surfactant, which showed interesting non-conventional features. Compared to the conventional hydrothermal synthesis of zeolite beta, the reported nonionic emulsion system showed a faster ...

  6. Efficacy of natural zeolite and pigments on yolk color and ...

    African Journals Online (AJOL)

    user

    2011-04-16

    Apr 16, 2011 ... The YI was significantly affected by zeolite and pigment levels. Hens fed zeolite tended (P = 0.062) to lay eggs with a lighter shell weight (%) during the entire period compared with the control group. This effect was signifi- cant in 49 to 50 weeks of age, in a quadratic manner. A linear decrease in YI between ...

  7. 3D Nanoscale Imaging and Quantitative Analysis of Zeolite Catalysts

    NARCIS (Netherlands)

    Zecevic, J.

    2013-01-01

    Zeolites are crystalline microporous aluminosilicates, one of the most versatile and widely used class of materials.The unique physico-chemical properties of zeolites are found to be irreplaceable in many industrial processes such as separation, adsorption and catalysis. To exploit their full

  8. Mesoporous zeolite and zeotype single crystals synthesized in fluoride media

    DEFF Research Database (Denmark)

    Egeblad, Kresten; Kustova, Marina; Klitgaard, Søren Kegnæs

    2007-01-01

    We report the synthesis and characterization of a series of new mesoporous zeolite and zeotype materials made available by combining new and improved procedures for directly introducing carbon into reaction mixtures with the fluoride route for conventional zeolite synthesis. The mesoporous...

  9. Defluorination of drinking water using surfactant modified zeolites ...

    African Journals Online (AJOL)

    This study focused on the removal of fluoridefrom groundwater by employing surfactant modified zeolites (SMZ) synthesized using locallyavailable kaolin material as precursor. The zeolite synthesis involved calcination of kaolin, alkaline fusion and hydrothermal treatment. The final product was modified with 5g/L ...

  10. Nonionic emulsion-mediated synthesis of zeolite beta

    Indian Academy of Sciences (India)

    Administrator

    Abstract. Zeolite beta synthesis was first carried out in a newly developed emulsion system containing nonionic polyoxyethylated alkylphenol surfactant, which showed interesting non-conventional features. Compared to the conventional hydrothermal synthesis of zeolite beta, the reported nonionic emulsion system showed ...

  11. Zeolite Membranes : Ozone Detemplation, Modeling, and Performance Characterization

    NARCIS (Netherlands)

    Kuhn, J.

    2009-01-01

    Membrane technology plays an increasingly important role in developing a more sustainable process industry. Zeolites are a novel class of membrane materials with unique properties enabling molecular sieving and affinity based separations. This thesis proposes some new concepts in zeolite membrane

  12. Zeolite H-BEA catalysed multicomponent reaction: One-pot ...

    Indian Academy of Sciences (India)

    attention because of their tunable acidity and the vari- ety of structures and pore dimensions. The other salient features of zeolite include their low cost and excel- lent thermal stability which make them economically and environmentally feasible.2 The use of zeolites as a catalyst is important in the development of clean tech-.

  13. FUNDAMENTALS AND APPLICATIONS OF PERVAPORATION THROUGH ZEOLITE MEMBRANES

    Science.gov (United States)

    Zeolite membranes are well suited for separating liquid-phase mixtures by pervaporation because of their molecular-sized pores and their hydrophilic/hydrophobic nature, and the first commercial application of zeolite membranes has been for dehydrating organics [1]. Because of ...

  14. A novel urea conductometric biosensor based on zeolite immobilized urease.

    Science.gov (United States)

    Kirdeciler, Salih Kaan; Soy, Esin; Oztürk, Seçkin; Kucherenko, Ivan; Soldatkin, Oleksandr; Dzyadevych, Sergei; Akata, Burcu

    2011-09-15

    A new approach was developed for urea determination where a thin film of silicalite and zeolite Beta deposited onto gold electrodes of a conductometric biosensor was used to immobilize the enzyme. Biosensor responses, operational and storage stabilities were compared with results obtained from the standard membrane methods for the same measurements. For this purpose, different surface modification techniques, which are simply named as Zeolite Membrane Transducers (ZMTs) and Zeolite Coated Transducers (ZCTs) were compared with Standard Membrane Transducers (SMTs). Silicalite and zeolite Beta with Si/Al ratios 40, 50 and 60 were used to modify the conductometric electrodes and to study the biosensor responses as a function of changing zeolitic parameters. During the measurements using ZCT electrodes, there was no need for any cross-linker to immobilize urease, which allowed the direct evaluation of the effect of changing Si/Al ratio for the same type of zeolite on the biosensor responses for the first time. It was seen that silicalite and zeolite Beta added electrodes in all cases lead to increased responses with respect to SMTs. The responses obtained from ZCTs were always higher than ZMTs as well. The responses obtained from zeolite Beta modified ZMTs and ZCTs increased as a function of increasing Si/Al ratio, which might be due to the increased hydrophobicity and/or the acid strength of the medium. Copyright © 2011 Elsevier B.V. All rights reserved.

  15. Generalized synthesis of mesoporous shells on zeolite crystals

    KAUST Repository

    Han, Yu

    2010-12-30

    A simple and generalized synthetic approach is developed for creating mesoporous shells on zeolite crystals. This method allows for the tailoring of thickness, pore size, and composition of the mesoporous shell, and can be applied to zeolites of various structures, compositions, and crystal sizes. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. Adsorption selectivity of benzene and propene mixtures for various zeolites

    NARCIS (Netherlands)

    Ban, S.|info:eu-repo/dai/nl/304837288; van Laak, A.N.C.|info:eu-repo/dai/nl/304833223; de Jongh, P.E.|info:eu-repo/dai/nl/186125372; van der Eerden, J.P.J.M.|info:eu-repo/dai/nl/068420471; Vlugt, T.J.H.|info:eu-repo/dai/nl/205040187

    2007-01-01

    The nine-site benzene model of Zhao et al. (J. Phys. Chem. B 2005, 109, 5368-5374) has been used to systematically study the adsorption of benzene, propene, and benzene-propene mixtures in zeolites mordenite, Y, , silicalite, and MCM22. Interaction parameters for the benzene-zeolite interactions

  17. Obtaining of iron particles of nanometer size in a natural zeolite

    International Nuclear Information System (INIS)

    Xingu C, E. G.

    2013-01-01

    The zeolites are aluminosilicates with cavities that can act as molecular sieve. Their crystalline structure is formed by tetrahedrons that get together giving place to a three-dimensional net, in which each oxygen is shared by two silicon atoms, being this way part of the tecto silicate minerals, its external and internal areas reach the hundred square meters for gram, they are located in a natural way in a large part of earth crust and also exist in a synthetic way. In Mexico there are different locations of zeolitic material whose important component is the clinoptilolite. In this work the results of three zeolitic materials coming from San Luis Potosi are shown, the samples were milled and sieved for its initial characterization, to know its chemical composition, crystalline phases, morphology, topology and thermal behavior before and after its homo-ionization with sodium chloride, its use as support of iron particles of nanometer size. The description of the synthesis of iron particles of nanometer size is also presented, as well as the comparison with the particles of nanometer size synthesized without support after its characterization. The characterization techniques used during the experimental work were: Scanning electron microscopy, X-ray diffraction, Infrared spectroscopy, specific area by means of BET and thermogravimetry analysis. (Author)

  18. Treatments of reverse osmosis concentrate using natural zeolites

    Directory of Open Access Journals (Sweden)

    Taherifar Hossein

    2015-06-01

    Full Text Available The purpose of the current study is to experimentally investigate the reduction of sodium adsorption ratio (SAR from a concentrated stream of reversed osmosis (RO using natural zeolites. In order to reduce the salinity of solution, experiments were carried out using zeolites of varying concentration, pretreatment of adsorbents, and the addition of Ethylenediaminetetraacetic acid (EDTA. The results show that both zeolites can be used in an RO brine treatment; however, Rhyolitic tuff is more effective than clinoptilolite for the reduction of water salinity. The experiments show that Rhyolitic tuff decreases salinity of RO concentrate to nearly one – third of the initial value. Statistical analyses show that the effect of zeolite concentration is negligible. Furthermore, the addition of EDTA and pretreatment of zeolite increase the SAR values.

  19. Tailoring the porosity of hierarchical zeolites by carbon-templating

    DEFF Research Database (Denmark)

    Zhu, Kake; Egeblad, Kresten; Christensen, Claus H.

    2008-01-01

    We report the synthesis and characterization of a series of hierarchical porous zeolite single crystal materials with a range of porosities made available by carbon-templating using differently-sized carbon particles as templates for the additional non-micropore porosity. The materials were...... prepared by adsorption of the required zeolite synthesis gel components onto various commercially available carbon black powders followed by crystallization of the zeolite crystals in the presence of the inert carbon matrix and subsequent removal of the carbon particles embedded in the zeolite crystals...... by combustion. It is shown that the additional porosity of the hierarchical zeolites can be tailored by encapsulation of the differently-sized carbon particles during crystallization....

  20. Synthesis and catalytic applications of combined zeolitic/mesoporous materials

    Directory of Open Access Journals (Sweden)

    Jarian Vernimmen

    2011-11-01

    Full Text Available In the last decade, research concerning nanoporous siliceous materials has been focused on mesoporous materials with intrinsic zeolitic features. These materials are thought to be superior, because they are able to combine (i the enhanced diffusion and accessibility for larger molecules and viscous fluids typical of mesoporous materials with (ii the remarkable stability, catalytic activity and selectivity of zeolites. This review gives an overview of the state of the art concerning combined zeolitic/mesoporous materials. Focus is put on the synthesis and the applications of the combined zeolitic/mesoporous materials. The different synthesis approaches and formation mechanisms leading to these materials are comprehensively discussed and compared. Moreover, Ti-containing nanoporous materials as redox catalysts are discussed to illustrate a potential implementation of combined zeolitic/mesoporous materials.

  1. Fly ash based zeolitic pigments for application in anticorrosive paints

    International Nuclear Information System (INIS)

    Shaw, Ruchi; Tiwari, Sangeeta

    2016-01-01

    The purpose of this work is to evaluate the utilization of waste fly ash in anticorrosive paints. Zeolite NaY was synthesized from waste fly ash and subsequently modified by exchanging its nominal cation Na + with Mg 2+ and Ca 2+ ions. The metal ion exchanged zeolite was then used as anticorrosive zeolitic pigments in paints. The prepared zeolite NaY was characterized using X-Ray diffraction technique and Scanning electron microscopy. The size, shape and density of the prepared fly ash based pigments were determined by various techniques. The paints were prepared by using fly ash based zeolitic pigments in epoxy resin and the percentages of pigments used in paints were 2% and 5%. These paints were applied to the mild steel panels and the anticorrosive properties of the pigments were assessed by the electrochemical spectroscopy technique (EIS).

  2. Obtaining and preliminary structural characterization of membranes of zeolite through the PLD technique

    International Nuclear Information System (INIS)

    Concepción-Rosabal, B.; Rodríguez-Iznaga, I.; Rodríguez, E.; Pentón-Madrigal, A.

    2008-01-01

    Full text: This paper presents the preliminary results of the obtaining of membranes of natural zeolites exchanged with metal species through the P ulsed Laser technique Deposition ( PLD). The ultimate goal of this work is to obtain membranes zeolite that can serve as matrices or different species (nanoparticles) supports Active stable and controlled environment release. This material is oriented to biomedical applications. The microbiocidal effect of zeolites containing ion or metallic nanoparticles with oligodynamic properties is widely reported in the literature. The material used zeolitic was purified natural clinoptilolite, NZ Site Tasajeras (Villa Clara, Cuba), which is a mixture of around 70% of clinoptilolite heulandita, and mordenite and 30% of other phases (feldspars, quartz). Ag-clinoptilolite and Feclinoptilota were obtained from the audio Exchange NZ natural zeolite with solutions of silver nitrate and sulphate of iron (II) respectively. The experimental arrangement used for the manufacture of the thin films of NZ consists of a vacuum chamber pumped up to a final pressure of - 1 x 10 - 7 mbar with a pump turbo molecular. Zeolite ablation was performed in atmosphere of Argon of high purity, using the second harmonic of a Quantel Brillant Nd: YAG laser (532nm, 4ns, 20 Hz) Q-Switch contract.) Pulse energy, measured at the surface of the target was 80 MJ, resulting in a yield of 20 J / cm2. The laser beam was focused with a lens of 30 cm of focus at 45° incidence on the target surface. The target was rotated during growth to prevent irradiation of the same area. The distance white glass substrate was maintained at 5 cm. The flow of Argon in the Chamber was regulated through a driver Shimadzu FC-40, keeping constant pressure of the Argon 0.5 mbar during growth. To improve the cleaning of the surface of the substrate and consequently the adhesion of the film in the same East was subjected to an initial treatment of RF. Preliminary analysis by diffraction

  3. Removal of pyridine and quinoline by bio-zeolite composed of mixed degrading bacteria and modified zeolite

    International Nuclear Information System (INIS)

    Bai Yaohui; Sun Qinghua; Xing Rui; Wen Donghui; Tang Xiaoyan

    2010-01-01

    In the process of the biodegradation of pyridine and quinoline, ammonium is often generated because of the transformation of N from pyridine and quinoline. Zeolite has been proven to be an effective sorbent for the removal of the ammonium. The natural zeolite can be modified to be the macroporous carrier in the biological wastewater treatment process. In this study, a specific bio-zeolite composed of mixed bacteria (a pyridine-degrading bacterium and a quinoline-degrading bacterium) and modified zeolite was used for biodegradation and adsorption in two types of wastewater: sterile synthetic and coking wastewater. The experimental results indicated that pyridine and quinoline could be degraded simultaneously by the mixed bacteria. Furthermore, NH 4 + -N transformed from pyridine and quinoline could be removed by the modified zeolite. In addition, the bacterial community structures of the coking wastewater and the bio-zeolite were monitored by the amplicon length heterogeneity polymerase-chain reaction (LH-PCR) technique. Both LH-PCR results and scanning electron microscope (SEM) observations indicated that the microorganisms, including BW001 and BW003, could be easily attached on the surface of the modified zeolite and that the bio-zeolite could be used in the treatment of wastewater containing pyridine and/or quinoline.

  4. Adsorption of Indigo Carmine Dye Using Cetyltrimethylammonium Bromide (CTAB) Surfactant Modified Zeolite

    OpenAIRE

    Fauziyah, Nurul; Sriatun, Sriatun; Pardoyo, Pardoyo

    2015-01-01

    Research of indigo carmine dye adsorption using natural zeolite modified by cetyltrimethylammonium bromide (CTAB) surfactant has been done. The purpose of this study was to modify the natural zeolite using CTAB surfactant and to determine its ability on the adsorption of indigo carmine dye. The stages of the study included the activation of zeolites, modifying zeolites using CTAB surfactant and adsorption test of indigo carmine dye. The results showed that the zeolites could be modified by CT...

  5. [Zeolite catalysis in conversion of cellulosics

    Energy Technology Data Exchange (ETDEWEB)

    Tsao, G.T.

    1992-12-31

    To transform biomass into fermentable substrate for yeast, we are using zeolites instead of enzymes to catalyze the two bottleneck reactions in biomass conversion, xylose isomerization and ceuobiose hydrolysis. The experimental results on these reactions carried out over various zeolites and other catalysts are presented herein. The advantages and disadvantages of using these catalysts over enzymes are also discussed. Heterogeneous solid catalysts other than zeolites has been employed for cellobiose-to-glucose hydrolysis. The size and shape selectivity that makes zeoutes unique for some reactions can add diffusional hindrance. We have spent some time screening various known solid acidic catalysts. We report that a class of cationic ion exchange resins in the acidified form (e.g. Amberlite) has worked well as an acidic catalyst in hydrolyzing cellobiose to glucose. Our experimental results, together with those obtained from a homogeneous acid catalyst (e.g. sulfuric acid) for comparison are provided. Having succeeded in finding an alternative solid acid catalyst for hydrolysis, we explored other solid resin or other homogeneous but non-enzyme catalyst to carry out the xylose-to-xylulose isomerization. A fairly extensive search has been made. We explored the use of sodium aluminates in the homogeneous phase isomerization of glucose to fructose and obtained a very high conversion of glucose to fructose with the final mixture containing 85% of fructose instead of the common 45%. Fructose apparently complexes with aluminates, and its equilibrium concentration is shifted to considerably higher values than permitted by simple glucose/fructose equilibrium. We have recently found a number of catalysts capable of promoting isomerization between aldoses and ketoses. One solid resin, known as polyvinyl pyridine (PVP), is able to convert xylose to xylulose at a pH below 7. Our usage of alternative isomerization catalysts, including PVP, are described.

  6. [Zeolite catalysis in conversion of cellulosics

    Energy Technology Data Exchange (ETDEWEB)

    Tsao, G.T.

    1992-01-01

    To transform biomass into fermentable substrate for yeast, we are using zeolites instead of enzymes to catalyze the two bottleneck reactions in biomass conversion, xylose isomerization and ceuobiose hydrolysis. The experimental results on these reactions carried out over various zeolites and other catalysts are presented herein. The advantages and disadvantages of using these catalysts over enzymes are also discussed. Heterogeneous solid catalysts other than zeolites has been employed for cellobiose-to-glucose hydrolysis. The size and shape selectivity that makes zeoutes unique for some reactions can add diffusional hindrance. We have spent some time screening various known solid acidic catalysts. We report that a class of cationic ion exchange resins in the acidified form (e.g. Amberlite) has worked well as an acidic catalyst in hydrolyzing cellobiose to glucose. Our experimental results, together with those obtained from a homogeneous acid catalyst (e.g. sulfuric acid) for comparison are provided. Having succeeded in finding an alternative solid acid catalyst for hydrolysis, we explored other solid resin or other homogeneous but non-enzyme catalyst to carry out the xylose-to-xylulose isomerization. A fairly extensive search has been made. We explored the use of sodium aluminates in the homogeneous phase isomerization of glucose to fructose and obtained a very high conversion of glucose to fructose with the final mixture containing 85% of fructose instead of the common 45%. Fructose apparently complexes with aluminates, and its equilibrium concentration is shifted to considerably higher values than permitted by simple glucose/fructose equilibrium. We have recently found a number of catalysts capable of promoting isomerization between aldoses and ketoses. One solid resin, known as polyvinyl pyridine (PVP), is able to convert xylose to xylulose at a pH below 7. Our usage of alternative isomerization catalysts, including PVP, are described.

  7. Epoxy Nanocomposites Containing Zeolitic Imidazolate Framework-8.

    Science.gov (United States)

    Liu, Cong; Mullins, Michael; Hawkins, Spencer; Kotaki, Masaya; Sue, Hung-Jue

    2018-01-10

    Zeolitic imidazole framework-8 (ZIF-8) is utilized as a functional filler and a curing agent in the preparation of epoxy nanocomposites. The imidazole group on the surface of the ZIF-8 initiates epoxy curing, resulting in covalent bonding between the ZIF-8 crystals and epoxy matrix. A substantial reduction in dielectric constant and increase in tensile modulus were observed. The implication of the present study for utilization of metal-organic framework to improve physical and mechanical properties of polymeric matrixes is discussed.

  8. Hydrogen storage in Chabazite zeolite frameworks.

    Science.gov (United States)

    Regli, Laura; Zecchina, Adriano; Vitillo, Jenny G; Cocina, Donato; Spoto, Giuseppe; Lamberti, Carlo; Lillerud, Karl P; Olsbye, Unni; Bordiga, Silvia

    2005-09-07

    We have recently highlighted that H-SSZ-13, a highly siliceous zeolite (Si/Al = 11.6) with a chabazitic framework, is the most efficient zeolitic material for hydrogen storage [A. Zecchina, S. Bordiga, J. G. Vitillo, G. Ricchiardi, C. Lamberti, G. Spoto, M. Bjørgen and K. P. Lillerud, J. Am. Chem. Soc., 2005, 127, 6361]. The aim of this new study is thus to clarify both the role played by the acidic strength and by the density of the polarizing centers hosted in the same framework topology in the increase of the adsorptive capabilities of the chabazitic materials towards H2. To achieve this goal, the volumetric experiments of H2 uptake (performed at 77 K) and the transmission IR experiment of H2 adsorption at 15 K have been performed on H-SSZ-13, H-SAPO-34 (the isostructural silico-aluminophosphate material with the same Brønsted site density) and H-CHA (the standard chabazite zeolite: Si/Al = 2.1) materials. We have found that a H2 uptake improvement has been obtained by increasing the acidic strength of the Brønsted sites (moving from H-SAPO-34 to H-SSZ-13). Conversely, the important increase of the Brønsted sites density (moving from H-SSZ-13 to H-CHA) has played a negative role. This unexpected behavior has been explained as follows. The additional Brønsted sites are in mutual interaction via H-bonds inside the small cages of the chabazitic framework and for most of them the energetic cost needed to displace the adjacent OH ligand is higher than the adsorption enthalpy of the OH...H2 adduct. From our work it can be concluded that proton exchanged chabazitic frameworks represent, among zeolites, the most efficient materials for hydrogen storage. We have shown that a proper balance between available space (volume accessible to hydrogen), high contact surface, and specific interaction with strong and isolated polarizing centers are the necessary characteristics requested to design better materials for molecular H2 storage.

  9. Mechanistic insights into aqueous phase propanol dehydration in H-ZSM-5 zeolite

    Energy Technology Data Exchange (ETDEWEB)

    Mei, Donghai [Pacific Northwest National Laboratory, Physical and Computational Sciences Directorate & Institute for Integrated Catalysis, Richland WA 99352; Lercher, Johannes A. [Pacific Northwest National Laboratory, Physical and Computational Sciences Directorate & Institute for Integrated Catalysis, Richland WA 99352; Dept. of Chemistry and Catalysis Research Institute, TU München, Lichtenbergstrasse 4 Garching 85748 Germany

    2016-10-06

    Aqueous phase dehydration of 1-propanol over H-ZSM-5 zeolite was investigated using density functional theory (DFT) calculations. The water molecules in the zeolite pores prefer to aggregate via the hydrogen bonding network and be protonated at the Brønsted acidic sites (BAS). Two typical configurations, i.e., dispersed and clustered, of water molecules were identified by ab initio molecular dynamics simulation of the mimicking aqueous phase H-ZSM-5 zeolite unit cell with 20 water molecules per unit cell. DFT calculated Gibbs free energies suggest that the dimeric propanol-propanol, the propanol-water complex, and the trimeric propanol-propanol-water are formed at high propanol concentrations, which provide a kinetically feasible dehydration reaction channel of 1-propanol to propene. However, calculation results also indicate that the propanol dehydration via the unimolecular mechanism becomes kinetically discouraged due to the enhanced stability of the protonated dimeric propanol and the protonated water cluster acting as the BAS site for alcohol dehydration reaction. This work was supported by the US Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences & Biosciences. Pacific Northwest National Laboratory (PNNL) is a multiprogram national laboratory operated for DOE by Battelle. Computing time was granted by the grand challenge of computational catalysis of the William R. Wiley Environmental Molecular Sciences Laboratory (EMSL). EMSL is a national scientific user facility located at Pacific Northwest National Laboratory (PNNL) and sponsored by DOE’s Office of Biological and Environmental Research.

  10. EPR, TEM and cell viability study of asbestiform zeolite fibers in cell media.

    Science.gov (United States)

    Cangiotti, Michela; Salucci, Sara; Battistelli, Michela; Falcieri, Elisabetta; Mattioli, Michele; Giordani, Matteo; Ottaviani, Maria Francesca

    2018-01-01

    Human monocyte U937 cell line was used as a model to verify the toxicity of erionite and offretite asbestiform zeolite fibers. As a presumed non-toxic reference, a fibrous scolecite zeolite was also used. To analyze the process of fiber ingestion into cells and the cells-fibers interactions, a spin-probe electron paramagnetic resonance (EPR) analysis was performed supported by transmission electron microscopy (TEM) and cell viability measurements as a function of the incubation time. Erionite fibers were fast internalized in the membrane mainly as aggregates with radical-solution drops trapped inside, and were found in the cytosol and at the nucleus. In 24h, first erionite fibers rich in sodium and potassium, and then calcium-rich erionite fibers, induced cell necrosis. The offretite fibers formed rounding electron-dense filaments which transformed in curved filaments, initially perturbing the cell structure and interacting at the external surface more than erionite fibers. Such interactions probably diminished the toxic effect of offretite on cells. Interestingly, the presumed non-toxic scolecite fibers were partially internalized, inducing formation of swollen mitochondria and squared cells. Overall, the toxic effect of the fibrous zeolites was related to fiber morphology, chemical distribution of sites, structural variations and formation of aggregates. Copyright © 2017 Elsevier B.V. All rights reserved.

  11. Catalytic behavior of Pt nanoparticles dealuminated Y-zeolite for some n-alkane hydroisomerization

    Directory of Open Access Journals (Sweden)

    S.A. Hanafi

    2014-06-01

    Full Text Available Dealuminated zeolite Y-supported platinum was prepared adopting two dealumination methods, viz. fast (1, 3 and 6 h and slow method (18 h. The content of Pt was constant at 0.5 wt% in all investigated catalysts. The prepared samples were characterized using TGA/DSC, XRD, FTIR techniques, nitrogen adsorption at −196 °C and TEM-connected with energy dispersive spectroscopy (EDS. Surface acidity was investigated via pyridine adsorption using FT-IR spectroscopy. The parent and dealuminated Y-zeolite samples were characterized by their microporous system. By increasing the dealumination time to 6 h, the increased specific surface area and total pore volume indicated a sort of pore opening taking place with an increase in the accessibility of nitrogen molecules. DSC confirmed the thermal stability of the dealuminated zeolite samples up to 800 °C. The prepared catalysts were tested through hydroisomerization reactions of n-hexane and n-heptane using a micro-catalytic pulse technique. Different catalytic behaviors could be distinguished for the dealuminated samples based on competitive reactions; hydro-isomerization, hydrocracking and cyclization. Slow dealumination leads to the most selective catalysts for hydroisomerization. n-Heptane was converted to higher extent than n-hexane; cracking process was more evident when the former was fed to the reactor.

  12. Experimental Study on Pressure Drop and Flow Dispersion in Packed Bed of Natural Zeolite

    Directory of Open Access Journals (Sweden)

    Ruya Petric Marc

    2018-01-01

    Full Text Available The use of conventional correlation for pressure drop and dispersion coefficient calculation may result in inaccurate values for zeolite packed bed as the correlations are generally developed for regularly shaped and uniformly sized particles. To support the research on the application of modified natural zeolite as tar cracking catalyst, the research on the hydrodynamic behaviour of zeolite packed bed has been conducted. Experiments were carried out using a glass column with diameter of 37.8 mm. Natural zeolite with particle size of about 2.91 to 6.4 mm was applied as packing material in the column, and the bed height was varied at 9, 19 and 29 cm. Air was used as the fluid that flows through the bed and nitrogen was used as a tracer for residence time distribution determination. Air flow rates were in the range of 20 to 100 mL/s which correspond to the laminar-transitional flow regime. The pressure drops through the bed were in the range of 1.7 to 95.6 Pa, depending on the air flow rate and bed height. From these values, the parameters in the Ergun equation were estimated, taking into account the contribution by wall effect when the ratio of column to particle diameter is low. The viscous and inertial term constants in the Ergun equation calculated ranges from 179 to 199 and 1.41 to 1.47 respectively while the particle sphericity ranges from 0.56 to 0.59. The reactor Peclet number were determined to range from 5.2 to 5.5, which indicated significant deviation from a plug flow condition.

  13. Introduction to chemistry of crystalline zeolites and its applications

    International Nuclear Information System (INIS)

    Lobo Cabezas, Raul Francisco

    2006-01-01

    Establishes the zeolites as the most important group of solid acids and its relation to the contemporaneous chemical industry. It describes that zeolites are used in the following applications: refineries, chemicals/petrochemicals, environmental chemistry, separation of gas, adsorbent ia and ionic exchange in water purification in mineral processes, medicine and agricultural industry. Zeolites are defined as crystalline aluminium silicates with a compound structure of interconnected tetrahedrons. It mentions the key components in zeolites structure. It focuses that structural basic unity of the zeolite is the tetrahedron and compound structural unities are: cells and columns. Besides, it describes that pore system defines a lot of all its properties; but chemical composition affects them. Composition and properties of zeolites are established: adsorption, molecular sieves, acidity, selectivity, transition state in the hydrocarbon's chemistry. It concludes that the newer application of zeolite is in oxidations: Titanium-Silicate-1; production of propylene's oxide using peroxide of hydrogen as oxidizing. The catalysis is an active area of research, and the most popular areas are related to chemicals and the environment [es

  14. Zeolite-catalyzed hydrogenation of carbon dioxide and ethene.

    Science.gov (United States)

    Chan, Bun; Radom, Leo

    2008-07-30

    Ab initio molecular orbital theory and density functional theory calculations have been used to study the three-stage zeolite-catalyzed hydrogenation of CO2 to methanol and the hydrogenation of C2H 4 to ethane, with the aim of designing an effective zeolite catalyst for these reactions. Both Brønsted acid (XH) and alkali metal (XM) sites in model zeolites (-X-Al-XH- or -X-Al-XM-) have been examined. It is found that appropriately designed zeolites can provide excellent catalysis for these reactions, particularly for the hydrogenation of CO2, HCO2H and CH2O, with uncatalyzed barriers of more than 300 kJ mol(-1) being reduced to as little as 17 kJ mol(-1) (in the case of CH2O). The reaction barrier depends on the acidity of the XH moiety or the nature of the metal cation M in the XM moiety, and the basicity of the adjacent X group in the catalyst. For a catalyst based on alkali metal zeolites (XM), the catalytic activity is relatively insensitive to the nature of X in the XM group. As a result, the catalytic activity for these types of zeolites increases as X becomes more basic. We propose that alkali metal zeolites with Ge and N incorporated into the framework could be very effective catalysts for hydrogenation processes.

  15. CoX zeolites and their exchange with deuterium

    International Nuclear Information System (INIS)

    Novakova, J.; Kubelkova, L.; Jiru, P.

    1976-01-01

    An analysis of the gaseous phase using a mass spectrometer and analysis of the solid phase using an infrared spectrophotometer was made to investigate the deuterium exchange with hydrogen mostly bound in hydroxyl groups of zeolites CoX(21 and 47%) and NaX. It was found that with the increasing amount of cobalt ions the number of exchangeable hydrogens of the zeolite increases; the respective types of the hydrogen are discussed with respect to the particular dehydration temperatures. The rate of the D 2 +OH exchange is substantially faster with the CoX than with the NaX zeolite, and exhibits a decrease with increasing dehydration. On the other hand, the rate of D 2 +H 2 exchange without zeolite hydrogen incorporation, catalyzed by CoX zeolites, increases with increasing dehydration. The increased activation of gaseous hydrogen molecules is related to the presence in the zeolite of cobalt ions whose properties change during dehydration with the change in their environment. Hydroxyl groups of the CoX zeolites are not equivalent during the exchange; the hydroxyl hydrogens of the 3740 cm -1 band are exchanged more slowly than are the other hydrogens. (author)

  16. Fabrication of 6FDA-durene membrane incorporated with zeolite T and aminosilane grafted zeolite T for CO2/CH4 separation

    Science.gov (United States)

    Jusoh, Norwahyu; Fong Yeong, Yin; Keong Lau, Kok; Shariff, Azmi Mohd

    2017-08-01

    In the present work, zeolite T and aminosilane grafted zeolite T are embedded into 6FDA-durene polyimide phase for the fabrication of mixed matrix membranes (MMMs). FESEM images demonstrated that the improvement of interfacial adhesion between zeolite and polymer phases in MMM loaded with aminosilane grafted zeolite T was not significant as compared to zeolite T/6FDA-durene MMM. From the gas permeation test, CO2/CH4 selectivity up to 26.4 was achieved using MMM containing aminosilane grafted zeolite T, while MMM loaded with ungrafted zeolite T showed CO2/CH4 selectivity of 19.1. In addition, MMM incorporated with aminosilane grafted zeolite T particles successfully lies on Robeson upper bound 2008, which makes it an attractive candidate for CO2/CH4 separation.

  17. Crafting tolerance

    DEFF Research Database (Denmark)

    Kirchner, Antje; Freitag, Markus; Rapp, Carolin

    2011-01-01

    Ongoing changes in social structures, orientation, and value systems confront us with the growing necessity to address and understand transforming patterns of tolerance as well as specific aspects, such as social tolerance. Based on hierarchical analyses of the latest World Values Survey (2005...... results show that specific institutional qualities, which reduce status anxiety, such as inclusiveness, universality, and fairness, prevail over traditional socio-economic, societal, cultural, and democratic explanations....

  18. Enhanced phosphorus removal from sewage in mesocosm-scale constructed wetland using zeolite as medium and artificial aeration.

    Science.gov (United States)

    Vera, I; Araya, F; Andrés, E; Sáez, K; Vidal, G

    2014-08-01

    Phosphorus (P) contained in sewage maybe removed by mesocosm-scale constructed wetlands (MCW), although removal efficiency is only between 20% and 60%. P removal can be enhanced by increasing wetland adsorption capacity using special media, like natural zeolite, operating under aerobic conditions (oxidation-reduction potential (ORP) above +300 mV). The objective of this study was to evaluate P removal in sewage treated by MCW with artificial aeration and natural zeolite as support medium for the plants. The study compared two parallel lines of MCW: gravel and zeolite. Each line consisted in two MCW in series, where the first MCW of each line has artificial aeration. Additionally, four aeration strategies were evaluated. During the operation, the following parameters were measured in each MCW: pH, temperature, dissolved oxygen and ORP. Phosphate (PO4(-3) - P) and chemical oxygen demand (COD), five-day biological oxygen demand (BOD5), total suspended solids (TSS) and ammonium. (NH4(+) - N) were evaluated in influents and effluents. Plant growth (biomass) and proximate analysis for P content into Schoenoplectus californicus were also performed. The results showed that PO4(-3) - P removal efficiency was 70% in the zeolite medium, presenting significant differences (p < .05) with the results obtained by the gravel medium. Additionally, aeration was found to have a significant effect (p < .05) only in the gravel medium with an increase in up to 30% for PO43 - P removal. Thus, S. californicus contributed to 10-20% of P removal efficiency.

  19. OPTIMATION OF TIME AND CATALYST/FEED RATIO IN CATALYTIC CRACKING OF WASTE PLASTICS FRACTION TO GASOLINE FRACTION USING Cr/NATURAL ZEOLITE CATALYST

    Directory of Open Access Journals (Sweden)

    Wega Trisunaryanti

    2010-06-01

    Full Text Available Optimation of time and catalyst/feed ratio in catalytic cracking of waste plastics fraction to gasoline fraction using Cr/Natural Zeolite catalyst has been studied.The natural zeolite was calcined by using nitrogen gas at 500 oC for 5 hours. The chromium supported on to the zeolite was prepared by ion exchange methode with Cr(NO33.9H2O solution with chromium/zeolite concentration of 1% (w/w. The zeolite samples were then calcined  with nitrogen gas at 500 oC for 2 hours, oxidyzed with oxygen gas and reduced with hydrogen at 400 oC for 2 hours. The characterization of the zeolite catalyst by means of Si/Al ratio by UV-Vis spectroscopy, acidity with pyridine vapour adsorption and Na, Ca and Cr contents by atomic adsorption spectroscopy (AAS. The catalyst activity test was carried out in the cracking process of waste plastics fraction with boiling point range of 150 - 250 °C (consisted of C12 - C16 hydrocarbons at 450 oC for 30 min, 60 min and 90 min, and catalyst/feed ratio 1/1, 1/2, 1/3, ¼ (w/w. The result of catalyst activity test  showed  that  the maximum number  conversion of gasoline fraction (C5-C11 is 53,27% with relatively low coke formation using 1/3 catalyst/feed ratio and the cracking time of 60 min.. This  catalyst has  Si/Al ratio = 1,21 (w/w , acidity = 0,16 mmol/g and Na content = 0,81%, Ca content = 0,15% and Cr content 0,24%.   Keywords: zeolite, catalytic cracking, gasoline, chromium.

  20. Sorption of 60 Co in natural zeolite (clinoptilolite)

    International Nuclear Information System (INIS)

    Hernandez B, E.

    1996-01-01

    A Mexican zeolite (clinoptilolite) from Taxco, Guerrero, was partially stabilized with sodium cations. Radioactive Cobalt ( 60 Co) was used to study the Co 2+ sorption in the stabilized zeolite (Na + ). It was found that sorption in general does not favour the diffusion of cobalt between framework, it explains because of it is a natural zeolite and its composition heterogeneous decrease its exchange capacity by the generated competence to the existence other type of exchange ions. The cobalt retention reached the highest level, around 0.408 m eq Co 2+ /g in the Na-Clinoptilolite. The crystallinity of the aluminosilicates was maintained during experiments, it was verified by XRD patterns. (Author)

  1. Zeolite-catalyzed isomerization of tetroses in aqueous medium

    DEFF Research Database (Denmark)

    Shunmugavel, Saravanamurugan; Riisager, Anders

    2014-01-01

    The isomerization of erythrose (ERO) was studied in water over commercially available large-pore zeolites such as, e.g. H-Y, H-USY and H-beta. Among the employed zeolites, H-USY(6) was found to efficiently isomerize the sugar yielding 45 % erythrulose (ERU), 42 % ERO and 3 % of the epimer threose...... in water. Hence, the results demonstrate water to be a preferred solvent compared to lower alcohols for zeolite-catalyzed tetrose isomerization, which is opposite to what previously have been found for analogous pentose and hexose isomerization. A reuse study revealed further that H-USY(6) could be applied...

  2. Zeolite-catalyzed biomass conversion to fuels and chemicals

    DEFF Research Database (Denmark)

    Taarning, Esben; Osmundsen, Christian Mårup; Yang, Xiaobo

    2011-01-01

    Heterogeneous catalysts have been a central element in the efficient conversion of fossil resources to fuels and chemicals, but their role in biomass utilization is more ambiguous. Zeolites constitute a promising class of heterogeneous catalysts and developments in recent years have demonstrated...... their potential to find broad use in the conversion of biomass. In this perspective we review and discuss the developments that have taken place in the field of biomass conversion using zeolites. Emphasis is put on the conversion of lignocellulosic material to fuels using conventional zeolites as well...

  3. Oxidation of Bioethanol using Zeolite-Encapsulated Gold Nanoparticles

    DEFF Research Database (Denmark)

    Mielby, Jerrik Jørgen; Abildstrøm, Jacob Oskar; Wang, Feng

    2014-01-01

    With the ongoing developments in biomass conversion, the oxidation of bioethanol to acetaldehyde may become a favorable and green alternative to the preparation from ethylene. Here, a simple and effective method to encapsulate gold nanoparticles in zeolite silicalite-1 is reported and their high...... zeolite crystals comprise a broad range of mesopores and contain up to several hundred gold nanoparticles with a diameter of 2-3nm that are distributed inside the zeolites rather than on the outer surface. The encapsulated nanoparticles have good stability and result in 50% conversion of ethanol with 98...

  4. Oxidation of Bioethanol using Zeolite-Encapsulated Gold Nanoparticles

    DEFF Research Database (Denmark)

    Mielby, Jerrik Jørgen; Abildstrøm, Jacob Oskar; Wang, Feng

    2014-01-01

    With the ongoing developments in biomass conversion, the oxidation of bioethanol to acetaldehyde may become a favorable and green alternative to the preparation from ethylene. Here, a simple and effective method to encapsulate gold nanoparticles in zeolite silicalite‐1 is reported and their high...... zeolite crystals comprise a broad range of mesopores and contain up to several hundred gold nanoparticles with a diameter of 2–3 nm that are distributed inside the zeolites rather than on the outer surface. The encapsulated nanoparticles have good stability and result in 50 % conversion of ethanol with 98...

  5. Method of preparing sodalite from chloride salt occluded zeolite

    Science.gov (United States)

    Lewis, M.A.; Pereira, C.

    1997-03-18

    A method is described for immobilizing waste chloride salts containing radionuclides and hazardous nuclear material for permanent disposal starting with a substantially dry zeolite and sufficient glass to form leach resistant sodalite with occluded radionuclides and hazardous nuclear material. The zeolite and glass are heated to a temperature up to about 1000 K to convert the zeolite to sodalite and thereafter maintained at a pressure and temperature sufficient to form a sodalite product near theoretical density. Pressure is used on the formed sodalite to produce the required density.

  6. Nanomodified natural zeolite as a fertilizer of prolonged activity

    Directory of Open Access Journals (Sweden)

    G. Tsintskaladze

    2016-09-01

    Full Text Available Natural zeolites of sedimentary origin are widely used in agriculture both as individual fertilizer and a mix of mineral and organic fertilizers. Natural zeolites are crystalline nanoporous hydrated aluminosilicates. Fertilizer of prolonged activity enriched with macro- and microelements is obtained by fusing zeolite with dehydrated ammonium using nanotechnological method of modification. The structure and some physical and chemical properties of a novel nanomaterial were studied by the methods of X-ray diffraction, IR-spectroscopy, absorption and thermal analysis. It was shown that the obtained fertilizer may be used in both protected and open grounds.

  7. Encapsulation of noble gas in zeolites

    International Nuclear Information System (INIS)

    Dorea, A.

    1987-04-01

    The noble gases neon, argon, krypton and xenon were encapsulated hydrothermally as pure gases as well as in the form of mixtures in type A zeolite of various cationic compositions. As opposed to the starting material the encapsulates are X-ray amorphous and posess a very small specific surface area. Irrespective of the thermal pretreatment of the zeolites the optimal loading occured within a certain temperature window. The amount of gas trapped was essentially a function of the fixation pressure. Within the pressure range 50-2200 bar the obtained loading was independent from the type of noble gas. When mixtures of noble gases were encapsulated a small enrichment of the heavier noble gas, caused by kinetic and thermodynamic effects, was observed. The thermal stability of the encapsulates was found to be very high. Even at temperatures as high as 750 0 C a recrystallization to anorthite was only observed after practically all the trapped gas had been released. Experiments destined to clarify the mechanism of gas leckage at temperatures below 750 0 C suggest a diffusion controlled mechanism described by a √t law. Even at loadings of 45 ml/(STP) Kr/g the leckage predicted under conditions as expected during longterm storage of Kr-85 is extremely small. Kinetic data demonstrate that the gas is not trapped in the form of agglomerates but rather exists homogeneously distributed within the encapsulate. This result is substantiated by electron beam microanalysis. (orig./RB) [de

  8. Multicolor photoluminescence in ITQ-16 zeolite film

    KAUST Repository

    Chen, Yanli

    2016-09-07

    Exploring the native defects of zeolites is highly important for understanding the properties of zeolites, such as catalysis and optics. Here, ITQ-16 films were prepared via the secondary growth method in the presence of Ge atoms. Various intrinsic defects of ITQ-16 films were fully studied through photoluminescence and FTIR characterizations. It was found that both the as-synthesized and calcined ITQ-16 films displayed multicolor photoluminescence including ultraviolet, blue, green and red emissions by exciting upon appropriate wavelengths. The results indicate that Si―OH and non-bridging oxygen hole centers(NBOHCs) are responsible for the origin of green and red emissions at 540―800 nm, while according to a variety of emission bands of calcined ITQ-16 film, blue emission bands at around 446 and 462 nm are attributed to peroxy free radicals(≡SiO2), ultraviolet emissions ranging from 250 nm to 450 nm are suggested originating from a singlet-to-triplet transition of two-fold-coordinated Si and Ge, respectively. © 2016, Jilin University, The Editorial Department of Chemical Research in Chinese Universities and Springer-Verlag GmbH.

  9. Catalytic pyrolysis using UZM-44 aluminosilicate zeolite

    Science.gov (United States)

    Nicholas, Christopher P; Boldingh, Edwin P

    2013-12-17

    A new family of aluminosilicate zeolites designated UZM-44 has been synthesized. These zeolites are represented by the empirical formula Na.sub.nM.sub.m.sup.k+T.sub.tAl.sub.1-xE.sub.xSi.sub.yO.sub.z where "n" is the mole ratio of Na to (Al+E), M represents a metal or metals from zinc, Group 1, Group 2, Group 3 and or the lanthanide series of the periodic table, "m" is the mole ratio of M to (Al+E), "k" is the average charge of the metal or metals M, T is the organic structure directing agent or agents, and E is a framework element such as gallium. The process involves contacting a carbonaceous biomass feedstock with UZM-44 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. Preparation, Processing, and Characterization of Oriented Polycrystalline Zeolite and Aluminophosphate Membranes

    Science.gov (United States)

    Stoeger, Jared Andrew

    Since the advent of zeolite membranes, speculation on their industrial applicability has been closely monitored, although widespread commercialization has been hampered by limitations in fabrication and post-synthesis processing. Economical, energy-efficient technology breakthroughs require an evaluation of a range of material candidates which show robustness and reliability. Straightforward manufacturing techniques should be devised to generate thousands of square meters of membrane area; however, this demands control of structural characteristics on the scale of nanometers. As described in this dissertation, the path forward will be forged by exploiting the intrinsic crystalline properties of zeolites or aluminophosphates for the next advancement in membrane technology. A facile method is described for the preparation of silicalite-1 (MFI zeolite type) membranes using the secondary growth technique on symmetric porous stainless steel tubes. Activation through rapid thermal processing (RTP), a lamp-based heat-treatment process used as a critical fabrication step in silicon integrated circuit manufacturing, is proven to reduce the density of non-zeolitic transport pathways which are detrimental to high-resolution molecular sieving. RTP-treated membranes are shown to have enhanced performance in the binary separation of vapor-phase isomers (p-/o-xylene), gas-phase isomers (n-/i-butane), and alcohol/water when compared to membranes activated at a much slower heating rate but otherwise similarly-prepared. The performance is discussed in the context of the market potential for industrially-attractive separations: the recovery of p-xylene from an isomeric mixture or alcohol biofuels from aqueous post-fermentation streams. Hydrothermal growth techniques for the preparation and characterization of continuous aluminophosphate (AFI zeolite type) membranes with a preferential crystallographic alignment on porous alpha-Al2O3 disc supports are demonstrated. A mechanism is

  11. Oxidative regeneration of toluene-saturated natural zeolite by gaseous ozone: The influence of zeolite chemical surface characteristics

    Energy Technology Data Exchange (ETDEWEB)

    Alejandro, Serguei [Laboratorio de Tecnologías Limpias (F. Ingeniería), Universidad Católica de la Santísima Concepción, Alonso de Ribera 2850, Concepción (Chile); Núcleo de Energías Renovables (F. Ingeniería), Universidad Católica de Temuco, Rudecindo Ortega 02950, Temuco (Chile); Valdés, Héctor, E-mail: hvaldes@ucsc.cl [Laboratorio de Tecnologías Limpias (F. Ingeniería), Universidad Católica de la Santísima Concepción, Alonso de Ribera 2850, Concepción (Chile); Manéro, Marie-Hélène [Université de Toulouse (France); INPT, UPS (France); Laboratoire de Génie Chimique, 4, Allée Emile Monso, F–31030 Toulouse (France); CNRS (France); Laboratoire de Génie Chimique, F–31030 Toulouse (France); Zaror, Claudio A. [Departamento de Ingeniería Química (F. Ingeniería), Universidad de Concepción, Concepción, Correo 3, Casilla 160–C (Chile)

    2014-06-01

    Highlights: • Surface acidity of modified natural zeolite is related to its chemical reactivity. • Brønsted acid sites are associated to toluene adsorption. • Lewis acid sites could decompose ozone generating surface active oxygen species. • Infrared spectra evidence active atomic oxygen and oxidation by-product formation. • 2NH4Z1 sample shows the highest reactivity toward adsorbed toluene. - Abstract: In this study, the effect of zeolite chemical surface characteristics on the oxidative regeneration of toluene saturated-zeolite samples is investigated. A Chilean natural zeolite (53% clinoptilolite, 40% mordenite and 7% quartz) was chemically modified by acid treatment with hydrochloric acid and by ion-exchange with ammonium sulphate. Thermal pre-treatments at 623 and 823 K were applied and six zeolite samples with different chemical surface characteristics were generated. Chemical modification of natural zeolite followed by thermal out-gassing allows distinguishing the role of acidic surface sites on the regeneration of exhausted zeolites. An increase in Brønsted acid sites on zeolite surface is observed as a result of ammonium-exchange treatment followed by thermal treatment at 623 K, thus increasing the adsorption capacity toward toluene. High ozone consumption could be associated to a high content of Lewis acid sites, since these could decompose ozone into atomic active oxygen species. Then, surface oxidation reactions could take part among adsorbed toluene at Brønsted acid sites and surface atomic oxygen species, reducing the amount of adsorbed toluene after the regenerative oxidation with ozone. Experimental results show that the presence of adsorbed oxidation by-products has a negative impact on the recovery of zeolite adsorption capacity.

  12. Oxidative regeneration of toluene-saturated natural zeolite by gaseous ozone: The influence of zeolite chemical surface characteristics

    International Nuclear Information System (INIS)

    Alejandro, Serguei; Valdés, Héctor; Manéro, Marie-Hélène; Zaror, Claudio A.

    2014-01-01

    Highlights: • Surface acidity of modified natural zeolite is related to its chemical reactivity. • Brønsted acid sites are associated to toluene adsorption. • Lewis acid sites could decompose ozone generating surface active oxygen species. • Infrared spectra evidence active atomic oxygen and oxidation by-product formation. • 2NH4Z1 sample shows the highest reactivity toward adsorbed toluene. - Abstract: In this study, the effect of zeolite chemical surface characteristics on the oxidative regeneration of toluene saturated-zeolite samples is investigated. A Chilean natural zeolite (53% clinoptilolite, 40% mordenite and 7% quartz) was chemically modified by acid treatment with hydrochloric acid and by ion-exchange with ammonium sulphate. Thermal pre-treatments at 623 and 823 K were applied and six zeolite samples with different chemical surface characteristics were generated. Chemical modification of natural zeolite followed by thermal out-gassing allows distinguishing the role of acidic surface sites on the regeneration of exhausted zeolites. An increase in Brønsted acid sites on zeolite surface is observed as a result of ammonium-exchange treatment followed by thermal treatment at 623 K, thus increasing the adsorption capacity toward toluene. High ozone consumption could be associated to a high content of Lewis acid sites, since these could decompose ozone into atomic active oxygen species. Then, surface oxidation reactions could take part among adsorbed toluene at Brønsted acid sites and surface atomic oxygen species, reducing the amount of adsorbed toluene after the regenerative oxidation with ozone. Experimental results show that the presence of adsorbed oxidation by-products has a negative impact on the recovery of zeolite adsorption capacity

  13. High temperature desulphuruzation of coal by zeolite-supported ...

    African Journals Online (AJOL)

    Journal of Mining and Geology. Journal Home · ABOUT THIS JOURNAL · Advanced Search · Current Issue · Archives · Journal Home > Vol 39, No 1 (2003) >. Log in or Register to get access to full text downloads.

  14. Preparation of natural zeolitic supports for potential biomedical applications

    Energy Technology Data Exchange (ETDEWEB)

    Farias, Tania; Ruiz-Salvador, A. Rabdel [Zeolites Engineering Laboratory, Institute of Materials Science and Technology (IMRE), University of Havana, Vedado, 10400 Havana (Cuba); Velazco, Lya [Electronic Department, Institute of Materials Science and Technology (IMRE), University of Havana, 10400 Havana (Cuba); Menorval, Louis Charles de [Institut Charles Gerhardt Montpellier, UMR 5253 CNRS-UM2, Equipe Agregats, Interfaces et Materiaux pour l' Energie, C.C. 1502, Place Eugene Bataillon, 34095 Montpellier cedex 5 (France); Rivera, Aramis, E-mail: aramis@fisica.uh.cu [Zeolites Engineering Laboratory, Institute of Materials Science and Technology (IMRE), University of Havana, Vedado, 10400 Havana (Cuba)

    2009-12-15

    Considering the biological properties reported for the purified natural clinoptilolite, NZ, we prepared K- and Li-enriched forms aimed at release matrices for biomedical applications. The raw material and the obtained solid samples were characterized by means of atomic absorption spectroscopy, X-ray diffraction, {sup 27}Al and {sup 29}Si MAS nuclear magnetic resonance, and nitrogen adsorption. The results demonstrated the structural stability of the materials after the different transformations applied. The chemical behavior of the samples in bi-distilled water and hydrochloric acid was studied by pH and conductivity measurements. A preliminary study related with the liberation of K and Li in aqueous medium was carried out by atomic absorption spectroscopy. The studies showed that the release of both ions from the solid samples is favored in HCl solutions, and that lithium is released faster than potassium in both dissolution media.

  15. A study on zeolite precipitation at alkaline conditions: effect of solution composition on mineralogy and crystallization rate

    International Nuclear Information System (INIS)

    Francisco, P.C.M.; Nakabayashi, R.; Sato, T.

    2012-01-01

    Document available in extended abstract form only. Designs for engineered barrier systems for the geologic confinement of radioactive wastes involve the extensive use of bentonite, a material known for its capability to retard radionuclide migration into the groundwater system due to its low permeability. Cement and concrete are used in conjunction with bentonite to serve as structural supports and to seal access routes. However, when concrete becomes saturated with groundwater, it produces alkaline fluids that may attack and degrade the bentonite over time. A key concern regarding bentonite alteration by alkaline fluids is the precipitation of secondary minerals, such as zeolites, which may produce changes in the transport properties of the bentonite and compromise the stability of the entire barrier system. More importantly, studies have shown that zeolites form at timescales that are of interest in determining the long-term integrity of the barrier system. It is thus important to understand zeolite precipitation at conditions operative during bentonite alteration. The objective of this study, therefore, is to determine the effects of fluid composition on the crystallization rate and zeolite mineralogy. Zeolites were synthesized in batches from solutions with varying ratios of Si and Al at pH 13.5 by combining appropriate amounts of NaOH, NaAlO 2 and Na 2 SiO 3 .9H 2 O. The Si and Al concentrations in the starting solutions both ranged from 0.03 to 0.24 M and the solution Si/Al ratios ranged from 0.125 to 8. The solutions were transferred to polypropylene bottles and stored in an oven set at a constant temperature of 70 deg. C for 1, 4, 7, 14 and 30 days. At appropriate reaction times, samples were extracted from the oven and then centrifuged to separate the solids from the liquid. The supernatant was filtered using 0.2 μm filter and the solids were washed several times before drying in a freeze dryer. The solids were characterized by XRD and SEM-EDX to

  16. Cation-Exchanged Zeolitic Chalcogenides for CO2 Adsorption.

    Science.gov (United States)

    Yang, Huajun; Luo, Min; Chen, Xitong; Zhao, Xiang; Lin, Jian; Hu, Dandan; Li, Dongsheng; Bu, Xianhui; Feng, Pingyun; Wu, Tao

    2017-12-18

    We report here the intrinsic advantages of a special family of porous chalcogenides for CO 2 adsorption in terms of high selectivity of CO 2 /N 2 , large uptake capacity, and robust structure due to their first-ever unique integration of the chalcogen-soft surface, high porosity, all-inorganic crystalline framework, and the tunable charge-to-volume ratio of exchangeable cations. Although tuning the CO 2 adsorption properties via the type of exchangeable cations has been well-studied in oxides and MOFs, little is known about the effects of inorganic exchangeable cations in porous chalcogenides, in part because ion exchange in chalcogenides can be very sluggish and incomplete due to their soft character. We have demonstrated that, through a methodological change to progressively tune the host-guest interactions, both facile and nearly complete ion exchange can be accomplished. Herein, a series of cation-exchanged zeolitic chalcogenides (denoted as M@RWY) were studied for the first time for CO 2 adsorption. Samples were prepared through a sequential ion-exchange strategy, and Cs + -, Rb + -, and K + -exchanged samples demonstrated excellent CO 2 adsorption performance. Particularly, K@RWY has the superior CO 2 /N 2 selectivity with the N 2 adsorption even undetected at either 298 or 273 K. It also has the large uptake of 6.3 mmol/g (141 cm 3 /g) at 273 K and 1 atm with an isosteric heat of 35-41 kJ mol -1 , the best among known porous chalcogenides. Moreover, it permits a facile regeneration and exhibits an excellent recyclability, as shown by the multicycling adsorption experiments. Notably, K@RWY also demonstrates a strong tolerance toward water.

  17. Current progress on zeolite membrane reactor for CO2 hydrogenation

    Science.gov (United States)

    Makertiharta, I. G. B. N.; Dharmawijaya, P. T.; Wenten, I. G.

    2017-01-01

    Carbon capture and storage via catalytic hydrogenation into methanol have been recognized as the most promising solution to not only global warming issue but also high fuel and methanol demand worldwide. However, methanol synthesis from CO2 involves equilibrium limited reaction that can be optimized using membrane reactor (MR). Among all selective membrane layer, the zeolite is the most promising material because it can selectively remove water and methanol from reaction mixture component, especially H2. To present a clear background of zeolite membrane reactor, this paper will bring the brief discussion on the recent progress towards utilization of zeolite membrane reactor for CO2 hydrogenation. The progress of selective layer used in said MR will be examined in detail. Critical issues related to zeolite membrane reactor will also be discussed to develop it further.

  18. Obtaining zeolite Y synthesized by hydrothermal treatment assisted by microwave

    International Nuclear Information System (INIS)

    Simoes, A.N.; Simoes, V.N.; Neiva, L.S.; Rodrigues, M.G.F.; Gama, L.; Oliveira, J. B.L.

    2011-01-01

    n search of new catalysts several man-made structures have been developed. The use of zeolites in catalysis is applied due to its ability to associate activity, selectivity and stability, the main conditions to have an effective catalyst. Thus, studies have been done on the hydrothermal synthesis of zeolites by microwave assisted, since the use of microwave radiation offers several advantages over conventional heating. In this context, this work aims to synthesis and characterization of zeolite Y via hydrothermal treatment in a microwave oven. The sample obtained was characterized by XRD, BET and SEM. XRD results showed the formation of zeolite Y in just 60 minutes. The sample showed high value of surface area, the latter being of 476.2 m² / g. The particles are agglomerated, but with a narrow distribution of size. (author)

  19. Ammoniacal nitrogen removal from groundwaters using natural and synthetic zeolites

    OpenAIRE

    Matsiyevska, Oksana; Chverenchuk, Andrii; Soprunko, Svitlana; Berezyuk, Roman; Pidlisny, Bogdan

    2013-01-01

    In article results of ammoniacal nitrogen occurrence ways into groundwaters analysis was represented. NH4+ removing effectivity from simulative solutions by natural (Sokyrnytsia minefield, Ukraine) and synthetic zeolites was compared.

  20. Catalytic Cracking of Used Palm Oil using Composite Zeolite

    International Nuclear Information System (INIS)

    Chang, W.H.; Tye, C.T.

    2013-01-01

    The rapid expansion of human society implies greater energy demand and environmental issues. In face of depletion energy resources, research is being carried out widely in order to convert the plant oil into biofuel. In this research, the production of liquid biofuels via catalytic cracking of used palm oil in the presence of composite zeolite was studied. The performance of composite zeolite of different properties in the reaction has been evaluated. The catalytic cracking reactions were carried out in a batch reactor at reaction temperature of 350 degree Celsius for an hour. In the present study, adjusting the ratio of meso porous coating to microporous zeolite and magnesium loading on composite zeolite catalyst were found to be able to increase the gasoline fraction and overall conversion of the reaction. (author)

  1. Solubilisation of dye-loaded zeolite L nanocrystals

    NARCIS (Netherlands)

    Devaux, A.; Popović, Z.; Bossart, O.; De Cola, L.; Kunzmann, A.; Calzaferri, G.

    2006-01-01

    Solubilisation of zeolite L nanocrystals in different solvents is reported. Grafting alkoxysilane derivatives with a hydrophobic part leads to transparent suspensions in non-polar solvents while modification with a positively charged complex leads to solubilisation in water.

  2. Characterization structural and morphology ZSM-5 zeolite by hydrothermal synthesis

    International Nuclear Information System (INIS)

    Silva, V.J.; Crispim, A.C.; Queiroz, M.B.; Laborde, H.M.; Rodrigues, M.G.F.; Menezes, R.R.

    2009-01-01

    Solid acids are catalytic materials commonly used in the chemical industry. Among these zeolites are the most important business processes including water treatment, gas separation, and cracking long hydrocarbon chains to produce high octane gasoline. Its synthesis, characterization and applications have been widely studied. The objective this study was to synthesize the ZSM-5 zeolite for future use in separation processes and catalysis. The zeolite ZSM-5 was prepared by hydrothermal synthesis at 170°C, using silica, deionized water and the director of structures (TPABr - tetrapropylammonium bromide). The materials were characterized by X ray diffraction (XRD), scanning electron microscopy (SEM) and semiquantitative chemical analysis by X ray fluorescence (XRF). According to the XRD was possible to observe the formation of ZSM-5 zeolite, with peaks intense and well defined. The SEM showed the formation of individual particles, clean, rounded shapes. (author)

  3. Iba of Zeolites Exchanged with Lithium for Co2 Retention

    Science.gov (United States)

    Andrade, E.; Alfaro, S.; Valenzuela, M. A.; Solis, C.; Zaval, E. P.; Rocha, M. F.; Cruz, J.; Pfeiffer, H.; Bosch, P.; Contreras, C.; Baptiste, J.

    2009-03-01

    A great concern on the global climatic change, partially due to industry CO2 expelled to the atmosphere, has motivated the search of new materials able to retain this gas. Clays, perovskites, zeolites and membranes have been utilized to trap the CO2. Zeolites are widely used as molecular sieves in different industrial processes related to gas purification or gas separation. Synthetic zeolites exchanged with lithium were prepared as potential material for CO2 retention. A NRA method using the 7Li (p,α)4He was performed in order to measure the the Li contents. With SEM-EDS the atomic concentrations of elements as C, Na, Si, Al, K, Ca, Fe, etc. were determined. Zeolites were also characterized by XRD.

  4. Moderate temperature zeolitic alternation in a cooling pyroclastic deposit

    International Nuclear Information System (INIS)

    Levy, S.S.; O'Neil, J.R.

    1984-01-01

    The locally zeolitized Topopah Spring Member of the Paintbrush Tuff, Yucca Mountain, Nevada, USA is part of a thick sequence of zeolitized pyroclastic units. Most of the zeolitized units are nonwelded tuffs that were altered during low temperature diagenesis, but the distribution and textural setting of zeolite (heulandite-clinoptilolite and smectite in the densely welded Topopah Spring tuff suggests that these hydrous minerals formed while the tuff was still cooling after pyroclastic emplacement and welding. The hydrous minerals are concentrated within a transition zone between devitrified tuff in the central part of the unit and underlying vitrophyre. Movement of liquid and convected heat along fractures from the devitrified tuff to the vitrophyre caused local devitrification and hydrous mineral crystallization. Oxygen isotope geothermometry of cogenetic quartz confirms the nondiagnetic moderate temperature origin of the hydrous minerals at temperatures of about 40 to 100 0 C, assuming a meteoric water source. 14 refs., 3 figs., 1 tab

  5. Microporous Cokes Formed in Zeolite Catalysts Enable Efficient Solar Evaporation

    KAUST Repository

    Wang, Jianjian

    2017-03-13

    Cokes are inevitably generated during zeolite-catalyzed reactions as deleterious side products that deactivate the catalyst. In this study, we in-situ converted cokes into carbons within the confined microporous zeolite structures and evaluated their performances as absorbing materials for solar-driven water evaporation. With a properly chosen zeolite, the cokederived carbons possessed ordered interconnected pores and tunable compositions. We found that the porous structure and the oxygen content in as-prepared carbons had important influences on their energy conversion efficiencies. Among various investigated carbon materials, the carbon derived from the methanol-to-olefins reaction over zeolite Beta gave the highest conversion efficiency of 72% under simulated sunlight with equivalent solar intensity of 2 suns. This study not only demonstrates the great potential of traditionally useless cokes for solar thermal applications but also provides new insights into the design of carbon-based absorbing materials for efficient solar evaporation.

  6. Zeolites and clays behavior in presence of radioactive solutions

    International Nuclear Information System (INIS)

    Carrera Garcia, L.M.

    1991-01-01

    Natural aluminosilicates have found application as selective ion exchangers for radioactive cations, present in liquid wastes arising from nuclear facilities. Among severals cations and complex mixtures of them, Co is a common constituent of liquid radioactive wastes. Two types of zeolites (Y zeolite, and natural mexican erionite), and two types of clays (natural bentonite, and Al-expanded bentonite (Al-B) were used. Previous to the experiments, the zeolites and the natural bentonite were stabilized to their respective Na + form using 5N NaCl solution. 2Na + → 60 Co 2+ ion exchange kinetics in zeolites and clays was followed by gamma spectrometry using a NaCl-Co(NO 3 ) 2 isonormal solution (0.1N) labeled with 60 Co-Co(NO 3 ) 2 (100 μ Ci). Before and after experiments, the structural changes in the cristallinity of aluminosilicates were determined by X-ray diffraction. XRD analyzes show that the cristallinity of the aluminosilicates was not affected by ion exchange. After Co exchange the cell parameters were determined in all samples. The efficiency of zeolites, natual clays and expanded clays to remove cobalt ions from solutions depends on the ion echange capacity of the material. Results for long contacts time, 18 days, show that Co is more effectively removed by Y zeolite ( 4.07 wt %), followed by erionite (3.09 wt %), then bentonite ( 2.36 wt %) and finally expanded bentonite ( 0.70 wt %). In Y zeolite an unusual fast soportion uptake of 4.51 % wt Co was observed followed by a desorption process to 4.07 %. This effect is due to the different hydration degree of zeolites during the contact time between the zeolite and the 60 Co solution. In erionite the exchange is lower than in Y-zeolite, frist because the Si/Al ratio is higher for erionite than for Y-zeolite and second because K ions in erionite cannot be exchanged during the stabilization of erionite in 5N NaCl solution. The low exchange in expanded bentonite was expected because its cation exchange

  7. Regioselective nitration of aromatic substrates in zeolite cages

    Indian Academy of Sciences (India)

    Unknown

    selective nitration with a nitrogen dioxide-oxygen-zeolite H-β/HY as a solid inorganic catalyst.14 Recently .... acetic anhydride/CCl4 with an isomer distribution of ortho 23, meta 1 and para 76%.18. Smith has shown that .... all the zeolites, except CaY, recovered mass balance was about 90%. 3.2c Nitration of toluene and ...

  8. Investigation of zeolites by solid state quadrapole NMR

    International Nuclear Information System (INIS)

    Janssen, R.

    1990-01-01

    The subject of this thesis is the NMR investigation of zeolites. The nature and properties of zeolites are discussed. Some of the basic priniples of NMR techniques on quadrupole nuclei are presented. A special technique, namely a two-dimensional nutation experiment is discussed in detail. The theory of the nutation experiment for quadrupole spin species with spin quantum number 3/2 as well as 5/2 is presented. For both spin spcies the theoretical spectra are compared with experimental results. It is also shown that the nutation expeirment can be performed with several pulse schemes. It is shown how phase-sensitive pure-absorption nutation spectra can be obtained and an NMR-probe is presented that is capable of performing NMR experiments at high (up to 500 degree C) temperatures. The two-dimensional nutation NMR technique has been applied to sodium cations in zeolite NaA. For this purpose a numbre of zeolite samples were prepared that contained different amounts of water. With the aid of nutation NMR the hydration of the zeolite can be studied and conclusions can be drawn about the symmetry of the surrounding of the sodium cations. With the aid of an extension of the nutation NMR experiment: Rotary Echo Nutation NMR, it is shown that in zeolite NaA, in various stages of hydration, the sodium cations or water molecules are mobile. Proof is given by means of high-temperature 23 Na-NMR that dehydrates zeolite NaA undergoes a phase transition at ca. 120 degree C. In a high-temperature NMR investigation of zeolite ZSM-5 it is shown that the sodium ions start to execute motions when the temperature is increased. (author). 198 refs.; 72 figs.; 6 tabs

  9. Zeolite and zeotype-catalysed transformations of biofuranic compounds

    DEFF Research Database (Denmark)

    Li, Hu; Yang, Song; Riisager, Anders

    2016-01-01

    ,5-furandicarboxylic acid can be obtained from hexoses and pentoses via selective dehydration and subsequent etherification, hydrogenation, oxidation reactions, which show great potential for industrial applications to replace petroleum-based chemicals and fuels. Zeolite and zeotype micro- and mesoporous materials...... introducing zeolite-catalysed hydrolysis of di-, oligo- and polysaccharides and isomerization reactions of monomeric sugars. Subsequently, the catalytic dehydration reactions of hexoses and pentoses to obtain HMF and furfural are reported. Particularly, a variety of reaction pathways towards upgrading...

  10. Catalytic transformation of methyl benzenes over zeolite catalysts

    KAUST Repository

    Al-Khattaf, S.

    2011-02-01

    Catalytic transformation of three methyl benzenes (toluene, m-xylene, and 1,2,4-trimethyl benzene) has been investigated over ZSM-5, TNU-9, mordenite and SSZ-33 catalysts in a novel riser simulator at different operating conditions. Catalytic experiments were carried out in the temperature range of 300-400 °C to understand the transformation of these alkyl benzenes over large pore (mordenite and SSZ-33) in contrast to medium-pore (ZSM-5 and TNU-9) zeolite-based catalysts. The effect of reaction conditions on the isomerization to disproportionation product ratio, distribution of trimethylbenzene (TMB) isomers, and p-xylene/o-xylene ratios are reported. The sequence of reactivity of the three alkyl benzenes depends upon the pore structure of zeolites. The zeolite structure controls primarily the diffusion of reactants and products while the acidity of these zeolites is of a secondary importance. In the case of medium pore zeolites, the order of conversion was m-xylene > 1,2,4-TMB > toluene. Over large pore zeolites the order of reactivity was 1,2,4-TMB > m-xylene > toluene for SSZ-33 catalyst, and m-xylene ∼ 1,2,4-TMB > toluene over mordenite. Significant effect of pore size between ZSM-5 and TNU-9 was observed; although TNU-9 is also 3D 10-ring channel system, its slightly larger pores compared with ZSM-5 provide sufficient reaction space to behave like large-pore zeolites in transformation of aromatic hydrocarbons. We have also carried out kinetic studies for these reactions and activation energies for all three reactants over all zeolite catalysts under study have been calculated. © 2011 Elsevier B.V.

  11. Pemanfaatan Zeolit Alam Untuk Pengeringan Karaginan Dengan Spray Dryer

    OpenAIRE

    M.H, Babar Priyadi; Afifi, Thufail Khoirul; Sasongko, Setia Budi

    2012-01-01

    The problem that will be faced in drying is quite high relative humidity, therefore carrageenan drying process using spray dryer with zeolite as humidity absorber becomes alternative option to achieve heat effectiveness of air dryer. The research is purposed to examine the effect of temperature and level of zeolite to relative humidity and product quality on carrageenan drying process. Spray dryer is a dryer used to produce powder material from feeds which have liquid and pasta form. The Resu...

  12. Synthesis of Zeolite Materials for Noble Gas Separation

    Energy Technology Data Exchange (ETDEWEB)

    Achey, R. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Rivera, O. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Wellons, M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Hunter, D. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2017-10-02

    Microporous zeolite adsorbent materials are widely used as a medium for separating gases. Adsorbent gas separation systems can run at ambient temperature and require minimal pressure to flow the input gas stream across the adsorbent bed. This allows for low energy consumption relative to other types of separation systems. Specific zeolites also have a high capacity and selectivity for the gases of interest, leading to compact and efficient separation systems. These characteristics are particularly advantageous for the application of signatures detection for non-proliferation, which often requires portable systems with low power draw. Savannah River National Laboratory currently is the leader in using zeolites for noble gas sampling for non-proliferation detection platforms. However, there is a constant customer need for improved sampling capabilities. Development of improved zeolite materials will lead to improved sampling technology. Microwave-assisted and conventional hydrothermal synthesis have been used to make a variety of zeolites tailored for noble gas separation. Materials characterization data collected in this project has been used to help guide the synthesis of improved zeolite materials. Candidate materials have been down-selected based on highest available surface area, maximum overall capacity for gas adsorption and highest selectivity. The creation of improved adsorbent materials initiated in this project will lead to development of more compact, efficient and effective noble gas collectors and concentrators. The work performed in this project will be used as a foundation for funding proposals for further material development as well as possible industrial applications.

  13. Effects of Zeolite (Clinoptelolite on Performance Characteristics of

    Directory of Open Access Journals (Sweden)

    A Hassan Abadim

    2011-12-01

    Full Text Available A 70-days experiment was conducted to investigate the effects of natural zeolite (clinoptelolite on the performance of commercial laying hens. 288 Hy-Line W36 strain laying hens (50 weeks old were allotted to 6 dietary treatments including basal diet as control and basal diet supplemented with 1, 2, 3, 4 and 5% zeolite that were fed ad -libitum throughout the experiment. Experimental diets for the 6 treatments were prepared to be iso-caloric and iso-nitrogenous. A completely randomized design with six treatments, eight replicates of six birds per replicate was used at this experiment. Daily feed intake (DFI, feed conversion ratio (FCR, egg production, egg weight, egg white quality, eggshell quality (thickness and percentage and body weight changes were measured during the experiment. Results of this experiment showed that DFI, FCR, egg production and egg abnormality were not significantly (P>0.05 affected by zeolite supplementation. Zeolite supplementation significantly increased egg weight, eggshell thickness and live body weight gain of the hens. Dietary zeolite significantly decreased haugh unit of the eggs. In conclusion, natural zeolite significantly improved egg weight and eggshell quality, decreased haugh unit and live weight gain, and had no significant effects on other parameters.

  14. Catalytic conversion of ethanol on H-Y zeolite

    Directory of Open Access Journals (Sweden)

    Čegar Nedeljko

    2005-01-01

    Full Text Available The catalytic activity of the H-form of synthetic zeolite NaY was examined in this study. The catalytic activity was determined according to the rate of ethanol conversion in a gas phase in the static system. In the conversion of ethanol on synthetic NaY zeolite at 585, 595, and 610 K, on which the reaction develops at an optimal rate, ethene and diethyl ether are evolved in approximately the same quantity. After transforming the NaY zeolite into the H-form, its catalytic activity was extremely increases so, the reaction develops at a significantly lower temperature with a very large increase in the reaction rate. The distribution of the products also changes, so that at lower temperatures diethyl ether is elvolved in most cases, and the development of ethene is favored at higher ones, and after a certain period of time there is almost complete conversion of ethanol into ethene. The increase in catalytic activity, as well as the change of selectivity of conversion of ethanol on the H-form of zeolite, is the result of removing Na+ cations in the NaY zeolite, so that more acidic catalyst is obtained which contains a number of acidic catalytically active centers, as well as a more powerful one compared to the original NaY zeolite.

  15. Inhibition of palm oil oxidation by zeolite nanocrystals.

    Science.gov (United States)

    Tan, Kok-Hou; Awala, Hussein; Mukti, Rino R; Wong, Ka-Lun; Rigaud, Baptiste; Ling, Tau Chuan; Aleksandrov, Hristiyan A; Koleva, Iskra Z; Vayssilov, Georgi N; Mintova, Svetlana; Ng, Eng-Poh

    2015-05-13

    The efficiency of zeolite X nanocrystals (FAU-type framework structure) containing different extra-framework cations (Li(+), Na(+), K(+), and Ca(2+)) in slowing the thermal oxidation of palm oil is reported. The oxidation study of palm oil is conducted in the presence of zeolite nanocrystals (0.5 wt %) at 150 °C. Several characterization techniques such as visual analysis, colorimetry, rheometry, total acid number (TAN), FT-IR spectroscopy, (1)H NMR spectroscopy, and Karl Fischer analyses are applied to follow the oxidative evolution of the oil. It was found that zeolite nanocrystals decelerate the oxidation of palm oil through stabilization of hydroperoxides, which are the primary oxidation product, and concurrently via adsorption of the secondary oxidation products (alcohols, aldehydes, ketones, carboxylic acids, and esters). In addition to the experimental results, periodic density functional theory (DFT) calculations are performed to elucidate further the oxidation process of the palm oil in the presence of zeolite nanocrystals. The DFT calculations show that the metal complexes formed with peroxides are more stable than the complexes with alkenes with the same ions. The peroxides captured in the zeolite X nanocrystals consequently decelerate further oxidation toward formation of acids. Unlike the monovalent alkali metal cations in the zeolite X nanocrystals (K(+), Na(+), and Li(+)), Ca(2+) reduced the acidity of the oil by neutralizing the acidic carboxylate compounds to COO(-)(Ca(2+))1/2 species.

  16. Xylenes transformation over zeolites ZSM-5 ruled by acidic properties

    Science.gov (United States)

    Gołąbek, Kinga; Tarach, Karolina A.; Góra-Marek, Kinga

    2018-03-01

    The studies presented in this work offer an insight into xylene isomerization process, followed by 2D COS analysis, in the terms of different acidity of microporous zeolites ZSM-5. The isomerisation reaction proceeded effectively over zeolites ZSM-5 of Si/Al equal of 12 and 32. Among them, the Al-poorer zeolite (Si/Al = 32) was found to offer the highest conversion and selectivity to p-xylene with the lowest number of disproportionation products, both in ortho- and meta-xylene transformation. Further reduction of Brønsted acidity facilitated the disproportionation path (zeolites of Si/Al = 48 and 750). The formation of intermediate species induced by the diffusion constraints for m-xylene in 10-ring channels was rationalized in the terms of the methylbenzenium ions formation inside the rigid micropore environment. Finally, both microporous character of zeolite and the optimised acidity were found to be crucial for high selectivity to the most desired product i.e. p-xylene. The analysis of asynchronous maps allowed for concluding on the order of the appearance of the respective products on the zeolite surface.

  17. Influence of zeolitized perlite on blended cement properties

    Directory of Open Access Journals (Sweden)

    Vaičiukynienė Danutė

    2016-01-01

    Full Text Available Perlite is the mineral of volcanic origin. Expanded perlite has good heat insulation and sound absorption properties. It is light, resistant to fire, moisture and micro-organisms, harmless to health. However, due to the presence of hyaline phase, its use in Portland cement mixture is problematic. In this paper, the zeolitization of expanded perlite was carried out to improve its hydraulic properties. The conversion of expanded perlite into zeolite material was carried out when Na2O : Al2O3 : SiO2 : H2O molar ratio was equal to 2: 1: 2: 10 and the suspension of starting materials was treated for 3 hours at 100°C temperature. Mechanical and physical properties of hardened cement paste containing 0%, 5%, 10%, and 15% of pure perlite admixtures, zeolitized perlite, and perlite altered to calcium (Ca2+ zeolite were researched. The results showed that zeolitization of expanded perlite activates its hydraulic properties; after 28 days of hydration under normal conditions, the compressive strength of the specimens modified with 5% of zeolitized perlite admixture was 49-50 MPa, whereas the compressive strength of the specimens containing 5% of pure perlite admixture was only 33 MPa.

  18. Synthesis of uniform-sized zeolite from windshield waste

    International Nuclear Information System (INIS)

    Kim, Jae-Chan; Choi, Mingu; Song, Hee Jo; Park, Jung Eun; Yoon, Jin-Ho; Park, Kyung-Soo; Lee, Chan Gi; Kim, Dong-Wan

    2015-01-01

    We demonstrate the synthesis of A-type zeolite from mechanically milled windshield waste via acid treatment and a low-temperature hydrothermal method. As-received windshield cullet was crushed to a fine powder and impurities were removed by HNO 3 treatment. The resulting glass powder was used as the source material for the hydrothermal synthesis of A-type zeolite. Crystal structure, morphology, and elemental composition changes of the windshield waste were evaluated at each step of the process through scanning electron microscopy, X-ray diffraction, X-ray fluorescence spectrometry, etc. After a high-energy milling process, the glass had an average particle size of 520 nm; after acid treatment, its composition was over 94% silica. Zeolite was successfully synthesized in the A-type phase with a uniform cubic shape. - Highlights: • Environmental-friendly recycling of windshield waste for high valuable product of zeolite. • Synthesis of zeolite form windshield waste via a low-temperature hydrothermal process. • High-energy milling effect on the uniform cubic shape and high-purity A-type zeolite.

  19. The application of silicalite-1/fly ash cenosphere (S/FAC) zeolite composite for the adsorption of methyl tert-butyl ether (MTBE).

    Science.gov (United States)

    Lu, Jia; Xu, Fang; Wang, Deju; Huang, Jue; Cai, Weimin

    2009-06-15

    Silicalite-1/fly ash cenosphere (S/FAC) zeolite composite has been applied for batch adsorption of methyl tert-butyl ether (MTBE) from water systems. Here the key experimental conditions, including the ratio of initial MTBE concentration to the amount weight of S/FAC, adsorption time and temperature, have been discussed in detail. The results show that approximately 93-95% MTBE could be adsorbed with initial concentration of MTBE solution 1000 microg l(-1). The column flow-through experiments also prove the high capacity of S/FAC composite for MTBE removal. The distinct advantages of S/FAC zeolite composite as adsorbent lie in (1) enhanced adsorption rate and capacity based on hierarchical micro and meso/macroporosity of S/FAC; (2) more easily operation and recycling process by assembly of nano-sized silicalite-1 zeolite on FAC support.

  20. Molecular exchange of n-hexane in zeolite sieves studied by diffusion-diffusion and T{sub 1}-diffusion nuclear magnetic resonance exchange spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Neudert, Oliver; Stapf, Siegfried; Mattea, Carlos, E-mail: carlos.mattea@tu-ilmenau.de [Fachgebiet Technische Physik II/Polymerphysik, Institute of Physics, Technische Universitaet Ilmenau, PO Box 100 565, 98684 Ilmenau (Germany)

    2011-03-15

    Molecular exchange properties and diffusion of n-hexane embedded in a bimodal pore structure with characteristic length scales in the order of nano and micrometres, respectively, formed by packing of zeolite particles, are studied. Two-dimensional (2D) nuclear magnetic resonance (NMR) diffusion correlation experiments together with relaxation-diffusion correlation experiments are performed at low magnetic field using a single-sided NMR scanner. The exchange time covers a range from 10{sup -3} to 10{sup -1} s. The molecular exchange properties are modulated by transport inside the zeolite particles. Different exchange regimes are observed for molecules starting from different positions inside the porous sample. The influence of the spin-lattice relaxation properties of the fluid molecules inside the zeolite particles on the signal intensity is also studied. A Monte Carlo simulation of the exchange process is performed and is used to support the analysis of the experimental data.

  1. Zeolites as alcohol adsorbents from aqueous solutions

    Directory of Open Access Journals (Sweden)

    Cekova Blagica

    2006-01-01

    Full Text Available The potential usage of zeolites as adsorbents for the removal of organic molecules from water was investigated in a series of experiments with aqueous solutions of lower alcohols. This could represent a simple solution to the problem of cleaning up industrial wastewater as well as recovering valuable chemicals at relatively low costs. Adsorption isotherms of the Langmuir type were applied, and calculations showed that the amount of propanol adsorbed on silicalite corresponded to approximately 70% of the pore volume. The adsorption process is simple, and recovery of the more concentrated products is easily done by heat treatment and/or at lowered pressures. Adsorption experiments with aqueous acetone showed that silicalite had approximately the same adsorption capacity for acetone as for n-propanol. Heats of adsorption were determined calorimetrically.

  2. Exchange of Co(II) Ions in H-BEA Zeolites. Identification of Aluminium Pairs in the Zeolite Framework

    Czech Academy of Sciences Publication Activity Database

    Bortnovsky, Oleg; Sobalík, Zdeněk; Wichterlová, Blanka

    2001-01-01

    Roč. 46, č. 2 (2001), s. 265-275 ISSN 1387-1811 R&D Projects: GA AV ČR IBS4040015; GA MŠk OC D15.20 Institutional research plan: CEZ:AV0Z4040901 Keywords : BEA zeolites * cobalt ion exchange * zeolite framework aluminium Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 2.497, year: 2001

  3. Pyrolysis of scrap tyres with zeolite USY

    International Nuclear Information System (INIS)

    Shen Boxiong; Wu Chunfei; Wang Rui; Guo Binbin; Liang Cai

    2006-01-01

    A zeolite catalyst of ultrastable Y-type (USY) was investigated in the research of two staged pyrolysis-catalysis of scrap tyres. Scrap tyres were pyrolysed in a fixed bed reactor and the evolved pyrolysis gases were passed through a secondary catalytic reactor. The main objective of this paper was to investigate the effect of zeolite USY on the yield of products and the composition of derived oil. The influences of several parameters such as pyrolysis temperature, catalytic temperature, catalyst/tyre ratio, heating rate, etc. on the yield of the derived oil, char and gas were investigated. It showed that the increase of catalytic temperature and catalyst/tyre ratio resulted in high yield of gas at the expense of the oil yield. For example, when the catalyst/tyre ratio increased from 0.25 to 1.0, the yield of gas increased from 30.5 to 49.9 wt.%, and the oil yield decreased nearly two-fold from 31.6 to 12.7 wt.%. The concentration of light naphtha (boiling point < 160 deg. C) was also investigated in this study. And the high catalyst/tyre ratio favored to increase the concentration of light naphtha (<160 deg. C) in oil. In order to study the composition of derived oil, a distilled fraction (<280 deg. C), which was 92.5 wt.% of the oil obtained from catalytic pyrolysis of scrap tyre at a pyrolysis temperature, catalytic temperature and catalyst/tyre ratio of 500, 400 deg. C and 0.5, respectively, was analyzed with gas chromatography/mass spectrometry (GC/MS). The distillate was found to contain 1.23 wt.% benzene, 9.35 wt.% toluene, 3.68 wt.% ethylbenzene, 12.64 wt.% xylenes, 1.81 wt.% limonene and 13.89 wt.% PAHs, etc., where the single ring aromatics represented a significant potential use as chemicals

  4. Pyrolysis of scrap tyres with zeolite USY.

    Science.gov (United States)

    Shen, Boxiong; Wu, Chunfei; Wang, Rui; Guo, Binbin; Liang, Cai

    2006-09-21

    A zeolite catalyst of ultrastable Y-type (USY) was investigated in the research of two staged pyrolysis-catalysis of scrap tyres. Scrap tyres were pyrolysed in a fixed bed reactor and the evolved pyrolysis gases were passed through a secondary catalytic reactor. The main objective of this paper was to investigate the effect of zeolite USY on the yield of products and the composition of derived oil. The influences of several parameters such as pyrolysis temperature, catalytic temperature, catalyst/tyre ratio, heating rate, etc. on the yield of the derived oil, char and gas were investigated. It showed that the increase of catalytic temperature and catalyst/tyre ratio resulted in high yield of gas at the expense of the oil yield. For example, when the catalyst/tyre ratio increased from 0.25 to 1.0, the yield of gas increased from 30.5 to 49.9 wt.%, and the oil yield decreased nearly two-fold from 31.6 to 12.7 wt.%. The concentration of light naphtha (boiling point tyre ratio favored to increase the concentration of light naphtha (composition of derived oil, a distilled fraction (tyre at a pyrolysis temperature, catalytic temperature and catalyst/tyre ratio of 500, 400 degrees C and 0.5, respectively, was analyzed with gas chromatography/mass spectrometry (GC/MS). The distillate was found to contain 1.23 wt.% benzene, 9.35 wt.% toluene, 3.68 wt.% ethylbenzene, 12.64 wt.% xylenes, 1.81 wt.% limonene and 13.89 wt.% PAHs, etc., where the single ring aromatics represented a significant potential use as chemicals.

  5. Intolerant tolerance.

    Science.gov (United States)

    Khushf, G

    1994-04-01

    The Hyde Amendment and Roman Catholic attempts to put restrictions on Title X funding have been criticized for being intolerant. However, such criticism fails to appreciate that there are two competing notions of tolerance, one focusing on the limits of state force and accepting pluralism as unavoidable, and the other focusing on the limits of knowledge and advancing pluralism as a good. These two types of tolerance, illustrated in the writings of John Locke and J.S. Mill, each involve an intolerance. In a pluralistic context where the free exercise of religion is respected, John Locke's account of tolerance is preferable. However, it (in a reconstructed form) leads to a minimal state. Positive entitlements to benefits like artificial contraception or nontherapeutic abortions can legitimately be resisted, because an intolerance has already been shown with respect to those that consider the benefit immoral, since their resources have been coopted by taxation to advance an end that is contrary to their own. There is a sliding scale from tolerance (viewed as forbearance) to the affirmation of communal integrity, and this scale maps on to the continuum from negative to positive rights.

  6. Solvation and Acid Strength Effects on Catalysis by Faujasite Zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Gounder, Rajamani P.; Jones, Andrew J.; Carr, Robert T.; Iglesia, Enrique

    2012-02-01

    Kinetic, spectroscopic, and chemical titration data indicate that differences in monomolecular isobutane cracking and dehydrogenation and methanol dehydration turnover rates (per H+) among FAU zeolites treated thermally with steam (H-USY) and then chemically with ammonium hexafluorosilicate (CDHUSY) predominantly reflect differences in the size and solvating properties of their supercage voids rather than differences in acid strength. The number of protons on a given sample was measured consistently by titrations with Na+, with CH3 groups via reactions of dimethyl ether, and with 2,6-di-tert-butylpyridine during methanol dehydration catalysis; these titration values were also supported by commensurate changes in acidic OH infrared band areas upon exposure to titrant molecules. The number of protons, taken as the average of the three titration methods, was significantly smaller than the number of framework Al atoms (Alf) obtained from X-ray diffraction and 27Al magic angle spinning nuclear magnetic resonance spectroscopy on H-USY (0.35 H+/Alf) and CD-HUSY (0.69 H+/Alf). These data demonstrate that the ubiquitous use of Alf sites as structural proxies for active H+ sites in zeolites can be imprecise, apparently because distorted Al structures that are not associated with acidic protons are sometimes detected as Alf sites. Monomolecular isobutane cracking and dehydrogenation rate constants, normalized non-rigorously by the number of Alf species, decreased with increasing Na+ content on both H-USY and CD-HUSY samples and became undetectable at sub-stoichiometric exchange levels (0.32 and 0.72 Na+/Alf ratios, respectively), an unexpected finding attributed incorrectly in previous studies to the presence of minority ‘‘super-acidic’’ sites. These rate constants, when normalized rigorously by the number of residual H+ sites were independent of Na+ content on both H-USY and CD-HUSY samples, reflecting the stoichiometric replacement of protons that are uniform in

  7. Post-synthesis incorporation of Al into germanosilicate ITH zeolites: The influence of treatment conditions on the acidic properties and catalytic behavior in tetrahydropyranylation

    Czech Academy of Sciences Publication Activity Database

    Shamzhy, Mariya; Opanasenko, Maksym; de O. Ramos, F. S.; Brabec, Libor; Horáček, Michal; Navarro-Rojas, M.; Morris, R. E.; de O. Pastore, H.; Čejka, Jiří

    2015-01-01

    Roč. 5, č. 5 (2015), s. 2973-2984 ISSN 2044-4753 R&D Projects: GA ČR(CZ) GP14-30898P; GA ČR GP13-17593P Institutional support: RVO:61388955 Keywords : bromine * zeolites * germanium Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 5.287, year: 2015

  8. Exploratory catalyst screening studies on the base free conversion of glycerol to lactic acid and glyceric acid in water using bimetallic Au-Pt compounds on acidic zeolites

    NARCIS (Netherlands)

    Pazhavelikkakath Purushothaman, Rajeesh Kumar; van Haveren, J.; Mayoral, A.; Melian Cabrera, I.; Heeres, H.J.

    2014-01-01

    The base free oxidation of glycerol with molecular oxygen in water using bimetallic Au-Pt catalysts on three different acidic zeolite supports (H-mordenite, H-beta and H-USY) was explored in a batch setup. At temperatures between 140 and 180 degrees C, lactic acid formation was significant and

  9. Exploratory Catalyst Screening Studies on the Base Free Conversion of Glycerol to Lactic Acid and Glyceric Acid in Water Using Bimetallic Au–Pt Nanoparticles on Acidic Zeolites

    NARCIS (Netherlands)

    Purushothaman, R.K.P.; Haveren, van J.; Mayoral, A.; Melian-Cabrera, I.; Heeres, H.J.

    2014-01-01

    The base free oxidation of glycerol with molecular oxygen in water using bimetallic Au-Pt catalysts on three different acidic zeolite supports (H-mordenite, H-beta and H-USY) was explored in a batch setup. At temperatures between 140 and 180 degrees C, lactic acid formation was significant and

  10. Static in-situ hydrothermal synthesis of small pore zeolite SSZ-16 (AFX) using heated and pre-aged synthesis mixtures

    Czech Academy of Sciences Publication Activity Database

    Hrabánek, Pavel; Zikánová, Arlette; Supiňková, Taťána; Drahokoupil, Jan; Fíla, V.; Lhotka, M.; Dragounová, H.; Laufek, František; Brabec, Libor; Jirka, Ivan; Bernauer, B.; Prokopová, Olga; Martin-Gil, V.; Kočiřík, Milan

    2016-01-01

    Roč. 228, JUL 2016 (2016), s. 107-115 ISSN 1387-1811 R&D Projects: GA ČR(CZ) GAP204/11/1206 Institutional support: RVO:61388955 ; RVO:68378271 Keywords : zeolite * synthesis * AFX Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 3.615, year: 2016

  11. Remarkably enhanced density and specific activity of active sites in Al-rich Cu-, Fe- and Co-beta zeolites for selective catalytic reduction of NOx

    Czech Academy of Sciences Publication Activity Database

    Sazama, Petr; Pilař, Radim; Mokrzycki, Lukasz; Vondrová, Alena; Kaucký, Dalibor; Plšek, Jan; Sklenák, Štěpán; Šťastný, Petr; Klein, Petr

    2016-01-01

    Roč. 189, JUL 2016 (2016), s. 65-74 ISSN 0926-3373 R&D Projects: GA TA ČR(CZ) TH01021259 Institutional support: RVO:61388955 Keywords : SCR- NOx * Al-rich beta zeolite (*BEA) * Cobalt Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 9.446, year: 2016

  12. Remarkably enhanced density and specific activity of active sites in Al-rich Cu-, Fe- and Co-beta zeolites for selective catalytic reduction of NOx

    Czech Academy of Sciences Publication Activity Database

    Sazama, Petr; Pilař, Radim; Mokrzycki, Lukasz; Vondrová, Alena; Kaucký, Dalibor; Plšek, Jan; Sklenák, Štěpán; Šťastný, Petr; Klein, Petr

    2016-01-01

    Roč. 189, JUL 2016 (2016), s. 65-74 ISSN 0926-3373 R&D Projects: GA TA ČR(CZ) TH01021259 Institutional support: RVO:61388955 Keywords : SCR-NOx * Al-rich beta zeolite (*BEA) * Cobalt Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 9.446, year: 2016

  13. PENJERAPAN P-KHLOROFENOL DALAM AIR LIMBAH DENGAN ZEOLIT (Adsorption of p-Chlorophenol from Wastewater using Zeolite

    Directory of Open Access Journals (Sweden)

    Sarto Sarto

    2007-07-01

    Full Text Available ABSTRAK Penelitian ini bertujuan untuk mempelajari kemampuan zeolit untuk menjerap p-khlorofenol dari limbah cair secara batch, pada suhu 30 °C dan tekanan 1 atmosfer. Hasil penelitian menunjukkan bahwa proses penjerapan mengikuti persamaan Freundlich dan bersifat reversibel sebagian. Nisbah kinerja desorbsi dan penjerapan adalah antara 31,85 % dan 49,36 %. Kemampuan zeolit untuk menjerap p-khlorofenol meningkat dengan semakin rendahnya pH. pada nilai pH 3,92, berat zeolit 30 g, dan konsentrasi awal p-khlorofenol 97,302 mg/L. Adapun jumlah p-khlorofenol yang terjerap adalah sebesar 8,319 mg/L.   ABSTRACT The aim of this research is to study the characteristics of zeolit to adsorb p-chlorophenol from wastewater in a batch reactor at 30 oC and atmospheric conditions. The experimental results show that the adsorbtion process is partially reversible and fits with Freundlich Equation. The ratio of  desorption and adsortion performance is between 31.85 % and 49.36 %.  The performance of zeolit to adsorb p-chlorophenol increases with decreasing pH. At  pH about 3.92, using 30 g zeolit and 97.302 mg  p-chlorophenol/L. The concentration of adsorbed p-chlorophenol is about 8.319 mg/L.

  14. Acid and redox activity of template-free Al-rich H-BEA* and Fe-BEA* zeolites

    Czech Academy of Sciences Publication Activity Database

    Sazama, Petr; Wichterlová, Blanka; Sklenák, Štěpán; Parvulescu, V. I.; Candu, N.; Sádovská, Galina; Dědeček, Jiří; Klein, Petr; Pashková, Veronika; Šťastný, Petr

    2014-01-01

    Roč. 318, OCT 2014 (2014), s. 22-33 ISSN 0021-9517 R&D Projects: GA ČR GAP106/11/0624; GA ČR(CZ) GA14-10251S; GA TA ČR TA01021377 Institutional support: RVO:61388955 Keywords : Acid strength * Alkylation of aromatics * Beta zeolite Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 6.921, year: 2014

  15. Effect of Enhanced Accessibility of Acid Sites in Micromesoporous Mordenite Zeolites on Hydroisomerization of n-Hexane

    Czech Academy of Sciences Publication Activity Database

    Pastvová, Jana; Kaucký, Dalibor; Morávková, Jaroslava; Rathouský, Jiří; Sklenák, Štěpán; Vorokhta, Maryna; Brabec, Libor; Pilař, Radim; Jakubec, Ivo; Tabor, Edyta; Klein, Petr; Sazama, Petr

    2017-01-01

    Roč. 7, č. 9 (2017), s. 5781-5795 ISSN 2155-5435 R&D Projects: GA ČR GA15-12113S; GA MŠk(CZ) LM2015073 Institutional support: RVO:61388955 ; RVO:61388980 ; RVO:67985891 Keywords : micromesoporous mordenite (MOR) zeolites * isomerization * n-hexane Subject RIV: CF - Physical ; Theoretical Chemistry; CA - Inorganic Chemistry (UACH-T) OBOR OECD: Physical chemistry; Inorganic and nuclear chemistry (UACH-T) Impact factor: 10.614, year: 2016

  16. Catalytic Properties of 3D Graphene-Like Microporous Carbons Synthesized in a Zeolite Template

    Czech Academy of Sciences Publication Activity Database

    Sazama, Petr; Pastvová, Jana; Rizescu, C.; Tirsoaga, A.; Parvulescu, V. I.; Garcia, H.; Kobera, Libor; Seidel, J.; Rathouský, Jiří; Klein, Petr; Jirka, Ivan; Morávková, Jaroslava; Blechta, Václav

    2018-01-01

    Roč. 8, č. 3 (2018), s. 1779-1789 ISSN 2155-5435 R&D Projects: GA ČR GA15-12113S; GA MŠk(CZ) LM2015073 Grant - others:GA MŠk(CZ) CZ.02.1.01/0.0/0.0/16_013/0001821 Institutional support: RVO:61388955 ; RVO:61389013 Keywords : catalytic hydrogenation * zeolite-templated carbon * 3D graphene-like microporous carbons Subject RIV: CF - Physical ; Theoretical Chemistry OBOR OECD: Physical chemistry Impact factor: 10.614, year: 2016

  17. Zeolite-based SCR catalysts and their use in diesel engine emission treatment

    Science.gov (United States)

    Narula, Chaitanya K; Yang, Xiaofan

    2015-03-24

    A catalyst comprising a zeolite loaded with copper ions and at least one trivalent metal ion other than Al.sup.+3, wherein the catalyst decreases NO.sub.x emissions in diesel exhaust. The trivalent metal ions are selected from, for example, trivalent transition metal ions, trivalent main group metal ions, and/or trivalent lanthanide metal ions. In particular embodiments, the catalysts are selected from Cu--Fe-ZSM5, Cu--La-ZSM-5, Fe--Cu--La-ZSM5, Cu--Sc-ZSM-5, and Cu--In-ZSM5. The catalysts are placed on refractory support materials and incorporated into catalytic converters.

  18. Fault tolerant software modules for SIFT

    Science.gov (United States)

    Hecht, M.; Hecht, H.

    1982-01-01

    The implementation of software fault tolerance is investigated for critical modules of the Software Implemented Fault Tolerance (SIFT) operating system to support the computational and reliability requirements of advanced fly by wire transport aircraft. Fault tolerant designs generated for the error reported and global executive are examined. A description of the alternate routines, implementation requirements, and software validation are included.

  19. Mordenite - Type Zeolite SCR Catalysts with Iron or Copper

    DEFF Research Database (Denmark)

    2012-01-01

    Cu/mordenite catalysts were found to be highly active for the SCR of NO with NH3 and exhibited high resistance to alkali poisoning. Redox and acidic properties of Cu/mordenite were well preserved after poisoning with potassium unlike that of vanadium catalysts. Fe-mordenite catalysts also reveale...... to be essential requirements for the high alkali resistance. Mordenite-type zeolite based catalysts could therefore be attractive alternatives to conventional SCR catalysts for biomass fired power plant flue gas treatment.......Cu/mordenite catalysts were found to be highly active for the SCR of NO with NH3 and exhibited high resistance to alkali poisoning. Redox and acidic properties of Cu/mordenite were well preserved after poisoning with potassium unlike that of vanadium catalysts. Fe-mordenite catalysts also revealed...... much higher alkali resistivity than that of commercial V2O5/WO3-TiO2 (VWT) SCR catalyst which is currently used for NOx abatement in stationary installations. Unique support properties like high surface area and surface acidity, which are not available in the commercial VWT catalyst, seem...

  20. The Effect of Zeolite on Aggregate Stability Indices

    Directory of Open Access Journals (Sweden)

    F. Sohrab

    2016-02-01

    Full Text Available Introduction: Soil structural stability affects the profitability and sustainability of agricultural systems. Particle size distribution (PSD and aggregate stability are the important characteristics of soil. Aggregate stability has a significant impact on the development of the root system, water and carbon cycle and soil resistance against soil erosion. Soil aggregate stability, defined as the ability of the aggregates to remain intact when subject to a given stress, is an important soil property that affects the movement and storage of water, aeration, erosion, biological activity and growth of crops. Dry soil aggregate stability (Mean Weight Diameter (MWD, Geometric Mean Diameter (GMD and Wet Aggregate Stability (WAS are important indices for evaluating soil aggregate stability.To improve soil physical properties, including modifying aggregate, using various additives (organic, inorganic and chemicals, zeolites are among what has been studied.According to traditional definition, zeolites are hydratealuminosilicates of alkaline and alkaline-earth minerals. Their structure is made up of a framework of[SiO4]−4 and [AlO4]−5 tetrahedron linked to each other's cornersby sharing oxygen atoms. The substitution of Si+4 by Al+3 intetrahedral sites results inmore negative charges and a high cation exchange capacity.Zeolites, as natural cation exchangers, are suitable substitutes to remove toxic cations. Among the natural zeolites,Clinoptilolite seems to be the most efficient ion exchanger and ion-selective material forremoving and stabilizing heavy metals.Due to theexisting insufficient technical information on the effects of using different levels of zeolite on physical properties of different types of soils in Iran, the aim of this research was to assess the effects of two different types of zeolite (Clinoptilolite natural zeolite, Z4, and Synthetic zeolite, A4 on aggregate stability indicesof soil. Materials and Methods: In this study at first

  1. Utilization of zeolites synthesized from coal fly ash for the purification of acid mine waters

    Energy Technology Data Exchange (ETDEWEB)

    Moreno, N.; Querol, X.; Ayora, C.; Pereira, C.F.; Janssen-Jurkovicova, M. [CSIC, Barcelona (Spain). Inst. of Earth Sciences ' Jaume Almera'

    2001-09-01

    Two pilot plant products containing 65 and 45% NaP1 zeolite were obtained from two Spanish coal fly ashes (Narcea and Teruel Power Station, respectively). The zeolitic product obtained showed a cation exchange capacity (CEC) of 2.7 and 2.0 mequiv/g, respectively. Decontamination tests of three acid mine waters from southwestern Spain were carried out using the zeolite derived from fly ash and commercial synthetic zeolite. The results demonstrate that the zeolitic material could be employed for heavy metal uptake in the water purification process. Doses of 5-30 g of zeolite/L have been applied according on the zeolite species and the heavy metal levels. Moreover, the application of zeolites increases the pH. This causes metal-bearing solid phases to precipitate and enhances the efficiency of the decontamination process. 31 refs., 4 figs., 5 tabs.

  2. Synthesis and characterization of zeolite material from coal ashes modified by surfactant

    International Nuclear Information System (INIS)

    Fungaro, D.A.; Borrely, S.I.

    2010-01-01

    Coal ash was used as starting material for zeolite synthesis by means of hydrothermal treatment. The surfactant-modified zeolite (SMZ) was prepared by adsorbing the cationic surfactant hexadecyltrimethylammonium bromide (HDTMA-Br) on the external surface of the zeolite from coal ash. The zeolite structure stability was monitored during the characterization of the materials by FTIR, XDR and SEM. The structural parameters of surfactant-modified zeolite are very close to that of corresponding non-modified zeolite which indicates that the crystalline nature of the zeolite remained intact after required chemical treatment with HDTMA-Br molecules and heating treatment for drying. The most intense peaks in the FTIR spectrum of HDTMA-Br were observed in SMZ spectrum confirming adsorption of surfactant on zeolites. (author)

  3. Antifungal activities against toxigenic Fusarium specie and deoxynivalenol adsorption capacity of ion-exchanged zeolites.

    Science.gov (United States)

    Savi, Geovana D; Cardoso, William A; Furtado, Bianca G; Bortolotto, Tiago; Zanoni, Elton T; Scussel, Rahisa; Rezende, Lucas F; Machado-de-Ávila, Ricardo A; Montedo, Oscar R K; Angioletto, Elidio

    2018-03-04

    Zeolites are often used as adsorbents materials and their loaded cations can be exchanged with metal ions in order to add antimicrobial properties. The aim of this study was to use the 4A zeolite and its derived ion-exchanged forms with Zn 2+ , Li + , Cu 2+ and Co 2+ in order to evaluate their antifungal properties against Fusarium graminearum, including their capacity in terms of metal ions release, conidia germination and the deoxynivalenol (DON) adsorption. The zeolites ion-exchanged with Li + , Cu 2+ , and Co 2+ showed an excellent antifungal activity against F. graminearum, using an agar diffusion method, with a zone of inhibition observed around the samples of 45.3 ± 0.6 mm, 25.7 ± 1.5 mm, and 24.7 ± 0.6 mm, respectively. Similar results using agar dilution method were found showing significant growth inhibition of F. graminearum for ion-exchanged zeolites with Zn 2+ , Li + , Cu 2+ , and Co 2+ . The fungi growth inhibition decreased as zeolite-Cu 2+ >zeolite-Li + >zeolite-Co 2+ >zeolite-Zn 2+ . In addition, the conidia germination was strongly affected by ion-exchanged zeolites. With regard to adsorption capacity, results indicate that only zeolite-Li + were capable of DON adsorption significantly (P concentration. The antifungal effects of the ion-exchanged zeolites can be ascribed to the interactions of the metal ions released from the zeolite structure, especially for zeolite-Li + , which showed to be a promising agent against F. graminearum and its toxin.

  4. Molecular interactions of alcohols with zeolite BEA and MOR frameworks.

    Science.gov (United States)

    Stückenschneider, Kai; Merz, Juliane; Schembecker, Gerhard

    2013-12-01

    Zeolites can adsorb small organic molecules such as alcohols from a fermentation broth. Also in the zeolite-catalyzed conversion of alcohols to biofuels, biochemicals, or gasoline, adsorption is the first step. Several studies have investigated the adsorption of alcohols in different zeolites experimentally, but computational investigations in this field have mostly been restricted to zeolite MFI. In this study, the adsorption of C1-C4 alcohols in BEA and MOR was investigated using density functional theory (DFT). Calculated adsorption geometries and the corresponding energies of the designed cluster models were comparable to periodic calculations, and the adsorption energies were in the same range as the corresponding computational and experimental values reported in the literature for zeolite MFI. Thus, BEA and MOR may be good adsorption materials for alcohols in the field of downstream processing and catalysis. Aside from the DFT calculations, adsorption isotherms were determined experimentally in this study from aqueous solutions. For BEA, the adsorption of significant amounts of alcohol from aqueous solution was observed experimentally. In contrast, MOR was loaded with only a very small amount of alcohol. Although differences were found between the affinities obtained from gas-phase DFT calculations and those observed experimentally in aqueous solution, the computational data presented here represent molecular level information on the geometries and energies of C1-C4 alcohols adsorbed in zeolites BEA and MOR. This knowledge should prove very useful in the design of zeolite materials intended for use in adsorption and catalytic processes, as it allows adsorption behavior to be predicted via judiciously designed computational models.

  5. Effect of hydrophilic defects on water transport in MFI zeolites.

    Science.gov (United States)

    Humplik, Thomas; Raj, Rishi; Maroo, Shalabh C; Laoui, Tahar; Wang, Evelyn N

    2014-06-10

    The subnanometer pore structure of zeolites and other microporous materials has been proposed to act as a molecular sieve for various water separation technologies. However, due to the increased interaction between the solid and water in these nanoconfined spaces, it is unclear which type of interface, be it hydrophilic or hydrophobic, offers an advantageous medium for enhancing transport properties. In this work, we probe the role of hydrophilic defects on the transport of water inside the microporous hydrophobic MFI zeolite pore structure via combined sorption and high-pressure infiltration experiments. While the inclusion of defects was observed to increase the amount of water within the zeolite pore network by up to 7 times at the saturation pressure, the diffusivity of this infiltrated water was lowered by up to 2 orders of magnitude in comparison to that of water within the nearly defect-free hydrophobic MFI zeolite. Subsequently, the permeability of water within the more defective MFI zeolite was an order of magnitude lower than that of the nearly defect-free zeolite. The results from these experiments suggest that the intrinsic hydrophobic pore structure of MFI zeolites can facilitate faster water transport due to the decreased attraction between the water and the defect-free surface. While the strong attraction of water to the defects allows for water to infiltrate the porous network at lower pressures, the results suggest that this strong attraction decreases the mobility of the infiltrated water. The insights gained from this study can be utilized to improve the design of future membranes for water desalination and other separation techniques.

  6. Sulphide phases in Y zeolite for hydro-treatment reactions; Phase sulfures dans une zeolithe Y pour l'hydrotraitement

    Energy Technology Data Exchange (ETDEWEB)

    Leyrit, P.

    1999-06-28

    Several types of single (Mo, Co, Pd, Pt) or binary (MoCo, PdCo, PtCo) sulphides phases supported on a HY zeolite were studied. The catalysts were first prepared and characterised in the oxide form. Their reactivity was then evaluated in toluene hydrogenation and 4.6-dimethyl-dibenzo-thiophene hydro-desulfurization reactions. Characterisation of sulphide phases supported on HY zeolite was carried out by elemental analysis, X-Ray Diffraction (XRD), Transmission Electron Microscopy and Scanning Transmission Electron Microscopy (STEM), Extended X-Ray Absorption Fine Structure (EXAFS) and Temperature Programmed Reduction coupled with HS analysis. The results show that. compared with alumina supported catalysts, zeolite used as a support enables extremely active catalysts to be obtained. It appears in particular that molybdenum sulphide phases inside the zeolite have a very high intrinsic activity at low molybdenum content. This activity is attributed to highly dispersed molybdenum sulphide phases differing from MoS{sub 2} slabs and probably present as clusters. The influence of cobalt depends of its concentration. Thus at low loadings cobalt has a strong negative effect. It has been shown, in the molybdenum case, that cobalt interaction leads to an increase in the sulphur content of the molybdenum phases. At higher cobalt loading, the formation of a mixed phase is possible but the degree of promotion remains limited. This work emphasises the advantages of using zeolite supported sulphide phases, and especially Mo and Pd phases, in the hydro-treatment reactions. It seems however that single phases present a greater interest than binary phases. (author)

  7. Tritium and deuterium NMR studies of zeolite catalyzed isotope exchange reactions

    International Nuclear Information System (INIS)

    Garnett, J.L.; Long, M.A.; Williams, P.G.

    1986-01-01

    The use of 3 H and 2 H nmr spectroscopy in studies of hydrogen isotope exchange over zeolites and metal loaded zeolites is important for both development of new catalytic methods of producing labelled compounds and for investigation of the mechanisms of catalysis over zeolites, as selected examples illustrate. 9 refs.; 1 figure; 2 tabs

  8. Effect of rare earth cations on activity of type Y zeolites in ethylene transformations

    International Nuclear Information System (INIS)

    Amezhnova, G.N.; Zhavoronkov, M.N.; Dorogochinskij, A.Z.; Proskurin, A.L.; Shmailova, V.I.

    1984-01-01

    The ethylene transformations on type Y rare earth zeolites with high degrees of sodium exchange are studied. It is shown that rare earth cations increase zeolites activity with growth of electronoacceptor capacity. The ethylene oligomerization occurs on polyvalent cations while subsequent oligomer transformations - on hydroxyl groups of zeolites

  9. Characterization of Mexican zeolite minerals; Caracterizacion de minerales zeoliticos mexicanos

    Energy Technology Data Exchange (ETDEWEB)

    Jimenez C, M.J

    2005-07-01

    50% of the Mexican territory is formed by volcanic sequences of the Pliocene type, which appear extensively in the northwest states (Sonora, Sinaloa, Chihuahua, Durango) and west of Mexico (Jalisco and Nayarit), in central Mexico (Zacatecas, Guanajuato, San Luis Potosi, Queretaro, Hidalgo) and south of Mexico (Guerrero, Oaxaca); therefore, it is to be expected that in our country big locations of natural zeolites exist in its majority of the clinoptilolite type. The present study was focused toward the characterization of two Mexican natural zeolite rocks presumably of the clinoptilolite and filipsite types, one of them comes from the state of Chihuahua and the other of a trader company of non metallic minerals, due that these materials are not characterized, its are not known their properties completely and therefore, the uses that can be given to these materials. In this investigation work it was carried out the characterization of two Mexican zeolite rocks, one coming from the Arroyo zone, municipality of La Haciendita, in the state of Chihuahua; and the other one was bought to a trader company of non metallic minerals. The two zeolites so much in their natural form as conditioned with sodium; they were characterized by means of X-ray diffraction, scanning electron microscopy of high vacuum and elementary microanalysis (EDS), surface area analysis (BET), thermal gravimetric analysis. To differentiate the heulandite crystalline phase of the other clinoptilolite rock, its were carried out thermal treatments. The quantification of Al, Na, Ca, K, Mg, Fe was carried out in solution, by means of atomic absorption spectroscopy and the quantity of Si was determined by gravimetry. The zeolite rocks presented for the major part the crystalline heulandite and clinoptilolite phases for the most part, and it was found that the zeolite coming from the state of Chihuahua possesses a bigger content of heulandite and the denominated filipsite it is really a zeolite

  10. Modification of Polyamide Knitted Fabric using Different Zeolites

    Directory of Open Access Journals (Sweden)

    Ojsteršek Alenka

    2017-05-01

    Full Text Available The aim of this research was to apply three different types of zeolites and the combination thereof in the form of a very fine powder, together with different chemicals and additives on polyamide knitted fabric according to an industrially acceptable exhaustion procedure in order to study changes in the morphology, optical properties and wettability of surfaces. Zeolites were analysed using Scanning Electron Microscopy (SEM, Fourier Transform Infrared Spectroscopy (FTIR and gas physiosorption. Additionally, the morphology of zeolite-coated surfaces was examined closely using SEM, while changes in molecular-chemical level were examined by means of IR spectroscopy. Optical properties were studied using CIE colour measurement and diffuse refl ectance profile determination, while the hydrophilic/hydrophobic character was examined using goniometry. The obtained results show the suitability of the employed exhaustion procedure, depending on the type of zeolite and the composition of the treatment bath. The results also provided evidence of the enhanced wettability of PA fabrics using 4A and 13X zeolites in combination with selected additives.

  11. Synthesis of type A zeolite from calcinated kaolin

    International Nuclear Information System (INIS)

    Rodrigues, E.C.; Neves, R.F.; Souza, J.A.S.; Moraes, C.G.; Macedo, E.N.

    2011-01-01

    The mineral production has caused great concern in environmental and industrial scenario due to the effects caused to the environment. The industries of processing kaolin for paper are important economically for the state of Para, but produce huge quantities of tailings, which depend on large areas to be stocked. This material is rich in silico-aluminates can be recycled and used as raw material for other industries. The objective is to synthesize zeolite A at different temperatures of calcination and synthesis. The starting materials and synthesis of zeolite A have been identified and characterized through analysis of X-ray diffraction (DRX) and scanning electron microscopy (MEV). The synthesis process of zeolite A, using as source of silica and the aluminum metakaolin, which was calcined at temperatures of 700 ° C and 800 ° C for 2 hours of landing in a burning furnace type muffle. Observed in relation to the calcination of kaolin as the main phase, the metakaolin. This is just a removal of water from its structure, so we opted for the lower temperature, less energy consumption. The synthesis process of zeolite A, produced good results for the formation of zeolites type A, which were characterized with high purities. (author)

  12. Copper removal using bio-inspired polydopamine coated natural zeolites.

    Science.gov (United States)

    Yu, Yang; Shapter, Joseph G; Popelka-Filcoff, Rachel; Bennett, John W; Ellis, Amanda V

    2014-05-30

    Herein, for the first time, natural clinoptilolite-rich zeolite powders modified with a bio-inspired adhesive, polydopamine (PDA), have been systematically studied as an adsorbent for copper cations (Cu(II)) from aqueous solution. Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS) and thermogravimetric analysis (TGA) revealed successful grafting of PDA onto the zeolite surface. The effects of pH (2-5.5), PDA treatment time (3-24h), contact time (0 to 24h) and initial Cu(II) ion concentrations (1 to 500mgdm(-3)) on the adsorption of Cu(II) ions were studied using atomic absorption spectroscopy (AAS) and neutron activation analysis (NAA). The adsorption behavior was fitted to a Langmuir isotherm and shown to follow a pseudo-second-order reaction model. The maximum adsorption capacities of Cu(II) were shown to be 14.93mgg(-1) for pristine natural zeolite and 28.58mgg(-1) for PDA treated zeolite powders. This impressive 91.4% increase in Cu(II) ion adsorption capacity is attributed to the chelating ability of the PDA on the zeolite surface. Furthermore studies of recyclability using NAA showed that over 50% of the adsorbed copper could be removed in mild concentrations (0.01M or 0.1M) of either acid or base. Copyright © 2014 Elsevier B.V. All rights reserved.

  13. Methanation of CO2 over Zeolite-Encapsulated Nickel Nanoparticles

    DEFF Research Database (Denmark)

    Goodarzi, Farnoosh; Kang, Liqun; Wang, Feng Ryan

    2018-01-01

    Efficient methanation of CO2 relies on the development of more selective and stable heterogeneous catalysts. Here we present a simple and effective method to encapsulate Ni nanoparticles in zeolite silicalite-1. In this method, the zeolite is modified by selective desilication, which creates intr...... Ni h-1. The encapsulated Ni nanoparticles show no change in activity or selectivity after 50 h of operation, although post-catalysis characteri-sation reveals some particle migration.......Efficient methanation of CO2 relies on the development of more selective and stable heterogeneous catalysts. Here we present a simple and effective method to encapsulate Ni nanoparticles in zeolite silicalite-1. In this method, the zeolite is modified by selective desilication, which creates intra......-particle voids and mesopores that facilitate the formation of small and well-dispersed nanoparticles upon impregnation and reduction. TEM and XPS analysis confirm that a significant part of the Ni nanoparticles are situated inside the zeolite rather than on the outer surface. The encapsulation results...

  14. Phenol removal from wastewater by adsorption on zeolitic composite.

    Science.gov (United States)

    Bizerea Spiridon, Otilia; Preda, Elena; Botez, Alexandru; Pitulice, Laura

    2013-09-01

    It is well known that adsorption is an efficient method of removal of various pollutants from wastewater. The present study examines the phenol removal from water by adsorption on a new material, based on zeolitic volcanic tuff. This compound contains zeolitic tuff and cellulose, another known adsorbent, in a mass ratio of 4 to 1. The performances of the new adsorbent composite were compared with those of a widely used adsorbent material, zeolitic volcanic tuff. The adsorbent properties were tested on batch synthetic solutions containing 1-10 mg L(-1) (1-10 ppm) phenol, at room temperature without pH adjustment. The influence of the adsorbent dose, pH and contact time on the removal degree of phenol from water was investigated. The experimental data were modeled using the Langmuir, Freundlich, and Temkin adsorption isotherms. The Langmuir model was found to best represent our data revealing a monolayer adsorption with a maximum adsorption capacity between 0.12 and 0.53 mg g(-1) at 25 °C, for 2.00 g of adsorbent, depending on the initial phenol concentration. The adsorption kinetic study was performed using a pseudo-first- and pseudo-second-order kinetic models illustrating that phenol adsorption on zeolite composite is well described by pseudo-first kinetic equations. Our results indicated that phenol adsorption on the new adsorbent composite is superior to that on the classic zeolite.

  15. Synthesis of high ion exchange zeolites from coal fly ash

    Energy Technology Data Exchange (ETDEWEB)

    Querol, X.; Moreno, N.; Alastuey, A.; Juan, R.; Andres, J.M.; Lopez-Soler, A.; Ayora, C.; Medinaceli, A.; Valero, A. [CSIC, Barcelona (Spain)

    2007-07-01

    This study focuses on the synthesis at a pilot plant scale of zeolitic material obtained from the coal fly ashes of the Teruel and Narcea power plants in Spain. After the optimisation of the synthesis parameters at laboratory scale, the Teruel and Narcea fly ashes were selected as low and high glass fly ashes. The pilot plant scale experiments were carried out in a 10 m{sup 3} reactor of Clariant SA (Barcelona, Spain). The results allowed obtaining 1.1 and 2.2 tonnes of zeolitic material with 40 and 55% of NaP1 content, in two single batch experiments of 24 and 8 hours, for Teruel and Narcea fly ashes, respectively. The cation exchange capacities (CEC) of the final product reached 2.0 and 2.7 meq g{sup -1} for Teruel and Narcea zeolitic material, respectively, which are very close to the usual values reached by the high quality natural zeolitic products. Finally, with the aim of testing possible applications of the commercial NaP1-IQE and pilot plant NaP1-Narcea zeolitic products in water decontamination, efficiency for metal uptake from waste waters from electroplating baths was investigated.

  16. Enhanced water transport and salt rejection through hydrophobic zeolite pores

    Science.gov (United States)

    Humplik, Thomas; Lee, Jongho; O’Hern, Sean; Laoui, Tahar; Karnik, Rohit; Wang, Evelyn N.

    2017-12-01

    The potential of improvements to reverse osmosis (RO) desalination by incorporating porous nanostructured materials such as zeolites into the selective layer in the membrane has spurred substantial research efforts over the past decade. However, because of the lack of methods to probe transport across these materials, it is still unclear which pore size or internal surface chemistry is optimal for maximizing permeability and salt rejection. We developed a platform to measure the transport of water and salt across a single layer of zeolite crystals, elucidating the effects of internal wettability on water and salt transport through the ≈5.5 Å pores of MFI zeolites. MFI zeolites with a more hydrophobic (i.e., less attractive) internal surface chemistry facilitated an approximately order of magnitude increase in water permeability compared to more hydrophilic MFI zeolites, while simultaneously fully rejecting both potassium and chlorine ions. However, our results also demonstrated approximately two orders of magnitude lower permeability compared to molecular simulations. This decreased performance suggests that additional transport resistances (such as surface barriers, pore collapse or blockages due to contamination) may be limiting the performance of experimental nanostructured membranes. Nevertheless, the inclusion of hydrophobic sub-nanometer pores into the active layer of RO membranes should improve both the water permeability and salt rejection of future RO membranes (Fasano et al 2016 Nat. Commun. 7 12762).

  17. Intensified Biobutanol Recovery by using Zeolites with Complementary Selectivity.

    Science.gov (United States)

    Van der Perre, Stijn; Gelin, Pierre; Claessens, Benjamin; Martin-Calvo, Ana; Cousin Saint Remi, Julien; Duerinck, Tim; Baron, Gino V; Palomino, Miguel; Sánchez, Ledys Y; Valencia, Susana; Shang, Jin; Singh, Ranjeet; Webley, Paul A; Rey, Fernando; Denayer, Joeri F M

    2017-07-21

    A vapor-phase adsorptive recovery process is proposed as an alternative way to isolate biobutanol from acetone-butanol-ethanol (ABE) fermentation media, offering several advantages compared to liquid phase separation. The effect of water, which is still present in large quantities in the vapor phase, on the adsorption of the organics could be minimized by using hydrophobic zeolites. Shape-selective all-silica zeolites CHA and LTA were prepared and evaluated with single-component isotherms and breakthrough experiments. These zeolites show opposite selectivities; adsorption of ethanol is favorable on all-silica CHA, whereas the LTA topology has a clear preference for butanol. The molecular sieving properties of both zeolites allow easy elimination of acetone from the mixture. The molecular interaction mechanisms are studied by density functional theory (DFT) simulations. The effects of mixture composition, humidity and total pressure of the vapor stream on the selectivity and separation behavior are investigated. Desorption profiles are studied to maximize butanol purity and recovery. The combination of LTA with CHA-type zeolites (Si-CHA or SAPO-34) in sequential adsorption columns with alternating adsorption and desorption steps allows butanol to be recovered in unpreceded purity and yield. A butanol purity of 99.7 mol % could be obtained at nearly complete butanol recovery, demonstrating the effectiveness of this technique for biobutanol separation processes. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Catalytic activities of zeolite compounds for decomposing aqueous ozone.

    Science.gov (United States)

    Kusuda, Ai; Kitayama, Mikito; Ohta, Yoshio

    2013-12-01

    The advanced oxidation process (AOP), chemical oxidation using aqueous ozone in the presence of appropriate catalysts to generate highly reactive oxygen species, offers an attractive option for removing poorly biodegradable pollutants. Using the commercial zeolite powders with various Si/Al ratios and crystal structures, their catalytic activities for decomposing aqueous ozone were evaluated by continuously flowing ozone to water containing the zeolite powders. The hydrophilic zeolites (low Si/Al ratio) with alkali cations in the crystal structures were found to possess high catalytic activity for decomposing aqueous ozone. The hydrophobic zeolite compounds (high Si/Al ratio) were found to absorb ozone very well, but to have no catalytic activity for decomposing aqueous ozone. Their catalytic activities were also evaluated by using the fixed bed column method. When alkali cations were removed by acid rinsing or substituted by alkali-earth cations, the catalytic activities was significantly deteriorated. These results suggest that the metal cations on the crystal surface of the hydrophilic zeolite would play a key role for catalytic activity for decomposing aqueous ozone. Copyright © 2013 The Research Centre for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.

  19. Impact protection behavior of a mordenite zeolite system

    Science.gov (United States)

    Xu, J.; Hu, R.; Chen, X.; Hu, D.

    2016-05-01

    By combining zeolite with water, a novel nanocomposite may exhibit extraordinary capability of energy absorption and impact mitigation. The multiple size of zeolite may lead to simultaneous yet different infiltration behaviors of water molecules, and thus multi-staged energy mitigation characteristics (which may benefit the scope of application). In this study, we investigate the dynamic infiltration behavior of water into mordenite zeolite (MOR) using molecular dynamics (MD) simulations. Thanks to its hydrophobicity and multi pore-sized structure, the MOR system has a decent energy mitigation performance upon high impact speed. Parametric studies are carried out to investigate the effects of various parameters, including the impact speed, mass, and water/zeolite ratio, on energy mitigating characteristics. The MOR/water mixture may perform better at a higher impact energy with higher MOR zeolite-water ratio. Upon unloading, the defiltration of water molecules is faster and more complete at higher impact speed. Results may guide the design and application of the energy mitigation nanosystem.

  20. Recent Advances on Bioethanol Dehydration using Zeolite Membrane

    Science.gov (United States)

    Makertihartha, I. G. B. N.; Dharmawijaya, P. T.; Wenten, I. G.

    2017-07-01

    Renewable energy has gained increasing attention throughout the world. Bioethanol has the potential to replace existing fossil fuel usage without much modification in existing facilities. Bioethanol which generally produced from fermentation route produces low ethanol concentration. However, fuel grade ethanol requires low water content to avoid engine stall. Dehydration process has been increasingly important in fuel grade ethanol production. Among all dehydration processes, pervaporation is considered as the most promising technology. Zeolite possesses high potential in pervaporation of bioethanol into fuel grade ethanol. Zeolite membrane can either remove organic (ethanol) from aqueous mixture or water from the mixture, depending on the framework used. Hydrophilic zeolite membrane, e.g. LTA, can easily remove water from the mixture leaving high ethanol concentration. On the other hand, hydrophobic zeolite membrane, e.g. silicate-1, can remove ethanol from aqueous solution. This review presents the concept of bioethanol dehydration using zeolite membrane. Special attention is given to the performance of selected pathway related to framework selection.

  1. Dissolution of Iron During Biochemical Leaching of Natural Zeolite

    Directory of Open Access Journals (Sweden)

    Lengauer C.

    2004-12-01

    Full Text Available Natural zeolite, including clinoptilolite, often contains iron and manganese which decrease the whiteness of this sharp angular material.The biological treatment of zeolite enables its use as an substitute for tripolyphosphates in wash powders which have to comply with strict requirements as far as whiteness is concerned and rounded off grain content. Insoluble Fe3+ and Mn4+ in the zeolite could be reduced to soluble Fe2+ and Mn2+ by silicate bacteria of Bacillus spp. These metals were efficiently removed from zeolite as documented by Fe2O3 decrease (from 1.37% to 1.08% and MnO decrease (from 0.022% to 0.005% after bioleaching. The whiteness of zeolite was increased by 8%. The leaching effect, observed by scanning electron microscopy, caused also a chamfer of the edges of sharp angular grains. Despite the enrichment by fine-grained fraction, the decrease of the surface area of clinoptilolite grains from the value 24.94 m2/g to value 22.53 m2/g was observed. This fact confirms the activity of bacteria of Bacillus genus in the edge corrosion of mineral grains.Removal of iron and manganese as well as of sharp edges together with the whiteness increase would provide a product suitable for industrial applications.

  2. Zeolite and wollastonite synthesis from rice hull ash

    International Nuclear Information System (INIS)

    Fernandes, Alberto de Andrade

    2006-01-01

    Rice hull ash (RHA) is a industry scrap rich in amorphous silica. A simple and low-energy cost method for the extraction of this silica was researched. A low level of impurity and high reactivity material was produced, which is appropriate for the synthesis of zeolites and wollastonite (CaSiO 3 ). The synthetic zeolites has not similar structures in nature, and they have been more and more valued in the market due to their purity and efficiency in specific applications like ion exchange, molecular sieve and catalysis areas. High purity wollastonite has many applications in manufacturing and agriculture. The mineral wollastonite can be formed in nature in different ways; it is generally accepted two forming processes, both encompassing limestone metamorphism (heat and pressure). In this work, a new process for the synthesis of zeolites and wollastonite from RHA colloidal silica was developed. Moreover, the process is aimed at lower energy costs, fewer stages and fewer reactants consume. In this work, zeolite A used in detergent and zeolite ZSM-5, employed in the petrochemical industry due to its high selectivity in catalytic reactions and its high thermo and acid stability, were synthesized. The first step of the wollastonite synthesis was studied, with the purpose of obtaining calcium hydrosilicate. Eleven different hydrosilicates occur in the system Ca(OH) 2 -SiO 2 -H 2 O, in the second step it was annealed to form the wollastonite phase. (author)

  3. Hierarchical porous structured zeolite composite for removal of ionic contaminants from waste streams and effective encapsulation of hazardous waste

    Energy Technology Data Exchange (ETDEWEB)

    Al-Jubouri, Sama M. [Chemical Engineering & Analytical Science, The University of Manchester, Oxford Road, Manchester M13 9PL (United Kingdom); Curry, Nicholas A. [Materials Science, The University of Manchester, Oxford Road, Manchester M13 9PL (United Kingdom); Holmes, Stuart M., E-mail: stuart.holmes@manchester.ac.uk [Chemical Engineering & Analytical Science, The University of Manchester, Oxford Road, Manchester M13 9PL (United Kingdom)

    2016-12-15

    A hierarchical structured composite made from clinoptilolite supported on date stones carbon is synthesized using two techniques. The composites are manufactured by fixing a natural zeolite (clinoptilolite) to the porous surface of date stones carbon or by direct hydrothermal synthesis on to the surface to provide a supported high surface area ion-exchange material for metal ion removal from aqueous streams. The fixing of the clinoptilolite is achieved using sucrose and citric acid as a binder. The composites and pure clinoptilolite were compared to test the efficacy for the removal of Sr{sup 2+} ions from an aqueous phase. The encapsulation of the Sr{sup 2+} using either vitrification or a geo-polymer addition was tested to ensure that the hazardous waste can be made safe for disposal. The hierarchical structured composites were shown to achieve a higher ion exchange capacity per gram of zeolite than the pure clinoptilolite (65 mg/g for the pure natural clinoptilolite and 72 mg/g for the pure synthesized clinoptilolite) with the synthesized composite (160 mg/g) having higher capacity than the natural clinoptilolite composite (95 mg/g). The rate at which the equilibria were established followed the same trend showing the composite structure facilitates diffusion to the ion-exchange sites in the zeolite.

  4. Infectious Tolerance

    OpenAIRE

    Jonuleit, Helmut; Schmitt, Edgar; Kakirman, Hacer; Stassen, Michael; Knop, Jürgen; Enk, Alexander H.

    2002-01-01

    Regulatory CD4+CD25+ T cells (Treg) are mandatory for maintaining immunologic self-tolerance. We demonstrate that the cell-cell contact–mediated suppression of conventional CD4+ T cells by human CD25+ Treg cells is fixation resistant, independent from membrane-bound TGF-β but requires activation and protein synthesis of CD25+ Treg cells. Coactivation of CD25+ Treg cells with Treg cell–depleted CD4+ T cells results in anergized CD4+ T cells that in turn inhibit the activation of conventional, ...

  5. 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.

  6. Nondestructive depth profiling of rare-earth and actinide zeolites via Rutherford backscattering methods

    International Nuclear Information System (INIS)

    Baumann, S.A.; Strathman, M.D.; Suib, S.L.

    1988-01-01

    Rutherford backscattering (RBS) methods have been used to study rare-earth and actinide-ion-exchanged small pore (A) and large pore (Y) zeolites. A theoretical discussion of the RBS method and a novel method of data treatment are given. Experimental data for zeolites have been simulated and theoretical depth profiles have been determined. Both experimental and theoretical data suggest that uranyl-exchanged A zeolite has a large uranium to oxygen surface ratio while the corresponding Y zeolite has a large uranium to oxygen bulk ratio. Relative atomic fractions of all zeolite elements are also given

  7. Water and water vapor sorption studies in polypropylene-zeolite composites

    OpenAIRE

    Pehlivan, H.; Özmıhçı, Filiz; Tıhmınlıoğlu, Funda; Balköse, Devrim; Ülkü, Semra

    2003-01-01

    Water and water vapor sorption to porous polypropylene-zeolite composites prepared by hot pressing have been studied as a function of zeolite loading. This work presents the first report on the effect of the zeolite as a filler on the water-sorption properties of PP composites. Water swelling experiments were conducted at 25°C using pure PP and PP-zeolite films samples having different zeolite loadings (6-40 wt %). Because PP is a hydrophobic polymer, it does not sorp any water, but the compo...

  8. Recent progress in the direct synthesis of hierarchical zeolites: synthetic strategies and characterization methods

    KAUST Repository

    Liu, Zhaohui

    2017-06-16

    Hierarchically structured zeolites combine the merits of microporous zeolites and mesoporous materials to offer enhanced molecular diffusion and mass transfer without compromising the inherent catalytic activities and selectivity of zeolites. This short review gives an introduction to the synthesis strategies for hierarchically structured zeolites with emphasis on the latest progress in the route of ‘direct synthesis’ using various templates. Several characterization methods that allow us to evaluate the ‘quality’ of complex porous structures are also introduced. At the end of this review, an outlook is given to discuss some critical issues and challenges regarding the development of novel hierarchically structured zeolites as well as their applications.

  9. Loading and leakage of krypton immobilized in zeolites and glass

    International Nuclear Information System (INIS)

    Christensen, A.B.; Del Debbio, J.A.; Knecht, D.A.; Tanner, J.E.

    1980-01-01

    Krypton-85 is formed in nuclear power reactors and remains trapped until the fuel is reprocessed. Federal regulations limit the release of 85 Kr to the environment, requiring recovery and storage of 85% of the 85 Kr produced in commercial light-water reactors after January 1, 1983. One of the long-term storage options involves encapsulating 85 Kr in zeolites or glasses at high pressure and temperature. This paper presents experimental results for krypton encapsulation and leakage in sodalite, zeolite 5A, and Vycor Thristy glass. The results show that all three materials are feasible for 85 Kr immobilization and long-term storage, although zeolite 5A and Thirsty Vycor are preferable due to lower leakage rates

  10. Methanol conversion to lower olefins over RHO type zeolite

    KAUST Repository

    Masih, Dilshad

    2013-07-01

    Eight-membered ring small-pore zeolite of RHO-type topology has been synthesized, characterized and tested for methanol-to-olefin (MTO) reaction. The zeolite was hydrothermally crystallized from the gel with Si/Al ratio of 5.0. It showed a high BET specific surface area (812 m2 g-1), micropore volume (0.429 cm3 g-1), and acid amount (2.53 mmol g-1). Scanning electron microscopy observations showed small crystallites of about 1 μm. The zeolite was active for MTO reaction with 100% methanol conversions at 623-723 K, whereas selectivity to lower olefins changed with time. © 2013 Elsevier B.V.

  11. Synthesis and Evaluation of Zeolite Surface-Modified Perlite

    Directory of Open Access Journals (Sweden)

    Kasai Makoto

    2017-01-01

    Full Text Available Perlite is volcanic glass mainly composed of amorphous aluminum silicate, mainly composed SiO2 and Al2O3 with less impurities such as heavy metals. Amorphous (glassy perlite is used in lightweight aggregate and insulation. In addition, it has also been used as a filter aid by grinding the expanded perlite. However, it has not been used as environmental cleanup materials, because the ion exchange capacity of the perlite is very low. In this study, we tried to synthesize the hybrid filter aid with chemical adsorption capacity by synthesizing the zeolite on the surface of the perlite. As a result, by using the hydrothermal synthesis method, zeolite surface modified perlite was synthesized in which the LTA type zeolites were generated on the surface of the perlite.

  12. The zeolite mediated isomerization of allyl phenyl ether

    Science.gov (United States)

    Pebriana, R.; Mujahidin, D.; Syah, Y. M.

    2017-04-01

    Allyl phenyl ether is an important starting material in organic synthesis that has several applications in agrochemical industry. The green transformation of allyl phenyl ether assisted by heterogeneous catalyst is an attractive topic for an industrial process. In this report, we investigated the isomerization of allyl phenyl ether by heating it in zeolite H-ZSM-5 and Na-ZSM-5. The conversion of allyl phenyl ether (neat) in H-ZSM-5 was 67% which produced 40% of 2-allylphenol, 17% of 2-methyldihydrobenzofuran, and other product (4:1.7:1), while in Na-ZSM-5 produced exclusively 2-allylphenol with 52% conversion. These results showed that zeolite properties can be tuned to give a selective transformation by substitution of metal ion into the zeolite interior.

  13. Evaluation of paddy quality dried with zeolite under medium temperature

    Science.gov (United States)

    Irfandy, F.; Djaeni, M.

    2018-01-01

    Drying becomes important role to obtain good quality product in post-harvest treatment for paddy. Adsorption drying process taken place on medium operation temperature can be an option to enhance paddy quality. The aim of this study was to evaluate the quality of paddy dried with zeolite as adsorbent. In case, paddy from local farmer in Semarang was dried from initial moisture content 23% (wet basis) under different temperature 40 and 60°C, both with and without zeolite. Moisture content was observed by gravimetry every 15 minutes during 60 minutes drying time. Furthermore, the quality of paddy represented by percentage of head rice and proximate was analyzed after drying process completed. Results showed that compared to conventional drying without zeolite, the adsorption dryer was more superior in term of drying time as well as product quality improvement and there are no much differences in proximate analyzed result.

  14. Zeolites as Catalysts for Fuels Refining after Indirect Liquefaction Processes

    Directory of Open Access Journals (Sweden)

    Arno de Klerk

    2018-01-01

    Full Text Available The use of zeolite catalysts for the refining of products from methanol synthesis and Fisher–Tropsch synthesis was reviewed. The focus was on fuels refining processes and differences in the application to indirect liquefaction products was compared to petroleum, which is often a case of managing different molecules. Processes covered were skeletal isomerisation of n-butenes, hydroisomerisation of n-butane, aliphatic alkylation, alkene oligomerisation, methanol to hydrocarbons, ethanol and heavier alcohols to hydrocarbons, carbonyls to hydrocarbons, etherification of alkenes with alcohols, light naphtha hydroisomerisation, catalytic naphtha reforming, hydroisomerisation of distillate, hydrocracking and fluid catalytic cracking. The zeolite types that are already industrially used were pointed out, as well as zeolite types that have future promise for specific conversion processes.

  15. Improvement of adsorption properties of zeolites and their characterization - 15133

    International Nuclear Information System (INIS)

    Mimura, H.; Rahman, M.S.; Yamagishi, I.; Matsukura, M.; Kuroda, A.

    2015-01-01

    The improvement of adsorption properties of radioactive Cs and Sr was evaluated for different kinds of zeolites treated with various methods; calcination, conditioning, surface alteration, fine-granulation, mixture-granulation, honeycomb modeling and loading. Their characteristics were examined by instrumental analyses (SEM, EPMA, XRD, IR) and batch and column adsorption methods. As for the calcination treatment, the calcined natural mordenite was prepared by heat treatment at different temperatures up to 1000 C. degrees. The improvement of adsorption rate was observed for the calcined mordenite at 500 C. degrees. The conditioning with H + , Na + and K + ions was ineffective for the enhancement of adsorption properties of mordenites. Comparing the adsorption properties of Sr 2+ for A-type zeolites having various particle sizes, the adsorption kinetics tended to increase with decreasing particle size in the order of A powder > A0.5(0.5 mm) > A0.5HP(0.5 mm) > A1.5(1.5 mm). In particular, A0.5HP with no binder exhibited a relatively large uptake (%) of Sr 2+ above 80% in seawater, which is the largest value in the conventional granular zeolites. For multi-nuclide decontamination, composite zeolites such as AMXα and AMXβ were prepared by mixing three kinds of zeolites; A zeolite, Mordenite and X zeolite. The mixing ratios of AMXα and AMXβ were 1: 1: 1 and 0.5: 1: 0.5, respectively. Composite zeolites had relatively large uptake (%) above 95% for Cs + , Sr 2+ and Co 2+ ions in 1/10 diluted seawater. Zeolites honeycomb can be used for the continuous concentration of Cs + and Sr 2+ ions in seawater. Uptake (%) of Cs + ions for mordenite honeycomb at V/m= 100 cm 3 /g was estimated to be 86.8% and 57.9% within 18 h in pure water and 15 h in seawater, respectively. Uptake (%) of Sr 2+ ions for A-type zeolite honeycomb was estimated to be 99.2% within 24 h and 69.0% within 3 h in pure water and seawater, respectively. As for the Cs adsorption on mordenite honeycomb at a

  16. Selective reduction of NO over copper-containing modified zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Halasz, J.; Varga, J.; Schoebel, G.; Kiricsi, I.; Hernadi, K.; Hannus, I.; Varga, K.; Fejes, P. [Applied Chemistry Dept., Jozsef Attila Univ., Szeged (Hungary)

    1995-12-31

    The most efficient method for NO removal from stationary and mobile sources is catalytic reduction with ammonia, hydrocarbons, CO or H{sub 2}. Modified zeolites are active catalysts in these processes. For Cu-ZSM-5 especially high activity and stability have been reported. In this work the properties of copper-containing ZSM-5 zeolites prepared by wet or solid state ion-exchange have been investigated. The Broensted acidity of the Cu{sup 2+}-exchanged samples was much lower than that of the parent zeolites, and they had high activity in selective reduction with ammonia, propene or propane. A comparison of Cu-ZSM-5 activity in the decomposition of NO and in the reaction of NO with propene or propane revealed that the hydrocarbons as well as the nitrogen oxides play important roles in the performance of NO reduction catalysis. 8 figs., 1 tab., 16 refs.

  17. D2-H2 equilibration over γ-irradiated zeolites

    International Nuclear Information System (INIS)

    Novakova, J.; Wichterlova, B.

    1987-01-01

    D 2 -H 2 equilibration was studied at 77 and 298 K over HY, AlHY, HZSM-5 and Alsub(x)Osub(y)HZSM-5 zeolites which had been γ-irradiated at 77 and/or 298 K. The exchange rate was found to be higher at the lower temperature regardless of the temperature of irradiation. Moreover, at 77 K the exchange rates were similar and more stable over the individual zeolites than at 298 K, thus indicating a common reaction path at 77 K. The exchange rate at 298 K depended on the zeolite type: it was more stable and higher over HZSM-5 than over HY, and extra-lattice Al increased both these properties on HY as well as on HZSM-5. The reaction mechanism is discussed in connection with the nature of defects generated by γ-irradiation. (author)

  18. Infectious Tolerance

    Science.gov (United States)

    Jonuleit, Helmut; Schmitt, Edgar; Kakirman, Hacer; Stassen, Michael; Knop, Jürgen; Enk, Alexander H.

    2002-01-01

    Regulatory CD4+CD25+ T cells (Treg) are mandatory for maintaining immunologic self-tolerance. We demonstrate that the cell-cell contact–mediated suppression of conventional CD4+ T cells by human CD25+ Treg cells is fixation resistant, independent from membrane-bound TGF-β but requires activation and protein synthesis of CD25+ Treg cells. Coactivation of CD25+ Treg cells with Treg cell–depleted CD4+ T cells results in anergized CD4+ T cells that in turn inhibit the activation of conventional, freshly isolated CD4+ T helper (Th) cells. This infectious suppressive activity, transferred from CD25+ Treg cells via cell contact, is cell contact–independent and partially mediated by soluble transforming growth factor (TGF)-β. The induction of suppressive properties in conventional CD4+ Th cells represents a mechanism underlying the phenomenon of infectious tolerance. This explains previously published conflicting data on the role of TGF-β in CD25+ Treg cell–induced immunosuppression. PMID:12119350

  19. Novel modified zeolites for energy-efficient hydrocarbon separations.

    Energy Technology Data Exchange (ETDEWEB)

    Arruebo, Manuel (University of Colorado, Boulder, CO); Dong, Junhang; Anderson, Thomas (Burns and McDonnell, Kansas City, MO); Gu, Xuehong; Gray, Gary (Goodyear Chemical Company, Akron, OH); Bennett, Ron (Goodyear Chemical Company, Akron, OH); Nenoff, Tina Maria; Kartin, Mutlu; Johnson, Kaylynn (Goodyear Chemical Company, Akron, OH); Falconer, John (University of Colorado, Boulder, CO); Noble, Richard (University of Colorado, Boulder, CO)

    2006-11-01

    We present synthesis, characterization and testing results of our applied research project, which focuses on the effects of surface and skeletal modification of zeolites for significant enhancements in current hydrocarbon (HC) separations. Zeolites are commonly used by the chemical and petroleum industries as catalysts and ion-exchangers. They have high potential for separations owing to their unique pore structures and adsorption properties and their thermal, mechanical and chemical properties. Because of zeolites separation properties, low cost, and robustness in industrial process, they are natural choice for use as industrial adsorbents. This is a multidisciplinary effort to research, design, develop, engineer, and test new and improved materials for the separation of branched vs. linear organic molecules found in commercially important HC streams via adsorption based separations. The focus of this project was the surface and framework modification of the commercially available zeolites, while tuning the adsorption properties and the selectivities of the bulk and membrane separations. In particular, we are interested with our partners at Goodyear Chemical, on how to apply the modified zeolites to feedstock isoprene purification. For the characterization and the property measurements of the new and improved materials powder X-ray diffraction (PXRD), Residual Gas Analyzer-Mass Spectroscopy (RGA-MS), Electron Microscopy (SEM/EDAX), temperature programmed desorption (TPD) and surface area techniques were utilized. In-situ carbonization of MFI zeolite membranes allowed for the maximum separation of isoprene from n-pentane, with a 4.1% enrichment of the binary stream with n-pentane. In four component streams, a modified MFI membrane had high selectivities for n-pentane and 1-3-pentadiene over isoprene but virtually no separation for the 2-methyl-2-butene/isoprene pair.

  20. Regeneration of clinoptilolite zeolite used for the ammonium removal

    International Nuclear Information System (INIS)

    Garcia G, M.C.

    2002-01-01

    The use of zeolites has been increased in the last years with different applications and with a great boom in the environmental area, but a little had been make about the regeneration of such zeolites. The presence of nitrogen-ammonia in water may cause serious pollution problems since it results to be toxic for fishes and other aquatic life forms, also it provokes the algae growing. The natural clinoptilolite contains interchangeable ions such as the sodium (Na + ), potassium (K + ), magnesium (Mg 2+ ) and calcium (Ca 2+ ) in different proportions depending on the mineral origin When the zeolite is upgraded to its sodium form, the cation exchange capacity and the preference by the nitrogen-ammonia are increased, allowing the reversible process of sorption. In this work it was proposed the regeneration to its sodium form about the ammonia clinoptilolite zeolite. The natural mineral was characterized using the methods such as: X-ray diffraction, Infrared spectroscopy, Thermal gravimetric analysis and surface area. The results show that the ammonium sorption was between 95% and 98.7% such an ambient temperature as a flow back. the zeolite was regenerated approximately from 60% in the first cycle up to 97% in the last cycle at flow back temperature and of 59.2% up to 96.9% at ambient temperature, it was not presented any significant effect which could be attributed to the temperature. During the exchange process, the cations present in the natural zeolite were exchanged with the ammonium ions, this process was not completed due to that retained ammonium quantity was major that of the desorpted ions, what shows that in addition of ion exchange, another type of sorption process exists. (Author)

  1. Copper removal using bio-inspired polydopamine coated natural zeolites

    International Nuclear Information System (INIS)

    Yu, Yang; Shapter, Joseph G.; Popelka-Filcoff, Rachel; Bennett, John W.; Ellis, Amanda V.

    2014-01-01

    Highlights: • Natural zeolites were modified with bio-inspired polydopamine. • A 91.4% increase in Cu(II) ion adsorption capacity was observed. • Atomic absorption and neutron activation analysis gave corroborative results. • Neutron activation analysis was used to provide accurate information on 30+ elements. • Approximately 90% of the adsorbed copper could be recovered by 0.1 M HCl treatment. - Abstract: Herein, for the first time, natural clinoptilolite-rich zeolite powders modified with a bio-inspired adhesive, polydopamine (PDA), have been systematically studied as an adsorbent for copper cations (Cu(II)) from aqueous solution. Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS) and thermogravimetric analysis (TGA) revealed successful grafting of PDA onto the zeolite surface. The effects of pH (2–5.5), PDA treatment time (3–24 h), contact time (0 to 24 h) and initial Cu(II) ion concentrations (1 to 500 mg dm −3 ) on the adsorption of Cu(II) ions were studied using atomic absorption spectroscopy (AAS) and neutron activation analysis (NAA). The adsorption behavior was fitted to a Langmuir isotherm and shown to follow a pseudo-second-order reaction model. The maximum adsorption capacities of Cu(II) were shown to be 14.93 mg g −1 for pristine natural zeolite and 28.58 mg g −1 for PDA treated zeolite powders. This impressive 91.4% increase in Cu(II) ion adsorption capacity is attributed to the chelating ability of the PDA on the zeolite surface. Furthermore studies of recyclability using NAA showed that over 50% of the adsorbed copper could be removed in mild concentrations (0.01 M or 0.1 M) of either acid or base

  2. [Biodegradation and adsorption of bio-zeolite on pyridine and quinoline].

    Science.gov (United States)

    Bai, Yao-Hui; Sun, Qing-Hua; Xing, Rui; Wen, Dong-Hui; Tang, Xiao-Yan

    2010-09-01

    The study was to explore the treatment of pyridine, quinoline and their transformation product, NH(4+) -N, by the biodegradation and adsorption of a natural and a modified bio-zeolites. The experiment results demonstrated that the mixed bacteria on the bio-zeolites, a pyridine-degrading bacterium and a quinoline-degrading bacterium, could degrade pyridine and quinoline simultaneously. The NH(4+) -N transformed from pyridine and quinoline could be adsorbed by the natural and modified zeolites. The adsorption capacity of the modified zeolite was lower than that of the natural zeolite. However, more microorganisms could attach on the surface of the modified zeolite, so the application of the modified bio-zeolite has a better prospect in actual treatment of pyridine and/ or quinoline pollution.

  3. Adsorpsi Ion Logam Tembaga Menggunakan Nano Zeolit Alam yang Diaktivasi

    OpenAIRE

    Yulianis Yulianis; Mahidin Mahidin; Syaifullah Muhammad

    2017-01-01

    This study was aimed to find out the ability of natural zeolite coming from Blang Pidie, South West Aceh District, Aceh Province, Indonesia, which was applied as an adsorbent to adsorp heavy metal copper (Cu²⁺) ions in aqueous solution. This research was conducted to enhance the performance of natural zeolite by downsizing it to nano particles, then activated physically and chemically using 0.05 M HCl, then calcined at temperature 350°C for 2 hours. Test of Cu²⁺ metal ion adsorption to nano n...

  4. Deuteration of piperylene on zeolite NaY

    International Nuclear Information System (INIS)

    Kharlamov, V.V.; Kadentsev, V.I.; Kharatishvili, N.G.; Minachev, Kh.M.

    1982-01-01

    In order to further refine the mechanism of hydrogenation reaction on zeolites, the deuteration of piperylene on NaY was studied. The kinetic isotope effect in the hydrogenation of piperylene on zeolite NaY indicates that hydrogen takes part in the limiting step of the process and the 1-pentene and 2-pentene formed in the deuteration of piperylene have a wide isotope distribution, with a maximum amount of the d 2 isotope, and an average number of deuterium atoms in the molecules equal to 2.25-2.36

  5. Nonlinear upconversion based infrared spectroscopy on ZSM-5 zeolite

    DEFF Research Database (Denmark)

    Kehlet, Louis Martinus; Beato, Pablo; Tidemand-Lichtenberg, Peter

    2017-01-01

    We present a spectroscopic measurement of zeolite ZSM-5 in the mid-IR following the methanol attachment to active sites at 200 °C. The spectra are measured using nonlinear frequency upconversion to the near-IR spectral region.......We present a spectroscopic measurement of zeolite ZSM-5 in the mid-IR following the methanol attachment to active sites at 200 °C. The spectra are measured using nonlinear frequency upconversion to the near-IR spectral region....

  6. Method for encapsulating nanoparticles in a zeolite matrix

    Science.gov (United States)

    Coker, Eric N.

    2007-12-11

    A method for preparing a metal nanocluster composite material. A porous zeolitic material is treated with an aqueous metal compound solution to form a metal ion-exchanged zeolitic material, heated at a temperature ramp rate of less than 2.degree. C./min to an elevated temperature, cooled, contacted with an organic monomer and heating to induce polymerization, and heating the composite material to greater than 350.degree. C. under non-oxidizing conditions to form a metal nanocluster-carbon composite material with nanocluster sizes between approximately 0.6 nm and 10 nm.

  7. Effect of zeolite on health condition of canines

    Directory of Open Access Journals (Sweden)

    Vučićević Ivana

    2008-01-01

    Full Text Available The paper shows the results of investigations of elementary hematological and biochemical blood parameters of German Shepherd dogs administered zeolite through feed daily for a period of 50 days. No undesired effects were established during the period of observation, and in fact there was a full normalization of the condition of the dogs that previously exhibited transitory symptoms of gastrointestinal tract disorders. No significant digressions were observed in the examined biochemical parameters of blood, either, that could indicate any harmful effects of zeolite, with the exception of the tendency toward a reduction in the concentrations of phosphorus and calcium, which was not manifest clinically as well during this period.

  8. Zeolite-like metal-organic frameworks with ana topology

    KAUST Repository

    Eddaoudi, Mohamed

    2017-04-20

    Embodiments of the present disclosure describe a zeolite-like metal-organic framework composition comprising a metal-organic framework composition with ana topology characterized by the formula [MIII(4, 5-imidazole dicarboxylic acid)2X(solvent)a]n wherein MIII comprises a trivalent cation of a rare earth element, X comprises an alkali metal element or alkaline earth metal element, and solvent comprises a guest molecule occupying pores. Embodiments of the present disclosure describe a method of separating paraffins comprising contacting a zeolite-like metal-organic framework with ana topology with a flow of paraffins, and separating the paraffins by size.

  9. Investigation of Y, FAU-zeolites containing rare earth cations

    International Nuclear Information System (INIS)

    Gardos, G.; De Jonge, A.; Halmos, F.; Kristof, J.; Redey, A.

    1984-01-01

    Polycationic zeolites were made of the H (NHsub(4))-Y, FAU form one. The change of Broensted acid sites was followed as a function of the pretreating temperature by infrared spectroscopy for mixed (La, Ce) form zeolites. It was stated that the 3630 cmsup(-1) absorption band can be related to the acidic OH-groups responsible for the catalytic activity in the alkylating reaction of isobutane with 1-butene, while the band at 3510 cmsup(-1) is characteristic of the non-acidic hydroxyl-groups and has no relation with the catalytic activity. (author)

  10. EFFECT OF GRAIN SIZE AND ACTIVATION TIME OF ZEOLITE TO ADSORPTION AND DESORPTION OF NH4OH AND KCL AS MODEL OF FERTILIZER-ZEOLITE MIX

    Directory of Open Access Journals (Sweden)

    Muhammad Prasantio Bimantio

    2017-10-01

    Full Text Available Zeolites can be used as adsorbent, ion exchange, catalyst, or catalyst carrier. Application of fertilizer use in the zeolite also be one of the interesting topic. Zeolites in a mixture of fertilizer can use to control the release of nutrients. The purpose of this research is to study the effect of grain size and time of the activation of zeolite to adsorption and desorption of NH4OH and KCl as modeling of ZA and KCl fertilizer, to obtain the value of adsorption rate constant (ka and desorption rate constant (kd. This research procedure include: the process of adsorption by adding zeolite with various size and time of activation into a sealed beaker glass and let the adsorption process occurs for 24 hours. After 24 hours, the solution was filtered, the zeolite then put in 100 ml of aquadest into a sealed beaker glass and let the desorption process happened for another 24 hours. Three samples with the largest difference solution concentrations looked for the value of the ka and kd. Zeolite configuration with the largest ka is trialed with fertilizer and compared with the value of ka obtained from modeling. The result for NH4OH adsorbate, -50+60 mesh 2 hours configuration zeolite give the largest ka. For KCl adsorbate, -30+40 mesh 4 hours configuration zeolite give the largest ka. The value between modeling and trials with fertilizers are not much different.

  11. Beyond Creation of Mesoporosity: The Advantages of Polymer-Based Dual-Function Templates for Fabricating Hierarchical Zeolites

    KAUST Repository

    Tian, Qiwei

    2016-02-05

    Direct synthesis of hierarchical zeolites currently relies on the use of surfactant-based templates to produce mesoporosity by the random stacking of 2D zeolite sheets or the agglomeration of tiny zeolite grains. The benefits of using nonsurfactant polymers as dual-function templates in the fabrication of hierarchical zeolites are demonstrated. First, the minimal intermolecular interactions of nonsurfactant polymers impose little interference on the crystallization of zeolites, favoring the formation of 3D continuous zeolite frameworks with a long-range order. Second, the mutual interpenetration of the polymer and the zeolite networks renders disordered but highly interconnected mesopores in zeolite crystals. These two factors allow for the synthesis of single-crystalline, mesoporous zeolites of varied compositions and framework types. A representative example, hierarchial aluminosilicate (meso-ZSM-5), has been carefully characterized. It has a unique branched fibrous structure, and far outperforms bulk aluminosilicate (ZSM-5) as a catalyst in two model reactions: conversion of methanol to aromatics and catalytic cracking of canola oil. Third, extra functional groups in the polymer template can be utilized to incorporate desired functionalities into hierarchical zeolites. Last and most importantly, polymer-based templates permit heterogeneous nucleation and growth of mesoporous zeolites on existing surfaces, forming a continuous zeolitic layer. In a proof-of-concept experiment, unprecedented core-shell-structured hierarchical zeolites are synthesized by coating mesoporous zeolites on the surfaces of bulk zeolites. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. Evaluation of synthetic zeolite as engineering passive permeable reactive barrier

    International Nuclear Information System (INIS)

    Ibrahim, O.A.A.

    2011-01-01

    The presence of toxic pollutants in groundwater brings about significant changes in the properties of water resources and has to be avoided in order to preserve the environmental quality. Heavy metals are among the most dangerous inorganic water pollutants, that related to many anthropogenic sources and their compounds are extremely toxic. The treatment of contaminated groundwater is among the most difficult and expensive environmental problems. Over the past years, permeable reactive barriers have provided an increasingly important role in the passive insitu treatment of contaminated groundwater. There are a large number of materials that are able to immobilize contaminants by sorption, including granulated active carbon, zeolite, montmorillonite, peat, compost, sawdust, etc. Zeolite X is a synthetic counterpart of the naturally occurring mineral Faujasite. It has one of the largest cavities and cavity entrances of any known zeolites. The main aim of this work is to examine the possibility of using synthetic zeolite X as an engineering permeable reactive barrier to remove heavy metals from a contaminated groundwater. Within this context, the following investigations were carried out: 1. Review on the materials most commonly used as engineered permeable reactive barriers to identify the important features to be considered in the examination of the proposed permeable reactive barrier material (zeolite X). 2. Synthesis of zeolite X and characterization of the synthesized material using different techniques. 3. Batch tests were carried out to characterize the equilibrium and kinetic sorption properties of the synthesized zeolite X towards the concerned heavy metals; zinc and cadmium ions. 4. Column tests were also performed to determine the design factors for permeable reactive barrier against zinc and cadmium ions solutions.Breakthrough curves measured in such experiments used to determine the hydrodynamic dispersion coefficients for both metal ions. 5. Analytical

  13. Experimental Determination of the Molar Absorption Coefficient of n-Hexane Adsorbed on High-Silica Zeolites.

    Science.gov (United States)

    Gatti, Giorgio; Olivas Olivera, Diana F; Sacchetto, Vittoria; Cossi, Maurizio; Braschi, Ilaria; Marchese, Leonardo; Bisio, Chiara

    2017-09-06

    Determination of the molar absorption coefficients of the CH 3 bending mode at ν˜ =1380 cm -1 (ϵ 1380 ) of n-hexane adsorbed from the gas phase on two different dealuminated zeolites is derived by a combination of IR spectroscopy and microgravimetric analysis. High-silica zeolite Y (HSZ-Y) and zeolite ZSM-5 (with SiO 2 /Al 2 O 3 ratios of 200 and 280, respectively) with different textural and surface features are selected to evaluate the effect of the pore structure and architecture on the value of ϵ 1380 of the adsorbed n-hexane. Experimental data indicate that the molecule experiences a different adsorption environment inside zeolites; thus resulting in a significant change of the dipole moment and very different ϵ 1380 values: (0.278±0.018) cm μmol -1 for HSZ-Y and (0.491±0.032) cm μmol -1 for ZSM-5. Experimental data are also supported by computational modeling, which confirms the effect of different matrices on the IR absorption intensity. This study reveals that the use of probe molecules for quantitative measurements of surface sites has to be judiciously adopted, especially if adsorption occurs in the restricted spaces of microporous materials. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  14. Disposal of Kr-85 in compressed gas cylinders and in zeolites; application of the zeolite method to other radioactive gases

    International Nuclear Information System (INIS)

    Penzhorn, R.D.

    1983-01-01

    Ultimate storage of Kr-85 in compressed gas cylinders of structural steel or austenic special steels is possible for the required storage time of 100 years at temperatures of up to 200 0 C, since Rb corrosion under ultimate storage conditions may be neglected. When Kr is stored in CaNaA zeolite at temperatures from 340-650 0 C, the pressure is of secondary importance. CO 2 and CH 4 can also be durably solidified in zeolites 4A and 5A. It is presently being assessed whether this method is applicable to T and J-129. (DG) [de

  15. Investigating the Influence of Mesoporosity in Zeolite Beta on its Catalytic Performance for the Conversion of Methanol to Hydrocarbons

    KAUST Repository

    Liu, Zhaohui

    2015-08-26

    Hierarchically porous zeolite Beta (Beta-MS) synthesized by a soft-templating method contains remarkable intra-crystalline mesoporosity, which reduces the diffusion length in zeolite channels down to several nanometers and alters the distribution of Al among distinct crystallographic sites. When used as a catalyst for the conversion of methanol to hydrocarbons (MTH) at 330 oC, Beta-MS exhibited a 2.7-fold larger conversion capacity, a 2.0-fold faster reaction rate, and a remarkably longer lifetime than conventional zeolite Beta (Beta-C). The superior catalytic performance of Beta-MS is attributed to its hierarchical structure, which offers full accessibility to all catalytic active sites. In contrast, Beta-C was easily deactivated because a layer of coke quickly deposited on the outer surfaces of the catalyst crystals, impeding access to interior active sites. This difference is clearly demonstrated by using electron microscopy combined with electron energy loss spectroscopy to probe the distribution of coke in the deactivated catalysts. At both low and high conversions, ranging from 20% to 100%, Beta-MS gave higher selectivity towards higher aliphatics (C4-C7) but lower ethene selectivity compared to Beta-C. Therefore, we conclude that a hierarchical structure decreases the residence time of methylbenzenes in zeolite micropores, disfavoring the propagation of the aromatic-based catalytic cycle. This conclusion is consistent with a recent report on ZSM-5 and is also strongly supported by our analysis of soluble coke species residing in the catalysts. Moreover, we identified an oxygen-containing compound, 4-methyl-benzaldehyde, in the coke, which has not been observed in the MTH reaction before.  

  16. Characterization of Cr/Bentonite and HZSM-5 Zeolite as Catalysts for Ethanol Conversion to Biogasoline

    Directory of Open Access Journals (Sweden)

    Robert Ronal Widjaya

    2012-04-01

    Full Text Available In this research it has been done characterization on Cr/Bentonit and Zeolit HZSM-5 catalysts for ethanol catalytic process to biogasoline (equal to gasoline. Cr/Bentonit has high acidity and resistant to a lot of moisture, so in addition to being able to processing feed which a lot of moisture (>15% from ethanol-water mixture, also it is not easy deactivated. Cr/Bentonit which is then used as the catalyst material on the process of ethanol conversion to be biogasoline and the result was compared with catalyst HZSM-5 zeolite. Several characterization methods: X-ray diffraction, Brunauer Emmett Teller (BET, thermogravimetry analysis (TGA, and catalyst activity tests using catalytic Muffler instrument and gas chromatography-mass spectrometry (GC-MS for product analysis were performed on both catalysts. From acidity measurement, it is known that acidity level of Cr/Bentonit is the highest and also from XRD result, it is known there is shift for 2theta in Cr/Bentonit, which indicates that Cr-pillar in the Bentonite can have interaction. It is also supported by BET data that shows the addition of specific surface are in Cr/Bentonite compared with natural Bentonite before pillarization. Futhermore catalyst activity test produced the results, analyzed by GC-MS, identified as butanol and also possibly formed hexanol, decane, dodecane, undecane, which are all included in gasoline range (C4 until C12.

  17. Preferable adsorption of phosphate using lanthanum-incorporated porous zeolite: Characteristics and mechanism

    Science.gov (United States)

    He, Yinhai; Lin, Hai; Dong, Yingbo; Wang, Liang

    2017-12-01

    The adsorbent, where lanthanum oxide was incorporated onto porous zeolite (La-Z), of preferable adsorption towards phosphate was prepared by hydrothermal synthesis. Based on pH effect results, La-Z would effectively sequestrate phosphate over wider pH range of 3.0-7.0, alkaline conditions were unfavorable for phosphate. The adsorption of phosphate was not significantly influenced by ionic strength and by coexisting anions of chloride, nitrate and sulfate but bicarbonate showed slightly greater negative effects, indicating La-Z possessed highly selectivity to phosphate. Adsorption of phosphate could be well fitted by pseudo-second-order model and the process was mainly controlled by intra-particle diffusion. Equilibrium adsorption demonstrated that Langmuir model was more suitable than Freundlich model for description phosphate adsorption and the adsorption capacity was 17.2 mg P g-1, which exhibited 95% utilization of incorporated La. Over 95% phosphate was eliminated in real effluent treatment when the dose was 2 g L-1. The underlying mechanism for phosphate capture was probed with Zeta potential and X-ray photoelectron spectroscope analysis, and the formation of La-P inner-sphere complexation was testified to be the dominant pathway. All the results suggested that the porous zeolite-supported lanthanum oxide can serve as a promising adsorbent for phosphate removal in realistic application.

  18. Hydrogen Separation by Natural Zeolite Composite Membranes: Single and Multicomponent Gas Transport

    Directory of Open Access Journals (Sweden)

    Afrooz Farjoo

    2017-10-01

    Full Text Available Single and multicomponent gas permeation tests were used to evaluate the performance of metal-supported clinoptilolite membranes. The efficiency of hydrogen separation from lower hydrocarbons (methane, ethane, and ethylene was studied within the temperature and pressure ranges of 25–600 °C and 110–160 kPa, respectively. The hydrogen separation factor was found to reduce noticeably in the gas mixture compared with single gas experiments at 25 °C. The difference between the single and multicomponent gas results decreased as the temperature increased to higher than 300 °C, which is when the competitive adsorption–diffusion mechanism was replaced by Knudsen diffusion or activated diffusion mechanisms. To evaluate the effect of gas adsorption, the zeolite surface isotherms of each gas in the mixture were obtained from 25 °C to 600 °C. The results indicated negligible adsorption of individual gases at temperatures higher than 300 °C. Increasing the feed pressure resulted in a higher separation efficiency for the individual gases compared with the multicomponent mixture, due to the governing effect of the adsorptive mechanism. This study provides valuable insight into the application of natural zeolites for the separation of hydrogen from a mixture of hydrocarbons.

  19. Desalination of aqueous solutions by LTA and MFI zeolite membranes using pervaporation method

    Directory of Open Access Journals (Sweden)

    A. Malekpour

    2011-12-01

    Full Text Available LTA and MFI zeolite membranes were hydrothermally grown on the surface of an α-alumina porous support. The synthesized membranes were used for removal of cationic and anionic species from aqueous solutions by the pervaporation method. The perfection of the membranes was improved by employing the multi-stage synthesis method. The membranes were characterized by XRD, SEM and IR methods. The membranes were initially evaluated by the pervaporation separation of water from aqueous 2-propanol mixtures. The separation factors obtained were 7081 and 105 for NaA and ZSM-5 membranes, respectively. The ability of membranes for desalination of some aqueous solutions containing I-, Cs+ and Sr2+ ions was examined in various conditions. These ionic species were chosen because of their importance in the nuclear sciences. Both membranes effectively removed (more than 99 wt% I-, Cs+ and Sr2+ from their singlesalt solutions (0.001mol dm-3 over a temperature range of 298-338 K. The effects of parameters such as time and temperature on the separation factors and fluxes were investigated. This work shows that, due to their excellent chemical, thermal and mechanical stability, the zeolitic membranes are useful for desalination of aqueous solutions and treating saline wastewaters by pervaporation. Therefore, this method has the ability to desalinate harsh environment solutions involving strong solvent and radioactive components.

  20. Effect of Zeolite, Selenium and Silicon on Yield, Yield Components and Some Physiological Traits of Canola under Salt Stress Conditions

    Directory of Open Access Journals (Sweden)

    A Bybordi

    2016-07-01

    Full Text Available Introduction Canola can be cultivated in large areas of the country due to its specific characteristics such as suitable composition of the fatty acids, its germination ability under low temperature, as well as its good compatibility with different climates. Canola is a high demanding crop in terms of fertilizers so that it uptakes considerable amount of nutrients from the soil during the growing season. Canola cultivation in poor soils or application of imbalanced fertilizers, especially nitrogen, can reduce qualitaty and quantity of final yield. On the other hand, salinity is known as one of the major limiting factors in canola production. Therefore, the aim of this study is the application of zeolite, selenium and silicon treatments to amend soil and increasing salinity tolerance in canola. Materials and Methods In order to study the effect of soil applied zeolite and foliar application of selenium and silicon on yield, yield components and some physiological traits of canola grown under salinity stress, a factorial experiment in randomized complete block design was conducted in Agriculture and Natural Resource Research Center in East Azerbaijan during 2011-2013 cropping seasons. Zeolite was applied at three levels (0, 5 and 10 ton ha-1 and foliar selenium and silicon were applied at three levels as well (each one zero, 2 and 4 g l-1. For this purpose, seedbed was prepared using plow and disk and then plot were designed. Canola seeds, cultivar Okapi, were sown in sandy loam soil with 4 dS.m-1 salinity at the depth of 2-3 cm. Irrigation was performed using local well based on 60% field capacity using the closed irrigation system. Potassium selentae and potassium silicate were used for selenium and silicon treatments. Treatments at rosette and stem elongation stages were sprayed on plants using a calibrated pressurized backpack sprayer. At flowering stage, photosynthesis rate was recorded. Then leaf samples were randomly collected to assay