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Sample records for bifunctional beta zeolite

  1. Selective Ring Opening of 1-Methylnaphthalene Over NiW-Supported Catalyst Using Dealuminated Beta Zeolite.

    Science.gov (United States)

    Kim, Eun-Sang; Lee, You-Jin; Kim, Jeong-Rang; Kim, Joo-Wan; Kim, Tae-Wan; Chae, Ho-Jeong; Kim, Chul-Ung; Lee, Chang-Ha; Jeong, Soon-Yong

    2016-02-01

    Nanoporous Beta zeolite was dealuminated by weak acid treatment for reducing the acidity. Bi-functional catalysts were prepared using commercial Beta zeolites and the dealuminated zeolites for acidic function, NiW for metallic function. 1-Methylnaphthalene was selected as a model compound for multi-ring aromatics in heavy oil, and its selective ring opening reaction has been investigated using the prepared bi-functional catalysts with different acidity in fixed bed reaction system. The dealuminated Beta zeolites, which crystal structure and nanoporosity were maintained, showed the higher SiO2/Al2O3 ratio and smaller acidity than their original zeolite. NiW-supported catalyst using the dealuminated Beta zeolite with SiO2/Al203 mole ratio of 55 showed the highest performance for the selective ring opening. The acidity of catalyst seemed to play an important role as active sites for the selective ring opening of 1-methylnaphthalene but there should be some optimum catalyst acidity for the reaction. The acidity of Beta zeolite could be controlled by the acid treatment and the catalyst with the optimum acidity for the selective ring opening could be prepared.

  2. Zr-zeolite beta: a new heterogeneous catalyst system for the highly selective cascade transformation of citral to (+/-)-menthol.

    Science.gov (United States)

    Nie, Yuntong; Jaenicke, Stephan; Chuah, Gaik-Khuan

    2009-01-01

    The transformation of citral to menthols involves hydrogenation steps as well as cyclisation of the intermediate, citronellal. The ability of Zr-zeolite beta to catalyse the cyclisation with high diastereoselectivity to (+/-)-isopulegol is the critical step in this cascade transformation. Bifunctional catalysts containing nickel or rhodium supported on Zr-zeolite beta gave menthols in yields of 87-89% and an excellent diastereoselectivity of 94% for the desired (+/-)-menthol. Dual catalyst systems of Zr-zeolite beta and nano-dispersed Ni on an MCM-41 support were equally effective and have the added advantage that the rates of the acid- and hydrogenation-catalysed steps can be independently varied. By applying a pressure ramp of 0.2-2 MPa, the yield of menthols could be increased to 95%, with 94% diastereoselectivity for (+/-)-menthol. The low initial pressure minimises the rates of competing hydrogenation reactions to byproducts such as citronellol and 3,7-dimethyloctanol. PMID:19132702

  3. Nonionic emulsion-mediated synthesis of zeolite beta

    Indian Academy of Sciences (India)

    Yuguo Shen; Ying Zhang; Chao Jin; Ying Cao; Wei Gao; Lishan Cui

    2011-07-01

    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 nucleation rate. Furthermore, the emulsion system could stabilize the beta product and retarded its further transformation to ZSM-5 even under the high crystallization temperature at 453 K. Additionally, the beta particle size could be tuned by the adoption of different lengths of alkyl chain in the surfactant and cosurfactant. Control experiments showed each emulsion component played a crucial role in the zeolite beta growth. The approach proposed in this paper might be extended to apply for the syntheses of other types of zeolites with particle size under control.

  4. Adsorptive desulfurization over hierarchical beta zeolite by alkaline treatment

    Institute of Scientific and Technical Information of China (English)

    Fuping Tian; Xiaojian Yang; Yanchun Shi; Cuiying Jia; Yongying Chen

    2012-01-01

    Hierarchical beta zeolites with SiO2/Al2O3 molar ratios of 16 to 25 were obtained by alkaline treatment in NaOH solution.The effects of treatment temperature on crystallinity,textural properties and chemical composites were studied by XRD,N2 sorption,FT-IR and XRF techniques.The desulfurization performance of parent and alkaline-treated beta zeolites was investigated by static absorption in four model fuels,containing four sulfur compounds of different molecular sizes like thiophene (TP),3-methylthiophene (3-MT),benzothiophene (BT) and dibenzothiophene (DBT),respectively.The crystallinity was observed to be successfully maintained when the treatment temperature was below 50℃.Mesoporosity of beta zeolite was evidently developed with alkaline treatment.The formation of mesopore remarkably improved the desulfurization performance for TP,3-MT,BT and DBT,especially for DBT with larger molecular diameter.Though the addition of toluene in the model fuels resulted in a significant drop of the desulfurization performance of mesoporous beta zeolite,the introduction of cerium ions to some extent mitigated the effect of toluene,which means that both the adsorbents porous structure and the adsorption mode are responsible for the desulfurization performance.The adsorbent of cerium ion-exchanged mesoporous beta showed about 80% recovery of desulfurization after the first regeneration.

  5. Synthesis of mesoporous Beta and Sn-Beta zeolites and their catalytic performances.

    Science.gov (United States)

    Jin, Junjiang; Ye, Xinxin; Li, Yongsheng; Wang, Yanqin; Li, Liang; Gu, Jinlou; Zhao, Wenru; Shi, Jianlin

    2014-06-14

    Mesoporous Beta zeolite has been successfully prepared through hydrothermal synthesis in the presence of cationic ammonium-modified chitosan as the meso-template. Through a subsequent solid-gas reaction between highly dealuminated mesoporous Beta zeolite and SnCl4 steam at an elevated temperature, mesoporous Sn-Beta has been facilely obtained. It was revealed that the addition of cationic chitosan induced the nanocrystal aggregation to particle sizes of ∼300 nm, giving rise to the intercrystalline/interparticle mesoporosity. In the Sn-implanting procedure, Sn species were demonstrated to be doped into the framework of the resulting mesoporous Beta zeolite in a tetrahedral environment without structural collapse. Due to the micro/mesoporous structures, both mesoporous Beta and Sn-Beta exhibited superior performances in α-pinene isomerization, Baeyer-Villiger oxidation of 2-adamantanone by hydrogen peroxide and the isomerization of glucose in water, respectively.

  6. Enhanced Activity of Nanocrystalline Beta Zeolite for Acylation of Veratrole with Acetic Anhydride.

    Science.gov (United States)

    Aisha Mahmood Abdulkareem, Al-Turkustani; Selvin, Rosilda

    2016-04-01

    Friedel-Craft acylation of veratrole using homogeneous acid catalysts such as AlCl3, FeCl3, ZnCl2, and HF etc. produces acetoveratrone, (3',4'-dimethoxyacetophenone), which is the intermediate for synthesis of papavarine alkaloids. The problems associated with these homogeneous catalysts can be overcome by using heterogeneous solid catalysts. Since acetoveratrone is a larger molecule, large pore Beta zeolites with smaller particle sizes are beneficial for the liquid-phase acylation of veratrole, for easy diffusion of reactants and products. The present study aims in the acylation of veratrole with acetic anhydride using nanocrystalline Beta Zeolite catalyst. A systematic investigation of the effects of various reaction parameters was done. The catalysts were characterized for their structural features by using XRD, TEM and DLS analyses. The catalytic activity of nanocrystalline Beta zeolite was compared with commercial Beta zeolite for the acylation and was found that nanocrystalline Beta zeolite possessed superior activity.

  7. Transalkylation of Multi-secbutylbenzenes with Benzene over Hierarchical Beta Zeolite

    Institute of Scientific and Technical Information of China (English)

    Yingxia Li; Can Luo; Xuan Wang; Chongpin Huang; Biaohua Chen

    2014-01-01

    A hierarchical beta zeolite synthesized by quasi-solid phase conversion method was characterized by BET, scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), temperature-programmed desorption of ammonia (NH3-TPD), 27Al and 29Si magic angle spinning nuclear magnetic resonance (27Al and 29Si MAS NMR), and its catalytic performance was compared with that of conventional microporous beta zeolite for liquid phase transalkylation of multi-secbutylbenzenes (MSBBs) with benzene. The results indicate that the hierarchical beta zeolite consists of nanosized crystals with a meso/microporous structure and has stronger acid strength than the microporous beta zeolite. The higher conversion of tri-secbutylbenzene (TSBB) and selectivity of sec-butylbenzene (SBB) are achieved on hierarchical beta zeolite than microporous beta zeolite, while the conversion of di-secbutylbenzene (DSBB) is slightly higher. The improvement of catalytic performance over hierarchical beta zeolite can be ascribed to the presence of mesopores, nanosized crystals and stronger acidity.

  8. Preparation and Characterization of Zeolite Beta with Low SiO2/Al2O3 Ratio

    Institute of Scientific and Technical Information of China (English)

    Kang Shanjiao; Gong Yanjun; Dou Tao; Zhang Ying; Zheng Yanying

    2007-01-01

    Zeolite beta with a low SiO2/Al2O3 ratio was synthesized by a novel two-step process. The synthesized sample was characterized with XRD,SEM,FTIR,and N2 adsorption-desorption and solid-state MAS NMR. The results showed that aluminium species were inserted into the framework of zeolite beta. The BET surface area,volume,and particle size of the zeolite beta sample decreased with decreasing SiO2/Al2O3 ratio. Our process was proved an efficient route to synthesize zeolite beta with a low SiO2/Al2O3 ratio.

  9. Oxidative dehydration of glycerol to acrylic acid over vanadium-impregnated zeolite beta

    International Nuclear Information System (INIS)

    The oxidative dehydration of glycerol to acrylic acid was studied over vanadium-impregnated zeolite Beta. Catalysts were prepared by wet impregnation of ammonium metavanadate over ammonium-exchanged zeolite Beta, followed by air calcination at 823 K. Impregnation reduced the specific surface area, but did not significantly affected the acidity (Bronsted and Lewis) of the zeolites. The catalytic evaluation was carried out in a fixed bed flow reactor using air as the carrier and injecting glycerol by means of a syringe pump. Acrolein was the main product, with acetaldehyde and hydroxy-acetone (acetol) being also formed. Acrylic acid was formed with approximately 25% selectivity at 548 K over the impregnated zeolites. The result can be explained by XPS (X-ray photoelectron spectroscopy) measurements, which indicated a good dispersion of the vanadium inside the pores. (author)

  10. Oxidative dehydration of glycerol to acrylic acid over vanadium-impregnated zeolite beta

    Energy Technology Data Exchange (ETDEWEB)

    Pestana, Carolina F.M.; Guerra, Antonio C.O.; Turci, Cassia C. [Universidade Federal do Rio de Janeiro, RJ (Brazil). Inst. de Quimica; Ferreira, Glaucio B. [Universidade Federal Fluminense, Niteroi, RJ (Brazil). Inst. de Quimica; Mota, Claudio J.A., E-mail: cmota@iq.ufrj.br [INCT Energia e Ambiente, Universidade Federal do Rio de Janeiro, RJ (Brazil)

    2013-01-15

    The oxidative dehydration of glycerol to acrylic acid was studied over vanadium-impregnated zeolite Beta. Catalysts were prepared by wet impregnation of ammonium metavanadate over ammonium-exchanged zeolite Beta, followed by air calcination at 823 K. Impregnation reduced the specific surface area, but did not significantly affected the acidity (Bronsted and Lewis) of the zeolites. The catalytic evaluation was carried out in a fixed bed flow reactor using air as the carrier and injecting glycerol by means of a syringe pump. Acrolein was the main product, with acetaldehyde and hydroxy-acetone (acetol) being also formed. Acrylic acid was formed with approximately 25% selectivity at 548 K over the impregnated zeolites. The result can be explained by XPS (X-ray photoelectron spectroscopy) measurements, which indicated a good dispersion of the vanadium inside the pores. (author)

  11. Highly mesoporous single-crystalline zeolite beta synthesized using a nonsurfactant cationic polymer as a dual-function template

    KAUST Repository

    Zhu, Jie

    2014-02-12

    Mesoporous zeolites are useful solid catalysts for conversion of bulky molecules because they offer fast mass transfer along with size and shape selectivity. We report here the successful synthesis of mesoporous aluminosilicate zeolite Beta from a commercial cationic polymer that acts as a dual-function template to generate zeolitic micropores and mesopores simultaneously. This is the first demonstration of a single nonsurfactant polymer acting as such a template. Using high-resolution electron microscopy and tomography, we discovered that the resulting material (Beta-MS) has abundant and highly interconnected mesopores. More importantly, we demonstrated using a three-dimensional electron diffraction technique that each Beta-MS particle is a single crystal, whereas most previously reported mesoporous zeolites are comprised of nanosized zeolitic grains with random orientations. The use of nonsurfactant templates is essential to gaining single-crystalline mesoporous zeolites. The single-crystalline nature endows Beta-MS with better hydrothermal stability compared with surfactant-derived mesoporous zeolite Beta. Beta-MS also exhibited remarkably higher catalytic activity than did conventional zeolite Beta in acid-catalyzed reactions involving large molecules. © 2014 American Chemical Society.

  12. The study of methanol transformation over Cu-modified ZSM-5, Beta zeolite and MCM-41 mesoporous silica using 11C-radioisotope labeling

    International Nuclear Information System (INIS)

    Complete text of publication follows. The copper-containing zeolites and mesoporous silica, among other metals, are suitable for dehydrogenation of methanol. The Cu transition metal determines the route of methanol conversion on supports of ZSM-5 and Beta zeolite as well as MCM-41 mesoporous silica. The catalysis mechanism and the catalytic property are concluded from the composition of methanol derivates over Cu-modified catalysts. The Cu ion-exchanged ZSM-5 and Beta zeolite and MCM-41 mesoporous silica were synthesized and characterized using X-ray power diffraction, scanning electron microscope, nitrogen and pyridine adsorption, X-ray fluorescency and FTIR spectroscopy. The 11C-radioactive labeling method (11C radioisotope, T1/2 = 20 min, is a gamma emitter by annihilation of its positron) is suitable for following the process of 11C-methanol con- version i.e. adsorption, desorption and catalytic transformation as well as for investigation of small amounts of molecules over catalysts by very sensitive radioactivity detectors.The 11C radioisotope was produced at cyclotron and the 11C-methanol was synthesized by a classical radiochemical method. After catalysis the 11C-radioactive and non radioactive volatile products were identified by radiogas chromatography hereby radiolabeled compound and -derivates were distinguished from other participant natural, nonradioactive carbon compounds. Along radioactive products dimethyl ether and small hydrocarbons products were formed by Bronsted acid sites of catalysts while formaldehyde and small methyl formate were formed by Cu metal over bifunctional Cu-ZSM-5, Cu-Beta zeolite and mesoporous Cu-MCM-41 silica at 240 deg C. The detection of methoxy methanol and dimethoxy methane confirmed the simultaneous presence of acid and basic sites of catalysts. At higher temperature (400 deg C) the CO and CO2 final products were dominated. In our previous works, methanol conversion to hydrocarbons was observed by dehydration over acid H

  13. Dynamic Nuclear Polarization NMR Enables the Analysis of Sn-Beta Zeolite Prepared with Natural Abundance 119Sn Precursors

    OpenAIRE

    Gunther, William R.; Michaelis, Vladimir K.; Caporini, Marc A.; Griffin, Robert G.; Román-Leshkov, Yuriy

    2014-01-01

    The catalytic activity of tin-containing zeolites, such as Sn-Beta, is critically dependent on the successful incorporation of the tin metal center into the zeolite framework. However, synchrotron-based techniques or solid-state nuclear magnetic resonance (ssNMR) of samples enriched with 119Sn isotopes are the only reliable methods to verify framework incorporation. This work demonstrates, for the first time, the use of dynamic nuclear polarization (DNP) NMR for characterizing zeolites contai...

  14. ASETILASI PADA FENOL DAN ANISOL MENGGUNAKAN ANHIDRIDA ASAM ASETAT BERKATALIS Zr4+-ZEOLIT BETA

    Directory of Open Access Journals (Sweden)

    DA Retnoningrum

    2015-07-01

    Full Text Available Zeolit beta pada umumnya memiliki keasaman tinggi dan berpotensi aktif sebagai katalis heterogen dalam asilasi Friedel-Crafts senyawa aromatik. Untuk meningkatkan stabilitas dan selektivitasnya, zeolit beta perlu diaktivasi dan dimodifikasi terlebih dahulu dengan mengembankan logam aktif zirkonium dengan metode pertukaran ion. Karakterisasi katalis meliputi analisis kristalinitas katalis dengan XRD, sifat permukaan katalis dengan Surface Area Analyzer dan uji keasaman dengan pengadsorbsi piridin. Dalam penelitian ini, dipelajari aktivitas dan selektivitas katalis Zr4+-zeolit beta dalam reaksi asetilasi fenol dan anisol. Reaksi dilakukan pada berbagai variasi suhu yaitu 100 dan 130C dengan waktu reaksi yaitu pada jam ke 4, 8 dan 12. Hasil asetilasi kemudian dianalisis menggunakan GC, FTIR dan analisis produk menggunakan GC-MS. Asetilasi fenol dengan katalis Zr4+-zeolit beta menghasilkan produk fenil etanoat dengan kadar 95,87% dan selektivitas 100%. Hasil ini didapatkan pada suhu reaksi 130C dan waktu reaksi 8 jam. Asetilasi pada cincin benzena baik pada fenol maupun anisol tidak terjadi, hal ini karena asetilasi pada cincin benzena lebih sukar dibandingkan asetilasi pada gugus OH fenol. Perlu adanya kondisi lain untuk melakukan asetilasi pada cincin benzena. Asetilasi anisol pada waktu reaksi 24 jam dan temperatur 130C didapatkan produk dengan kadar 74%.Beta zeolite generally has a high acidity and potentially active as heterogeneous catalyst in the Friedel-Crafts acylation of aromatic compounds. To improve its stability and selectivity, beta zeolite needs to be activated and modified in advance with zirconium to elicit active metal using ion exchange method. Characterization of catalyst include catalyst’s crystallinity using XRD analysis, the nature of the catalyst surface with the Surface Area Analyzer and the acidity test using pyridine adsorption. In the current study the activity and the selectivity of catalyst Zr4+-beta zeolite

  15. Influence of the aluminium impregnation [ Al(NO33] in the beta zeolite over its acidity

    Directory of Open Access Journals (Sweden)

    Francisco José Sánchez Castellanos

    2010-04-01

    Full Text Available Beta zeolite was impregnated with [ Al(NO33], increasing the aluminium content in increments of 0.05% from 0.00% to 0.25%. A parallel treatment with 0.05% sulphuric acid was also performed; in both cases, methanol was used as solvent (disperse phase. Cation exchange capacity (CEC, ammonia chemisorption, infrared spectroscopy (FIT-IR, scanning electronic microscopy (SEM, X-Ray powder diffraction (XRD, atomic absorption spectroscopy (AAS, titration with sodium hydroxide and nitrogen physisorption at 77K were used to carry out the physical and chemical characterization of the catalysts. Futhermore, the catalysts were employed in the esterification of ethanol with acetic acid, to quantify the effect of aluminium impregnation over the beta zeolite.

  16. Direct evidence of advantage of using nanosized zeolite Beta for ISFET-based biosensor construction

    International Nuclear Information System (INIS)

    Analytical characteristics of urease- and butyrylcholinesterase (BuChE)- based ion sensitive field-effect transistor (ISFET) biosensors were investigated by the incorporation of zeolite Beta nanoparticles with varying Si/Al ratios. The results obtained by the zeolite-modified ISFET transducers suggested that the Si/Al ratio strongly influenced the biosensor performances due to the electrostatic interactions among enzyme, substrate, and zeolite surface as well as the nature of the enzymatic reaction. Using relatively small nanoparticles (62.7 ± 10, 76.2 ± 10, and 77.1 ± 10 nm) rather than larger particles, that are widely used in the literature, allow us to produce more homogenous products which will give more control over the quantity of materials used on the electrode surface and ability to change solely Si/Al ratio without changing other parameters such as particle size, pore volume, and surface area. This should enable the investigation of the individual effect of changing acidic and electronic nature of this material on the biosensor characteristics. According to our results, high biosensor sensitivity is evident on nanosize and submicron size particles, with the former resulting in higher performance. The sensitivity of biosensors modified by zeolite particles is higher than that to the protein for both types of biosensors. Most significantly, our results show that the performance of constructed ISFET-type biosensors strongly depends on Si/Al ratio of employed zeolite Beta nanoparticles as well as the type of enzymatic reaction employed. All fabricated biosensors demonstrated high signal reproducibility and stability for both BuChE and urease.

  17. Tight bifunctional hierarchical catalyst.

    Science.gov (United States)

    Højholt, Karen T; Vennestrøm, Peter N R; Tiruvalam, Ramchandra; Beato, Pablo

    2011-12-28

    A new concept to prepare tight bifunctional catalysts has been developed, by anchoring CoMo(6) clusters on hierarchical ZSM-5 zeolites for simultaneous use in HDS and hydrocracking catalysis. The prepared material displays a significant improved activity in HDS catalysis compared to the impregnated counterpart. PMID:22048337

  18. Pure Silica Zeolite Beta Membrane: A Potential Low Dielectric Constant Material For Microprocessor Application

    Science.gov (United States)

    Fong, Yeong Yin; Bhatia, Subhash

    The semiconductor industry needs low dielectric constant (low k-value) materials for more advance microprocessor and chips by reducing the size of the device features. In fabricating these contents, a new material with lower k-value than conventional silica (k = 3.9-4.2) is needed in order to improve the circuit performance. The choice of the inorganic zeolite membrane is an attractive option for low k material and suitable for microprocessor applications. A pure silica zeolite beta membrane was synthesized and coated on non-porous stainless steel support using insitu crystallization in the presence of tetraethylammonium hydroxide, TEA (OH), as structure directing agent, fumed silica, HF and deionized water at pH value of 9. The crystallization was carried out for the duration of 14 days under hydrothermal conditions at 130°C. The membrane was characterized by thermogravimetric analysis (TGA), nitrogen adsorption and Scanning Electron Microscope (SEM). SEM results show a highly crystalline; with a truncated square bipyramidal morphology of pure silica zeolite beta membrane strongly adhered on the non-porous stainless steel support. In the present work, the k-value of the membrane was measured as 2.64 which make it suitable for the microprocessor applications.

  19. Elaboration of new method of enzyme adsorption on silicalite and nano beta zeolite for amperometric biosensor creation

    Directory of Open Access Journals (Sweden)

    Soldatkin O. O.

    2014-07-01

    Full Text Available Aim. Optimization of a new method of enzyme immobilization for amperometric biosensor creation. Methods. The amperometric biosensor with glucose oxidase immobilized on zeolites as bioselective elements and platinum disk electrode as transducers of biochemical signal into the electric one was used in the work. Results. The biosensors based on glucose oxidase adsorbed on zeolites were characterized by a higher sensitivity to glucose and a better inter-reproducibility. The best analytical characteristics were obtained for the biosensors based on nano beta zeolite. It has been found that an increase in the amount of zeolite on the surface of amperometric transducer may change such biosensor parameters as sensitivity to the substrate and duration of the analysis. Conclusions. The proposed method of enzyme immobilization by adsorption on zeolites is shown to be quite promising in the development of amperometric biosensors and therefore should be further investigated.

  20. Synthesis of zeolite beta with pretreated rice husk silica and its transformation to ZSM-12

    Energy Technology Data Exchange (ETDEWEB)

    Loiha, Sirinuch [Material Chemistry Research Unit, School of Chemistry, Institute of Science, Suranaree University of Technology, Nakhon Ratchasima 30000 (Thailand); Synchrotron Light Research Institute (Public Organization), Nakhon Ratchasima 30000 (Thailand); Prayoonpokarach, Sanchai [Material Chemistry Research Unit, School of Chemistry, Institute of Science, Suranaree University of Technology, Nakhon Ratchasima 30000 (Thailand); Songsiriritthigun, Prayoon [Synchrotron Light Research Institute (Public Organization), Nakhon Ratchasima 30000 (Thailand); Wittayakun, Jatuporn, E-mail: jatuporn@sut.ac.th [Material Chemistry Research Unit, School of Chemistry, Institute of Science, Suranaree University of Technology, Nakhon Ratchasima 30000 (Thailand); Center of Environmental and Hazardous Waste Management (EHWM), Thammasat University, Pathumtani 12120 (Thailand)

    2009-06-15

    Silica with 98% purity was prepared from rice husk by acid leaching and used as a silica source for the syntheses of zeolite beta (Beta) under hydrothermal conditions with gel Si/Al ratios of 8, 13, 15, 20, 50, 100, 150, and 200. Based on powder X-ray diffraction patterns, samples with gel Si/Al ratios of 8-20 contained only the pure phase of Beta and the highest relative crystallinity was observed in the Beta with gel Si/Al ratio of 13. This sample was further characterized by scanning electron microscopy, particle size analyzer and N{sub 2} adsorption analysis. The Beta particles were sphere shaped with the average particle size of 1.5 {mu}m and a surface area of 670 m{sup 2} g{sup -1}. The samples with gel Si/Al ratios ranging from 50 to 200 showed mixed phases of Beta and ZSM-12, and the latter phase was more dominant as the Si/Al ratio increased.

  1. Synthesis of zeolite beta with pretreated rice husk silica and its transformation to ZSM-12

    International Nuclear Information System (INIS)

    Silica with 98% purity was prepared from rice husk by acid leaching and used as a silica source for the syntheses of zeolite beta (Beta) under hydrothermal conditions with gel Si/Al ratios of 8, 13, 15, 20, 50, 100, 150, and 200. Based on powder X-ray diffraction patterns, samples with gel Si/Al ratios of 8-20 contained only the pure phase of Beta and the highest relative crystallinity was observed in the Beta with gel Si/Al ratio of 13. This sample was further characterized by scanning electron microscopy, particle size analyzer and N2 adsorption analysis. The Beta particles were sphere shaped with the average particle size of 1.5 μm and a surface area of 670 m2 g-1. The samples with gel Si/Al ratios ranging from 50 to 200 showed mixed phases of Beta and ZSM-12, and the latter phase was more dominant as the Si/Al ratio increased.

  2. Effects of Dealumination and Desilication of Beta Zeolite on Catalytic Performance in n-Hexane Cracking

    Directory of Open Access Journals (Sweden)

    Yong Wang

    2016-01-01

    Full Text Available Catalytic cracking of n-hexane to selectively produce propylene on Beta zeolite was carried out. The H-Beta (HB (Si/Al = 77 zeolite showed higher catalytic stability and propylene selectivity than the Al-rich HB (Si/Al = 12, due to its smaller number of acid sites, especially Lewis acid sites (LAS. However, catalytic stability and propylene selectivity in high n-hexane conversions were still not satisfactory. After dealumination with HNO3 treatment, catalytic stability was improved and propylene selectivity during high n-hexane conversions was increased. On the other hand, catalytic stability was not improved after desilication with NaOH treatment, although mesopores were formed. This may be related to the partially destroyed structure. However, propylene selectivity in high n-hexane conversions was increased after alkali treatment. We successfully found that the catalytic stability was improved and the propylene selectivity in high n-hexane conversions was further increased after the NaOH treatment followed by HNO3 treatment. This is due to the decrease in the number of acid sites and the increase in mesopores which are beneficial to the diffusion of coke precursor.

  3. 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.  

  4. Scope and limitations of reactant shape selectivity in hydrocracking on zeolite catalysts. Moeglichkeiten und Grenzen des formselektiven Hydrocrackens an Zeolith-Katalysatoren

    Energy Technology Data Exchange (ETDEWEB)

    Weitkamp, J.; Ernst, S. (Stuttgart Univ. (Germany, F.R.). Inst. fuer Technische Chemie)

    1990-01-01

    The paper reports on model investigations on isomerization and hydrocracking of long-chain n-alkanes on bifunctional zeolite catalysts. The investigations are aimed at developing the basics of a method for middle distillate and lobe fraction dewaxing by means of isomerization. On certain high-silicate zeolites considerable yields, invariably greater than isomere yields achieved with carefully optimized Y-zeolites, can be obtained. This leads to improved low-temperature properties of the feedstock without the drawback of matter loss in the boiling range of the goal product, as is the case in dewaxing by hydrocracking with reactant shape selectivity. The bifunctional forms of zeolites Beta, ZSM-12, ZSM-22 and ZSM-23 are particularly suitable as catalysts. (orig.).

  5. Intergrown new zeolite beta polymorphs with interconnected 12-ring channels solved by combining electron crystallography and single-crystal X-ray diffraction

    KAUST Repository

    Yu, Zhengbao

    2012-10-09

    Two new polymorphs of zeolite beta, denoted as SU-78A and SU-78B, were synthesized by employing dicyclohexylammonium hydroxides as organic structure-directing agents. The structure was solved by combining transmission electron microscopy and single-crystal X-ray diffraction. SU-78 is an intergrowth of SU-78A and SU-78B and contains interconnected 12-ring channels in three directions. The two polymorphs are built from the same building layer, similar to that for the zeolite beta family. The layer stacking in SU-78, however, is different from those in zeolite beta polymorph A, B, and C, showing new zeolite framework topologies. SU-78 is thermally stable up to 600 °C. © 2012 American Chemical Society.

  6. S+X-I+ route to mesostructured materials from Fau and Beta zeolite precursors: A comparative study of their assembly behaviors in extremely acidic media

    International Nuclear Information System (INIS)

    Mesoporous molecular sieves were synthesized from Beta and Fau zeolite precursors through S+X-I+ route under extremely acidic conditions in parallel (designated as MBeta and MFau, respectively). The textural properties of MFau were different from its MBeta counterpart but resembled normal MCM-41 silica from TEOS. Al content in MBeta was almost equivalent to that in the initial Beta zeolite precursors, whereas only trace Al species was present in MFau from elemental analysis results. The hydrothermal stability of MBeta after post-synthesis ammonia treatment was considerably improved compared with normal MCM-41 aluminosilicates, whereas the MFau after the same procedure was as unstable as normal MCM-41 silica. Thus, the assembly behaviors of Beta and Fau zeolite precursors were comparatively studied based on these results. The microstructure of Fau zeolite precursors were degraded by the extremely acidic condition, and Al species was dissolved into the synthesis mixture. However, Beta zeolite precursors survived the chemical attack of extremely acidic media and were incorporated into mesostructured framework as primary building units

  7. Performance of Adsorption Desulfurization on NiY/Beta Zeolites%NiY/Beta 复合分子筛吸附脱硫性能研究

    Institute of Scientific and Technical Information of China (English)

    庄新玲; 秦玉才; 阮艳军; 董世伟; 胡志君; 范跃超; 秦波; 段林海; 宋丽娟

    2013-01-01

    采用液相离子交换法制备了NiY及NiY/Beta分子筛,利用智能重量分析仪测定了噻吩、苯在NiY、NiY/Beta分子筛上的吸附-脱附等温线,计算比较了噻吩、苯在分子筛上的扩散系数,同时使用固定床技术考查了改性后的分子筛对催化裂化汽油的吸附脱硫性能。结果表明,复合分子筛 NiY/Beta仍然保持着较好的微孔结构,对噻吩的饱和吸附量大于苯的。而且噻吩在 NiY/Beta分子筛上的相对扩散系数明显增大,而苯的扩散系数有所减少,这有利于噻吩在分子筛上的扩散过程,抑制了苯在分子筛上的吸附,从而提高了NiY/Beta复合分子筛对噻吩的选择性脱除能力。对于FCC汽油NiY/Beta复合分子筛也表现出更好的深度脱硫能力。%The adsorption-desorption isotherms of thiophene and benzene in the NiY and NiY/Beta zeolites ,prepared by liquid phase ion exchange ,have been investigated by an intelligent gravimetric analyzer (IGA) and the diffusion coefficients were also calculated .Properties of selective adsorptive desulfurization of FCC gasoline on the zeolites were evaluated by a fixed-bed adsorption experiment . The results show that the NiY/Beta zeolites remain the microporous structure . The saturated adsorption amount of thiophene is larger than that of benzene and so it is to the diffusion coefficients .The better diffusivity of thiophene inhibits the adsorption of benzene , resulting in the absorption desulfurization capability of the NiY/Beta zeolites improved .

  8. Investigation of Aluminum Site Changes of Dehydrated Zeolite H-Beta during a Rehydration Process by High Field Solid State NMR

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Zhenchao; Xu, Suochang; Hu, Mary Y.; Bao, Xinhe; Peden, Charles HF; Hu, Jian Z.

    2015-01-22

    Aluminum site changes for dehydrated H-Beta zeolite during rehydration process are systematically investigated by ²⁷Al MAS and MQ MAS NMR at high magnetic fields up to 19.9 T. Benefiting from the high magnetic field, more detailed information is obtained from the considerably broadened and overlapped spectra of dehydrated H-beta zeolite. Dynamic changes of aluminum sites are demonstrated during rehydration process. In completely dehydrated H-Beta, invisible aluminum can reach 29%. The strength of quadrupole interactions for framework aluminum sites decreases gradually during water adsorption processes. The number of extra-framework aluminum (EFAL) species, i.e., penta- (34 ppm) and octa- (4 ppm) coordinated aluminum atoms rises initially with increasing water adsorption, and finally change into either tetra-coordinated framework or extra-framework aluminum in saturated water adsorption samples, with the remaining octa-coordinated aluminum lying at 0 and -4 ppm, respectively. Quantitative ²⁷Al MAS NMR analysis combined with ¹H MAS NMR indicates that some active EFAL species formed during calcination can reinsert into the framework during this hydration process. The assignment of aluminum at 0 ppm to EFAL cation and -4 ppm to framework aluminum is clarified for H-Beta zeolite.

  9. Dynamic nuclear polarization NMR enables the analysis of Sn-Beta zeolite prepared with natural abundance ¹¹⁹Sn precursors.

    Science.gov (United States)

    Gunther, William R; Michaelis, Vladimir K; Caporini, Marc A; Griffin, Robert G; Román-Leshkov, Yuriy

    2014-04-30

    The catalytic activity of tin-containing zeolites, such as Sn-Beta, is critically dependent on the successful incorporation of the tin metal center into the zeolite framework. However, synchrotron-based techniques or solid-state nuclear magnetic resonance (ssNMR) of samples enriched with (119)Sn isotopes are the only reliable methods to verify framework incorporation. This work demonstrates, for the first time, the use of dynamic nuclear polarization (DNP) NMR for characterizing zeolites containing ~2 wt % of natural abundance Sn without the need for (119)Sn isotopic enrichment. The biradicals TOTAPOL, bTbK, bCTbK, and SPIROPOL functioned effectively as polarizing sources, and the solvent enabled proper transfer of spin polarization from the radical's unpaired electrons to the target nuclei. Using bCTbK led to an enhancement (ε) of 75, allowing the characterization of natural-abundance (119)Sn-Beta with excellent signal-to-noise ratios in <24 h. Without DNP, no (119)Sn resonances were detected after 10 days of continuous analysis. PMID:24697321

  10. Method for purifying zeolitic material

    Energy Technology Data Exchange (ETDEWEB)

    Kokotailo, G.T.; Rohrman, A.C. Jr.

    1987-10-27

    A method is described for purifying an impure zeolitic material which contains crystalline zeolite phases of varying solubility in the presence of hydroxide ion whereby crystalline phases of greater solubility are removed from the zeolitic material. The zeolitic material contacts an aqueous solution having a hydroxide ion concentration sufficient to substantially solubilize at least one but not all of the phases in such a way that the solution does not substantially enter the zeolitic channel system of the material, and thereafter washing the zeolitic material to remove the solubilized phases. The method of claim 1 is described wherein the solution is a 1 to 50 weight percent aqueous solution of alkali metal hydroxide. The method of claim 1 is described wherein the impure zeolitic material contains a component selected from the group consisting of zeolite beta, ZSM-5, ZSM-11, ZSM-5/ZSM-11 intermediate, ZSM-12, ZSM-23, ZSM-35, ZSM-38 and ZSM-48.

  11. Elaboration of new method of enzyme adsorption on silicalite and nano beta zeolite for amperometric biosensor creation

    OpenAIRE

    Soldatkin O. O.; Ozansoy Kasap B.; Akata Kurc B.; Soldatkin A. P.; Dzyadevych S. V.; El’skaya A. V.

    2014-01-01

    Aim. Optimization of a new method of enzyme immobilization for amperometric biosensor creation. Methods. The amperometric biosensor with glucose oxidase immobilized on zeolites as bioselective elements and platinum disk electrode as transducers of biochemical signal into the electric one was used in the work. Results. The biosensors based on glucose oxidase adsorbed on zeolites were characterized by a higher sensitivity to glucose and a better inter-reproducibility. The best analytical charac...

  12. One-pot hydrothermal synthesis of CuBi co-doped mesoporous zeolite Beta for the removal of NOx by selective catalytic reduction with ammonia

    Science.gov (United States)

    Xie, Zhiguo; Zhou, Xiaoxia; Wu, Huixia; Chen, Lisong; Zhao, Han; Liu, Yan; Pan, Linyu; Chen, Hangrong

    2016-07-01

    A series of CuBi co-doped mesoporous zeolite Beta (CuxBiy-mBeta) were prepared by a facile one-pot hydrothermal treatment approach and were characterized by XRD, N2 adsorption-desorption, TEM/SEM, XPS, H2-TPR, NH3-TPD and in situ DRIFTS. The catalysts CuxBiy-mBeta were applied to the removal of NOx by selective catalytic reduction with ammonia (NH3-SCR), especially the optimized Cu1Bi1-mBeta achieved the high efficiency for the removal of NOx and N2 selectivity, superior water and sulfur resistance as well as good durability. The excellent catalytic performance could be attributed to the acid sites of the support and the synergistic effect between copper and bismuth species. Moreover, in situ DRIFTS results showed that amides NH2 and NH4+ generated from NH3 adsorption could be responsible for the high selective catalytic reduction of NOx to N2. In addition, a possible catalytic reaction mechanism on Cu1Bi1-mBeta for the removal of NOx by NH3-SCR was proposed for explaining this catalytic process.

  13. One-pot hydrothermal synthesis of CuBi co-doped mesoporous zeolite Beta for the removal of NOx by selective catalytic reduction with ammonia.

    Science.gov (United States)

    Xie, Zhiguo; Zhou, Xiaoxia; Wu, Huixia; Chen, Lisong; Zhao, Han; Liu, Yan; Pan, Linyu; Chen, Hangrong

    2016-01-01

    A series of CuBi co-doped mesoporous zeolite Beta (CuxBiy-mBeta) were prepared by a facile one-pot hydrothermal treatment approach and were characterized by XRD, N2 adsorption-desorption, TEM/SEM, XPS, H2-TPR, NH3-TPD and in situ DRIFTS. The catalysts CuxBiy-mBeta were applied to the removal of NOx by selective catalytic reduction with ammonia (NH3-SCR), especially the optimized Cu1Bi1-mBeta achieved the high efficiency for the removal of NOx and N2 selectivity, superior water and sulfur resistance as well as good durability. The excellent catalytic performance could be attributed to the acid sites of the support and the synergistic effect between copper and bismuth species. Moreover, in situ DRIFTS results showed that amides NH2 and NH4(+) generated from NH3 adsorption could be responsible for the high selective catalytic reduction of NOx to N2. In addition, a possible catalytic reaction mechanism on Cu1Bi1-mBeta for the removal of NOx by NH3-SCR was proposed for explaining this catalytic process. PMID:27445009

  14. One-pot hydrothermal synthesis of CuBi co-doped mesoporous zeolite Beta for the removal of NOx by selective catalytic reduction with ammonia

    Science.gov (United States)

    Xie, Zhiguo; Zhou, Xiaoxia; Wu, Huixia; Chen, Lisong; Zhao, Han; Liu, Yan; Pan, Linyu; Chen, Hangrong

    2016-01-01

    A series of CuBi co-doped mesoporous zeolite Beta (CuxBiy-mBeta) were prepared by a facile one-pot hydrothermal treatment approach and were characterized by XRD, N2 adsorption-desorption, TEM/SEM, XPS, H2-TPR, NH3-TPD and in situ DRIFTS. The catalysts CuxBiy-mBeta were applied to the removal of NOx by selective catalytic reduction with ammonia (NH3-SCR), especially the optimized Cu1Bi1-mBeta achieved the high efficiency for the removal of NOx and N2 selectivity, superior water and sulfur resistance as well as good durability. The excellent catalytic performance could be attributed to the acid sites of the support and the synergistic effect between copper and bismuth species. Moreover, in situ DRIFTS results showed that amides NH2 and NH4+ generated from NH3 adsorption could be responsible for the high selective catalytic reduction of NOx to N2. In addition, a possible catalytic reaction mechanism on Cu1Bi1-mBeta for the removal of NOx by NH3-SCR was proposed for explaining this catalytic process. PMID:27445009

  15. Preparation of catalyst composition comprising a boron containing crystalline material having the structure of zeolites ZSM-5, ZSM-11, ZSM-12, Beta or NU-1

    Energy Technology Data Exchange (ETDEWEB)

    Kuehl, G.H.

    1987-04-28

    A method is described for preparing a catalyst composition for processing high nitrogen-containing oils comprising a boron-containing crystalline material having the structure of zeolite ZSM-5, ZSM-11, ZSM-12, Beta or Nu-1. The sequential steps of synthesizing a boron-containing crystalline material having the structure of zeolite ZSM-5, ZSM-11, ZSM-12, Beta or Nu-1 are: drying the crystalline material at a temperature of from about ambient to less than about 170/sup 0/C; calcining the dried crystalline material in an oxygen- and water-free environment of anhydrous ammonia, anhydrous nitrogen, other anhydrous inert gases or a mixture thereof at a temperature of from about 200/sup 0/ to about 600/sup 0/C to minimize hydrolysis of boron in the boron-containing crystalline material; adsorbing ammonia on the calcined crystalline material; contacting the crystalline material with an ion-exchange solution at a pH of from about 7 to about 11; compositing the ion-exchange solution contacted crystalline material with an inorganic oxide material; drying the composite at a temperature of from about ambient to less than about 170/sup 0/C and calcining the dried composite at a temperature of from about 200/sup 0/ to about 600/sup 0/C.

  16. Chemical Imaging of Catalyst Deactivation during the Conversion of Renewables at the Single Particle Level: The Etherification of Biomass-based Polyols with Alkenes over H-Beta Zeolites

    Energy Technology Data Exchange (ETDEWEB)

    A Parvulescu; D Mores; E Stavitski; C Teodorescu; P Bruijnicx; R Klein Gebbing; B Weckhuysen

    2011-12-31

    The etherification of biomass-based alcohols with various linear {alpha}-olefins under solvent-free conditions was followed in a space- and time-resolved manner on 9 {micro}m large H-Beta zeolite crystals by confocal fluorescence microscopy. This allowed us to visualize the interaction with the substrate and distribution of the coke products into the catalyst at the level of an individual zeolite crystal during the etherification process. The spectroscopic information obtained on the micrometer-scale zeolite was in line with the results obtained with bulk characterization techniques and further confirmed by the catalytic results obtained both for micrometer-scale and nanoscale zeolites. This allowed us to explain the influence of the substrate type (glycerol, glycols, and alkenes) and zeolite properties (Si/Al ratio and particle size) on the etherification activity. The etherification of the biomass-based alcohols takes place mainly on the external surface of the zeolite particles. The gradual blockage of the external surface of the zeolite results in a partial or total loss of etherification activity. The deactivation could be attributed to olefin oligomerization. The high conversions obtained in the etherification of 1,2-propylene glycol with long linear alkenes (up to 80%) and the pronounced deactivation of the zeolite observed in the etherification of glycerol with long linear alkenes (max. 20% conversion) were explained by the spectroscopic measurements and is due to differences in the adsorption, i.e., in the center of the zeolite particle for glycerol and on the external surface in the case of glycols.

  17. 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...

  18. Nanoscale intimacy in bifunctional catalysts for selective conversion of hydrocarbons

    Science.gov (United States)

    Zecevic, Jovana; Vanbutsele, Gina; de Jong, Krijn P.; Martens, Johan A.

    2015-12-01

    The ability to control nanoscale features precisely is increasingly being exploited to develop and improve monofunctional catalysts. Striking effects might also be expected in the case of bifunctional catalysts, which are important in the hydrocracking of fossil and renewable hydrocarbon sources to provide high-quality diesel fuel. Such bifunctional hydrocracking catalysts contain metal sites and acid sites, and for more than 50 years the so-called intimacy criterion has dictated the maximum distance between the two types of site, beyond which catalytic activity decreases. A lack of synthesis and material-characterization methods with nanometre precision has long prevented in-depth exploration of the intimacy criterion, which has often been interpreted simply as ‘the closer the better’ for positioning metal and acid sites. Here we show for a bifunctional catalyst—comprising an intimate mixture of zeolite Y and alumina binder, and with platinum metal controllably deposited on either the zeolite or the binder—that closest proximity between metal and zeolite acid sites can be detrimental. Specifically, the selectivity when cracking large hydrocarbon feedstock molecules for high-quality diesel production is optimized with the catalyst that contains platinum on the binder, that is, with a nanoscale rather than closest intimacy of the metal and acid sites. Thus, cracking of the large and complex hydrocarbon molecules that are typically derived from alternative sources, such as gas-to-liquid technology, vegetable oil or algal oil, should benefit especially from bifunctional catalysts that avoid locating platinum on the zeolite (the traditionally assumed optimal location). More generally, we anticipate that the ability demonstrated here to spatially organize different active sites at the nanoscale will benefit the further development and optimization of the emerging generation of multifunctional catalysts.

  19. Nanoscale intimacy in bifunctional catalysts for selective conversion of hydrocarbons

    Science.gov (United States)

    Zečević, Jovana; Vanbutsele, Gina; de Jong, Krijn P.; Martens, Johan A.

    2016-01-01

    The ability to precisely control nanoscale features is increasingly exploited to develop and improve monofunctional catalysts1–4. Striking effects might also be expected in the case of bifunctional catalysts, which play an important role in hydrocracking of fossil and renewable hydrocarbon sources to provide high-quality diesel fuel5–7. Such bifunctional hydrocracking catalysts contain metal sites and acid sites, and for more than 50 years the so-called ‘intimacy criterion’8 has dictated the maximum distance between the two site types beyond which catalytic activity decreases. The lack of synthesis and material characterization methods with nanometer precision has long prevented in-depth exploration of the criterion, which has often been interpreted simply as ‘the closer the better’ for positioning metal and acid sites8–11. Here we show for a bifunctional catalyst, comprised of an intimate mixture of zeolite Y and alumina binder and with platinum (Pt) metal controllably deposited20,21 on either the zeolite or the binder, that close proximity between metal and zeolite acid sites can be detrimental: the selectivity when cracking large hydrocarbon feedstock molecules for high-quality diesel production is optimized with the catalyst that contains Pt on the binder, i.e. with a larger distance between metal and acid sites. Cracking of the large and complex hydrocarbon molecules typically derived from alternative sources such as gas-to-liquid technology, vegetable oil or algal oil6–7 should thus benefit especially from bifunctional catalysts that avoid locating Pt on the zeolite as the traditionally assumed optimal location. More generally, we anticipate that the ability to spatially organize different active sites at the nanoscale demonstrated here will benefit the further development and optimization of the newly emerging generation of multifunctional catalysts12–15. PMID:26659185

  20. Titanium-Beta Zeolites Catalyze the Stereospecific Isomerization of D-Glucose to L-Sorbose via Intramolecular C5-C1 Hydride Shift

    Energy Technology Data Exchange (ETDEWEB)

    Gounder, Rajamani [California Inst. of Technology (CalTech), Pasadena, CA (United States); Davis, Mark E. [California Inst. of Technology (CalTech), Pasadena, CA (United States)

    2013-06-03

    Pure-silica zeolite beta containing Lewis acidic framework Ti4+ centers (Ti-Beta) is shown to catalyze the isomerization of D-glucose to L-sorbose via an intramolecular C5–C1 hydride shift. Glucose–sorbose isomerization occurs in parallel to glucose–fructose isomerization on Ti-Beta in both water and methanol solvents, with fructose formed as the predominant product in water and sorbose as the predominant product in methanol (at 373 K) at initial times and over the course of >10 turnovers. Isotopic tracer studies demonstrate that 13C and D labels placed respectively at the C1 and C2 positions of glucose are retained respectively at the C6 and C5 positions of sorbose, consistent with its formation via an intramolecular C5–C1 hydride shift isomerization mechanism. This direct Lewis acid-mediated pathway for glucose–sorbose isomerization appears to be unprecedented among heterogeneous or biological catalysts and sharply contrasts indirect base-mediated glucose–sorbose isomerization via 3,4-enediol intermediates or via retro-aldol fragmentation and recombination of sugar fragments. Measured first-order glucose–sorbose isomerization rate constants (per total Ti; 373 K) for Ti-Beta in methanol are similar for glucose and glucose deuterated at the C2 position (within a factor of ~1.1), but are a factor of ~2.3 lower for glucose deuterated at each carbon position, leading to H/D kinetic isotope effects expected for kinetically relevant intramolecular C5–C1 hydride shift steps. Optical rotation measurements show that isomerization of D-(+)-glucose (92% enantiomeric purity) with Ti-Beta in water (373 K) led to the formation of L-(-)-sorbose (73% enantiomeric purity) and D-(-)-fructose (87% enantiomeric purity) as the predominant stereoisomers, indicating that stereochemistry is preserved at carbon centers not directly involved in intramolecular C5–C1 or C2–C1 hydride shift steps, respectively. This new Lewis acid

  1. Application of novel Polypyrrole/thiol-functionalized zeolite Beta/MCM-41 type mesoporous silica nanocomposite for adsorption of Hg2+ from aqueous solution and industrial wastewater: Kinetic, isotherm and thermodynamic studies

    International Nuclear Information System (INIS)

    Hierarchical zeolite consists of both microporous and unordered mesoporous structures. A composite of Polypyrrole/thiol-functionalized Beta/MCM-41 (PPy/SH-Beta/MCM-41) was prepared, characterized by FE-SEM, FT-IR, XRD, TGA and BET analysis and applied in the investigation of its adsorption characteristics for the removal of Hg2+ ions from aqueous solutions. Thiol-functionalized Beta/MCM-41 (SH-Beta/MCM-41) was prepared by 3-mercaptopropyltrimethoxysilane (MPTMS) in the presence of aerosil-200 as a silica source by two-step hydrothermal crystallization procedure. Batch mode experiments were conducted and three kinetic models were used to describe the adsorption process. The experimental data fitted very well with the Pseudo-second-order kinetic model. The calculated thermodynamic parameters (ΔH, ΔS and ΔG) revealed that the adsorption of Hg2+ onto PPy/SH-Beta/MCM-41 is an endothermic and spontaneous process. It was found that temperature has a positive effect on the removal efficiency and that PPy/SH-Beta/MCM-41 is potentially able to remove Hg2+ ions from aqueous solutions at even high concentrations (400 mg L−1). The recovery of Hg2+ from the PPy/SH-Beta/MCM-41 adsorbent was found to be more than 90% using 0.5 M H2SO4, and the ability of the absorbent to be reused for removal of Hg2+ was investigated.

  2. Application of novel Polypyrrole/thiol-functionalized zeolite Beta/MCM-41 type mesoporous silica nanocomposite for adsorption of Hg2+ from aqueous solution and industrial wastewater: Kinetic, isotherm and thermodynamic studies

    Science.gov (United States)

    Javadian, Hamedreza; Taghavi, Mehdi

    2014-01-01

    Hierarchical zeolite consists of both microporous and unordered mesoporous structures. A composite of Polypyrrole/thiol-functionalized Beta/MCM-41 (PPy/SH-Beta/MCM-41) was prepared, characterized by FE-SEM, FT-IR, XRD, TGA and BET analysis and applied in the investigation of its adsorption characteristics for the removal of Hg2+ ions from aqueous solutions. Thiol-functionalized Beta/MCM-41 (SH-Beta/MCM-41) was prepared by 3-mercaptopropyltrimethoxysilane (MPTMS) in the presence of aerosil-200 as a silica source by two-step hydrothermal crystallization procedure. Batch mode experiments were conducted and three kinetic models were used to describe the adsorption process. The experimental data fitted very well with the Pseudo-second-order kinetic model. The calculated thermodynamic parameters (ΔH, ΔS and ΔG) revealed that the adsorption of Hg2+ onto PPy/SH-Beta/MCM-41 is an endothermic and spontaneous process. It was found that temperature has a positive effect on the removal efficiency and that PPy/SH-Beta/MCM-41 is potentially able to remove Hg2+ ions from aqueous solutions at even high concentrations (400 mg L-1). The recovery of Hg2+ from the PPy/SH-Beta/MCM-41 adsorbent was found to be more than 90% using 0.5 M H2SO4, and the ability of the absorbent to be reused for removal of Hg2+ was investigated.

  3. Bifunctional alkaline oxygen electrodes

    Science.gov (United States)

    Swette, L.; Kackley, N.; Mccatty, S. A.

    1991-01-01

    The authors describe the identification and testing of electrocatalysts and supports for the positive electrode of moderate-temperature, single-unit, rechargeable alkaline fuel cells. Recent work on Na(x)Pt3O4, a potential bifunctional catalyst, is described, as well as the application of novel approaches to the development of more efficient bifunctional electrode structures. The three dual-character electrodes considered here showed similar superior performance; the Pt/RhO2 and Rh/RhO2 electrodes showed slightly better performance than the Pt/IrO2 electrode. It is concluded that Na(x)Pt3O4 continues to be a promising bifunctional oxygen electrode catalyst but requires further investigation and development.

  4. β沸石中Fe(Ⅱ)Salen络合物的合成及性能研究%SYNTHESIS AND CHARACTERIZATION OF Fe( Ⅱ )SALEN COMPLEX IN ZEOLITE BETA

    Institute of Scientific and Technical Information of China (English)

    马静红; 李瑞丰; 谢克昌

    2001-01-01

    Fe( Ⅱ )Salen( N, N',-bis(salicylaldehyde)ethylenediimine) was synthesized inside the cavity of zeolite Beta by the flexible ligand method and characterized by various physicochemical methods such as XRD, SEM, TG-DTA, UVVis. Evidences indicate by elemental analysis and thermal analysis that Fe( Ⅱ ) ion complexes stoichiometrically associated with Salen molecule in zeolite Beta. The encapsulated Fe( Ⅱ )Salen complexes were found to catalyze the cyclohexene oxidation reaction effectually.%采用自由配体法在β沸石的空腔内合成了Fe(Ⅱ)Salen络合物.XRD,SEM,TG-DTA,UV-Vis和元素分析等物理化学方法的分析结果表明,在沸石中的Fe(Ⅱ)Salen是由金属离子与配体以化学计量(摩尔比为1)络合而成,并体现了Fe(Ⅱ)Salen络合物的本征特性.环己烯的催化氧化揭示了β沸石中Fe(Ⅱ)Salen络合物的独特反应性.

  5. Application of novel Polypyrrole/thiol-functionalized zeolite Beta/MCM-41 type mesoporous silica nanocomposite for adsorption of Hg{sup 2+} from aqueous solution and industrial wastewater: Kinetic, isotherm and thermodynamic studies

    Energy Technology Data Exchange (ETDEWEB)

    Javadian, Hamedreza, E-mail: Hamedreza.Javadian@yahoo.com [Department of Chemical Engineering, Shahrood Branch, Islamic Azad University, Shahrood, Islamic Republic of Iran (Iran, Islamic Republic of); Taghavi, Mehdi [Polymer Chemistry Research Laboratory, Department of Chemistry, University of Mazandaran, Babolsar, 47416-95447, Islamic Republic of Iran (Iran, Islamic Republic of)

    2014-01-15

    Hierarchical zeolite consists of both microporous and unordered mesoporous structures. A composite of Polypyrrole/thiol-functionalized Beta/MCM-41 (PPy/SH-Beta/MCM-41) was prepared, characterized by FE-SEM, FT-IR, XRD, TGA and BET analysis and applied in the investigation of its adsorption characteristics for the removal of Hg{sup 2+} ions from aqueous solutions. Thiol-functionalized Beta/MCM-41 (SH-Beta/MCM-41) was prepared by 3-mercaptopropyltrimethoxysilane (MPTMS) in the presence of aerosil-200 as a silica source by two-step hydrothermal crystallization procedure. Batch mode experiments were conducted and three kinetic models were used to describe the adsorption process. The experimental data fitted very well with the Pseudo-second-order kinetic model. The calculated thermodynamic parameters (ΔH, ΔS and ΔG) revealed that the adsorption of Hg{sup 2+} onto PPy/SH-Beta/MCM-41 is an endothermic and spontaneous process. It was found that temperature has a positive effect on the removal efficiency and that PPy/SH-Beta/MCM-41 is potentially able to remove Hg{sup 2+} ions from aqueous solutions at even high concentrations (400 mg L{sup −1}). The recovery of Hg{sup 2+} from the PPy/SH-Beta/MCM-41 adsorbent was found to be more than 90% using 0.5 M H{sub 2}SO{sub 4}, and the ability of the absorbent to be reused for removal of Hg{sup 2+} was investigated.

  6. 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 c...

  7. Synthesis of 2,3-Butanedione over TS-1, Ti-NCl, TiMCM-41, Ti-Beta, Fe-Si, Fe-Beta and VS-1 Zeolites

    OpenAIRE

    Oscar Anunziata; Liliana Pierella; Marcos Gomez; Andrea Beltramone

    2000-01-01

    The purpose of this work is the synthesis of 2,3-butanedione (diacetyl) by selective oxidation of 2-butanone (methyl ethyl ketone) in the presence of O2 and H2O2 30% as oxidants. All the tests were performed over several selective oxidation zeolite catalysts, synthesized and characterized in our laboratory.

  8. Synthesis of Novel Perfluoroalkylglucosides on Zeolite and Non-Zeolite Catalysts

    Directory of Open Access Journals (Sweden)

    Janusz Nowicki

    2015-04-01

    Full Text Available Perfluoroalkylglucosides comprise a very important class of fluorine-containing surfactants. These compounds can be synthesized by using the Fisher reaction, starting directly from glucose and the required perfluoroalcohols. We wish to report on the use of zeolite catalysts of different structure and composition for the synthesis of perfluoroalkylglucosides when using glucose and 1-octafluoropentanol as substrates. Zeolites of different pore architecture have been chosen (ZSM-5, ZSM-12, MCM-22 and Beta. Zeolites were characterized by XRD, nitrogen sorption, scanning electron microscopy (SEM and solid-state 27Al MAS NMR spectroscopy. The activity of the zeolite catalysts in the glycosidation reaction was studied in a batch reactor at 100 °C below atmospheric pressure. The performance of zeolites was compared to other catalysts, an ion-exchange resin (Purolite and a montmorillonite-type layered aluminosilicate. The catalytic performance of zeolite Beta was the highest among the zeolites studied and the results were comparable to those obtained over Purolite and montmorillonite type catalysts.

  9. Synthesis of novel perfluoroalkylglucosides on zeolite and non-zeolite catalysts.

    Science.gov (United States)

    Nowicki, Janusz; Mokrzycki, Łukasz; Sulikowski, Bogdan

    2015-01-01

    Perfluoroalkylglucosides comprise a very important class of fluorine-containing surfactants. These compounds can be synthesized by using the Fisher reaction, starting directly from glucose and the required perfluoroalcohols. We wish to report on the use of zeolite catalysts of different structure and composition for the synthesis of perfluoroalkylglucosides when using glucose and 1-octafluoropentanol as substrates. Zeolites of different pore architecture have been chosen (ZSM-5, ZSM-12, MCM-22 and Beta). Zeolites were characterized by XRD, nitrogen sorption, scanning electron microscopy (SEM) and solid-state 27Al MAS NMR spectroscopy. The activity of the zeolite catalysts in the glycosidation reaction was studied in a batch reactor at 100 °C below atmospheric pressure. The performance of zeolites was compared to other catalysts, an ion-exchange resin (Purolite) and a montmorillonite-type layered aluminosilicate. The catalytic performance of zeolite Beta was the highest among the zeolites studied and the results were comparable to those obtained over Purolite and montmorillonite type catalysts.

  10. ZEOLITES: EFFECTIVE WATER PURIFIERS

    Science.gov (United States)

    Zeolites are known for their adsorption, ion exchange and catalytic properties. Various natural zeolites are used as odor and moisture adsorbents and water softeners. Due to their acidic nature, synthetic zeolites are commonly employed as solid acid catalysts in petrochemical ind...

  11. Study of the hydro-isomerization of paraffins with 7 and 8 carbon atoms on bifunctional catalysts; Etude de l'hydroisomerisation des paraffines a 7 et 8 atomes de carbone sur catalyseurs bifonctionnels

    Energy Technology Data Exchange (ETDEWEB)

    Patrigeon, A.

    2000-10-11

    Due to the suppression of lead additives and the trend to decrease the aromatic and olefinic content in gasoline, the interest for new octane enhancement processes has increased, particularly for isomerization of C{sub 7} and C{sub 8} linear paraffins into higher octane number multi-branched paraffins. Up to the present day, no industrial bifunctional catalyst exists due to the high tendency of the paraffins to be cracked limiting the amount of multi-branched products. The aim of this work is to study the possibility of isomerizing linear C{sub 7} and C{sub 8} paraffins in two steps in order to increase the amount of formed multi-branched paraffins. The first step converts linear paraffins into mono-branched paraffins (that step is supposed to be the slowest one) carried out using one bifunctional catalyst. The second step converts the formed mono-branched paraffins into multi-branched paraffins using a second bifunctional catalyst. The aim is to determine the characteristics of the two catalysts. To study the first step, Pt/zeolite or Pt/meso-porous solid catalysts, with different acidities and porosities, were tested in n-heptane and n-octane hydro-conversion. The role of solid porosity on selectivities was clearly established. Molecular modelling was utilised to explain the observed selectivities. To study the second step, the 2-methyl-hexane and 2-methyl-heptane hydro-conversion on Pt/H-beta and Pt/H-Y was carried out. This lead to maximum multi-branched yields similar to those obtained with the n-heptane and n-octane hydro-conversion. That result shows that the two steps isomerization process is not necessarily required because no more multi-branched products are formed. A kinetic study on the n-heptane hydro-conversion was performed. The decomposition of isomerization and cracking reactions into elementary steps has shown the major role of the paraffins physio-sorption step in the zeolite pores. (author)

  12. New zeolites in Fischer-Tropsch synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Hammer, H.; Joisten, M.; Luengen, S.; Winkler, D. (RWTH Aachen, Aachen (Germany). Inst. fuer Brennstoffchemie und Physikalisch-Chemische Verfahrenstechnik)

    1994-03-01

    Liquid fuels as well as liquid chemical feedstock can be produced from abundantly available sources such as coal or natural gas via syngas and subsequent Fischer-Tropsch synthesis (FTS). Continuing earlier investigations of various authors on zeolites A,X,Y or ZSM-5 in FTS, this paper deals with mordenite, erionite, ZSM-11, ZSM-12, and zeolites L, omega and beta, combined with Fe (promoted with Cu and K), or Co, by coprecipitation, by impregnation with carbonyls, or by ion exchange. It was the aim of this investigation to measure the effect of these zeolites on the composition of FTS products. Catalyst screening was executed at medium pressure (10 to 15 bar) in fixed bed and in bubble column reactors. It was found that the product spectra in the gaseous phase as well as in the liquid phase can be significantly different from those of classical straight-chain FTS products, and that they branch into more isomers, olefins and oxygenates, owing to the shape selectivity and acidity of the zeolites. Furthermore, it was found that zeolites with large pores were more resistant to fast blocking by carbon deposition. From the point of view of environmental protection, it should be emphasized that the FTS product is absolutely sulphur-free. 4 refs., 7 figs., 6 tabs.

  13. Infrared Spectroscopic Characterization of CIT-6 and a Family of *BEA Zeolites

    OpenAIRE

    Tomlinson, Sean R.; Tyler McGown; Schlup, John R.; Jennifer L. Anthony

    2013-01-01

    Infrared spectroscopy is known to be a useful tool for identifying local structure changes in zeolites. Infrared spectroscopy is often employed to complement X-ray diffraction data. Local structure changes in zeolite CIT-6 and its zeolite beta (*BEA) analogs caused by calcination, altering framework composition, and ion exchange have been identified with mid- and far-infrared spectroscopy. Differences in the local structures of the samples were observed in mid- and far-infrared spectra, inclu...

  14. Dimerization of norbornene on zeolite catalysts

    Institute of Scientific and Technical Information of China (English)

    N. G. Grigor’eva; S. V. Bubennov; L. M. Khalilov; B. I. Kutepov

    2015-01-01

    The high activity and selectivity of H‐Beta and H‐ZSM‐12 zeolites in the dimerization of norbornene was established. The norbornene conversion reached 100%in chlorinated paraffin and argon gas medium, with a selectivity of dimer formation of 88%–98%. Four stereo‐isomers of the bis‐2,2’‐norbornylidene structure were identified in the dimer fraction, with the (Z)‐anti‐bis‐2,2’‐norbornylidene prevailing over the others.

  15. Thermodynamic Parameters Evaluation of Alpha- and Beta-cages in Na/sup +/, Ba/sup 2+/, Fe/sup 3+/, Co/sup 2+/, Ni/sup 2+/ and Cu/sup 2+/ Exchanged Zeolite a Using Quantum Mechanical Theory and Fermi Dirac Statistics

    International Nuclear Information System (INIS)

    The aim of present paper is to investigate the effects of non-framework cations, their hydration capacity and the role of phonons (acoustical and optical) on the thermodynamic characteristics of Type-A zeolite using Quantum Mechanical theory and Fermi Dirac Statistics. This study is motivated by the lack of an accurate measurement capability of thermodynamic properties of zeolites by the existing methods reported in literature, that is why we have suggested the quantum mechanical and Fermi Dirac statistical approaches. Thermal analysis data for zeolite samples were obtained by thermogravimetric and differential thermal analysis (TG-DTG) technique at a heating rate of 10 K min-1 in order to evaluate the desorption behavior of water. The results showed that the thermal stability of these samples was found to be dependent mainly on the electropositive non-framework cations. Meanwhile, on the basis of thermodynamic parameters, the sizes of alpha- and beta-cages in Na-A and its derivative zeolite were calculated using Fermi Dirac Statistics. Thereafter, semi-quantum effects (logarithmic behavior) of specific heat, entropy and enthalpy were observed in all samples as manifestations of the production of photons due to gaining of thermal energy. As a result, Debye temperature would increase due to localization of heat energy in the Brillouin zone, and the calculated specific heat capabilities showed almost no changes after cation exchange. However entropy and enthalpy first exceeds NaA in Ba/sup 2+/, Ni/sup 2+/ and Cu/sup 2+/ and then decrease in Fe/sup 3+/ and Co/sup 2+/. These demonstrations indicated that Ba/sup 2+/, Ni/sup 2+/, Cu/sup 2+/, Fe/sup 3+/ and Co/sup 2+/ cations influenced both the entropy and enthalpy as a result of the interaction of cations with the zeolite framework, which confirmed that the changes in the lattice mode were dependent on the increase or decrease in the electrostatic interactions between the cations and the framework zeolite. (author)

  16. Lanthanum-catalysed synthesis of microporous 3D graphene-like carbons in a zeolite template.

    Science.gov (United States)

    Kim, Kyoungsoo; Lee, Taekyoung; Kwon, Yonghyun; Seo, Yongbeom; Song, Jongchan; Park, Jung Ki; Lee, Hyunsoo; Park, Jeong Young; Ihee, Hyotcherl; Cho, Sung June; Ryoo, Ryong

    2016-07-01

    Three-dimensional graphene architectures with periodic nanopores—reminiscent of zeolite frameworks—are of topical interest because of the possibility of combining the characteristics of graphene with a three-dimensional porous structure. Lately, the synthesis of such carbons has been approached by using zeolites as templates and small hydrocarbon molecules that can enter the narrow pore apertures. However, pyrolytic carbonization of the hydrocarbons (a necessary step in generating pure carbon) requires high temperatures and results in non-selective carbon deposition outside the pores. Here, we demonstrate that lanthanum ions embedded in zeolite pores can lower the temperature required for the carbonization of ethylene or acetylene. In this way, a graphene-like carbon structure can be selectively formed inside the zeolite template, without carbon being deposited at the external surfaces. X-ray diffraction data from zeolite single crystals after carbonization indicate that electron densities corresponding to carbon atoms are generated along the walls of the zeolite pores. After the zeolite template is removed, the carbon framework exhibits an electrical conductivity that is two orders of magnitude higher than that of amorphous mesoporous carbon. Lanthanum catalysis allows a carbon framework to form in zeolite pores with diameters of less than 1 nanometre; as such, microporous carbon nanostructures can be reproduced with various topologies corresponding to different zeolite pore sizes and shapes. We demonstrate carbon synthesis for large-pore zeolites (FAU, EMT and beta), a one-dimensional medium-pore zeolite (LTL), and even small-pore zeolites (MFI and LTA). The catalytic effect is a common feature of lanthanum, yttrium and calcium, which are all carbide-forming metal elements. We also show that the synthesis can be readily scaled up, which will be important for practical applications such as the production of lithium-ion batteries and zeolite-like catalyst

  17. Lanthanum-catalysed synthesis of microporous 3D graphene-like carbons in a zeolite template

    Science.gov (United States)

    Kim, Kyoungsoo; Lee, Taekyoung; Kwon, Yonghyun; Seo, Yongbeom; Song, Jongchan; Park, Jung Ki; Lee, Hyunsoo; Park, Jeong Young; Ihee, Hyotcherl; Cho, Sung June; Ryoo, Ryong

    2016-07-01

    Three-dimensional graphene architectures with periodic nanopores—reminiscent of zeolite frameworks—are of topical interest because of the possibility of combining the characteristics of graphene with a three-dimensional porous structure. Lately, the synthesis of such carbons has been approached by using zeolites as templates and small hydrocarbon molecules that can enter the narrow pore apertures. However, pyrolytic carbonization of the hydrocarbons (a necessary step in generating pure carbon) requires high temperatures and results in non-selective carbon deposition outside the pores. Here, we demonstrate that lanthanum ions embedded in zeolite pores can lower the temperature required for the carbonization of ethylene or acetylene. In this way, a graphene-like carbon structure can be selectively formed inside the zeolite template, without carbon being deposited at the external surfaces. X-ray diffraction data from zeolite single crystals after carbonization indicate that electron densities corresponding to carbon atoms are generated along the walls of the zeolite pores. After the zeolite template is removed, the carbon framework exhibits an electrical conductivity that is two orders of magnitude higher than that of amorphous mesoporous carbon. Lanthanum catalysis allows a carbon framework to form in zeolite pores with diameters of less than 1 nanometre; as such, microporous carbon nanostructures can be reproduced with various topologies corresponding to different zeolite pore sizes and shapes. We demonstrate carbon synthesis for large-pore zeolites (FAU, EMT and beta), a one-dimensional medium-pore zeolite (LTL), and even small-pore zeolites (MFI and LTA). The catalytic effect is a common feature of lanthanum, yttrium and calcium, which are all carbide-forming metal elements. We also show that the synthesis can be readily scaled up, which will be important for practical applications such as the production of lithium-ion batteries and zeolite-like catalyst

  18. Hydraulic conductivity of compacted zeolites.

    Science.gov (United States)

    Oren, A Hakan; Ozdamar, Tuğçe

    2013-06-01

    Hydraulic conductivities of compacted zeolites were investigated as a function of compaction water content and zeolite particle size. Initially, the compaction characteristics of zeolites were determined. The compaction test results showed that maximum dry unit weight (γ(dmax)) of fine zeolite was greater than that of granular zeolites. The γ(dmax) of compacted zeolites was between 1.01 and 1.17 Mg m(-3) and optimum water content (w(opt)) was between 38% and 53%. Regardless of zeolite particle size, compacted zeolites had low γ(dmax) and high w(opt) when compared with compacted natural soils. Then, hydraulic conductivity tests were run on compacted zeolites. The hydraulic conductivity values were within the range of 2.0 × 10(-3) cm s(-1) to 1.1 × 10(-7) cm s(-1). Hydraulic conductivity of all compacted zeolites decreased almost 50 times as the water content increased. It is noteworthy that hydraulic conductivity of compacted zeolite was strongly dependent on the zeolite particle size. The hydraulic conductivity decreased almost three orders of magnitude up to 39% fine content; then, it remained almost unchanged beyond 39%. Only one report was found in the literature on the hydraulic conductivity of compacted zeolite, which is in agreement with the findings of this study.

  19. Neurodegeneration in D-bifunctional protein deficiency: diagnostic clues and natural history using serial magnetic resonance imaging

    Energy Technology Data Exchange (ETDEWEB)

    Khan, Aneal [University of Calgary, Department of Medical Genetics and Pediatrics, Alberta Children' s Hospital, Calgary, AB (Canada); Wei, Xing-Chang [University of Calgary, Department of Radiology, Alberta Children' s Hospital, Calgary, AB (Canada); Snyder, Floyd F. [Alberta Children' s Hospital, Biochemical Genetics Laboratory, Calgary, AB (Canada); Mah, Jean K. [University of Calgary, Division of Neurology, Department of Pediatrics, Calgary, AB (Canada); Waterham, Hans; Wanders, Ronald J.A. [University of Amsterdam, Academic Medical Center, Lab Genetic Metabolic Diseases, Amsterdam (Netherlands)

    2010-12-15

    We report serial neurodegenerative changes on neuroimaging in a rare peroxisomal disease called D-bifunctional protein deficiency. The pattern of posterior to anterior demyelination with white matter disease resembles X-linked adrenoleukodystrophy. We feel this case is important to (1) highlight that D-bifunctional protein deficiency should be considered in cases where the neuroimaging resembles X-linked adrenoleukodystrophy, (2) to show different stages of progression to help identify this disease using neuroimaging in children, and (3) to show that neuroimaging suggesting a leukodystrophy can warrant peroxisomal beta-oxidation studies in skin fibroblasts even when plasma very long chain fatty acids are normal. (orig.)

  20. β分子筛在加氢裂化反应中催化性能特点研究%STUDY ON THE CATALYTIC PERFORMANCE OF ZEOLITE BETA IN HYDROCRACKING

    Institute of Scientific and Technical Information of China (English)

    杜艳泽; 乔楠森; 王凤来; 关明华

    2011-01-01

    A brief introduction of the characteristics of zeolite p structure was presented. The hydrocracking performance of catalyst containing zeolite pwas studied on a 200 mL hydrocracking device,and compared with catalyst containing zeolite Y and amorphous silica-alumina catalyst. Results show that under the same process conditions,catalysts containing zeolite p exhibit better catalytic performance during hydrocracking than the others; the selectivity of middle distillates is more than two percentage points higher,the setting point of diesel fractions is 4-12℃ lower,as well as good isomerization property, high cracking activity and strong nitrogen tolerance, which indicates that hydrocracking catalyst containing zeolite β can be used for maximizing middle distillates production.%对β分子筛结构特点进行介绍,在200 mL小型加氢实验装置上考察β分子筛催化剂的加氢裂化性能,并与Y型分子筛和无定形硅铝催化剂的性能进行对比.结果表明:在相同工艺条件下,与Y型分子筛和无定形硅铝催化剂相比,β分子筛加氢裂化催化剂的中间馏分油选择性提高2.0百分点以上,柴油凝点降低4~12℃.β分子筛在加氢裂化反应中表现出异构性能好、裂化活性高、中间馏分油选择性好、产品质量好、抗氮能力强等特点,可应用于最大量生产中间馏分油的加氢裂化催化剂.

  1. Zeolite H-BEA catalysed multicomponent reaction: One-pot synthesis of amidoalkyl naphthols - Biologically active drug-like molecules

    Indian Academy of Sciences (India)

    Sunil R Mistry; Rikesh S Joshi; Kalpana C Maheria

    2011-07-01

    Zeolite has been used as an efficient and a novel heterogeneous catalyst for one-pot synthesis of biologically active drug-like molecules, amidoalkyl naphthols. This green route involves multicomponent reaction of 2-naphthol, aromatic aldehydes and amide in the presence of a catalytic amount of zeolite H-Beta (H-BEA) under solvent reflux as well as solvent-free conditions.

  2. GSK-3: A Bifunctional Role in Cell Death Pathways

    Directory of Open Access Journals (Sweden)

    Keith M. Jacobs

    2012-01-01

    Full Text Available Although glycogen synthase kinase-3 beta (GSK-3β was originally named for its ability to phosphorylate glycogen synthase and regulate glucose metabolism, this multifunctional kinase is presently known to be a key regulator of a wide range of cellular functions. GSK-3β is involved in modulating a variety of functions including cell signaling, growth metabolism, and various transcription factors that determine the survival or death of the organism. Secondary to the role of GSK-3β in various diseases including Alzheimer’s disease, inflammation, diabetes, and cancer, small molecule inhibitors of GSK-3β are gaining significant attention. This paper is primarily focused on addressing the bifunctional or conflicting roles of GSK-3β in both the promotion of cell survival and of apoptosis. GSK-3β has emerged as an important molecular target for drug development.

  3. GSK-3β: A Bifunctional Role in Cell Death Pathways

    Science.gov (United States)

    Jacobs, Keith M.; Bhave, Sandeep R.; Ferraro, Daniel J.; Jaboin, Jerry J.; Hallahan, Dennis E.; Thotala, Dinesh

    2012-01-01

    Although glycogen synthase kinase-3 beta (GSK-3β) was originally named for its ability to phosphorylate glycogen synthase and regulate glucose metabolism, this multifunctional kinase is presently known to be a key regulator of a wide range of cellular functions. GSK-3β is involved in modulating a variety of functions including cell signaling, growth metabolism, and various transcription factors that determine the survival or death of the organism. Secondary to the role of GSK-3β in various diseases including Alzheimer's disease, inflammation, diabetes, and cancer, small molecule inhibitors of GSK-3β are gaining significant attention. This paper is primarily focused on addressing the bifunctional or conflicting roles of GSK-3β in both the promotion of cell survival and of apoptosis. GSK-3β has emerged as an important molecular target for drug development. PMID:22675363

  4. 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.

  5. 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 at least five reaction runs with essentially unchanged activity and without significant aluminium leaching from the catalyst. The use of benign reaction conditions and an industrially pertinent solid catalyst in combination with water establishes a new, green tetrose isomerization protocol...

  6. Synthesis of zeolite membranes

    Institute of Scientific and Technical Information of China (English)

    JIANG Haiyang; ZHANG Baoquan; Y. S. Lin; LI Yongdan

    2004-01-01

    Zeolite membranes offer great application potentials in membrane separation and/or reaction due to their excellent separation performance and catalytic ability. Up to present, various synthesis methods of zeolite membranes have been developed, including embedded method,in-situ hydrothermal synthesis method, and secondary growth method etc. Compared with the in-situ hydrothermal synthesis method, the secondary growth method possesses a variety of advantages such as easier operation, higher controllability in crystal orientation, microstructure and film thickness, leading to much better reproducibility. This review provides a concise summary and analysis of various synthesis methods reported in the literature. In particular, the secondary growth method was discussed in detail in terms of crystal orientation, defects and crystal grain layers. Some critical issues were also highlighted, which were conducive to the improvement in the synthesis technology of zeolite membranes.

  7. Effect of NiW Modified HZSM-5 and HY Zeolites on Hydrocracking Conversion of Crude Palm Oil to Liquid Hydrocarbons

    Directory of Open Access Journals (Sweden)

    Maliwan Subsadsana

    2016-05-01

    Full Text Available The catalytic conversion of crude palm oil over HZSM-5 and HY zeolites modified with NiW as catalysts in the hydrocracking process was investigated. These zeolites supported by NiW catalysts were prepared employing the impregnation technique. NiW was added to the zeolites in order to induce bi-functional properties (both acid and metal sites in the catalysts. Subsequently, the catalysts were characterized by X-ray diffraction spectrometry (XRD, scanning electron microscope (SEM, transmission electron microscope (TEM, ammonia temperature programmed desorption (NH3-TPD andnitrogen adsorption-desorption isotherms analysis. The catalytic activity of prepared catalysts was evaluated through the conversion of crude palm oil to biofuels. These results indicate that the incorporation of NiW over HZSM-5 and HY zeolites improves the conversion efficiency and enhances the yield of biofuel (gasoline, kerosene, and diesel, possibly due to NiW promote of hydrogenation and dehydrogenation reaction.

  8. Infrared Spectroscopic Characterization of CIT-6 and a Family of *BEA Zeolites

    Directory of Open Access Journals (Sweden)

    Sean R. Tomlinson

    2013-01-01

    Full Text Available Infrared spectroscopy is known to be a useful tool for identifying local structure changes in zeolites. Infrared spectroscopy is often employed to complement X-ray diffraction data. Local structure changes in zeolite CIT-6 and its zeolite beta (*BEA analogs caused by calcination, altering framework composition, and ion exchange have been identified with mid- and far-infrared spectroscopy. Differences in the local structures of the samples were observed in mid- and far-infrared spectra, including changes in the intratetrahedral asymmetric stretch, the double-ring mode, and the intratetrahedral bending mode regions. The infrared spectra indicate that calcination or acetic acid extraction changed the structure of CIT-6 to that of zeolite beta (*BEA. Zinc ion exchange or the substitution of aluminum into the framework structure of acetic acid extracted samples retained the CIT-6 structure.

  9. Catalysis with hierarchical zeolites

    DEFF Research Database (Denmark)

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

    2011-01-01

    Hierarchical (or mesoporous) zeolites have attracted significant attention during the first decade of the 21st century, and so far this interest continues to increase. There have already been several reviews giving detailed accounts of the developments emphasizing different aspects of this resear...

  10. Acid-Base Pairs in Lewis Acidic Zeolites Promote Direct Aldol Reactions by Soft Enolization.

    Science.gov (United States)

    Lewis, Jennifer D; Van de Vyver, Stijn; Román-Leshkov, Yuriy

    2015-08-17

    Hf-, Sn-, and Zr-Beta zeolites catalyze the cross-aldol condensation of aromatic aldehydes with acetone under mild reaction conditions with near quantitative yields. NMR studies with isotopically labeled molecules confirm that acid-base pairs in the Si-O-M framework ensemble promote soft enolization through α-proton abstraction. The Lewis acidic zeolites maintain activity in the presence of water and, unlike traditional base catalysts, in acidic solutions. PMID:26138135

  11. Influence of zeolitic structure on photoreduction property and hydrogen evolution reaction

    Energy Technology Data Exchange (ETDEWEB)

    Chatti, Ravikrishna V.; Dubey, Nidhi; Joshi, Meenal V.; Labhsetwar, Nitin K.; Rayalu, Sadhana S. [National Environmental Engineering Research Institute (NEERI-CSIR), Environmental Materials Unit, Nehru Marg, 440020 Nagpur, Maharashtra (India); Joshi, P.N. [National Chemical Laboratory (NCL-CSIR), Pune (India)

    2010-03-15

    A new photocatalytic material developed by supporting TiO{sub 2} in combination with transition metal ion like cobalt and heteropolyacid (HPA) on the surface is facilitating enhanced photoreduction of water and methyl orange. Zeolites being a solid acid play an important role in the electron transfer reaction, facilitated by the Lewis acid sites in the form of aluminium ions. In the present work, four different zeolite matrices namely, NaY zeolite, ultrastable zeolite Y, beta zeolite and titanium silicate-1 have been used for the synthesis of new photocatalytic materials. These materials have been evaluated for water splitting by an initial screening procedure using methyl orange photoreduction. The photocatalyst containing Na Y has emerged as a potential photocatalyst with hydrogen evolution rate of 2730 {mu}mol/h/g of TiO{sub 2}. Hydrogen evolution was not observed for the composite photocatalysts synthesized using the other zeolite matrices. It has been observed that physico-chemical properties like Si/Al ratio, acidity and basicity of the zeolite support have a tremendous influence on the photoreduction property of these zeolite matrices. (author)

  12. Zeolite crystal growth in space

    Science.gov (United States)

    Sacco, Albert, Jr.; Thompson, Robert W.; Dixon, Anthony G.

    1991-01-01

    The growth of large, uniform zeolite crystals in high yield in space can have a major impact on the chemical process industry. Large zeolite crystals will be used to improve basic understanding of adsorption and catalytic mechanisms, and to make zeolite membranes. To grow large zeolites in microgravity, it is necessary to control the nucleation event and fluid motion, and to enhance nutrient transfer. Data is presented that suggests nucleation can be controlled using chemical compounds (e.g., Triethanolamine, for zeolite A), while not adversely effecting growth rate. A three-zone furnace has been designed to perform multiple syntheses concurrently. The operating range of the furnace is 295 K to 473 K. Teflon-lined autoclaves (10 ml liquid volume) have been designed to minimize contamination, reduce wall nucleation, and control mixing of pre-gel solutions on orbit. Zeolite synthesis experiments will be performed on USML-1 in 1992.

  13. Zeolite Catalyzed Aldol Condensation Reactions

    OpenAIRE

    Adedayo I. Inegbenebor; Raphael C. Mordi; Oluwakayode M. Ogunwole

    2015-01-01

    The review is based on the description of zeolite structure, uses, synthesis, and catalytic aldol reaction in aldol condensation. An internal aldolcondensation reaction has been achieved over ZSM-5 zeolite with high silica-alumina ratio at 350oC. It therefore follows that zeolite canfunction as a catalyst in aldol type condensation reactions and that weak acid sites as well as a small number of active sites favor the aldolcondensation reaction of carbonyl compounds. However, the mixed condens...

  14. 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

    Recently, a new family of crystalline zeolitic materials was reported, the so-called mesoporous zeolite single crystals featuring individual zeolite single crystals with an additional noncrystalline mesopore system interconnected with the usual micropore system of the zeolite, resulting in a hier...... transport. Importantly, the mesoporous zeolites show significant improved resistance to poisoning by carbon formation....

  15. 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...

  16. Potential of sustainable hierarchical zeolites in the valorization of α-pinene.

    Science.gov (United States)

    Nuttens, Nicolas; Verboekend, Danny; Deneyer, Aron; Van Aelst, Joost; Sels, Bert F

    2015-04-13

    In the valorization of α-pinene, which is an important biomass intermediate derived from turpentine oil, hierarchical (mesoporous) zeolites represent a superior class of catalysts. Hierarchical USY, ZSM-5, and beta zeolites have been prepared, characterized, and catalytically evaluated, with the aim of combining the highest catalytic performance with the most sustainable synthetic protocol. These zeolites are prepared by alkaline treatment in aqueous solutions of NH4 OH, NaOH, diethylamine, and NaOH complemented with tetrapropylammonium bromide. The hierarchical USY zeolite is the most attractive catalyst of the tested series, and is able to combine an overall organic-free synthesis with an up to sixfold activity enhancement and comparable selectivity over the conventional USY zeolite. This superior performance relates to a threefold greater activity than that of the commercial standard, namely, H2 SO4 /TiO2 . Correlation of the obtained benefits to the amount of solid lost during the postsynthetic modifications highlights that the highest activity gains are obtained with minor leaching. Furthermore, a highly zeolitic character, as determined by bulk XRD, is beneficial, but not crucial, in the conversion of α-pinene. The alkaline treatments not only result in a higher overall activity, but also a more functional external surface area, attaining up to four times the pinene conversions per square nanometer. The efficiency of the hierarchical USY zeolite is concomitantly demonstrated in the conversion of limonene and turpentine oil, which emphasizes its industrial potential.

  17. Oxygen and hydrogen isotope geochemistry of zeolites

    Science.gov (United States)

    Karlsson, Haraldur R.; Clayton, Robert N.

    1990-01-01

    Oxygen and hydrogen isotope ratios for natural samples of the zeolites analcime, chabazite, clinoptilolite, laumontite, mordenite, and natrolite have been obtained. The zeolite samples were classified into sedimentary, hydrothermal, and igneous groups. The ratios for each species of zeolite are reported. The results are used to discuss the origin of channel water, the role of zeolites in water-rock interaction, and the possibility that a calibrated zeolite could be used as a low-temperature geothermometer.

  18. Zeolite ITQ-30

    OpenAIRE

    Corma, Avelino; Díaz Cabañas, María José

    2005-01-01

    [EN] The invention relates to a laminar microporous crystalline zeolite material known as ITQ-30 which, as when synthesized, has a chemical composition in the anhydrous state with the following molar relations: x (M 1/n XO 2 ): y YO 2 . SiO 2 z R, wherein: x represents a value less than 0.1, which can be equal to zero; y has a value of less than 0.1, which can be equal to zero; z has a value of less than 0.1; M is selected from among H + , NH 4+ , one or more +n inorganic cations and combinat...

  19. Performance of ultrasonic – Treated nano-zeolites employed in the preparation of dimethyl ether

    Directory of Open Access Journals (Sweden)

    Sanaa M. Solyman

    2013-06-01

    Full Text Available Catalytic dehydration of methanol to dimethyl ether was carried out over nano-zeolites and their modified samples via ultrasonic technique. Parent H-Beta and Parent H-Mordenite zeolites are used as synthesized and after sonication. H-Mordenite sonicated for 20 and 120 min whereas H-Beta sonicated for 20 min only. The reaction temperature was varied between 100 and 225 °C at three different contact times. The different catalyst samples were characterized using: XRD, FTIR, TEM, SEM and NH3-TPD techniques. The results revealed that sonication of parent zeolite samples affects on the unit cell dimensions and their crystal size. FTIR-spectroscopic analysis indicated that sonication may decrease the pore opening and cause framework structure defects. TEM and SEM micrographs showed that sonication broke-up and re-ordered zeolite crystals with longer time resulted in a different morphology relative to parents and also change the particle size. Sonicated samples have a good performance in methanol dehydration with complete conversion and complete selectivity to dimethyl ether at lower temperature relative to the corresponding parent zeolites. TPD results indicated that the concentration of strong acid sites decreased in sonicated H-Mordenite samples leading to an increase of their catalytic activity and the selectivity to DME. On the other hand, ultrasonic treatment of H-Beta sample decreased its catalytic activity.

  20. Process for preparing noble metal-containing zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Tsao, Y.-Y.P.

    1989-11-21

    The patent describes a process for preparing noble metal- containing zeolite material of enhanced noble metal dispersion. It comprises: contacting a zeolite material with a cationic noble metal complex; calcining the resulting material in the presence of molecular oxygen at about 300 {degrees} to 375 {degrees} C. for a period of time sufficient to cause decomposition of the noble metal complex into a product containing cationic noble metal species; purging oxygen and water from the resulting material by exposing the material to an atmosphere of inert gas at 200 {degrees} to 350 {degrees} C. and reducing the resulting material with hydrogen at 200 {degrees} to 350 {degrees} C. for a period of time sufficient to reduce the cationic noble metal species to highly dispersed free metal. This paper also describes the same process wherein the zeolite is selected from the group consisting of zeolite beta, ZSM-5, ZSM-11, ZSM-12, ZSM-18, ZSM- 20, ZSM-22, ZSM-23, ZSM-35 and ZSM-48. This paper also describes the same process wherein the noble metal is selected from the group consisting of platinum, palladium, rhodium, ruthenium, silver, rhenium, and iridium.

  1. Mesostructured zeolites: bridging the gap between zeolites and MCM-41.

    Science.gov (United States)

    Prasomsri, Teerawit; Jiao, Wenqian; Weng, Steve Z; Garcia Martinez, Javier

    2015-05-28

    Surfactant-templating is one of the most versatile and useful techniques to implement mesoporous systems into solid materials. Various strategies based on various interactions between surfactants and solid precursors have been explored to produce new structures. Zeolites are invaluable as size- and shape-selective solid acid catalysts. Nevertheless, their micropores impose limitations on the mass transport of bulky feed and/or product molecules. Many studies have attempted to address this by utilizing surfactant-assisting technology to alleviate the diffusion constraints. However, most efforts have failed due to micro/mesopore phase separation. Recently, a new technique combining the uses of cationic surfactants and mild basic solutions was introduced to synthesise mesostructured zeolites. These materials sustain the unique characteristics of zeolites (i.e., strong acidity, crystallinity, microporosity, and hydrothermal stability), including tunable mesopore sizes and degrees of mesoporosity. The mesostructured zeolites are now commercially available through Rive Technology, and show superior performance in VGO cracking. This feature article provides an overview of recent explorations in the introduction of mesoporosity into zeolites using surfactant-templating techniques. Various porous materials, preparation methods, physical and catalytic properties of mesostructured zeolites will be discussed. PMID:25866848

  2. Zeolite Catalyzed Aldol Condensation Reactions

    Directory of Open Access Journals (Sweden)

    Adedayo I. Inegbenebor

    2015-03-01

    Full Text Available The review is based on the description of zeolite structure, uses, synthesis, and catalytic aldol reaction in aldol condensation. An internal aldolcondensation reaction has been achieved over ZSM-5 zeolite with high silica-alumina ratio at 350oC. It therefore follows that zeolite canfunction as a catalyst in aldol type condensation reactions and that weak acid sites as well as a small number of active sites favor the aldolcondensation reaction of carbonyl compounds. However, the mixed condensation product was found to be favored at temperatures above 300oCand the self-condensation of ethanal to crotonaldehyde was favored at temperatures below 300oC. It has also been suggested that both Brønstedand Lewis acids are involved in aldol reactions with Lewis acid sites the most probable catalytic sites. The zeolite group of minerals has founduse in many chemical and allied industries.

  3. Astaxanthin diferulate as a bifunctional antioxidant

    DEFF Research Database (Denmark)

    Papa, T.B.R.; Pinho, V.D.; Nascimento, E.P. do;

    2015-01-01

    Abstract Astaxanthin when esterified with ferulic acid is better singlet oxygen quencher with k2 = (1.58 ± 0.1) 10(10) L mol(- 1)s(- 1) in ethanol at 25°C compared with astaxanthin with k2 = (1.12 ± 0.01) 10(9) L mol(- 1)s(- 1). The ferulate moiety in the astaxanthin diester is a better radical s....... The mutual enhancement of antioxidant activity for the newly synthetized astaxanthin diferulate becoming a bifunctional antioxidant is rationalized according to a two-dimensional classification plot for electron donation and electron acceptance capability....

  4. MOFs as multifunctional catalysts: one-pot synthesis of menthol from citronellal over a bifunctional MIL-101 catalyst.

    Science.gov (United States)

    Cirujano, F G; Llabrés i Xamena, F X; Corma, A

    2012-04-14

    A bifunctional MOF catalyst containing coordinatively unsaturated Cr(3+) sites and palladium nanoparticles (Pd@MIL-101) has been used for the cyclization of citronellal to isopulegol and for the one-pot tandem isomerization/hydrogenation of citronellal to menthol. The MOF was found to be stable under the reaction conditions used, and the results obtained indicate that the performance of this bifunctional solid catalyst is comparable with other state-of-the-art materials for the tandem reaction: Full citronellal conversion was attained over Pd@MIL-101 in 18 h, with 86% selectivity to menthols and a diastereoselectivity of 81% to the desired (-)-menthol, while up to 30 h were necessary for attaining similar values over Ir/H-beta under analogous reaction conditions. PMID:22382815

  5. Síntesis y caracterización de la zeolita Beta

    Directory of Open Access Journals (Sweden)

    Mahiceth Quintero

    2012-12-01

    Full Text Available Beta zeolite is normally obtained with Si/Al 5 and infinity ratios, using tetraethylammonium (TEA as templante. Important parameters in the TEA-Beta synthesis are alkali cation concentration, the type of cation used, the concentration of hydroxide, and the amount of templante, the temperature and the source of silica used. The synthesis with ratios Si:Al above 80 are generally quite difficult to achieve, but have recently been reported with all silica synthesis using TEA as templante. Their main applications are in the catalytic processes of hydrocarbon transformation (alkylation, in the inorganic membrane preparation and like “seed” in the synthesis of other zeolites. It is a microporous solid, with a unique system of channels and characteristic a chemical composition. In this work Beta zeolite was synthesized with aluminum sulfate like aluminum source. The phase identified in the pattern of X-ray diffraction obtained, coincides with the structure of the zeolite Beta.

  6. Bifunctional electrocatalyst for oxygen/air electrodes

    International Nuclear Information System (INIS)

    Highlights: • Nano-Silver powder was prepared by chemical method. • Ag catalyst was characterized by SEM and XRD studies. • Ag was investigated as bi-functional electrocatalyst for oxygen/air electrodes. • Ag shows good electrochemical activity towards OER and ORR reactions. - Abstract: Nano-Silver powder has been studied as bi-functional electrocatalyst for both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in alkaline medium. Ag nano-powder has been prepared by a simple wet chemical method with Silver nitrate as precursor and Glucose as reducing agent. X-ray Diffraction and Scanning Electron Microscopy studies were carried out to characterize the Silver catalyst. Electrochemical oxygen evolution characterization shows anodic peak typically at the range between 0.350 and 0.514 V Vs Hg/HgO corresponding to Silver oxidation followed by the onset of oxygen evolution at 0.706 V. Oxygen reduction reaction studies carried out using Rotating Disc Electrode (RDE) confirm the four electron reaction mechanism. Ag catalyst shows promising characteristics for oxygen evolution and oxygen reduction

  7. 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...... on the four different zeolite supports H-beta, H-Y, H-mordenite, and H-ZSM-5 with 1–10 wt% vanadia loading were prepared and characterized by nitrogen physisorption, X-ray powder diffraction, scanning electron  microscopy, ammonia temperature-programmed desorption, Raman spectroscopy and UV...

  8. Preparation by the nano-casting process of novel porous carbons from large pore zeolite templates

    Energy Technology Data Exchange (ETDEWEB)

    F Gaslain; J Parmentier; V Valtchev; J Patarin [Laboratoire de Materiaux a Porosite Controlee (LMPC), UMR CNRS 7016, ENSCMu Universite de Haute Alsace, 3 rue Alfred Werner, 68093 Mulhouse Cedex, (France); C Vix Guterl [Institut de Chimie des Surfaces et Interfaces (ICSI), UPR CNRS 9069, 15 rue Jean Starky, 68057 Mulhouse Cedex (France)

    2005-07-01

    The development of new growing industrial applications such as gas storage (e.g.: methane or hydrogen) or electric double-layer capacitors has focussed the attention of many research groups. For this kind of application, porous carbons with finely tailored micro-porosity (i.e.: pore size diameter {<=} 1 nm) appear as very promising materials due to their high surface area and their specific pore size distribution. In order to meet these requirements, attention has been paid towards the feasibility of preparing microporous carbons by the nano-casting process. Since the sizes and shapes of the pores and walls respectively become the walls and pores of the resultant carbons, using templates with different framework topologies leads to various carbon replicas. The works performed with commercially available zeolites employed as templates [1-4] showed that the most promising candidate is the FAU-type zeolite, which is a large zeolite with three-dimensional channel system. The promising results obtained on FAU-type matrices encouraged us to study the microporous carbon formation on large pore zeolites synthesized in our laboratory, such as EMC-1 (International Zeolite Association framework type FAU), zeolite {beta} (BEA) or EMC-2 (EMT). The carbon replicas were prepared following largely the nano-casting method proposed for zeolite Y by the Kyotani research group [4]: either by liquid impregnation of furfuryl alcohol (FA) followed by carbonization or by vapour deposition (CVD) of propylene, or by an association of these two processes. Heat treatment of the mixed materials (zeolite / carbon) could also follow in order to improve the structural ordering of the carbon. After removal of the inorganic template by an acidic treatment, the carbon materials obtained were characterised by several analytical techniques (XRD, N{sub 2} and CO{sub 2} adsorption, electron microscopy, etc...). The unique characteristics of these carbons are discussed in details in this paper and

  9. Characterization of Mexican zeolite minerals

    International Nuclear Information System (INIS)

    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. Comparison of adsorption efficiency of Triton X-100 surfactant from industrial wastewater using synthetic and natural zeolites: isotherm and kinetic studies

    Directory of Open Access Journals (Sweden)

    A Shahbazi

    2016-01-01

    Full Text Available Background and Objectives: Rapid growing of Triton X-100 application in industries results in its appearance in effluents  and threaten the aqueous ecosystems. Triton X-100 is not biodegradable and can accumulate in food chain. Materials and Methods: In this study, sorption capacity of six synthesized zeolites with different regular porous structure was studied for triton X-100 (TX-100 surfactant and the results were compared with Clinoptilolite natural zeolite of Damavand region. Results: Within all zeolite studied, Beta(200 showed the highest sorption capacity (about 575 mg/g, which is due to its regular pore structure with large pore diameter, channel intersections, high SiO2/Al2O3 ratio and high surface area. Langmuir monolayer isotherm and pseudo-second-order kinetic equation could provide well-fitted to the experimental data in simulating adsorption behavior of TX-100 over Beta(200 zeolite. Conclusion: The adsorption feature was internal sorption and the intraparticle diffusion might be a rate-limiting control for Beta(200 zeolite. Results of experiments demonstrated that the hydrophobic zeolites with large pore diameter such as Beta(200 could be effective sorbents for industrial wastewater treatment features.

  11. Zeolite synthesis: an energetic perspective.

    Science.gov (United States)

    Zwijnenburg, Martijn A; Bromley, Stefan T

    2010-11-21

    Taking |D(H(2)O)(x)|[AlSiO(4)] based materials (where D is Li, Na, K, Rb or Cs) as an archetypal aluminosilicate system, we use accurate density functional theory calculations to demonstrate how the substitution of silicon cations in silica, with pairs of aluminium and (alkali metal) cations, changes the energetic ordering of different competing structure-types. For large alkali metal cations we further show that the formation of porous aluminosilicate structures, the so-called zeolites, is energetically favored. These findings unequivocally demonstrate that zeolites can be energetic preferred reaction products, rather than being kinetically determined, and that the size of the (hydrated) cations in the pore, be it inorganic or organic, is critical for directing zeolite synthesis.

  12. Zeolite-dye micro lasers

    CERN Document Server

    Vietze, U; Laeri, F; Ihlein, G; Schüth, F; Limburg, B; Abraham, M

    1998-01-01

    We present a new class of micro lasers based on nanoporous molecular sieve host-guest systems. Organic dye guest molecules of 1-Ethyl-4-(4-(p-Dimethylaminophenyl)-1,3-butadienyl)-pyridinium Perchlorat were inserted into the 0.73-nm-wide channel pores of a zeolite AlPO$_4$-5 host. The zeolitic micro crystal compounds where hydrothermally synthesized according to a particular host-guest chemical process. The dye molecules are found not only to be aligned along the host channel axis, but to be oriented as well. Single mode laser emission at 687 nm was obtained from a whispering gallery mode oscillating in a 8-$\\mu$m-diameter monolithic micro resonator, in which the field is confined by total internal reflection at the natural hexagonal boundaries inside the zeolitic microcrystals.

  13. Nanoscale intimacy in bifunctional catalysts for selective conversion of hydrocarbons

    OpenAIRE

    Zecevic, Jovana; Vanbutsele, Gina; de Jong, Krijn P.; Martens, Johan

    2015-01-01

    The ability to precisely control nanoscale features is increasingly exploited to develop and improve monofunctional catalysts1–4. Striking effects might also be expected in the case of bifunctional catalysts, which play an important role in hydrocracking of fossil and renewable hydrocarbon sources to provide high-quality diesel fuel5–7. Such bifunctional hydrocracking catalysts contain metal sites and acid sites, and for more than 50 years the so-called ‘intimacy criterion’8 has dictated the ...

  14. Nanoparticle Superlattices as Efficient Bifunctional Electrocatalysts for Water Splitting.

    Science.gov (United States)

    Li, Jun; Wang, Yongcheng; Zhou, Tong; Zhang, Hui; Sun, Xuhui; Tang, Jing; Zhang, Lijuan; Al-Enizi, Abdullah M; Yang, Zhongqin; Zheng, Gengfeng

    2015-11-18

    The solar-driven water splitting process is highly attractive for alternative energy utilization, while developing efficient, earth-abundant, bifunctional catalysts for both oxygen evolution reaction and hydrogen evolution reaction has remained as a major challenge. Herein, we develop an ordered CoMnO@CN superlattice structure as an efficient bifunctional water-splitting electrocatalyst, in which uniform Co-Mn oxide (CoMnO) nanoparticles are coated with a thin, continuous nitrogen-doped carbon (CN) framework. The CoMnO nanoparticles enable optimized OER activity with effective electronic structure configuration, and the CN framework serves as an excellent HER catalyst. Importantly, the ordered superlattice structure is beneficial for enhanced reactive sites, efficient charge transfer, and structural stability. This bifunctional superlattice catalyst manifests optimized current densities and electrochemical stability in overall water splitting, outperforming most of the previously reported single- or bifunctional electrocatalysts. Combining with a silicon photovoltaic cell, this CoMnO@CN superlattice bifunctional catalyst enables unassisted solar water splitting continuously for ∼5 days with a solar-to-hydrogen conversion efficiency of ∼8.0%. Our discovery suggests that these transition metal oxide-based superlattices may serve as a unique structure modality for efficient bifunctional water splitting electrocatalysts with scale-up potentials. PMID:26496655

  15. Nanoparticle Superlattices as Efficient Bifunctional Electrocatalysts for Water Splitting.

    Science.gov (United States)

    Li, Jun; Wang, Yongcheng; Zhou, Tong; Zhang, Hui; Sun, Xuhui; Tang, Jing; Zhang, Lijuan; Al-Enizi, Abdullah M; Yang, Zhongqin; Zheng, Gengfeng

    2015-11-18

    The solar-driven water splitting process is highly attractive for alternative energy utilization, while developing efficient, earth-abundant, bifunctional catalysts for both oxygen evolution reaction and hydrogen evolution reaction has remained as a major challenge. Herein, we develop an ordered CoMnO@CN superlattice structure as an efficient bifunctional water-splitting electrocatalyst, in which uniform Co-Mn oxide (CoMnO) nanoparticles are coated with a thin, continuous nitrogen-doped carbon (CN) framework. The CoMnO nanoparticles enable optimized OER activity with effective electronic structure configuration, and the CN framework serves as an excellent HER catalyst. Importantly, the ordered superlattice structure is beneficial for enhanced reactive sites, efficient charge transfer, and structural stability. This bifunctional superlattice catalyst manifests optimized current densities and electrochemical stability in overall water splitting, outperforming most of the previously reported single- or bifunctional electrocatalysts. Combining with a silicon photovoltaic cell, this CoMnO@CN superlattice bifunctional catalyst enables unassisted solar water splitting continuously for ∼5 days with a solar-to-hydrogen conversion efficiency of ∼8.0%. Our discovery suggests that these transition metal oxide-based superlattices may serve as a unique structure modality for efficient bifunctional water splitting electrocatalysts with scale-up potentials.

  16. Synthesis and testing of nanosized zeolite Y

    Science.gov (United States)

    Karami, Davood

    This work focuses on the synthesis and testing of nanosized zeolite Y. The synthesis formulations of faujasite-type structure of zeolite Y prepared in nanosized form are described. The synthetic zeolite Y is the most widely employed for the preparation of fluid catalytic cracking (FCC) catalysts. The synthesis of zeolite Y is very complicated process. The mean particle size of zeolite Y is 1800 nm. The major challenge of this work involved reducing this average particle size to less than 500 nm. The preliminary experiments were conducted to obtain the pure zeolite Y using the soluble silicates as a silica source. This was achieved by applying the experimental design approach to study the effects of many parameters. The ageing time turned out to be the most significant variable affecting product purity. Based on the preliminary results, a detailed investigation was carried out to determine the effects of silica-alumina precursor preparations on zeolite Y synthesis. Aluminosilicate precursors were prepared by gelling and precipitation of soluble silicate. The as-prepared precursors were used for the hydrothermal synthesis of zeolite Y. The procedure of the precipitation of soluble silicate yielded pure zeolite Y at the conventional synthesis conditions. The extent of purity of zeolite Y depends on the surface areas of aluminosilicate precursors. A novel approach to zeolite Y synthesis was employed for the preparation of the pure nanosized zeolite Y. This was achieved by applying the method of impregnation of precipitated silica. This novel method of impregnation for zeolite Y preparation allows eliminating the vigorous agitation step required for the preparation of a homogeneous silica solution, thereby simplifying the synthesis of zeolite Y in one single vessel. In case of the synthesis of nanosized zeolite Y, the effect of varying the organic templates on the formation of nanosized particles of zeolite Y was investigated, while all other reaction parameters were

  17. Hydrodewaxing with mixed zeolite catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Chester, A.W.; McHale, W.D.; Yen, J.H.

    1986-03-11

    A process is described for catalytically dewaxing a hydrocarbon lubricating oil feedstock comprising contacting the feedstock with a dewaxing catalyst, the dewaxing catalyst comprising, in combination: (a) a zeolite catalyst having a Constraint Index not less than 1, (b) an acidic catalytic material selected from the group consisting of Mordenite, TEA Mordenite, Dealuminized Y, Ultrastable Y, Rare Earth Y, amorphous silica-alumina chlorinated alumina, ZSM-4 and ZSM-20, and (c) a hydrogenation component, and recovering a dewaxed product. A process is also described for catalytically dewaxing a hydrocarbon lubricating oil feedstock comprising contacting the feedstock with a dewaxing catalyst, the dewaxing catalyst comprising, in combinations: (a) a first zeolite catalyst selected from the group consisting of ZSM-5, ZMS-11, ZSM-12, ZSM-22, ZSM-23, ZSM-34, ZSM-35, ZSM-38, ZSM-48, TMA Offretite and Erionite, (b) a second catalyst selected from the group consisting of ZSM-12, ZSM-22, ZSM-38 and ZSM-48, the second zeolite catalyst being different from the first zeolite catalyst, and (c) a hydrogenation component, and recovering a dewaxed product.

  18. 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

  19. Zeolite and high silica zeotype microporous materials used for the removal of toxic elements

    International Nuclear Information System (INIS)

    Breakthrough properties and kinetics of barium (Ba/sup 2+/ sorption in high silica zeolite-beta and zeotype beta-Fe and beta-B have been studied. Exchange diffusion coefficients and activation energies were measured at temperatures between 298 to 333 K and thermodynamic parameters delta S/sup */ and delta G/sup */ were also calculated. The sodium forms of zeolite-beta, zeotype materials beta-B and beta-Fe were synthesized hydrothermally from the aqueous silicate gels of Na/sub 2/O-SiO/sub 2/-Al/sub 2/O/sub 3/-B/sub 2/O/sub 3/-Fe/sub 2/O/sub 3/-[(C/sub 4/H/sub 9)/ sub 4/ N]/sub 2/O-H/sub 2/O. The crystalline products have been characterised by a wide range of analytical techniques like X-ray powder diffraction (DSC). /sup 57/Fe Moessbauer spectroscopic studies on synthesized and calcined samples have confirmed the uniform dispersion of Fe/sup 3+/ ion sin the tetrahedral framework of zeotype beta-Fe. (authors)

  20. Process for producing zeolite adsorbent and process for treating radioactive liquid waste with the zeolite adsorbent

    International Nuclear Information System (INIS)

    Zeolite is contacted with an aqueous solution containing at least one of copper, nickel, cobalt, manganese and zinc salts, preferably copper and nickel salts, particularly preferably copper salt, in such a form as sulfate, nitrate, or chloride, thereby adsorbing the metal on the zeolite in its pores by ion exchange, then the zeolite is treated with a water-soluble ferrocyanide compound, for example, potassium ferrocyanide, thereby forming metal ferrocyanide on the zeolite in its pores. Then, the zeolite is subjected to ageing treatment, thereby producing a zeolite adsorbent impregnated with metal ferrocyanide in the pores of zeolite. The adsorbent can selectively recover cesium with a high percent cesium removal from a radioactive liquid waste containing at least radioactive cesium, for example, a radioactive liquid waste containing cesium and such coexisting ions as sodium, magnesium, calcium and carbonate ions at the same time at a high concentration. The zeolite adsorbent has a stable adsorbability for a prolonged time

  1. 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

    During the last years, several new routes to produce zeolites with controlled mesoporosity have appeared. Moreover, an improved catalytic performance of the resulting mesoporous zeolites over conventional zeolites has been demonstrated in several reactions. In most cases, the mesoporous zeolites...... exhibit higher catalytic activity, but in some cases also improved selectivity and longer catalyst lifetime has been reported. The beneficial effects of introducing mesopores into the zeolites has in most instances been attributed to improved mass transport to and from the active sites located...... 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...

  2. Resonant diffusion of normal alkanes in zeolites: Effect of the zeolite structure and alkane molecule vibrations

    CERN Document Server

    Tsekov, R

    2015-01-01

    Diffusion of normal alkanes in one-dimensional zeolites is theoretically studied on the basis of the stochastic equation formalism. The calculated diffusion coefficient accounts for the vibrations of the diffusing molecule and zeolite framework, molecule-zeolite interaction, and specific structure of the zeolite. It is shown that when the interaction potential is predominantly determined by the zeolite pore structure, the diffusion coefficient varies periodically with the number of carbon atoms of the alkane molecule, a phenomenon called resonant diffusion. A criterion for observable resonance is obtained from the balance between the interaction potentials of the molecule due to the atomic and pore structures of the zeolite. It shows that the diffusion is not resonant in zeolites without pore structure, such as ZSM-12. Moreover, even in zeolites with developed pore structure no resonant dependence of the diffusion constant can be detected if the pore structure energy barriers are not at least three times high...

  3. Bimetallic Pt-Ni catalysts supported on usy zeolite for n-hexane isomerization

    Directory of Open Access Journals (Sweden)

    F. V. Barsi

    2009-06-01

    Full Text Available Isomerization of linear alkanes has had considerable importance for the refining industry because the isomers formed in this reaction have high octane number. Most works reported in the literature studied the use of bifunctional catalysts, i.e., ones that have acid sites and metallic sites. In this study, bifunctional monometallic (Ni or Pt and bimetallic catalysts (Pt-Ni, using HUSY zeolite as the support, were prepared in order to verify the role of the metal content and composition on the catalytic properties for n-hexane isomerization. The method used for metal dispersion in the zeolite was competitive ion exchange using ammine complexes [Ni(NH36]Cl2 and [Pt(NH34]Cl2 as precursors. Four series of catalysts with constant atomic metal content had total metal amounts between 130 and 280 µmol M/g cat. Catalysts were characterized by temperature programmed reduction (TPR and subjected to catalytic evaluation for n-hexane isomerization at 250 ºC and 1 atm using H2/C6 = 9 molar ratio. TPR results show an easier reducibility of Ni+2 cations in the presence of Pt, which was evidenced by the displacement of the reduction peak of those cations towards lower temperatures in bimetallic catalysts. The bimetallic catalysts presented a higher activity in the isomerization of n-hexane when compared to the monometallic ones, as well better stability as the Pt content in the solid increases. The results of the activity as a function of the Pt content in the bimetallic catalysts show a maximum value around 50% of Pt. An addition of Pt above this critical value leads to a small decrease of the catalytic activity.

  4. Catalytic Acylation of Ethylidenecyclohexane over Zeolite Catalysts

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Some environmentally friendly catalysts such as HY and H-β zeolites,various cation-exchanged β zeolites,and some other solids have been used in the acylation reaction of ethylidenecyclohexane with acetic anhydride at room temperature to synthesize 3-(1-cyclohexenyl)-2-butanone instead of conventional catalysts.The effect of the amount of HY zeolite used on the acylation reaction was investigated.The yield of the acylated product was 72% in the case of n(ethylidenecyclohexane)∶n(acetic anhydride)∶m(HY zeolite)=1 mmol∶10 mmol∶0.100 g,reaction temperature:25 ℃,and reaction time:2 h.The regenerated HY zeolite showed almost the same catalytic activity as the fresh zeolite.

  5. Zeolites for Sensors for Reducing Gases

    Institute of Scientific and Technical Information of China (English)

    Ralf Moos; Kathy Sahner; Gunter Hagen; Andreas Dubbe

    2006-01-01

    Due to their unique properties, zeolites can be used either as passive filters to greatly enhance selectivity or as very selective sensor materials. Some well known principles are briefly reviewed and the following three novel application modes are discussed. Zeolites can be applied as cover layers for specificity improvement of p-type semiconducting hydrocarbon sensors. Furthermore, a novel combination of metal oxides with zeolites leading to a very selective hydrocarbon sensor is described. In this application, it is shown that the interface chromium oxide / zeolite plays an essential role. And, in a very recent approach, Na+ ion conducting zeolites are applied as an auxiliary phase in a potentiometric gas sensor. The cell voltage shows a Nernstian response, which is selective towards propane. Here, the proposed mechanism assumes Na+ activity changes in the zeolite pores due to hydrocarbon sorption.

  6. Zeolite from fly ash: synthesis and characterization

    Indian Academy of Sciences (India)

    Keka Ojha; Narayan C Pradhan; Amar Nath Samanta

    2004-12-01

    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. The synthesis conditions were optimized to obtain highly crystalline zeolite with maximum BET surface area. The maximum surface 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.

  7. [What a physician should know about zeolites].

    Science.gov (United States)

    Boranić, M

    2000-01-01

    Zeolites are natural and synthetic hydrated crystalline aluminosilicates endowed with absorptive and ion exchange properties. They have found numerous and multifarous applications--in industry as catalysts and absorbents, in water sanitation for the removal of ammonia and heavy metals, in agriculture as fertilizers, and in animal husbandry as the absorbents of excreted material and as food additives. Medical applications have included the use in filtration systems for anesthesia or dialysis and as the contrast materials in NMR imaging. Recently, zeolite powders for external use have found application as deodorants, antimycotic agents and wound dressings. Peroral use of encapsulated zeolite powders enriched with vitamins, oligoelements or other ingredients has been claimed to exert beneficial medical effects. Ingestion of zeolites may be considered analogous to the clay eating (geophagia), considered in traditional medicine as a remedy for various illnesses. Being amphoteric, zeolites are partly soluble in acid or alkaline media, but within the physiological pH range the solubility is generally low. Minimal amounts of free aluminium or silicium from the ingested zeolites are resorbed from the gut. The bulk of ingested zeolite probably remains undissolved in the gut. In view of the ion exchange properties, zeolites may be expected to change the ionic content, pH and buffering capacity of the gastrointestinal secretions and to affect the transport through the intestinal epithelium. In addition, zeolites could affect the bacterial flora and the resorption of bacterial products, vitamins and oligoelements. The contact of zeolite particles with gastrointestinal mucosa may elicit the secretion of cytokines with local and systemic actions. Reactive silicium ions might react with biomolecules of the intestinal epithelium, and if resorbed, do so in other cells. Mutagenic and carcinogenic effects of zeolite particles have been described, resembling such effects of asbestos

  8. Catalytic Acylation of Anisole over Some Zeolites

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    4-Methoxyacetophenone(4-MAP) was synthesized by the acylation of anisole with acetic anhydride in the presence of HY zeolite.The addition of an appropriate amount of some solvent such as dichloromethane,chloroform,carbon disulfide or chlorobenzene to the reaction system can improve the yield of the acylated product to a certain extent.HY zeolite used can be recovered,and reused after being regenerated,obtaining almost the same yield of 4-MAP as the fresh zeolite.

  9. Bifunctional Nanostructured Base Catalysts: Opportunities for BioFuels

    Energy Technology Data Exchange (ETDEWEB)

    Connor, William

    2010-12-30

    ABSTRACT This research studied and develop novel basic catalysts for production of renewable chemicals and fuels from biomass. We will focus on the development of unique porous structural-base catalysts formed by two techniques: from (mixed) metal-oxide bases and by nitrogen substitution for oxygen in zeolites. These catalysts will be compared to conventional solid base materials for aldol condensation, catalytic fast pyrolysis, and transesterification reactions. These reactions are important in processes that are currently being commercialized for production of fuels from biomass and will be pivotal in future biomass conversion to fuels and chemicals. Specifically, we have studied the aldol-condensation of acetone with furfural over oxides and zeolites, the conversion of sugars by rapid pyrolysis over zeolites and the trans-esterification of vegetable oil with methanol over mixed oxide catalysts. Our previous research has indicated that the base strength of framework nitrogen in nitrogen-substituted zeolites (NH-zeolites) is nearly twice as strong as in standard zeolites. Nitrogen substituted catalysts have been synthesized from several zeolites (including FAU, MFI, BEA, and LTL) using NH3 treatment.

  10. 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.

  11. Adsorption of radioactive iodide by natural zeolites

    International Nuclear Information System (INIS)

    Two natural zeolites from Iranian deposits (clinoptilolite and natrolite) were characterized and their ability for adsorption of iodide from nuclear wastewaters was evaluated. The adsorption behavior was studied on natural and modified zeolites by γ-spectrometry using 131I as radiotracer. Adsorption isotherms and distribution coefficient (Kd) were measured. The results showed that clinoptilolite is a more promising zeolite for removal of iodide compared to natrolite. Furthermore, the adsorption was higher in silver, lead and thallium forms, whereas the lowest desorption was observed in lead modified zeolite. (author)

  12. Removal of Toluene over NaX Zeolite Exchanged with Cu2+

    Directory of Open Access Journals (Sweden)

    Douglas Romero

    2015-09-01

    Full Text Available Toluene is a major air pollutant emitted from painting and metal coating processes and might have some health effects. Adsorption and catalytic complete oxidation are promising ways to retain or convert toluene into harmless products. The present work aims to develop a bifunctional material which can be used as an adsorbent and catalyst for low-temperature toluene removal. Copper zeolites were obtained by exchanging the sodium in the parent NaX zeolite with copper from aqueous solutions of Cu(NO32∙2.5H2O. Several characterization techniques, H2-TPR, XPS, XRD and N2 physisorption, were used in order to evaluate the redox, surface, structural and textural properties of the materials, respectively. The various materials were tested in adsorption and catalytic processes. The sample with low copper content (1 wt. % exhibited promising features in terms of toluene adsorption capacity and total oxidation. The results can be correlated to the presence of micropores and well-dispersed CuO species.

  13. Natural zeolites - origin and mechanism of action

    International Nuclear Information System (INIS)

    The chemical composition and the crystalline structure explain ion exchange, adsorption selectivity, acidity and stability of zeolites. The properties of the two most important natural zeolites, e.g. Klinoptilolite and mordenite are described in detail. This includes petrography, chemical modification and applications. (orig.)

  14. Moessbauer spectroscopy study of a natural zeolite

    International Nuclear Information System (INIS)

    With the help of Moessbauer spectroscopy, it was established that iron in natural zeolites occupies positions in the aluminosilicate structure in place of aluminium; the positions of iron are octahedricals, and the valency is 3+; it was shown too, that the zeolite is geometrically stable to acid treatment, notwithstanding the formation of vacancies during acid treatments. (author)

  15. 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 nanopart......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...... template and structure directing agent and isolating the resulting zeolite, zeolite-like or zeotype encapsulated metal nanoparticles...

  16. Preparation of Zeolite-metal Composite Membrane

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A NaA zeolite membrane was synthesized on the surface of the stainless steel slab. The membrane was characterized by XRD and SEM. The membrane was continuous and highly intergrown. The size of NaA zeolite crystals was about 5 ~ 6 mm.

  17. Dynamics Studies on Molecular Diffusion in Zeolites

    Institute of Scientific and Technical Information of China (English)

    王秋霞; 樊建芬; 肖鹤鸣

    2003-01-01

    A review about the applications of molecular dynamics(MD)simulation in zeolites is presented. MD simulation has been proved to be a useful tool due to its applications in this field for the recent two decades. The fundamental theory of MD is introduced and the hydrocarbon diffusion in zeolites is mainly focused on in this paper.

  18. Nuclear waste treatment using Iranian natural zeolites (a brief review)

    International Nuclear Information System (INIS)

    The natural zeolite research in Iran is a relatively new subject, which has started about 12 years ago. This paper intends to review some performed research in the field of nuclear wastewater using zeolites in our laboratory. The results of various research work on the natural zeolites as well as on some relevant synthetic zeolites will be discussed in this article. (author)

  19. Ion exchange investigation on the Syrian zeolite

    International Nuclear Information System (INIS)

    We have studied the ion exchange process by using Syrian zeolite from the region of Tell-Assis with four solutions containing these ions: Ag+, NH4+, Pb2+, and Cu2+. It was found that the required time to reach the equilibrium is 6-8 hours, and depends on the type of ion. the exchange capacity mainly depends on the type of ions, and range between 0.5-1.57 m. mol/g. The effect of pH on ion exchange capacity was obvious and the best results were reached when the pH ranged between 5+ will exchange with univalent and bivalent ions in the zeolite, whereas the bivalent ions as Pb+2 will preferentially exchange with the bivalent ions in the zeolite. we concluded that the used zeolite gave good results compared with some known zeolite. (Author)

  20. Single flexible nanofiber to simultaneously realize electricity-magnetism bifunctionality

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Ming; Sheng, Shujuan; Ma, Qianli; Lv, Nan; Yu, Wensheng; Wang, Jinxian; Dong, Xiangting; Liu, Guixia, E-mail: wenshengyu2009@sina.com, E-mail: dongxiangting888@163.com [Key Laboratory of Applied Chemistry and Nanotechnology at Universities of Jilin Province, Changchun University of Science and Technology, Changchun (China)

    2016-03-15

    In order to develop new-typed multifunctional composite nanofibers, PANI/Fe{sub 3}O{sub 4}/PVP flexible bifunctional composite nanofibers with simultaneous electrical conduction and magnetism have been successfully fabricated via a facile electrospinning technology. Polyvinyl pyrrolidone (PVP) is used as a matrix to construct composite nanofibers containing different amounts of polyaniline (PANI) and Fe{sub 3}O{sub 4} nanoparticles (NPs). The bifunctional composite nanofibers simultaneously possess excellent electrical conductivity and magnetic properties. The electrical conductivity reaches up to the order of 10{sup -3} S·cm{sup -1}. The electrical conductivity and saturation magnetization of the composite nanofibers can be respectively tuned by adding various amounts of PANI and Fe{sub 3}O{sub 4} NPs. The obtained electricity-magnetism bifunctional composite nanofibers are expected to possess many potential applications in areas such as electromagnetic interference shielding, special coating, microwave absorption, molecular electronics and future nanomechanics. More importantly, the design concept and construct technique are of universal significance to fabricate other bifunctional one-dimensional nanostructures. (author)

  1. Bifunctional mesoporous silicas with clearly distinguished localization of grafted groups

    Science.gov (United States)

    Roik, N. V.; Belyakova, L. A.

    2013-12-01

    Bifunctional mesoporous silicas with clearly distinguished localization of grafted groups on the surface of particles and inside their pores were obtained by means of sol-gel synthesis with postsynthetic vapor-phase treatment in vacuum. It was found that the synthesized materials have the hexagonally ordered porous structure typical of MCM-41 type silica.

  2. Nanoscale intimacy in bifunctional catalysts for selective conversion of hydrocarbons

    NARCIS (Netherlands)

    Zecevic, Jovana; Vanbutsele, Gina; de Jong, Krijn P.; Martens, Johan A.

    2015-01-01

    The ability to control nanoscale features precisely is increasingly being exploited to develop and improve monofunctional catalysts(1-4). Striking effects might also be expected in the case of bifunctional catalysts, which are important in the hydrocracking of fossil and renewable hydrocarbon source

  3. 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.

  4. Tin-containing zeolites are highly active catalysts for the isomerization of glucose in water

    Energy Technology Data Exchange (ETDEWEB)

    Moliner, Manuel [California Inst. of Technology (CalTech), Pasadena, CA (United States); Roman-Leshkov, Yuriy [California Inst. of Technology (CalTech), Pasadena, CA (United States); Davis, Mark E. [California Inst. of Technology (CalTech), Pasadena, CA (United States)

    2010-04-06

    The isomerization of glucose into fructose is a large-scale reaction for the production of high-fructose corn syrup (HFCS; reaction performed by enzyme catalysts) and recently is being considered as an intermediate step in the possible route of biomass to fuels and chemicals. Here, it is shown that a large-pore zeolite that contains tin (Sn-Beta) is able to isomerize glucose to fructose in aqueous media with high activity and selectivity. Specifically, a 10% (wt/wt) glucose solution containing a catalytic amount of Sn-Beta (1:50 Sn:glucose molar ratio) gives product yields of approximately 46% (wt/wt) glucose, 31% (wt/wt) fructose, and 9% (wt/wt) mannose after 30 min and 12 min of reaction at 383 K and 413 K, respectively. This reactivity is achieved also when a 45 wt% glucose solution is used. The properties of the large-pore zeolite greatly influence the reaction behavior because the reaction does not proceed with a medium-pore zeolite, and the isomerization activity is considerably lower when the metal centers are incorporated in ordered mesoporous silica (MCM-41). The Sn-Beta catalyst can be used for multiple cycles, and the reaction stops when the solid is removed, clearly indicating that the catalysis is occurring heterogeneously. Most importantly, the Sn-Beta catalyst is able to perform the isomerization reaction in highly acidic, aqueous environments with equivalent activity and product distribution as in media without added acid. This enables Sn-Beta to couple isomerizations with other acid-catalyzed reactions, including hydrolysis/isomerization or isomerization/dehydration reaction sequences [starch to fructose and glucose to 5-hydroxymethylfurfural (HMF) demonstrated here].

  5. Preparation by the nano casting process of novel porous carbons from large pore zeolite templates

    Energy Technology Data Exchange (ETDEWEB)

    Gaslain, F.; Parmentier, J.; Valtchev, V.; Patarin, J. [Universite de Haute Alsace, Lab. de Materiaux a Porosite Controlee (LMPC), UMR CNRS 7016, ENSCMu, 68 - Mulhouse (France); Vix-Guterl, C. [Institut de Chimie des Surfaces et Interfaces (ICSI), UPR CNRS 9069, 68 - Mulhouse (France)

    2005-07-01

    The development of new growing industrial applications such as gas storage (e.g.: methane or hydrogen) or electric double-layer capacitors has focussed the attention of many research groups. For this kind of application, porous carbons with finely tailored micro-porosity (i.e.: pore size diameter {<=} 1 nm) appear as very promising materials due to their high surface area and their specific pore size distribution. In order to meet these requirements, attention has been paid towards the feasibility of preparing microporous carbons by the nano-casting process. Since the sizes and shapes of the pores and walls respectively become the walls and pores of the resultant carbons, using templates with different framework topologies leads to various carbon replicas. The works performed with commercially available zeolites employed as templates [1-4] showed that the most promising candidate is the FAU-type zeolite, which is a large zeolite with three-dimensional channel system. The promising results obtained on FAU-type matrices encouraged us to study the microporous carbon formation on large pore zeolites synthesized in our laboratory, such as EMC-1 (International Zeolite Association framework type FAU), zeolite {beta} (BEA) or EMC-2 (EMT). The carbon replicas were prepared following largely the nano-casting method proposed for zeolite Y by the Kyotani research group [4]: either by liquid impregnation of furfuryl alcohol (FA) followed by carbonisation or by vapour deposition (CVD) of propylene, or by an association of these two processes. Heat treatment of the mixed materials (zeolite / carbon) could also follow in order to improve the structural ordering of the carbon. After removal of the inorganic template by an acidic treatment, the carbon materials obtained were characterised by several analytical techniques (XRD, N{sub 2} and CO{sub 2} adsorption, electron microscopy, etc...). The unique characteristics of these carbons are discussed in details in this paper and

  6. Evaluación de la estructura porosa de los materiales MCM-22, MCM-36 e ITQ-2 empleando el test catalitico del n-decano Evaluation of the pore structure of MCM-22, MCM-36 and ITQ-2 materials using the n-decane catalytic test

    Directory of Open Access Journals (Sweden)

    Sibele B. C. Pergher

    2003-12-01

    Full Text Available The void structure of zeolites MCM-22, MCM-36 and ITQ-2 were discussed on the bases of catalytic reaction tests. The hydromerization of n-decane on bifunctional Pt/Zeolite Catalysts have been used as model reactions. Beta and ZSM-5 zeolites were used for comparison. It is concluded that all materials show features of 10MR zeolites and have also pores bigger than 12MR in this order MCM-22

  7. Ultrasound-assisted dealumination of zeolite Y

    Indian Academy of Sciences (India)

    M Hosseini; M A Zanjanchi; B Ghalami-Choobar; H Golmojdeh

    2015-01-01

    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, acidic and neutralized zeolite were used for dealumination. Parts of the framework aluminumatoms are removed from their sites in the structure of zeolite Y upon the use of either acetylacetone on its own or simultaneous use of acetylacetone and ultrasound waves. Higher dealumination was observed for those samples subjected to both ultrasound irradiation and acetylacetone extraction.

  8. First Principles Simulations of Hydrocarbon Conversion Processes in Functionalized Zeolitic Materials

    Science.gov (United States)

    Mazar, Mark Nickolaus

    is responsible for the largest activation energy of the catalytic cycle. This assessment is similar to the findings of alkane metathesis studies on alumina/silica supports and indicates that the entire AM cycle can be performed in zeolites by isolated single-atom transition metal hydrides. Performed over acid form zeolites, MTH is used in the conversion of methanol into a broad range of hydrocarbons, including alkenes, alkanes, and aromatics. For reasons that are not yet rigorously quantified, product selectivities vary dramatically based on the choice of catalyst and reaction conditions. The methylation of species containing double bonds (i.e., co-catalysts) is central to the overall process. Distinct structure-function relationships were found with respect to the elementary steps in the methylation and beta-scission of olefins. In Chapter 4, the role of zeolite topology in the step-wise methylation of ethene by surface methoxides is investigated. Elementary steps are studied across multiple frameworks (i.e., BEA, CHA, FER, MFI, and MOR) constituting a wide variety of confinement environments. The reaction of surface methoxides with ethene is found to require a transition state containing a primary carbocation. The barrier height is found to decrease nearly monotonically with respect to the degree of dispersion interactions stabilizing the primary carbocationic species in the transition state. In addition, quantification of the ``local'' dispersion energy indicates that confinement effects can not be simply correlated to pore size. The beta-scission of olefins plays an important role in the product selectivities of many important chemical processes, including MTH. In Chapter 5, beta-scission modes involving C6 and C8 isomers are investigated at a single, isolated Bronsted acid site within H-ZSM-5. We find that the relative enthalpic barriers of beta-scission elementary steps can be rationalized by the substitution order of the two different carbocationic carbon

  9. Growth of ZSM-5 crystals within hollow β-zeolite

    Institute of Scientific and Technical Information of China (English)

    Qing Hu Zeng; Xiang Bai; Jia Jun Zheng; Jia Qi Chen; Rui Feng Li

    2011-01-01

    A zeolite composite composed of ZSM-5 and β-zeolites has been synthesized by a procedure of the nucleation and crystallization of ZSM-5 zeolite in the hollow β-zeolite. The property of β-zeolite crystals with aluminum-poor interior and aluminum-rich outer rim results in silicon extraction favorably in the aluminum-poor bulk rather than the aluminum-rich external surface. Subsequently, alkaline treatment of β-zeolite crystals during the second-step synthesis leads to a preferential dissolution of the aluminum-poor center and the formation of hollow β-zeolite crystals. ZSM-5 zeolite crystals are therefore embedded and grown within the hollow β-zeolite. The catalytic activities of Co-Hβ, Co-HZSM-5 and Co-HZSM-5/BEA are investigated during the reaction of methane catalytic reduction NO in the presence of O2.

  10. Catalytic Upgrading of 5-Hydroxymethylfurfural to Drop-in Biofuels by Solid Base and Bifunctional Metal-Acid Catalysts.

    Science.gov (United States)

    Bohre, Ashish; Saha, Basudeb; Abu-Omar, Mahdi M

    2015-12-01

    Design and synthesis of effective heterogeneous catalysts for the conversion of biomass intermediates into long chain hydrocarbon precursors and their subsequent deoxygenation to hydrocarbons is a viable strategy for upgrading lignocellulose into distillate range drop-in biofuels. Herein, we report a two-step process for upgrading 5-hydroxymethylfurfural (HMF) to C9 and C11 fuels with high yield and selectivity. The first step involves aldol condensation of HMF and acetone with a water tolerant solid base catalyst, zirconium carbonate (Zr(CO3 )x ), which gave 92 % C9 -aldol product with high selectivity at nearly 100 % HMF conversion. The as-synthesised Zr(CO3 )x was analysed by several analytical methods for elucidating its structural properties. Recyclability studies of Zr(CO3 )x revealed a negligible loss of its activity after five consecutive cycles over 120 h of operation. Isolated aldol product from the first step was hydrodeoxygenated with a bifunctional Pd/Zeolite-β catalyst in ethanol, which showed quantitative conversion of the aldol product to n-nonane and 1-ethoxynonane with 40 and 56 % selectivity, respectively. 1-Ethoxynonane, a low oxygenate diesel range fuel, which we report for the first time in this paper, is believed to form through etherification of the hydroxymethyl group of the aldol product with ethanol followed by opening of the furan ring and hydrodeoxygenation of the ether intermediate. PMID:26549016

  11. Investigation of new bifunctional agents. D-Penicillamine

    International Nuclear Information System (INIS)

    Somatostatin inhibits the release of growth hormone (somatotropin) from the Anterior Pituitary. The main use of derivatives of somatostatin is to diagnose growth hormone problems and to use against some forms of cancer which involve growth hormone. Also somatostatin suppresses gastric acid secretion, gallbladder contractions, and pancreatic enzyme secretion. The aim of the current study is to investigate new bifunctional agents for labeling with 99mTc. Therefore D-Penicillamine was used as a bifunctional agent and compared to DTPA in the labeling with 99mTc. Quality controls were established using thin layer radio chromatography (TLRC) and electrophoresis techniques. In addition, high performance liquid radio chromatography (HPLRC) was also performed for elimination of possible uncertainties. The radiolabeled complexes maintained their stabilities throughout the study. The results obtained showed that 99mTc-D-Penicillamine-somatostatin is a promising potential radiopharmaceutical and an alternative of 99mTc-DTPA-somatostatin for in vivo and in vitro applications. (author)

  12. The aminoindanol core as a key scaffold in bifunctional organocatalysts.

    Science.gov (United States)

    G Sonsona, Isaac; Marqués-López, Eugenia; Herrera, Raquel P

    2016-01-01

    The 1,2-aminoindanol scaffold has been found to be very efficient, enhancing the enantioselectivity when present in organocatalysts. This may be explained by its ability to induce a bifunctional activation of the substrates involved in the reaction. Thus, it is easy to find hydrogen-bonding organocatalysts ((thio)ureas, squaramides, quinolinium thioamide, etc.) in the literature containing this favored structural core. They have been successfully employed in reactions such as Friedel-Crafts alkylation, Michael addition, Diels-Alder and aza-Henry reactions. However, the 1,2-aminoindanol core incorporated into proline derivatives has been scarcely explored. Herein, the most representative and illustrative examples are compiled and this review will be mainly focused on the cases where the aminoindanol moiety confers bifunctionality to the organocatalysts. PMID:27340443

  13. Factors affecting the MTW zeolite cristallization process

    Energy Technology Data Exchange (ETDEWEB)

    Katovic, A.; Giordano, G. [Universita della Calabria, Rende (Italy)

    1995-12-01

    The synthesis mechanism of the high silica zeolite types other than MFI is rarely studied in the open literature. This work is devoted to the role of different parameters governing the zeolite MTW crystallization process. The influence of the most important factors: the nature of the silica and alumina source, the type of the organic cation, the alkalinity of the reaction mixture and the crystallization temperature, was studied. The molar composition of the initial hydrogel was varied in other to determine the crystallization field of the zeolite MTW. The observed morphology and particle size of the crystallites are related to the corresponding reaction conditions. The competitive formation of the other zeolite types (prevalently MFI and BEA) is discussed.

  14. Diagenetic Quartz Morphologies and Zeolite formation

    DEFF Research Database (Denmark)

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

    the Siri Canyon wells.  Volcanic lithoclasts are strongly altered and associated with diagenetic opal/ microquartz coatings and zeoliteZeolite crystals formed simultaneously with opal and prior to microquartz but dissolved with increased burial depth.  The dissolution of zeolite followed two steps...... in samples where no volcanic ash is demonstrated; it seems that a rapid supply of dissolved silica from dissolution of siliceous fossils was the main reason for the early co-precipitation of opal and zeolite. There are two important sources for Si: 1) Biogenic opal from diatoms or radiolarians, which...... 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...

  15. Characteristics of some Iranian natural zeolites

    International Nuclear Information System (INIS)

    Zeolites are hydrated crystalline aluminosilicates of alkali and alkaline earth cations. Their three dimensional framework consist of (SIO4) and (AlO4) tetrahedra. Beside their low price and abundance, three main properties of zeolites i.e: adsorption, ion exchange and catalytically properties promote their versatile industrial applications. In Iran, lack of a systematic and comprehensive research on the characterization of natural zeolites causes these valuable minerals to be relatively unknown. The aim of this research is to characterize some of the Iranian natural zeolites by means of thermal analysis methods including thermogravimetry (TG), and derivative thermogravimetry (DTG). In some cases, X-ray diffractometry and chemical analysis were used as complementary methods

  16. Preparation of Zeolite X Membranes on Porous Ceramic Substrates with Zeolite Seeds

    Institute of Scientific and Technical Information of China (English)

    Zhongqiang Xu; Qingling Chen; Guanzhong Lu

    2002-01-01

    Zeolite X membranes were investigated by in-situ hydrothermal synthesis on porous ceramic tubes precoated with zeolite X seeds or precursor amorphous aluminosilicate, and porous α-Al2O3 ceramic tubes with a pore size of 50 200 nm were employed as supports. Zeolite X crystals were synthesized by the classic method and mixed into deionized water as a slurry with a concentration of 0.2 0.5wt%, having a range of crystal sizes from 0.2 to 2μm. Crystal seeds were pressed into the pores near the inner surface of the ceramic tubes, and crystallization took place at 95℃ for 24-96 h. It was also investigated that Boehmite sol added with zeolite X seeds was precoated on ceramic supports to form a layer of γ-Al2O3 by heating, and hydrothermal crystallization could then take place to prepare the zeolite membranes on the composite ceramic tubes. The crystal species were characterized by XRD, and the morphology of the supports subjected to crystallization was characterized by SEM. The composite zeolite membranes have zeolitic top-layers with a thickness of 10-25 μm, and zeolite crystals can be intruded into pores of the supports as deeply as 100μm. The experimental results indicate that the precoating of zeolitic seeds on supports is beneficial to crystallization by shortening the synthesis time and improving the membrane strength. The resulting zeolite X membrane shows permselectivity to tri-n-butylamine((C4H9)3N) over perfluro-tributyl-amine ((C4Fg)3N), and a permeance ratio of 57 for ((C4Hg)3N to (C4F9)3N could be reached at 350℃. Permeances of BZ, EB and TIPB through the zeolite membrane were also measured and were found to slightly increase with temperature.

  17. Effects of Hydrothermal Aging on NH3-SCR reaction over Cu/zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Kwak, Ja Hun; Tran, Diana N.; Burton, Sarah D.; Szanyi, Janos; Lee, Jong H.; Peden, Charles HF

    2012-02-06

    The effects of hydrothermal treatment on model Cu/zeolite catalysts were investigated to better understand the nature of Cu species for the selective catalytic reduction of NO{sub x} by NH{sub 3}. After hydrothermal aging at 800 C for 16 h, the NO{sub x} reduction performance of Cu-ZSM-5 and Cu-beta were significantly reduced at low temperatures, while that of Cu-SSZ-13 was not affected. When the zeolite framework aluminum species were probed using solid state {sup 27}Al-NMR, significant reduction in the intensities of the tetrahedral aluminum peak was observed for Cu-ZSM-5 and Cu-beta, although no increase in the intensities of the octahedral aluminum peak was observed. When the redox behavior of Cu species was examined using H{sub 2}-TPR, it was found that Cu{sup 2+} could be reduced to Cu{sup +} and to Cu{sup 0} fir Cu-ZSM-5 and Cu-beta catalysts, while Cu{sup 2+} could be reduced to Cu{sup +} only for Cu-SSZ-13. After hydrothermal aging, CuO and Cu-aluminate species were found to form in Cu-ZSM-5 and Cu-beta, while little changes were observed for Cu-SSZ-13.

  18. Synthesis and peculiarities of the cesium zeolite crystal structure (cesite)

    International Nuclear Information System (INIS)

    An attempt is made to synthesize cesium zeolite by introduction of amorphous seed crystals which correspond by composition with cesium-containing zeolite into the aluminosilicate gel, since this method can produce zeolite with a crystal structure it would not adopt under the usual conditions. It is seen that during crystablization upon introduction of a seed crystal the cesium content in zeolite decreases. A more complete structural elucidation of zeolite obtained by the suggested method was carried out by x0ray and IR spectral analyses. The data of x-ray analysis showed that the structures of synthesized zeolite and binary octagonal pores are similar

  19. Catalytic Cracking of Heptane Using Prepared Zeolite

    OpenAIRE

    Mohammed Nsaif; Ahmed Abdulhaq; Ali Farhan; Safa Neamat

    2012-01-01

    This investigation was conducted to study the potential of type Y-zeolite prepared locally from Iraqi Rice Husk (IRH) (which considered as a type of agricultural waste that difficult to discard it in conventional methods in Iraq) on the removal of one heavy metals pollutant which was divalent zinc (Zn+2) ions from industrial wastewater using different design parameters by adsorption process. The design parameters studied to remove (Zn+2) ions using zeolite prepared locally from (IRH) as an ad...

  20. Acetylene diffusion in Na-Y zeolite

    Indian Academy of Sciences (India)

    S Mitra; S Sumitra; A M Umarji; R Mukhopadhyay; S Yashonath; S L Chaplot

    2004-08-01

    Study of diffusivity of acetylene adsorbed in Na-Y zeolite by quasi-elastic neutron scattering (QENS) measurements at temperatures of 300, 325 and 350 K is reported. A model in which the acetylene molecules undergo random-walk diffusion characterized by a Gaussian distribution of jump lengths inside zeolite cages describes the data consistently. The diffusion constant, residence time between jumps and root mean square jump length are determined.

  1. ADSORPTION MALACHITE GREEN ON NATURAL ZEOLITE

    Directory of Open Access Journals (Sweden)

    Eko Ariyanto

    2012-02-01

    Full Text Available A natural zeolite was employed as adsorbent for reducing of malachite green from aqueous solution. A batch system was applied to study the adsorption of malachite green in single system on natural zeolite. The adsorption studies indicate that malachite green in single component system follows the second-order kinetics and the adsorption is diffusion process with two stages for malachite green. Malachite green adsorption isotherm follows the Langmuir model.

  2. Multidiagnostic Analysis to Track Zeolite Formation

    OpenAIRE

    Castro, M.; Haouas, M.; Taulelle, Francis; Lim, I; Breynaert, Eric; Brabants, Gert; Kirschhock, Christine; Schmidt, W.

    2014-01-01

    Introduction The formation of zeolites in presence of tetraalkylammonium cations from so-called clear solutions using silicon alkoxides is a highly complex process. Our research aims to identify the key mechanisms on a molecular scale with the goal of understanding the factors that drive the formation of zeolites [1]. For this purpose we have used electrospray ionization mass spectrometry (ESI-MS), 29Si and 27Al liquid-NMR spectrometry, DOSY NMR (diffusion experi...

  3. Modelling active sites for the Beckmann rearrangement reaction in boron-containing zeolites and their interaction with probe molecules.

    Science.gov (United States)

    Lezcano-González, Inés; Vidal-Moya, Alejandro; Boronat, Mercedes; Blasco, Teresa; Corma, Avelino

    2010-06-28

    Theoretical calculations and in situ solid state NMR spectroscopy have been combined to get insight on the nature of the active sites for the Beckmann rearrangement reaction in borosilicate zeolites. The interaction of a B site in zeolite Beta with a series of probe molecules (ammonia, pyridine, acetone and water) has been modelled and the (15)N and (11)B NMR isotropic chemical shift of the resulting complexes calculated and compared with experimental in situ NMR results. This approach has allowed validation of the methodology to model the adsorption on a zeolite boron site of molecules of varying basicity which are either protonated or non-protonated. The limitation is that theoretical calculations overestimate the effect of molecular adsorption through hydrogen bonds on the calculated isotropic (11)B NMR chemical shift.Theoretical and experimental results on the adsorption of acetophenone and cyclohexanone oximes on zeolite B-Beta indicate that Brønsted acid sites protonate the oximes, changing the boron coordination from trigonal to tetrahedral. Comparison of theoretical and experimental (15)N NMR chemical shifts of the adsorbed amides (acetanilide and epsilon-caprolactam) indicates that they are non-protonated, and the (11)B NMR spectra show that, as expected, boron remains in trigonal coordination with an isotropic delta(11)B(exp) which differs from the calculated value delta(11)B(calc).

  4. Kinetics of zeolite dealumination in steam

    Energy Technology Data Exchange (ETDEWEB)

    Hughes, C.D.; Labouriau, A.; Crawford, S.N.; Romero, R.; Quirin, J.; Earl, W.L.

    1998-08-01

    Zeolite dealumination is a well known phenomenon that contributes to the deactivation or activation of catalysts in several different applications. The most obvious effect is in acid catalysis where dealumination under reaction conditions removes the Broensted sites, thus deactivating the catalyst. The authors are interested in the use of cation exchanged zeolites as selective reduction catalysts for removal of NO{sub x} from exhaust streams, particularly from automotive exhaust. In this case, copper exchanged ZSM-5 has been shown to be an effective catalyst for the generic reaction of NO{sub x} with hydrocarbons. However, high temperature and steam in combustion exhaust causes dealumination and consequent migration of copper out of the zeolite structure resulting in rapid deactivation of the catalyst. Dealumination of zeolites has been reported by many authors in uncountable papers and cannot be reviewed here. However, to the authors` knowledge there are no reports on the kinetics of dealumination under varying conditions of temperature and steam. By measuring the kinetics of dealumination with different zeolites and exchange cations they expect to develop working models of the dealumination process that will allow control of zeolite deactivation. This manuscript is a description of the basic techniques used and a progress report on the very beginning of this study.

  5. Probing zeolites by vibrational spectroscopies.

    Science.gov (United States)

    Bordiga, Silvia; Lamberti, Carlo; Bonino, Francesca; Travert, Arnaud; Thibault-Starzyk, Frédéric

    2015-10-21

    This review addresses the most relevant aspects of vibrational spectroscopies (IR, Raman and INS) applied to zeolites and zeotype materials. Surface Brønsted and Lewis acidity and surface basicity are treated in detail. The role of probe molecules and the relevance of tuning both the proton affinity and the steric hindrance of the probe to fully understand and map the complex site population present inside microporous materials are critically discussed. A detailed description of the methods needed to precisely determine the IR absorption coefficients is given, making IR a quantitative technique. The thermodynamic parameters of the adsorption process that can be extracted from a variable-temperature IR study are described. Finally, cutting-edge space- and time-resolved experiments are reviewed. All aspects are discussed by reporting relevant examples. When available, the theoretical literature related to the reviewed experimental results is reported to support the interpretation of the vibrational spectra on an atomic level.

  6. Organosilver radicals in gamma-irradiated Ag-NaA zeolite with methanol adsorbate

    Energy Technology Data Exchange (ETDEWEB)

    Wasowicz, T.; Mikosz, J.; Sadio, J.; Michalik, J. (Institute of Nuclear Chemistry and Technology, Warsaw (Poland))

    1992-09-01

    Hydroxyalky silver radicals, Ag.CH[sub 2]OH[sup +] in [gamma]-irradiated Ag-NaA zeolites with adsorbed methanol have been studied by EPR spectroscopy. These adducts, for silver loadings greater than one Ag[sup +] per unit cell, are formed directly after irradiation at 77 K. For lower Ag[sup +] content they appear on annealing above 140 K. It is postulated that the Ag[sup +] location in the zeolite lattice plays a crucial role in this process, and two different mechanisms of Ag[center dot]CH[sub 2]OH[sup +] formation are discussed depending on Ag[sup +] location inside a [beta]-cage. (Author).

  7. Effect of different glasses in glass bonded zeolite

    International Nuclear Information System (INIS)

    A mineral waste form has been developed for chloride waste salt generated during the pyrochemical treatment of spent nuclear fuel. The waste form consists of salt-occluded zeolite powders bound within a glass matrix. The zeolite contains the salt and immobilizes the fission products. The zeolite powders are hot pressed to form a mechanically stable, durable glass bonded zeolite. Further development of glass bonded zeolite as a waste form requires an understanding of the interaction between the glass and the zeolite. Properties of the glass that enhance binding and durability of the glass bonded zeolite need to be identified. Three types of glass, boroaluminosilicate, soda-lime silicate, and high silica glasses, have a range of properties and are now being investigated. Each glass was hot pressed by itself and with an equal amount of zeolite. MCC-1 leach tests were run on both. Soda-lime silicate and high silica glasses did not give a durable glass bonded zeolite. Boroaluminosilicate glasses rich in alkaline earths did bind the zeolite and gave a durable glass bonded zeolite. Scanning electron micrographs suggest that the boroaluminosilicate glasses wetted the zeolite powders better than the other glasses. Development of the glass bonded zeolite as a waste form for chloride waste salt is continuing

  8. EFFICIENCY OF HOTYNETS NATURAL ZEOLITES UTILIZATION IN LIVESTOCK INDUSTRY

    OpenAIRE

    Yarovan, N.; Boytsova, O.; Novikova, I.; Petrushina, M.

    2014-01-01

    The article presents data on efficiency of Hotynets natural zeolites in combination with other biological additives in dairy cattle breeding. It shows the economic effect of the complexes: "hotynets zeolites + thyme" under transport and industry stress; "hotynets zeolites + lecithin" under industrial stress and in the treatment of subclinical ketosis of heavy milking cows the main treatment. Utilization of hotynets natural zeolites and thyme as means of adaptogenic action of heavy milking cow...

  9. First Principles Simulations of Hydrocarbon Conversion Processes in Functionalized Zeolitic Materials

    Science.gov (United States)

    Mazar, Mark Nickolaus

    is responsible for the largest activation energy of the catalytic cycle. This assessment is similar to the findings of alkane metathesis studies on alumina/silica supports and indicates that the entire AM cycle can be performed in zeolites by isolated single-atom transition metal hydrides. Performed over acid form zeolites, MTH is used in the conversion of methanol into a broad range of hydrocarbons, including alkenes, alkanes, and aromatics. For reasons that are not yet rigorously quantified, product selectivities vary dramatically based on the choice of catalyst and reaction conditions. The methylation of species containing double bonds (i.e., co-catalysts) is central to the overall process. Distinct structure-function relationships were found with respect to the elementary steps in the methylation and beta-scission of olefins. In Chapter 4, the role of zeolite topology in the step-wise methylation of ethene by surface methoxides is investigated. Elementary steps are studied across multiple frameworks (i.e., BEA, CHA, FER, MFI, and MOR) constituting a wide variety of confinement environments. The reaction of surface methoxides with ethene is found to require a transition state containing a primary carbocation. The barrier height is found to decrease nearly monotonically with respect to the degree of dispersion interactions stabilizing the primary carbocationic species in the transition state. In addition, quantification of the ``local'' dispersion energy indicates that confinement effects can not be simply correlated to pore size. The beta-scission of olefins plays an important role in the product selectivities of many important chemical processes, including MTH. In Chapter 5, beta-scission modes involving C6 and C8 isomers are investigated at a single, isolated Bronsted acid site within H-ZSM-5. We find that the relative enthalpic barriers of beta-scission elementary steps can be rationalized by the substitution order of the two different carbocationic carbon

  10. REDUCTIVE ACTIVATION OF DIOXYGEN FOR DEGRADATION OF METHYL TERT-BUTYL ETHER BY BIFUNCTION

    Science.gov (United States)

    Bifunctional aluminum is prepared by sulfating aluminum metal with sulfuric acid. The use of bifunctional aluminum to degrade methyl tert-butyl ether (MTBE) in the presence of dioxygen has been examined using batch systems. Primary degradation products were tert-butyl alcohol, ...

  11. 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 c

  12. Influencing the selectivity of zeolite Y for triglycine adsorption

    NARCIS (Netherlands)

    Wijntje, R.; Bosch, H.; Haan, de A.B.; 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 ar

  13. Zeolite and swine inoculum effect on poultry manure biomethanation

    DEFF Research Database (Denmark)

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

    2013-01-01

    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...

  14. Preparation of hollow-fibre composite carbon-zeolite membranes

    NARCIS (Netherlands)

    Smith, S.P.J.; Linkov, V.M.; Sanderson, R.D.; Petrik, L.F.; O'Connor, C.T.; Keizer, K.

    1995-01-01

    Carbon membranes, produced by thermo-oxidative stabilization of polyacrylonitrile (PAN) precursors, were used as porous supports for continuous zeolite layers to give composite zeolite-carbon membranes. Different zeolite growth techniques were used, and the membranes were characterized by means of s

  15. Organometallics in confined geometries. Ferrocene in zeolite Y

    NARCIS (Netherlands)

    Kemner, E.

    2001-01-01

    Zeolites are crystalline aluminosilicates with a three-dimensional open framework structure of channels and cavities of molecular dimensions. Zeolites can thus act as molecular sieves, making catalytic centres in the interior of the zeolite only accessible to molecules of the correct size. Such cata

  16. Monitoring early zeolite formation via in situ electrochemical impedance spectroscopy.

    Science.gov (United States)

    Brabants, G; Lieben, S; Breynaert, E; Reichel, E K; Taulelle, F; Martens, J A; Jakoby, B; Kirschhock, C E A

    2016-04-01

    Hitherto zeolite formation has not been fully understood. Although electrochemical impedance spectroscopy has proven to be a versatile tool for characterizing ionic solutions, it was never used for monitoring zeolite growth. We show here that EIS can quantitatively monitor zeolite formation, especially during crucial early steps where other methods fall short.

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

    Directory of Open Access Journals (Sweden)

    Hayami Takeda

    2013-05-01

    Full Text Available 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, 29Si and 27Al 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.

  18. Italian zeolitized rocks of technological interest

    Science.gov (United States)

    de'Gennaro, M.; Langella, A.

    1996-09-01

    Large areas of Italian territory are covered by thick and widespread deposits of zeolite-bearing volcaniclastic products. The main zeolites are phillipsite and chabazite spread over the whole peninsula, and clinoptilolite recorded only in Sardinia. A trachytic to phonolitic glassy precursor accounts for the formation of the former zeolites characterized by low Si/Al ratios (?3.00), while clinoptilolite is related to more acidic volcanism. The genesis of most of these zeolitized deposits is linked to pyroclastic flow emplacement mechanisms characterized by quite high temperatures and by the presence of abundant fluids. The main utilization of these materials has been and still is as dimension stones in the building industry. Currently, limited amounts are also employed in animal farming (dietary supplement, pet litter and manure deodorizer) and in agriculture as soil improvement and slow-release fertilizers. New fields of application have been proposed for these products on account of their easy availability, very low cost, their high-grade zeolites (50 70%), and good technological features such as high cation exchange capacities and adsorption properties.

  19. Strong white photoluminescence from annealed zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Bai, Zhenhua, E-mail: baizh46@gmail.com [School of Chemical and Biomedical Engineering, Nanyang Technological University, Singapore 637457 (Singapore); Fujii, Minoru; Imakita, Kenji; Hayashi, Shinji [Department of Electrical and Electronic Engineering, Graduate School of Engineering, Kobe University, Rokkodai, Nada, Kobe 657-8501 (Japan)

    2014-01-15

    The optical properties of zeolites annealed at various temperatures are investigated for the first time. The annealed zeolites exhibit strong white photoluminescence (PL) under ultraviolet light excitation. With increasing annealing temperature, the emission intensity of annealed zeolites first increases and then decreases. At the same time, the PL peak red-shifts from 495 nm to 530 nm, and then returns to 500 nm. The strongest emission appears when the annealing temperature is 500 °C. The quantum yield of the sample is measured to be ∼10%. The PL lifetime monotonously increases from 223 μs to 251 μs with increasing annealing temperature. The origin of white PL is ascribed to oxygen vacancies formed during the annealing process. -- Highlights: • The optical properties of zeolites annealed at various temperatures are investigated. • The annealed zeolites exhibit strong white photoluminescence. • The maximum PL enhancement reaches as large as 62 times. • The lifetime shows little dependence on annealing temperature. • The origin of white emission is ascribed to the oxygen vacancies.

  20. Hydrothermal synthesis of zeolites from natural stellerite

    Institute of Scientific and Technical Information of China (English)

    李酽; 汪信; 董元彩; 朱俊武

    2002-01-01

    Y and P zeolites were synthesized hydrothermally from natural stellerite under different conditions and were characterized via XRD and FT-IR.The results show that the higher crystallinity of Y zeolite can be obtained in hydrothermal system with low alkalinity,low Ca2+/Na+ ratio,and high SiO2/Al2O3 ratio.The lattice space of the samples decreases as crystallization time increases.P Zeolite is prompted under condition of higher alkalinity and higher Ca2+/Na+ ratio.The intensity and number of bands in the range of 400 cm-1~900 cm-1 increases with reaction time.Bands at 680 cm-1,760 cm-1 and 860 cm-1 corresponding to Y zeolite appear during the crystallization stage.Most of these bands shift to higher wavenumbers when SiO2/Al2O3 ratio increases generally.In the hydrothermal system with reverse condition above,bands at 600 cm-1,420 cm-1~470 cm-1 hardly change as the crystallization time increases and the main crystal phase of P zeolite is obtained.

  1. Bifunctional chelating agents for targeted α-particle radiotherapy

    International Nuclear Information System (INIS)

    An α-emitting radionuclide is proposed as a better choice for application in radiotherapy of either leukemias or lymphomas due to very high cytotoxicity, short emission path length, and immediate energy deposition minimizing collateral cytotoxicity. Metallic α-emitters that have been studied are 212Bi and 213Bi. Bifunctional derivatives of diethylenetriamine pentaacetic acid (DTPA) were found to form Bi(III) complexes that were labile in vivo. Pre-clinical experiments confirmed both the stability of the CHX-DTPA ligands for the Bi(III) isotopes and the therapeutic applicability of these α-emitting isotopes

  2. A bifunctional perovskite catalyst for oxygen reduction and evolution.

    Science.gov (United States)

    Jung, Jae-Il; Jeong, Hu Young; Lee, Jang-Soo; Kim, Min Gyu; Cho, Jaephil

    2014-04-25

    La0.3(Ba0.5Sr0.5)0.7Co0.8Fe0.2O3d is a promising bifunctional perovskite catalyst for the oxygen reduction reaction and the oxygen evolution reaction. This catalyst has circa 10 nm-scale rhombohedral LaCoO3 cobaltite particles distributed on the surface. The dynamic microstructure phenomena are attributed to the charge imbalance from the replacement of A-site cations with La3+ and local stress on Cosite sub-lattice with the cubic perovskite structure.

  3. Bifunctional xylanases and their potential use in biotechnology

    Digital Repository Service at National Institute of Oceanography (India)

    Khandeparker, R.; Numan, M.Th.

    showed signiWcant similarity (33– 40% identical residues) to a diVerent group of bacterial xylanases and exoglucanases exempliWed by the Caldocel- lum saccharolyticum xynA and celB products. The xynA product is, therefore, a bifunctional enzyme having two... biochemistry of fungal and bacterial cellulolytic enzyme system. In: Aubert JP, Be- guin P, Millet J (eds) Biochemistry and genetics of cellulose deg- radation. Academic Press, London, pp 11–30 19. Cui W, Wood PJ, Blackwell B, Nikiforuk J (2000) Physicochemi...

  4. Hydrogen Purification Using Natural Zeolite Membranes

    Science.gov (United States)

    DelValle, William

    2003-01-01

    The School of Science at Universidad del Turabo (UT) have a long-lasting investigation plan to study the hydrogen cleaning and purification technologies. We proposed a research project for the synthesis, phase analysis and porosity characterization of zeolite based ceramic perm-selective membranes for hydrogen cleaning to support NASA's commitment to achieving a broad-based research capability focusing on aerospace-related issues. The present study will focus on technology transfer by utilizing inorganic membranes for production of ultra-clean hydrogen for application in combustion. We tested three different natural zeolite membranes (different particle size at different temperatures and time of exposure). Our results show that the membranes exposured at 900 C for 1Hr has the most higher permeation capacity, indicated that our zeolite membranes has the capacity to permeate hydrogen.

  5. Cupric natural zeolites as microbic ides

    International Nuclear Information System (INIS)

    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)

  6. Preparation and Characterization of Natural Zeolite Modified with Iron Nanoparticles

    Directory of Open Access Journals (Sweden)

    Alvaro Ruíz-Baltazar

    2015-01-01

    Full Text Available This study is aimed at investigating the structural and morphological characterization of natural and modified zeolite obtained from the state of Oaxaca (Mexico. Iron nanoparticles were used for the zeolite modification. The iron nanoparticles were loaded on the zeolite surface by homogeneous nucleation. Adsorption kinetic models of pseudo first and second order were surveyed. The characterization of pristine and modified zeolite was performed by Fourier transform infrared (FTIR, transmission electron microscopy (TEM, and X-ray diffraction (XRD. From the results, three main phases were identified: clinoptilolite, mordenite, and feldspar. We could also determine the adsorption capacity of the zeolites by means of adsorption kinetic models.

  7. Study on Synthesis and Catalytic Performance of Hierarchical Zeolite

    Institute of Scientific and Technical Information of China (English)

    Zhang Lingling; Li Fengyan; ZhaoTianbo; Sun Guida

    2007-01-01

    A kind of hierarchical zeolite catalyst was synthesized by hydrothermal method.X-ray diffraction (XRD)and nitrogen adsorption-desorption method were used to study the phase and aperture structure of the prepared catalyst.Infrared(IR)spectra of pyridine adsorbed on the sample showed that the hierarchical zeolite really had much more Bronsted and Lewis acidic sites than the HZSM-5 zeolite.The catalytic cracking of large hydrocarbon molecules showed that the hierarchical zeolite had a higher catalytic activity than the HZSM-5 zeolite.

  8. Cobalt sulfide/N,S codoped porous carbon core-shell nanocomposites as superior bifunctional electrocatalysts for oxygen reduction and evolution reactions

    Science.gov (United States)

    Chen, Binling; Li, Rong; Ma, Guiping; Gou, Xinglong; Zhu, Yanqiu; Xia, Yongde

    2015-12-01

    Exploring highly-efficient and low-cost bifunctional electrocatalysts for both oxygen reduction reaction (ORR) and oxygen evolution reactions (OER) in the renewable energy area has gained momentum but still remains a significant challenge. Here we present a simple but efficient method that utilizes ZIF-67 as the precursor and template for the one-step generation of homogeneous dispersed cobalt sulfide/N,S-codoped porous carbon nanocomposites as high-performance electrocatalysts. Due to the favourable molecular-like structural features and uniform dispersed active sites in the precursor, the resulting nanocomposites, possessing a unique core-shell structure, high porosity, homogeneous dispersion of active components together with N and S-doping effects, not only show excellent electrocatalytic activity towards ORR with the high onset potential (around -0.04 V vs. -0.02 V for the benchmark Pt/C catalyst) and four-electron pathway and OER with a small overpotential of 0.47 V for 10 mA cm-2 current density, but also exhibit superior stability (92%) to the commercial Pt/C catalyst (74%) in ORR and promising OER stability (80%) with good methanol tolerance. Our findings suggest that the transition metal sulfide-porous carbon nanocomposites derived from the one-step simultaneous sulfurization and carbonization of zeolitic imidazolate frameworks are excellent alternative bifunctional electrocatalysts towards ORR and OER in the next generation of energy storage and conversion technologies.Exploring highly-efficient and low-cost bifunctional electrocatalysts for both oxygen reduction reaction (ORR) and oxygen evolution reactions (OER) in the renewable energy area has gained momentum but still remains a significant challenge. Here we present a simple but efficient method that utilizes ZIF-67 as the precursor and template for the one-step generation of homogeneous dispersed cobalt sulfide/N,S-codoped porous carbon nanocomposites as high-performance electrocatalysts. Due to the

  9. Studies of anions sorption on natural zeolites.

    Science.gov (United States)

    Barczyk, K; Mozgawa, W; Król, M

    2014-12-10

    This work presents results of FT-IR spectroscopic studies of anions-chromate, phosphate and arsenate - sorbed from aqueous solutions (different concentrations of anions) on zeolites. The sorption has been conducted on natural zeolites from different structural groups, i.e. chabazite, mordenite, ferrierite and clinoptilolite. The Na-forms of sorbents were exchanged with hexadecyltrimethylammonium cations (HDTMA(+)) and organo-zeolites were obtained. External cation exchange capacities (ECEC) of organo-zeolites were measured. Their values are 17mmol/100g for chabazite, 4mmol/100g for mordenite and ferrierite and 10mmol/100g for clinoptilolite. The used initial inputs of HDTMA correspond to 100% and 200% ECEC of the minerals. Organo-modificated sorbents were subsequently used for immobilization of mentioned anions. It was proven that aforementioned anions' sorption causes changes in IR spectra of the HDTMA-zeolites. These alterations are dependent on the kind of anions that were sorbed. In all cases, variations are due to bands corresponding to the characteristic Si-O(Si,Al) vibrations (occurring in alumino- and silicooxygen tetrahedra building spatial framework of zeolites). Alkylammonium surfactant vibrations have also been observed. Systematic changes in the spectra connected with the anion concentration in the initial solution have been revealed. The amounts of sorbed CrO4(2-), AsO4(3-) and PO4(3-) ions were calculated from the difference between their concentrations in solutions before (initial concentration) and after (equilibrium concentration) sorption experiments. Concentrations of anions were determined by spectrophotometric method. PMID:25002191

  10. 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

  11. Relationship between structure and catalytic performance of dealuminated Y zeolites

    International Nuclear Information System (INIS)

    Dealuminated Y zeolites which have been prepared by hydrothermal and chemical treatments show differences in catalytic performance when tested fresh; however, these differences disappear after the zeolites have been steamed. The catalytic behavior of fresh and steamed zeolites is directly related to zeolite structural and chemical characteristics. Such characteristics determine the strength and density of acid sites for catalytic cracking. Dealuminated zeolites were characterized using x-ray diffraction, porosimetry, solid-state NMR and elemental analysis. Hexadecane cracking was used as a probe reaction to determine catalytic properties. Cracking activity was found to be proportional to total aluminum content in the zeolite. Product selectivity was dependent on unit cell size, presence of extra framework alumina and spatial distribution of active sites. The results from this study elucidate the role that zeolite structure plays in determining catalytic performance

  12. Ammonium removal by modified zeolite from municipal wastewater

    Institute of Scientific and Technical Information of China (English)

    ZHAO Ya-ping; GAO Ting-yao; JIANG Shang-ying; CAO Da-wen

    2004-01-01

    Ammonium removal by modified zeolite, H-form and Na-form zeolite, were examined by batch-type methods. The adsorption of ammonium on modified zeolite was exothermic process. The saturation adsorption capacity of ammonium on H-form and Na-form zeolite were 21.23 and 41.15 mg/g, respectively. After ten times adsorption- desorption-readsorption cycles the standard deviations of H-form and Na-form zeolite were 6.34% and 6.59%. The zeolite adsorption process has proved cost effective and practical in reducing ammonium by H-form and Na-form zeolite in municipal wastewater from concentration 27.68 mg/L to 2.80 mg/L and 5.91 mg/L.

  13. 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%.

  14. Natural zeolite reactivity towards ozone: The role of compensating cations

    International Nuclear Information System (INIS)

    Highlights: ► Chemical and thermal treatment enhances catalytic activity of natural zeolite. ► Modified natural zeolite exhibits high stability after thermal treatment. ► Reducing the compensating cation content leads to an increase on ozone abatement. ► Surface active atomic oxygen was detected using the DRIFT technique. ► The highest reactivity toward ozone was performed by NH4Z3 zeolite sample. - Abstract: Among indoor pollutants, ozone is recognised to pose a threat to human health. Recently, low cost natural zeolites have been applied as alternative materials for ozone abatement. In this work, the effect of compensating cation content of natural zeolite on ozone removal is studied. A Chilean natural zeolite is used here as starting material. The amount of compensating cations in the zeolite framework was modified by ion exchange using an ammonium sulphate solution (0.1 mol L−1). Characterisation of natural and modified zeolites were performed by X-ray powder diffraction (XRD), nitrogen adsorption at 77 K, elemental analysis, X-ray fluorescence (XRF), thermogravimetric analysis coupled with mass spectroscopy (TGA-MS), and temperature-programmed desorption of ammonia (NH3-TPD). Ozone adsorption and/or decomposition on natural and modified zeolites were studied by diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). Results show that the zeolite compensating cation content affects ozone interaction with zeolite active sites. Ammonium ion-exchange treatments followed by thermal out-gassing at 823 K, reduces ozone diffusion resistance inside the zeolite framework, increasing ozone abatement on zeolite surface active sites. Weak and strong Lewis acid sites of zeolite surface are identified here as the main active sites responsible of ozone removal.

  15. Natural zeolite reactivity towards ozone: The role of compensating cations

    Energy Technology Data Exchange (ETDEWEB)

    Valdes, Hector, E-mail: hvaldes@ucsc.cl [Laboratorio de Tecnologias Limpias (F. Ingenieria), Universidad Catolica de la Santisima Concepcion, Alonso de Ribera 2850, Concepcion (Chile); Alejandro, Serguei; Zaror, Claudio A. [Departamento de Ingenieria Quimica (F. Ingenieria), Universidad de Concepcion, Concepcion (Chile)

    2012-08-15

    Highlights: Black-Right-Pointing-Pointer Chemical and thermal treatment enhances catalytic activity of natural zeolite. Black-Right-Pointing-Pointer Modified natural zeolite exhibits high stability after thermal treatment. Black-Right-Pointing-Pointer Reducing the compensating cation content leads to an increase on ozone abatement. Black-Right-Pointing-Pointer Surface active atomic oxygen was detected using the DRIFT technique. Black-Right-Pointing-Pointer The highest reactivity toward ozone was performed by NH4Z3 zeolite sample. - Abstract: Among indoor pollutants, ozone is recognised to pose a threat to human health. Recently, low cost natural zeolites have been applied as alternative materials for ozone abatement. In this work, the effect of compensating cation content of natural zeolite on ozone removal is studied. A Chilean natural zeolite is used here as starting material. The amount of compensating cations in the zeolite framework was modified by ion exchange using an ammonium sulphate solution (0.1 mol L{sup -1}). Characterisation of natural and modified zeolites were performed by X-ray powder diffraction (XRD), nitrogen adsorption at 77 K, elemental analysis, X-ray fluorescence (XRF), thermogravimetric analysis coupled with mass spectroscopy (TGA-MS), and temperature-programmed desorption of ammonia (NH{sub 3}-TPD). Ozone adsorption and/or decomposition on natural and modified zeolites were studied by diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). Results show that the zeolite compensating cation content affects ozone interaction with zeolite active sites. Ammonium ion-exchange treatments followed by thermal out-gassing at 823 K, reduces ozone diffusion resistance inside the zeolite framework, increasing ozone abatement on zeolite surface active sites. Weak and strong Lewis acid sites of zeolite surface are identified here as the main active sites responsible of ozone removal.

  16. Photovoltachromic device with a micropatterned bifunctional counter electrode.

    Science.gov (United States)

    Cannavale, Alessandro; Manca, Michele; De Marco, Luisa; Grisorio, Roberto; Carallo, Sonia; Suranna, Gian Paolo; Gigli, Giuseppe

    2014-02-26

    A photovoltachromic window can potentially act as a smart glass skin which generates electric energy as a common dye-sensitized solar cell and, at the same time, control the incoming energy flux by reacting to even small modifications in the solar radiation intensity. We report here the successful implementation of a novel architecture of a photovoltachromic cell based on an engineered bifunctional counter electrode consisting of two physically separated platinum and tungsten oxide regions, which are arranged to form complementary comb-like patterns. Solar light is partially harvested by a dye-sensitized photoelectrode made on the front glass of the cell which fully overlaps a bifunctional counter electrode made on the back glass. When the cell is illuminated, the photovoltage drives electrons into the electrochromic stripes through the photoelectrochromic circuit and promotes the Li(+) diffusion towards the WO3 film, which thus turns into its colored state: a photocoloration efficiency of 17 cm(2) min(-1) W(-1) at a wavelength of 650 nm under 1.0 sun was reported along with fast response (coloration time photovoltaic functionality was also retained due to the copresence of the independently switchable micropatterned platinum electrode.

  17. Comparative study of zeolite 5A and zeolite 13X in air separation by pressure swing adsorption

    Energy Technology Data Exchange (ETDEWEB)

    Shokroo, Ehsan Javadi; Meymandi, Hadiseh Khalilpour; Yadollahi, Nadia [PART-SHIMI Knowledge Based Company, Shiraz (Iran, Islamic Republic of); Farsani, Danial Jafari [Bidboland Refining Co., NIGC, Bidboland (Iran, Islamic Republic of)

    2016-04-15

    The performance of zeolites 5A and 13X is numerically investigated in oxygen separation from air by a two-bed PSA system. The effect of operating variables such as adsorption step time, PH/PL ratio and cycle time was investigated on product purity and recovery. The simulation results showed that nitrogen adsorption capacity on zeolite 13X was slightly more than the one on zeolite 5A. In the completely same operating conditions, zeolite 5A had a larger mass transfer zone than zeolite 13X. Therefore, the adsorption and desorption rate of nitrogen on zeolite 5A is less than zeolite 13X. Moreover, for the equal volume of adsorbed nitrogen on both adsorbents, zeolite 5A is more capable rather than zeolite 13X to desorb much more volume of nitrogen at certain time. Furthermore, for achieving oxygen with purity of 96%, utilizing zeolite 5A is more economical than zeolite 13X, when 5.5

  18. Cristalización de zeolita beta mediante conversión asistida por vapor: influencia de los parámetros de síntesis

    Directory of Open Access Journals (Sweden)

    Salvador Alfaro

    2013-01-01

    Full Text Available In the present work, beta zeolites were prepared by an alternative route called steam-assisted conversion (SAC. Several zeolites were synthesized using amorphous dry gels with a low SDA concentration (0.09 mol, TEAOH. Temperature and crystallization time were the main parameters studied. X-ray diffraction (XRD, infrared spectroscopy (IR and scanning electron microscopy (SEM were the characterization techniques employed. The zeolites prepared showed mixed phases such as beta, MTW and ZSM-5 while only one sample treated at 150ºC with 24 h of crystallization time showed a pure ZSM-5 phase (SAC-5. These preliminary results serve as a starting point for optimizing the synthesis of a specific type of zeolite using the SAC method.

  19. Catalytic Fast Pyrolysis of Cellulose Using Nano Zeolite and Zeolite/Matrix Catalysts in a GC/Micro-Pyrolyzer.

    Science.gov (United States)

    Lee, Kyong-Hwan

    2016-05-01

    Cellulose, as a model compound of biomass, was catalyzed over zeolite (HY,.HZSM-5) and zeolite/matrix (HY/Clay, HM/Clay) in a GC/micro-pyrolyzer at 500 degrees C, to produce the valuable products. The catalysts used were pure zeolite and zeolite/matrix including 20 wt% matrix content, which were prepared into different particle sizes (average size; 0.1 mm, 1.6 mm) to study the effect of the particle size of the catalyst for the distribution of product yields. Catalytic pyrolysis had much more volatile products as light components and less content of sugars than pyrolysis only. This phenomenon was strongly influenced by the particle size of the catalyst in catalytic fast pyrolysis. Also, in zeolite and zeolite/matrix catalysts the zeolite type gave the dominant impact on the distribution of product yields.

  20. Theoretical Study on Adsorption of Methanol on Zeolite and Phosphorus Modified Zeolite

    Institute of Scientific and Technical Information of China (English)

    Lü Renqing; Li Ting; Gu Jun; Liu Chenguang

    2004-01-01

    Methanol adsorption in zeolite and phosphorus modified zeolite has been investigated within the cluster model framework of quantum chemical calculation. Full optimization and frequency analysis of all cluster model have been carried out using Gaussian 94 soft package with Hartree-Fock method and B3LYP, B3P86 hybrid methods of density functional theory at 3-2 1 G, 6-31G basis set level for hydrogen atoms and 6-31G+(d) basis set level for the other atoms performed on small cluster model for CH3OH, H3Al(OH)SiH2(H2PO4), H3Al(OH)SiH2(H3SiO4), H3Al(OH-CH3OH)SiH2(H2PO4) and H3Al(OHCH3OH)SiH2(H3SiO4). The results show that phosphorus grafting in the zeolite framework has modified the chemical environment in the vicinity of the zeolite bridging hydroxyl. Phosphorus modification can enhance the acid strength of zeolite bridging hydroxyl, which was suggested by the lengthening of zeolite bridging hydroxyl O-H bond and the increasing methanol adsorption energy. This may be favorable to the initial CH3OCH3 formation in the methanol to gasoline (MTG) process.

  1. 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.

  2. Dehydrogenation of light alkanes over zeolites

    NARCIS (Netherlands)

    Narbeshuber, Thomas F.; Brait, Axel; Seshan, Kulathuiyer; Lercher, Johannes A.

    1997-01-01

    The conversion of light paraffins to olefins and the secondary reactions of the unsaturated compounds were investigated on H-ZSM5 and H-Y zeolites between 733 and 823 K. Steady state- and transient response-isotope tracing studies revealed that two mechanisms of dehydrogenation are operative. The ma

  3. 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.

  4. Chemical interactions in multimetal/zeolite catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Sachtler, W.M.H.

    1992-02-07

    Mechanistic explanations have been found for the migration of atoms and ions through the zeolite channels leading to specific distribution of ions and the metal clusters. In this report, we summarize the state of understanding attained on a number of topics in the area of mono- and multimetal/zeolite systems, to which our recent research has made significant contributions. The following topics are discussed: (1) Formation of isolated metal atoms in sodalite cages; (2) differences of metal/zeolite systems prepared by ion reduction in channels or via isolated atoms; (3) rejuvenation of Pd/NaY and Pd/HY catalysts by oxidative redispersion of the metal; (4) formation of mono- or bimetal particles in zeolites by programmed reductive decomposition of volatile metal complexes; (5) cation-cation interaction as a cause of enhanced reducibility; (6) formation of palladium carbonyl clusters in supercages; (7) enhanced catalytic activity of metal particle-proton complexes for hydrocarbon conversion reactions; (8) stereoselectivity of catalytic reactions due to geometric constraints of particles in cages.

  5. 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...

  6. Zeolite 5A Catalyzed Etherification of Diphenylmethanol

    Science.gov (United States)

    Cooke, Jason; Henderson, Eric J.; Lightbody, Owen C.

    2009-01-01

    An experiment for the synthetic undergraduate laboratory is described in which zeolite 5A catalyzes the room temperature dehydration of diphenylmethanol, (C[subscript 6]H[subscript 5])[subscript 2]CHOH, producing 1,1,1',1'-tetraphenyldimethyl ether, (C[subscript 6]H[subscript 5])[subscript 2]CHOCH(C[subscript 6]H[subscript 5])[subscript 2]. The…

  7. Synthesis and Characterization of a New Bifunctional Dye Containing Spirobenzopyran and Cinnamoyl Moiety

    Institute of Scientific and Technical Information of China (English)

    申凯华; 崔东熏

    2005-01-01

    A novel bifunctional dye containing spirobenzopyran and cinnaznoyl moiety has been prepared and its photochromic behavior following irradiation at different wavelengths of monochrome UV light was investigated.The colourless bifunctional dye in film or solution exhibits unusual photochromism through structural and geometrical transformation from spirobenzopyran to merocyanine accompanying with photocrosslinking reaction in cinnamoyl moieties. Two kinds of photochemical reaction were achieved by irradiation at the different wavelengths of monochrome UV light (275 nm, 365 nm) selectively. The photochromic process of the bifunctional dye was discussed and the dynamic behaviors of the decolorization process were investigated.

  8. Thermal Treatment of Salt-Loaded Zeolite

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Jeong Guk; Lee, Jae Hee; Kim, Eung Ho; Kim, Joon Hyung [Korea Atomic Energy Research Institute, Taejon (Korea, Republic of)

    2005-07-01

    For disposal in a geological repository, the waste salts such as molten LiCl salt from an oxide fuel reduction process and molten LiCl-KCl eutectic salt from an electro refining process must meet the acceptance criteria. For a waste form containing chloride salt, two of the more important criteria are known to be leach resistance and waste form durability. US Argonne National Laboratory (ANL) developed a ceramic waste form (CWF) fabrication technology for LiCl-KCl eutectic salt from ANL Experimental Breeder Reactor-II (EBR-II). The CWF, which was made by first occluding salt in zeolite A at 730 K and then encapsulating the zeolite in a borosilicate binder glass by a hot isostatic press (HIP) method or pressureless consolidation (PC) method, has the phase composition of about 70% sodalite, 25% binder glass, and a 5% total of inclusion phases (halite, nepheline, and various oxides and silicates). US ANL showed that the chemical durability and leach resistance of the CWF were higher than those of glass waste form for high level waste from aqueous process, by a 7-day product consistency test (PCT). However, the waste form fabrication process for waste LiCl salt is somewhat different in mixing temperature from that for LiCl-KCl eutectic salt at US ANL. The former is mixed at 920 K, whereas, the later mixing is accomplished at 730 K. Such difference in mixing temperature results in the different major phase of SLZ, that is, zeolite Li-A from LiCl salt, and unchanged zeolite A from LiCl-KCl eutectic salt. This unchanged phase of zeolite A during an immobilization step is transformed to sodalite, which was known to be very high leach-resistant, in the step of encapsulating with borosilicate glass. In this work, we tried to investigate the transformation of major phase of SLZ, from zeolite Li-A to Na{sub 8}Cl{sub 2}-Sod using zeolite only sodalite, by a quantitative analysis with a software for X-ray diffractometer during the thermal treatment under 1170 K.

  9. Ethylenediamine effect on No2+ uptake by zeolite Y

    International Nuclear Information System (INIS)

    Co2+ ion exchange, at room temperature, form aqueous cobalt-sodium chloride solutions with NaY zeolite has been studied. The effect of contact time on the shape of the sorption curves of Co2+ using zeolite Y dehydrated at 600 deg C is similar to the one found in our previous work with a zeolite dehydrated at 150 deg C. A fast sorption uptake is observed in which 1.8 meq of Na= ions/g zeolite are replaced by cobalt ions followed by a desorption process where the uptake decreases to 1.2 meq/g zeolite. The Co2+ sorption using zeolite Y dehydrated at 600 deg C is increased when ethylenediamine solution is passed through the zeolite. The Co2+ sorption uptake, initially 2.0 meq/g, increases to 2.8 meq/g, of zeolite. This behavior is explained by the location and coordination of cobalt in zeolite Y sites. It is suggested that the highest uptake process is due to the blocking of zeolite sites by a Co complex compound. (author) 17 refs.; 4 figs

  10. Zeolite Nanoparticles for Selective Sorption of Plasma Proteins

    Science.gov (United States)

    Rahimi, M.; Ng, E.-P.; Bakhtiari, K.; Vinciguerra, M.; Ahmad, H. Ali; Awala, H.; Mintova, S.; Daghighi, M.; Bakhshandeh Rostami, F.; de Vries, M.; Motazacker, M. M.; Peppelenbosch, M. P.; Mahmoudi, M.; Rezaee, F.

    2015-11-01

    The affinity of zeolite nanoparticles (diameter of 8-12 nm) possessing high surface area and high pore volume towards human plasma proteins has been investigated. The protein composition (corona) of zeolite nanoparticles has been shown to be more dependent on the plasma protein concentrations and the type of zeolites than zeolite nanoparticles concentration. The number of proteins present in the corona of zeolite nanoparticles at 100% plasma (in vivo state) is less than with 10% plasma exposure. This could be due to a competition between the proteins to occupy the corona of the zeolite nanoparticles. Moreover, a high selective adsorption for apolipoprotein C-III (APOC-III) and fibrinogen on the zeolite nanoparticles at high plasma concentration (100%) was observed. While the zeolite nanoparticles exposed to low plasma concentration (10%) exhibited a high selective adsorption for immunoglobulin gamma (i.e. IGHG1, IGHG2 and IGHG4) proteins. The zeolite nanoparticles can potentially be used for selectively capture of APOC-III in order to reduce the activation of lipoprotein lipase inhibition during hypertriglyceridemia treatment. The zeolite nanoparticles can be adapted to hemophilic patients (hemophilia A (F-VIII deficient) and hemophilia B (F-IX deficient)) with a risk of bleeding, and thus might be potentially used in combination with the existing therapy.

  11. Energetics of sodium-calcium exchanged zeolite A.

    Science.gov (United States)

    Sun, H; Wu, D; Guo, X; Shen, B; Navrotsky, A

    2015-05-01

    A series of calcium-exchanged zeolite A samples with different degrees of exchange were prepared. They were characterized by powder X-ray diffraction (XRD) and differential scanning calorimetry (DSC). High temperature oxide melt drop solution calorimetry measured the formation enthalpies of hydrated zeolites CaNa-A from constituent oxides. The water content is a linear function of the degree of exchange, ranging from 20.54% for Na-A to 23.77% for 97.9% CaNa-A. The enthalpies of formation (from oxides) at 25 °C are -74.50 ± 1.21 kJ mol(-1) TO2 for hydrated zeolite Na-A and -30.79 ± 1.64 kJ mol(-1) TO2 for hydrated zeolite 97.9% CaNa-A. Dehydration enthalpies obtained from differential scanning calorimetry are 32.0 kJ mol(-1) H2O for hydrated zeolite Na-A and 20.5 kJ mol(-1) H2O for hydrated zeolite 97.9% CaNa-A. Enthalpies of formation of Ca-exchanged zeolites A are less exothermic than for zeolite Na-A. A linear relationship between the formation enthalpy and the extent of calcium substitution was observed. The energetic effect of Ca-exchange on zeolite A is discussed with an emphasis on the complex interactions between the zeolite framework, cations, and water.

  12. Incorporação de dióxido de titânio em zeólitas para emprego em fotocatálise heterogênea Titanium oxide incorporation on zeolites for heterogeneous photocatalisis

    Directory of Open Access Journals (Sweden)

    Jean C. Merg

    2010-01-01

    Full Text Available This work proposes the study of heterogeneous photocatalysis using TiO2 impregnated in zeolites beta, ZSM-5, mordenite, NaXb, NaXp and NaY for the decomposition of methylene blue. The catalysts were characterized by XRD, IR, textural analyses by N2 adsorption, SEM, DRS and the reaction of decomposition was monitored by UV visible. The results indicated that didn't have structural changes in the catalysts after Ti impregnations, only in the case of NaY and NaX zeolites. The better photocatalyst to metylene blue decomposition was beta/Ti zeolite due had one structure more accessible (with bigger porous helping in TiO2 dispersion and catalytic active.

  13. Solidification of cesium and strontium with zeolites

    International Nuclear Information System (INIS)

    The thermal change of zeolites and the elution property of nuclides from calcined matters were experimentally studied in order to produce the solid of low leaching property. The method includes the ion exchange of nuclides in radioactive waste solution and the calcination at a high temperature. Differential thermal analysis, thermal gravity analysis and X-ray diffraction method were employed to see the occurrence of recrystallization of Na type, Cs type, Sr type of the zeolites at a high temperature. Samples were synthetic zeolites including A type, X type, Y type and mordenite (zolen, hereafter referred to as S.M.), and natural mordenite. The ion exchanging capacity for Cs and Sr was measured, using the above zeolites. The adsorption was measured by the column method, using Cs-135 and Sr-85 as tracers. The leaching test of the zeolites calcined at 8000C, 9000C, 1,0000C and 1,1000C for 3 hours was performed by the atomic light absorption method. The daily change of the leaching ratio was observed according to the method of IAEA. The experiment revealed that CsA and CsX recrystallized at 1,0000C or above, whereas mordenite did not recrystallize even at the calcining temperature of 1,1000C, and it was leachable. The calcined CsY showed much lower leaching value than the other methods such as cement solidification and glass solidification. The leaching into sea water was five times as much as that into distilled water. (Iwakiri, K.)

  14. Altering bio-oil composition by catalytic treatment of pinewood pyrolysis vapors over zeolites using an auger - packed bed integrated reactor system

    Directory of Open Access Journals (Sweden)

    Vamshi Krishna Guda

    2016-09-01

    Full Text Available Pine wood pyrolysis vapors were catalytically treated using Zeolite catalysts. An auger fed reactor was used for the pinewood pyrolysis while a packed bed reactor mounted on the top of the auger reactor housed the catalyst for the treatment of pinewood pyrolytic vapors. The pyrolytic vapors produced at 450 oC were passed through zeolite catalysts maintained at 425 oC at a weight hourly space velocity (WHSV of 12 h-1. Five zeolites, including ZSM-5, mordenite, ferrierite, Zeolite-Y, and Zeolite-beta (all in H form, were used to study the effect of catalyst properties such as acidity, pore size, and pore structure on catalytic cracking of pinewood pyrolysis vapors. Product bio-oils were analyzed for their chemical composition using GC-MS, water content, density, viscosity, acid value, pH, and elemental compositions. Thermogravimetric analysis (TGA was performed to analyze the extent of coking on zeolite catalysts. Application of catalysis to biomass pyrolysis increased gas product yields at the expense of bio-oil yields. While all the zeolites deoxygenated the pyrolysis vapors, ZSM-5 was found to be most effective. The ZSM-5 catalyzed bio-oil, rich in phenolics and aromatic hydrocarbons, was less viscous, had relatively lower acid number and high pH, and possessed oxygen content nearly half that of un-catalyzed bio-oil. Brønsted acidity, pore size, and shape-selective catalysis of ZSM-5 catalyst proved to be the determining factors for its activity. TGA results implied that the pore size of catalysts highly influenced coking reactions. Regeneration of the used catalysts was successfully completed at 700 oC.

  15. 3D-modelling of bifunctional core-shell catalysts for the production of fuels from biomass-based synthesis gas

    Energy Technology Data Exchange (ETDEWEB)

    Ding, Wenjin; Lee, Seung Cheol; Li, Hui; Pfeifer, Peter; Dittmeyer, Roland [Karlsruhe Institute of Technology (KIT), Eggenstein-Leopoldshafen (Germany). Inst. for Micro Process Engineering (IMVT)

    2013-09-01

    Until now, the main route for the production of DME from synthesis gas in industry is methanol synthesis on a metallic catalyst and subsequent dehydration of methanol on an acid catalyst (two-step process). A single-step process using bifunctional catalysts to perform the two steps simultaneously would be preferred e.g. due to thermodynamic considerations; but this is impeded by the higher volumetric heat release which may cause deactivation of the methanol synthesis catalyst function. Thus we propose to conduct the reaction in a microchannel reactor. However, in order to increase the productivity of the microchannel reactor and to lower the investment costs, we aim at a high selectivity and activity of the catalyst. The continuously removal of methanol by dehydration on an acidic ZSM-5 catalyst as shell improves the thermodynamic conditions of methanol synthesis in the CuO/ZnO/Al{sub 2}O{sub 3} core; thus, the synthesis gas conversion can be higher than that determined by the thermodynamics of pure methanol synthesis. The molecular sieving in the zeolite layer can further lead to higher selectivity of DME at milder reaction conditions. However, mass transport limitation of the synthesis gas to the catalyst core should not hinder the reaction, and therefore a more detailed investigation is required. In order to computer-aided optimize the catalyst structure and the operating conditions for core-shell catalysts, a simulation model should be developed to study the coupled reaction and transport processes in core-shell catalysts. In this simulation model the complicated interaction of diffusion and reaction in the zeolite layer (shell) must be detailed by a network model to describe its structure and the mechanisms effectively. In addition, suitable diffusion and kinetic models are required to describe the mass transport and reactions in the layer. Suitable networks, diffusion and kinetic models are discussed for 3D simulations in this contribution. (orig.)

  16. Fabrication of Zeolite A Rods with Irregular Macropores by Self-assembly of Zeolite A Microcrystals Using Microwave-assisted Hydrothermal Synthesis

    Institute of Scientific and Technical Information of China (English)

    程志林; 万惠霖; 刘赞

    2004-01-01

    Zeolite A rods by self-assembly of zeolite A microcrystal were successfully synthesized by microwave-assisted hydrothermal synthesis. The average size of zeolite crystals consisting of self-assembling materials was about 300 nm and the length of zeolite rods was in the range of 15-30 μm.

  17. characterization of alumino and ferosilicate high siliceous zeolites by thermo analytical and Moessbauer spectroscopic techniques

    International Nuclear Information System (INIS)

    Simultaneous thermogravimetric/differential thermal analysis (TG/DTA) and differential scanning calorimetric (DSC) techniques were used to measure quantitatively the degree of crystallization and confirmation of tetrapropylammonium (TPA /sup +/) and tetraethylammonium (TEA /sup +/) species incorporated in ZSM5 and BETA-zeolite structure framework respectively. It is observed from thermal analysis that 3.3 to 3.8 TPA entities are normally present per unit cell of the ZSM-5 structure while for BETA the corresponding values are 6.2 to 6.7 for TEA. The propyl organic molecule was found to be located preferentially in the zigzag channel of ZSM5-AL and ZSM5-Fe in agreement with the results of the other techniques. 67Fe Moessbauer spectroscopic studies on as-synthesized and calcined samples have confirmed the uniform dispersion of Fe/sup 3+/ in the tetrahedral framework of ZSM5-Fe zeotype. Crystallinity and unit cell parameters of the materials were determined by powder x-ray diffraction, which are the function of Al and Fe content of the zeolites. A good correlation was obtained between the degree of crystallinity as established by TG/DSC techniques and x-ray diffraction crystallinity. (author)

  18. Bifunctional chelates of RH-105 and AU199 as potential radiotherapeutic agents

    Energy Technology Data Exchange (ETDEWEB)

    Droege, P.

    1997-03-01

    Research is presented on new bifunctional chelating ligand systems with stability on the macroscopic and radiochemical levels. The synthesis of the following complexes are described: rhodium 105, palladium 109, and gold 198.

  19. Chemoselective Reactivity of Bifunctional Cyclooctynes on Si(001)

    CERN Document Server

    Reutzel, Marcel; Lipponer, Marcus A; Länger, Christian; Höfer, Ulrich; Koert, Ulrich; Dürr, Michael

    2016-01-01

    Controlled organic functionalization of silicon surfaces as integral part of semiconductor technology offers new perspectives for a wide range of applications. The high reactivity of the silicon dangling bonds, however, presents a major hindrance for the first basic reaction step of such a functionalization, i.e., the chemoselective attachment of bifunctional organic molecules on the pristine silicon surface. We overcome this problem by employing cyclooctyne as the major building block of our strategy. Functionalized cyclooctynes are shown to react on Si(001) selectively via the strained cyclooctyne triple bond while leaving the side groups intact. The achieved selectivity originates from the distinctly different adsorption dynamics of the separate functionalities: A direct adsorption pathway is demonstrated for cyclooctyne as opposed to the vast majority of other organic functional groups. The latter ones react on Si(001) via a metastable intermediate which makes them effectively unreactive in competition wi...

  20. The bi-functional organization of human basement membranes.

    Science.gov (United States)

    Halfter, Willi; Monnier, Christophe; Müller, David; Oertle, Philipp; Uechi, Guy; Balasubramani, Manimalha; Safi, Farhad; Lim, Roderick; Loparic, Marko; Henrich, Paul Bernhard

    2013-01-01

    The current basement membrane (BM) model proposes a single-layered extracellular matrix (ECM) sheet that is predominantly composed of laminins, collagen IVs and proteoglycans. The present data show that BM proteins and their domains are asymmetrically organized providing human BMs with side-specific properties: A) isolated human BMs roll up in a side-specific pattern, with the epithelial side facing outward and the stromal side inward. The rolling is independent of the curvature of the tissue from which the BMs were isolated. B) The epithelial side of BMs is twice as stiff as the stromal side, and C) epithelial cells adhere to the epithelial side of BMs only. Side-selective cell adhesion was also confirmed for BMs from mice and from chick embryos. We propose that the bi-functional organization of BMs is an inherent property of BMs and helps build the basic tissue architecture of metazoans with alternating epithelial and connective tissue layers.

  1. The bi-functional organization of human basement membranes.

    Directory of Open Access Journals (Sweden)

    Willi Halfter

    Full Text Available The current basement membrane (BM model proposes a single-layered extracellular matrix (ECM sheet that is predominantly composed of laminins, collagen IVs and proteoglycans. The present data show that BM proteins and their domains are asymmetrically organized providing human BMs with side-specific properties: A isolated human BMs roll up in a side-specific pattern, with the epithelial side facing outward and the stromal side inward. The rolling is independent of the curvature of the tissue from which the BMs were isolated. B The epithelial side of BMs is twice as stiff as the stromal side, and C epithelial cells adhere to the epithelial side of BMs only. Side-selective cell adhesion was also confirmed for BMs from mice and from chick embryos. We propose that the bi-functional organization of BMs is an inherent property of BMs and helps build the basic tissue architecture of metazoans with alternating epithelial and connective tissue layers.

  2. The Effect of K and Acidity of NiW-Loaded HY Zeolite Catalyst for Selective Ring Opening of 1-Methylnaphthalene.

    Science.gov (United States)

    Lee, You-Jin; Kim, Eun-Sang; Kim, Jeong-Rang; Kim, Joo-Wan; Kim, Tae-Wan; Chae, Ho-Jeong; Kim, Chul-Ung; Lee, Chang-Ha; Jeong, Soon-Yong

    2016-05-01

    Bi-functional catalysts were prepared using HY zeolites with various SiO2/Al2O3 ratios for acidic function, NiW for metallic function, and K for acidity control. 1-Methylnaphthalene was selected as a model compound for multi-ring aromatics in heavy oil, and its selective ring opening reaction was investigated using the prepared bi-functional catalysts with different levels of acidity in a fixed bed reactor system. In NiW/HY catalysts without K addition, the acidity decreased with the SiO2/Al2O3 mole ratio of the HY zeolite. Ni1.1W1.1/HY(12) catalyst showed the highest acidity but slightly lower yields for the selective ring opening than Ni1.1W1.1/HY(30) catalyst. The acidity of the catalyst seemed to play an important role as the active site for the selective ring opening of 1-methylnaphthalene but there should be some optimum catalyst acidity for the reaction. Catalyst acidity could be controlled between Ni1.1W1.1/HY(12) and Ni1.1W1.1/HY(30) by adding a moderate amount of K to Ni1.1W1.1/HY(12) catalyst. K0.3Ni1.1W1.1/HY(12) catalyst should have the optimum acidity for the selective ring opening. The addition of a moderate amount of K to the NiW/HY catalyst must improve the catalytic performance due to the optimization of catalyst acidity.

  3. A conductive composite of polythiophene with 13X-zeolite

    International Nuclear Information System (INIS)

    A composite of polythiophene (PTP) with 13X-zeolite was prepared via chemical oxidative polymerization of thiophene (TP) in presence of a dispersion of 13X-zeolite (powder) in CHCl3 solvent using anhydrous FeCl3 oxidant. Formation of PTP and its subsequent incorporation in the PTP-13X composite was confirmed by FTIR spectral studies and X-ray diffraction (XRD) pattern analysis. Scanning electron microscopic (SEM) analysis revealed formation of composite particles with average diameter in the range of 5-10 μm. XRD analyses indicated typical structural differences between 13X-zeolite and PTP-13X-zeolite composite. DC conductivity value of the PTP-13X-zeolite composite was in the order of 10-2 S/cm, which was indeed high compared to that of PTP, produced under identical conditions as above without the presence of 13X-zeolite

  4. Study on Crystallization of Titanium Silicalite Zeolite (Ⅱ)

    Institute of Scientific and Technical Information of China (English)

    Lin Min; Zhu Bin; Shu Xingtian; Wang Xieqing

    2009-01-01

    In order to investigate the rules on formation of zeolite during crystallization of titanium silicalite zeolite (TS-1) the X-ray diffractometry and Foulier transform infra-red spectrometry were applied to track the process of crystallization of titanium silicalite zeolite. The research results revealed that at the initial stage of crystallization the interactions between silica gel and titania gel in the polymer blend could gradually lead to the formation of tiny crystal nuclei with complicated structure that could slowly grow up to form molecular sieves. Quite different from the conventional zeolites that use the acid sites as the catalytically active centers, the oxidative reactivity of the titanium silicalite zeolite was not proportional to its crystallinity and is associated with the oxidative centers of titanium contained in the zeolite.

  5. Natural zeolites: structures, classification, origin, occurrence and importance

    International Nuclear Information System (INIS)

    Zeolite are hydrated aluminosilicates composed of SiO/sub 4/ and AlO/sub 4/ tetrahedra. The aluminosilicate frameworks contain well defined channels (pores) and cavities . The cavities contain exchangeable cation, in particular sodium, potasium, magnesium, calcium and barium. The dehydrated zeolite behaves like molecular sieve. The zeolites occur both as minerals and as material synthesized in laboratory and on industrial scale. The old classification of recognized species of zeolites was based on morphological properties. A modified classification in based on secondary building units of frameworks. There are different opinions about the origin and occurrence of zeolite minerals. The zeolites have gained much importance as molecular sieves and catalysts. They are also very important for their unique structural properties. (authors)

  6. Synthesis and characterization of carbon cryogel/zeolite composites

    Directory of Open Access Journals (Sweden)

    Biljana Babić

    2011-06-01

    Full Text Available A novel method for synthesis of carbon cryogel/zeolite composites was obtained. Method considers forming of carbon cryogel from the sol-gel polycondenzation of resorcinol and formaldehyde, followed by freeze drying, and subsequent pyrolysis in presence of different amount of zeolite. Characterization of composite materials by nitrogen adsorption shows that samples are micro- and mesoporous and that specific surface area decrease with increasing the amount of zeolite in samples. XRD method confirms amorphous structure of carbon cryogel and crystalline structure of zeolite, i.e. structure of zeolite has not been destroyed by carbonization process. SEM and EDX analyses reveal homogenous distribution of zeolite through out carbon cryogel and corresponding composition.

  7. Opioid bifunctional ligands from morphine and the opioid pharmacophore Dmt-Tic.

    Science.gov (United States)

    Balboni, Gianfranco; Salvadori, Severo; Marczak, Ewa D; Knapp, Brian I; Bidlack, Jean M; Lazarus, Lawrence H; Peng, Xuemei; Si, Yu Gui; Neumeyer, John L

    2011-02-01

    Bifunctional ligands containing an ester linkage between morphine and the δ-selective pharmacophore Dmt-Tic were synthesized, and their binding affinity and functional bioactivity at the μ, δ and κ opioid receptors determined. Bifunctional ligands containing or not a spacer of β-alanine between the two pharmacophores lose the μ agonism deriving from morphine becoming partial μ agonists 4 or μ antagonists 5. Partial κ agonism is evidenced only for compound 4. Finally, both compounds showed potent δ antagonism.

  8. Zeolitic tuffs as raw materials for lightweight aggregates

    OpenAIRE

    de Gennaro, R.; P. Cappelletti; Cerri, G.; Gennaro, M; Dondi, M.; A. Langella

    2004-01-01

    The aim of this research is to assess the possible use of Italian zeolitic rocks for the production of lightweight aggregates. In particular, both the expansion at high temperature and the technological features of fired products were investigated. Fifteen zeolite-bearing volcanoclastites from Northern Sardinia and three zeolitized tuffs from Campania and Tuscany (Sorano and Campanian ignimbrites and Neapolitan Yellow Tuff) were taken into account. The firing expansion turned out to be mainly...

  9. Fundamental aspects of water methane separation in zeolites

    OpenAIRE

    Leirvik, Kim Nes

    2013-01-01

    The main objective of this thesis was to use molecular dynamics to investigate the methane interactions with zeolite, specifically the Linde Type A-3A, alongside with an investigation into the use of polynomial path integration for water in zeolite. This thesis is a part of a larger collaboration between the separation group at the University of Bergen and Statoil, with the main goal of explaining the reduced lifetime of zeolites. This thesis continued from the work done by ...

  10. Composites obtained from magnesium clusters and zeolite 4A

    International Nuclear Information System (INIS)

    Zeolite-supported metal clusters have most commonly been prepared by ion exchange, followed by calcination and reduction. Proper activation and reduction treatment give the highest metal dispersion into zeolite mass. This work presents composites obtained from metal magnesium clusters and zeolite 4 A. It was determined the structure and properties by studies of texture, X-ray diffraction and transmission electron microscopy (TEM). These samples offer an opportunity to determine the catalytic properties of metal magnesium clusters. (authors)

  11. Zeolite for strontium separation from concentrated sodium salt solutions

    International Nuclear Information System (INIS)

    Strontium sorption from solutions with concentration of 5 mol/l sodium chloride on zeolites of different structure is investigated. Synthetic potassium zeolite of the K-G(13) chabasite type is established to be used to purify the solutions given from strontium radionuclides. Capacity of K-G(13) zeolite for strontium in the solution with concentration of 5 mol/l sodium chloride is 0.65 mmol/g

  12. 3D Nanoscale Imaging and Quantitative Analysis of Zeolite Catalysts

    OpenAIRE

    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 potential and optimize their properties for specific applications, zeolites are often subjected to several post-synthesis modifications. The work presented in this thesis aims to provide a deeper underst...

  13. Fluoride-assisted synthesis of bimodal microporous SSZ-13 zeolite.

    Science.gov (United States)

    Zhu, Xiaochun; Kosinov, Nikolay; Hofmann, Jan P; Mezari, Brahim; Qian, Qingyun; Rohling, Roderigh; Weckhuysen, Bert M; Ruiz-Martínez, Javier; Hensen, Emiel J M

    2016-02-21

    The presence of small amount of fluoride in alkaline hydrothermal synthesis of SSZ-13 zeolite yields bimodal microporous particles with substantially improved performance in the methanol-to-olefins (MTO) reaction. Hydrocarbon uptake measurements and fluorescence microspectroscopy of spent catalysts demonstrate enhanced diffusion through micropores at the grain boundaries of nanocrystals running through the zeolite particles. Fluoride-assisted SSZ-13 synthesis is a cheap and scalable approach to optimize the performance of MTO zeolite catalysts. PMID:26810114

  14. Removal of Ammonia from Air, using Three Iranian Natural Zeolites

    OpenAIRE

    H. Asilian; SB Mortazavi; Kazemian, H; S Phaghiehzadeh; Sj Shahtaheri; Salem, M.

    2004-01-01

    Ammonia in air can be hazardous to human and animal life and should be removed from the environment. Recently the removal of environmental pollutants such as ammonia by means of natural and modified zeolites has attracted a lot of attention and interests. In this study the capability of three Iranian natural zeolites (Clinoptilolite) in point of view of removal of ammonia from air was investigated. Through this research, different zeolites from various regions of Iran including Semnan, Meyane...

  15. Application of natural zeolites in anaerobic digestion processes: A review

    OpenAIRE

    Montalvo, Silvio; Borja Padilla, Rafael; Sánchez, Enrique; Milán, Zhenia; Cortés, Isel; Rubia, M. Ángeles de la

    2012-01-01

    This paper reviews the most relevant uses and applications of zeolites in anaerobic digestion processes. The feasibility of using natural zeolites as support media for the immobilization of microorganisms in different high-rate reactor configurations (fixed bed, fluidized bed, etc.) is also reviewed. Zeolite, with its favorable characteristics for microorganism adhesion, has also been widely used as an ion exchanger for the removal of ammonium in anaerobic digestion due to the presence of Na ...

  16. Selective adsorption of heavy and light metals by natural zeolites

    OpenAIRE

    Fosso-Kankeu, Elvis; Reitz, Magdali; Waanders, Frans

    2014-01-01

    Recent studies have shown that zeolite can be applied through an ion-exchange process to remove metals from solutions. In this paper the potential of two zeolites to perform as sorbents for treatment of multi-metal system is investigated. Parameters such as initial metal concentration, contact time, zeolite type and affinity for heavy versus light metals are taken into consideration. All the samples were prepared and characterized by XRD, XRF and FTIR. Evaluating suitable model for the det...

  17. 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...

  18. Properties of natural zeolites in benefit of nutrition and health

    OpenAIRE

    Irina Smical

    2011-01-01

    Due to their remarkable properties, natural zeolites have come to the attention of medicineresearchers to find new ways of treating various diseases and ensure an improved supply of mineralsin nutrition. The research results have shown the beneficial effects of application of various types ofnatural zeolites in healing or ameliorating especially gastrointestinal and diarrhea disease and cancerdisease, as well. Because natural zeolites have a very good ability as ion exchangers they are largel...

  19. Zeolitization of Tuffaceous Rocks in the Kesan Region, Thrace, Turkey

    OpenAIRE

    Esenli, F.; Uz, B.; Suner, F.; Esenli, V.; Ece, O.I.; Kumbasar, I.

    2005-01-01

    A 33 metre thick pyroclastic-rich zone of the Mezardere formation of Oligocene age is exposed in the Kesan region of Thrace, Turkey. In this zone, vitreous tuffs of dacitic composition have altered primarily to zeolites, including mordenite, heulandite–clinoptilolite and analcime. Silicification and alteration to clay minerals are common. Zeolite minerals have developed from volcanic glass, whereas some mordenites have formed from dissolution of heulandite-group zeolites. Although authigenic ...

  20. Association of indigo with zeolites for improved colour stabilization

    OpenAIRE

    Dejoie, Catherine; Martinetto, Pauline; Dooryhee, Eric; Van Eslande, Elsa; Blanc, Sylvie; Bordat, Patrice; Brown, Ross; Porcher, Florence; Anne, Michel

    2010-01-01

    The durability of an organic colour and its resistance against external chemical agents and exposure to light can be significantly enhanced by hybridizing the natural dye with a mineral. In search for stable natural pigments, the present work focuses on the association of indigo blue with several zeolitic matrices (LTA zeolite, mordenite, MFI zeolite). The manufacturing of the hybrid pigment is tested under varying oxidising conditions, using Raman and UV-visible spectrometric techniques. Ble...

  1. Multi-elemental characterization of Cuban natural zeolites

    International Nuclear Information System (INIS)

    Concentration of 38 elements in samples from four important Cuban zeolite beds have been obtained by Instrumental Neutron Activation (INAA) and X-ray Fluorescence analyses (XRFA). In comparison with other analytical techniques good agreement was reached. 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. (author)

  2. Extraction and immobilization of simulated pyrometallurgical chloride waste in Zeolite

    International Nuclear Information System (INIS)

    Zeolites are effective media for the removal and immobilization of fission products waste from pyrometallurgical reprocessing of nuclear fuels. In the present study, equilibration experiments between zeolite 4A and a simulated: pyrometallurgical chloride waste were carried out. Several batches of equilibration were carried out by varying the zeolite to salt (Z/S) ratio. The effects of Z/S on the extraction behaviour of the waste chloride salts were explored. (author)

  3. Green Process for Synthesis of Zeolite with MFI Structure

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    A clean and environmentally friendly new process for synthesis of zeolite with MFI structure was presented. This process through recycling of vented gas and mother liquor can reduce or avoid discharge of nitrogen-containing offgas and waste liquid without affecting the physical and chemical properties of synthetic zeolite, leading to green synthesis of zeolite. This process can help to cut corners on production cost to achieve the sustainable development.

  4. Cation locations and dislocations in zeolites

    Science.gov (United States)

    Smith, Luis James

    The focus of this dissertation is the extra-framework cation sites in a particular structural family of zeolites, chabazite. Cation sites play a particularly important role in the application of these sieves for ion exchange, gas separation, catalysis, and, when the cation is a proton, acid catalysis. Structural characterization is commonly performed through the use of powder diffraction and Rietveld analysis of powder diffraction data. Use of high-resolution nuclear magnetic resonance, in the study of the local order of the various constituent nuclei of zeolites, complements well the long-range order information produced by diffraction. Recent developments in solid state NMR techniques allow for increased study of disorder in zeolites particularly when such phenomena test the detection limits of diffraction. These two powerful characterization techniques, powder diffraction and NMR, offer many insights into the complex interaction of cations with the zeolite framework. The acids site locations in SSZ-13, a high silica chabazite, and SAPO-34, a silicoaluminophosphate with the chabazite structure, were determined. The structure of SAPO-34 upon selective hydration was also determined. The insensitivity of X-rays to hydrogen was avoided through deuteration of the acid zeolites and neutron powder diffraction methods. Protons at inequivalent positions were found to have different acid strengths in both SSZ-13 and SAPO-34. Other light elements are incorporated into zeolites in the form of extra-framework cations, among these are lithium, sodium, and calcium. Not amenable by X-ray powder diffraction methods, the positions of such light cations in fully ion-exchanged versions of synthetic chabazite were determined through neutron powder diffraction methods. The study of more complex binary cation systems were conducted. Powder diffraction and solid state NMR methods (MAS, MQMAS) were used to examine cation site preferences and dislocations in these mixed-akali chabazites

  5. Peculiarities of the dielectric response of natural zeolite composites prepared by using zeolite and silicon powders

    Science.gov (United States)

    Ozturk Koc, S.; Orbukh, V. I.; Eyvazova, G. M.; Lebedeva, N. N.; Salamov, B. G.

    2016-03-01

    We present the real and imaginary part of the dielectric permittivity of natural zeolite composites prepared by using zeolite and silicon powders. The dielectric response (DR) dependences on the frequency (3-300 GHz) of electric field and different Si concentrations (5-33%) are non-monotonic and a maximum peak is observed. This peak position is practically independent on the frequency and its maximum is observed in zeolite composites which included 9% of the Si-powder. Also the maximum peak is decreased by about an order of magnitude when frequency increases from 500 Hz to 5 kHz. Addition of the conductive Si-particles to zeolite-powder leads to two opposite effects. Firstly, the movement of electrons in the Si-particles provides increase of DR. Secondly, cations which leaving from zeolite pores can be neutralized by the particles of Si in the intercrystalline-space. Such a peculiar mechanism for recombination of Si electrons and cations from pores leads to a reduction of DR for large silicon concentrations. Due to the fact that the contribution of free carriers in the decreasing of the DR as the frequency increases, it is consistent with the suggestion that the maximum peak decreases with increasing frequency.

  6. Synthesis of Zeolite ZSM-2 Using Zeolite NaX as Seeds

    Institute of Scientific and Technical Information of China (English)

    YI, Hong-Jiang(易洪江); WU, Tai-Liu(吴泰琉); WANG, Li-Ping(王力平); SUN, Yao-Jun(孙尧俊)

    2004-01-01

    A method is presented for the synthesis of zeolite ZSM-2 by adding zeolite X as seeds in the synthetic mixture containing both lithium and sodium. At the presence of zeolite X seeds, highly crystalline zeolite ZSM-2 with composition of (0.3-0.7)Li2O·(0.7-0.3)Na2O·Al2O3·(2.5-4.0)SiO2·nH2O can be obtained in a wide range of SiO2/Al2O3 ratios from 2.5 to 16, and the optimum Li2O/(Li2O+Na2O) fraction is between 0.3 and 0.7. The ZSM-2 products were characterized by XRD, SEM, IR, 29Si MAS NMR and DTA/TG analysis etc. By 29Si MAS NMR spectroscopy, it was found that ZSM-2 contained nearly equal FAU and EMT phase, and the Si/Al ratios in FAU were slightly lower than those in EMT domains in most cases. The lithium form zeolite ZSM-2 has comparable N2 adsorption capacity with LiX.

  7. Zeolite occurrence and genesis in the Late-Cretaceous Cayo arc of Coastal Ecuador: Evidence for zeolite formation in cooling marine pyroclastic flow deposits

    OpenAIRE

    Machiels, L.; Garces, D. (D.); Snellings, R.; Vilema, W.; Morante, F.; C Paredes; ELSEN, J

    2014-01-01

    This paper describes the quantitative mineralogy, the mineral chemistry and the distribution of natural zeolites over the outcrop area of the Late Cretaceous Cayo Formation of Coastal Ecuador (>1000 km(2)) and develops a model for zeolite alteration in the Cayo volcanic arc. Different zeolite types were identified: Ca-heulandite-type zeolites (clinoptilolite and heulandite), mordenite, laumontite, analcime, stilbite, epistilbite, chabazite, thomsonite and erionite. Zeolites occur over nearly ...

  8. KINERJA ZEOLIT DALAM MEMPERBAIKI MUTU MINYAK GORENG BEKAS [Zeolit Performance in Improving the Quality of Used Oil

    Directory of Open Access Journals (Sweden)

    Kusumastuti

    2004-08-01

    Full Text Available The aim of this study was to improve the used oil by treatment with zeolite in order to absorb the undesirable components in the oil. Sample of used oil were heated with active zeolite (A1 and natural zeolite (A2 at 2% (B1, 6% (B2 and 10% (B3 in boiled water-bath for 30 minutes. The control was used oil without treatment. After filtered, the oil were analyzed for moisture content, acid number, peroxide value, clearness, colour and viscosity. The results indicated that treating used oil with 10% zeolite could reduce the initial level of tested parameters The reductions were: moisture content and volatile matters 50%, acid number 7% , clearness 3.9% and reduction of peroxide value was 33,8%. However the color and viscosity of the treated oils were not different from the used oil. Active zeolite was more effective than natural zeolite in absorbing the undesirable contaiment

  9. Dealuminization treatment effect of krypton gas adsorption on zeolite

    Energy Technology Data Exchange (ETDEWEB)

    Shin, J. M.; Shin, S. W.; Park, J. J.; Lee, H. H.; Yang, M. S. [KAERI, Taejon (Korea, Republic of)

    2003-10-01

    During the OREOX process of DUPIC fuel fabrication, krypton is released as a noble fission gas. In order to treat Kr safely, adsorption method on solids havs been selected. In order to determine the optimum extraction conditions of zeolite for Kr adsorption, the preliminary experiments for the concentration of hydrochloric acid were conducted. It was found that zeolite treated with 2N hydrochloric acid solution is superior to the zeolite untreated with HCl solution. When the zeolite was treated with 2N hydrochloric acid, it was found that the surface area was decreased. The micropores and the pore volume were increased and the adsorption amount of Kr gas was increased.

  10. Regioselective nitration of aromatic substrates in zeolite cages

    Indian Academy of Sciences (India)

    T Esakkidurai; M Kumarraja; K Pitchumani

    2003-04-01

    Phenol is nitrated regioselectively by fuming nitric acid inside the cages of faujasite zeolites (dependent on the loading level) and a remarkable orthoselectivity is observed in solid state nitration. Toluene and chlorobenzene also containing ortho-/para-orienting substituents, undergo faster nitration, though the regioselectivity is less significant in zeolite media. The results are explained on the basis of diffusion and binding of phenol inside zeolite, which facilitate regioselectivity (and which is absent in toluene and chlorobenzene). Other advantages of employing zeolites as media for mild and selective nitration are also highlighted.

  11. Natural zeolites in diet or litter of broilers.

    Science.gov (United States)

    Schneider, A F; Almeida, D S De; Yuri, F M; Zimmermann, O F; Gerber, M W; Gewehr, C E

    2016-04-01

    This study aims to analyse the influence of adding natural zeolites (clinoptilolite) to the diet or litter of broilers and their effects on growth performance, carcass yield and litter quality. Three consecutive flocks of broilers were raised on the same sawdust litter, from d 1 to d 42 of age, and distributed in three treatments (control with no added zeolites, addition of 5 g/kg zeolite to diet and addition of 100 g/kg zeolites to litter). The addition of zeolites to the diet or litter did not affect growth performance or carcass yield. The addition of zeolites to the diet did not influence moisture content of the litter, ammonia volatilisation was reduced only in the first flock and pH of litter was reduced in the second and third flock. However, the addition of zeolites to the litter reduced moisture content, litter pH and ammonia volatilisation in all flocks analysed. The addition of 5 g/kg zeolite to the diet in three consecutive flocks was not effective in maintaining litter quality, whereas the addition of 100 g/kg natural zeolites to sawdust litter reduced litter moisture and ammonia volatilisation in three consecutive flocks raised on the same litter. PMID:26879673

  12. Influence of temperature on natural and chemically modified zeolites

    International Nuclear Information System (INIS)

    Zeolites from Nizny Hrabovec (Slovak Republic) were modified with solutions of NaOH. The changes of zeolites in the temperature range 20-1200 deg C were studied by thermal analysis (DTA, TG, ETA), X-ray analysis and REM analysis. Thermal analysis showed that the process of dehydration started between temperatures 20 and 600 deg C, over this temperature the dealumination and structural changes have taken place. X-ray analysis and REM analysis showed the structural changes of natural zeolites and gradual loss of cristallinity of the chemically modified zeolites. (author)

  13. 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.

  14. Human bile sorption by cancrinite-type zeolites

    International Nuclear Information System (INIS)

    A nitrated cancrinite-type zeolite was synthesized from zeolite X, NaOH and NaNO3 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

  15. Acidity of two-dimensional zeolites.

    Science.gov (United States)

    Rybicki, Marcin; Sauer, Joachim

    2015-11-01

    Hybrid quantum mechanics:molecular mechanics (QM/MM) calculations of absolute deprotonation energies are performed with periodic boundary conditions for Brønsted sites of aluminosilicate bilayers with various Al/Si ratios (two-dimensional zeolite). The supercell method is applied and density functional theory is used. Much lower values are obtained (1042, 1069 and 1091 kJ mol(-1) for Al/Si = 1/63, 1/7 and 1/3, respectively) than those for bulk zeolites (1233 kJ mol(-1) for H-chabazite with Al/Si = 1/11). We ascribe the much lower deprotonation energy to the smaller effective dielectric constant (1.6-1.9) of an ultra-thin dielectric in a vacuum compared to that of the corresponding bulk systems (3.0 for H-chabazite), which leads to a better stabilization of the charge created upon deprotonation. PMID:26437870

  16. Computer simulation of molecular sorption in zeolites

    CERN Document Server

    Calmiano, M D

    2001-01-01

    The work presented in this thesis encompasses the computer simulation of molecular sorption. In Chapter 1 we outline the aims and objectives of this work. Chapter 2 follows in which an introduction to sorption in zeolites is presented, with discussion of structure and properties of the main zeolites studied. Chapter 2 concludes with a description of the principles and theories of adsorption. In Chapter 3 we describe the methodology behind the work carried out in this thesis. In Chapter 4 we present our first computational study, that of the sorption of krypton in silicalite. We describe work carried out to investigate low energy sorption sites of krypton in silicalite where we observe krypton to preferentially sorb into straight and sinusoidal channels over channel intersections. We simulate single step type I adsorption isotherms and use molecular dynamics to study the diffusion of krypton and obtain division coefficients and the activation energy. We compare our results to previous experimental and computat...

  17. 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.

  18. Concerted bifunctionality of the dCTP deaminase-dUTPase from Methanocaldococcus jannaschii: A structural and pre-steady state kinetic analysis

    DEFF Research Database (Denmark)

    Siggaard, Julie; Johansson, Eva; Vognsen, Tina Reinholdt;

    2009-01-01

    complexes and closed over the active site by interacting with the phosphate backbone of the nucleotide or with the diphosphate. A magnesium ion was readily observed to complex with all three phosphoryls in the nucleotide complex or with the diphosphate. A water molecule that is likely to be involved...... in the nucleotidyl diphosphorylase reaction was observed in the E145A:alpha,beta-imido-dUTP complex and positioned similarly as in the monofunctional trimeric dUTPase. A comparison of the active sites of the bifunctional enzyme and the monofunctional family members, dCTP deaminase and dUTPase, suggests similar...... reaction mechanisms. The similar side chain conformations in the deaminase site between the nucleotide and diphosphate complexes indicated a concerted re-arrangement, or induced fit, of the whole active site promoted by enzyme and nucleotide phosphoryl interactions. A pre-steady state kinetic analysis...

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

    Science.gov (United States)

    Salim, Mashitah Mad; Malek, Nik Ahmad Nizam Nik

    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, 5h) and this material has excellent performance as an antibacterial agent after silver ions loading.

  20. 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.

  1. Zeolite-Nafion composites as ion conducting membrane materials

    International Nuclear Information System (INIS)

    Composite membranes formed of zeolitic fillers embedded in Nafion can be made by evaporating the solvents from a suspension of small zeolite crystals in a Nafion solution. Two natural zeolites were selected as fillers: chabazite and clinoptilolite. Membranes with various zeolite content were obtained. Composite membranes with zeolite content up to 40 vol.% exhibited uniform distribution of the zeolite fillers throughout the thickness, as ascertained by scanning electron microscopy (SEM), energy dispersive X-rays absorption (EDX) and ion conductivity measurements. Although more brittle than Nafion, these composite sheets retain--when hydrated--reasonable flexibility below 40 vol.% zeolite content. We have determined the hydrogen ion conductivity and the permeability of methanol molecules through these membranes (in the H+-form as well as in the Na+-form) in the temperature range 22-60 deg. C. We found that the presence of the zeolitic fillers in the membranes can bear notable changes of conductivity, permeability and selectivity with respect to membranes made out of sole Nafion

  2. Innovations in the synthesis of Fe-(exchanged)-zeolites

    NARCIS (Netherlands)

    Melian-Cabrera, [No Value; Kapteijn, F; Moulijn, JA; Melián-Cabrera, I.

    2005-01-01

    Several aspects on the preparation of Fe-zeolites are discussed. In contrast to the many studies highlighting the characterisation of the active sites, new approaches for incorporation of Fe are presented. Full utilization of exchange capacity of zeolites has been achieved by a controlled alkaline t

  3. 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 potent

  4. Arrangement and dynamics of water in natural zeolites

    International Nuclear Information System (INIS)

    Elastic, inelastic and quasielastic neutron scattering experiments are performed on natural zeolites. Hydrogen atoms at the water molecules could be located in the fibrous zeolites natrolite and edingtonite. Inelastic neutron spectra can be divided into translational (δE -5 cm sec-1 at T = 295 K for the full amount of water. (author) 6 refs., 4 figs., 1 tab

  5. Cleaning of liquid radioactive wastes using natural zeolites

    International Nuclear Information System (INIS)

    Natural zeolite, clinoptilolite, was used to eliminate liquid radioactive wastes (LRW) 137Cs and 90Sr. The influence of several factors (pH of solution, grain size of the zeolite, etc.) on the process effectivity was studied. It was shown that clinoptilolite is an effective filter of the nuclides above

  6. A zeolite ion exchange membrane for redox flow batteries.

    Science.gov (United States)

    Xu, Zhi; Michos, Ioannis; Wang, Xuerui; Yang, Ruidong; Gu, Xuehong; Dong, Junhang

    2014-03-01

    The zeolite-T membrane was discovered to have high proton permselectivity against vanadium ions and exhibit low electrical resistance in acidic electrolyte solutions because of its enormous proton concentration and small thickness. The zeolite membrane was demonstrated to be an efficient ion exchange membrane in vanadium redox flow batteries. PMID:24396857

  7. Zeolite Nanoparticles for Selective Sorption of Plasma Proteins

    NARCIS (Netherlands)

    Rahimi, Mehran; Ng, E. -P.; Bakhtiari, K.; Vinciguerra, M.; Ahmad, H. Ali; Awala, H.; Mintova, S.; Daghighi, M.; Rostami, F. Bakhshandeh; de Vries, Marcel; Motazacker, M. M.; Peppelenbosch, M. P.; Mahmoudi, M.; Rezaee, F.

    2015-01-01

    The affinity of zeolite nanoparticles (diameter of 8-12 nm) possessing high surface area and high pore volume towards human plasma proteins has been investigated. The protein composition (corona) of zeolite nanoparticles has been shown to be more dependent on the plasma protein concentrations and th

  8. Zeolite Nanoparticles for Selective Sorption of Plasma Proteins

    NARCIS (Netherlands)

    M. Rahimi (Mehran); E.-P. Ng; K. Bakhtiari (Kamran); M. Vinciguerra (Manlio); H.A. Ahmad (H. Ali); H. Awala; S. Mintova; M. Daghighi (Mojtaba); F. Bakhshandeh Rostami; M. de Vries (Marieke); M.M. Motazacker (Mohammad); M.P. Peppelenbosch (Maikel); M. Mahmoudi; F. Rezaee (Farhad)

    2015-01-01

    textabstractThe affinity of zeolite nanoparticles (diameter of 8-12 nm) possessing high surface area and high pore volume towards human plasma proteins has been investigated. The protein composition (corona) of zeolite nanoparticles has been shown to be more dependent on the plasma protein concentra

  9. 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 ...

  10. Incorporation of copper histidine complexes into a zeolite Y matrix

    NARCIS (Netherlands)

    Mesu, J.G.; Baute, D.; Tromp, H.J.; Faassen, E.E.H. van; Weckhuysen, B.M.

    2003-01-01

    Preformed copper-histidine complexes were loaded into zeolite Y by ion exchange. The zeolite was found to contain a mixture of two different encaged complexes: a mono-histidine complex (A) and a bis-histidine complex (B). The initial copper concentration affects the composition of this mixture, with

  11. Adsorption and thermodynamic behavior of uranium on natural zeolite

    International Nuclear Information System (INIS)

    Adsorptive behavior of natural clinoptilolite-rich zeolite from Balikesir deposites in Turkey was assessed for the removal of uranium from aqueous solutions. The uranium uptake and cation exchange capacities of zeolite were determined. The effect of initial uranium concentrations in solution was studied in detail at the optimum conditions determined before (pH 2.0, contact time: 60 minutes, temperature: 20 deg C). The uptake equilibrium is best described by Langmuir adsorption isotherm. Some thermodynamic parameters (ΔH deg, ΔS deg, ΔG deg) of the adsorption system were also determined. Application to fixation of uranium to zeolite was performed. The uptake of uranium complex on zeolite followed Langmuir adsorption isotherm for the initial concentration (25 to 100 μg/ml). Thermodynamic values of ΔG deg, ΔS deg and ΔH deg found show the spontaneous and exothermic nature of the process of uranium ions uptake by natural zeolite. (author)

  12. Ethylenediamine complexes of transition metals in zeolite X

    International Nuclear Information System (INIS)

    Single-crystal X-ray diffraction studies of two ion-exchanged zeolite forms of the faujasite type are performed. Form I, NaCu[Cu(en)2]X [a=25.013(5) A, space group Fd3, 315F(hkl), R=0.050], is obtained by the treatment of zeolite NaX crystals with a [Cu(en)2]SO4 solution. Form II, NaCo[Co(en)x]X [a=25.000(5) A, space group Fd3, 532F(hkl), R=0.051], is obtained by the treatment of zeolite NaCoX with an ethylenediamine solution. Along with Na, Cu, and Co ions situated at the positions typical of zeolite X, the cationic complexes [Cu(en)2]2+ and [Co(en)x]2+ are found to be located in the large-sized zeolite cavities

  13. Rheological Influence of Synthetic Zeolite on Cement Pastes

    Science.gov (United States)

    Baldino, N.; Gabriele, D.; Frontera, P.; Crea, F.; de Cindio, B.

    2008-07-01

    Self Compacting Concrete (SCC) is characterized by specific and particular mechanical properties, often due to the addition of components, able to modify the paste rheology. Concrete properties are strongly affected by characteristics of the fresh cement paste that is the continuous phase dispersing larger aggregates. Therefore, aiming to characterize mechanical properties of final concrete is relevant to know rheological properties of the base cement paste. In this work cement pastes for SCC were prepared by using, as additive, synthetic zeolite 5A in different amounts and they were analyzed by small amplitude oscillations. Experimental results have shown a relationship between dynamic moduli and zeolite content, identifying a proper level of zeolite addition. Moreover samples containing traditional fine additives, such as silica fume and limestone, were prepared and experimental data were compared to those obtained by using zeolite. It was found that zeolite seems to give better properties to cement paste than other additives can do.

  14. The charge transport in the nanoporous natural zeolite

    International Nuclear Information System (INIS)

    It was presented the electrical characterization of a natural zeolite plate and charge transport, it is studied the functions of pressure (4-760 Torr), temperatures (295-435 K) and diameter (5-25 mm) of the cathode areas in the gas discharge electronic devices (GDED) with nanoporous zeolite cathode (NZC) for the first time. There are not enough investigations devoted to conductivity of zeolites in a dc voltage mode. Comparison of current from GDED is used for the determination of the stabilization under low- and atmospheric pressure glow microdischarges conditions. It is found that the gas in zeolite pores ionizes and accordingly the number of electrons in the pores grows. It is of importance to have knowledge in peculiarities of operation of GDED. It can be supposed that cheap natural zeolite will be effective in low-power GDED

  15. 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.

  16. 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.

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

    DEFF Research Database (Denmark)

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

    2005-01-01

    Zeolitcs are crystalline materials, which are widely used as solid acid catalysts and supports in many industrial processes. Recently, mesoporous MFI-type zeolite single crystals were synthesized by use of carbon particles as a mesopore template and sodium aluminate as the aluminum Source....... 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...... 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...

  18. Physico-chemical Characterization of Mo-Hβ Zeolite Catalysts

    Institute of Scientific and Technical Information of China (English)

    LIU Sheng-lin; HUANG Sheng-jun; XIN Wen-jie; QIN xin-hua; XIE Su-juan; XU Long-ya

    2004-01-01

    A series of Mo-impregnated Hβ samples, with MoO3 loading in Hβ zeolite in the mass fraction range of 0. 5%-6.0%, were studied by means of XRD and IR in order to characterize their structures. Mo/Hβ samples' crystallinity almost linearly decreases with increasing the amount of MoO3 loaded. The IR spectra and XRD patterns suggest that the progressive destabilization of the Hβ zeolite structure is caused by increasing Mo loading in (MoO3+Hβ zeolite). During the calcination, Al2(MoO4)3 formed from the dealumination of Hβ zeolite, causes the substantially partial breakdown of the zeolite framework when the Mo loading in MoO3 +Hβ is relatively high.

  19. Fly ash based zeolitic pigments for application in anticorrosive paints

    Science.gov (United States)

    Shaw, Ruchi; Tiwari, Sangeeta

    2016-04-01

    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 Mg2+ and Ca2+ 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).

  20. Zeolite stability constraints on radioactive waste isolation in zeolite-bearing volcanic rocks

    International Nuclear Information System (INIS)

    Silicic tuffs of the southern Great Basin and basalts of the Columbia River Plateau are under investigation as potential host rocks for high- and intermediate-level radioactive wastes. Non-welded and partially welded tuffs may contain major amounts (> 50%) of the zeolite minerals: clinoptilolite, mordenite, and analcime. Densely welded tuffs and some basalt flows may contain clinoptilolite as fracture filling which limits permeability of these rocks. The cation exchange properties of these zeolite minerals allow them to pose a natural barrier to the migration of cationic species of various radionuclides in aqueous solutions. However, these minerals are unstable at elevated temperatures and at low water vapor pressures, and they may break down either by reversible dehydration or by irreversible mineralogical reactions. All of the breakdown reactions occurring with increased temperature involve a net volume reduction and evolution of fluids. Thus, they may provide both a pathway (shrinkage fractures) and a driving force (fluid pressure) for release of radionuclides to the biosphere. These reactions may be avoided by keeping zeolite-bearing horizons saturated with water and below about 850C. This may restrict allowable gross thermal loadings in radioactive waste repositories in zeolite-bearing volcanic rocks. 3 figures

  1. Radiation-induced silver agglomeration in molecular sieves: a comparison between A and X zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Sadlo, J.; Wasowicz, T.; Michalik, J. [Institute of Nuclear Chemistry and Technology, Warsaw (Poland)

    1995-06-01

    The stabilization conditions of silver atoms and clusters in hydrated and dehydrated AgNa-A and AgNa-X zeolites {gamma}-irradiated at 77 K have been studied by ESR. It was found that silver agglomeration mechanisms in hydrated A and X zeolites are very similar and are controlled by the migration of silver atoms into the {alpha}-cages. In dehydrated zeolites agglomeration leads to completely different silver clusters in A and X zeolites. Small cationic clusters are stabilized in A zeolites and metallic clusters in X zeolites. Various factors affecting the agglomeration process in A and X zeolites are discussed. (author).

  2. Gold-Copper Nanoparticles: Nanostructural Evolution and Bifunctional Catalytic Sites

    Energy Technology Data Exchange (ETDEWEB)

    Yin, Jun; Shan, Shiyao; Yang, Lefu; Mott, Derrick; Malis, Oana; Petkov, Valeri; Cai, Fan; Ng, Mei; Luo, Jin; Chen, Bing H.; Engelhard, Mark H.; Zhong, Chuan-Jian

    2012-12-12

    Understanding of the atomic-scale structure is essential for exploiting the unique catalytic properties of any nanoalloy catalyst. This report describes novel findings of an investigation of the nanoscale alloying of gold-copper (AuCu) nanoparticles and its impact on the surface catalytic functions. Two pathways have been explored for the formation of AuCu nanoparticles of different compositons, including wet chemical synthesis from mixed Au- and Cu-precursor molecules, and nanoscale alloying via an evolution of mixed Au- and Cu-precursor nanoparticles near the nanoscale melting temperatures. For the evolution of mixed precursor nanoparticles, synchrotron x-ray based in-situ real time XRD was used to monitor the structural changes, revealing nanoscale alloying and reshaping towards an fcc-type nanoalloy (particle or cube) via a partial melting–resolidification mechanism. The nanoalloys supported on carbon or silica were characterized by in-situ high-energy XRD/PDFs, revealing an intriguing lattice "expanding-shrinking" phenomenon depending on whether the catalyst is thermochemically processed under oxidative or reductive atmosphere. This type of controllable structural changes is found to play an important role in determining the catalytic activity of the catalysts for carbon monoxide oxidation reaction. The tunable catalytic activities of the nanoalloys under thermochemically oxidative and reductive atmospheres are also discussed in terms of the bifunctional sites and the surface oxygenated metal species for carbon monoxide and oxygen activation.

  3. Gold(I) catalysts with bifunctional P, N ligands.

    Science.gov (United States)

    Wetzel, Corinna; Kunz, Peter C; Thiel, Indre; Spingler, Bernhard

    2011-08-15

    A series of phosphanes with imidazolyl substituents were prepared as hemilabile PN ligands. The corresponding gold(I) complexes were tested as bifunctional catalysts in the Markovnikov hydration of 1-octyne, as well as in the synthesis of propargylamines by the three component coupling reaction of piperidine, benzaldehyde, and phenylacetylene. While the activity in the hydration of 1-octyne was low, the complexes are potent catalysts for the three component coupling reaction. In homogeneous solution the conversions to the respective propargylamine were considerably higher than under aqueous biphasic conditions. The connectivity of the imidazolyl substituents to the phosphorus atom, their substitution pattern, as well as the number of heteroaromatic substituents have pronounced effects on the catalytic activity of the corresponding gold(I) complexes. Furthermore, formation of polymetallic species with Au(2), Au(3), and Au(4) units has been observed and the solid-state structures of the compounds [(5)(2)Au(3)Cl(2)]Cl and [(3c)(2)Au(4)Cl(2)]Cl(2) (3c = tris(2-isopropylimidazol-4(5)-yl phosphane, 5 = 2-tert-butylimidazol-4(5)-yldiphenyl phosphane) were determined. The gold(I) complexes of imidazol-2-yl phosphane ligands proved to be a novel source for bis(NHC)gold(I) complexes (NHC = N-heterocyclic carbene). PMID:21761834

  4. Bifunctional alkyl nitrates - trace constituents of the atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Kastler, J. [Department of Analytical and Environmental Chemistry, University of Ulm (Germany); Ballschmiter, K. [Center of Technology Assessment in Baden-Wuerttemberg, Stuttgart (Germany)

    1998-04-01

    Mono- and multifunctional esters of nitric acid (alkyl nitrates or organonitrates) form very complex mixtures of organic trace constituents in air. An analytical method was developed which combines selectivity in separation and detection in order to simplify this complexity in analytical terms. Mononitrates, dinitrates, keto nitrates, hydroxy nitrates of alkanes and alkenes, respecitvely, and bifunctional terpene nitrates were synthesized as reference substances. A specially developed new HPLC stationary phase (organonitrate phase) allows a group separation of mono-, di-, and hydroxy nitrates. After the HPLC preseparation the single components were finally separated by capillary HRGC-ECD and HRGC-MSD on polar and non-polar stationary phases. Mass spectrometric detection in the selected-ion-mode using the highly selective NO{sub 2}{sup +} fragment (m/z = 46 amu) led to very good selectivities for the nitric acid ester moiety. The analysis of a 100 m{sup 3} ambient air sample using this new analytical protocol allowed the identification of seven hydroxy nitrates and 24 dinitrates ranging from C2 to C7, 22 of them for the first time ever. (orig.) With 3 figs., 3 tabs., 20 refs.

  5. Bioinspired Bifunctional Membrane for Efficient Clean Water Generation.

    Science.gov (United States)

    Liu, Yang; Lou, Jinwei; Ni, Mengtian; Song, Chengyi; Wu, Jianbo; Dasgupta, Neil P; Tao, Peng; Shang, Wen; Deng, Tao

    2016-01-13

    Solving the problems of water pollution and water shortage is an urgent need for the sustainable development of modern society. Different approaches, including distillation, filtration, and photocatalytic degradation, have been developed for the purification of contaminated water and the generation of clean water. In this study, we explored a new approach that uses solar light for both water purification and clean water generation. A bifunctional membrane consisting of a top layer of TiO2 nanoparticles (NPs), a middle layer of Au NPs, and a bottom layer of anodized aluminum oxide (AAO) was designed and fabricated through multiple filtration processes. Such a design enables both TiO2 NP-based photocatalytic function and Au NP-based solar-driven plasmonic evaporation. With the integration of these two functions into a single membrane, both the purification of contaminated water through photocatalytic degradation and the generation of clean water through evaporation were demonstrated using simulated solar illumination. Such a demonstration should also help open up a new strategy for maximizing solar energy conversion and utilization.

  6. Oxidative regeneration of toluene-saturated natural zeolite by gaseous ozone: the influence of zeolite chemical surface characteristics.

    Science.gov (United States)

    Alejandro, Serguei; Valdés, Héctor; Manéro, Marie-Hélène; Zaror, Claudio A

    2014-06-15

    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 823K 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 623K, 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. PMID:24794812

  7. Oxidative regeneration of toluene-saturated natural zeolite by gaseous ozone: the influence of zeolite chemical surface characteristics.

    Science.gov (United States)

    Alejandro, Serguei; Valdés, Héctor; Manéro, Marie-Hélène; Zaror, Claudio A

    2014-06-15

    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 823K 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 623K, 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.

  8. Single flexible nanofiber to achieve simultaneous photoluminescence-electrical conductivity bifunctionality.

    Science.gov (United States)

    Sheng, Shujuan; Ma, Qianli; Dong, Xiangting; Lv, Nan; Wang, Jinxian; Yu, Wensheng; Liu, Guixia

    2015-02-01

    In order to develop new-type multifunctional composite nanofibers, Eu(BA)3 phen/PANI/PVP bifunctional composite nanofibers with simultaneous photoluminescence and electrical conductivity have been successfully fabricated via electrospinning technology. Polyvinyl pyrrolidone (PVP) is used as a matrix to construct composite nanofibers containing different amounts of Eu(BA)3 phen and polyaniline (PANI). X-Ray diffractometry (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM), fluorescence spectroscopy and a Hall effect measurement system are used to characterize the morphology and properties of the composite nanofibers. The results indicate that the bifunctional composite nanofibers simultaneously possess excellent photoluminescence and electrical conductivity. Fluorescence emission peaks of Eu(3+) ions are observed in the Eu(BA)3 phen/PANI/PVP photoluminescence-electrical conductivity bifunctional composite nanofibers. The electrical conductivity reaches up to the order of 10(-3)  S/cm. The luminescent intensity and electrical conductivity of the composite nanofibers can be tuned by adjusting the amounts of Eu(BA)3 phen and PANI. The obtained photoluminescence-electrical conductivity bifunctional composite nanofibers are expected to possess many potential applications in areas such as microwave absorption, molecular electronics, biomedicine and future nanomechanics. More importantly, the design concept and construction technique are of universal significance to fabricate other bifunctional one-dimensional naonomaterials.

  9. Novel Polyamide Proton Exchange Membranes with Bi-Functional Sulfonimide Bridges for Fuel Cell Applications

    International Nuclear Information System (INIS)

    Graphical abstract: A polymer proton conductor crosslinked with bi-functional sulfonamide bridges is synthesized for PEM fuel cell applications. The architecture simultaneously enhances mechanical strength and improves water retention of the PEMs. With an appropriate degree of crosslinking, the bi-functional PEM exhibits comparable performance to that of a commercial Nafion membrane tested in a direct methanol fuel cell. - Abstract: We design and successfully synthesize non-fluorinated polyamides with controlled crosslinking using sulfonimide as a bi-functional linker to interconnect polymer backbones and as a bridge for proton conduction. We show that the bi-functional linkers are highly beneficial not only for mechanical enforcement of the proton exchange membranes but also for enhancement of water retention capacity. With an appropriate degree of crosslinking, higher water retention capacity than that of commercial Nafion membranes can be obtained. The maximum proton conductivity of the membranes is found to be as high as 0.139 S cm−1 at 80 °C, almost the same as that of a Nafion 117 membrane. Excellent performance with the bi-functional polymer membranes in an air-breathing direct methanol fuel cell prototype, comparable to the performance of a Nafion 117 membrane, is demonstrated

  10. 氧化钙改性分子筛对一步法合成二甲醚的影响%One-step synthesis of dimethyl ether over a bi-functional catalyst containing CaO-modified HZSM-5

    Institute of Scientific and Technical Information of China (English)

    许庆利; 李廷琛; 颜涌捷

    2008-01-01

    Synthesis of dimethyl ether (DME) was carried out in a fixed bed reactor over a bifunctional catalyst CaO/HZSM-5+JC207,which was composed of a methanol-synthesis catalyst JC207 (Jingjing Catalyst Plant,China) and a dehydrator HZSM-5 (Si/Al = 38) modified with CaO. The effects of zeolite modification with CaO on the performance of the bifunctional catalyst in one-step synthesis of DME were investigated. XRD analysis of the modified zeolite CaO/HZSM-5 indicates that CaO is highly dispersed on the zeolite HZSM-5 without any new species formed. Pyridine-IR analysis shows that the modification of HZSM-5 with CaO not only brings on significant changes in acid type and acid amount but also turns some of Bronstead acid sites into Lewis acid sites. NH3-temperature programming desorption analysis indicates that the number of acid sites on the zeolite surface,especially,that of the strong acid sites decreases with the increase of CaO loading. Modification of zeolite HZSM-5 with appropriate dose of CaO turns the strong acid sites into weak or less strong acid sites;such a redistribution of acid sites may be beneficial for the increase of DME selectivity.%采用浸渍法制备了一系列CaO改性的HZSM-5 (Si/Al=38)分子筛,并以CaO/HZSM-5为脱水剂 与JC207甲醇合成催化剂(靖江催化剂厂)按照一定的比例组成双功能催化剂,在固定床反应器上考察了其对一步法合成二甲醚的影响.XRD结果表明,CaO在HZSM-5上呈高度分散状态,没有发现新的物种生成.Pyridine-IR结果表明,CaO引入HZSM-5后,酸中心的类型和数量发生明显的变化,CaO的加人促使部分酸中心由B酸中心转变为L酸中心.NH3-TPD结果表明,随着CaO含量的增加,HZSM-5分子筛表面酸性较强的酸中心数目下降,总酸中心数目也下降,但酸性较强的酸中心下降较快.表明适量的CaO改性HZSM-5分子筛不是除去表面所有的酸中心,而是通过与表面强酸中心的作用,使其向弱酸和中强

  11. The use of clinoptilolite and synthetic zeolites for removal of petroleum substances

    OpenAIRE

    Bandura, L.; Panek, R; Franus, W.

    2014-01-01

    In the present paper the sorption of petroleum substances such as diesel fuels on zeolite beds was investigated. A natural occurring zeolite clinoptilolite, and mixtures of clinoptilolite and synthetic zeolites Na-P1 and Na-X type, in the ratio 3:1, were used in this study. Natural zeolite acquired from the mine tuffs in Sokyrnytsya (Ukraine). In order to obtain synthetic zeolites, F-class fly ash (Kozienice Power Plant, Poland) with sodium hydroxide was u...

  12. Mechanish of dTTP Inhibition of the Bifunctional dCTP Deaminase:dUTPase Encoded by Mycobacterium tuberculosis

    DEFF Research Database (Denmark)

    Helt, Signe Smedegaard; Thymark, Majbritt; Harris, Pernille;

    2008-01-01

    Recombinant deoxycytidine triphosphate (dCTP) deaminase from Mycobacterium tuberculosis was produced in Escherichia coli and purified. The enzyme proved to be a bifunctional dCTP deaminase:deoxyuridine triphosphatase. As such, the M. tuberculosis enzyme is the second bifunctional enzyme to be cha...

  13. Characteristics of Lead Sorption by Zeolite Minerals

    Science.gov (United States)

    Al-Sewailem, M. S.

    Lead adsorption behavior was investigated using four Zeolite minerals (clinoptilolite, analcime, phillipsite and chabazite). The used Pb2+ concentrations were 0, 0.1, 0.5, 1.0, 2.0, 3.0 and 5 µmol mL-1. Results indicated that Pb2+ sorption followed the Langmuir adsorption isotherm, but over limited concentration ranges for clinoptilolite and analcime. The bindg energy (Kd) reached, 2.400 and 0.875 g L-1 for phillipsite and chabazite, respectively. The maximum adsorption capacity for such minerals reached 208.33 and 204.08 mg g-1 with correlation coefficient (R2) reached, 0.997 and 0.995, respectively. Meanwhile, two stages for Pb2+adsorption were observed with clinoptilolite and analcime in the low and high concentrations of the applied Pb2+. Data also was applicable to the Freundlich adsorption isotherm over the used entire Pb2+ concentration ranges. The binding energy (n) reached, 1.014, 1.005, 1.001 and 1.001 g L-1 for clinoptilolite, analcime, phillipsite and chabazite, respectively. However, the b values (maximum adsorption capacity) reached 202.582, 201.651, 207.062 and 206.871 mg g-1 with correlation coefficient (R2) nearly one for all studying minerals, respectively. Desorption data indicated that most of the sorbed Pb2+ was extractedin the 1st extraction following the adsorption experiment. The ability of the used zeolite minerals to retain Pb2+ was high and there were differences between the studied minerals in sorption of Pb2+. In conclusion, data eliminated that, zeolite minerals especially, philipsite and chabazite, could be successfully used as packing material in subsurface reactive barriers intercepting ground water plumes and for fixed bed reactors designed to remove Pb2+ from industrial wastewater.

  14. [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.

  15. [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.

  16. 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 antifouling coatings. When zeolites are incorporated into polymer thin films in the form of nanocrystals, we also show that the resultant composite membranes can significantly improve the performance of reverse osmosis membranes for sea water desalination and proton exchange membrane fuel cells. These diverse applications of zeolites have the potential to initiate new industries while revolutionizing

  17. The effect of physical and chemical treatment on nano-zeolite characterization and their performance in dimethyl ether preparation

    Directory of Open Access Journals (Sweden)

    Sanaa M. Solyman

    2015-09-01

    Full Text Available Catalytic dehydration of methanol to dimethyl ether (DME was investigated using physically and chemically modified H-Mordenite and H-Beta zeolites as catalysts. Physical modification was carried out using ultrasonic wave’s energy, while chemical modification was performed through impregnation in aluminum nitrate followed by calcination. The produced solid catalysts were evaluated as selective catalysts for the dehydration of methanol to dimethyl ether at 100–250 °C performed at three different contact times. Chemical and structural characterizations of the solid catalysts were identified using XRD, FT-IR, TEM, SEM and NH3-TPD. Ultrasonication physical mixing of solids proved as useful tool of preparation, producing fine reordered crystals of nanocomposite zeolites with novel morphology. The newly ordered crystals were distinguished by their frame work structure, acidic properties, crystal and particle sizes, unit cell volume, pore opening, and favorable catalytic activity of 100% selectivity to DME at 200 °C for all contact times studied. The effects of Al2O3 on the dispersion and interaction within the nano-zeolite crystals and hence on the catalytic dehydration of methanol were verified as the major influence toward utmost selectivity.

  18. Structural analysis of hierarchically organized zeolites

    Science.gov (United States)

    Mitchell, Sharon; Pinar, Ana B.; Kenvin, Jeffrey; Crivelli, Paolo; Kärger, Jörg; Pérez-Ramírez, Javier

    2015-10-01

    Advances in materials synthesis bring about many opportunities for technological applications, but are often accompanied by unprecedented complexity. This is clearly illustrated by the case of hierarchically organized zeolite catalysts, a class of crystalline microporous solids that has been revolutionized by the engineering of multilevel pore architectures, which combine unique chemical functionality with efficient molecular transport. Three key attributes, the crystal, the pore and the active site structure, can be expected to dominate the design process. This review examines the adequacy of the palette of techniques applied to characterize these distinguishing features and their catalytic impact.

  19. 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

    2005-09-01

    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. PMID:16240032

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

    Science.gov (United States)

    Barbosa, Gustavo P; Debone, Henrique S; Severino, Patrícia; Souto, Eliana B; da Silva, Classius F

    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.

  1. Laccase-mediated oxidation of small organics: bifunctional roles for versatile applications.

    Science.gov (United States)

    Jeon, Jong-Rok; Chang, Yoon-Seok

    2013-06-01

    Laccases have been widely used in several biotechnological areas, including organic synthesis, bioremediation, and pulp/textile bleaching. In most applications, the enzymatic actions start with single-electron oxidation of small organics followed by formation of the corresponding radicals. These radicals are subsequently involved in either oxidative coupling (i.e., bond formation) or bond cleavage of target organics. These bifunctional actions--catabolic versus anabolic--are readily identifiable in in vivo metabolic processes involving laccases. Here, we characterize the bifunctionality of laccase-mediated oxidation of small organics and present the view that knowledge of the biological functions of these metabolic processes in vivo can illuminate potential biotechnological applications of this bifunctionality.

  2. Enhanced Bifunctional Oxygen Catalysis in Strained LaNiO3 Perovskites

    Energy Technology Data Exchange (ETDEWEB)

    Petrie, Jonathan R.; Cooper, Valentino R.; Freeland, John W.; Meyer, Tricia L.; Zhang, Zhiyong; Lutterman, Daniel A.; Lee, Ho Nyung

    2016-03-02

    Strain is known to greatly influence low temperature oxygen electro catalysis on noble metal films, leading to significant enhancements in bifunctional activity essential for fuel cells and Metal-air batteries. However, its catalytic impact on transition-metal oxide thin films, such as perovskites, is not widely understood. Here, we epitaxially strain the conducting perovskite LaNiO3 to systematically determine its influence on both the oxygen reduction and oxygen evolution reaction. Uniquely, we found that compressive strain could significantly enhance both reactions, yielding a bifunctional catalyst that surpasses the performance of noble metals' such as Pt. We attribute the improved bifunctionality to strain induced splitting of the e(g) Orbitals, which can customize orbital asymmetry at the surface. Analogous to strain induced shifts in the d-band center of noble metals relative to the Fermi level, :such splitting can dramatically affect catalytic activity in this perovskite and other potentially more active Oxides.

  3. Nickel sulfide microsphere film on Ni foam as an efficient bifunctional electrocatalyst for overall water splitting.

    Science.gov (United States)

    Zhu, Wenxin; Yue, Xiaoyue; Zhang, Wentao; Yu, Shaoxuan; Zhang, Yuhuan; Wang, Jing; Wang, Jianlong

    2016-01-25

    Developing low-cost, efficient, and bifunctional electrocatalysts for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is an appealing yet challenging task. Herein, for the first time, a NiS microsphere film was grown in situ on Ni foam (NiS/Ni foam) via a sulfurization reaction as an efficient bifunctional electrocatalyst for overall water splitting with superior activity and good durability. This NiS/Ni foam electrode delivers 20 mA cm(-2) at an overpotential of 158 mV for the HER and 50 mA cm(-2) at an overpotential of 335 mV for the OER in 1.0 M KOH. This bifunctional electrode also enables a high-efficiency alkaline water electrolyzer with 10 mA cm(-2) at a cell voltage of only 1.64 V, which could be promising in water splitting devices for large-scale hydrogen production. PMID:26661579

  4. Polymer-Supported Reagents: The Role of Bifunctionality in the Design of Ion-Selective Complexants

    Energy Technology Data Exchange (ETDEWEB)

    Alexandratos, S. D.

    2001-06-01

    The importance of multi-functionality in the preparation of ion-selective polymers is evident from the structure of enzymes where specific metal ions are bound through cooperative interactions among different amino acids. In synthetic polymers, ionic selectivity is enhanced when a chemical reaction is superimposed on an ion-exchange process. The concept of reactive ion exchange has been extended through the synthesis of crosslinked polymers whose metal ion selectivity is a function of reduction, coordination or precipitation reactions as determined by various covalently bound ligands. Development of three classes of dual mechanism bifunctional polymers, a new series of bifunctional diphosphonate polymers, and novel bifunctional ion-selective polymers with enhanced ionic accessibility has been accomplished.

  5. Electrochemical Investigation of Interaction between a Bifunctional Probe and GG Mismatch Duplex.

    Science.gov (United States)

    Li, Jiao; He, Hanping; Peng, Xiaoqian; Huang, Min; Zhang, Xiuhua; Wang, Shengfu

    2015-01-01

    A bifunctional probe (FecNC), containing a recognition part and an electrochemical active center, was applied to electrochemical detection of GG mismatch duplexes. The preparation of gold electrodes modified by mismatch and complementatry duplexes was characterized by electrochemical impedance spectroscopy (EIS) and optimized for better detection in terms of self-assembly time, hybridization time, and incubation time. The interaction between FecNC and DNA duplexes modified on the surface of a gold electrode was explored by square wave voltammetry (SWV) and EIS. The results showed that the DNA duplexes with GG mismatch on the surface of a gold electrode was easily detected by the largest electrochemical signal of the bifunctional probe because of its selective binding to GG mismatches. The bifunctional probe could offer a simple, effective electrochemical detection of GG mismatches, and theoretical bases for development of electrochemical biosensors. Further, the method would be favorable for diagnosis of genetic diseases.

  6. Introduction to chemistry of crystalline zeolites and its applications

    International Nuclear Information System (INIS)

    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

  7. Distribution of metal and adsorbed guest species in zeolites

    International Nuclear Information System (INIS)

    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 129Xe NMR spectroscopy an important diagnostic probe of metal clustering and adsorbate distribution processes in zeolites. The utility of 129Xe 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, 129Xe NMR is insensitive to fine structural details at room temperature

  8. 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.

  9. Copper cation removal in an electrokinetic cell containing zeolite.

    Science.gov (United States)

    Elsayed-Ali, Omar H; Abdel-Fattah, Tarek; Elsayed-Ali, Hani E

    2011-01-30

    Zeolites are used in environmental remediation of soil or water to immobilize or remove toxic materials by cation exchange. An experiment was conducted to test the use a low electric field to direct the toxic cations towards the zeolite. An electrokinetic cell was constructed using carbon electrodes. Synthetic Linde Type A (LTA) zeolite was placed in the cell. Copper(II) chloride dissolved in water was used as a contaminant. The Cu(2+) concentration was measured for ten hours with and without an applied electric field. The removal of the Cu(2+) ions was accelerated by the applied field in the first two hours. For longer time, the electric field did not improve the removal rate of the Cu(2+) ions. The presence of zeolite and applied electric field complicates the chemistry near the cathode and causes precipitation of Cu(2+) ions as copper oxide on the surface of the zeolite. With increased electric field the zeolite farther away from the cathode had little cation exchange due to the higher drift velocity of the Cu(2+) ions. The results also show that, in the LTA Zeolite A pellets, the cation exchange of Cu is limited to a shell of several tens of micrometers. PMID:21109348

  10. 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.)

  11. Synthesis of NaA zeolite from kaolin source

    Institute of Scientific and Technical Information of China (English)

    Qian MIAO; Zhihui ZHOU; Jianhua YANG; Jinming LU; Shiwei YAN; Jinqu WANG

    2009-01-01

    In this work, zeolite NaA was successfully synthesized by a hydrothermal method using kaolin as a combined source for silica and alumina. Zeolite NaA with high static water adsorption was synthesized from the low-cost raw material, kaolin, and the reaction parameters were optimized. Metakaolin was obtained by calcining kaolin at temperatures ranged from 953 K to 1173 K. The synthesis mixture was pre-crystallized at 343 K and crystallized at 373 K successively. Zeolite NaA was obtained, which was confirmed by SEM, XRD and the water adsorption analysis. The optimized metakaolinization temperature was found at 973 K. The influence of Na2O/SiO2 molar ratio, pre-crystallization time and seed on the crystal- lization of NaA zeolite was investigated. A thorough mixing of metakaolin and NaOH solution was favourable for the nucleation/crystallization rate. The obtained NaA zeolite under the optimized conditions shows excellent crystallinity and static water adsorption of 28.0wt-%,which was higher than 25.9 wt-% of the commercial NaA zeolite. Kaolin was suggested to be a feasible and economical raw material for the practical industrial applications for NaA zeolite.

  12. Potential applications of synthetic zeolites for in situ land reclamation

    Energy Technology Data Exchange (ETDEWEB)

    Rebedea, I.; Edwards, R. [Liverpool John Moores University (United Kingdom). School of Chemical and Physical Sciences Byrom Street; Lepp, N.W. [Liverpool John Moores University (United Kingdom). School of Biological and Earth Science Byrom Street; Lovell, A.J. [Crosfield Chemicals, Warrington, Cheshire (United Kingdom)

    1997-12-31

    The results of a detailed study on the use of synthetic zeolites for the amelioration of contaminated soils are presented. Binary exchange isotherms (25 C) for the systems Na/M (where M is Cd{sup 2+}, Cu{sup 2+}, Pb{sup 2+} and Zn{sup 2+}) and three synthetic zeolites have been derived. The zeolites studied, 4A, P and Y, showed a preference for the exchanging divalent metal cation over sodium. The effect of the three zeolites on the pool of plant available heavy metals of three contaminated soils (mine spoil and sewage sludge application) has been determined, with all three zeolites showing beneficial effects at differing levels of application. The phyto-toxicity and metal bioavailability in the soils, with and without zeolite application, was assessed by growing test species, Lolium perenne, Helianthus annuus and Zea mays and determining the resulting plant metal concentrations and plant biomass. The optimum application rates for the various zeolites were determined

  13. Synthesis, characterization and catalytic activity of acid-base bifunctional materials through protection of amino groups

    Energy Technology Data Exchange (ETDEWEB)

    Shao, Yanqiu [College of Chemistry, Jilin University, Changchun 130023 (China); College of Chemistry, Mudanjiang Normal University, Mudanjiang 157012 (China); Liu, Heng; Yu, Xiaofang [College of Chemistry, Jilin University, Changchun 130023 (China); Guan, Jingqi, E-mail: guanjq@jlu.edu.cn [College of Chemistry, Jilin University, Changchun 130023 (China); Kan, Qiubin, E-mail: qkan@mail.jlu.edu.cn [College of Chemistry, Jilin University, Changchun 130023 (China)

    2012-03-15

    Graphical abstract: Acid-base bifunctional mesoporous material SO{sub 3}H-SBA-15-NH{sub 2} was successfully synthesized under low acidic medium through protection of amino groups. Highlights: Black-Right-Pointing-Pointer The acid-base bifunctional material SO{sub 3}H-SBA-15-NH{sub 2} was successfully synthesized through protection of amino groups. Black-Right-Pointing-Pointer The obtained bifunctional material was tested for aldol condensation. Black-Right-Pointing-Pointer The SO{sub 3}H-SBA-15-NH{sub 2} catalyst containing amine and sulfonic acid groups exhibited excellent acid-basic properties. -- Abstract: Acid-base bifunctional mesoporous material SO{sub 3}H-SBA-15-NH{sub 2} was successfully synthesized under low acidic medium through protection of amino groups. X-ray diffraction (XRD), N{sub 2} adsorption-desorption, transmission electron micrographs (TEM), back titration, {sup 13}C magic-angle spinning (MAS) NMR and {sup 29}Si magic-angle spinning (MAS) NMR were employed to characterize the synthesized materials. The obtained bifunctional material was tested for aldol condensation reaction between acetone and 4-nitrobenzaldehyde. Compared with monofunctional catalysts of SO{sub 3}H-SBA-15 and SBA-15-NH{sub 2}, the bifunctional sample of SO{sub 3}H-SBA-15-NH{sub 2} containing amine and sulfonic acid groups exhibited excellent acid-basic properties, which make it possess high activity for the aldol condensation.

  14. Reaction Current Phenomenon in Bifunctional Catalytic Metal-Semiconductor Nanostructures

    Science.gov (United States)

    Hashemian, Mohammad Amin

    Energy transfer processes accompany every elementary step of catalytic chemical processes on material surface including molecular adsorption and dissociation on atoms, interactions between intermediates, and desorption of reaction products from the catalyst surface. Therefore, detailed understanding of these processes on the molecular level is of great fundamental and practical interest in energy-related applications of nanomaterials. Two main mechanisms of energy transfer from adsorbed particles to a surface are known: (i) adiabatic via excitation of quantized lattice vibrations (phonons) and (ii) non-adiabatic via electronic excitations (electron/hole pairs). Electronic excitations play a key role in nanocatalysis, and it was recently shown that they can be efficiently detected and studied using Schottky-type catalytic nanostructures in the form of measureable electrical currents (chemicurrents) in an external electrical circuit. These nanostructures typically contain an electrically continuous nanocathode layers made of a catalytic metal deposited on a semiconductor substrate. The goal of this research is to study the direct observations of hot electron currents (chemicurrents) in catalytic Schottky structures, using a continuous mesh-like Pt nanofilm grown onto a mesoporous TiO2 substrate. Such devices showed qualitatively different and more diverse signal properties, compared to the earlier devices using smooth substrates, which could only be explained on the basis of bifunctionality. In particular, it was necessary to suggest that different stages of the reaction are occurring on both phases of the catalytic structure. Analysis of the signal behavior also led to discovery of a formerly unknown (very slow) mode of the oxyhydrogen reaction on the Pt/TiO2(por) system occurring at room temperature. This slow mode was producing surprisingly large stationary chemicurrents in the range 10--50 microA/cm2. Results of the chemicurrent measurements for the bifunctional

  15. Oriented growth and assembly of zeolite crystals on substrates

    Institute of Scientific and Technical Information of China (English)

    ZHOU Ming; ZHANG BaoQuan; LIU XiuFeng

    2008-01-01

    The aligned array and thin film of zeolites and molecular sieves possess a variety of potential applica-tions in membrane separation and catalysis, chemical sensors, and microelectronic devices. There are two main synthesis methods for manufacturing the aligned arrays and thin films of zeolites and mo-lecular sieves, i.e. in situ hydrothermal reaction and self-assembly of crystal grains on substrates. Both of them have attracted much attention in the scientific community worldwide. A series of significant progress has been made in recent years. By the in situ hydrothermal synthesis, the oriented nucleation and growth of zeolite and molecular sieve crystals can be achieved by modifying the surface properties of substrates or by changing the composition of synthesis solutions, leading to the formation of uni-formly oriented multicrystal-aligned arrays or thin films. On the other hand, the crystal grains of zeo-lites and molecular sieves can be assembled onto the substrate surface in required orientation using different bondages, for instance, the microstructure in the array or thin film can be controlled. This review is going to summarize and comment the significant results and progress reported recently in manufacturing highly covered and uniformly aligned arrays or thin films of zeolites and molecular sieves. It involves (1) in situ growth of highly aligned zeolite arrays and thin films via embedding func-tional groups on the substrate surface, modifying the surface microstructure of substrates, as well as varying the composition of synthesis solutions; (2) assembly of zeolite and molecular sieve crystals on various substrates to form aligned arrays and thin films with full coverage by covalent, ionic, and in-termolecular coupling interactions between crystals and substrates; (3) coupling surface assembly with microcontact printing or photoetching technique to produce patterned zeolite arrays and thin films. Finally, the functionality and applications of zeolite

  16. Physical properties of bifunctional BST/LSMO nanocomposites

    International Nuclear Information System (INIS)

    We report the fabrication of bifunctional nanocomposites consisting of ferroelectric Ba0.7Sr0.3TiO3 (BST) and ferromagnetic La0.67Sr0.33MnO3 (LSMO) at different concentrations via a high-temperature solid state route. The structural, dielectric, electrical, magnetodielectric (MD), magnetoelectric (ME) and magnetic properties of BST/LSMO nanocomposites were systematically investigated over a wide range of temperatures and frequencies. The X-Ray Diffraction analyses reveal the nanocrystalline nature of the heterostructures, wherein both perovskite phases co-exist. No parasitic phases were observed. The study of the dielectric properties shows that the nanocomposites exhibit relaxor ferroelectric character, with ferroelectric-paraelectric phase transition temperatures around 287–292 K that do not follow the Curie-Weiss law. The electrical measurements indicate that ac conductivities of the nanocomposites follow the Jonscher's universal power law, with activation energies of 0.42–0.63 eV based on Arrhenius-type behavior at high temperatures. The nanocomposites exhibit well-defined ferromagnetic hysteresis loops at room temperature (RT). The MD and ME measurements at RT indicate that BST/LSMO exhibits a nonlinear ME effect at low frequencies, with a threshold near 0.5 T. The magnetocapacitance (MCp) measurements evidence a quadratic dependence on magnetic field, further confirming the multiferroic nature of BST/LSMO. The order of MCp was found to be ∼7% per Tesla. The analysis of the MCp measurements indicates that one of the BST/LSMO compositions studied can be considered as a new multiferroic compound

  17. Physical properties of bifunctional BST/LSMO nanocomposites

    Energy Technology Data Exchange (ETDEWEB)

    Beltran-Huarac, Juan, E-mail: baristary26@gmail.com; Morell, Gerardo [Institute for Functional Nanomaterials, University of Puerto Rico, San Juan, Puerto Rico 00931 (United States); Department of Physics, University of Puerto Rico, Rio Piedras Campus, San Juan, Puerto Rico 00936 (United States); Martinez, Ricardo [Department of Mathematics and Physics, University of Puerto Rico, Cayey Campus, Cayey, Puerto Rico 00737 (United States)

    2014-02-28

    We report the fabrication of bifunctional nanocomposites consisting of ferroelectric Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} (BST) and ferromagnetic La{sub 0.67}Sr{sub 0.33}MnO{sub 3} (LSMO) at different concentrations via a high-temperature solid state route. The structural, dielectric, electrical, magnetodielectric (MD), magnetoelectric (ME) and magnetic properties of BST/LSMO nanocomposites were systematically investigated over a wide range of temperatures and frequencies. The X-Ray Diffraction analyses reveal the nanocrystalline nature of the heterostructures, wherein both perovskite phases co-exist. No parasitic phases were observed. The study of the dielectric properties shows that the nanocomposites exhibit relaxor ferroelectric character, with ferroelectric-paraelectric phase transition temperatures around 287–292 K that do not follow the Curie-Weiss law. The electrical measurements indicate that ac conductivities of the nanocomposites follow the Jonscher's universal power law, with activation energies of 0.42–0.63 eV based on Arrhenius-type behavior at high temperatures. The nanocomposites exhibit well-defined ferromagnetic hysteresis loops at room temperature (RT). The MD and ME measurements at RT indicate that BST/LSMO exhibits a nonlinear ME effect at low frequencies, with a threshold near 0.5 T. The magnetocapacitance (MC{sub p}) measurements evidence a quadratic dependence on magnetic field, further confirming the multiferroic nature of BST/LSMO. The order of MC{sub p} was found to be ∼7% per Tesla. The analysis of the MC{sub p} measurements indicates that one of the BST/LSMO compositions studied can be considered as a new multiferroic compound.

  18. Monodisperse Magneto-Fluorescent Bifunctional Nanoprobes for Bioapplications

    Science.gov (United States)

    Zhang, Hongwang; Huang, Heng; Pralle, Arnd; Zeng, Hao

    2013-03-01

    We present the work on the synthesis of dye-doped monodisperse Fe/SiO2 core/shell nanoparticles as bifunctional probes for bioapplications. Magnetic nanoparticles (NP) have been widely studied as nano-probes for bio-imaging, sensing as well as for cancer therapy. Among all the NPs, Fe NPs have been the focus because they have very high magnetization. However, Fe NPs are usually not stable in ambient due to the fast surface oxidation of the NPs. On the other hand, dye molecules have long been used as probes for bio-imaging. But they are sensitive to environmental conditions. It requires passivation for both so that they can be stable for applications. In this work, monodisperse Fe NPs with sizes ranging from 13-20 nm have been synthesized through the chemical thermal-decomposition in a solution. Silica shells were then coated on the Fe NPs by a two-phase oil-in-water method. Dye molecules were first bonded to a silica precursor and then encapsulated into the silica shell during the coating process. The silica shells protect both the Fe NPs and dye molecules, which makes them as robust probes. The dye doped Fe/SiO2 core/shell NPs remain both highly magnetic and highly fluorescent. The stable dye doped Fe/SiO2NPs have been used as a dual functional probe for both magnetic heating and local nanoscale temperature sending, and their performance will be reported. Research supported by NSF DMR 0547036, DMR1104994.

  19. Janus nanobelts: fabrication, structure and enhanced magnetic-fluorescent bifunctional performance

    Science.gov (United States)

    Ma, Qianli; Yu, Wensheng; Dong, Xiangting; Wang, Jinxian; Liu, Guixia

    2014-02-01

    A new nanostructure of magnetic-fluorescent bifunctional Janus nanobelts with Fe3O4/PMMA as one half and Tb(BA)3phen/PMMA as the other half has been successfully fabricated by a specially designed parallel spinneret electrospinning technology. The morphology and properties of the final products were investigated in detail by X-ray diffractometry (XRD), scanning electron microscopy (SEM), energy dispersive spectrometry (EDS), biological microscopy (BM), vibrating sample magnetometry (VSM) and fluorescence spectroscopy. The results revealed that the [Fe3O4/PMMA]//[Tb(BA)3phen/PMMA] magnetic-fluorescent bifunctional Janus nanobelts possess superior magnetic and fluorescent properties due to their special nanostructure. Compared with Fe3O4/Tb(BA)3phen/PMMA composite nanobelts, the magnetic-fluorescent bifunctional Janus nanobelts provided better performance. The new magnetic-fluorescent bifunctional Janus nanobelts have potential applications in novel nano-bio-label materials, drug target delivery materials and future nanodevices due to their excellent magnetic-fluorescent properties, flexibility and insolubility. Moreover, the construction technique for the Janus nanobelts is of universal significance for the fabrication of other multifunctional Janus nanobelts.A new nanostructure of magnetic-fluorescent bifunctional Janus nanobelts with Fe3O4/PMMA as one half and Tb(BA)3phen/PMMA as the other half has been successfully fabricated by a specially designed parallel spinneret electrospinning technology. The morphology and properties of the final products were investigated in detail by X-ray diffractometry (XRD), scanning electron microscopy (SEM), energy dispersive spectrometry (EDS), biological microscopy (BM), vibrating sample magnetometry (VSM) and fluorescence spectroscopy. The results revealed that the [Fe3O4/PMMA]//[Tb(BA)3phen/PMMA] magnetic-fluorescent bifunctional Janus nanobelts possess superior magnetic and fluorescent properties due to their special

  20. Structural basis for bifunctional peptide recognition at human δ-opioid receptor.

    Science.gov (United States)

    Fenalti, Gustavo; Zatsepin, Nadia A; Betti, Cecilia; Giguere, Patrick; Han, Gye Won; Ishchenko, Andrii; Liu, Wei; Guillemyn, Karel; Zhang, Haitao; James, Daniel; Wang, Dingjie; Weierstall, Uwe; Spence, John C H; Boutet, Sébastien; Messerschmidt, Marc; Williams, Garth J; Gati, Cornelius; Yefanov, Oleksandr M; White, Thomas A; Oberthuer, Dominik; Metz, Markus; Yoon, Chun Hong; Barty, Anton; Chapman, Henry N; Basu, Shibom; Coe, Jesse; Conrad, Chelsie E; Fromme, Raimund; Fromme, Petra; Tourwé, Dirk; Schiller, Peter W; Roth, Bryan L; Ballet, Steven; Katritch, Vsevolod; Stevens, Raymond C; Cherezov, Vadim

    2015-03-01

    Bifunctional μ- and δ-opioid receptor (OR) ligands are potential therapeutic alternatives, with diminished side effects, to alkaloid opiate analgesics. We solved the structure of human δ-OR bound to the bifunctional δ-OR antagonist and μ-OR agonist tetrapeptide H-Dmt-Tic-Phe-Phe-NH2 (DIPP-NH2) by serial femtosecond crystallography, revealing a cis-peptide bond between H-Dmt and Tic. The observed receptor-peptide interactions are critical for understanding of the pharmacological profiles of opioid peptides and for development of improved analgesics. PMID:25686086

  1. A nanostructured bifunctional Pd/C gas-diffusion electrode for metal-air batteries

    OpenAIRE

    McKerracher, R.D.; Alegre, C.; Baglio, V.; Aricò, A.S.; Ponce de León, C.; Mornaghini, F.; Rodlert, M.; Walsh, F. C.

    2015-01-01

    Designing a bifunctional air electrode which catalyses both the oxygen reduction and oxygen evolution reactions is an essential part of progress towards fully rechargeable metal-air batteries, such as the iron-air battery which is environmentally friendly, low cost, and does not suffer risk of thermal runaway like lithium-ion batteries. This paper reports the development of a lightweight carbon-based bifunctional air electrode, catalysed by a small (0.5 mg cm?2) loading of 30 wt.% palladium o...

  2. Catalytic pyrolysis using UZM-44 aluminosilicate zeolite

    Energy Technology Data Exchange (ETDEWEB)

    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.

  3. Catalytic pyrolysis using UZM-44 aluminosilicate zeolite

    Energy Technology Data Exchange (ETDEWEB)

    Nicholas, Christopher P; Boldingh, Edwin P

    2014-04-29

    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.

  4. Formaldehyde removal from wastewater applying natural zeolite

    Directory of Open Access Journals (Sweden)

    Dovilė Kulikauskaitė

    2015-10-01

    Full Text Available Formaldehyde is one of the most chemically active compounds which is discharged with untreated or just partially treated industrial wastewater. It is hazardous for environment and humans. Formaldehyde vapors can strongly irritate skin, can cause damage to eyes and harm respiratory tract. As long as formaldehyde causes a toxic effect on environment and living organisms, it is necessary to remove it from wastewater which is directed to natural water. There are many methods used for formaldehyde removal from wastewater: biological method, evaporation, membrane separation method. Most of them have disadvantages. Adsorption method has many advantages: it is fast, cheap, and universal, and can be widely used, therefore it was chosen for this research. Experiment was carried out with natural zeolite in different contact time with different concentration formaldehyde solutions. Concentration of formaldehyde was determined applying the Photocolorimetric Method. Method is based on reaction of formaldehyde with chromotropic acid and determination of formaldehyde concentration. Determined average sorption efficiency was highest when formaldehyde concentration was lowest, e. g. 2 mg/l (45.94% after eight hours of contact time with adsorbent. Sorption efficiency was increasing when the contact time increased, but when the contact time increased to 12 hours, sorption efficiency stayed the same because of the saturation of zeolite.

  5. Structural, thermal and electrical properties of natural zeolite in Syria

    International Nuclear Information System (INIS)

    we have applied, in this work, the techniques of X-Ray Diffraction (XRD), Differential Thermal Analysis (DTA), X-Ray Florescence (XRF), Electron Microscopy (EM) and Scanning of Electronic Microscope (SEM) in order to investigate some samples taken from Sis mountain located in Syrian territory where geological exploration efforts carried out by the General Establishment of Geology and Mineral Resources. The study indicates that zeolite could be existed there in an economical quantities. This work is intended to determine zeolite types and their concentrations as well as to investigate thermal and electrical properties of samples containing zeolite minerals. (author)

  6. Properties of natural zeolites in benefit of nutrition and health

    Directory of Open Access Journals (Sweden)

    Irina Smical

    2011-11-01

    Full Text Available Due to their remarkable properties, natural zeolites have come to the attention of medicineresearchers to find new ways of treating various diseases and ensure an improved supply of mineralsin nutrition. The research results have shown the beneficial effects of application of various types ofnatural zeolites in healing or ameliorating especially gastrointestinal and diarrhea disease and cancerdisease, as well. Because natural zeolites have a very good ability as ion exchangers they are largelyused in nutrition for supplying the essential minerals in nutrition of animals.

  7. Ion exchange of ammonium in natural and synthesized zeolites

    International Nuclear Information System (INIS)

    In this study, zeolite Na-P and Na-Y was prepared by hydrothermal treatment of the Chinese natural clinoptilolite with NaOH. The ion exchange of NH4+ into the three zeolites in the temperature range of 288-333 K was also investigated, and the thermodynamic parameters were calculated. The selectivity sequence for NH4+ entering the sodium form of the three materials was Na-clinoptilolite > Na-Y > Na-P, as indicated by values of ΔGo. The results demonstrated that the Si/Al molar ratio of zeolites determined the selectivity for NH4+

  8. Sorption of 60 Co in natural zeolite (clinoptilolite)

    International Nuclear Information System (INIS)

    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 Co2+ /g in the Na-Clinoptilolite. The crystallinity of the aluminosilicates was maintained during experiments, it was verified by XRD patterns. (Author)

  9. Splicing growth of zeolite 4A in hydrothermal system

    Institute of Scientific and Technical Information of China (English)

    李酽; 汪信; 杨绪杰; 张术根

    2002-01-01

    The morphology evolution of zeolite 4A in hydrothermal system was studied via XRD, TEM and electron diffractometry. A phenomenon of aggregation of nano-crystals of zeolite 4A exists in the crystallization process, and microcrystals are derived from nano-crystal aggregating directly. The splicing growth model of zeolite 4A is described as: 1)an induction period which exists at the beginning of crystallization, 2)followed by many nano-meter crystals initiating immediately, and 3)the nanocrystals congregated as slices and spliced with each other to form a larger crystal.

  10. 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

  11. Oxidative regeneration of toluene-saturated natural zeolite by gaseous ozone: The influence of zeolite chemical surface characteristics

    International Nuclear Information System (INIS)

    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

    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.

  13. BETA-S, Multi-Group Beta-Ray Spectra

    International Nuclear Information System (INIS)

    1 - Description of program or function: BETA-S calculates beta-decay source terms and energy spectra in multigroup format for time-dependent radionuclide inventories of actinides, fission products, and activation products. Multigroup spectra may be calculated in any arbitrary energy-group structure. The code also calculates the total beta energy release rate from the sum of the average beta-ray energies as determined from the spectral distributions. BETA-S also provides users with an option to determine principal beta-decaying radionuclides contributing to each energy group. The CCC-545/SCALE 4.3 (or SCALE4.2) code system must be installed on the computer before installing BETA-S, which requires the SCALE subroutine library and nuclide-inventory generation from the ORIGEN-S code. 2 - Methods:Well-established models for beta-energy distributions are used to explicitly represent allowed, and 1., 2. - and 3. -forbidden transition types. Forbidden non-unique transitions are assumed to have a spectral shape of allowed transitions. The multigroup energy spectra are calculated by numerically integrating the energy distribution functions using an adaptive Simpson's Rule algorithm. Nuclide inventories are obtained from a binary interface produced by the ORIGEN-S code. BETA-S calculates the spectra for all isotopes on the binary interface that have associated beta-decay transition data in the ENSDF-95 library, developed for the BETA-S code. This library was generated from ENSDF data and contains 715 materials, representing approximately 8500 individual beta transition branches. 3 - Restrictions on the complexity of the problem: The algorithms do not treat positron decay transitions or internal conversion electrons. The neglect of positron transitions in inconsequential for most applications involving aggregate fission products, since most of the decay modes are via electrons. The neglect of internal conversion electrons may impact on the accuracy of the spectrum in the low

  14. Xenon NMR studies of dynamics and exchange in zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Moudrakovski, I.L.; Ratcliffe, C.I.; Ripmeester, J.A. [Steacie Institute for Molecular Sciences, Ottawa, Ontario (Canada)

    1996-10-01

    We have found, despite earlier reports to the contrary, that for many microporous solids with one-dimensional channels (ZSM-12, ALPO-5, VPI-5, SSZ-24) the chemical shift has an anisotropic component. For ALPO-11, a detailed model has been developed which accounts for the loading-dependent chemical shift in terms of intraparticle exchange of statistical distributions of xenon atoms with 0, 1 or 2 nearest neighbors. A similar model can be applied to ZSM-12 up to moderate loadings. At higher loading levels 2D exchange methods show that interparticle exchange occurs as well. The same approach was used to study interparticle exchange in X and Y zeolite mixtures, exchange amongst zeolite clusters of up to 8 xenon atoms in the supercages of AgA zeolite, and main channel - side pocket exchange in mordenite. The parameters derived are directly relevant to the understanding of sorption and diffusion processes in zeolites.

  15. Metal loaded zeolite adsorbents for hydrogen cyanide removal

    Institute of Scientific and Technical Information of China (English)

    Ping Ning; Juan Qiu; Xueqian Wang; Wei Liu; Wei Chen

    2013-01-01

    Metal (Cu,Co,or Zn) loaded ZSM-5 and Y zeolite adsorbents were prepared for the adsorption of hydrogen cyanide (HCN) toxic gas.The results showed that the HCN breakthrough capacity was enhanced significantly when zeolites were loaded with Cu.The physical and chemical properties of the adsorbents that influence the HCN adsorption capacity were analyzed.The maximal HCN breakthrough capacities were about the same for both zeolites at 2.2 mol of HCN/mol of Cu.The Cu2p XPS spectra showed that the possible species present were Cu2O and CuO.The N1s XPS data and FT-IR spectra indicated that CN-would be formed in the presence of Cu+/Cu2+and oxygen gas,and the reaction product could be adsorbed onto Cu/ZSM-5 zeolite more easily than HCN.

  16. Modelling of copper and zinc adsorption onto zeolite

    Directory of Open Access Journals (Sweden)

    H. Pavolová

    2016-10-01

    Full Text Available Adsorption of Cu(II and Zn(II ions from metallurgical solutions has been studied and the adsorption capacity of zeolite (Nižný Hrabovec, SK has been determined. Zeolites are characterized by relatively high sorption capacity, i.e. Cu(II and Zn(II can be removed even at relatively low concentrations. The experiments were realised in a batch system and evaluated using isotherms. According to the results of the experiments the adsorption equilibrium of Cu(II and Zn(II on zeolite was best described by Freundlich isotherm. The maximum sorption capacity was 1,48 and 1,49 mg/g for Cu(II and Zn(II, respectively. The experimental results of this study demonstrate that zeolite is suitable for adsorption of copper and zinc from aqueous solutions at low concentrations.

  17. Preparation of Natural Zeolite for Air Dehumidification in Food Drying

    Directory of Open Access Journals (Sweden)

    Mohamad Djaeni

    2015-03-01

    Full Text Available Drying with air dehumidification with solid adsorbent improves the quality of food product as well as energy efficiency. The natural zeolite is one of adsorbent having potential to adsorb the water.  Normally, the material was activated to open the pore, remove the organic impurities, and increase Si/Al rate. Hence, it can enhance the adsorbing capacity. This research studied the activation of natural zeolite mined from Klaten, Indonesia as air dehumidification for food drying. Two different methods were used involving activation by heat and NaOH introduction.  As indicators, the porosity and water loaded were evaluated. Results showed both methods improved the adsorbing capacity significantly. With NaOH, the adsorbing capacity was higher. The simple test in onion and corn drying showed the presence of activated natural zeolite can speed up water evaporation positively. This performance was also comparable with Zeolite 3A

  18. Zeolite - A Natural Filter Material for Lead Polluted Water

    Science.gov (United States)

    Neamţu, Corina Ioana; Pică, Elena Maria; Rusu, Tiberiu

    2014-11-01

    Reducing the concentration of lead ions in a wastewater using zeolite has proven to be a successful water treatement method, all over the world. Putting the two media (solid and liquid) in contact in static conditions had good results regarding the concentration of the filtered solution, the pH and the electric conductivity, depending on the values of certain parameters such as the amount of the zeolite, volume of the solution or interaction time. The present study highlights the zeolite ability to retain the lead ions from a solution, in dynamic interaction conditions between the two environments, in a short interaction time. The results confirmed the effectiveness of ion exchange water treatment method in the conditions set, emphasizing once again the properties of the filter material - the zeolite

  19. Mesoporous zeolite single crystals for catalytic hydrocarbon conversion

    DEFF Research Database (Denmark)

    Schmidt, I.; Christensen, C.H.; Hasselriis, Peter;

    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, a...

  20. 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.

  1. Properties of zeolite a synthesized by natural bentonite

    International Nuclear Information System (INIS)

    Synthetic zeolite was prepared by using of natural bentonite from Kampo area and the application of detergent builder was investigated. The optimum synthetic condition was SiO2/Al2O3 = 2, Na2O/Al2O3 = 1, H2O/Al2O3 30 at 90 deg C for 3 hr and it was found by XRD analysis that the zeolite synthesized under this condition was type A. When the zeolite A synthesized under the optimum condition was contacted with 40 deg Dh CaCl2 solution at 30 deg C for 15 min, the cation exchange capacity was 264.9 mg CaO/g-zeolite. And the whiteness of the sample was 89% and the mean particle size was 9.95μm. (author)

  2. Theoretical models for NO decomposition in Cu-exchanged zeolites

    CERN Document Server

    Tsekov, R

    2015-01-01

    A unified description of the catalytic effect of Cu-exchanged zeolites is proposed for the decomposition of NO. A general expression for the rate constant of NO decomposition is obtained by assuming that the rate-determining step consists of the transferring of a single atom associated with breaking of the N-O bond. The analysis is performed on the base of the generalized Langevin equation and takes into account both the potential interactions in the system and the memory effects due to the zeolite vibrations. Two different mechanisms corresponding to monomolecular and bimolecular NO decomposition are discussed. The catalytic effect in the monomolecular mechanism is related to both the Cu+ ions and zeolite O-vacancies, while in the case of the bimolecular mechanism the zeolite contributes through dissipation only. The comparison of the theoretically calculated rate constants with experimental results reveals additional information about the geometric and energetic characteristics of the active centers and con...

  3. 不同结构分子筛的甲醇制丙烯催化性能%Methanol to propylene reaction over zeolite catalysts with different topologies

    Institute of Scientific and Technical Information of China (English)

    胡思; 巩雁军; 张卿; 张军亮; 张亚飞; 杨飞鹰; 窦涛

    2012-01-01

    Conversion of methanol to propylene (MTP) was comparatively studied over four zeolites with different topologies,i. e. SAPO-34,ZSM-48,ZSM-5 and beta at atmospheric pressure,450℃ and WHSV=1. 5 h-1 . The correlations between product selectivity,catalyst stability and zeolite topology were investigated. Besides,coking behavior of the four zeolite catalysts during the reaction was also discussed. Among the studied catalysts,SAPO-34 with narrow 8-member ring openings showed the highest selectivity to light olefins (ethylene and propylene). However,it seems that the high density of acid site and the large cages of SAPO-34 resulted in an extremely fast coking deactivation. Beta zeolite with wide pore structure exhibited high propylene/ethylene (P/E) ratio,but the propylene selectivity was somewhat low due to the product distribution shifting towards heavier hydrocarbons. In contrast,ZSM-48 and ZSM-5 zeolite with 10-member ring openings gave higher propylene selectivity,but their deactivation rates were quite different. ZSM-48 zeolite with symmetrical straight channels underwent fast deactivation after a few hours on stream,while ZSM-5 zeolite with intersecting channel system presented superior resistance to coke deactivation. The significant difference in catalytic performance of the four zeolites could be mainly ascribed to the combined effect of shape selectivity for intermediates and products controlled by zeolites topology.%在常压、空速为1.5h-1、反应温度为450℃条件下,考察了4种具有不同拓扑结构的分子筛(SAPO-34、ZSM-48、ZSM-5和beta)在甲醇转化制丙烯(MTP)反应中的催化性能,并对催化剂的积炭失活行为进行了研究.结果表明,从8元环到12元环,分子筛孔口尺寸越小,低碳烯烃(乙烯+丙烯)选择性越高,积炭失活速率也越快.孔道尺寸越大,丙烯/乙烯(P/E)比越高,但产物分布向C4以上组分偏移,丙烯选择性降低.10元环分子筛具有较高的丙烯选择性,但催化剂

  4. Use of Natural Zeolite to Upgrade Activated Sludge Process

    OpenAIRE

    Hrenović, Jasna; Büyükgüngör, Hanife; Orhan, Yüksel

    2003-01-01

    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 act...

  5. Electrocatalytic oxidation of ethanol using zeolite modified carbon paste electrode

    Directory of Open Access Journals (Sweden)

    Maryam Abrishamkar

    2014-12-01

    Full Text Available In this research application of synthesized ZSM-5 zeolite to prepare the modified carbon paste electrodes was studied. To prepare of modified electrode, the nickel ions as mediator for electrochemical oxidation of ethanol were doped to ZSM-5 zeolite framework through ion exchange mechanism and oxidation of ethanol on the surface of proposed electrode in the alkaline solution was investigated using cyclic voltammetry and chronoamperometry methods. Also, the catalytic rate constant for oxidation of ethanol (k was reported.

  6. Effect of zeolite formation on borosilicate glass dissolution kinetics

    Energy Technology Data Exchange (ETDEWEB)

    Fournier, Maxime; Frugier, Pierre; Gin, Stephane [CEA, DEN-Marcoule, F30207, Bagnols-sur-Ceze (France)

    2013-07-01

    This study is a preliminary work on the description and the modeling of physico-chemical mechanisms potentially causing nuclear glass alteration to accelerate, as observed under experimental specific conditions. A better understanding of the mechanisms of alteration resumption, linked to the precipitation of zeolite, is necessary to model these phenomena. Leaching tests of a nuclear borosilicate glass show guidelines for designing experiments that promote alteration resumption and evidence the role of developed crystalline surfaces and aluminum on nucleation kinetics of zeolites. (authors)

  7. Effects of Zeolite on Seed Quality of Organic Upland Rice

    OpenAIRE

    Raumjit Nokkoul; Teerayut Wichitparp

    2014-01-01

    The production of high quality seeds is an important strategy for organic seed producers. In particular, organic farming is a production system which avoids the use of synthetic fertilizers, insecticides and plant growth regulators. Alternative management organic farming system is reducing nutrient loss and improving soil quality. Zeolite is organic matter and alternative for organic upland rice production. Our objective was to determine the effects of zeolite on seed quality of organic uplan...

  8. Sorption behavior of tritiated water on Armenian natural zeolites

    International Nuclear Information System (INIS)

    The sorptive behavior of tritiated water on natural, irradiated, chemically treated and heated at high temperatures Armenian zeolites was studied and their capacity for the separation and enrichment of tritiated water was evaluated. The distribution coefficients from the batch experiments were calculated for different zeolites and vary between 0.23 and 3.01. The influence of temperature, acidity, basicity, specific activity, electron and gamma-irradiation on sorption has been studied. (author)

  9. DIELECTRIC PROPERTIES OF NATURAL SYRIAN AND ARMENIAN ZEOLITES

    OpenAIRE

    Sahakyan, A.; Soulayman, S.; Nikogosyan, S.; Yunusova, S.

    2007-01-01

    Using an experimental arrangement, designed and manufactured locally, the electric permittivity ε = ε' iε" and alternative current (a.c.) conductivity σac of natural Syrian and Armenian zeolites were investigated in order to understand the mechanism of the electrical properties in these materials. The frequency dependence of angle tangents (tan δ = ε" /ε') of dielectric losses was also studied for both zeolites. The mentioned measuring arrangement has a configuration of an electrical bridge. ...

  10. Phosphate recovery using calcium zeolite in ultrafiltration pilot plant

    OpenAIRE

    La Rotonda Ferrer, Pablo

    2015-01-01

    One of the most important ecological problems is the eutrophication, this process consist in the uncontrolled growing of algae and phytoplankton, which can destroy entire aquatic ecosystems. The reason of this process is the excess of nutrients, as for example, phosphate coming from human activities. This project focus on the study of synthetic zeolites capacity to absorb phosphate from wastewater. Zeolites are porous minerals of the alumina-silicates family with high capacity ...

  11. 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.

  12. High surface area carbon for bifunctional air electrodes applied in zinc-air batteries

    Energy Technology Data Exchange (ETDEWEB)

    Arai, H. [on leave from NTT Laboratories (Japan); Mueller, S.; Haas, O. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1999-08-01

    Bifunctional air electrodes with high surface area carbon substrates showed low reduction overpotential, thus are promising for enhancing the energy efficiency and power capability of zinc-air batteries. The improved performance is attributed to lower overpotential due to diffusion of the reaction intermediate, namely the peroxide ion. (author) 1 fig., 2 refs.

  13. Radiation Induced Crosslinking of Polyethylene in the Presence of Bifunctional Vinyl Monomers

    DEFF Research Database (Denmark)

    Joshi, M. S.; Singer, Klaus Albert Julius; Silverman, J.

    1977-01-01

    Several reports have been published showing that the radiation induced grafting of bifunctional vinyl monomers to low density polyethylene results in a product with an unusually high density of crosslinks. The same grafting reactions are shown to reduce the incipient gel dose by more than a facto...

  14. Oxidations of amines with molecular oxygen using bifunctional gold–titania catalysts

    DEFF Research Database (Denmark)

    Klitgaard, Søren Kegnæs; Egeblad, Kresten; Mentzel, Uffe Vie;

    2008-01-01

    Over the past decades it has become clear that supported gold nanoparticles are surprisingly active and selective catalysts for several green oxidation reactions of oxygen-containing hydrocarbons using molecular oxygen as the stoichiometric oxidant. We here report that bifunctional gold–titania c...

  15. Direct catalytic transformation of carbohydrates into 5-ethoxymethylfurfural with acid–base bifunctional hybrid nanospheres

    DEFF Research Database (Denmark)

    Li, Hu; Khokarale, Santosh Govind; Kotni, Ramakrishna;

    2014-01-01

    carbohydrates. A high EMF yield of 76.6%, 58.5%, 42.4%, and 36.5% could be achieved, when fructose, inulin, sorbose, and sucrose were used as starting materials, respectively. Although, the acid–base bifunctional nanocatalysts were inert for synthesis of EMF from glucose based carbohydrates, ethyl...

  16. Direct catalytic transformation of carbohydrates into 5-ethoxymethylfurfural with acid–base bifunctional hybrid nanospheres

    International Nuclear Information System (INIS)

    Graphical abstract: Catalytic conversion of carbohydrates into HMF and EMF in ethanol/DMSO with acid–base bifunctional hybrid nanospheres prepared from self-assembly of corresponding basic amino acids and HPA. - Highlights: • Acid–base bifunctional nanospheres were efficient for production of EMF from sugars. • Synthesis of EMF in a high yield of 76.6% was realized from fructose. • Fructose based biopolymers could also be converted into EMF with good yields. • Ethyl glucopyranoside was produced in good yields from glucose in ethanol. - Abstract: A series of acid–base bifunctional hybrid nanospheres prepared from the self-assembly of basic amino acids and phosphotungstic acid (HPA) with different molar ratios were employed as efficient and recyclable catalysts for synthesis of liquid biofuel 5-ethoxymethylfurfural (EMF) from various carbohydrates. A high EMF yield of 76.6%, 58.5%, 42.4%, and 36.5% could be achieved, when fructose, inulin, sorbose, and sucrose were used as starting materials, respectively. Although, the acid–base bifunctional nanocatalysts were inert for synthesis of EMF from glucose based carbohydrates, ethyl glucopyranoside in good yields could be obtained from glucose in ethanol. Moreover, the nanocatalyst functionalized with acid and basic sites was able to be reused several times with no significant loss in catalytic activity

  17. Bifunctional catalysts for the direct production of liquid fuels from syngas

    NARCIS (Netherlands)

    Sartipi, S.

    2014-01-01

    Design and development of catalyst formulations that maximize the direct production of liquid fuels by combining Fischer-Tropsch synthesis (FTS), hydrocarbon cracking, and isomerization into one single catalyst particle (bifunctional FTS catalyst) have been investigated in this thesis. To achieve th

  18. First-Principles Study of Structure Property Relationships of Monolayer (Hydroxy)Oxide-Metal Bifunctional Electrocatalysts

    DEFF Research Database (Denmark)

    Zeng, Zhenhua; Kubal, Joseph; Greeley, Jeffrey Philip

    2015-01-01

    step towards accurate identification and prediction of a variety of oxide/electrode interfacial structure-properties relationships, but also provides the foundation for rational design and control of ‘targeted active phases’ at catalytic interfaces. The successful design of bifunctional...

  19. The Golgi localized bifunctional UDP-rhamnose/UDP-galactose transporter family of Arabidopsis

    DEFF Research Database (Denmark)

    Rautengarten, Carsten; Ebert, Berit; Moreno, Ignacio;

    2014-01-01

    that are specifically presumed to deliver the diverse array of nucleotide sugars found in plants. This study has developed a novel approach that enabled functional characterization of six bifunctional UDP-rhamnose (Rha)/UDP-galactose (Gal) transporters from Arabidopsis. An analysis of loss...

  20. Bifunctional phage-based pretargeted imaging of human prostate carcinoma

    Energy Technology Data Exchange (ETDEWEB)

    Newton-Northup, Jessica R. [Department of Biochemistry, University of Missouri, Columbia, MO 65211 (United States)], E-mail: newtonj@missouri.edu; Figueroa, Said D. [Department of Radiology, University of Missouri, Columbia, MO 65211 (United States); Quinn, Thomas P.; Deutscher, Susan L. [Department of Biochemistry, University of Missouri, Columbia, MO 65211 (United States); Research Service, Harry S. Truman Veterans Memorial Hospital, Columbia, MO 65201 (United States)

    2009-10-15

    Introduction: Two-step and three-step pretargeting systems utilizing biotinylated prostate tumor-homing bacteriophage (phage) and {sup 111}In-radiolabeled streptavidin or biotin were developed for use in cancer radioimaging. The in vivo selected prostate carcinoma-specific phage (G1) displaying up to five copies of the peptide IAGLATPGWSHWLAL was the focus of the present study. Methods: The ability of G1 phage to extravasate and target prostate tumor cells was investigated using immunohistochemistry. G1 phages were biotinylated, streptavidin was conjugated to diethylenetriaminepentaacetic acid (DTPA) and biotin was conjugated to 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA). Biodistribution studies and single-photon emission computed tomography (SPECT)/CT imaging of xenografted PC-3 tumors via two-step pretargeted {sup 111}In-labeled streptavidin and three-step pretargeted {sup 111}In-labeled biotin were performed in SCID mice to determine the optimal pretargeting method. Results: The ability of G1 phage to extravasate the vasculature and bind directly to human PC-3 prostate carcinoma tumor cells in vivo was demonstrated via immunocytochemical analysis. Comparative biodistribution studies of the two-step and three-step pretargeting strategies indicated increased PC-3 human prostate carcinoma tumor uptake in SCID mice of 4.34{+-}0.26 %ID g{sup -1} at 0.5 h postinjection of {sup 111}In-radiolabeled biotin (utilized in a three-step protocol) compared to 0.67{+-}0.06 %ID g{sup -1} at 24 h postinjection of {sup 111}In radiolabeled streptavidin (employed in a two-step protocol). In vivo SPECT/CT imaging of xenografted PC-3 tumors in SCID mice with the three-step pretargeting method was superior to that of the two-step pretargeting method, and, importantly, blocking studies demonstrated specificity of tumor uptake of {sup 111}In-labeled biotin in the three-step pretargeting scheme. Conclusion: This study demonstrates the use of multivalent bifunctional

  1. Comparison of bifunctional chelates for {sup 64}Cu antibody imaging

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Cara L.; Crisp, Sarah; Bensimon, Corinne [MDS Nordion, Vancouver, BC (Canada); Yapp, Donald T.T.; Ng, Sylvia S.W. [British Columbia Cancer Agency Research Centre, Vancouver, BC (Canada); University of British Columba, The Faculty of Pharmaceutical Sciences, Vancouver, BC (Canada); Sutherland, Brent W. [British Columbia Cancer Agency Research Centre, Vancouver, BC (Canada); Gleave, Martin [Prostate Centre at Vancouver General Hospital, Vancouver, BC (Canada); Jurek, Paul; Kiefer, Garry E. [Macrocyclics Inc., Dallas, TX (United States)

    2010-11-15

    Improved bifunctional chelates (BFCs) are needed to facilitate efficient {sup 64}Cu radiolabeling of monoclonal antibodies (mAbs) under mild conditions and to yield stable, target-specific agents. The utility of two novel BFCs, 1-Oxa-4,7,10-triazacyclododecane-5-S-(4-isothiocyanatobenzyl)-4,7,10-triacetic acid (p-SCN-Bn-Oxo-DO3A) and 3,6,9,15-tetraazabicyclo[9.3.1]pentadeca-1(15),11,13-triene-4-S-(4-isothiocyanatobenzyl)-3,6,9-triacetic acid (p-SCN-Bn-PCTA), for mAb imaging with {sup 64}Cu were compared to the commonly used S-2-(4-isothiocyanatobenzyl)-1,4,7,10-tetraazacyclododecane-tetraacetic acid (p-SCN-Bn-DOTA). The BFCs were conjugated to trastuzumab, which targets the HER2/neu receptor. {sup 64}Cu radiolabeling of the conjugates was optimized. Receptor binding was analyzed using flow cytometry and radioassays. Finally, PET imaging and biodistribution studies were done in mice bearing either HER2/neu-positive or HER2/neu-negative tumors. {sup 64}Cu-Oxo-DO3A- and PCTA-trastuzumab were prepared at room temperature in >95% radiochemical yield (RCY) in <30 min, compared to only 88% RCY after 2 h for the preparation of {sup 64}Cu-DOTA-trastuzumab under the same conditions. Cell studies confirmed that the immunoreactivity of the mAb was retained for each of the bioconjugates. In vivo studies showed that {sup 64}Cu-Oxo-DO3A- and PCTA-trastuzumab had higher uptake than the {sup 64}Cu-DOTA-trastuzumab at 24 h in HER2/neu-positive tumors, resulting in higher tumor to background ratios and better tumor images. By 40 h all three of the {sup 64}Cu-BFC-trastuzumab conjugates allowed for clear visualization of the HER2/neu-positive tumors but not the negative control tumor. The antibody conjugates of PCTA and Oxo-DO3A were shown to have superior {sup 64}Cu radiolabeling efficiency and stability compared to the analogous DOTA conjugate. In addition, {sup 64}Cu-PCTA and Oxo-DO3A antibody conjugates may facilitate earlier imaging with greater target to background ratios than

  2. Seed-Directed and Organotemplate-free Synthesis of Zeolites%无有机模板条件下晶种导向合成微孔分子筛晶体材料

    Institute of Scientific and Technical Information of China (English)

    张海燕; 杨承广; 孟祥举; 肖丰收

    2012-01-01

    沸石分子筛晶体材料(例如Beta,ZSM-34)由于具有独特的物理及化学性质,被广泛应用于催化,吸附与分离、离子交换等领域.一般来说,人多数分子筛晶体材料需要在有机模板刺存在的条件下合成.然而,有机模板刺的使用会带水很多问题。例如,提高分予筛品体材料的合成成本、亿高温煅烧去除模板剂的过程中,消耗人链的能鼙以及带水环境污染.因此,开发无有机模板剂合成沸“分子筛新路线具有十分重要的研究意义和史川价值.近年束,我们研究小组首先开发了无有机馍板条件下品种导向合成分了筛的新方法,相继合成出了Beta,ZSM-34,FER和LEV等微孔分子筛晶体材料.将对这几种沸石的合成进行简要的评论.%Zeolites with unique physical and chemical properties, such as Beta, ZSM-34 have been extensively studied for a long time as important materials in the chemical industries such as shape selective catalysis, adsorption, ion exchange etc. Normally, most of zeolites were synthesized in the presence of organic templates, and the use of them usually results in more or less shortcomings including high cost of organic templates and production of environmentally undesirable gases by high temperature calcination for removing these organic templates, which strongly influence their applications. Thus, it is very important to develop an organotemplate-free route for synthesizing zeolites. Addition of seeds crystals has been demonstrated as an effective method to accelerate the crystallization of zeolite, improving the purity of the crystal product. Based on the effect of seeds, we have successfully developed a seed-directed and organotemplate-free (SDS) synthesis of zeolites such as Beta, FER, ZSM-34 and LEV, where zeolite seeds play similar roles to the "templates" that direct crystallization of zeolites from the amorphous aluminosilicate gels. When no zeolites seeds

  3. Reduction volume of radioactive wastes using natural zeolite

    International Nuclear Information System (INIS)

    The aim of this experience was to know of the characteristics of zeolite as the sorbent for reduction volume of liquid waste with the Pb contaminant contain. The experiment was done by sorption method a batch performed by using zeolite from Gedangsari Gunung Kidul with the grain size (-60+80) mesh, (-80+100) mesh dan (-100+120) mesh which was activated by (NH4) CI and NH4N03 1.0 M. Weight of sorbent was added was variated from 5.0 to 40.0 %, and variation of silica sand to added from 0.5 to 2.5 % of weight sorbent. Stirring speed was varied from 30 to 180 rpm and the stirring time of 10 to 120 minutes, and filtrates from filtering process to analyzed by Absorption Analysis Spectrophotometry utilities. From the experience can be achieved of data that the best sorption to obtained at the condition of zeolite on (-80+100) mesh, sorbent added of 25 %, stirring speed of 120 rpm, time of stirring of 90 minutes, and the setting time of 120 minutes. At this condition to obtained sorption efficiency are 64.162 % for natural zeolite, 7.034 % for zeolite be activated with NH4N03 and 77.414 % for zeolite be activated with NH4Cl 1.0 M. (author)

  4. On the role of small amines in zeolite synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Rollmann, L.D.; Schlenker, J.L.; Lawton, S.L.; Kennedy, C.L.; Kennedy, G.J. [Mobil Technology Co., Paulsboro, NJ (United States). Strategic Research Center; Doren, D.J. [Univ. of Delaware, Newark, DE (United States). Dept. of Chemistry and Biochemistry

    1999-08-26

    A crystallization study was undertaken to relate the structure of small amines to the zeolite product obtained. At SiO{sub 2}/Al{sub 2}O{sub 3} = 200, certain noncyclic amines (some not previously recognized) were specific for the formation of 10-ring zeolites, e.g., ZSM-22 and ZSM-23. For example, ethylmethylamine and diethylamine yielded highly crystalline ZSM-22, while ethylamine and isopropylamine yielded ZSM-12. At lower SiO{sub 2}/Al{sub 2}O{sub 3} ratios (40), a different set of zeolites was obtained, as expected, ZSM-35 and MCM-22. Again, a specific relationship was observed between the amine employed and the zeolite obtained. In both SiO{sub 2}/Al{sub 2}O{sub 3} regimes, several amines played non-structure-specific pore- and pH-stabilizing roles and yielded ZSM-5. With relatively few exceptions, the zeolite products were fully porefilled with amine and low in Na (Na/Al < 1). Computer simulations confirmed a pore-stabilizing role for both structure-specific and non-structure-specific amines. At the same time, among structure-specific (structure-directing) amines, they showed that the interaction energy differences between alternative amine-pore combinations were often quite small (0.5--2.0 kcal/mol, for example). Nevertheless, the changes in amine-pore interaction energies for this group of amines consistently tracked the changes in zeolite products observed.

  5. 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.

  6. Activity of titania and zeolite samples dosed with triethylamine

    Energy Technology Data Exchange (ETDEWEB)

    Baker, Caitlin; Gole, James L.; Brauer, Jonathann I.; Graham, Samuel; Hu, Jian Z.; Kenvin, Jeff; D' Amico, Andrew D.; White, Mark

    2016-01-15

    Certain properties of titania and the ammonium- and proton-form of Y zeolites (silica/alumina ratio of 5.2) were explored before and after treatment by triethylamine (TEA). The effect of the triethylamine upon the physical and chemical properties of both titania and the zeolite were characterized by physical and chemical adsorption methods. BET surface area data showed enhanced surface area of the TEA-treated nanotitania over the untreated nanotitania whereas the TEA-treated zeolite showed a considerable decrease in surface area compared to the untreated zeolite. TPD of the TEA-treated Y zeolite showed that weakly adsorbed TEA left the surface between 150 and 300 oC; strongly adsorbed TEA decomposed to ethylene and ammonia at higher temperatures. XPS, IR, and Raman spectroscopies, powder XRD, and 27Al MAS-NMR spectroscopy were used to further characterize the changes introduced by in-situ nitridation. Pre-adsorbed triethylamine decorated acid sites so as to neutralize these sites for the reaction of methanol to dimethylether. Carbon monoxide and ormaldehyde, products of the methanol probe reaction, were observed-- suggesting that basic sites are present in this treated zeolite and titania.

  7. Removal of Heavy Metals from Textile Wastewater using Zeolite

    Directory of Open Access Journals (Sweden)

    Normala Halimoon

    2010-01-01

    Full Text Available Heavy metals such as lead (Pb, chromium (Cr, cadmium (Cd and copper (Cu are widely used for production of colour pigments of textile dyes. Textile dyes pollutants are being released to the environment at various stages of operation therefore it is necessary that the pollutants are treated before discharge using zeolite with and without alum. A study was carried out to compare the effectiveness of treatment using zeolite with and without alum for the removal of heavy metals (Pb, Cu, Cd, Cr in textile effluent. The concentrations of these heavy metals in the textile wastewater samples were reduced to more than 50 percent after treating with zeolite. The sequence in increasing order of removal efficiency of these heavy metals using zeolite was Cd < Pb < Cr < Cu. When the textile wastewater sample was treated using zeolite and 10 mg/L of alum, 80% of the heavy metals (Cd and Cu were removed. The most effective treatment prior to removal of heavy metals from textile wastewater sample is by using zeolite with the addition of 10 mg/L of alum as flocculants.

  8. Removal of Ammonia from Air, using Three Iranian Natural Zeolites

    Directory of Open Access Journals (Sweden)

    H Asilian

    2004-06-01

    Full Text Available Ammonia in air can be hazardous to human and animal life and should be removed from the environment. Recently the removal of environmental pollutants such as ammonia by means of natural and modified zeolites has attracted a lot of attention and interests. In this study the capability of three Iranian natural zeolites (Clinoptilolite in point of view of removal of ammonia from air was investigated. Through this research, different zeolites from various regions of Iran including Semnan, Meyaneh, and Firoozkooh resources were considered to be studied. These samples of zeolites were ground and granulized into 425 µm to 4 mm and were utilized in dynamic sorption experiments. Curves of sorption were plotted and breakthrough and saturated points of zeolite samples were obtained. The adsorption capacities at different ammonia concentrations, temperatures, and flow – rates were also calculated. Results obtained showed that, the natural Iranian zeolite (Clinoptilolite was identified to be more efficient adsorbent than the others to remove ammonia from the air. In the same conditions, the obtained breakthrough time for clinoptilolite sample of Meyaneh was longer than the others ( 135min , while, the adsorption capacity of Semnan clinoptilolite was higher than adsorbents ( 6.30 mg /g (P<0.0001.

  9. Removal of ammonium from municipal landfill leachate using natural zeolites.

    Science.gov (United States)

    Ye, Zhihong; Wang, Jiawen; Sun, Lingyu; Zhang, Daobin; Zhang, Hui

    2015-01-01

    Ammonium ion-exchange performance of the natural zeolite was investigated in both batch and column studies. The effects of zeolite dosage, contact time, stirring speed and pH on ammonium removal were investigated in batch experiments. The result showed that ammonium removal efficiency increased with an increase in zeolite dosage from 25 to 150 g/L, and an increase in stirring speed from 200 to 250 r/min. But further increase in zeolite dosage and stirring speed would result in an unpronounced increase of ammonium removal. The optimal pH for the removal of ammonium was found as 7.1. In the column studies, the effect of flow rate was investigated, and the total ammonium removal percentage during 180 min operation time decreased with the flow rate though the ion-exchange capacity varied to a very small extent with the flow rate ranging from 4 to 9 mL/min. The spent zeolite was regenerated by sodium chloride solution and the ammonia removal capacity of zeolite changed little or even increased after three regeneration cycles. PMID:26510611

  10. The Influence of Zeolites on Radical Formation During Lignin Pyrolysis.

    Science.gov (United States)

    Bährle, Christian; Custodis, Victoria; Jeschke, Gunnar; van Bokhoven, Jeroen A; Vogel, Frédéric

    2016-09-01

    Lignin from lignocellulosic biomass is a promising source of energy, fuels, and chemicals. The conversion of the polymeric lignin to fuels and chemicals can be achieved by catalytic and noncatalytic pyrolysis. The influence of nonporous silica and zeolite catalysts, such as silicalite, HZSM5, and HUSY, on the radical and volatile product formation during lignin pyrolysis was studied by in situ high-temperature electron paramagnetic resonance spectroscopy (HTEPR) as well as GC-MS. Higher radical concentrations were observed in the samples containing zeolite compared to the sample containing only lignin, which suggests that there is a stabilizing effect by the inorganic surfaces on the formed radical fragments. This effect was observed for nonporous silica as well as for HUSY, HZSM5, and silicalite zeolite catalysts. However, the effect is far larger for the zeolites owing to their higher specific surface area. The zeolites also showed an effect on the volatile product yield and the product distribution within the volatile phase. Although silicalite showed no effect on the product selectivity, the acidic zeolites such as HZSM5 or HUSY increased the formation of deoxygenated products such as benzene, toluene, xylene (BTX), and naphthalene.

  11. Tribomechanical micronization and activation of whey protein concentrate and zeolite

    Indian Academy of Sciences (India)

    Z Herceg; V Lelas; M Brnčić; B Tripalo; D Ježek

    2004-02-01

    Tribomechanics is a part of physics that is concerned with the study of phenomena that appear during milling under dynamic conditions. Tribomechanical micronization and activation (TMA) of whey protein concentrates (WPC) and zeolites (type clinoptilolite) were carried out. Samples of powdered WPC and zeolite were treated with the laboratory TMA equipment. The treatment was carried out at two various rotor speeds: 16,000 and 22,000 r.p.m. at ambient temperature. Analyses of the particle size and distribution as well as the specific area and scanning electron microscopy were carried out on the powdered WPC and zeolite, before and after the TMA treatment. Suspensions of the WPC and zeolite were treated with ultrasound, just before determining the particle size distribution, at 50 kHz. The results showed that tribomechanical treatment causes significant decrease in particle size, change in particle size distribution and increase in specific area of WPC and zeolite. These changes of the treated materials depend on the type of the material, the level of inserting particles, the planned angle of the impact, internal rubbing and the planned number of impacts. The effects found became stronger as the rotor speed of the TMA equipment increased (16,000 to 22,000 rpm). Ultrasonic treatment of suspension of tribomechanically treated WPC resulted infurther breakdown of partly damaged protein globules as proved with the statistic analyses. No further changes in their granulometric composition were caused by ultrasonic treatment of a suspension of tribomechanically treated zeolite.

  12. Nanocellulose-Zeolite Composite Films for Odor Elimination.

    Science.gov (United States)

    Keshavarzi, Neda; Mashayekhy Rad, Farshid; Mace, Amber; Ansari, Farhan; Akhtar, Farid; Nilsson, Ulrika; Berglund, Lars; Bergström, Lennart

    2015-07-01

    Free standing and strong odor-removing composite films of cellulose nanofibrils (CNF) with a high content of nanoporous zeolite adsorbents have been colloidally processed. Thermogravimetric desorption analysis (TGA) and infrared spectroscopy combined with computational simulations showed that commercially available silicalite-1 and ZSM-5 have a high affinity and uptake of volatile odors like ethanethiol and propanethiol, also in the presence of water. The simulations showed that propanethiol has a higher affinity, up to 16%, to the two zeolites compared with ethanethiol. Highly flexible and strong free-standing zeolite-CNF films with an adsorbent loading of 89 w/w% have been produced by Ca-induced gelation and vacuum filtration. The CNF-network controls the strength of the composite films and 100 μm thick zeolite-CNF films with a CNF content of less than 10 vol % displayed a tensile strength approaching 10 MPa. Headspace solid phase microextraction (SPME) coupled to gas chromatography-mass spectroscopy (GC/MS) analysis showed that the CNF-zeolite films can eliminate the volatile thiol-based odors to concentrations below the detection ability of the human olfactory system. Odor removing zeolite-cellulose nanofibril films could enable improved transport and storage of fruits and vegetables rich in odors, for example, onion and the tasty but foul-smelling South-East Asian Durian fruit.

  13. Synthesis and Characterization of Hollow Titanium Silicalite Zeolite(HTS)

    Institute of Scientific and Technical Information of China (English)

    Lin Min; Zhu Bin; Shu Xingtian; Wang Xieqing

    2008-01-01

    29Si-NMR and 1H-NMR were used to follow up the basic hydrolysis of tetraethyl orthosilicate (TOES) and the results showed that species of monomer, dimer, trimer, cyclic and polymer silicates were formed. The monomer and dimer were favorable for the high activity of zeolite. XRD, 13C CP/MAS and 29Si NMR were used to trace the crystallization process of hollow titanium silicalite zeolites (HTS). The results showed that the induction period of HTS was 80 min, and subsequently it took next 10 min to form HTS and the remaining time of the crystallization period might function for cleaning up the pores and/or washing off the impurities from the HTS zeolite. The catalytic oxidation performance of HTS zeolite is different from that of the acid activity of zeolite in which the conventional definition of crystallinity does not reflect the catalytic oxidation activity proportionally. The synthesized HTS samples were character-ized by XRD, FT-IR, UV-Vis and Raman spectra. It was confirmed that Ti was incorporated into the zeolite framework. The synthesized HTS samples revealed good repeatability and high activity for oxidation of phenol into diphenol.

  14. 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.

  15. Preparation and gas permeabilities of zeolite membranes

    Energy Technology Data Exchange (ETDEWEB)

    Jinqu Wang; Yongfeng Wang; Shuanshi Fan [Dalian Univ. of Technology (China)] [and others

    1994-12-31

    Zeolites with less than 10 {angstrom} pore are desirable membrane materials, due to their crystallinity, resistance to high temperature, and chemical inertness. A variety of new membranous materials were synthesized composed of a continuous intergrowth of 5-50 micrometer type A, X, Y, or ZSM-5 crystals. The membranes were crystallized under hydrothermal conditions at 90 to 220{degrees}C on the external surface of a porous ceramics. The reagents used were aluminum sulphate, water glass (20.1 wt% SiO{sub 2}, 6.09 wt% Na{sub 2}O, 73.8 wt% water), sodium hydroxide, sulphuric acid, deionized water and templating agents. The molar composition was: 0.1-0.5 Na{sub 2}O:1 SiO{sub 2}:0.04-0.05 Al{sub 2}O{sub 3}:20-60H{sub 2}O.

  16. 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.

  17. Polypropylene obtained through zeolite supported catalysts

    International Nuclear Information System (INIS)

    Propylene polymerizations were carried out with φ2C(Flu)(Cp)ZrCl2 and SiMe2(Ind)2ZrCl2 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)(Cp)ZrCl2, 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 stereo regularity. (author)

  18. Hierarchical Porous ZSM-5 Zeolite Synthesized by in situ Zeolitization and Its Coke Deposition Resistance in Aromatization Reaction

    Institute of Scientific and Technical Information of China (English)

    张珂; 柳云骐; 赵晋翀; 刘晨光

    2012-01-01

    Hierarchical ZSM-5 zeolites with micro-, meso- and macroporosity were prepared from diatomite zeolitization through a vapor-phase transport process on solid surfaces. The aromatization performance of the catalysts was in- vestigated on a fixed bed reactor by using FCC gasoline as feedstock. The crystal phase, morphology, pore struc- tures, acidity and coke depositions of the hierarchical ZSM-5 zeolites were characterized by means of X-ray diffrac- tion (XRD), scanning electron microscope (SEM), N2 adsorption/desorption, Fourier transform infrared (FT-IR) and thermogravimetry-mass spectrogram (TG-MS), respectively. The results show that the prepared hierarchical ZSM-5 zeolite possesses excellent porosity and high crystallinity, displaying an improved aromatization performance and carbon deposition resistance due to its meso- and macroporous structures.

  19. Pyrolysis of scrap tyres with zeolite USY

    International Nuclear Information System (INIS)

    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

  20. Zeolite ZSM-12: Hydrothermal synthesis and catalytic properties

    Energy Technology Data Exchange (ETDEWEB)

    Weitkamp, J.; Kumar, R.; Ernst, S.

    1987-02-01

    ZSM-12 was produced by hydrothermal synthesis. To obtain detailed information on the catalytic and type-selective properties of the bi-functional type (Pd/HZSM-12), the hydrocracking of butyl cyclohexane and the isomerisation and hydrocracking of long-chain n-alkanes were investigated as test reactions.

  1. X-ray electron probe microanalysis of zeolite powder particles

    International Nuclear Information System (INIS)

    Complete text of publication follows. The zeolite powders of various trademarks are used for production of petroleum-refining catalysts. In this connection, it is very important have information not only about chemical composition and distribution of impurity elements, but about shape, surface, structure and size of particles. That allows a more detailed analysis of the physical-chemical characteristics of catalysts, affecting their activity at different stages of technological process. The X-ray electron probe microanalysis (EPMA) technique is developed for individual particles of fine-dispersed zeolite powders of various trademarks: ZSM-5, ZSM-12, MOR, BEA. The investigations were conducted using Superprobe-733 and Superprobe JXA-8200 (JEOL Ltd, Japan) devices with energy-dispersive and wavelength-dispersive spectrometers. The dependencies of the relative intensity on the time of electron probe influence have been studied at the different accelerating voltages and currents of probe for the selecting of optimum condition of analytical signal registration. The phase and chemical composition of zeolite powders, the surface, shape of particles and their distribution in sizes were studied. The results of phase analysis showed, that particles of different shape and various size were separated in all samples of zeolites. The particles of flaky, orbicular, rounded and oval shape with size of 10 m are separated in zeolite sample ZSM-12. The particles of faceted shape with size of 5-10 μm are observed in zeolite samples MOR and BEA. Larger particles of different shape with size of 5-20 μm are separated in zeolite sample ZSM-5, while the finer-dispersed fraction of particles with size of 3-10 μm are observed in this sample after gel decomposition (aging of gel). The data of zeolite powders chemical composition showed the heterogeneous distribution of silicon. The increased contents of silicon are observed towards the edge of particles that connected with aggregation and

  2. Metal clusters in zeolite 4A obtained by synthesis process

    Directory of Open Access Journals (Sweden)

    E. David

    2006-09-01

    Full Text Available Purpose: The goal of this paper is to study the possibility of obtaining of the supported metal clusters in zeolite 4A that are a new class of composite materials with application in sorption and catalytic processes.Design/methodology/approach: The materials were fabricated by synthesis process involving organo-metallic chemistry on surfaces, gas-phase cluster chemistry and chemistry in zeolite cages. The magnesium clusters in zeolite 4A(Mg/Z4A has been prepared by ion exchange, followed by calcination and reduction processes. The metals are introduced as cationic form, which replace cations such as natrium from zeolite and then treated by heating in oxidized mixture or air and reduced in hydrogen. The activation and reduction treatments give the highest metal dispersions. The texture studies, X-ray diffraction , transmission electron microscopy (TEM and atomic absorption were used for to characterize these materials.Findings: Through this study it was determined the structures and properties of (Mg/Z4A composites and then these properties were compared with zeolite 4A properties without metal addition. It was found that Mg/Z4A have new properties, with high catalytic effect and the reducing process are decisively regarding the size and the placement of the metal magnesium particles into zeolite 4A.Research limitations/implications: It is noticed, that increase of the reducing temperature over 600ºC promotes the forming of metal clusters with great sizes at the external surface of zeolite 4A and the catalitycal activity is diminished. The activation and reduction treatments give the highest metal dispersions, but the most uniform metal clusters are not easily formed.Practical implications: Obtained results allowed to optimize the catalytic activity of the supported metals on zeolite.Originality/value: This work contains several new aspects, which are: the conditions for performing the magnesium metal clusters in zeolite 4A cages, wide range of

  3. Synthesis and characterization of zeolite material from coal ashes modified by surfactant

    International Nuclear Information System (INIS)

    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)

  4. Preparation of zeolite NaA for CO2 capture from nickel laterite residue

    Institute of Scientific and Technical Information of China (English)

    Tao Du; Li-ying Liu; Penny Xiao; Shuai Che; He-ming Wang

    2014-01-01

    Zeolite NaA was successfully prepared from nickel laterite residue for the first time via a fusion-hydrothermal procedure. The structure and morphology of the as-synthesized zeolite NaA were characterized with a range of experimental techniques, such as X-ray diffraction, scanning electronic microscopy, and infrared spectroscopy. It was revealed that the structures of the produced zeolites were dependent on the molar ratios of the reactants and hydrothermal reaction conditions, so the synthesis conditions were optimized to obtain pure zeolite NaA. Adsorption of nitrogen and carbon dioxide on the prepared zeolite NaA was also measured and analyzed. The results showed that zeolite NaA could be prepared with reasonable purity, it had physicochemical properties comparable with zeolite NaA made from other methods, and it had excellent gas adsorption properties, thus demonstrating that zeolite NaA could be prepared from nickel laterite residue.

  5. CaE-T zeolite - a new effective adsorber for vacuum technique

    International Nuclear Information System (INIS)

    Adsorption of air at low pressures on type E zeolites was studied as a function of their composition and dehydration regime. It was shown that zeolite CaE-T has a greatly increased sorption capacity for air at low pressures and that this is more than 3 times that of industrial zeolites currently used in vacuum technology. Mass-spectrometer studies were made of the gas phase over zeolites type E and A after adsorption of air at pressures from 10-8 to 10-5 mm Hg at liquid nitrogen temperatures under conditions approximating equilibrium. It was shown that zeolite CaE-T has a high adsorption capacity for Ar, O2, and H2. Adsorption of H2 and Ar by zeolites of different structural types at low pressures was studied. It was shown that zeolite CaE-T has a significantly higher adsorption capacity for hydrogen and argon than all industrial zeolites

  6. Sorption and migration of radiocaesium in natural zeolite-water systems

    International Nuclear Information System (INIS)

    The sorption properties for caesium and its migration in a system zeolite-aqueous solution were studied for natural zoelites from Zaloshka gorica. It was found that zeolites are rather efficient sorbents for caesium even in the presence of some other electrolytes. A correlation between the rate of migration of caesium in the system zeolite-water and the sorption intensity was established. Migration of caesium from a zeolite layer by diffusion is described. (author) 7 refs.; 2 figs,; 1 tab

  7. SYNTHESIS AND CHARACTERISATION OF HIERARCHICAL ZEOLITIC MATERIALS FOR HEAVY METALS ADSORPTION

    OpenAIRE

    De Haro del rio, David

    2015-01-01

    This thesis explains a method based on the homogenisation of zeta potential charges on carbon supports for the production of hierarchical structured zeolitic composites. The modification of carbons’ surface chemistry allowed zeolite particles to be fixed to the support by electrostatic interactions. In order to achieve this, the size reduction of zeolite particles was carried out by two different methods: a) ball milling and b) a synthetic route to produce zeolite colloidal dispersions. Also, th...

  8. Influence of zeolites on the sintering and technological properties of porcelain stoneware tiles

    OpenAIRE

    de Gennaro, R.; Cappelletti, P.; G. Cerri; Gennaro, M.; Dondi, M.; Guarini, G.; Langella, A.; Naimo, D.

    2003-01-01

    Low-cost zeolitic rocks are promising substitutes for feldspathic fluxes in ceramic bodies, since their fusibility, modest hardness and high cation exchange capacity (CEC) should improve grinding and sintering. Five large-scale Italian deposits of natural zeolites with different mineralogy were characterised and tested in porcelain stoneware bodies. Their behaviour during processing was appraised and compared with that of zeolite-free bodies. Zeolites increased the slip viscosity during wet g...

  9. BTX abatement using Chilean natural zeolite: the role of Brønsted acid sites

    OpenAIRE

    Alejandro, S.; Valdés, Héctor; Manero, Marie-Hélène; Zaror, Claudio A.

    2012-01-01

    In wastewater treatment facilities, air quality is not only affected by conventional unpleasant odour compounds; toxic volatile organic compounds (VOCs) are also found. In this study, the adsorptive capacity of Chilean natural zeolite toward VOC removal was evaluated. Moreover, the influence of zeolite chemical surface properties on VOC elimination was also investigated. Three modified zeolite samples were prepared from a natural Chilean zeolite (53% clinoptilolite, 40% mordenite and 7% quart...

  10. Na-noparticles of activated natural zeolite on textiles for protection and therapy

    OpenAIRE

    Ivančica Kovaček; Anita Tarbuk; Ana Marija Grancarić

    2009-01-01

    Activated natural zeolite clinoptilolite is microporous hydrated aluminosilicates crystals with well-defined structures containing AlO4 and SiO4 tetrahedral linked through the common oxygen atoms. It is to point out that zeolites act as strong adsorbents and ion-exchangers but having many other useful properties. Due to its cationexchange ability, zeolites have catalytic properties and, for that, multiple uses in medicine and industry, agriculture, water purification and detergents. Zeolites ...

  11. Enhancement of Sudan Gasoline Octane Number by Natural and Synthetic Zeolites

    OpenAIRE

    *M. A. M. El Hassan

    2014-01-01

    The sample of natural zeolite is collected from the Sudan area, (scolecite) from Buda desert. And the other one is synthetic zeolite (Y). The study characterized the natural zeolite (scolecite) and synthetic (Y). Using thin sections for natural zeolite to recognize it. Beside different techniques as follow: Atomic absorption, x- ray diffraction (XRD), inferared spectroscopy (FTIR), acidity measured by pyridine FTIR, scanning electron microscopy (SEM). The study was carried out for selected na...

  12. In vitro studies on the ability of natural zeolites to sorb some radionuclides

    International Nuclear Information System (INIS)

    The aim of our work was to study sorption and sorption kinetics of 85Sr, 137Cs and 131I from rumen liquid after application of zeolite (clinoptilolite) under laboratory conditions. Zeolite dump corresponded with usual (3%) and high (9%) dose of zeolite in feed. We have ascertained that zeolite is characterized with a high sorption ability for 85Sr and 137Cs from rumen liquid. 84% of 85Sr and 98% of 137Cs was bound after 24 hours. (orig.)

  13. The Microwave Direct Heating of Zeolite FAU in an Open System

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Zeolite FAU was heated directly by microwave irradiation at 2450 MHz in an open system without special loading materials. It was discovered that zeolite X was heated to 1473 K about 90 seconds at power output of 400 W. HY type zeolite was also heated to 1373 K although it needed relative long time (about 11 minutes). Influences of exchangeable cations and adsorbed substances on zeolite1s ability to absorb microwaves were also discussed.

  14. Adsorption of alkali and alkaline earth radionuclides on zeolite from water solutions

    International Nuclear Information System (INIS)

    The adsorption of cesium and strontium ions from water solutions on zeolite has been investigated in presence of sodium, potassium, magnesium and calcium ions. Distribution ratios of cesium and strontium on the zeolite were determined in solutions of various compositions and solution volume to sorbent weight ratios (batch factor). Breakthrough curves for zeolite layers are reported. (author) 7 refs.; 4 figs

  15. Solid state uptake of manganese from KMnO4 by zeolite-13X

    International Nuclear Information System (INIS)

    The solid state reaction between KMnO4 and zeolite-13X at a temperature below the melting point of the salt presumably results in inclusion of manganese in the zeolite. Quantitative measurements of manganese uptake at various proportions of KMnO4 in the mixture were achieved by neutron activation analysis of the Mn-zeolite. (author)

  16. Influence of Different Factors on Sorption of 90Sr by natural and Synthetic Zeolites

    International Nuclear Information System (INIS)

    The paper researches into factors influencing sorption and selective properties of natural zeolite clinoptilolite from the Sokirnitsky deposit of Ukraine and synthetic zeolites in relation to radionuclide 90Sr. It also studies the effect of competing ions on the sorption of 90Sr by zeolites

  17. Leachability of cobalt and cesium from natural and chemically treated zeolites

    International Nuclear Information System (INIS)

    The determination of leachability of radioisotopes of cesium and cobalt from preloaded zeolites in distilled water, base solution and acid solution has been studied. For the experiment, we used natural and chemically treated zeolites. The zeolites before leaching were calcined at different temperatures. (author). 8 refs., 5 figs., 2 tabs

  18. Zeolite catalysts and their use in selective catalytic reduction of NOx

    NARCIS (Netherlands)

    Seijger, G.B.F.; Van den Bleek, C.M.; Calis, H.P.A.

    2003-01-01

    The invention is directed to catalyst compositions comprising a zeolite, as well as to processes for the reduction of nitrogen oxides (NOx) employing these catalyst compositions. The catalyst compositions of the invention comprise a zeolite of the ferrierite type (FER), which zeolite is ion exchange

  19. A study of highly concentrated fission product salt loading into zeolite-A

    International Nuclear Information System (INIS)

    A study investigating the loading of highly contaminated electrorefiner salt into zeolite-4A is currently underway. The objective of the study is to optimize the absorption process in order to maximize fission product sorption into zeolite, which should result in reduction of waste associated with the pyrochemical processing of spent nuclear fuel. The study is based on both experimental and theoretical investigations to develop a fundamental understanding of the transport of LiCl-KCl and fission product chlorides in zeolite-A. A diffusion-limited sorption rate model has been formulated, while data have been collected using molten salt-zeolite contacting experiments. Solid-state salt-zeolite contacts have also been performed to probe single salt sorption characteristics in the absence of LiCl-KCl. Experimental data suggest that the rate of fission product sorption into the zeolite can be increased by pre-loading the zeolite with LiCl-KCl. Additionally, experiments involving variable zeolite particle size were performed in an effort to further support the theory that the salt sorption is diffusion-limited. X-ray fluorescence imaging of the cross section of a zeolite pellet after solid-state salt-zeolite contacting was performed to examine salt distribution through the zeolite pellet. The findings will be used to design practical processes that can be used for absorbing high fission product content salt into zeolite-A. (author)

  20. Bayberry-like ZnO/MFI zeolite as high performance methanol-to-aromatics catalyst.

    Science.gov (United States)

    Wang, Ning; Qian, Weizhong; Shen, Kui; Su, Chang; Wei, Fei

    2016-02-01

    Unique bayberry-like MFI zeolites are synthesized through a quasi-solid-state crystallization approach. This hierarchical zeolite structure has a relatively thick shell, densely grown nanocrystals with an ordered packed channel, high mechanical stability, high surface area and a low Si/Al ratio. Its catalytic efficiency for methanol-to-aromatics is significantly higher than that of conventional MFI zeolites.

  1. ZEOLITE PERFORMANCE AS AN ANION EXCHANGER FOR ARSENIC SEQUESTRATION IN WATER

    Science.gov (United States)

    Zeolites are well known for their use in ion exchange and acid catalysis reactions. The use of zeolites in anion or ligand exchange reactions is less studied. The NH4+ form of zeolite Y (NY6, Faujasite) has been tested in this work to evaluate its performance for arsenic removal...

  2. 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

  3. 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

  4. PENINGKATAN KECEPATAN PROSES PENGERINGAN KARAGINAN MENGGUNAKAN PENGERING ADSORPSI DENGAN ZEOLIT

    Directory of Open Access Journals (Sweden)

    Mohamad Djaeni

    2012-07-01

    Full Text Available Drying carrageenan product still deals with low product quality and energy efficiency. The drying with airdehumidified by activated natural zeolite has a potential for drying the product. In this concept, air as dryingmedium was contacted with zeolite to reduce its relative humidity. Hence, the driving force of drying increasesand the process can be conducted at moderate temperature (40-60oC to retain the quality. This research looksinto the effectiveness of adsorption dryer with zeolite for drying carrageenan. The natural zeolite is activated byheating 300-400oC for 2-3 hours. The zeolite is then used to dehumidify the ambient air as drying medium. Inthis work, the effect of drying temperature and carrageenan thickness on water content in carrageenan duringthe drying were studied. Results showed with air velocity 3.0 m/sec, thickness of carrageenan 1-2 mm,operational drying time 3 hours and air temperature 40-60oC, water content in carrageenan can be reducedfrom 82.0% to 25%. This result is very promising for industrial application.

  5. 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.

  6. Risk assessment for the transportation of radioactive zeolite liners

    Energy Technology Data Exchange (ETDEWEB)

    1982-01-01

    The risk is estimated for the shipment of radioactive zeolite liners in support of the Zeolite Vitrification Demonstration Program currently underway at Pacific Northwest Laboratory under the sponsorship of the US Department of Energy. This program will establish the feasibility of zeolite vitrification as an effective means of immobilizing high-specific-activity wastes. In this risk assessment, it is assumed that two zeolite liners, each loaded around July 1, 1981 to 60,000 Ci, will be shipped by truck around January 1, 1982. However, to provide a measure of conservatism, each liner is assumed to initially hole 70,000 Ci, with the major radioisotopes as follow: /sup 90/Sr = 3000 Ci, /sup 134/Cs = 7000 Ci, /sup 137/Cs = 60,000 Ci. Should shipment take place with essentially no delay after initial loading (regardless of loading date), the shipment loading would be only 2.7% higher than that for the assumed six-month delay. This would negligibly affect the overall risk. As a result of this risk assessment, it is concluded that the transport of the radioactive zeolite liners from TMI to PNL by truck can be conducted at an insignificant level of risk to the public.

  7. Electron beam irradiation and zeolites adsorption applied to dyeing effluents

    International Nuclear Information System (INIS)

    Wastewater generated from the textile industries contain large amount of azo dyes and many of them present low biodegradability capability. Today several countries are facing with evidences that water pollution is related to toxicity, mutagenicity and carcinogenic nature. Once reactive dyes are commercial products they will be discharged to the waterways and rivers causing ecological damages and health problems. The aim of this paper was to consider the potential of two techniques for colour and toxicity removal: ionizing radiation and adsorption by zeolites synthesized from fly ash. Real effluents from chemical and textile industries (hardly coloured) were submitted to radiation and adsorption using zeolites. It was necessary to dilute some effluents prior the treatments in order to get any success. When electrons irradiation was performed radiation doses applied were from 0.5 kGy up to 20 kGy. This radiation process accounted for a partial decolouring as higher doses were implemented. Coal fly ashes were used as starting material for zeolite synthesis by means of hydrothermal treatment with alkaline medium. The adsorption was performed by batch experiments. It was obtained about 77% - 90% color removal from dye wastewater after 24h of contact time with two types of zeolite. The irradiation accounted for 72% of the initial toxicity. The ionizing radiation and adsorption by zeolites synthesized from fly ash can be used as an alternative for the treatment of aqueous waste containing dyes. (author)

  8. [Adsorption of phenol chemicals by surfactant-modified zeolites].

    Science.gov (United States)

    Xie, Jie; Wang, Zhe; Wu, De-Yi; Li, Chun-Jie

    2012-12-01

    Two kinds of zeolites were prepared from fly ash and modified by surfactant subsequently. Surfactant-modified zeolites were studied for adsorption of phenol chemicals (phenol, p-chlorphenol, bisphenol A). It showed that the adsorption affinity of zeolite to phenol chemicals was significantly improved after surfactant modification. The adsorption isotherms of phenol chemicals were well fitted by the Langmuir isotherm. For the two surfactant-surfactant modified zeolites, the maximum adsorption amounts of phenol, p-chlorphenol, and bisphenol A calculated from the Langmuir equation were 37.7, 52.36, 90.9 mg x g(-1) and 10.7, 22.83, 56.8 mg x g(-1), respectively. When pH values of solutions were higher than the pK(a) values of phenol chemicals, the removal efficiencies were getting higher with the increase of pH values. The octanol/water partition coefficient (K(ow)) was also found to be an important factor affecting adsorption of phenol chemicals by the modified zeolites. Higher K(ow) value, which means the greater hydrophobicity of the chemicals, resulted in a higher removal.

  9. Zeolite A effect on calcium homeostasis in growing goats.

    Science.gov (United States)

    Schwaller, D; Wilkens, M R; Liesegang, A

    2016-04-01

    The purpose of this study was to investigate the influence of 2 different concentrations of zeolite A on calcium homeostasis. Seventeen growing goats were divided into 3 groups. Whereas the control group (5 animals) received no supplementation, 2 treatment groups were supplemented with zeolite A at either 1.2 (6 animals) or 1.6 g/kg BW (6 animals), respectively. Blood and urine samples were continually drawn and bone mineral density was measured weekly by peripheral quantitative computed tomography. After 3 wks, the animals were slaughtered and samples were taken from the rumen, duodenum, and kidneys. Plasma concentrations of phosphate ( Ussing chamber technique and quantification of RNA and protein expression of genes known to be involved in active calcium absorption did not reveal any stimulating effect of zeolite. Plasma calcium concentrations were not altered, probably because of the sufficient dietary calcium supply. However due to the effects of zeolite on 1,25 dihydroxycholecalciferol, bone metabolism and serum concentrations of phosphate and magenesium shown in the present study, potential negative long-termin effects on the animals should be considered whenever rations with zeolite are designed. PMID:27136016

  10. USE OF NATURAL ZEOLITES (KLINOPTILOLIT IN WATER SOFTENING PROCESS

    Directory of Open Access Journals (Sweden)

    Yurdanur SABAH

    1999-03-01

    Full Text Available In this work, the potential for the elimination of hardness of the water by using zeolitic tuff (klinoptilolit obtained from the upper layer tuff of Balıkesir-Bigadiç, where the richest deposits are located in our country, has been investigated; as a means of water supply, daily usage water of campus, Selçuk University, was utilized to wich none of the pre-refining process was applied apart from chloring. At first, zeolite samples of -0.85+0.60 mm were regenerated by NaOH and the change in the hardness of water passing through zeolitic bad in ion exchange column at a constant rate was abserved. After optimizing the regeneration conditions in this way, the effect of the velocity of water fed into zeolitic bad and the water left in the column on the elimination of water hardness were also searched. As a result, the lowest value of water hardness was obtained by taking the water feeding rates at 10 ml/sec. and using zeolite regenerated with 0.75 M NaOH. Additionally, it was seen that the highest working capacity will be reached under these circumstances.

  11. 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. PMID:24731937

  12. Ion exchangers in radioactive waste management: Natural Iranian zeolites

    International Nuclear Information System (INIS)

    Five samples of natural zeolites from different parts of Iran were chosen for this study. In order to characterize and determine their structures, X-ray diffraction and infrared spectrometry were carried out for each sample. The selective absorption properties of each zeolite were found by calculating the distribution coefficient (K d) of various simulated wastes which were prepared by spiking the radionuclides with 131I, 99Mo, 153Sm, 140La and 147Nd. All the zeolite samples used in this study had extremely high absorption value towards 140La; clinoptolite from Mianeh and analsite from Ghalehkhargoshi showed good absorption for 147Nd; clinoptolite from Semnan and clinoptolite from Firozkoh showed high absorption for 153Sm; mesolite from Arababad Tabas showed good absorption for 99Mo; and finally mesolite from Arababad Tabas, clinoptolite from Semnan and clinoptolite from Firozkoh could be used to selectively absorb 131I from the stimulated waste which was prepared. The natural zeolites chosen for these studies show a similar pattern to those synthetic ion exchangers in the literature and in some cases an extremely high selectivity towards certain radioactive elements. Hence the binary separation of radioactive elements could easily be carried out. Furthermore, these zeolites, which are naturally occurring ion exchangers, are viable economically and extremely useful alternatives in this industry

  13. 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.

  14. Hydrothermal preparation and crystal habit of X-zeolite powder

    Institute of Scientific and Technical Information of China (English)

    SHEN Shao-hua; ZHANG Shu-gen; WANG Da-wei; FANG Ke-ming

    2005-01-01

    The preparation of X-zeolite powder was investigatedin hydrothermal system, the crystal growth process of X-zeolite in hydrothermal condition was characterized by means of X-ray diffraction, scanning electron microscope and infrared ray. The results show that X-zeolite powder with uniform granularity and intact crystal shape can be obtained in hydrothermal system of acid-treated stellerite-NaOH-NaAl(OH)4-H2O; the crystallite size is in the range of 2 - 3μm. The best reaction time of hydrothermal preparation is 6 h. The formation phases of X-zeolite crystal are as follows: dissolution of feedstocks → formation of [SiO4]4- and [AlO4]5- tetrahedron, many-membered ring,β cage → formation of crystal nucleus and nano-particle → aggregation growth of nano-particle → coalescence growth of crystallite. The crystal habits of X-zeolite are intimately related with crystallization orientation ofβ cage in crystal and with its coupling stability on every crystal face family.

  15. Electron beam irradiation and zeolites adsorption applied to dyeing effluents

    Energy Technology Data Exchange (ETDEWEB)

    Higa, Marcela C.; Fungaro, Denise A.; Somessari, Elizabeth S.R.; Magdalena, Carina P.; Grosche, Lucas C.; NNeto, Antonio C.; Borrely, Sueli I. [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2007-07-01

    Wastewater generated from the textile industries contain large amount of azo dyes and many of them present low biodegradability capability. Today several countries are facing with evidences that water pollution is related to toxicity, mutagenicity and carcinogenic nature. Once reactive dyes are commercial products they will be discharged to the waterways and rivers causing ecological damages and health problems. The aim of this paper was to consider the potential of two techniques for colour and toxicity removal: ionizing radiation and adsorption by zeolites synthesized from fly ash. Real effluents from chemical and textile industries (hardly coloured) were submitted to radiation and adsorption using zeolites. It was necessary to dilute some effluents prior the treatments in order to get any success. When electrons irradiation was performed radiation doses applied were from 0.5 kGy up to 20 kGy. This radiation process accounted for a partial decolouring as higher doses were implemented. Coal fly ashes were used as starting material for zeolite synthesis by means of hydrothermal treatment with alkaline medium. The adsorption was performed by batch experiments. It was obtained about 77% - 90% color removal from dye wastewater after 24h of contact time with two types of zeolite. The irradiation accounted for 72% of the initial toxicity. The ionizing radiation and adsorption by zeolites synthesized from fly ash can be used as an alternative for the treatment of aqueous waste containing dyes. (author)

  16. 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.

  17. Levered and unlevered Beta

    OpenAIRE

    Fernandez, Pablo

    2003-01-01

    We prove that in a world without leverage cost the relationship between the levered beta ( L) and the unlevered beta ( u) is the No-costs-of-leverage formula: L = u + ( u - d) D (1 - T) / E. We also analyze 6 alternative valuation theories proposed in the literature to estimate the relationship between the levered beta and the unlevered beta (Harris and Pringle (1985), Modigliani and Miller (1963), Damodaran (1994), Myers (1974), Miles and Ezzell (1980), and practitioners) and prove that all ...

  18. Realized Beta GARCH

    DEFF Research Database (Denmark)

    Hansen, Peter Reinhard; Lunde, Asger; Voev, Valeri Radkov

    2014-01-01

    as the beta. We apply the model to a large set of assets and find the conditional betas to be far more variable than usually found with rolling-window regressions based exclusively on daily returns. In the empirical part of the paper, we examine the cross-sectional as well as the time variation...... of the conditional beta series during the financial crises....

  19. Catalytic pyrolysis using UZM-39 aluminosilicate zeolite

    Energy Technology Data Exchange (ETDEWEB)

    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.

  20. Advanced NMR characterization of zeolite catalysts

    Science.gov (United States)

    Welsh, L. B.

    1985-04-01

    The program discussed in this report is a two-year two-phase joint UOP-University of Illinois study of the application of improved high resolution solid state nuclear magnetic resonance (NMR) techniques to the characterization of zeolite catalysts. During the first phase of this program very pure, and in some cases isotopically enriched faujasites will be prepared and studied by magic angle sample spinning NMR (MASS NMR) and variable engine sample spinning NMR (VASS NMR) on 500 and 360 MHz (proton frequency) NMR spectrometers. The NMR techniques that will be emphasized are the measurement and analysis of the (17)O NMR properties, (27)Al NMR intensity quantitation, and (27)Al and (29)Si NMR relaxation rates. During the second phase of this program these NMR techniques will be used to study the effects of impurity concentration, dealumination treatments and cation exchange on the NMR properties of faujasites. The initial emphasis of this program during Phase I is on the preparation and measurement of the NMR properties of (17)O enriched Na-Y faujasties.

  1. Catalytic pyrolysis using UZM-39 aluminosilicate zeolite

    Energy Technology Data Exchange (ETDEWEB)

    Nicholas, Christopher P; Boldingh, Edwin P

    2014-10-07

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

  2. Sorption of melanoidin onto surfactant modified zeolite

    Directory of Open Access Journals (Sweden)

    Onyango Maurice S.

    2011-01-01

    Full Text Available Melanoidin is responsible for the dark brown colour of distillery wastewater. Discharge of coloured wastewater has a major environmental impact on the biota of the receiving water body. Consequently, this study explores the removal of melanodin from aqueous solution. The equilibrium, kinetics and thermodynamics of melanoidin sorption are studied by varying initial solution pH, initial concentration, adsorbent dose and temperature. Kinetically, the melanoidin removal from solution by a surfactant modified zeolite is rapid and the amount adsorbed is dependent on pH, initial concentration, adsorbent dose and temperature. The equilibrium sorption data are fitted to the Freundlich and Langmuir models while the sorption, kinetics is described by the Ho pseudo-second order and Elovich models. The thermodynamic analysis indicates that the sorption is spontaneous and endothermic in nature. The FTIR spectra analyses show no new peaks or shift in peaks after sorption indicating that the melanoidin sorption may have occurred by a physical process. The results from desorption studies showed that melanoidin eluted back easily to the solution using distilled water which corroborates the physical sorption mechanism.

  3. Bifunctional Nb/Ti-MCM-41 catalyst in oxidative acidic reaction of cyclohexene to diol

    International Nuclear Information System (INIS)

    Bifunctional oxidative and acidic catalyst was prepared by incorporating titanium ion (Ti4+) and niobic acid in meso porous molecular sieves MCM-41 structure. The catalyst is active both in oxidation, and acid-catalyzed reaction of olefin to diol. Nb/ Ti-MCM-41 catalyst was prepared by first synthesizing Ti-MCM-41 by hydrothermal method, followed by subsequent impregnation of niobic acid (Nb) into Ti-MCM-41 at various % wt Nb loading. The framework structure of Ti-MCM-41 collapsed after incorporation of Nb but the tetrahedral form of Ti4+ still maintained with octahedral Nb species. Both Bronsted and Lewis acid sites are present in all Nb/ Ti-MCM-41 samples. The formation of cyclohexanediol in the epoxidation of cyclohexene proved the bifunctional oxidative and acidic catalyst through the formation of cyclohexane oxide. The yield increased with the increase amount of the Bronsted acid sites provided by niobium species. (author)

  4. Sorption of Pu(IV) from nitric acid by bifunctional anion-exchange resins

    International Nuclear Information System (INIS)

    Anion exchange is attractive for separating plutonium because the Pu(IV) nitrate complex is very strongly sorbed and few other metal ions form competing anionic nitrate complexes. The major disadvantage of this process has been the unusually slow rate at which the Pu(IV) nitrate complex is sorbed by the resin. The paper summarizes the concept of bifunctional anion-exchange resins, proposed mechanism for Pu(IV) sorption, synthesis of the alkylating agent, calculation of Kd values from Pu(IV) sorption results, and conclusions from the study of Pu(IV) sorption from 7M nitric acid by macroporous anion-exchange resins including level of crosslinking, level of alkylation, length of spacer, and bifunctional vs. monofunctional anion-exchange resins

  5. Increasing round trip efficiency of hybrid Li-air battery with bifunctional catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Huang, K; Li, YF; Xing, YC

    2013-07-30

    Previously it was shown that Pt as cathode catalyst ha's a large overpotential during charge in rechargeable hybrid Li-air battery with sulfuric acid catholyte. This article demonstrates that a bifunctional catalyst composed of Pt and IrO2 supported on carbon nanotubes can address this problem. The specially designed and synthesized bifunctional catalyst showed significant overpotential reduction and achieved a round trip energy efficiency of 81% after 10 cycles, higher than many achieved in aprotic Li-O-2 batteries. The hybrid Li-air battery was discharged and recharged for 20 cycles at 0.2 mA/cm(2), showing a fairly stable cell performance. A specific capacity of 306 mAh/g and a specific energy of 1110 Wh/kg were obtained for the hybrid Li-air battery in terms of acid weight. (c) 2013 Elsevier Ltd. All rights reserved.

  6. Tethering metal ions to photocatalyst particulate surfaces by bifunctional molecular linkers for efficient hydrogen evolution

    KAUST Repository

    Yu, Weili

    2014-08-19

    A simple and versatile method for the preparation of photocatalyst particulates modified with effective cocatalysts is presented; the method involves the sequential soaking of photocatalyst particulates in solutions containing bifunctional organic linkers and metal ions. The modification of the particulate surfaces is a universal and reproducible method because the molecular linkers utilize strong covalent bonds, which in turn result in modified monolayer with a small but controlled quantity of metals. The photocatalysis results indicated that the CdS with likely photochemically reduced Pd and Ni, which were initially immobilized via ethanedithiol (EDT) as a linker, were highly efficient for photocatalytic hydrogen evolution from Na2S-Na2SO3-containing aqueous solutions. The method developed in this study opens a new synthesis route for the preparation of effective photocatalysts with various combinations of bifunctional linkers, metals, and photocatalyst particulate materials. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  7. Bifunctional metamaterials with simultaneous and independent manipulation of thermal and electric fields

    Science.gov (United States)

    Lan, Chuwen; Bi, Ke; Fu, Xiaojian; Li, Bo; Zhou, Ji

    2016-10-01

    Metamaterials offer a powerful way to manipulate a variety of physical fields ranging from wave fields (electromagnetic field, acoustic field, elastic wave, etc.), static fields (static magnetic field, static electric field) to diffusive fields (thermal field, diffusive mass). However, the relevant reports and studies are usually conducted on a single physical field or functionality. In this study, we proposed and experimentally demonstrated a bifunctional metamaterial which can manipulate thermal and electric fields simultaneously and independently. Specifically, a composite with independently controllable thermal and electric conductivity was introduced, on the basis of which a bifunctional device capable of shielding thermal flux and concentrating electric current simultaneously was designed, fabricated and characterized. This work provides an encouraging example of metamaterials transcending their natural limitations, which offers a promising future in building a broad platform for manipulation of multi-physics field.

  8. A bifunctional nonprecious metal catalyst for oxygen reduction and water oxidation.

    Science.gov (United States)

    Gorlin, Yelena; Jaramillo, Thomas F

    2010-10-01

    There is a growing interest in oxygen electrochemistry as conversions between O(2) and H(2)O play an important role in a variety of renewable energy technologies. The goal of this work is to develop active bifunctional catalyst materials for water oxidation and oxygen reduction. Drawing inspiration from a cubane-like CaMn(4)O(x), the biological catalyst found in the oxygen evolving center (OEC) in photosystem II, nanostructured manganese oxide surfaces were investigated for these reactions. Thin films of nanostructured manganese oxide were found to be active for both oxygen reduction and water oxidation, with similar overall oxygen electrode activity to the best known precious metal nanoparticle catalysts: platinum, ruthenium, and iridium. Physical and chemical characterization of the nanostructured Mn oxide bifunctional catalyst reveals an oxidation state of Mn(III), akin to one of the most commonly observed Mn oxidation states found in the OEC. PMID:20839797

  9. Improving stability and biocompatibility of alginate/chitosan microcapsule by fabricating bi-functional membrane.

    Science.gov (United States)

    Zheng, Guoshuang; Liu, Xiudong; Wang, Xiuli; Chen, Li; Xie, Hongguo; Wang, Feng; Zheng, Huizhen; Yu, Weiting; Ma, Xiaojun

    2014-05-01

    Cell encapsulation technology holds promise for the cell-based therapy. But poor mechanical strength and biocompatibility of microcapsule membrane are still obstacles for the clinical applications. A novel strategy is presented to prepare AC₁ C₂ A microcapsules with bi-functional membrane (that is, both desirable biocompatibility and membrane stability) by sequentially complexing chitosans with higher deacetylation degree (C₁) and lower deacetylation degree (C₂) on alginate (A) gel beads. Both in vitro and in vivo evaluation of AC₁C₂ A microcapsules demonstrate higher membrane stability and less cell adhesion, because the introduction of C₂ increases membrane strength and decreases surface roughness. Moreover, diffusion test of AC₁C₂ A microcapsules displays no inward permeation of IgG protein suggesting good immunoisolation function. The results demonstrate that AC₁C₂ A microcapsules with bi-functional membrane could be a promising candidate for microencapsulated cell implantation with cost effective usage of naturally biocompatible polysaccharides.

  10. Long n-alkanes isomerization by medium pore zeolites with pore mouth and key lock mechanisms; Isomerisation des paraffines longues par des zeolithes a pores moyens selon les mecanismes ouverture de pore et cle serrure

    Energy Technology Data Exchange (ETDEWEB)

    Claude, M.

    1999-10-01

    Skeletal isomerization of long n-alkanes is practiced to improve cold flow properties of diesel and lubricant fractions. In this work, model long n-alkanes (n-C{sub 10} - n-C{sub 24}) were hydro-isomerized in a fixed bed down flow vapour phase reactor loaded with bifunctional Pt/H-ZSM-22 zeolite catalyst. The skeletal isomers were analysed and identified with GC/MS. High isomer yields were obtained. The distribution of positional mono-methyl-branched isomers obtained from n-C{sub 12} to n-C{sub 24} are typically bimodal. This is explained by adsorption and reaction of the alkanes in pore mouths and locks on the external surface of the zeolite crystals. The pore mouth mode favours branching at C{sub 2} and C{sub 3}. The 'key lock' type proceeds by penetration of the two ends of the hydrocarbon chain into a different pore opening and favours more central mono-branching of the chain. The contribution of the key lock mode increases with increasing chain length and with the reaction temperature. The preferentially formed dimethyl-branched isomers have a separation between branchings of three up to fourteen carbon atoms. The formation of the second methyl-branching occurs preferentially from a centrally branched mono-methyl-branched isomer, so that the second branching is generated always more toward the end of the chain. Owing to the differences in adsorption entropy among the locks, at higher temperatures the largest lock is preferred and the distance between the two branching along the carbon chain in the preferred isomers is biggest. Thus the work resulted in the formulation of structure-selectivity relationships. n-C{sub 18} was hydro-isomerized on other zeolites. The nature and distribution of the isomers obtained suggest that the tubular 10-ring zeolites ZSM-23, ZSM-35 and SAPO-11 also operate according to pore mouth and key lock concepts. Zeolites with 12-rings show typical product patterns for catalysis in absence of steric hindrance. (author)

  11. PERVAPORATION OF ETHANOL/WATER MIXTURES WITH HIGH FLUX BY ZEOLITE-FILLED PDMS/PVDF COMPOSITE MEMBRANES

    Institute of Scientific and Technical Information of China (English)

    李继定

    2009-01-01

    Thin-film zeolite-filled silicone/PVDF composite membranes were fabricated by incorporating zeolite particles into PDMS(poly(dimethylsiloxane)) membranes.The morphology of zeolite particles and zeolite filled silicone composite membranes were characterized by SEM.The zeolite-filled PDMS/PVDF composite membranes were applied for the pervaporation of ethanol/water mixtures and showed higher flux compared with that reported in literatures.The effect of zeolite loading and Si/Al ratio of zeolite particles on...

  12. Coke formation over zeolites and CeO2-zeolites and its influence on selective catalytic reduction of NOx

    International Nuclear Information System (INIS)

    Selective catalytic reduction, various possible reasons of coke formation, and temperature programmed oxidation of coke deposits are studied over HFER, HZSM-5 and 15|wt% CeO2-H zeolites. The materials are characterised by TGA, NH3-TPD and in-situ FTIR measurements. HFER based catalysts showed superior NOx (NO+NO2) conversion in SCR with propene compared with HZSM-5 based catalysts. It is found that NO2 (formed by the oxidation of NO) is not the only important intermediate in determining the extent of NOx conversion. The topology and acidity of the zeolites play an important role in selective activation of propene and its reaction with NO2. Over HZSM-5 based catalysts the rate of deposition of carbonaceous compounds is higher than the rate of reaction of activated propene with NO2, leading to unselective reduction to NO. The nature and the amount of the carbonaceous products deposited over the zeolites are found to depend on the acidity, structure of the zeolite and reaction conditions (inert or oxidative atmosphere). Coke deposition rate is enhanced in the presence of oxygen and most of the coke is retained by the zeolite which is detrimental for NOx reduction. in-situ IR studies show that hydrocarbon deposits are more heterogeneous and carbon rich over HZSM-5 compared with HFER. TPO studies show that only a negligible fraction of hydrocarbon deposits are active in NOx conversion

  13. Bifunctional silica nanoparticles for the exploration of biofilms of Pseudomonas aeruginosa

    OpenAIRE

    Mauline, Léïla; Gressier, Marie; Roques, Christine; Hammer, Peter,; Ribeiro, Sidney J. L.; Caiut, José Maurício A.; Menu, Marie-Joëlle

    2013-01-01

    Luminescent silica nanoparticles are frequently employed for biotechnology applications mainly because of their easy functionalization, photo-stability, and biocompatibility. Bifunctional silica nanoparticles (BSNPs) are described here as new efficient tools for investigating complex biological systems such as biofilms. Photoluminescence is brought about by the incorporation of a silylated ruthenium (II) complex. The surface properties of the silica particles were designed by reaction with am...

  14. L-Proline Derived Bifunctional Organocatalysts: Enantioselective Michael Addition of Dithiomalonates to trans-β-Nitroolefins.

    Science.gov (United States)

    Jin, Hui; Kim, Seung Tae; Hwang, Geum-Sook; Ryu, Do Hyun

    2016-04-15

    A series of novel L-proline derived tertiary amine bifunctional organocatalysts 9 are reported, which were applied to the asymmetric Michael addition of dithiomalonates 2 to trans-β-nitroolefins 1. The reaction proceeded in high yields (up to 99%) with high enantioselectivities (up to 97% ee). The synthetic utility of this methodology was demonstrated in the short synthesis of (R)-phenibut in high yield. PMID:26989804

  15. A new bifunctional hybrid nanostructure as an active platform for photothermal therapy and MR imaging

    OpenAIRE

    Mona Khafaji; Manouchehr Vossoughi; M. Reza Hormozi-Nezhad; Rassoul Dinarvand; Felix Börrnert; Azam Irajizad

    2016-01-01

    As a bi-functional cancer treatment agent, a new hybrid nanostructure is presented which can be used for photothermal therapy by exposure to one order of magnitude lower laser powers compared to similar nanostructures in addition to substantial enhancment in magnetic resonance imaging (MRI) contrast. This gold-iron oxide hybrid nanostructure (GIHN) is synthesized by a cost-effective and high yield water-based approach. The GIHN is sheilded by PEG. Therefore, it shows high hemo and biocompatib...

  16. Bifunctional catalysts for the direct production of liquid fuels from syngas

    OpenAIRE

    Sartipi, S.

    2014-01-01

    Design and development of catalyst formulations that maximize the direct production of liquid fuels by combining Fischer-Tropsch synthesis (FTS), hydrocarbon cracking, and isomerization into one single catalyst particle (bifunctional FTS catalyst) have been investigated in this thesis. To achieve this aim, a second functionality (other than FTS) has to be added to the catalyst formulation to break the limitation of a classical Anderson-Schulz-Flory (ASF) distribution of FTS products. Since up...

  17. GST-TAT-SOD: Cell Permeable Bifunctional Antioxidant Enzyme—A Potential Selective Radioprotector

    OpenAIRE

    Jianru Pan; Huocong He; Ying Su; Guangjin Zheng; Junxin Wu; Shutao Liu; Pingfan Rao

    2016-01-01

    Superoxide dismutase (SOD) fusion of TAT was proved to be radioprotective in our previous work. On that basis, a bifunctional recombinant protein which was the fusion of glutathione S-transferase (GST), SOD, and TAT was constructed and named GST-TAT-SOD. Herein we report the investigation of the cytotoxicity, cell-penetrating activity, and in vitro radioprotective effect of GST-TAT-SOD compared with wild SOD, single-function recombinant protein SOD-TAT, and amifostine. We demonstrated that wi...

  18. Synthesis of acid-base bifunctional mesoporous materials by oxidation and thermolysis

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Xiaofang [College of Chemistry, Jilin University, Jiefang Road 2519, Changchun 130023 (China); Zou, Yongcun [State Key Laboratory of Inoranic Synthesis and Preparative Chemistryg, College of Chemistry, Jilin University, Changchun 130012 (China); Wu, Shujie; Liu, Heng [College of Chemistry, Jilin University, Jiefang Road 2519, Changchun 130023 (China); Guan, Jingqi, E-mail: guanjq@jlu.edu.cn [College of Chemistry, Jilin University, Jiefang Road 2519, Changchun 130023 (China); Kan, Qiubin, E-mail: qkan@jlu.edu.cn [College of Chemistry, Jilin University, Jiefang Road 2519, Changchun 130023 (China)

    2011-06-15

    Graphical abstract: A novel and efficient method has been developed for the synthesis of acid-base bifunctional catalyst. The obtained sample of SO{sub 3}H-MCM-41-NH{sub 2} containing amine and sulfonic acids exhibits excellent catalytic activity in aldol condensation reaction. Research highlights: {yields} Synthesize acid-base bifunctional mesoporous materials SO{sub 3}H-MCM-41-NH{sub 2}. {yields} Oxidation and then thermolysis to generate acidic site and basic site. {yields} Exhibit good catalytic performance in aldol condensation reaction between acetone and various aldehydes. -- Abstract: A novel and efficient method has been developed for the synthesis of acid-base bifunctional catalyst SO{sub 3}H-MCM-41-NH{sub 2}. This method was achieved by co-condensation of tetraethylorthosilicate (TEOS), 3-mercaptopropyltrimethoxysilane (MPTMS) and (3-triethoxysilylpropyl) carbamicacid-1-methylcyclohexylester (3TAME) in the presence of cetyltrimethylammonium bromide (CTAB), followed by oxidation and then thermolysis to generate acidic site and basic site. X-ray diffraction (XRD) and transmission electron micrographs (TEM) show that the resultant materials keep mesoporous structure. Thermogravimetric analysis (TGA), X-ray photoelectron spectra (XPS), back titration, solid-state {sup 13}C CP/MAS NMR and solid-state {sup 29}Si MAS NMR confirm that the organosiloxanes were condensed as a part of the silica framework. The bifunctional sample (SO{sub 3}H-MCM-41-NH{sub 2}) containing amine and sulfonic acids exhibits excellent acid-basic properties, which make it possess high activity in aldol condensation reaction between acetone and various aldehydes.

  19. Phase-Transfer Catalysis via a Proton Sponge: A Bifunctional Role for Biscyclopropenimine.

    Science.gov (United States)

    Belding, Lee; Stoyanov, Peter; Dudding, Travis

    2016-01-15

    The use of a bis(diisopropylamino)cyclopropenimine-substituted bis-protonated proton sponge as a bifunctional phase-transfer catalyst is reported. Experimental studies and DFT calculations suggest it operates simultaneously as a hydrogen bond donor and a phase-transfer catalyst, facilitating the movement of charged intermediates from the interface to the organic phase via favorable partitioning of hydrophilic/hydrophobic surface areas, resulting in high catalytic activity. PMID:26649566

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

    Indian Academy of Sciences (India)

    V K Sharma; Mala N Rao; Siddharth Gautam; A K Tripathi; V S Kamble; S L Chaplot; R Mukhopadhyay

    2008-11-01

    We report here the quasielastic neutron scattering (QENS) studies on the dynamics of propylene inside Na-Y zeolite using triple axis spectrometer (TAS) at Dhruva reactor, Trombay. Molecular dynamics (MD) simulations performed on the system had shown that the rotational motion involves energy larger than that involved in the translational motion. Therefore, rotational motion was not observed in our earlier QENS studies on propylene adsorbed Na-Y zeolite using a higher resolution spectrometer at Dhruva. Analysis of the TAS spectra revealed that the quasielastic broadening observed in propylene-loaded zeolite spectra is due to the rotational motion of the propylene molecules. This is consistent with our simulation result. Further, the rotational motion is found to be isotropic. The rotational diffusion coefficient has been obtained.

  1. 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...... characterized by XRPD, SEM, TEM and N-2 physisorption measurements. For the zeolite materials it A as found that mesoporous MFI and MEL structured single crystals could indeed be crystallized from fluoride media using an improved carbon-templating approach. More importantly, it was found that mesoporous BEA......-type single crystals could be crystallized from fluoride media by a newly developed procedure presented here. Thus, we here present the only known route to mesoporous BEA-type single crystals, since crystallization of this framework structure from basic media is known to give only nanosized crystals...

  2. Dealumination treatment of zeolite for krypton gas adsorption

    Energy Technology Data Exchange (ETDEWEB)

    Shin, Jin Myeong; Shin, Seol Woo; Park, Jang Jin; Lee, Ho Hee; Yang, Myoung Seung [Korea Atomic Energy Research Institute, Taejon (Korea, Republic of)

    2005-07-01

    The concept of the direct use of spent fuel in CANDU reactors (DUPIC) is a dry processing technology to manufacture CANDU fuel from spent PWR fuel material. The heart of the DUPIC fuel cycle is the OREOX (Oxidation and Reduction of Oxide fuels) process. During this dry process, uranium from spent PWR fuel is oxidized and reduced to a fine powder, which forms the starting material for fabrication of DUPIC fuel pellets. During the OREOX process of DUPIC fuel fabrication, krypton is released as a noble fission gas. As fuel burnup proceeds, more fission products are formed. About 15 % of the fission products are inert gases such as xenon and krypton. The dealumination of zeolite is examined in this study in order to know that the structural changes in zeolite and the effect of krypton adsorption on zeolite.

  3. Formulation of cracking catalyst based on zeolite and natural clays

    Energy Technology Data Exchange (ETDEWEB)

    Aliev, R.R.; Lupina, M.I.

    1995-11-01

    Domestically manufactured cracking catalysts are based on a synthetic amorphous aluminosilicate matrix and Y zeolite. A multistage {open_quotes}gel{close_quotes} technology is used in manufacturing the catalysts. The process includes mixing solutions of sodium silicate and acidic aluminum sulfate, forming, syneresis, and activation of the beaded gel. In the manufacture of bead catalysts, the next steps in the process are washing, drying, and calcining; in the manufacture of microbead catalysts, the next steps are dispersion and formation of a hydrogel slurry, spray-drying, and calcining. The Y zeolite is either introduced into the alumina-silica sol in the stage of forming the beads, or introduced in the dispersion stage. With the aim of developing an active and selective cracking catalyst based on Y zeolite and natural clays, with improved physicomechanical properties, the authors carried out a series of studies, obtaining results that are set forth in the present article.

  4. Phenol Tert-Butylation Catalyzed by Zeolite H-Mordenite

    Institute of Scientific and Technical Information of China (English)

    HAN Sen; LI Zhenhua; ZHANG Kui

    2005-01-01

    Para-tert-butyl phenol (p-TBP) and 2,4-di-tert-butyl phenol (2,4-DTBP) are widely used for the preparation of antioxidants. Zeolite catalysts showed good performance for the synthesis of p-TBP and 2,4-DTBP. In this work, zeolite H-mordenite (HM) catalyst was prepared and the alkylation of phenol with tert-butyl alcohol over zeolite HM catalyst was investigated at different reaction conditions. It is found that increasing temperature enhances the selectivity to p-TBP and the optimum reaction temperature for phenol conversion is 438 K. Increasing flow rate decreases phenol conversion apparently while the selectivity to p-TBP has a little increase. The suitable tert-butyl alcohol/phenol molar ratio is 2. Lower alcohol/phenol molar ratios are beneficial to p-TBP while higher ones are helpful for producing 2,4-DTBP.

  5. Inelastic neutron scattering studies of water in natural zeolites

    International Nuclear Information System (INIS)

    Results on the motion of water molecules in six natural zeolites (natrolite, phillipsite, harmotome, heulandite, stilbite and chabazite) from incoherent inelastic neutron scattering are presented. The spectra for five zeolite samples exhibit broad maxima and few resolved peaks. Only for natrolite with water molecules tightly bound to the alumosilicate framework a spectrum with well-resolved peaks is observed. A detailed interpretation is attempted for the Ba-zeolite harmotome where data were recorded at various temperatures and different amount of water. - Differential scanning calorimetry gave a broad dehydration peak for chabazite (T=443 K) and a sharp single peak for natrolite (T=633 K), whereas three maxima (T=433, 523 and 673 K) were observed for harmotome. (orig.)

  6. Cerium uptake by zeolite A synthesized from natural clinoptilolite tuffs

    International Nuclear Information System (INIS)

    Natural clinoptilolite tuffs from the Semnan region in Iran was used for the synthesis of zeolite A. The tuffs and synthesized zeolites were characterized by XRD and XRF. The sorption behavior of the synthesized zeolite toward cerium was studied. Using the Lagergren's equation, the absorption constant was calculated. The measured distribution coefficient values (Kd) indicated that cerium uptake is higher in lower initial concentrations, higher temperature and higher pH values. Thermodynamic parameters of the exchange were calculated through construction of ion-exchange isotherms at three temperatures of 298, 323 and 343 K. The dynamic absorption of cerium was also studied by passing the solution through a column in the presence and absence of sodium ions. (author)

  7. Wet gringing of zeolite in stirred media mill

    Science.gov (United States)

    Mucsi, G.; Bohács, K.

    2016-04-01

    In the present study the results of systematic experimental series are presented with the specific goal of optimizing the zeolite nanoparticles' production using a wet stirred media mill. The diameter of the grinding media as well as the rotor velocity were varied in the experiments. Particle size distribution and "outer" specific surface area of the ground samples were measured by a laser particle size analyser. Additionally, BET, XRD and FT-IR analyses were performed for the characterization of the "total" specific surface area as well as the crystalline and material structure, respectively. Based on the results of the laboratory experiments it was found that wet stirred media milling provided significant reductions in the particle size of zeolite. Furthermore, the crystallinity of the samples also decreased, so not only the physical but the mineralogical characteristics of zeolite can be controlled by stirred media milling.

  8. 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.

  9. Zeolites and their utilizations in radioactive waste treatment

    International Nuclear Information System (INIS)

    Applications of natural zeolites make use of one or more of the following properties: (I) cation exchange, (II) adsorption and related molecular sieving, (III) catalytic, (IV) dehydration and rehydration, and (v) biological reactivity. Extrinsic properties of the rock (e.g., siliceous composition, color, porosity, attrition resistance, and bulk density) are also important in many applications. Thus, the ideal zeolitic tuff for both cation exchange and adsorption applications should be mechanically strong to resist abrasion and disintegration, highly porous to allow solutions and gases to diffuse readily in and out of the rock, and soft enough to be easily crushed. In the present work, the removal of cesium+, strontium-2 and UO2+2 from nuclear wastewaters were investigated under static and dynamic conditions using two Iranian natural Clinoptilolite, their modified forms as well as a relevant synthetic zeolite-P

  10. Mechanochemical approach for selective deactivation of external surface acidity of ZSM-5 zeolite catalyst.

    Science.gov (United States)

    Inagaki, Satoshi; Sato, Koki; Hayashi, Shunsuke; Tatami, Junichi; Kubota, Yoshihiro; Wakihara, Toru

    2015-03-01

    The acid sites associated with the external surface of zeolite particles are responsible for undesirable consecutive reactions, such as isomerization, alkylation, and oligomerization, resulting in a lower selectivity to a target product; therefore, the selective modification (deactivation) of the external surface of zeolite particles has been an important issue in zeolite science. Here, a new method for surface deactivation of zeolite catalyst was tested via a mechanochemical approach using powder composer. Postsynthetic mechanochemical treatment of ZSM-5 zeolite causes a selective deactivation of catalytically active sites existing only on the external surface, as a potentially useful catalyst for highly selective production of p-xylene. PMID:25654542

  11. Solidification of radioactive resins by using ASC cement and zeolite blends

    International Nuclear Information System (INIS)

    The solidification of simulated spent radioactive resins is investigated using ASC cement and zeolite blends. The compress strengths and leaching rates of the solidified objects with various added amount of zeolite were compared. The microstructures of the matrix were investigated by SEM in order to explain the effect of zeolite amount on the performance of solidified object. The experimental results indicate that the addition of zeolite causes a structural shift of solidified object from pinhead crystal to layer crystal, and addition of 10%-20% zeolite can decrease the leaching rate of Cs greatly, however, it had little influence on the compress strengths. (authors)

  12. Synthesis of zeolites using fly ash and their application in removing heavy metals from waters

    Institute of Scientific and Technical Information of China (English)

    WANG; Yanxin(王焰新); GUO; Yonglong(郭永龙); YANG; Zhihua(杨志华); CAI; Hesheng(蔡鹤生); Xavier; Querol

    2003-01-01

    Three types of zeolite (NaP1 zeolite, analcime and chabazite) were hydrothermally synthesized by reacting fly ash with NaOH solution. The maximum conversion rate from fly ash to single zeolite is about 40%-75%, and the total conversion rate 60%-80%. The synthesis experimental results indicate that factors including vortex, viscosity, temperature, reaction time, and NaOH concentration in the reaction system strongly affect the type and conversion rate of zeolites. The batch experiments of removing Cu2+, Pb2+ and Cd2+ from wastewaters show that the adsorption capacity of zeolites synthesized is higher than that of fly ash.

  13. The use of clinoptilolite olite and synthetic zeolites for removal of petroleum subtances

    OpenAIRE

    Bandura, L.; Panek, R; Franus, W.

    2014-01-01

    In the present paper the sorption of petroleum substances such as diesel fuels on zeolite beds was investigated. A natural occurring zeolite clinoptilolite, and mixtures of clinoptilolite and synthetic zeolites Na-P1 and Na-X type, in the ratio 3:1, were used in this study. Natural zeolite acquired from the mine tuffs in Sokyrnytsya (Ukraine). In order to obtain synthetic zeolites, F-class fly ash (Kozienice Power Plant, Poland) with sodium hydroxide was used and later it under...

  14. Fabrication of Macro-porous β-zeolite by Using Colloidal Polystyrene Spheres as a Template

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    A β-zeolite/polystyrene composite material was synthesized by co-deposition of mono-disperse polystyrene spheres and nano β-zeolite particles in aqueous suspension on a vertical substrate. Macro-porous β-zeolite was obtained after the polystyrene template was removed by calcination. The micro/macro-pore structure of the prepared β-zeolite was highly ordered. In comparison with other assembly methods, the co-deposition method could obtain a highly ordered macro-porous material with relatively large zeolite filling particles, and therefore the co-deposition of particles with different size is a promising method for the fabrication of macro-porous materials.

  15. Collagen/chitosan based two-compartment and bi-functional dermal scaffolds for skin regeneration

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Feng [Department of Plastic Surgery and Burns, Shenzhen Second People' s Hospital, Shenzhen 518035 (China); Wang, Mingbo [Key Laboratory of Biomedical Materials and Implants, Research Institute of Tsinghua University in Shenzhen, Shenzhen 518057 (China); She, Zhending [Key Laboratory of Biomedical Materials and Implants, Research Institute of Tsinghua University in Shenzhen, Shenzhen 518057 (China); Shenzhen Lando Biomaterials Co., Ltd., Shenzhen 518057 (China); Fan, Kunwu; Xu, Cheng [Department of Plastic Surgery and Burns, Shenzhen Second People' s Hospital, Shenzhen 518035 (China); Chu, Bin; Chen, Changsheng [Key Laboratory of Biomedical Materials and Implants, Research Institute of Tsinghua University in Shenzhen, Shenzhen 518057 (China); Shi, Shengjun, E-mail: shengjunshi@yahoo.com [The Burns Department of Zhujiang Hospital, Southern Medical University, Guangzhou 510280 (China); Tan, Rongwei, E-mail: tanrw@landobiom.com [Key Laboratory of Biomedical Materials and Implants, Research Institute of Tsinghua University in Shenzhen, Shenzhen 518057 (China); Shenzhen Lando Biomaterials Co., Ltd., Shenzhen 518057 (China)

    2015-07-01

    Inspired from the sophisticated bilayer structures of natural dermis, here, we reported collagen/chitosan based two-compartment and bi-functional dermal scaffolds. Two functions refer to mediating rapid angiogenesis based on recombinant human vascular endothelial growth factor (rhVEGF) and antibacterial from gentamicin, which were encapsulated in PLGA microspheres. The gentamicin and rhVEGF encapsulated PLGA microspheres were further combined with collagen/chitosan mixtures in low (lower layer) and high (upper layer) concentrations, and molded to generate the two-compartment and bi-functional scaffolds. Based on morphology and pore structure analyses, it was found that the scaffold has a distinct double layered porous and connective structure with PLGA microspheres encapsulated. Statistical analysis indicated that the pores in the upper layer and in the lower layer have great variations in diameter, indicative of a two-compartment structure. The release profiles of gentamicin and rhVEGF exceeded 28 and 49 days, respectively. In vitro culture of mouse fibroblasts showed that the scaffold can facilitate cell adhesion and proliferation. Moreover, the scaffold can obviously inhibit proliferation of Staphylococcus aureus and Serratia marcescens, exhibiting its unique antibacterial effect. The two-compartment and bi-functional dermal scaffolds can be a promising candidate for skin regeneration. - Highlights: • The dermal scaffold is inspired from the bilayer structures of natural dermis. • The dermal scaffold has two-compartment structures. • The dermal scaffold containing VEGF and gentamicin encapsulated PLGA microspheres • The dermal scaffold can facilitate cell adhesion and proliferation.

  16. A New Synthesis of TE2A-a Potential Bifunctional Chelator for {sup 64}Cu

    Energy Technology Data Exchange (ETDEWEB)

    Pandya, Darpan N.; Kwak, Won Jung; Park, Jeong Chan; Gawande, Manoj B.; Yoo, Jeong Soo [Kyungpook National University, Daegu (Korea, Republic of); Kim, Jung Young; An, Gwang Il [Molecular Imaging Research Center, Seoul (Korea, Republic of); Ryu, Eun Kyoung [Korea Basic Science Institute, Chungbuk (Korea, Republic of)

    2010-09-15

    The development of a new bifunctional chelator, which holds radio metals strongly in living systems, is a prerequisite for the successful application of disease-specific biomolecules to medical diagnosis and therapy. Recently, TE2A was reported to make kinetically more stable Cu({Pi}) complexes than TETA. Herein, we report a new synthetic route to TE2A and explore its potential as a bifunctional chelator. TE2A was synthesized using the regioselective alkylation of benzyl bromoacetate and successive de protection of the methylene bridge and benzyl group. Salt-free TE2A was radiolabeled with {sup 64}Cu and micro PET imaging was performed to follow the clearance pattern of the {sup 64}Cu-TE2A complex. TE2A was conjugated with cyclic RGD peptide and the TE2A-c(RGDyK) conjugate was radiolabeled with {sup 64}Cu. TE2A was prepared in salt-free form cyclam in an overall yield of 74%. The micro PET images showed that {sup 64}Cu-TE2A is excreted rapidly from the body by the kidney and liver. TE2A was successfully conjugated with c(RGDyK) peptide through on carboxylate group and the TE2A-c(RGDyK) conjugate was radiolabeled with {sup 64}Cu in 94% yield within 30 min. TE2A can be used by itself as a bifunctional chelator without any further structural modification.

  17. Bifunctional Catalysts for Upgrading of Biomass-Derived Oxygenates: A Review

    Energy Technology Data Exchange (ETDEWEB)

    Robinson, Allison M.; Hensley, Jesse E.; Medlin, J. Will

    2016-08-05

    Deoxygenation is an important reaction in the conversion of biomass-derived oxygenates to fuels and chemicals. A key route for biomass refining involves the production of pyrolysis oil through rapid heating of the raw biomass feedstock. Pyrolysis oil as produced is highly oxygenated, so the feasibility of this approach depends in large part on the ability to selectively deoxygenate pyrolysis oil components to create a stream of high-value finished products. Identification of catalytic materials that are active and selective for deoxygenation of pyrolysis oil components has therefore represented a major research area. One catalyst is rarely capable of performing the different types of elementary reaction steps required to deoxygenate biomass-derived compounds. For this reason, considerable attention has been placed on bifunctional catalysts, where two different active materials are used to provide catalytic sites for diverse reaction steps. Here, we review recent trends in the development of catalysts, with a focus on catalysts for which a bifunctional effect has been proposed. We summarize recent studies of hydrodeoxygenation (HDO) of pyrolysis oil and model compounds for a range of materials, including supported metal and bimetallic catalysts as well as transition-metal oxides, sulfides, carbides, nitrides, and phosphides. Particular emphasis is placed on how catalyst structure can be related to performance via molecular-level mechanisms. These studies demonstrate the importance of catalyst bifunctionality, with each class of materials requiring hydrogenation and C-O scission sites to perform HDO at reasonable rates.

  18. Comparison of Dynamical Behaviors Between Monofunctional and Bifunctional Two-Component Signaling Modules

    Science.gov (United States)

    Yang, Xiyan; Wu, Yahao; Yuan, Zhanjiang

    2015-06-01

    Two-component signaling modules exist extensively in bacteria and microbes. These modules can be, based on their distinct network structures, divided into two types: the monofunctional system (denoted by MFS) where the sensor kinase (SK) modulates only phosphorylation of the response regulator (RR), and the bifunctional system (denoted by BFS) where the SK catalyzes both phosphorylation and dephosphorylation of the RR. Here, we analyze dynamical behaviors of these two systems based on stability theory, focusing on differences between them. The analysis of the deterministic behavior indicates that there is no difference between the two modules, that is, each system has the unique stable steady state. However, there are significant differences in stochastic behavior between them. Specifically, if the mean phosphorylated SK level is kept the same for the two modules, then the variance and the Fano factor for the phosphorylated RR in the BFS are always no less than those in the MFS, indicating that bifunctionality always enhances fluctuations. The correlation between the phosphorylated SK and the phosphorylated RR in the BFS is always positive mainly due to competition between system components, but this correlation in the MFS may be positive, almost zero, or negative, depending on the ratio between two rate constants. Our overall analysis indicates that differences between dynamical behaviors of monofunctional and bifunctional signaling modules are mainly in the stochastic rather than deterministic aspect.

  19. Bifunctional Perovskite Oxide Catalysts for Oxygen Reduction and Evolution in Alkaline Media.

    Science.gov (United States)

    Gupta, Shiva; Kellogg, William; Xu, Hui; Liu, Xien; Cho, Jaephil; Wu, Gang

    2016-01-01

    Oxygen electrocatalysis, namely of the oxygen reduction reaction (ORR) and the oxygen evolution reaction (OER), governs the performance of numerous electrochemical energy systems such as reversible fuel cells, metal-air batteries, and water electrolyzers. However, the sluggish kinetics of these two reactions and their dependency on expensive noble metal catalysts (e.g, Pt or Ir) prohibit the sustainable commercialization of these highly innovative and in-demand technologies. Bifunctional perovskite oxides have emerged as a new class of highly efficient non-precious metal catalysts (NPMC) for oxygen electrocatalysis in alkaline media. In this review, we discuss the state-of-the-art understanding of bifunctional properties of perovskites with regards to their OER/ORR activity in alkaline media and review the associated reaction mechanisms on the oxides surface and the related activity descriptors developed in the recent literature. We also summarize the present strategies to modify their electronic structure and to further improve their performance for the ORR/OER through highlighting the new concepts relating to the role of surface redox chemistry and oxygen deficiency of perovskite oxides for the ORR/OER activity. In addition, we provide a brief account of recently developed advanced perovskite-nanocarbon hybrid bifunctional catalysts with much improved performances. PMID:26247625

  20. Regeneration of clinoptilolite zeolite used for the ammonium removal

    International Nuclear Information System (INIS)

    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 (Mg2+) and calcium (Ca2+) 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)

    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. Sorption of Lithium on Bentonite, Kaolin and Zeolite

    Directory of Open Access Journals (Sweden)

    Mandy Hoyer

    2015-04-01

    Full Text Available Li sorption was studied on natural bentonite, kaolin and zeolite in batch experiments at variable Li and Na concentrations (0, 1.5, 15, 150, 750 mM LiCl and 0.01, 0.1, 1, 3, 5 M NaCl. The solid-to-solution ratio was 1:4 and pH ranged from 2 to 10. Maximum Li sorption was determined at 0.01 M NaCl and 750 mM LiCl concentration in solution. It was 3800 ± 380 ppm, 1300 ± 130 ppm and 3900 ± 390 ppm on bentonite, kaolin and zeolite, respectively, which is in the average to upper range typical for clay minerals. Under these conditions, kaolin was saturated with Li, whereas Li in bentonite and zeolite occupied only about 55%–79% and 9%–26% of the typical cation exchange capacity (CEC of smectites and zeolites, respectively. This is explained by differences in the way Li is bound in the materials studied. Li sorption on bentonite was independent of pH due to strong pH buffering. Above pH 5, kaolin was transformed to gibbsite, which completely changed its Li sorption capabilities. Extremely low as well as extremely high pH destabilized the crystal lattice of zeolite. All in all it was shown that, under the studied conditions, Li sorption on the studied materials occurs in detectable quantities. So, clay minerals and zeolites can act as a sink for Li if Li concentrations in solution are sufficiently high.

  3. Copper removal using bio-inspired polydopamine coated natural zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Yang; Shapter, Joseph G. [Flinders Centre for Nanoscale Science and Technology, School of Chemical and Physical Sciences, Flinders University, Sturt Road, Bedford Park, Adelaide 5042, SA (Australia); Popelka-Filcoff, Rachel [School of Chemical and Physical Sciences, Flinders University, Sturt Road, Bedford Park, Adelaide 5042, SA (Australia); Bennett, John W. [Centre for Nuclear Applications, Australian Nuclear Science and Technology Organisation, Lucas Heights 2234, NSW (Australia); Ellis, Amanda V., E-mail: Amanda.Ellis@flinders.edu.au [Flinders Centre for Nanoscale Science and Technology, School of Chemical and Physical Sciences, Flinders University, Sturt Road, Bedford Park, Adelaide 5042, SA (Australia)

    2014-05-01

    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{sup −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{sup −1} for pristine natural zeolite and 28.58 mg g{sup −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.

  4. 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.

  5. Deuteration of piperylene on zeolite NaY

    Energy Technology Data Exchange (ETDEWEB)

    Kharlamov, V.V.; Kadentsev, V.I.; Kharatishvili, N.G.; Minachev, Kh.M.

    1982-04-20

    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/sub 2/ isotope, and an average number of deuterium atoms in the molecules equal to 2.25-2.36.

  6. Exploring Mass Transfer in Mesoporous Zeolites by NMR Diffusometry

    Directory of Open Access Journals (Sweden)

    Ryong Ryoo

    2012-04-01

    Full Text Available With the advent of mesoporous zeolites, the exploration of their transport properties has become a task of primary importance for the auspicious application of such materials in separation technology and heterogeneous catalysis. After reviewing the potential of the pulsed field gradient method of NMR (PFG NMR for this purpose in general, in a case study using a specially prepared mesoporous zeolite NaCaA as a host system and propane as a guest molecule, examples of the attainable information are provided.

  7. Adsorption of cobalt on some natural zeolites occuring in CSFR

    International Nuclear Information System (INIS)

    The subject of this paper was to study Co2+-ion removal from aqueous solutions by means of natural mordenite and clinoptilolite. The mentioned zeolites were of Slovak origin (CSFR). The static and dynamic equilibrium adsorption of Co2+-ions by zeolites, the influence of pH, quality and quantity of interfering ions on adsorbate/adsorbent system were investigated. The influence of flow rate, activation and initial concentration on the shape of the breakthrough curve was examined in dynamic regime. Mathematical expression was found for the breakthrough curve description. (author) 4 refs.; 6 figs.; 3 tabs

  8. Synthesis of high ion exchange zeolites from coal fly ash

    OpenAIRE

    Ayora, Carlos; Querol, Xavier; Moreno, N.; Alastuey, Andrés; Juan Mainar, Roberto; Andrés Gimeno, José Manuel; López Soler, Ángel; Medinaceli, Alejandro; Valero, Antonio

    2007-01-01

    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 m3 reactor of Clariant SA (Barcelona, Spain). The results allowed obtaining 1.1 and 2.2 tonnes of zeolitic material with 40 an...

  9. Zeolites replacing plant fossils in the Denver formation, Lakewood, Colorado.

    Science.gov (United States)

    Modreski, P.J.; Verbeek, E.R.; Grout, M.A.

    1984-01-01

    Well-developed crystals of heulandite and stilbite, within fossil wood, occur in sedimentary rocks in Lakewood, Jefferson County. The rocks belong to the Denver formation, a locally fossiliferous deposit of fluvial claystone, siltstone, sandstone and conglomerate, containing some volcanic mudflows (andesitic) of late Cretaceous to Palaeocene age. Altered volcanic glass released Na and Ca into the ground-water and subsequently zeolites were crystallized in the open spaces between grains and within fossil plant structures. Minor pyrite, quartz (jasper), calcite and apatite also occur as replacements of fossil wood. Similar zeolite occurrences in other areas are reviewed.-R.S.M.

  10. 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.

  11. 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.

  12. SINTESIS ZEOLIT DARI ABU DASAR BATUBARADAN APLIKASINYA SEBAGAI ADSORBEN LOGAM MERKURI (II

    Directory of Open Access Journals (Sweden)

    Ma’rifat

    2014-05-01

    Full Text Available Telah dilakukan sintesis zeolit dari abu dasar batubara dan aplikasinya sebagai adsorbenuntuk logam merkuri (II. Zeolit disintesis dengan metode alkali hidrotermal dan dikarakterisasi menggunakan Spektrofotometer FTIR dan Difraktometer Sinar-X (XRD. Kajian adsorpsi zeolit terhadap logam merkuri (II dilakukan dengan variasi pH,waktu kontak dan konsentrasi merkuri. Karakterisasi FTIR menunjukkan bahwa zeolit telah terbentuk dengan serapan pspesifik pada bilangan gelombang 457,31 cm-1.Hasil karakterisasi XRD menunjukkan bahwa zeolit hasil sintesis mempunyai struktur material zeolit faujasit yang ditunjukkan dengan difraksi utama pada 6,29°; 26,89°; dan 31,19°. Adsorpsi zeolit terhadap logam merkuri (II optimum terjadi pada pH 6, kesetimbangan adsorpsi cenderung mengikuti pola isoterm Freundlich dengan konstanta yaitu 1,803 x 10-4 mol/gram dan kinetika adsorpsi cenderung mengikuti persamaan pseudo orde dua dengan konstanta laju reaksi (k yaitu 8,687 x 10-3(g/mg min.

  13. Experimental adsorption equilibrium study and comparison of zeolite with water and ethanol for cooling systems

    Institute of Scientific and Technical Information of China (English)

    MAIGA Abdoulaye Siddeye; CHEN Guang-ming; WANG Qin

    2007-01-01

    Two adsorption refrigeration working pairs of zeolite with water and ethanol were studied and the parameters of Dubinin-Astakhov model were regressed using the experimental data of equilibrium. The coefficient of heterogeneity varied from 1.305 to 1.52 for the zeolite-water pair and from 1.73 to 2.128 for zeolite-ethanol pair. The maximum adsorption capacity varied from 0.315 to 0.34 for zeolite-water and 0.23 to 0.28 for zeolite-ethanol, respectively. The results showed that the zeolite-water pair is suitable for solar energy cooling not only because of the high latent heat of vaporization of water but also because of the better equilibrium performance. On the other hand, zeolite-ethanol gives a high adsorption capacity at high regeneration temperature, which means it can be used in heat engine systems like buses and cars.

  14. Systems including catalysts in porous zeolite materials within a reactor for use in synthesizing hydrocarbons

    Science.gov (United States)

    Rolllins, Harry W.; Petkovic, Lucia M.; Ginosar, Daniel M.

    2012-07-24

    Catalytic structures include a catalytic material disposed within a zeolite material. The catalytic material may be capable of catalyzing a formation of methanol from carbon monoxide and/or carbon dioxide, and the zeolite material may be capable of catalyzing a formation of hydrocarbon molecules from methanol. The catalytic material may include copper and zinc oxide. The zeolite material may include a first plurality of pores substantially defined by a crystal structure of the zeolite material and a second plurality of pores dispersed throughout the zeolite material. Systems for synthesizing hydrocarbon molecules also include catalytic structures. Methods for synthesizing hydrocarbon molecules include contacting hydrogen and at least one of carbon monoxide and carbon dioxide with such catalytic structures. Catalytic structures are fabricated by forming a zeolite material at least partially around a template structure, removing the template structure, and introducing a catalytic material into the zeolite material.

  15. Methods of using structures including catalytic materials disposed within porous zeolite materials to synthesize hydrocarbons

    Science.gov (United States)

    Rollins, Harry W.; Petkovic, Lucia M.; Ginosar, Daniel M.

    2011-02-01

    Catalytic structures include a catalytic material disposed within a zeolite material. The catalytic material may be capable of catalyzing a formation of methanol from carbon monoxide and/or carbon dioxide, and the zeolite material may be capable of catalyzing a formation of hydrocarbon molecules from methanol. The catalytic material may include copper and zinc oxide. The zeolite material may include a first plurality of pores substantially defined by a crystal structure of the zeolite material and a second plurality of pores dispersed throughout the zeolite material. Systems for synthesizing hydrocarbon molecules also include catalytic structures. Methods for synthesizing hydrocarbon molecules include contacting hydrogen and at least one of carbon monoxide and carbon dioxide with such catalytic structures. Catalytic structures are fabricated by forming a zeolite material at least partially around a template structure, removing the template structure, and introducing a catalytic material into the zeolite material.

  16. Fast formation of NaA zeolite membrane in the microwave field

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    NaA zeolite membrane was successfully synthesized on the porous α-Al2O3 support by microwave heating. The synthesis of NaA zeolite membrane in the microwave field only needs 15 min and the synthesis time is 10 times shorter than that by conventional heating. SEM characterization indicates that the zeolite crystals in the NaA zeolite membrane synthesized by microwave heating are uniform in size; the membrane thickness is about 4 μm and is thinner than that of the NaA zeolite membrane synthesized by conventional heating. Gas permeation studies indicate that the permeances of the NaA zeolite membrane synthesized by microwave heating are 3-4 times higher than those of the NaA zeolite membrane synthesized by conventional heating, while their permselectivities are comparable.

  17. 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.

  18. Evaluation of synthetic zeolite as engineering passive permeable reactive barrier

    International Nuclear Information System (INIS)

    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

  19. The growth of zeolites A, X and mordenite in space

    Science.gov (United States)

    Sacco, Albert, Jr.; Bac, N.; Coker, E. N.; Dixon, A. G.; Warzywoda, J.; Thompson, R. W.

    1994-01-01

    Zeolites are a class of crystalline aluminosilicate materials that form the backbone of the chemical process industry worldwide. They are used primarily as adsorbents and catalysts and support to a significant extent the positive balance of trade realized by the chemical industry in the United States (around $19 billion in 1991). The magnitude of their efforts can be appreciated when one realizes that since their introduction as 'cracking catalysts' in the early 1960's, they have saved the equivalent of 60 percent of the total oil production from Alaska's North Slope. Thus the performance of zeolite catalysts can have a profound effect on the U.S. economy. It is estimated that a 1 percent increase in yield of the gasoline fraction per barrel of oil would represent a savings of 22 million barrels of crude oil per year, representing a reduction of $400 million in the United States' balance of payments. Thus any activity that results in improvement in zeolite catalyst performance is of significant scientific and industrial interest. In addition, due to their 'stability,' uniformity, and, within limits, their 'engineerable' structures, zeolites are being tested as potential adsorbents to purify gases and liquids at the parts-per-billion levels needed in today's electronic, biomedical, and biotechnology industries and for the environment. Other exotic applications, such as host materials for quantum-confined semiconductor atomic arrays, are also being investigated. Because of the importance of this class of material, extensive efforts have been made to characterize their structures and to understand their nucleation and growth mechanisms, so as to be able to custom-make zeolites for a desired application. To date, both the nucleation mechanics and chemistry (such as what are the 'key' nutrients) are, as yet, still unknown for many, if not all, systems. The problem is compounded because there is usually a 'gel' phase present that is assumed to control the degree of

  20. 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.

  1. Preparation and characteristics of Fe3O4-YVO4:Eu3+ bifunctional magnetic-luminescent nanocomposites

    International Nuclear Information System (INIS)

    Graphical abstract: Highlights: → Bifunctional magnetic-luminescent nanocomposites with Fe3O4 nanoparticles as the core and YVO4:Eu3+ as the shell. → A cubic spinel structrue of Fe3O4 core and a tetragonal phase of YVO4 shell were obtained. → The nanocomposites displayed a strong red emission and superparamagnetic behavior at room temperature. - Abstract: A facile direct precipitation method has been developed for the synthesis of bifunctional magnetic-luminescent nanocomposites with Fe3O4 nanoparticles as the core and YVO4:Eu3+ as the shell. Transmission electron microscopy (TEM) images revealed that the obtained bifunctional nanocomposites had a core-shell structure and a spherical morphology. The average size was ∼150 nm, and the thickness of the shell was ∼15 nm. The X-ray diffraction (XRD) patterns showed that a cubic spinel structure of Fe3O4 core and a tetragonal phase of YVO4 shell were obtained. Fourier transform infrared (FT-IR) spectra confirmed that the YVO4:Eu3+ had been successfully deposited on the surface of Fe3O4 nanoparticles. Photoluminescence (PL) spectra indicated that the nanocomposites displayed a strong red characteristic emission of Eu3+. Magnetic measurements showed that the obtained bifunctional nanocomposites exhibited superparamagnetic behavior at room temperature. Therefore, the bifunctional nanocomposites are expected to develop many potential applications in biomedical fields.

  2. Betting Against Beta

    DEFF Research Database (Denmark)

    Frazzini, Andrea; Heje Pedersen, Lasse

    We present a model with leverage and margin constraints that vary across investors and time. We find evidence consistent with each of the model’s five central predictions: (1) Since constrained investors bid up high-beta assets, high beta is associated with low alpha, as we find empirically for U.......S. equities, 20 international equity markets, Treasury bonds, corporate bonds, and futures; (2) A betting-against-beta (BAB) factor, which is long leveraged low beta assets and short high-beta assets, produces significant positive risk-adjusted returns; (3) When funding constraints tighten, the return...... of the BAB factor is low; (4) Increased funding liquidity risk compresses betas toward one; (5) More constrained investors hold riskier assets....

  3. Betting against Beta

    DEFF Research Database (Denmark)

    Frazzini, Andrea; Heje Pedersen, Lasse

    2014-01-01

    We present a model with leverage and margin constraints that vary across investors and time. We find evidence consistent with each of the model's five central predictions: (1) Because constrained investors bid up high-beta assets, high beta is associated with low alpha, as we find empirically...... for US equities, 20 international equity markets, Treasury bonds, corporate bonds, and futures. (2) A betting against beta (BAB) factor, which is long leveraged low-beta assets and short high-beta assets, produces significant positive risk-adjusted returns. (3) When funding constraints tighten......, the return of the BAB factor is low. (4) Increased funding liquidity risk compresses betas toward one. (5) More constrained investors hold riskier assets....

  4. Roughing up Beta

    DEFF Research Database (Denmark)

    Bollerslev, Tim; Li, Sophia Zhengzi; Todorov, Viktor

    Motivated by the implications from a stylized equilibrium pricing framework, we investigate empirically how individual equity prices respond to continuous, or \\smooth," and jumpy, or \\rough," market price moves, and how these different market price risks, or betas, are priced in the cross......-section of expected returns. Based on a novel highfrequency dataset of almost one-thousand individual stocks over two decades, we find that the two rough betas associated with intraday discontinuous and overnight returns entail significant risk premiums, while the intraday continuous beta is not priced in the cross......-section. An investment strategy that goes long stocks with high jump betas and short stocks with low jump betas produces significant average excess returns. These higher risk premiums for the discontinuous and overnight market betas remain significant after controlling for a long list of other firm characteristics...

  5. 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 i

  6. Pemanfaatan Zeolit Alam Teraktivasi untuk Adsorpsi Logam Krom (Cr3+

    Directory of Open Access Journals (Sweden)

    Lisanti Emelda

    2013-12-01

    Full Text Available Pertukaran ion antara Cr3+ dan H+ menggunakan zeolit sebagai penukar ion adalah salah satu metode untuk memurnikan air dari ion kromium. Zeolit adalah senyawa aluminosilikat tetrahedral dengan struktur ikatan 3-dimesi, memiliki pori bagian dalam, dan luas permukaan yang tinggi, karena itu dapat digunakan sebagai adsorben. Tujuan penelitian ini adalah untuk mengevaluasi pengaruh waktu kontak optimum, suhu, dan konsentrasi kromium terhadap kapasitas penyerapan. Tahap pertama adalah mencampur zeolit yang telah diaktifkan dengan larutan kromium (10 ppm kromium dalam tangki berpengaduk pada 25oC. Selanjutnya larutan diambil setiap 60 menit hingga konsentrasi residu larutan kromium konstan. Proses adsorpsi dilangsungkan pada suhu berbeda yaitu:  25, 30, 35, 40, 45, dan 50 oC. Untuk uji adsorpsi isotermal, pada suhu dengan hasil penyerapan terbaik divariasikan konsentrasi kromiumnya yaitu: 10, 20, 40, 60, dan 100 ppm. Dosis adsorben yang digunakan adalah 3 gram adsorbent/200 mL larutan krommium dengan kecepatan pengaduk 240 rpm. Larutan kromium dideteksi dengan menggunakan Atomic Absorption Spectroscopy (AAS atau Spektroskopi Serapan Atom. Waktu kontak optimum diperoleh 3 jam menggunakan zeolit yang diaktifkan dengan asam, diperoleh nilai adsorpsi optimum 99,275%. Proses adsorpsi berjalan secara eksoterm, memiliki ?Ho = -3.9574,6 J/mol dan ?So = -117.227 J/moloK. Model isotermal adsorpsi mengikuti isoterm Freundlich menurut persamaan Qe = 0,044463C1/2,5125, kapasitas penyerapan Kf = 0,044463 mmol/gram adsorben, dan intensitas adsorpsi n = 2,5125.

  7. Enriching the diet of dairy cows natural zeolite

    OpenAIRE

    Svetlana Dejatkina; Ekaterina Goryacheva; Vladimir Kozlov; Mihail Dejatkin

    2016-01-01

    Analysis of economic rations of dairy cows reveals a lack of these minerals, it found that the data on the nutritional diets meet the necessary requirements. Introduction to the diet of natural zeolite cows completely fills the mineral deficiency and enhances milk production.

  8. Enriching the diet of dairy cows natural zeolite

    Directory of Open Access Journals (Sweden)

    Svetlana Dejatkina

    2016-02-01

    Full Text Available Analysis of economic rations of dairy cows reveals a lack of these minerals, it found that the data on the nutritional diets meet the necessary requirements. Introduction to the diet of natural zeolite cows completely fills the mineral deficiency and enhances milk production.

  9. Preparation of Na-zeolite with Kaolinite for Wastewater Treatment

    Institute of Scientific and Technical Information of China (English)

    LIU Qiongqiong; TAN Xin; SHAO Xiaolong

    2015-01-01

    Kaolinite as a raw material was modified to prepare a Na-zeolite productvia calcination and alkaline treat-ment. According to the measurement of the cation-exchange capacity, the prepared Na-zeolite product with an ammo-nium ion-exchange capacity of >75 mg/g can be used to remove ammonia nitrogen in water. The Na-zeolite products were characterized by scanning electron microscopy, infrared spectroscopy and X-ray diffraction, respectively. The re-finement of the structure was simulated by a software named Full Prof. The results show that the Si–O stretching vibra-tions of the prepared product in the range of 1008–1115 cm–1 disappear, only a small bend appears at 1103 cm–1 and the Al–OH vibration peaks at 912 cm–1 and 940 cm–1 both disappear. It is indicated that after calcination and alkaline treat-ment, the Si–O tetrahedral and Al–O octahedral structures are severely damaged, resulting in changes in the flexural vi-brations of Si–O and Al–OH. Kaolinite is a lamellar structure with the space group of C1, classified into a triclinic sys-tem, and cell parameters (such asa=0.5154 nm,b=0.8941 nm, andc=0.74 nm). Kaolinite with a lamellar structure is completely dissolved after calcination and alkaline treatment, resulting in the formation of Na-zeolite with a cage cubic structure.

  10. Computer Simulation of Zeolites : Adsorption, Diffusion and Dealumination

    NARCIS (Netherlands)

    Ban, S.

    2009-01-01

    Zeolites are microporous materials with pores that have about the same size as small molecules like water or benzene. They are important catalysts in the petrochemical industry, for example for catalytic cracking, and isomerization- and alkylation reactions. This thesis deals with molecular aspects

  11. The Density Functional Study of Thiophene Adsorption on Zeolite Clusters

    Institute of Scientific and Technical Information of China (English)

    Lü Renqing; Cao Zuogang; Shen Guoping

    2007-01-01

    The density functional theory and the cluster model methods have been employed to investigate the interactions between thiophene and the HZSM-5 zeolites. The molecular complexes formed by the adsorption of thiophene on silanol H3SiOH with two coordination forms, and the model Br(o)nsted acid sites of zeolite cluster H3Si(OH)Al(OH)2SiH3 upon the interaction with thiophene have been comparatively studied.Full optimization and frequency analysis of all cluster models have been carried out using the B3LYP hybrid method at 6-31G basis level for hydrogen atoms and 6-31+G(d) basis set level for silicon, aluminum, oxygen,carbon, and sulfur atoms. The calculated results showed that the nature of interactions leading to the formation of the zeolite cluster-thiophene and silanol-thiophene complexes was associated with the van der Waals force confirmed by a slight change of geometric structures and properties. Thiophene is adsorbed on bridging hydroxyl group prior to silanol OH group judging from the magnitude of adsorption heat. The cluster model calculation reproducing the experimental prediction to form the experimental adsorption spectra of thiophene in HZSM-5 zeolite has illustrated the validity of the proposed adsorption models.

  12. 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...

  13. 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...

  14. Phosphatation of Zeolites : A Combined Spectroscopy, Microscopy and Catalysis Study

    NARCIS (Netherlands)

    van der Bij, Hendrik

    2014-01-01

    The scope of this dissertation is to gain a fundamental understanding of phosphorus interaction with zeolites. These interactions can be either promotional or poisonous. Therefore, the main focus of this PhD thesis will be on the understanding of the physicochemical effects that occur upon phosphoru

  15. Synthesis of Zeolites by Alkaline Activation of Fly Ash

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    In terms of mineral transformation, and chemical composition of acid-soluble component as a function of reaction time, the effect of alkaline solution on zeolite-like fly ash was studied by employing fly ash and NaOH solution as starting materials. When fly ash and 1€? 0mol/L NaOH solution were processed at 100℃ for 24h with 1:10 W/S rat io in a relatively closed system, powder XRD patterns of resulting pro ducts indicated the formation of various zeolites. Zeolite P crystalli zed early at low alkaline concentration, which was replaced then by ze olites X and A. At high concentration, hydroxy sodalite was the only n ew phase. Quartz, in fly ash and NaOH solution system, gradually disso lved, and mullite, however, remained stable. It was concluded that, wi th Al/Si and Na/Si finally reaching equilibrium in molar ratio, compos ition of starting mixtures affects the crystallization of zeolite from fly ash.

  16. Mobil/Badger to market zeolite-based cumene technology

    International Nuclear Information System (INIS)

    Badger (Cambridge, MA) and Mobil (Fairfax, VA) are ready to jointly license a new cumene technology that they say achieves higher yields and product purity than existing processes. The zeolite-based technology is scheduled to be introduced at next month's DeWitt Petrochemical Review in Houston. The Mobil/Badger technology aims to challenge the dominant position of UOP's (Des Plaines, IL) solid phosphoric acid (SPA) catalyst process - which accounts for 80%-90% of the world's cumene production. In addition, Monsanto/Kellogg's aluminum chloride-based technology has gained significant momentum since its introduction in the 1980s. And late last year, ABB Lummus Crest (Bloomfield, NJ) also began marketing a zeolite-based cumene technology. While all the technologies make cumene via the alkylation of benzene with propylene, the Mobil/Badger process uses a zeolite-containing catalyst designed by Mobil to selectively catalyze the benzene/propylene reaction, avoiding unwanted propylene oligomerization. Because the olefin reactions are so fast, says Frank A. Demers, Badger's v.p./technology development and marketing, other zeolite technologies are forced to use complex reactor arrangements to stop the propylene-propylene reactions. However, he says, 'Mobil has designed a catalyst that wants to react benzene with propylene to make cumene.'

  17. Synthesis of mesoporous zeolite single crystals with cheap porogens

    Science.gov (United States)

    Tao, Haixiang; Li, Changlin; Ren, Jiawen; Wang, Yanqin; Lu, Guanzhong

    2011-07-01

    Mesoporous zeolite (silicalite-1, ZSM-5, TS-1) single crystals have been successfully synthesized by adding soluble starch or sodium carboxymethyl cellulose (CMC) to a conventional zeolite synthesis system. The obtained samples were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), nitrogen sorption analysis, 27Al magic angle spinning nuclear magnetic resonance ( 27Al MAS NMR), temperature-programmed desorption of ammonia (NH 3-TPD) and ultraviolet-visible spectroscopy (UV-vis). The SEM images clearly show that all zeolite crystals possess the similar morphology with particle size of about 300 nm, the TEM images reveal that irregular intracrystal pores are randomly distributed in the whole crystal. 27Al MAS NMR spectra indicate that nearly all of the Al atoms are in tetrahedral co-ordination in ZSM-5, UV-vis spectra confirm that nearly all of titanium atoms are incorporated into the framework of TS-1. The catalytic activity of meso-ZSM-5 in acetalization of cyclohexanone and meso-TS-1 in hydroxylation of phenol was also studied. The synthesis method reported in this paper is cost-effective and environmental friendly, can be easily expended to prepare other hierarchical structured zeolites.

  18. [Denitrification water treatment with zeolite composite filter by intermittent operation].

    Science.gov (United States)

    Qing, Cheng-Song; Bao, Tao; Chen, Tian-Hu; Chen, Dong; Xie, Jing-Jing

    2012-12-01

    The zeolite composite filters (ZCF) with the size of4-8 mm were prepared using raw zeolite (0.15-0.18 mm) as the main material and the cement as binder. After a combination of material characterizations, such as the void fraction, apparent density, compression strength and surface area, the optimal prepared conditions of composite filters were obtained as follow: weight ratio of m (zeolite): m (cement) = 7 : 3, curing for 15 d under the moisture condition and ambient temperature. Through upflow low-concentration ammonia nitrogen wastewater, ZCF filled in the experimental column was hung with the biological membrane. Thus, intermittent dynamic experiments were conducted, the intermittent operation cycle included adsorption, biological regeneration and drip washing. Until concentration of ammonia nitrogen was more than 2 mg x L(-1) of effluent standards, water in experiment column was firstly emptied, and then blast biological regeneration was conducted. After the filters were bathed with water, the zeolite adsorption-biological regeneration cycle was performed repeatedly. The experimental results show that under conditions of 24 h blast and 5 d of continuous operation period, ammonia nitrogen removal rate is up to 87.6% on average, total nitrogen removal rate reaches 51.2% on average. PMID:23379168

  19. Zeolitic imidazolate frameworks for kinetic separation of propane and propene

    Energy Technology Data Exchange (ETDEWEB)

    Li, Jing; Li, Kunhao; Olson, David H.

    2014-08-05

    Zeolitic Imidazolate Frameworks (ZIFs) characterized by organic ligands consisting of imidazole ligands that are either essentially all 2-chloroimidazole ligands or essentially all 2-bromoimidazole ligands are disclosed. Methods for separating propane and propene with the ZIFs of the present invention, as well as other ZIFs, are also disclosed.

  20. Characterization of natural zeolite clinoptilolite for sorption of contaminants

    Science.gov (United States)

    Xingu-Contreras, E.; García-Rosales, G.; García-Sosa, I.; Cabral-Prieto, A.; Solache-Ríos, M.

    2015-06-01

    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∘ (2 𝜃), inferring the presence of nanocrystals of Fe2B as identified from Mössbauer Spectroscopy. The size of these Fe2B 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 %.

  1. Characterization of natural zeolite clinoptilolite for sorption of contaminants

    International Nuclear Information System (INIS)

    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∘ (2θ), inferring the presence of nanocrystals of Fe2B as identified from Mössbauer Spectroscopy. The size of these Fe2B 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 %

  2. Study on Thermal Insulation Zeolite by Coal Fly Ash

    Directory of Open Access Journals (Sweden)

    Huiping Song

    2014-01-01

    Full Text Available This paper takes the coal fly ash as the material and makes zeolite with low thermal conductivity under a two-step synthesis for the purpose of thermal insulation. It studies main factors affecting zeolite such as the different concentration of NaOH, the solid-liquid ratio, the silica-alumina ratio, and the crystallization temperature. The optimal conditions were obtained that the NaOH concentration was 3 mol/L, the solid-liquid ratio was 10 : 1, the silica-alumina ratio was 2, and the crystallization temperature was 12°C. Zeolites have multiple pores and skeletal structures under SEM observation. The mean particle size was 2.78 um of concentrated distribution. The pore volume was 0.148 m3/g measured by BET analysis, the specific surface was 118.6 m2/g, and the thermal conductivity was 0.153 W/(m·K. Zeolite was proved to be a qualified insulation material which can be used in thermal insulation coating as a new material of energy conservation.

  3. 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 %.

  4. Martian zeolites as a source of atmospheric methane

    Science.gov (United States)

    Mousis, Olivier; Simon, Jean-Marc; Bellat, Jean-Pierre; Schmidt, Frédéric; Bouley, Sylvain; Chassefière, Eric; Sautter, Violaine; Quesnel, Yoann; Picaud, Sylvain; Lectez, Sébastien

    2016-11-01

    The origin of the martian methane is still poorly understood. A plausible explanation is that methane could have been produced either by hydrothermal alteration of basaltic crust or by serpentinization of ultramafic rocks producing hydrogen and reducing crustal carbon into methane. Once formed, methane storage on Mars is commonly associated with the presence of hidden clathrate reservoirs. Here, we alternatively suggest that chabazite and clinoptilolite, which belong to the family of zeolites, may form a plausible storage reservoir of methane in the martian subsurface. Because of the existence of many volcanic terrains, zeolites are expected to be widespread on Mars and their Global Equivalent Layer may range up to more than ∼1 km, according to the most optimistic estimates. If the martian methane present in chabazite and clinoptilolite is directly sourced from an abiotic source in the subsurface, the destabilization of a localized layer of a few millimeters per year may be sufficient to explain the current observations. The sporadic release of methane from these zeolites requires that they also remained isolated from the atmosphere during its evolution. The methane release over the ages could be due to several mechanisms such as impacts, seismic activity or erosion. If the methane outgassing from excavated chabazite and/or clinoptilolite prevails on Mars, then the presence of these zeolites around Gale Crater could explain the variation of methane level observed by Mars Science Laboratory.

  5. Synthesis and Separating Performance of SAPO-44 Zeolite Membrance

    Institute of Scientific and Technical Information of China (English)

    Zan LIU; Zhi Lin CHENG

    2005-01-01

    A defect-free SAPO-44 zeolite membrane firmly anchored the porous α-Al2O3 plate substrate was successfully synthesized. The separating results showed that the H2/N2 and H2/CO permselectivities were higher than those of the corresponding Knudsen diffusion and the substrate,attaining 5.78 and 7.15 respectively.

  6. Biogas cleaning and upgrading with natural zeolites from tuffs.

    Science.gov (United States)

    Paolini, Valerio; Petracchini, Francesco; Guerriero, Ettore; Bencini, Alessandro; Drigo, Serena

    2016-01-01

    CO2 adsorption on synthetic zeolites has become a consolidated approach for biogas upgrading to biomethane. As an alternative to synthetic zeolites, tuff waste from building industry was investigated in this study: indeed, this material is available at a low price and contains a high fraction of natural zeolites. A selective adsorption of CO2 and H2S towards CH4 was confirmed, allowing to obtain a high-purity biomethane (CO2 <2 g m(-3), i.e. 0.1%; H2S <1.5 mg m(-3)), suitable for injection in national grids or as vehicle fuel. The loading capacity was found to be 45 g kg(-1) and 40 mg kg(-1), for CO2 and H2S, respectively. Synthetic gas mixtures and real biogas samples were used, and no significant effects due to biogas impurities (e.g. humidity, dust, moisture, etc.) were observed. Thermal and vacuum regenerations were also optimized and confirmed to be possible, without significant variations in efficiency. Hence, natural zeolites from tuffs may successfully be used in a pressure/vacuum swing adsorption process. PMID:26563442

  7. High-pressure alchemy on a small-pore zeolite

    Science.gov (United States)

    Lee, Y.

    2011-12-01

    While an ever-expanding variety of zeolites with a wide range of framework topology is available, it is desirable to have a way to tailor the chemistry of the zeolitic nanopores for a given framework topology via controlling both the coordination-inclusion chemistry and framework distortion/relaxation. This is, however, subjected to the ability of a zeolitic nanopore to allow the redistribution of cations-water assembly and/or insertion of foreign molecules into the pores and channels. Small-pore zeolites such as natrolite (Na16Al16Si24O80x16H2O), however, have been known to show very limited capacity for any changes in the confinement chemistry. We have recently shown that various cation-exchanged natrolites can be prepared under modest conditions from natural sodium natrolite and exhibit cation-dependent volume expansions by up to 18.5% via converting the elliptical channels into progressively circular ones. Here, we show that pressure can be used as a unique and clean tool to further manipulate the chemistry of the natrolite nanopores. Our recent crystallographic and spectroscopic studies of pressure-insertion of foreign molecules, trivalent-cation exchange under pressure, and pressure-induced inversion of cation-water coordination and pore geometry in various cation-exchanged natrolites will be presented.

  8. Acetalization of furfural with zeolites under benign reaction conditions

    DEFF Research Database (Denmark)

    Rubio-Caballeroa, Juan Miguel; Shunmugavel, Saravanamurugan; Maireles-Torres, Pedro;

    2014-01-01

    Acetalization is a viable method to protect carbonyl functionalities in organic compounds and offers apotential synthetic strategy for synthesizing derived chemicals. In this work, several families of commer-cial zeolites have been employed as solid acid catalysts in the acetalization of furfural...

  9. Phase transitions on dehydration of the natural zeolite thomsonite

    DEFF Research Database (Denmark)

    Ståhl, Kenny

    2001-01-01

    The dehydration of the natural zeolite thomsonite, Na4CasAl20Si20O80 24H(2)O, has been studied using a combination of conventional and synchrotron X-ray powder diffraction. A preliminary in situ dehydration study revealed two distinct unit cell changes at approximately 540 and 570 K, respectively...

  10. DIFFUSION MEASUREMENTS DURING PERVAPORATION THROUGH A ZEOLITE MEMBRANE

    Science.gov (United States)

    An isotopic-transient technique was used to directly measure diffusion times of H2O, methanol, ethanol, 2-propanol, and acetone in pure and binary mixture feeds transporting through a zeolite membrane under steady-state pervaporation conditions. Diffusivities can be determ...

  11. Enhanced relative photonic efficiency of titania/zeolite composite photocatalysts

    Energy Technology Data Exchange (ETDEWEB)

    Shankar, M.V.; Cheralathan, K.K.; Arabindoo, B.; Palanichamy, M.; Murugesan, V. [Dept. of Chemistry, Anna Univ., Chennai (India)

    2003-07-01

    The photocatalytic degradation of 2,4-dichlorophenoxyacetic acid, an endocrine disrupter using TiO{sub 2} and supported TiO{sub 2} has been attempted in the present investigation. Batch studies were carried out to optimise various experimental parameters for maximum degradation efficiency. As the adsorption capacity of the photocatalyst is important to provide maximum pollutant concentration environment surrounding the catalyst, zeolites, which are good adsorbents were chosen as supports for TiO{sub 2}. Studies were conducted with three different zeolites differing in Si/Al ratio which governs the hydrophilicity of the support. The wt% loading of TiO{sub 2} on the support was found to be important for effective degradation. Though immobilised system requires high wt% loading the amount of TiO{sub 2} used is only 50% compared to TiO{sub 2} system. Zeolite being less expensive than TiO{sub 2}, TiO{sub 2}/zeolite composite system makes the process cost effective. The efficiencies of various systems were compared in terms of relative photonic efficiency. The relative photonic efficiency value for all these systems is more than one showing the effectiveness of this process. (orig.)

  12. 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...

  13. A continuous flow strategy for the coupled transfer hydrogenation and etherification of 5-(hydroxymethyl)furfural using Lewis acid zeolites.

    Science.gov (United States)

    Lewis, Jennifer D; Van de Vyver, Stijn; Crisci, Anthony J; Gunther, William R; Michaelis, Vladimir K; Griffin, Robert G; Román-Leshkov, Yuriy

    2014-08-01

    Hf-, Zr- and Sn-Beta zeolites effectively catalyze the coupled transfer hydrogenation and etherification of 5-(hydroxymethyl)furfural with primary and secondary alcohols into 2,5-bis(alkoxymethyl)furans, thus making it possible to generate renewable fuel additives without the use of external hydrogen sources or precious metals. Continuous flow experiments reveal nonuniform changes in the relative deactivation rates of the transfer hydrogenation and etherification reactions, which impact the observed product distribution over time. We found that the catalysts undergo a drastic deactivation for the etherification step while maintaining catalytic activity for the transfer hydrogenation step. (119) Sn and (29) Si magic angle spinning (MAS) NMR studies show that this deactivation can be attributed to changes in the local environment of the metal sites. Additional insights were gained by studying effects of various alcohols and water concentration on the catalytic reactivity.

  14. Exploitation of Unique Properties of Zeolites in the Development of Gas Sensors

    Directory of Open Access Journals (Sweden)

    Prabir K. Dutta

    2012-04-01

    Full Text Available The unique properties of microporous zeolites, including ion-exchange properties, adsorption, molecular sieving, catalysis, conductivity have been exploited in improving the performance of gas sensors. Zeolites have been employed as physical and chemical filters to improve the sensitivity and selectivity of gas sensors. In addition, direct interaction of gas molecules with the extraframework cations in the nanoconfined space of zeolites has been explored as a basis for developing new impedance-type gas/vapor sensors. In this review, we summarize how these properties of zeolites have been used to develop new sensing paradigms. There is a considerable breadth of transduction processes that have been used for zeolite incorporated sensors, including frequency measurements, optical and the entire gamut of electrochemical measurements. It is clear from the published literature that zeolites provide a route to enhance sensor performance, and it is expected that commercial manifestation of some of the approaches discussed here will take place. The future of zeolite-based sensors will continue to exploit its unique properties and use of other microporous frameworks, including metal organic frameworks. Zeolite composites with electronic materials, including metals will lead to new paradigms in sensing. Use of nano-sized zeolite crystals and zeolite membranes will enhance sensor properties and make possible new routes of miniaturized sensors.

  15. Synthesis and Characterization of ZSM-5/β Co-Crystalline Zeolite

    Institute of Scientific and Technical Information of China (English)

    Tianbo Zhao; Huiying Zhang; Fengyan Li; Chao Yang; Baoning Zong

    2005-01-01

    ZSM-5/β co-crystalline zeolites with different content of ZSM-5 have been synthesized by adding different amount of ZSM-5 to the synthetic system ofβ zeolite with NaAlO2, silica sol as the source of aluminum and silica, respectively, and TEA+ as the template under controlled condition of the synthesis. The ZSM-5/β co-crystalline zeolite was studied by XRD, SEM, BET and NH3-TPD. The reaction activity of toluene alkylation was investigated with a mixture of toluene-methanol as the feedstock in a pulse micro-reactor over the ZSM-5/β co-crystalline zeolite. It is found that ZSM-5/β co-crystalline zeolite has two kinds of zeolite structure including ZSM-5 and β zeolite, not in the form of a physical mixture. The pore structure of ZSM-5/β co-crystalline zeolites is different from that forβ zeolite, ZSM-5and their physical mixture. In addition, the peaks of both high and low temperature desorption of ammonia over the ZSM-5/β co-crystalline zeolite shift 23 ℃ to lower temperatures and the acid amount of its strong acid is 3% more than the physical mixture. So the ZSM-5/β co-crystalline zeolite produces the highest content of xylene, which is 10.4% higher than the physical mixture. And the ZSM-5/β co-crystalline zeolite has better selectivity for toluene alkylation and weaker de-methylation than β zeolite, ZSM-5 and their physical mixture.

  16. Synthesis of highly effective adsorbents from natural raw materials (zeolites)

    International Nuclear Information System (INIS)

    Natural raw materials bentonite, silica tuff and diatomaceous earth from Macedonia were used in synthesis of zeolites type A, ZSM-5 and multilayer silicate magadiite-adsorbents. The bentonite was subject to pretreatment with acids (HCl and H2SO4 - 5, 10, 15 and W%) or NaOH, and used in synthesis of zeolite type A having molar ratio of: 2Na2O : Al2O3 : 2SiO2 : 100H2O. Silicate tuff was applied (without any pretreatment, in a two stage reaction) in a high temperature synthesis, using butylamine as an organic 'template' component in order to get high silica zeolite type ZSM-5 having molar ratio of: 59.37SiO2 : Al2O3 : 3.84Na2O : 1.90R2O : 2025.10H2O. Multilayer silicate magadiite MS-H was synthesized from natural raw material diatomaceous earth. The product with a molar ratio of: 8SiO2 : Na2O : 75H2O showed the best characteristics. The proposed method of alkaline pretreatment is a new one and it is acceptable from the economy point of view due to low energy consumption. The conclusion shows that the final result of the synthesis was not perfect, i.e. it has 70% of zeolite ZSM-5 and the rest were some amorphous phases. This product is suitable for industrial application in catalytic processes due to the fact that commercial catalyst contain typically 20 to 50% of zeolite type ZSM-5. On the other hand, the magadiite being multilayer silicate with no aluminium inside, is well suited as a carrier due to its ability of intercalation. The experimental results indicate that natural raw materials from Macedonia could be used for synthesis of synthetical silicates with high qualities and acceptable overall costs, specially when alkaline pretreatment is used. 14 refs., 4 tabs., 11 figs

  17. Adsorption of nicotine on different zeolite types, from aqueous solutions

    Directory of Open Access Journals (Sweden)

    Stošić Dušan K.

    2007-01-01

    Full Text Available The plant alkaloid, nicotine, is a strongly toxic heterocyclic compound: the lethal dose for an adult human being (40-60 mg is importantly lower in comparison with the other known poisons such as arsenic or strychni­ne. Cigarettes represent "the most toxic and addictive form of nicotine". Besides the negative effects of nicotine on public health produced by self-administration, recently another potentially very dangerous effect has been recognized: because of its miscibility with water, nicotine can be found in industrial wastewaters, and consequently, in groundwater. Therefore, the problem of nicotine removal from aqueous solutions has became an interesting topic. In this work, the removal of nicotine has been probed by adsorption on solid materials. Adsorption of nicotine on different zeolites (clinoptilolite, ZSM-5 and β zeolite and on activated carbon was investigated from aqueous solutions, at 298 K. The obtained results are presented as adsorption isotherms: the amount of adsorbed nicotine as a function of equilibrium concentration. These data were obtained from the residual amount of nicotine in the aqueous phase, by the use of UV spectroscopy. The highest amounts of adsorbed nicotine was found for activated carbon and p zeolite (~ mmol·g-1. The attempt to modify the adsorption properties of ZSM-5 zeolite has been also done: ZSM-5 was modified by ion-exchange with VIII group metal (Cu2+ and Fe3+. In addition, the adsorption of nicotine on ZSM-5 zeolite with different Si/Al ratios has been done. It has been noticed that ion-exchange did not improve the adsorption possibilities, while the adsorption was importantly lower in the case of higher silicon content in ZMS-5 structure. 13C NMR spectra were collected for suspensions formed of solid adsorbent and aqueous solution of nicotine; in this way, the part of nicotine molecule which is most probably connected with the adsorbent was recognized.

  18. The use of natural zeolites for radioactive waste treatment. Studies on leaching from zeolite/cement composites

    International Nuclear Information System (INIS)

    Samples of the natural zeolites chabazite, clinoptilolite and a clinoptilolite-rich tuff, were loaded with the isotope 137Cs. Composites of these labeled materials were made with cement and blast furnace slag. Standard leaching experiments were carried out with synthetic sea, ground and 'pond' waters, as well as distilled water. Rates of leaching were calculated and compared to similar systems. (author)

  19. Antimicrobial properties of zeolite-X and zeolite-A ion-exchanged with silver, copper, and zinc against a broad range of microorganisms.

    Science.gov (United States)

    Demirci, Selami; Ustaoğlu, Zeynep; Yılmazer, Gonca Altın; Sahin, Fikrettin; Baç, Nurcan

    2014-02-01

    Zeolites are nanoporous alumina silicates composed of silicon, aluminum, and oxygen in a framework with cations, water within pores. Their cation contents can be exchanged with monovalent or divalent ions. In the present study, the antimicrobial (antibacterial, anticandidal, and antifungal) properties of zeolite type X and A, with different Al/Si ratio, ion exchanged with Ag(+), Zn(2+), and Cu(2+) ions were investigated individually. The study presents the synthesis and manufacture of four different zeolite types characterized by scanning electron microscopy and X-ray diffraction. The ion loading capacity of the zeolites was examined and compared with the antimicrobial characteristics against a broad range of microorganisms including bacteria, yeast, and mold. It was observed that Ag(+) ion-loaded zeolites exhibited more antibacterial activity with respect to other metal ion-embedded zeolite samples. The results clearly support that various synthetic zeolites can be ion exchanged with Ag(+), Zn(2+), and Cu(2+) ions to acquire antimicrobial properties or ion-releasing characteristics to provide prolonged or stronger activity. The current study suggested that zeolite formulations could be combined with various materials used in manufacturing medical devices, surfaces, textiles, or household items where antimicrobial properties are required.

  20. Formation of carbon nanotubes on iron/cobalt oxides supported on zeolite-Y : Effect of zeolite textural properties and particle morphology

    NARCIS (Netherlands)

    Triantafyllidis, K. S.; Karakoulia, S. A.; Gournis, D.; Delimitis, A.; Nalbandian, L.; Maccallini, E.; Rudolf, P.

    2008-01-01

    The effect of the textural properties and morphology of zeolite Y, used as support of iron (Fe) or cobalt (Co) oxides, on the quantity and quality of the multi-wall carbon nanotubes (MWNTs) synthesized by catalytic chemical vapour deposition (CCVD) of acetylene was studied. The parent zeolite Y was