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Sample records for voc carbon zeolite

  1. Development of metal organic fromwork-199 immobilized zeolite foam for adsorption of common indoor VOCs.

    Science.gov (United States)

    Saini, Vipin K; Pires, João

    2017-05-01

    Reticulated foam shaped adsorbents are more efficient for the removal of volatile organic compounds (VOCs), particularly from low VOC-concentration indoor air streams. In this study composite structure of zeolite and metal organic frameworks (MOFs), referred as ZMF, has been fabricated by immobilization of fine MOF-199 powder on foam shaped Zeolite Socony Mobil-5 (ZSM-5) Zeolitic structure, referred as ZF. The ZMF possess a uniform and well-dispersed coating of MOF-199 on the porous framework of ZF. It shows higher surface area, pore volume, and VOCs adsorption capacity, as compared to ZF-structure. Post-fabrication changes in selective adsorption properties of ZMF were studied with three common indoor VOCs (benzene, n-hexane, and cyclohexane), using gravimetric adsorption technique. The adsorption capacity of ZMF with different VOCs follow the order of benzene>n-hexane>cyclohexane. In comparison with MOF-199 and ZF, the composite structure ZMF shows improvement in selectivity for benzene from other two VOCs. Further, improvement in efficiency and stability of prepared ZMF was found to be associated with its high MOF loading capacity and unique morphological and structural properties. The developed composite structure with improved VOCs removal and recyclability could be a promising material for small to limited scale air pollution treatment units. Copyright © 2016. Published by Elsevier B.V.

  2. Preparation of a MFI zeolite coating on activated carbon

    NARCIS (Netherlands)

    Vaart, van der R.; Bosch, H.; Keizer, K.; Reith, T.

    1997-01-01

    A new and simple method for the preparation of MFI zeolite coated activated carbon is presented. Suitable nucleation sites for the growth of zeolites were introduced to the carbon by adding hydrophilic montmorillonite clay to the carbon substrate. A gas tight MFI zeolite coating was obtained on this

  3. 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.

  4. Tailoring the porosity of hierarchical zeolites by carbon-templating

    DEFF Research Database (Denmark)

    Zhu, Kake; Egeblad, Kresten; Christensen, Claus H.

    2008-01-01

    We report the synthesis and characterization of a series of hierarchical porous zeolite single crystal materials with a range of porosities made available by carbon-templating using differently-sized carbon particles as templates for the additional non-micropore porosity. The materials were...... prepared by adsorption of the required zeolite synthesis gel components onto various commercially available carbon black powders followed by crystallization of the zeolite crystals in the presence of the inert carbon matrix and subsequent removal of the carbon particles embedded in the zeolite crystals...... by combustion. It is shown that the additional porosity of the hierarchical zeolites can be tailored by encapsulation of the differently-sized carbon particles during crystallization....

  5. Synthesis of a hierarchically structured zeolite-templated carbon starting from fly ash-derived zeolite X

    CSIR Research Space (South Africa)

    Musyoka, Nicholas M

    2014-05-01

    Full Text Available the same morphological features as the parent zeolite and was composed of more than 96% carbon which confirmed that the zeolite template was successfully removed. It is important to emphasize that the hierarchically structured zeolite was produced without...

  6. Zeolite-catalyzed methylation of pyrazole with dimethyl carbonate

    Energy Technology Data Exchange (ETDEWEB)

    Born, S.; Weichert, J.; Hartmann, M.; Ernst, S. [Dept. of Chemistry, Chemical Technology, Kaiserslautern Univ. (Germany)

    2002-07-01

    The present paper describes our attempts to explore the potential of acidic and nonacidic zeolites for the alkylation of pyrazole with dimethyl carbonate to 1-methyl pyrazole, which is a useful intermediate in the manufacture of pharmaceuticals and pesticides. (orig.)

  7. Application of high silica zeolite ZSM-5 in a hybrid treatment process based on sequential adsorption and ozonation for VOCs elimination.

    Science.gov (United States)

    Zaitan, Hicham; Manero, Marie Hélène; Valdés, Héctor

    2016-03-01

    In this study, a hydrophobic synthetic zeolite, namely ZSM-5 is chosen as an adsorbent/catalyst for toluene removal. Experimental results showed that toluene adsorption onto ZSM-5 was favourable, following a Langmuir adsorption isotherm model. ZSM-5 zeolite was regenerated using gaseous ozone at low temperature. Adsorbed toluene was oxidised, releasing mainly CO2 and H2O. Traces of oxidation by-products such as acetic acid and acetaldehyde were formed and remained adsorbed after the oxidativate regeneration with ozone. After four successive cycles of adsorption/ozonation, the adsorption efficiency was not affected (92%-99%). These results showed that volatile organic compound (VOC) removal by adsorption onto ZSM-5 zeolite followed by ozone regeneration could be used as a promising hybrid process for the control of VOC emissions in terms of efficiency.

  8. Efficient control of odors and VOC emissions via activated carbon technology.

    Science.gov (United States)

    Mohamed, Farhana; Kim, James; Huang, Ruey; Nu, Huong Ton; Lorenzo, Vlad

    2014-07-01

    This research study was undertaken to enhance the efficiency and economy of carbon scrubbers in controlling odors and volatile organic compounds (VOCs) at the wastewater collection and treatment facilities of the Bureau of Sanitation, City of Los Angeles. The butane activity and hydrogen sulfide breakthrough capacity of activated carbon were assessed. Air streams were measured for odorous gases and VOCs and removal efficiency (RE) determined. Carbon towers showed average to excellent removal of odorous compounds, VOCs, and siloxanes; whereas, wet scrubbers demonstrated good removal of odorous compounds but low to negative removal of VOCs. It was observed that the relative humidity and empty bed contact time are one of the most important operating parameters of carbon towers impacting the pollutant RE. Regular monitoring of activated carbon and VOCs has resulted in useful information on carbon change-out frequency, packing recommendations, and means to improve performance of carbon towers.

  9. Fixation of carbon dioxide into dimethyl carbonate over titanium-based zeolitic thiophene-benzimidazolate framework

    Data.gov (United States)

    U.S. Environmental Protection Agency — A titanium-based zeolitic thiophene-benzimidazolate framework has been designed for the direct synthesis of dimethyl carbonate (DMC) from methanol and carbon...

  10. 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

  11. Wide band gap carbon allotropes: Inspired by zeolite-nets

    Science.gov (United States)

    Wei, Zhi-Jing; Zhao, Hui-Yan; Wang, Jing; Liu, Ying

    2016-10-01

    Based on the topologies proposed for zeolites, six metastable semiconductor carbon allotropes with band gaps of 2.72-3.89 eV are predicted using ab initio density functional calculations. The hardnesses of these allotropes are about 90%-94% that of diamond, indicating that they may be superhard materials. We also present simulated X-ray diffraction spectra of these new carbon allotropes to provide a basis for possible experimental observations and synthesis. These new carbon structures with a range of band gaps and with hardnesses comparable to diamond could be potential targets for the synthesis of hard and transparent materials.

  12. Fixation of carbon dioxide into dimethyl carbonate over titanium-based zeolitic thiophene-benzimidazolate framework

    Science.gov (United States)

    A titanium-based zeolitic thiophene-benzimidazolate framework has been designed for the direct synthesis of dimethyl carbonate (DMC) from methanol and carbon dioxide. The developed catalyst activates carbon dioxide and delivers over 16% yield of DMC without the use of any dehydra...

  13. The growth of carbon nanotubes on montmorillonite and zeolite (clinoptilolite)

    Energy Technology Data Exchange (ETDEWEB)

    Kadlecikova, M. [Department of Microelectronics, Faculty of Electrical Engineering and Information Technology, Slovak University of Technology, Ilkovicova 3, 812 19 Bratislava (Slovakia); Breza, J. [Department of Microelectronics, Faculty of Electrical Engineering and Information Technology, Slovak University of Technology, Ilkovicova 3, 812 19 Bratislava (Slovakia)], E-mail: juraj.breza@stuba.sk; Jesenak, K.; Pastorkova, K.; Luptakova, V. [Department of Inorganic Chemistry, Faculty of Natural Sciences, Comenius University, Mlynska Dolina, 842 15 Bratislava (Slovakia); Kolmacka, M.; Vojackova, A. [Department of Microelectronics, Faculty of Electrical Engineering and Information Technology, Slovak University of Technology, Ilkovicova 3, 812 19 Bratislava (Slovakia); Michalka, M. [International Laser Centre, Ilkovicova 3, 812 19 Bratislava (Slovakia); Vavra, I. [Institute of Electrical Engineering, Slovak Academy of Sciences, Dubravska Cesta 9, 841 04 Bratislava (Slovakia); Krizanova, Z. [Department of Microelectronics, Faculty of Electrical Engineering and Information Technology, Slovak University of Technology, Ilkovicova 3, 812 19 Bratislava (Slovakia)

    2008-06-15

    Synthesis of carbon nanotubes described in the present work is based on activation of methane in a hot filament CVD reactor and subsequent creation of nanostructures on a catalyst pre-treated polished surface of silicon. An essential step of the synthesis is the use of natural minerals as catalysts. We have studied the catalyst parameters, the way of its application and the amount of Fe{sup 3+} cations on the surface of aluminosilicates on the quality of the grown nanotube layers. The growth of carbon nanotubes catalyzed by montmorillonite and zeolite (clinoptilolite) was confirmed by scanning electron microscopy and Raman spectroscopy.

  14. The growth of carbon nanotubes on montmorillonite and zeolite (clinoptilolite)

    Science.gov (United States)

    Kadlečíková, M.; Breza, J.; Jesenák, K.; Pastorková, K.; Luptáková, V.; Kolmačka, M.; Vojačková, A.; Michalka, M.; Vávra, I.; Križanová, Z.

    2008-06-01

    Synthesis of carbon nanotubes described in the present work is based on activation of methane in a hot filament CVD reactor and subsequent creation of nanostructures on a catalyst pre-treated polished surface of silicon. An essential step of the synthesis is the use of natural minerals as catalysts. We have studied the catalyst parameters, the way of its application and the amount of Fe 3+ cations on the surface of aluminosilicates on the quality of the grown nanotube layers. The growth of carbon nanotubes catalyzed by montmorillonite and zeolite (clinoptilolite) was confirmed by scanning electron microscopy and Raman spectroscopy.

  15. Zeolites

    Science.gov (United States)

    1992-01-01

    Zeolites are crystalline aluminosilicates that have complex framework structures. However, there are several features of zeolite crystals that make unequivocal structure determinations difficult. The acquisition of reliable structural information on zeolites is greatly facilitated by the availability of high-quality specimens. For structure determinations by conventional diffraction techniques, large single-crystal specimens are essential. Alternatively, structural determinations by powder profile refinement methods relax the constraints on crystal size, but still require materials with a high degree of crystalline perfection. Studies conducted at CAMMP (Center for Advanced Microgravity Materials Processing) have demonstrated that microgravity processing can produce larger crystal sizes and fewer structural defects relative to terrestrial crystal growth. Principal Investigator: Dr. Albert Sacco

  16. Investigation on Using SBS and Active Carbon Filler to Reduce the VOC Emission from Bituminous Materials

    Directory of Open Access Journals (Sweden)

    Peiqiang Cui

    2014-08-01

    Full Text Available Bituminous materials are playing a vital role in pavement design and the roofing industry because of outstanding properties. Unfortunately, bituminous materials will release volatile organic compounds (VOC, making them non-environmentally friendly. Therefore, technologies that can be used to decrease the VOC emission are urgently required. In this research, the VOC emission and material behaviors were analyzed and compared to investigate the possibility of adding styrene butadiene styrene (SBS and active carbon filler into bituminous materials to develop environmentally-friendly materials. Thermal gravimetric analysis-mass spectrometry (TG-MS and ultraviolet-visible spectroscopy testing (UV-Vis were employed to characterize the VOC emission process. Temperature sweep testing and frequency sweep testing were conducted to evaluate the rheological properties of bituminous materials. Research results indicated that the combined introduction of 4 wt% styrene butadiene styrene (SBS and 4 wt% active carbon filler cannot only significantly lower the VOC emission speed and amount, but also improve the deformation resistance behavior at a higher temperature. SBS and active carbon filler can be used to reduce the VOC emission form bituminous materials.

  17. Titanium-based zeolitic imidazolate framework for chemical fixation of carbon dioxide

    Science.gov (United States)

    A titanium-based zeolitic imidazolate framework (Ti-ZIF) with high surface area and porous morphology was synthesized and itsefficacy was demonstrated in the synthesis of cyclic carbonates from epoxides and carbon dioxide.

  18. Titanium-based zeolitic imidazolate framework for chemical fixation of carbon dioxide

    Science.gov (United States)

    A titanium-based zeolitic imidazolate framework (Ti-ZIF) with high surface area and porous morphology was synthesized and itsefficacy was demonstrated in the synthesis of cyclic carbonates from epoxides and carbon dioxide.

  19. Synthesis of Na-A and/or Na-X zeolite/porous carbon composites from carbonized rice husk

    Science.gov (United States)

    Katsuki, Hiroaki; Komarneni, Sridhar

    2009-07-01

    Na-A and/or Na-X zeolite/porous carbon composites were prepared under hydrothermal conditions by NaOH dissolution of silica first from carbonized rice husk followed by addition of NaAlO 2 and in situ crystallization of zeolites i.e., using a two-step process. When a one-step process was used, both Na-A and Na-X zeolites crystallized on the surface of carbon. Na-A or Na-X zeolite crystals were prepared on the porous carbonized rice husk at 90 °C for 2-6 h by changing the SiO 2/Al 2O 3, H 2O/Na 2O and Na 2O/SiO 2 molar ratios of precursors in the two-step process. The surface area and NH 4+-cation exchange capacity (CEC) of Na-A zeolite/porous carbon were found to be 171 m 2/g and 506 meq/100 g, respectively, while those of Na-X zeolite/porous carbon composites were 676 m 2/g and 317 meq/100 g, respectively. Na-A and Na-X zeolites are well-known microporous and hydrophilic materials while carbonized rice husk was found to be mesoporous (pores of ˜3.9 nm) and hydrophobic. These hybrid microporous-mesoporous and hydrophilic-hydrophobic composites are expected to be useful for decontamination of metal cations as well as organic contaminants simultaneously.

  20. ECOS E-MATRIX Methane and Volatile Organic Carbon (VOC) Emissions Best Practices Database

    Energy Technology Data Exchange (ETDEWEB)

    Parisien, Lia [The Environmental Council Of The States, Washington, DC (United States)

    2016-01-31

    This final scientific/technical report on the ECOS e-MATRIX Methane and Volatile Organic Carbon (VOC) Emissions Best Practices Database provides a disclaimer and acknowledgement, table of contents, executive summary, description of project activities, and briefing/technical presentation link.

  1. Synthesis of templated carbons starting from clay and clay-derived zeolites for hydrogen storage applications

    CSIR Research Space (South Africa)

    Musyoka, Nicholas M

    2014-10-01

    Full Text Available Clay and its recrystallized zeolitic derivatives were used in this study as templating agents for carbon nanostructured materials. The conventional nanocasting process that involves impregnation with furfural alcohol and subsequent chemical vapour...

  2. 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

  3. 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

  4. SEPARATION OF Ca AND Fe METAL ION IN SOURCE WATER BY ADSORPTION COLUMN TECHNIC WITH LOCAL ZEOLITE AND ACTIVE CARBON

    Directory of Open Access Journals (Sweden)

    Suyanta Suyanta

    2016-04-01

    Full Text Available This research aims are to separate of Ca and Fe metal ion in source water, with local zeolite and active carbon by adsorption column technic. Efficiency of separation are control by adsorption time and size of zeolite. Method that used was column adsorption with a flow system in which sample is applied to the filtration tube containing zeolite and active carbon. Initial and final concentrations of the samples were analyzed using Atomic Adsorption Spectrophotometer instrument. The results obtained shows that ability adsorption of zeolite to Ca and Fe metal ion are a good. Zeolite 1 (10 mesh can reduce iron concentration until 93.98 % and zeolite 2 (5mesh until 98.88% for 1 – 4 week range time. Whereas reducing of calcium concentration is not good, until 2 week period time adsorption of calcium ion is about 50%.   Keywords: adsorption, zeolite, source water

  5. Superconducting characteristics of 4-Å carbon nanotube-zeolite composite

    KAUST Repository

    Lortz, Rolf W.

    2009-04-15

    We have fabricated nanocomposites consisting of 4-A carbon nanotubes embedded in the 0.7-nm pores of aluminophosphate- five (AFI) zeolite that display a superconducting specific heat transition at 15 K. MicroRaman spectra of the samples show strong and spatially uniform radial breathing mode (RBM) signals at 510 cm-1 and 550 cm-1, characteristic of the (4,2) and (5,0) nanotubes, respectively. The specific heat transition is suppressed at >2T, with a temperature dependence characteristic of finite-size effects. Comparison with theory shows the behavior to be consistent with that of a type II BCS superconductor, characterized by a coherence length of 14 ± 2 nm and a magnetic penetration length of 1.5 ± 0.7 μm. Four probe and differential resistance measurements have also indicated a superconducting transition initiating at 15 K, but the magnetoresistance data indicate the superconducting network to be inhomogeneous, with a component being susceptible to magnetic fields below 3 T and other parts capable of withstanding a magnetic field of 5Tor beyond.

  6. Development of NaY zeolite derived from biomass and environmental assessment of carbon dioxide reduction

    Directory of Open Access Journals (Sweden)

    Worathanakul Patcharin

    2016-01-01

    Full Text Available Carbon dioxide is one of greenhouse gases. The carbon dioxide caused by the industry activities and impact to the global warming. The objectives of this research were to synthesize NaY zeolite from bagasse ash as silica source and loaded with different weight percentage of Cu(II for carbon dioxide reduction. The carbon footprint of Cu/Y zeolite for carbon dioxide reduction was calculated. The synthesized NaY zeolite from bagasse ash can be easily formed at Si/Al ratio of 0.75 with the additional heat after crystallization 70 °C for 1 hour. The crystal size of NaY zeolite was approximately 0.22−0.37 μm diameter. The results of carbon dioxide adsorption were increased when the flow rate of carbon dioxide decreased. Finally, the carbon footprint value was shown that synthesis step was shown the highest of greenhouse gas emission. This research can increase the value of wastes and reduce pollution emission.

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

    DEFF Research Database (Denmark)

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

    2016-01-01

    nanoparticles supported on silica, a carbon–silica composite is obtained and exploited as a combined carbon template/silica source for the zeolite synthesis. The mesoporous zeolite materials were all prepared by hydrothermal crystallization in alkaline media followed by removal of the carbon template...

  8. Treatment by adsorption on zeolites of volatile organic compounds (VOC). Study of the absorption/adsorption coupling applied to air treatment; Traitement des composes organiques volatils (COV) par adsorption sur zeolithe. Etude du couplage absorption/adsorption applique au traitement de l'air

    Energy Technology Data Exchange (ETDEWEB)

    Brosillon, St.

    2000-11-01

    Absorption and adsorption are the most suitable techniques to treat strong flow rates of gaseous effluents with low concentrations of volatile organic compounds (VOCs). This works deals with the adsorption on zeolites of pure VOCs or VOC mixtures. The competitive adsorption phenomena, the adsorption equilibria and the adsorption kinetics are analyzed for the dimensioning of industrial facilities. The selectiveness of zeolites depends on 4 parameters: the polarity, the volatility and the composition of the gaseous mixture compounds, and the filling up ratio of zeolites. The modeling of adsorption isotherms has been done using the Langmuir model for pure compounds and using the ideal adsorbed solution theory for mixtures. The simulation results obtained are relatively different from the experimental ones. The adsorbed VOCs seem to form non-ideal adsorbates. The saturation curves obtained by simulation are in good agreement with experimental curves when the proper value of the internal transfer coefficient is used. The different values of this parameter have permitted to deduce the average value of the effective diffusion of the zeolite for the 4 VOCs studied. In the last part, it is shown that the coupling of absorption and adsorption can be efficient for the treatment of mixtures of water soluble and water insoluble VOCs. The poor efficiency of water curtains for the treatment of industrial solvents has been demonstrated and a VOC adsorption process that use two concentrator wheels is proposed. (J.S.)

  9. Surface modification of coconut shell based activated carbon for the improvement of hydrophobic VOC removal.

    Science.gov (United States)

    Li, Lin; Liu, Suqin; Liu, Junxin

    2011-08-30

    In this study, coconut shell based carbons were chemically treated by ammonia, sodium hydroxide, nitric acid, sulphuric acid, and phosphoric acid to determine suitable modification for improving adsorption ability of hydrophobic volatile organic compounds (VOCs) on granular activated carbons (GAC). The saturated adsorption capacities of o-xylene, a hydrophobic volatile organic compound, were measured and adsorption effects of the original and modified activated carbons were compared. Results showed that GAC modified by alkalis had better o-xylene adsorption capacity. Uptake amount was enhanced by 26.5% and reduced by 21.6% after modification by NH(3)H(2)O and H(2)SO(4), respectively. Compared with the original, GAC modified by acid had less adsorption capacity. Both SEM/EDAX and BET were used to identify the structural characteristics of the tested GAC, while IR spectroscopy and Boehm's titration were applied to analysis the surface functional groups. Relationships between physicochemical characteristics of GAC and their adsorption performances demonstrated that o-xylene adsorption capacity was related to surface area, pore volume, and functional groups of the GAC surface. Removing surface oxygen groups, which constitute the source of surface acidity, and reducing hydrophilic carbon surface favors adsorption capacity of hydrophobic VOCs on carbons. The performances of modified GACs were also investigated in the purification of gases containing complex components (o-xylene and steam) in the stream.

  10. TOPICAL REVIEW Advances in principal factors influencing carbon dioxide adsorption on zeolites

    Directory of Open Access Journals (Sweden)

    Danielle Bonenfant et al

    2008-01-01

    Full Text Available We report the advances in the principal structural and experimental factors that might influence the carbon dioxide (CO2 adsorption on natural and synthetic zeolites. The CO2 adsorption is principally govern by the inclusion of exchangeable cations (countercations within the cavities of zeolites, which induce basicity and an electric field, two key parameters for CO2 adsorption. More specifically, these two parameters vary with diverse factors including the nature, distribution and number of exchangeable cations. The structure of framework also determines CO2 adsorption on zeolites by influencing the basicity and electric field in their cavities. In fact, the basicity and electric field usually vary inversely with the Si/Al ratio. Furthermore, the CO2 adsorption might be limited by the size of pores within zeolites and by the carbonates formation during the CO2 chemisorption. The polarity of molecules adsorbed on zeolites represents a very important factor that influences their interaction with the electric field. The adsorbates that have the most great quadrupole moment such as the CO2, might interact strongly with the electric field of zeolites and this favors their adsorption. The pressure, temperature and presence of water seem to be the most important experimental conditions that influence the adsorption of CO2. The CO2 adsorption increases with the gas phase pressure and decreases with the rise of temperature. The presence of water significantly decreases adsorption capacity of cationic zeolites by decreasing strength and heterogeneity of the electric field and by favoring the formation of bicarbonates. The optimization of the zeolites structural characteristics and the experimental conditions might enhance substantially their CO2 adsorption capacity and thereby might give rise to the excellent adsorbents that may be used to capturing the industrial emissions of CO2.

  11. Measurement and modeling of single- and multi-component adsorption equilibria of VOC on high-silica zeolites.

    Science.gov (United States)

    Monneyron, Pierre; Manero, Marie-Helene; Foussard, Jean-Noel

    2003-06-01

    From pure and binary gas adsorption equilibria measurements carried out using a volumetric method for three volatile organic compounds (methyl ethyl ketone, toluene (TOL), and 1,4-dioxane) on two high-silica zeolites, desaluminated faujasite Y (Fau Y) and ZSM-5 (Sil Z), co-adsorption was investigated and modeled. Apart from steric exclusion taking place with TOL-containing mixtures on Sil Z, micropore filling was similar to distillation since the component with the lower volatility adsorbed preferentially. At low coverage, chemisorption on specific sites happened in favor of polar or major compound, whereas at saturation the adsorbent was selective for the minor compound. Second, a quantitative prediction of binary equilibria was performed using the ideal adsorbed solution theory (IAST), examining the influence of pure component adsorption fitting model. The efficiency of correlations when extending AST to real mixture behavior was satisfactory in most cases. For engineering purposes, Fau Y is to be considered as a high-adsorption capacity adsorbent, whose selectivity can be described qualitatively by the distillation analogy and predicted quantitatively with the IAST in case of quasi-ideal mixtures.

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

    DEFF Research Database (Denmark)

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

    2016-01-01

    oxide, a carbon-silica composite is obtained and exploited as a combined carbon template/silica source for zeolite synthesis. This approach has several advantages in comparison with conventional carbon templating methods, where relatively complicated preparative strategies involving multistep...... impregnation procedures and rather expensive chemicals are used. Removal of the carbon template by combustion results in zeolite single crystals with intracrystalline pore volumes between 0.28 and 0.48 cm3/g. The prepared zeolites are characterized by XRD, SEM, TEM and physisorption analysis. The isomerization...

  13. Electrospun zeolite-templated carbon composite fibres for hydrogen storage applications

    CSIR Research Space (South Africa)

    Annamalai, Perushini

    2017-01-01

    Full Text Available -defined hierarchical pore structure. The study involved encapsulation of highly porous zeolite-templated carbon (ZTC) into electrospun fibres and testing of the resulting composites for hydrogen storage. The hydrogen storage capacity of the composite fibres was 1...

  14. Monte-Carlo simulations of methane/carbon dioxide and ethane/carbon dioxide mixture adsorption in zeolites and comparison with matrix treatment of statistical mechanical lattice model

    Science.gov (United States)

    Dunne, Lawrence J.; Furgani, Akrem; Jalili, Sayed; Manos, George

    2009-05-01

    Adsorption isotherms have been computed by Monte-Carlo simulation for methane/carbon dioxide and ethane/carbon dioxide mixtures adsorbed in the zeolite silicalite. These isotherms show remarkable differences with the ethane/carbon dioxide mixtures displaying strong adsorption preference reversal at high coverage. To explain the differences in the Monte-Carlo mixture isotherms an exact matrix calculation of the statistical mechanics of a lattice model of mixture adsorption in zeolites has been made. The lattice model reproduces the essential features of the Monte-Carlo isotherms, enabling us to understand the differing adsorption behaviour of methane/carbon dioxide and ethane/carbon dioxide mixtures in zeolites.

  15. FTIR study of carbon monoxide adsorption on ion-exchanged X, Y and mordenite type zeolites

    Directory of Open Access Journals (Sweden)

    R. HERCIGONJA

    2003-05-01

    Full Text Available In this work Fourier transform infrared (FTIR study has been applied to study the adsorption of carbon monoxide on transition metal (Mn+, Co2+, Ni2+ ion-exchanged zeolites type Y, X and mordenites. The adsorption of CO at room temperature produces overlapping IR absorption bands in the 2120–2200 cm-1 region. The frequency of the band around 2200 cm-1 is found to be dependent not only on the charge-balancing transition metal cation, but also on the framework composition. The frequencies of the band near 1600 cm-1 was found to be dependent on the Si/Al ratio of the investigated zeolites.

  16. Imprinted zeolite modified carbon paste electrode as a potentiometric sensor for uric acid

    Science.gov (United States)

    Khasanah, Miratul; Widati, Alfa Akustia; Fitri, Sarita Aulia

    2016-03-01

    Imprinted zeolite modified carbon paste electrode (carbon paste-IZ) has been developed and applied to determine uric acid by potentiometry. The imprinted zeolite (IZ) was synthesized by the mole ratio of uric acid/Si of 0.0306. The modified electrode was manufactured by mass ratio of carbon, IZ and solid paraffin was 40:25:35. The modified electrode had shown the measurement range of 10-5 M to 10-2 M with Nernst factor of 28.6 mV/decade, the detection limit of 5.86 × 10-6 M and the accuracy of 95.3 - 105.0%. Response time of the electrode for uric acid 10-5 M - 10-2 M was 25 - 44 s. The developed electrode showed the high selectivity toward uric acid in the urea matrix. Life time of the carbon paste-IZ electrode was 10 weeks.

  17. Adsorption separation of carbon dioxide, methane and nitrogen on monoethanol amine modified β-zeolite

    Institute of Scientific and Technical Information of China (English)

    Xiaoliang Xu; Xingxiang Zhao; Linbing Sun; Xiaoqin Liu

    2009-01-01

    A new type of composite adsorbents was synthesized by incorporating monoethanol amine (MEA) into β-zeolite. The parent and MEA-functionalized β-zeolites were characterized by X-ray diffraction (XRD), N2 adsorption, and thermogravimetric analysis (TGA). The adsorp-tion behavior of carbon dioxide (CO2), methane (CH4), and nitrogen (N2) on these adsorbents was investigated at 303 K. The results show that the structure of zeolite was well preserved after MEA modification. In comparison with CH4 and N2, CO2 was preferentially adsorbed on the adsorbents investigated. The introduction of MEA significantly improved the selectivity of both CO2/CH4 and CO2/N2, the optimal selectivity of CO2/CH4 can reach 7.70 on 40 wt% of MEA-functionalized β-zeolite (MEA(40)-β) at 1 atm. It is worth noticing that a very high selectivity of CO2/N2 of 25.67 was obtained on MEA(40)-β. Steric effect and chemical adsorbate-adsorbent interaction were responsible for such high adsorption selectivity of CO2. The present MEA-functionalized β-zeolite adsorbents may be a good candidate for applications in flue gas separation, as well as natural gas and landfill gas purifications.

  18. Controlling the Cross-Sensitivity of Carbon Nanotube-Based Gas Sensors to Water Using Zeolites.

    Science.gov (United States)

    Evans, Gwyn P; Buckley, David J; Adedigba, Abdul-Lateef; Sankar, Gopinathan; Skipper, Neal T; Parkin, Ivan P

    2016-10-05

    Carbon nanotube-based gas sensors can be used to detect harmful environmental pollutants such as NO2 at room temperature. Although they show promise as low-powered, sensitive, and affordable monitoring devices, cross-sensitivity of functionalized carbon nanotubes to water vapor often obscures the detection of target molecules. This is a barrier to adoption for monitoring of airborne pollutants because of the varying humidity levels found in real world environments. Zeolites, also known as molecular sieves because of their selective adsorption properties, are used in this work to control the cross-sensitivity of single-walled carbon nanotube (SWCNT)-based sensors to water vapor. Zeolites incorporated into the sensing layer are found to reduce interference effects that would otherwise obscure the identification of NO2 gas, permitting repeatable detection over a range of relative humidities. This significant improvement is found to depend on the arrangement of the SWCNT-zeolite layers in the sensing device, as well as the hydrophilicity of the chosen zeolite.

  19. A comparison of hydrogen storage capacity of commercial and fly ash-derived zeolite X together with their respective templated carbon derivatives

    CSIR Research Space (South Africa)

    Musyoka, Nicholas M

    2015-10-01

    Full Text Available –6]. Among the many studied porous materials (such as zeolites, metal organic frameworks (MOFs), activated carbons etc.), templated carbons have been identified and ear-marked as having attractive properties for hydrogen storage [11–15]. Templated carbons... diffraction pattern (SAED) is indicative of scattering from an amorphous material meaning that, unlike the parent zeolite, the templated carbon derivative was amorphous in nature. elsevier_HE_16341 Comparing the XRD pattern of fly ash-derived zeolite X...

  20. Controllable cyanation of carbon-hydrogen bonds by zeolite crystals over manganese oxide catalyst

    Science.gov (United States)

    Wang, Liang; Wang, Guoxiong; Zhang, Jian; Bian, Chaoqun; Meng, Xiangju; Xiao, Feng-Shou

    2017-05-01

    The synthesis of organic nitriles without using toxic cyanides is in great demand but challenging to make. Here we report an environmentally benign and cost-efficient synthesis of nitriles from the direct oxidative cyanation of primary carbon-hydrogen bonds with easily available molecular oxygen and urea. The key to this success is to design and synthesize manganese oxide catalysts fixed inside zeolite crystals, forming a manganese oxide catalyst with zeolite sheath (MnOx@S-1), which exhibits high selectivity for producing nitriles by efficiently facilitating the oxidative cyanation reaction and hindering the side hydration reaction. The work delineates a sustainable strategy for synthesizing nitriles while avoiding conventional toxic cyanide, which might open a new avenue for selective transformation of carbon-hydrogen bonds.

  1. The study of dehumidifying of carbon monoxide and ammonia adsorption by Iranian natural clinoptilolite zeolite

    Science.gov (United States)

    Tehrani, R. M. A.; Salari, A. A.

    2005-10-01

    The natural zeolite (clinoptilolite type) was obtained from the Neibagh region of Mianeh, the city in the west of Iran. The raw zeolite was tested for quality and quantity measurements including surface area and volumetric characteristics as well as thermogravimetry analysis. The acid activation process was used to increase the adsorption rate of zeolite and in order to obtain the optimum conditions: the effect of acid concentration, reaction time and the temperature were studied. A surface area measurement test was performed in each stage to get the best results. Thus, efficient condition was selected according to the produced highest surface area. The reaction was first obtained with hydrochloric acid, and then a comparison was made using the sulfuric acid. The hydrochloric reaction proved to be better. The result of activation was 2.5 times the increase in the surface area in relation to the raw sample. The result of elemental analysis conducted once again on the activated sample showed an increase in the ratio of Si/Al (approximately 0.6). Then, using CO, NH 3 and steam, the gas adsorption capacity of both the raw and activated samples was measured and compared. Since CO was not adsorbed at ambient temperature, but steam was adsorbed relatively well, the natural clinoptilolite zeolite of Iran was suggested as a suitable material for adsorbing humidity form carbon monoxide as well as synthesis gas (H 2 and CO mixture).

  2. Immobilizing of catalyst using Bayah's natural zeolite to reduce the chemical oxygen demand (COD) and total organic carbon (TOC)

    Science.gov (United States)

    Jayanudin, Kustiningsih, Indar; Sari, Denni Kartika

    2017-05-01

    Indonesia is rich of natural minerals, many of which had not been widely used. One potential natural mineral is zeolite from Bayah Banten that can be used to support catalyst in the process of waste degradation. The purpose of this research is to characterize the Bayah's zeolite and to figure out the effectiveness of the zeolite as supporting agent to the Fe catalyst in the process of phenol degradation, with the main purposes are to reduce the Chemical Oxygen Demand (COD) and Total Organic Carbon (TOC). This research consists of three steps, activation of natural zeolite using 1M, 2M, and 3M NaOH solution, impregnation process with 0.025M, 0.05 M and 0.075M Fe(NO3)3.9H2O solution, and calcination at 500°C. Bayah's natural zeolite was characterize using Brauner-Emmet-Teller (BET) for its pore area, X-ray Fluorescence (XRF) for analyzing zeolite's component before and after activation process and after impregnation process, and Scanning Electron Microscope (SEM) for analyzing zeolite's morphology. The result showed that the highest pore area was 9Å, Fe metal from Fe(NO3)3.9H2O 0,075 M solution remained in zeolite pore was 7,73%, the reduction of COD and TOC was yielded at H2O2: phenol ratio of 1 : 6.

  3. Carbon dioxide and methane transport in DDR zeolite: insights from molecular simulations into carbon dioxide separations in small pore zeolites

    Science.gov (United States)

    Jee, Sang Eun; Sholl, David

    2009-03-01

    Zeolites are good candidates as a membranes for chemical separations because of their excellent chemical and thermal stability. Cage type zeolites are promising materials for gas separation since their narrow windows are expected to control molecular transport. DDR is one of the strongest candidates for light gas separations because of its narrow 8MR window. In our study, we examined the separation selectivity of DDR for CO2/CH4 separation using atomistic simulation methods. We introduced new force fields which can reproduce experimental single component adsorption and diffusion data for this material for the first time. Previously interatomic potentials that have been applied to DDR overestimate experimental diffusivities at least one order of magnitude. We characterized single-component and binary adsorption using Grand Canonical Monte Carlo, and single-component. diffusion using a combination of Molecular Dynamics and Transition State Theory. The most important observation from our calculation is that CO2/CH4 diffusion in DDR is very different from the usual situation in nanoporous materials, where the presence of a slowly diffusing species retards transport rates of a more rapidly diffusing species. In DDR, we show that CO2 diffusion rates are only weakly affected by the presence of CH4, despite the very slow diffusion of the latter species. The physical origins of this unusual behavior are explained by analyzing the adsorption sites and diffusion mechanism for each species.

  4. From zeolite nets to sp(3) carbon allotropes: a topology-based multiscale theoretical study.

    Science.gov (United States)

    Baburin, Igor A; Proserpio, Davide M; Saleev, Vladimir A; Shipilova, Alexandra V

    2015-01-14

    We present a comprehensive computational study of sp(3)-carbon allotropes based on the topologies proposed for zeolites. From ≈600,000 zeolite nets we identified six new allotropes, lying by at most 0.12 eV per atom above diamond. The analysis of cages in the allotropes has revealed close structural relations to diamond and lonsdaleite phases. Besides the energetic and mechanical stability of new allotropes, three of them show band gaps by ca. 1 eV larger than that of diamond, and therefore represent an interesting technological target as hard and transparent materials. A structural relation of new allotropes to continuous random networks is pointed out and possible engineering from diamond thin films and graphene is suggested.

  5. Carbon dioxide selective adsorption within a highly stable mixed-ligand Zeolitic Imidazolate Framework

    KAUST Repository

    Huang, Lin

    2014-08-01

    A new mixed-ligand Zeolitic Imidazolate Framework Zn4(2-mbIm) 3(bIm)5·4H2O (named JUC-160, 2-mbIm = 2-methylbenzimidazole, bIm = benzimidazole and JUC = Jilin University China) was synthesized with a solvothermal reaction of Zn(NO3) 2·6H2O, bIm and 2-mbIm in DMF solution at 180 °C. Topological analysis indicated that JUC-160 has a zeolite GIS (gismondine) topology. Study of the gas adsorption and thermal and chemical stability of JUC-160 demonstrated its selective adsorption property for carbon dioxide, high thermal stability, and remarkable chemical resistance to boiling alkaline water and organic solvent for up to one week. © 2014 Elsevier B.V.

  6. Heterogeneous Catalysts for VOC Oxidation from Red Mud and Bagasse Ash Carbon

    Science.gov (United States)

    Pande, Gaurav

    A range of VOC oxidation catalysts have been prepared in this study from agricultural and industrial waste as the starting point. The aim is to prepare catalysts with non-noble metal oxides as the active catalytic component (iron in red mud). The same active component was also supported on activated carbon obtained from unburned carbon in bagasse ash. Red mud which is an aluminum industry waste and rich in different phases of iron as oxide and hydroxide is used as the source for the catalytically active species. It is our aim to enhance the catalytic performance of red mud which though high in iron concentration has a low surface area and may not have the properties of an ideal catalyst by itself. In one of the attempts to enhance the catalytic performance, we have tried to leach red mud for which we have explored a range of leaching acids for effecting the leaching most efficiently and then precipitated the iron from the leachate as its hydroxide by precipitating with alkali solution followed by drying and calcination to give high surface area metal oxide material. Extensive surface characterization and VOC oxidation catalytic testing were performed for these solids. In a step to further enhance the catalytic activity towards oxidation, copper was introduced by taking another industrial waste from the copper tubing industry viz. the pickling acid. Copper has a more favourable redox potential making it catalytically more effective than iron. To make the mixed metal oxide, red mud leachate was mixed with the pickling acid in a pre-decided ratio before precipitating with alkali solution followed by drying and calcination as was done with the red mud leachate. The results from these experiments are encouraging. The temperature programmed reduction (TPR) of the solids show that the precipitate of red mud leachates show hydrogen uptake peak at a lower temperature than for just the calcined red mud. This could be due to the greatly enhanced surface area of the prepared

  7. Adsorption and photocatalytic degradation of pharmaceuticals and pesticides by carbon doped-TiO2 coated on zeolites under solar light irradiation.

    Science.gov (United States)

    An, Ye; de Ridder, David Johannes; Zhao, Chun; Schoutteten, Klaas; Bussche, Julie Vanden; Zheng, Huaili; Chen, Gang; Vanhaecke, Lynn

    2016-01-01

    To evaluate the performance of zeolite-supported carbon-doped TiO(2) composite catalysts toward target pollutants under solar light irradiation, the adsorption and photocatalytic degradation of 18 pharmaceuticals and pesticides with distinguishing features (molecular size and volume, and photolysis) were investigated using mordenite zeolites with SiO(2)/Al(2)O(3) ratios of 18 and 240. Different quantities of carbon-doped TiO(2) were coated on the zeolites, and then the finished composite catalysts were tested in demineralized, surface, and hospital wastewater samples, respectively. The composite photocatalysts were characterized by X-ray diffraction, field emission scanning electron microscopy, and surface area and porosity analyses. Results showed that a dispersed layer of carbon-doped TiO(2) is formed on the zeolite surface; this layer blocks the micropores of zeolites and reduces their surface area. However, these reductions did not significantly affect adsorption onto the zeolites. Our results demonstrated that zeolite-supported carbon-doped TiO(2) systems can effectively degrade 18 pharmaceuticals and pesticides in demineralized water under natural and simulated solar light irradiation. In surface and hospital wastewaters, zeolite-supported carbon-doped TiO(2) systems present excellent anti-interference capability against radical scavengers and competitive organics for pollutants removal, and higher pollutants adsorption on zeolites evidently enhances the removal rate of target pollutants in surface and hospital wastewater samples with a complicated matrix.

  8. Glycerol Dehydration to Acrolein Catalyzed by ZSM‐5 Zeolite in Supercritical Carbon Dioxide Medium

    Science.gov (United States)

    Zou, Bin; Ren, Shoujie

    2016-01-01

    Abstract Supercritical carbon dioxide (SC‐CO2) has been used for the first time as a reaction medium for the dehydration of glycerol to acrolein catalyzed by a solid acid. Unprecedented catalyst stability over 528 hours of time‐on‐stream was achieved and the rate of coke deposition on the zeolite catalyst was the lowest among extensive previous studies, showing potential for industrial application. Coking pathways in SC‐CO2 were also elucidated for future development. The results have potential implications for other dehydration reactions catalyzed by solid acids. PMID:27796088

  9. Tailoring the Surface Chemistry of Zeolite Templated Carbon by Electrochemical Methods

    Directory of Open Access Journals (Sweden)

    R. Berenguer

    2013-01-01

    Full Text Available One option to optimize carbon materials forsupercapacitor applications is the generation ofsurface functional groups that contribute to thepseudocapacitance without losing the designedphysical properties. This requires suitablefunctionalization techniques able to selectivelyintroduce a given amount of electroactive oxygengroups. In this work, the influence of the chemical andelectrochemical oxidation methods, on the chemicaland physical properties of a zeolite templated carbon(ZTC, as a model carbon material, have beenstudied and compared. Although both oxidationmethods generally produce a loss of the originalZTC physical properties with increasing amount ofoxidation, the electrochemical method shows muchbetter controllability and, unlike chemical treatments,enables the generation of a large number of oxygengroups (O = 11000- 3300 μmol/g, with a higherproportion of active functionalities, while retaining ahigh surface area (ranging between 1900-3500 m2/g,a high microporosity and an ordered 3-D structure.

  10. Method of producing zeolite encapsulated nanoparticles

    DEFF Research Database (Denmark)

    2015-01-01

    nanoparticles on the surface of the silica or alumina source; 3) Passing a gaseous hydrocarbon, alkyl alcohol or alkyl ether over the silica or alumina supported metal nanoparticles to form a carbon template coated zeolite, zeolite-like or zeotype precursor composition; 4a) Adding a structure directing agent...... to the carbon template coated zeolite, zeolite-like or zeotype precursor composition thereby creating a zeolite, zeolite-like or zeotype gel composition; 4b) Crystallising the zeolite, zeolite-like or zeotype gel composition by subjecting said composition to a hydrothermal treatment; 5) Removing the carbon...

  11. Method for producing zeolites and zeotypes

    DEFF Research Database (Denmark)

    2015-01-01

    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...

  12. A zeolite modified carbon paste electrode as useful sensor for voltammetric determination of acetaminophen

    Energy Technology Data Exchange (ETDEWEB)

    Ahmadpour-Mobarakeh, Leila; Nezamzadeh-Ejhieh, Alireza, E-mail: arnezamzadeh@iaush.ac.ir

    2015-04-01

    The voltammetric behavior of a carbon paste electrode modified with Co(II)-exchanged zeolite A (Co(II)-A/ZMCPE) for determination of acetaminophen was studied. The proposed electrode showed a diffusion controlled reaction with the electron transfer rate constant (K{sub s}) of 0.44 s{sup −1} and charge transfer coefficient of 0.73 in the absence of acetaminophen. A linear voltammetric response was obtained in the range of 0.1 to 190 μmol L{sup −1} of acetaminophen [r{sup 2} = 0.9979, r = 0.9989 (n = 10)] with a detection limit of 0.04 μmol L{sup −1}. The method was successfully applied to the analysis of acetaminophen in some drugs. - Highlights: • Modified carbon paste electrode with Co(II)-zeolite A improved the voltammetric current in determination of acetaminophen. • Modified electrode is applicable for acetaminophen in real samples. • The proposed method has good reproducibility and repeatability.

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

    Science.gov (United States)

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

  14. Catalyst screening for the VOC decomposition using adsorption and oxygen plasma

    Energy Technology Data Exchange (ETDEWEB)

    Kim, H.H.; Ogata, A. [National Inst. of Advanced Industrial Science and Technology, Tokyo (Japan)

    2010-07-01

    Emissions of volatile organic compounds (VOCs) are directly related to the formation of photochemical smog and the secondary aerosol formation, particularly in urban areas. As such, VOC pollution control is a high priority in air quality management. Non-thermal plasmas (NTPs) have been considered for the abatement of VOCs, but 3 key factors must be addressed, notably improve the energy efficiency, have less NOx formation and acceptable material balance. A recent trend in the use of NTP for air pollution control is the combination of NTP with a catalyst. This combined process is subdivided into single-stage and two-stage depending on the position of the catalyst. Ozone-assisted catalysis is the two-stage system. This study focused on the decomposition of VOCs using a single-stage plasma-driven catalysis (PDC) system, and demonstrated the effectiveness of the PDC in terms of energy efficiency, product selectivity and carbon balance. The PDC reactor has a strong dependence on the oxygen content in the oxidation of VOCs. The potentials of various catalysts for cycled system were evaluated in terms of adsorption capability of VOC and enhancement factor (EF). The study focused on zeolites with a large surface area. Nanometer-sized active metals were also loaded on the zeolite surfaces, and their catalytic activity was tested. The metal nanoparticles supported on zeolites enhanced the catalytic activities considerably. ICCD camera observation of the discharge plasma on the surface of catalyst provided an important insight into the understanding of discharge plasma and catalyst. The area of discharge plasma expanded over a wide range by the metal nanoparticles. This physical influence was found to be closely related to the enhanced performance of the plasma-driven catalyst process. 15 refs., 5 figs.

  15. Selectivity of Chemoresistive Sensors Made of Chemically Functionalized Carbon Nanotube Random Networks for Volatile Organic Compounds (VOC

    Directory of Open Access Journals (Sweden)

    Jean-François Feller

    2014-01-01

    Full Text Available Different grades of chemically functionalized carbon nanotubes (CNT have been processed by spraying layer-by-layer (sLbL to obtain an array of chemoresistive transducers for volatile organic compound (VOC detection. The sLbL process led to random networks of CNT less conductive, but more sensitive to vapors than filtration under vacuum (bucky papers. Shorter CNT were also found to be more sensitive due to the less entangled and more easily disconnectable conducting networks they are making. Chemical functionalization of the CNT’ surface is changing their selectivity towards VOC, which makes it possible to easily discriminate methanol, chloroform and tetrahydrofuran (THF from toluene vapors after the assembly of CNT transducers into an array to make an e-nose. Interestingly, the amplitude of the CNT transducers’ responses can be enhanced by a factor of five (methanol to 100 (chloroform by dispersing them into a polymer matrix, such as poly(styrene (PS, poly(carbonate (PC or poly(methyl methacrylate (PMMA. COOH functionalization of CNT was found to penalize their dispersion in polymers and to decrease the sensors’ sensitivity. The resulting conductive polymer nanocomposites (CPCs not only allow for a more easy tuning of the sensors’ selectivity by changing the chemical nature of the matrix, but they also allow them to adjust their sensitivity by changing the average gap between CNT (acting on quantum tunneling in the CNT network. Quantum resistive sensors (QRSs appear promising for environmental monitoring and anticipated disease diagnostics that are both based on VOC analysis.

  16. Single-walled Carbon Nanotubes Regularly Aligned in Channels of Zeolite Single Crystal

    Institute of Scientific and Technical Information of China (English)

    Zi Kang Tang; Handong Sun; Jiannong Wang

    2000-01-01

    @@ We report the synthesis of single-wall carbon nanotubes (SWCNs) formed in 1-nm-sized channels of zeolite crystal by pyrolysis of tripropylamine molecules. The SWCNs are mono-sized and parallelly aligned along the crystal direction. In the present paper, we report the polarized Raman spectra measured for the wellaligned SWCNs, which gives us information about structural symmetry. Electrical transport properties of the SWNTs are measured in the temperature range of 0.3 K ~ 300 K. The conductivity of the SWCNs is monotonically decreased with decreasing temperature. The observed temperature dependence of zero-field conductance, In(σ) ~ 1/√T, could be explained well in terms of electron localization caused by imperfections and impurities in the nanotubes.

  17. A zeolite modified carbon paste electrode as useful sensor for voltammetric determination of acetaminophen.

    Science.gov (United States)

    Ahmadpour-Mobarakeh, Leila; Nezamzadeh-Ejhieh, Alireza

    2015-04-01

    The voltammetric behavior of a carbon paste electrode modified with Co(II)-exchanged zeolite A (Co(II)-A/ZMCPE) for determination of acetaminophen was studied. The proposed electrode showed a diffusion controlled reaction with the electron transfer rate constant (Ks) of 0.44s(-1) and charge transfer coefficient of 0.73 in the absence of acetaminophen. A linear voltammetric response was obtained in the range of 0.1 to 190μmolL(-1) of acetaminophen [r(2)=0.9979, r=0.9989 (n=10)] with a detection limit of 0.04μmolL(-1). The method was successfully applied to the analysis of acetaminophen in some drugs.

  18. Adsorption of carbon monoxide on H-FAU and Li-FAU zeolites: an embedded cluster approach

    Science.gov (United States)

    Limtrakul, J.; Jungsuttiwong, S.; Khongpracha, P.

    2000-07-01

    The interaction of carbon monoxide with H-faujasite (H-FAU) and metal-exchange Li-FAU zeolites has been investigated by means of cluster and embedded cluster approaches at the HF/6-31G(d,p) level of theory. In the case of the protonated zeolite, the adsorption energy of the bare quantum cluster is evaluated to be -1.90 kcal/mol for the H-FAU/CO complex. Inclusion of the Madelung potential field from the zeolite framework has an effect of lengthening the OH distance, hence enhancing the binding energies of the H-FAU/CO (-3.20 kcal/mol). For adsorption of CO on the metal-exchanged zeolites, the Madelung potential was found to differentiate the different types of zeolites (ZSM-5 and FAU), that cannot be drawn from the typical 3T-quantum cluster. This finding clearly demonstrates that acidity does not depend only on the Brønsted group center, but also on the dimension of the channel where the Brønsted group is located. The adsorption energy of the embedded cluster model (-6.69 kcal/mol) lies between those of the bare quantum cluster model (-5.81 kcal/mol) and the simple naked Li(I)/CO system (-13.14 kcal/mol). Correction of the 3T cluster model to take into account the long range contribution of the electrostatic potential of the zeolite crystal is found to agree with the experimental observation.

  19. Recovery of manganese oxides from spent alkaline and zinc–carbon batteries. An application as catalysts for VOCs elimination

    Energy Technology Data Exchange (ETDEWEB)

    Gallegos, María V., E-mail: plapimu@yahoo.com.ar [Pla.Pi.Mu-Planta Piloto Multipropósito, (CICPBA-UNLP) Cno. Centenario y 505, M.B. Gonnet, Buenos Aires (Argentina); Falco, Lorena R., E-mail: mlfalco@quimica.unlp.edu.ar [Pla.Pi.Mu-Planta Piloto Multipropósito, (CICPBA-UNLP) Cno. Centenario y 505, M.B. Gonnet, Buenos Aires (Argentina); Peluso, Miguel A., E-mail: apelu@quimica.unlp.edu.ar [Centro de Investigación y Desarrollo en Ciencias Aplicadas, “Dr. J. Ronco” CINDECA (CONICET CCT La Plata), 47 N°257, La Plata, Buenos Aires (Argentina); Sambeth, Jorge E., E-mail: sambeth@quimica.unlp.edu.ar [Centro de Investigación y Desarrollo en Ciencias Aplicadas, “Dr. J. Ronco” CINDECA (CONICET CCT La Plata), 47 N°257, La Plata, Buenos Aires (Argentina); Thomas, Horacio J. [Pla.Pi.Mu-Planta Piloto Multipropósito, (CICPBA-UNLP) Cno. Centenario y 505, M.B. Gonnet, Buenos Aires (Argentina)

    2013-06-15

    Highlights: • Manganese oxides were synthesized using spent batteries as raw materials. • Spent alkaline and zinc–carbon size AA batteries were used. • A biohydrometallurgical process was employed to bio-lixiviate batteries. • Manganese oxides were active in the oxidation of VOCs (ethanol and heptane). - Abstract: Manganese, in the form of oxide, was recovered from spent alkaline and zinc–carbon batteries employing a biohydrometallurgy process, using a pilot plant consisting in: an air-lift bioreactor (containing an acid-reducing medium produced by an Acidithiobacillus thiooxidans bacteria immobilized on elemental sulfur); a leaching reactor (were battery powder is mixed with the acid-reducing medium) and a recovery reactor. Two different manganese oxides were recovered from the leachate liquor: one of them by electrolysis (EMO) and the other by a chemical precipitation with KMnO{sub 4} solution (CMO). The non-leached solid residue was also studied (RMO). The solids were compared with a MnO{sub x} synthesized in our laboratory. The characterization by XRD, FTIR and XPS reveal the presence of Mn{sub 2}O{sub 3} in the EMO and the CMO samples, together with some Mn{sup 4+} cations. In the solid not extracted by acidic leaching (RMO) the main phase detected was Mn{sub 3}O{sub 4}. The catalytic performance of the oxides was studied in the complete oxidation of ethanol and heptane. Complete conversion of ethanol occurs at 200 °C, while heptane requires more than 400 °C. The CMO has the highest oxide selectivity to CO{sub 2}. The results show that manganese oxides obtained using spent alkaline and zinc–carbon batteries as raw materials, have an interesting performance as catalysts for elimination of VOCs.

  20. Hydrogenation of carbon monoxide over mixed catalysts. Co-Ni/MnO-ZrO sub 2 to zeolite kara naru kongo shokubai wo mochiita issankatanso no suisoka

    Energy Technology Data Exchange (ETDEWEB)

    Ishihara, T.; Iwakuni, H.; Eguchi, K.; Arai, H. (Graduate School of Engineering Sciences, Kyushu Univ., Fukuoka (Japan). Department of Materials Science and Technology)

    1990-07-10

    The mechanical mixtures of Co-Ni/MnO-ZrO {sub 2} and zeolite were used as catalysts for the selective synthesis of gasoline by CO hydrogenation. Formation of branched-paraffins was promoted but that of higher hydrocarbons than carbon number of 10 was suppressed by combination with zeolite. The product distribution strongly depended on the type of zeolite catalyst. Pentasil zeolite was active for the formation of branched-paraffins, probably because of the cracking reaction occurring on the strong acid sites. The formation of branched paraffin was further promoted by ion-exchange with Pt. The mixture of Co-Ni/MnO-ZrO {sub 2} and PtH-pentasil zeolite was very active for the formation of gasoline with high octane number. 34 refs., 10 figs., 2 tabs.

  1. Investigations of the ratios of stable carbon isotopes in atmospheric relevant VOC using simulation and field experiments; Untersuchungen der Verhaeltnisse stabiler Kohlenstoffisotope in atmosphaerisch relevanten VOC in Simulations- und Feldexperimenten

    Energy Technology Data Exchange (ETDEWEB)

    Spahn, Holger

    2010-07-01

    Volatile organic compounds (VOC) play an important role in the regional and global atmospheric chemistry. The author of the contribution under consideration reports on the analysis of the ratios of stable carbon isotopes ({delta}({sup 13}C) analysis) in atmospheric VOCs. At first, the state of the art of this analytical technique is described. For the first time {delta}({sup 13}C) values of different monoterpenes have been determined in the investigation of vegetable emissions at a plant chamber. By means of the oxidation of {beta}-pinene by ozone in an aerosol chamber, the kinetic isotope effect of this reaction was determined. In southern Germany, air samples for the {delta}({sup 13}C) analysis were collected using a zeppelin. This enables a height-resolved measurement of {delta}({sup 13}C) values. Based on these measurements, the average photochemical age for methanol, toluene and p-xylene at different heights was calculated.

  2. Removal of Volatile Organic Contaminants (VOCs) from the Groundwater Sources of Drinking Water via Granular Activated Carbon Treatment (WaterRF Report 4440)

    Science.gov (United States)

    The overall goal of this project was to assess the feasibility of granular activated carbon (GAC) for the treatment of selected carcinogenic volatile organic compounds (cVOC) to sub-μg/L levels. The project consisted of three tasks. The task objectives are: Task I - determine c...

  3. Hydrogenation of carbon monoxide over the mixed catalysts composed of cobalt-nickel/manganese oxide-zirconium oxide and zeolite catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Ishihara, Tatsumi; Iwakuni, Hideharu; Eguchi, Koichi; Arai, Hiromichi (Kyushu Univ., Fukuoka (Japan))

    1991-08-15

    Mechanical mixtures of Co-Ni/MnO-ZrO2 and zeolite were used as catalysts for the selective synthesis of gasoline by carbon monoxide hydrogenation. Formation of branched alkanes was promoted, but that of hydrocarbons higher than a carbon number of 10 was suppressed by a combination with zeolite. The reactivity of zeolite for higher hydrocarbons has the decisive role in the product distribution as result of using these mixed catalysts, and thus the product distribution strongly depends on the type of zeolite. Since the hydrogenolysis of higher hydrocarbons proceeds on the strong acid sites, the formation of branched alkanes was promoted by increasing the aluminium content in the zeolite. Ammonia temperature-programmed desorption suggests that increasing the aluminium content in the zeolite increases the number of strong acid sites, but weakens the average strength of the acid sites. Pentasil zeolite with an aluminium content of 1.32 mmolg{sup -1} is effective for enhancing the yield of gasoline as well as its octane number. 8 figs., 1 tab., 20 refs.

  4. Carbon dioxide capture utilizing zeolites synthesized with paper sludge and scrap-glass.

    Science.gov (United States)

    Espejel-Ayala, F; Corella, R Chora; Pérez, A Morales; Pérez-Hernández, R; Ramírez-Zamora, R M

    2014-12-01

    The present work introduces the study of the CO2 capture process by zeolites synthesized from paper sludge and scrap glass. Zeolites ZSM-5, analcime and wairakite were produced by means of two types of Structure Directing Agents (SDA): tetrapropilamonium (TPA) and ethanol. On the one hand, zeolite ZSM-5 was synthesized using TPA; on the other hand, analcime and wairakite were produced with ethanol. The temperature programmed desorption (TPD) technique was performed for determining the CO2 sorption capacity of these zeolites at two sorption temperatures: 50 and 100 °C. CO2 sorption capacity of zeolite ZSM-5 synthesized at 50 °C was 0.683 mmol/g representing 38.2% of the value measured for a zeolite ZSM-5 commercial. Zeolite analcime showed a higher CO2 sorption capacity (1.698 mmol/g) at 50 °C and its regeneration temperature was relatively low. Zeolites synthesized in this study can be used in the purification of biogas and this will produce energy without increasing the atmospheric CO2 concentrations.

  5. Electrocatalytic behavior of modified carbon paste electrode with Ni(ii-zeolite for oxidation of methanol in a basic solution

    Directory of Open Access Journals (Sweden)

    Maryam Abrishamkar

    2014-12-01

    Full Text Available In this research, the electrochemical behavior of Ni-zeolite modified carbon paste electrode in the form of Ni/NiZSM-5/CPE and unmodified carbon paste electrode were studied using cyclic voltammetry and chronoamperometric techniques. It was found that methanol was oxidized by NiOOH generated with further electrooxidation of Ni ions which were doped in modified electrode during the anodic sweep. Also, the rate constant for the catalytic reaction (K of methanol was calculated 2.64* 10⁵cm³s⁻¹mol⁻¹ via Cottrell equation.

  6. Electrocatalytic behavior of modified carbon paste electrode with Ni(ii)-zeolite for oxidation of methanol in a basic solution

    OpenAIRE

    Maryam Abrishamkar; Nassrin Kiamehr

    2014-01-01

    In this research, the electrochemical behavior of Ni-zeolite modified carbon paste electrode in the form of Ni/NiZSM-5/CPE and unmodified carbon paste electrode were studied using cyclic voltammetry and chronoamperometric techniques. It was found that methanol was oxidized by NiOOH generated with further electrooxidation of Ni ions which were doped in modified electrode during the anodic sweep. Also, the rate constant for the catalytic reaction (K) of methanol was calculated 2.64* 10⁵cm³s⁻¹mo...

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

    Directory of Open Access Journals (Sweden)

    Ashraf Aly Hassan

    2012-01-01

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

  8. Hierarchical Zeolites with Amine-Functionalized Mesoporous Domains for Carbon Dioxide Capture.

    Science.gov (United States)

    Nguyen, Tien Hoa; Kim, Sungjune; Yoon, Minyoung; Bae, Tae-Hyun

    2016-03-08

    To prepare materials with high CO2 adsorption, a series of hierarchical LTA zeolites possessing various mesopore spaces that are decorated with alkylamines was designed and synthesized. The highest CO2 uptake capacity was achieved when (3-aminopropyl)trimethoxysilane (APTMS) was grafted onto the hierarchical LTA zeolite having the largest mesopores. Owing to the contributions of both alkylamine groups grafted onto the mesopore surfaces and active sites in the LTA zeolites, the amount of CO2 that can be taken up on these materials is much higher than for conventional aminosilicas such SBA-15 and MCM-41. Furthermore, the adsorbent shows good CO2 uptake capacity and recyclability in dynamic flow conditions.

  9. Stable Carbon Isotope Ratios in Atmospheric VOC across the Asian Summer Monsoon Anticyclone obtained during the OMO-ASIA campaign

    Science.gov (United States)

    Krebsbach, Marc; Koppmann, Ralf; Meisehen, Thomas

    2017-04-01

    The automated high volume air sampling system (MIRAH) has been deployed during the atmospheric measurement campaign OMO-ASIA (Oxidation Mechanism Observations) with the German High Altitude - Long-range research aircraft (HALO) in July and August 2015. The intensive measurement period with base stations in Paphos (Cyprus) and Gan (Maldives) focussed on oxidation processes and air pollution chemistry downwind of the South Asia summer monsoon anticyclone, a pivot area critical for air quality and climate change, both regionally and worldwide. The measurement region covered the Eastern Mediterranean region, the Arabian Peninsula, Egypt, and the Arabian Sea. In total 194 air samples were collected on 17 flights in a height region from 3 km up to 15 km. The air samples were analysed for stable carbon isotope ratios in VOC with GC-C-IRMS in the laboratory afterwards. We determined stable carbon isotope ratios and mixing ratios of several aldehydes, ketones, alcohols, and aromatics. The large extent of the investigated area allowed for encountering air masses with different origin, characteristic, and atmospheric processing, e.g. Mediterranean air masses, crossing of polluted filaments and remnants of the Asian monsoon outflow, split of the Asian monsoon anticyclone. In this presentation we will show first results and interpretations supported by HYSPLIT backward trajectories.

  10. Recovery of manganese oxides from spent alkaline and zinc-carbon batteries. An application as catalysts for VOCs elimination.

    Science.gov (United States)

    Gallegos, María V; Falco, Lorena R; Peluso, Miguel A; Sambeth, Jorge E; Thomas, Horacio J

    2013-06-01

    Manganese, in the form of oxide, was recovered from spent alkaline and zinc-carbon batteries employing a biohydrometallurgy process, using a pilot plant consisting in: an air-lift bioreactor (containing an acid-reducing medium produced by an Acidithiobacillus thiooxidans bacteria immobilized on elemental sulfur); a leaching reactor (were battery powder is mixed with the acid-reducing medium) and a recovery reactor. Two different manganese oxides were recovered from the leachate liquor: one of them by electrolysis (EMO) and the other by a chemical precipitation with KMnO4 solution (CMO). The non-leached solid residue was also studied (RMO). The solids were compared with a MnOx synthesized in our laboratory. The characterization by XRD, FTIR and XPS reveal the presence of Mn2O3 in the EMO and the CMO samples, together with some Mn(4+) cations. In the solid not extracted by acidic leaching (RMO) the main phase detected was Mn3O4. The catalytic performance of the oxides was studied in the complete oxidation of ethanol and heptane. Complete conversion of ethanol occurs at 200°C, while heptane requires more than 400°C. The CMO has the highest oxide selectivity to CO2. The results show that manganese oxides obtained using spent alkaline and zinc-carbon batteries as raw materials, have an interesting performance as catalysts for elimination of VOCs.

  11. Iron and activated carbon to remove the VOC; Fer et charbon actif pour eliminer les COV

    Energy Technology Data Exchange (ETDEWEB)

    Batra, V.S. [Institut des Ressources et de l' Energie, New Delhi (India); Lamonier, J.F. [Lille-1 Univ., UMR CNRS 8181, Unite de Catalyse et de Chimie du solide, 59 (France)

    2010-11-15

    This work proposes an adsorbent/catalyst material synthesized from sugarcane activated carbon and red muds coming from the aluminium industry. A low cost solution to treat the volatile organic compounds. (O.M.)

  12. Titanium-based zeolitic imidazolate framework for chemical fixation of carbon dioxide

    Data.gov (United States)

    U.S. Environmental Protection Agency — A titanium-based zeolitic imidazolate framework (Ti-ZIF) with high surface area and porous morphology has been synthesized and its application as a recyclable...

  13. A preconcentrator chip employing μ-SPME array coated with in-situ-synthesized carbon adsorbent film for VOCs analysis.

    Science.gov (United States)

    Wong, Ming-Yee; Cheng, Wei-Rui; Liu, Mao-Huang; Tian, Wei-Cheng; Lu, Chia-Jung

    2012-11-15

    We report the design, fabrication, and evaluation of a μ-preconcentrator chip that utilizes an array of solid-phase microextraction (SPME) needles coated with in-situ-grown carbon adsorbent film. The structure of the SPME needle (diameter=100 μm, height=250 μm) array inside the sampling chamber was fabricated using a deep reactive-ion etching (DRIE) process to enhance the attachable surface area for adsorbent film. Heaters and temperature sensors were fabricated onto the back of a μ-preconcentrator chip using lithography patterning and a metal lift-off process. The devices were sealed by anodic bonding and diced prior to the application of the adsorbent film. An adsorbent precursor, cellulose was dissolved in water and dynamically coated onto the SPME needle array. The coated cellulose film was converted into a porous carbon film via pyrolysis at 600 °C in a N(2) atmosphere. The surface area of the carbon adsorbent film was 308 m(2)/g, which is higher than that of a commercial adsorbent Carbopack X. A preconcentration factor as high as 13,637-fold was demonstrated using toluene. Eleven volatile organic compounds (VOCs) of different volatilities and functional groups were sampled and analyzed by GC-FID, and the desorption peak widths at half height were all less than 2.6 s after elution from a 15m capillary GC column. There was no sign of performance degradation after continuous operation for 50 cycles in air. Copyright © 2012 Elsevier B.V. All rights reserved.

  14. MHDA-Functionalized Multiwall Carbon Nanotubes for detecting non-aromatic VOCs

    Science.gov (United States)

    Thamri, Atef; Baccar, Hamdi; Struzzi, Claudia; Bittencourt, Carla; Abdelghani, Adnane; Llobet, Eduard

    2016-01-01

    The chemical modification of multiwalled carbon nanotubes (MWCNTs) with a long chain mercapto acid is reported as a way to improve sensitivity and response time of gas sensors for detecting alcohols, acetone and toxic gases such as DMMP. We have developed sensors employing MWCNTs decorated with gold nanoparticles and modified with a 16-mercaptohexadecanoic acid (MHDA) monolayer. Morphological and compositional analysis by Transmission Electron Microscopy (TEM), Fourier Transform Infra-red Spectroscopy (FTIR) and X-ray photoelectron spectroscopy were performed to characterize the gold nanoparticles and to check the bonding of the thiol monolayer. The detection of aromatic and non-aromatic volatiles and DMMP vapors by MWCNT/Au and MWCNT/Au/MHDA shows that the presence of the self-assembled layer increases sensitivity and selectivity towards non-aromatics. Furthermore, it ameliorates response dynamics, and significantly reduces nitrogen dioxide and moisture cross-sensitivity. PMID:27721503

  15. MHDA-Functionalized Multiwall Carbon Nanotubes for detecting non-aromatic VOCs

    Science.gov (United States)

    Thamri, Atef; Baccar, Hamdi; Struzzi, Claudia; Bittencourt, Carla; Abdelghani, Adnane; Llobet, Eduard

    2016-10-01

    The chemical modification of multiwalled carbon nanotubes (MWCNTs) with a long chain mercapto acid is reported as a way to improve sensitivity and response time of gas sensors for detecting alcohols, acetone and toxic gases such as DMMP. We have developed sensors employing MWCNTs decorated with gold nanoparticles and modified with a 16-mercaptohexadecanoic acid (MHDA) monolayer. Morphological and compositional analysis by Transmission Electron Microscopy (TEM), Fourier Transform Infra-red Spectroscopy (FTIR) and X-ray photoelectron spectroscopy were performed to characterize the gold nanoparticles and to check the bonding of the thiol monolayer. The detection of aromatic and non-aromatic volatiles and DMMP vapors by MWCNT/Au and MWCNT/Au/MHDA shows that the presence of the self-assembled layer increases sensitivity and selectivity towards non-aromatics. Furthermore, it ameliorates response dynamics, and significantly reduces nitrogen dioxide and moisture cross-sensitivity.

  16. Combination of powdered activated carbon and powdered zeolite for enhancing ammonium removal in micro-polluted raw water.

    Science.gov (United States)

    Liao, Zhen-Liang; Chen, Hao; Zhu, Bai-Rong; Li, Huai-Zheng

    2015-09-01

    Even zeolite is promising in ammonia pollution disposing, its removal efficiency is frequently interfered by organics. As activated carbon has good removal efficiency on organic contaminants, combination of two adsorbents may allow their respective adsorption characteristics into full play. This paper provides a performance assessment of the combination for enhancing ammonium removal in micro-polluted raw water. Gel-filtration chromatography (GFC) was carried out to quantify the molecular weight (MW) range of organic contaminants that powdered activated carbon (PAC) and powdered zeolite (PZ) can remove. The polydispersity difference which also calculated from GFC may indicate the wider organic contaminants removal range of PAC and the relatively centralized removal range of PZ. The jar tests of combination dosing confirm a synergistic effect which promotes ammonium removing. Nevertheless, it also shows an antagonism hindering the due removal performance of the two adsorbents on CODMn, while it is not much evident on UV254. Furthermore, a comparison study with simulated coagulation-sedimentation process was conducted to evaluate the optimum dosing points (spatial and temporal) of PAC and PZ among follows: suction well, pipeline mixer, early and middle phase of flocculation. We suggest to dose both two adsorbents into the early phase of flocculation to maximize the versatile removal efficiency on turbidity, ammonium and organic contaminants. Copyright © 2015 Elsevier Ltd. All rights reserved.

  17. Tracing groundwater with low-level detections of halogenated VOCs in a fractured carbonate-rock aquifer, Leetown Science Center, West Virginia, USA

    Science.gov (United States)

    Plummer, L. Niel; Sibrell, Philip L.; Casile, Gerolamo C.; Busenberg, Eurybiades; Hunt, Andrew G.; Schlosser, Peter

    2013-01-01

    Measurements of low-level concentrations of halogenated volatile organic compounds (VOCs) and estimates of groundwater age interpreted from 3H/3He and SF6 data have led to an improved understanding of groundwater flow, water sources, and transit times in a karstic, fractured, carbonate-rock aquifer at the Leetown Science Center (LSC), West Virginia. The sum of the concentrations of a set of 16 predominant halogenated VOCs (TDVOC) determined by gas chromatography with electron-capture detector (GC–ECD) exceeded that possible for air–water equilibrium in 34 of the 47 samples (median TDVOC of 24,800 pg kg−1), indicating that nearly all the water sampled in the vicinity of the LSC has been affected by addition of halogenated VOCs from non-atmospheric source(s). Leakage from a landfill that was closed and sealed nearly 20 a prior to sampling was recognized and traced to areas east of the LSC using low-level detection of tetrachloroethene (PCE), methyl chloride (MeCl), methyl chloroform (MC), dichlorodifluoromethane (CFC-12), and cis-1,2-dichloroethene (cis-1,2-DCE). Chloroform (CHLF) was the predominant VOC in water from domestic wells surrounding the LSC, and was elevated in groundwater in and near the Fish Health Laboratory at the LSC, where a leak of chlorinated water occurred prior to 2006. The low-level concentrations of halogenated VOCs did not exceed human or aquatic-life health criteria, and were useful in providing an awareness of the intrinsic susceptibility of the fractured karstic groundwater system at the LSC to non-atmospheric anthropogenic inputs. The 3H/3He groundwater ages of spring discharge from the carbonate rocks showed transient behavior, with ages averaging about 2 a in 2004 following a wet climatic period (2003–2004), and ages in the range of 4–7 a in periods of more average precipitation (2008–2009). The SF6 and CFC-12 data indicate older water (model ages of 10s of years or more) in the low-permeability shale of the Martinsburg

  18. A Complete Transport Validated Model on a Zeolite Membrane for Carbon Dioxide Permeance and Capture

    CERN Document Server

    Gkanas, Evangelos I; Stubos, Athanasios K; Makridis, Sofoklis S

    2013-01-01

    The CO2 emissions from major industries cause serious global environment problems and their mitigation is urgently needed. The use of zeolite membranes is a very efficient way in order to capture CO2 from some flue gases. The dominant transport mechanism at low temperature andor high pressure is the diffusion through the membrane. This procedure can be divided in three steps: Adsorption of the molecules of the species in the surface of the membrane, then a driving force gives a path where the species follow inside the membrane and finally the species desorbed from the surface of the membrane. The current work is aimed at developing a simulation model for the CO2 transport through a zeolite membrane and estimate the diffusion phenomenon through a very thin membrane of 150 nm in a Wicke-Kallenbach cell. The cell is cylindrical in shape with diameter of 19 mm and consists of a retentate gas chamber, a permeate gas chamber which are separated by a cylindrical zeolite membrane. This apparatus have been modeled wit...

  19. A Five-year Performance Study of Low VOC Coatings over Zinc Thermal Spray for the Protection of Carbon Steel at the Kennedy Space Center

    Science.gov (United States)

    Kolody, Mark R.; Curran, Jerome P.; Calle, Luz Marina

    2014-01-01

    The launch facilities at the Kennedy Space Center (KSC) are located approximately 1000 feet from the Atlantic Ocean where they are exposed to salt deposits, high humidity, high UV degradation, and acidic exhaust from solid rocket boosters. These assets are constructed from carbon steel, which requires a suitable coating to provide long-term protection to reduce corrosion and its associated costs. While currently used coating systems provide excellent corrosion control performance, they are subject to occupational, safety, and environmental regulations at the Federal and State levels that limit their use. Many contain high volatile organic compounds (VOCs), hazardous air pollutants, and other hazardous materials. Hazardous waste from coating operations include vacuum filters, zinc dust, hazardous paint related material, and solid paint. There are also worker safety issues such as exposure to solvents and isocyanates. To address these issues, top-coated thermal spray zinc coating systems were investigated as a promising environmentally friendly corrosion protection for carbon steel in an acidic launch environment. Additional benefits of the combined coating system include a long service life, cathodic protection to the substrate, no volatile contaminants, and high service temperatures. This paper reports the results of a performance based study to evaluate low VOC topcoats (for thermal spray zinc coatings) on carbon steel for use in a space launch environment.

  20. Nuclear quantum effect on hydrogen adsorption site of zeolite-templated carbon model using path integral molecular dynamics

    Energy Technology Data Exchange (ETDEWEB)

    Suzuki, Kimichi, E-mail: ki-suzuki@aist.go.jp [Research Institute for Nanosystem, National Institute of Advanced Industrial Science and Technology, Chuo-2, 1-1-1, Umezono, Tsukuba, Ibaraki 305-8568 (Japan); Kayanuma, Megumi [Institut de Chimie, UMR 7177 CNRS/Universite de Strasbourg, 4 rue Blaise Pascal 67000, Strasbourg (France); Tachikawa, Masanori [Quantum Chemistry Division, Graduate School of Science, Yokohama-city University, Seto 22-2, Kanazawa-ku, Yokohama 236-0027 (Japan); Ogawa, Hiroshi [Research Institute for Nanosystem, National Institute of Advanced Industrial Science and Technology, Chuo-2, 1-1-1, Umezono, Tsukuba, Ibaraki 305-8568 (Japan); Nishihara, Hirotomo; Kyotani, Takashi [Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Nagashima, Umpei [Research Institute for Nanosystem, National Institute of Advanced Industrial Science and Technology, Chuo-2, 1-1-1, Umezono, Tsukuba, Ibaraki 305-8568 (Japan)

    2011-09-15

    Research highlights: > The stable hydrogen adsorption sites on C{sub 36}H{sub 12} were evaluated at 300 K using path integral molecular dynamics. > In the static MO calculation and conventional MD simulation, five stable adsorption sites of hydrogen atom were found. > In path integral simulation, only four stable adsorption sites were obtained. > The thermal and nuclear quantum effects are key role to settle the hydrogen adsorption sites on carbon materials. - Abstract: To settle the hydrogen adsorption sites on buckybowl C{sub 36}H{sub 12}, which is picked up from zeolite-templated carbon (ZTC), we have performed path integral molecular dynamics (PIMD) simulation including thermal and nuclear quantum fluctuations under semi-empirical PM3 method. In the static PM3 calculation and classical simulation the five stable adsorption sites of hydrogen atom are optimized inside a buckybowl C{sub 36}H{sub 12}, which are labeled as {alpha}-, {beta}{sub 1}-, {beta}{sub 2}-, {gamma}-, and {delta}-carbons from edge to innermost carbon. In PIMD simulation, meanwhile, stable adsorption site is not appeared on {delta}-carbon, but on only {alpha}-, {beta}{sub 1}-, {beta}{sub 2}-, and {gamma}-carbons. This result is due to the fact that the adsorbed hydrogen atom can easily go over the barrier for hydrogen transferring from {delta}- to {beta}{sub 1}-carbons by thermal and nuclear quantum fluctuations. The thermal and nuclear quantum effects are key role to settle the hydrogen adsorption sites on carbon materials.

  1. Comparisons of kinetics, thermodynamics and regeneration of tetramethylammonium hydroxide adsorption in aqueous solution with graphene oxide, zeolite and activated carbon

    Science.gov (United States)

    Chang, Shenteng; Lu, Chungsying; Lin, Kun-Yi Andrew

    2015-01-01

    Graphene oxide (GO), sodium Y-type zeolite (NaY) and granular activated carbon (GAC) are selected as adsorbents to study their kinetics, thermodynamics and regeneration of tetramethylammonium hydroxide (TMAH) adsorption from water. The adsorption kinetics follows the pseudo-second-order rate law while the adsorption thermodynamics shows an exothermic reaction with GO and GAC but displays an endothermic reaction with NaY. The adsorbed TMAH can be readily desorbed from the surface of GO and NaY by 0.05 M NaCl solution. A comparative study on the cyclic TMAH adsorption with GO, NaY and GAC is also conducted and the results reveal that GO exhibits the greatest TMAH adsorption capacity as well as superior reversibility of TMAH adsorption over 10 cycles of adsorption and desorption process. These features indicate that GO is a promising and efficient adsorbent for TMAH removal in wastewater treatment.

  2. The Variety of Carbon-Metal Bonds inside Cu-ZSM-5 Zeolites: A Density Functional Theory Study

    Directory of Open Access Journals (Sweden)

    Takashi Yumura

    2010-04-01

    Full Text Available Large-scale density functional theory calculations (DFT found various types of binding of an unsaturated hydrocarbon (C2H2 and C2H4 to a ZSM-5 zeolite extraframework copper cation. We employed the DFT calculations based on the B3LYP functional to obtain local minima of an unsaturated hydrocarbon adsorbed on one or two copper cations embedded inside ZSM-5, and then compared their stabilization energies. The DFT results show that the stabilization energies are strongly dependent on the copper coordination environment as well as configurations of two copper cations. Consequently, the inner copper-carbon bonds are influenced substantially by a nanometer-scale cavity of ZSM-5.

  3. 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.

  4. Comparisons of kinetics, thermodynamics and regeneration of tetramethylammonium hydroxide adsorption in aqueous solution with graphene oxide, zeolite and activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Chang, Shenteng; Lu, Chungsying, E-mail: clu@nchu.edu.tw; Lin, Kun-Yi Andrew

    2015-01-30

    Graphical abstract: A comparison of TMAH adsorption capacity with GO, NaY and GAC is conducted and the result reveals that the magnitude of qe follows the order of GO > NaY > GAC. The adsorption capacity of GO is significantly higher than those of zeolite and activated carbon in this and reported studies, showing its encouraging potential. GO also exhibits good reversibility of TMAH adsorption through 10 cycles of adsorption and desorption process. This reflects that GO is a promising and efficient adsorbent for TMAH removal in wastewater treatment. - Highlights: • Adsorption kinetics and isotherms of TMAH to GO, NaY and GAC are compared. • Thermodynamics of TMAH adsorption to GO, NaY and GAC is determined. • GO exhibits the highest TMAH adsorption capacity, followed by NaY and GAC. • Recyclabilities of NaY and GO remain above 95% but that of GAC dropped to 70%. - Abstract: Graphene oxide (GO), sodium Y-type zeolite (NaY) and granular activated carbon (GAC) are selected as adsorbents to study their kinetics, thermodynamics and regeneration of tetramethylammonium hydroxide (TMAH) adsorption from water. The adsorption kinetics follows the pseudo-second-order rate law while the adsorption thermodynamics shows an exothermic reaction with GO and GAC but displays an endothermic reaction with NaY. The adsorbed TMAH can be readily desorbed from the surface of GO and NaY by 0.05 M NaCl solution. A comparative study on the cyclic TMAH adsorption with GO, NaY and GAC is also conducted and the results reveal that GO exhibits the greatest TMAH adsorption capacity as well as superior reversibility of TMAH adsorption over 10 cycles of adsorption and desorption process. These features indicate that GO is a promising and efficient adsorbent for TMAH removal in wastewater treatment.

  5. Zeolitic imidazole framework templated synthesis of nanoporous carbon as a novel fiber coating for solid-phase microextraction.

    Science.gov (United States)

    Zhang, Shuaihua; Yang, Qian; Li, Zhi; Wang, Wenchang; Wang, Chun; Wang, Zhi

    2016-02-07

    A new solid-phase microextraction (SPME) fiber coating material, a zeolitic imidazole framework-67 (ZIF-67) templated nanoporous carbon, Co-NPC, was fabricated by one-step direct carbonization of ZIF-67 without using any other carbon precursors. The prepared Co-NPC was then coated onto a functionalized stainless steel wire by a simple physical coating method to prepare SPME fibers. By coupling the Co-NPC coated fiber based SPME with gas chromatography/micro-electron capture detection (GC/μECD), the developed method exhibited low limits of detection (0.07-0.45 ng g(-1)) and a wide linearity (0.30-50 ng g(-1)) for the determination of five organochlorine pesticides (OCPs) in vegetable samples. The method was applied to the analysis of cabbage, cucumber and celery cabbage samples, and the recoveries of the analytes were in the range of 87.9-103.9% with the relative standard deviations (RSDs) ranging from 5.1% to 10.4% (n = 5). Single fiber repeatability and fiber-to-fiber reproducibility values expressed as RSDs were in the range of 4.9-9.6% and 5.8-11.0%, respectively. The method was simple, convenient and feasible for the determination of OCPs in real samples.

  6. Zeolitic imidazolate framework-8 derived nanoporous carbon as an effective and recyclable adsorbent for removal of ciprofloxacin antibiotics from water.

    Science.gov (United States)

    Li, Siqi; Zhang, Xiaodan; Huang, Yuming

    2017-01-05

    The nanoporous carbons (NPC) derived from a one-step carbonization of zeolitic imidazolate framework-8 (ZIF-8) were synthesized and used for ciprofloxacin (CIP) removal from water. The resultant products were characterized by SEM, TEM, FT-IR, Raman, N2 adsorption-desorption analysis, XRD, TGA and Zeta potential. The optimized NPC-700 (carbonized at 700°C for 2h) exhibited an optimal performance in CIP adsorption removal. CIP adsorption on NPC-700 as a function of contact time, initial CIP concentration, adsorbent dosage, pH, ionic strength and humic acid concentration were investigated. Kinetics of CIP removal was found to follow pseudo-second-order rate equation. Both Langmuir and Freundlich models fitted the adsorption data well and gave similar correlation coefficients (>0.96). However, Freundlich isotherm gave a better fit (r(2)=0.9969), suggesting a multilayer adsorption of CIP onto surface of NPC-700 adsorbent. The maximum adsorption capacity for CIP based on Langmuir model was 416.7mg/g, which was higher than those of other adsorbents. The NPC-700 material showed no apparent loss in CIP adsorption after seven cycles. These features reveal that the metal-organic framework (MOF) derived NPC may be a promising adsorbent for CIP removal from water. Copyright © 2016 Elsevier B.V. All rights reserved.

  7. 活性炭与分子筛吸附性能比较研究%Study on Adsorption of Activated Carbon and Zeolite

    Institute of Scientific and Technical Information of China (English)

    李文明; 袁东; 付大友; 李红然; 谭文渊

    2011-01-01

    设计一套动态吸附装置.选取了三种室内空气中含量较大的有害气体:甲醛、苯和甲苯作为吸附质.利用气相色谱仪测定其穿透曲线,对活性炭和分子筛的吸附性能进行了比较.结果显示分子筛吸收低浓度的甲醛和甲苯性能较好,而活性炭吸收低浓度的苯性能较好.综合平衡吸附量、穿透时间和平衡时间三个指标进行比较,活性炭的吸附性能要优于分子筛.%A dynamic adsorption device was designed for the study. Three types of harmful gases with high level in indoor air that were formaldehyde, benzene and toluene were selected as adsorbate. Its breakthrough curves were determined by gas chromatograph. The adsorption of activated carbon and zeolite were compared. The conclusion is that zeolite is better to adsorpt low concentration of formaldehyde and toluene and activated carbon is better to adsorpt low concentration of benzene. The adsorption of activated carbon is better than zeolite through the comparison of equilibrium adsorption capacity ,breakthrough time and equilibration time.

  8. Determination of carbon monoxide with a modified zeolite sorbent and methanization-gas chromatography.

    Science.gov (United States)

    Juntarawijit, C; Poovey, H G; Rando, R J

    2000-01-01

    The purpose of this study was to develop an alternative sorbent sampling technique to concentrate CO from an air sample for subsequent instrumental analysis. Y52 zeolite doped with 9.4 wt % cuprous ions was found to have high capacity, stability to air, and thermal reversibility for CO. The Cu(I)-modified zeolite was packed in glass tubes, preceded by a drying tube containing silica gel. Air was sampled through the tubes at the flow rate of 100 mL/min. Collected CO was thermally desorbed at 300 degrees C and determined by gas chromatography with reduction of CO to methane and flame ionization detection (TD-GC-CH4-FID). Breakthrough capacity of the sorbent was found to be 2.74 mg CO per gram of sorbent. For 2-L air samples containing 12.5 to 100 ppm CO and 50% relative humidity at room temperature, recovery of CO was found to be 96.6% with pooled relative standard deviation of 5.8%. The estimated detection limit for a 2-L sample was 0.2 ppm. Collected CO was stable at room temperature for 1 day and up to 7 days at 4 degrees C if the sorbent tube was flushed with helium before storage. In field testing, the ratio of CO measured by the new technique and by a reference technique was found to be 0.93 with pooled relative standard deviation of 6.3%. This unique new sorbent coupled with TD-GC-CH4-FID shows promise as a sensitive and specific alternative for measurement of CO in air.

  9. Composition of gaseous organic carbon during ECOCEM in Beirut, Lebanon: new observational constraints for VOC anthropogenic emission evaluation in the Middle East

    Science.gov (United States)

    Salameh, Thérèse; Borbon, Agnès; Afif, Charbel; Sauvage, Stéphane; Leonardis, Thierry; Gaimoz, Cécile; Locoge, Nadine

    2017-01-01

    The relative importance of eastern Mediterranean emissions is suspected to be largely underestimated compared to other regions worldwide. Here we use detailed speciated measurements of volatile organic compounds (VOCs) to evaluate the spatial heterogeneity of VOC urban emission composition and the consistency of regional and global emission inventories downscaled to Lebanon (European Monitoring and Evaluation Programme, EMEP; Atmospheric Chemistry and Climate Model Intercomparison Project, ACCMIP; and MACCity, Monitoring Atmospheric Composition and Climate and megaCITY Zoom for the Environment). The assessment was conducted through the comparison of the emission ratios (ERs) extracted from the emission inventories to the ones obtained from the hourly observations collected at a suburban site in Beirut, Lebanon, during summer and winter ECOCEM (Emissions and Chemistry of Organic Carbon in the Eastern Mediterranean) campaigns. The observed ERs were calculated using two independent methods. ER values from both methods agree very well and are comparable to the ones of the road transport sector from near-field measurements for more than 80 % of the species. There is no significant seasonality in ER for more than 90 % of the species, unlike the seasonality usually observed in other cities worldwide. Regardless of the season, ERs agree within a factor of 2 between Beirut and other representative cities worldwide, except for the unburned fuel fraction and ethane. ERs of aromatics (except benzene) are higher in Beirut compared to northern post-industrialized countries and even the Middle Eastern city Mecca. The comparison of the observed ER to the ones extracted from the ACCMIP and MACCity global emission inventories suggests that the overall speciation of anthropogenic sources for major hydrocarbons that act as ozone and secondary organic aerosol (SOA) precursors in ACCMIP is better represented than other species. The comparison of the specific road transport ERs, relative

  10. 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...

  11. Sn-Beta zeolites with borate salts catalyse the epimerization of carbohydrates via an intramolecular carbon shift.

    Science.gov (United States)

    Gunther, William R; Wang, Yuran; Ji, Yuewei; Michaelis, Vladimir K; Hunt, Sean T; Griffin, Robert G; Román-Leshkov, Yuriy

    2012-01-01

    Carbohydrate epimerization is an essential technology for the widespread production of rare sugars. In contrast to other enzymes, most epimerases are only active on sugars substituted with phosphate or nucleotide groups, thus drastically restricting their use. Here we show that Sn-Beta zeolite in the presence of sodium tetraborate catalyses the selective epimerization of aldoses in aqueous media. Specifically, a 5 wt% aldose (for example, glucose, xylose or arabinose) solution with a 4:1 aldose:sodium tetraborate molar ratio reacted with catalytic amounts of Sn-Beta yields near-equilibrium epimerization product distributions. The reaction proceeds by way of a 1,2 carbon shift wherein the bond between C-2 and C-3 is cleaved and a new bond between C-1 and C-3 is formed, with C-1 moving to the C-2 position with an inverted configuration. This work provides a general method of performing carbohydrate epimerizations that surmounts the main disadvantages of current enzymatic and inorganic processes.

  12. Utilization of Human Urine as Fertilizer with Magnesium Oxide (MgO, Zeolite and Activated Carbon as Absorbent

    Directory of Open Access Journals (Sweden)

    Hijrah Purnama Putra

    2014-01-01

    Full Text Available Urine is residual fluid excreted by kidneys through urinary tract to outside of the human body, to maintain homeostasis of fluid in the body. Normally urine still contains high amount of nitrogen, which is 87%, phosphor 50%, potassium 54% and low bacterial content. With these contents urine potentially becomes organic fertilizer rich with nitrogen, phosphor and potassium contents and is beneficial to plants. However, until today the utilization or urine in Indonesia is very low. The urine produced is dispose with feces in toilets. This study aimed to utilize urine as solid organic fertilizer using magnesium oxide (MgO, zeolite, and actived carbon as absorbents of ammonium and phosphor. The study started with collecting urine, time variations of urine storage were 24; 48 and 72 hours, and urine was mixed with water as an assumption that urine mixes with water when flushed in urinals. The result showed effectiveness of optimum urine absorption in urine stored for 48 hours by adding 8 gram MgO, producing ammonium and phosphor contents 56.100 ppm and 3.610 ppm, respectively. From environmental perspective, utilization of urine as organic fertilizer was applicable because it satisfied the ecological principle of sanitation to prevent soil pollution, ground and surface water pollution and its utilization as agricultural resources.

  13. Mesoporous carbon prepared from carbohydrate as hard template for hierarchical zeolites

    DEFF Research Database (Denmark)

    Egeblad, Kresten; Christensen, Claus H.

    2007-01-01

    treatment of a mixture of sucrose and ammonia followed by carbonization of the mixture in N-2 at high temperatures. The porous carbon produced by this method was subsequently applied as a hard template in the synthesis of mesoporous silicalite-1 and removed by combustion after synthesis. X-ray diffraction...

  14. 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.

  15. Sensitive amperometric determination of hydrazine using a carbon paste electrode modified with silver-doped zeolite L nanoparticles

    Indian Academy of Sciences (India)

    NEDA SALEK GILANI; SEYED NASER AZIZI; SHAHRAM GHASEMI

    2017-02-01

    Silver-loaded nanozeolite-L-modified carbon paste electrode (Ag/L–CPE) was used as a novel sensing platform for enhanced electrocatalytic oxidation and determination of hydrazine. Zeolite L nanoparticles were synthesized via hydrothermal approach and then characterized using various techniques such as X-ray diffraction (XRD), Fourier transform infrared (FTIR), scanning electronic microscopy (SEM) and Brunauer–Emmett–Teller (BET). Silver-exchanged nanozeolite L (Ag/L) was prepared and mixed with carbon paste to prepare the modified electrode. Cyclic voltammetry studies revealed the high performance of Ag/L–CPE for electrocatalytic oxidation of hydrazine. Two linear ranges were detected in the amperometric detection of hydrazine. The first range was from10 $\\mu$M to 0.4 mM with sensitivity of 103.13 $\\mu$A mM$^{−1}$ and the second one was from 0.4 to 4mM with sensitivity of 58.131 $\\mu$A mM$^{−1}$. The response time and detection limit ($S/N = 3$) of this sensor were determined to be 2 s and 1.5 $\\mu$M, respectively. The unique porous structure of nanozeolite L offers a promising catalyst support candidate for efficient electrochemical sensing of hydrazine. The sensor exhibited appreciable repeatability, reproducibility and stability, and was able to detect hydrazine in the presence of even 500-fold excess concentrations of interfering species. Also, the sensor was used to determine hydrazine concentration in water samples with satisfactory results.

  16. The usage of activated carbon from teak sawdust (tectona grandis l.f.) and zeolite for the adsorption of Cr(VI) and its analysis using solid-phase spectrophotometry (sps)

    Science.gov (United States)

    Saputro, S.; Masykuri, M.; Mahardiani, L.; Mulyani, B.; Qorina, I.; Yoshimura, K.; Takehara, K.; Matsuoka, S.

    2017-02-01

    This study aims to evaluate the usage of teak sawdust and zeolite as an adsorbent of Cr(VI) ion; optimal composition ratio of the composite adsorbent; and the sensitivity of solid-phase spectrophotometry (SPS) as a method to determine the levels of Cr(VI) ion as an adsorption results of adsorbents. The adsorbent used were teak sawdust activated carbon and zeolite as a single and composite adsorbents. The teak sawdust carbonization using muffle furnace and then activated with H3PO4 10% while the zeolite with H2SO4 10%. The contacting process of the adsorbents with Cr(VI) was done by varying the compositions. Analysis of Cr(VI) level was done using SPS method. Characterization of adsorbent before and after being activated is done using a FTIR. The results showed that teak sawdust and zeolite can be used as adsorbents to adsorb Cr(VI) in the simulated liquid waste with the adsorption capacity 1.19 µg/g the optimum composition ratio of teak sawdust activated carbon and zeolite was 75%:25% with the percentage of adsorption was 62.72%. Solid-phase spectrophotometry is a sensitive method to analyze the decreased levels of Cr(VI) as an adsorption results in µg/L level with the limit of detection (LOD) was 0.03 µg/L.

  17. VOC emissions chambers

    Data.gov (United States)

    Federal Laboratory Consortium — In order to support the development of test methods and reference materials for volatile organic compounds (VOC) emissions from building materials and furnishings,...

  18. Synthesis and electrochemical capacitive properties of nitrogen-doped porous carbon micropolyhedra by direct carbonization of zeolitic imidazolate framework-11

    Energy Technology Data Exchange (ETDEWEB)

    Hao, Fei; Li, Li; Zhang, Xiaohua, E-mail: mickyxie@hnu.edu.cn; Chen, Jinhua, E-mail: chenjinhua@hnu.edu.cn

    2015-06-15

    Highlights: • Nitrogen-doped porous carbon micropolyhedra (N-PCMPs) were prepared from ZIF-11. • The activated N-PCMPs with fused KOH (N-PCMPs-A) have high specific surface area. • N-PCMPs-A exhibits high specific capacitance. • N-PCMPs-A reveals good cycling performance even at a high current density. - Abstract: Nitrogen-doped porous carbon micropolyhedra (N-PCMPs) were successfully prepared by direct carbonization of ZIF-11 polyhedra and further activated with fused KOH to obtain N-PCMPs-A. The morphology and microstructure of samples were examined by scanning electron microscopy, X-ray diffraction, and micropore and chemisorption analyzer. Electrochemical properties were characterized by cyclic voltammetry and galvanostatic charge/discharge method in 1.0 M H{sub 2}SO{sub 4} aqueous solution on a standard three-electrode system. Results show that, compared with N-PCMPs, N-PCMPs-A has higher specific surface area (2188 m{sup 2} g{sup −1}) and exhibits improved electrochemical capacitive properties (307 F g{sup −1} at 1.0 A g{sup −1}). The mass specific capacitance of N-PCMPs-A is also higher than that of most MOF-derived carbons, some carbide-derived carbons and carbon aerogel-derived carbons. In addition, the capacitance of the N-PCMPs-A retains 90% after 4000 cycles even at a high current density of 10 A g{sup −1}. These imply that N-PCMPs-A is the promising materials for the construction of a high-performance supercapacitor.

  19. Are Some Fungal Volatile Organic Compounds (VOCs) Mycotoxins?

    OpenAIRE

    Bennett, Joan W.; Arati A. Inamdar

    2015-01-01

    Volatile organic compounds (VOCs) are carbon-compounds that easily evaporate at room temperature. Toxins are biologically produced poisons; mycotoxins are those toxins produced by microscopic fungi. All fungi emit blends of VOCs; the qualitative and quantitative composition of these volatile blends varies with the species of fungus and the environmental situation in which the fungus is grown. These fungal VOCs, produced as mixtures of alcohols, aldehydes, acids, ethers, esters, ketones, terpe...

  20. VOCs in Arid soils: Technology summary

    Energy Technology Data Exchange (ETDEWEB)

    1994-02-01

    The Volatile Organic Compounds In Arid Soils Integrated Demonstration (VOC-Arid ID) focuses on technologies to clean up volatile organic compounds and associated contaminants in soil and groundwater at arid sites. The initial host site is the 200 West Area at DOE`s Hanford site in southeastern Washington state. The primary VOC contaminant is carbon tetrachloride, in association with heavy metals and radionuclides. An estimated 580--920 metric tons of carbon tetrachloride were disposed of between 1955 and 1973, resulting in extensive soil and groundwater contamination. The VOC-Arid ID schedule has been divided into three phases of implementation. The phased approach provides for: rapid transfer of technologies to the Environmental Restoration (EM-40) programs once demonstrated; logical progression in the complexity of demonstrations based on improved understanding of the VOC problem; and leveraging of the host site EM-40 activities to reduce the overall cost of the demonstrations. During FY92 and FY93, the primary technology demonstrations within the ID were leveraged with an ongoing expedited response action at the Hanford 200 West Area, which is directed at vapor extraction of VOCs from the vadose (unsaturated) zone. Demonstration efforts are underway in the areas of subsurface characterization including: drilling and access improvements, off-gas and borehole monitoring of vadose zone VOC concentrations to aid in soil vapor extraction performance evaluation, and treatment of VOC-contaminated off-gas. These current demonstration efforts constitute Phase 1 of the ID and, because of the ongoing vadose zone ERA, can result in immediate transfer of successful technologies to EM-40.

  1. [Life support of the Mars exploration crew. Control of a zeolite system for carbon dioxide removal from space cabin air within a closed air regeneration cycle].

    Science.gov (United States)

    Chekov, Iu F

    2009-01-01

    The author describes a zeolite system for carbon dioxide removal integrated into a closed air regeneration cycle aboard spacecraft. The continuous operation of a double-adsorbent regeneration system with pCO2-dependable productivity is maintained through programmable setting of adsorption (desorption) semicycle time. The optimal system regulation curve is presented within the space of statistical performance family obtained in quasi-steady operating modes with controlled parameters of the recurrent adsorption-desorption cycle. The automatically changing system productivity ensures continuous intake of concentrated CO2. Control of the adsorption-desorption process is based on calculation of the differential adsorption (desorption) heat from gradient of adsorbent and test inert substance temperatures. The adaptive algorithm of digital control is implemented through the standard spacecraft interface with the board computer system and programmable microprocessor-based controllers.

  2. Conversion of methanol to hydrocarbons over ZSM-5 zeolite: an examination of the role of aromatic hydrocarbons using /sup 13/carbon and deuterium-labeled feeds

    Energy Technology Data Exchange (ETDEWEB)

    Mole, T.; Bett, G.; Seddon, D.

    1983-12-01

    A mechanism is suggested for the acceleration by aromatic hydrocarbons of zeolite-catalyzed methanol conversion. According to this mechanism, the aromatic hydrocarbon undergoes successive ring methylation, prototropic conversion to an exo-methylene-cyclohexadiene, side-chain methylation, and ring de-ethylation. The overall result is that two methanol molecules give an ethylene molecule. The mechanism is supported by various reactions observed over ZSM-5 catalyst at methanol conversion temperatures: (I) deuteration of p-xylene by D/sub 2/O in the ring and methyl positions; (II) de-alkylation of p-ethyltoluene and n-propylbenzene; and (III) incorporation of the aromatic carbon of benzenes and alkylbenzenes into ethylene product, as revealed by /sup 13/C-labeling studies. 3 tables.

  3. Volatile organic compounds (VOCs) in surface coating materials: Their compositions and potential as an alternative fuel.

    Science.gov (United States)

    Dinh, Trieu-Vuong; Choi, In-Young; Son, Youn-Suk; Song, Kyu-Yong; Sunwoo, Young; Kim, Jo-Chun

    2016-03-01

    A sampling system was designed to determine the composition ratios of VOCs emitted from 31 surface coating materials (SCMs). Representative architectural, automotive, and marine SCMs in Korea were investigated. Toluene, ethylbenzene, and xylene were the predominant VOCs. The VOC levels (wt%) from automotive SCMs were significantly higher than those from architectural and marine paints. It was found that target SCMs comprised mainly VOCs with 6-10 carbon atoms in molecules, which could be adsorbed by activated carbon. The saturated activated carbon which had already adsorbed toluene, ethylbenzene, and m-xylene was combusted. The saturated activated carbon was more combustible than new activated carbon because it comprised inflammable VOCs. Therefore, it could be an alternative fuel when using in a "fuelization system". To use the activated carbon as a fuel, a control technology of VOCs from a coating process was also designed and introduced.

  4. 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...... crystals, nanosized zeolite crystals, and supported zeolite crystals. For the pure zeolite materials in the first two categories, the additional meso- or macroporosity can be classified as being either intracrystalline or intercrystalline, whereas for supported zeolite materials, the additional porosity...... originates almost exclusively from the support material. The methods for introducing mesopores into zeolite materials are discussed and categorized. In general, mesopores can be templated in zeolite materials by use of solid templating, supramolecular templating, or indirect templating...

  5. Co@Pt Core@Shell nanoparticles encapsulated in porous carbon derived from zeolitic imidazolate framework 67 for oxygen electroreduction in alkaline media

    Science.gov (United States)

    Wang, Likai; Tang, Zhenghua; Yan, Wei; Wang, Qiannan; Yang, Hongyu; Chen, Shaowei

    2017-03-01

    Nanocomposites based on Co@Pt core@shell nanoparticles encapsulated in nitrogen-doped porous carbons were prepared as a new type of high-performance electrocatalysts for oxygen reduction reaction (ORR). Controlled pyrolysis of zeolitic imidazolate framework 67 (ZIF-67) led to the formation of Co nanoparticles encapsulated in nitrogen-doped porous carbon (Co-NC), which underwent galvanic replacement reactions with K2PtCl4 forming Co@Pt core@shell nanoparticles. The surface microstructure and composition of the resulting Co@Pt-NC nanocomposite were examined by electron microscopic as well as X-ray photoelectron spectroscopic (XPS) measurements. With the Co@Pt particles encapsulated in nitrogen-doped porous carbon, the hybrids exhibited a high specific surface area and abundant catalytically active sites for ORR. Electrochemically, the specific activity and mass activity of the Co@Pt-NC composite at +0.85 V (0.145 mA cm-2 and 71.9 A g-1) were superior to those of commercial Pt/C (0.123 mA cm-2 and 38.4 A g-1). Furthermore, the Co@Pt-NC composite also exhibited remarkably higher durability and more robust tolerance against methanol crossover than commercial Pt/C.

  6. Diffuse emissions of Volatile Organic Compounds (VOCs) from soil in volcanic and hydrothermal systems: evidences for the influence of microbial activity on the carbon budget

    Science.gov (United States)

    Venturi, Stefania; Tassi, Franco; Fazi, Stefano; Vaselli, Orlando; Crognale, Simona; Rossetti, Simona; Cabassi, Jacopo; Capecchiacci, Francesco

    2017-04-01

    Soils in volcanic and hydrothermal areas are affected by anomalously high concentrations of gases released from the deep reservoirs, which consists of both inorganic (mainly CO2 and H2S) and organic (volatile organic compounds; VOCs) species. VOCs in volcanic and hydrothermal fluids are mainly composed of saturated and unsaturated hydrocarbons (alkanes, aromatics, alkenes, and cyclics), with variable concentrations of O- and S-bearing compounds and halocarbons, depending on the physicochemical conditions at depth. VOCs in interstitial soil gases and fumarolic emissions from four volcanic and hydrothermal systems in the Mediterranean area (Solfatara Crater, Poggio dell'Olivo and Cava dei Selci, in Italy, and Nisyros Island, in Greece) evidenced clear compositional differences, suggesting that their behavior is strongly affected by secondary processes occurring at shallow depths and likely controlled by microbial activity. Long-chain saturated hydrocarbons were significantly depleted in interstitial soil gases with respect to those from fumarolic discharges, whereas enrichments in O-bearing compounds (e.g. aldehydes, ketones), DMSO2 and cyclics were commonly observed. Benzene was recalcitrant to degradation processes, whereas methylated aromatics were relatively instable. The chemical and isotopic (δ13C in CO2 and CH4) composition of soil gases collected along vertical profiles down to 50 cm depth at both Solfatara Crater and Poggio dell'Olivo (Italy) showed evidences of relevant oxidation processes in the soil, confirming that microbial activity likely plays a major role in modifying the composition of deep-derived VOCs. Despite their harsh conditions, being typically characterized by high temperatures, low pH, and high toxic gases and metal contents, the variety of habitats characterizing volcanic and hydrothermal environments offers ideal biomes to extremophilic microbes, whose metabolic activity can consume and/or produce VOCs. In the Solfatara Crater, microbial

  7. 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.

  8. Systems including catalysts in porous zeolite materials within a reactor for use in synthesizing hydrocarbons

    Science.gov (United States)

    Rolllins, Harry W [Idaho Falls, ID; Petkovic, Lucia M [Idaho Falls, ID; Ginosar, Daniel M [Idaho Falls, ID

    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.

  9. 用修正的Polanyi-Dubinin方程描述有机蒸气-水蒸气在活性炭上的吸附平衡%MODIFIED POLANYI-DUBININ EQUATION TO ORRELATE ADSORPTION EQUILIBRIUM OF VOC-WATER VAPOR MIXTURES ON ACTIVATED CARBON

    Institute of Scientific and Technical Information of China (English)

    高华生; 汪大翚; 叶芸春; 谭天恩

    2001-01-01

    Long-column method was used to determine the adsorption isotherms of 4 VOCs (benzene, toluene, chloroform and acetone) in concentration range of 250~5000?mg*m-3 on a commercial activated-carbon under different humidity levels at 30?℃.A modified Polanyi-Dubinin equation was proposed to correlate the adsorption equilibrium of different VOC-water vapor systems. Among 3 methods of calculating the Relative Affinity Coefficient β used,the Molar Volume method and the Molecular Parachor method proved to be suitable for the calculation with better precision than the Electronic Polarization method. Calculation results were satisfactory for the benzene-, toluene-, and chloroform-water vapor/activated carbon systems, but poor for acetone possibly because of its strong polarity.The equation could be used to estimate the detaining effect of atmospheric humidity on the adsorption equilibrium of VOCs on activated carbon.

  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. Microporous Cokes Formed in Zeolite Catalysts Enable Efficient Solar Evaporation

    KAUST Repository

    Wang, Jianjian

    2017-03-13

    Cokes are inevitably generated during zeolite-catalyzed reactions as deleterious side products that deactivate the catalyst. In this study, we in-situ converted cokes into carbons within the confined microporous zeolite structures and evaluated their performances as absorbing materials for solar-driven water evaporation. With a properly chosen zeolite, the cokederived carbons possessed ordered interconnected pores and tunable compositions. We found that the porous structure and the oxygen content in as-prepared carbons had important influences on their energy conversion efficiencies. Among various investigated carbon materials, the carbon derived from the methanol-to-olefins reaction over zeolite Beta gave the highest conversion efficiency of 72% under simulated sunlight with equivalent solar intensity of 2 suns. This study not only demonstrates the great potential of traditionally useless cokes for solar thermal applications but also provides new insights into the design of carbon-based absorbing materials for efficient solar evaporation.

  12. Low Absorption Vitreous Carbon Reactors for Operando XAS: A Case Study on Cu/Zeolites for Selective Catalytic Reduction of NOx by NH3

    Energy Technology Data Exchange (ETDEWEB)

    Kispersky, Vincent F.; Kropf, Jeremy; Ribeiro, Fabio H; Miller, Jeffrey T

    2012-01-01

    We describe the use of vitreous carbon as an improved reactor material for an operando X-ray absorption spectroscopy (XAS) plug-flow reactor. These tubes significantly broaden the operating range for operando experiments. Using selective catalytic reduction (SCR) of NOx by NH₃ on Cu/Zeolites (SSZ-13, SAPO-34 and ZSM-5) as an example reaction, we illustrate the high-quality XAS data achievable with these reactors. The operando experiments showed that in Standard SCR conditions of 300 ppm NO, 300 ppm NH₃, 5% O₂, 5% H₂O, 5% CO₂ and balance He at 200 °C, the Cu was a mixture of Cu(I) and Cu(II) oxidation states. XANES and EXAFS fitting found the percent of Cu(I) to be 15%, 45% and 65% for SSZ-13, SAPO-34 and ZSM-5, respectively. For Standard SCR, the catalytic rates per mole of Cu for Cu/SSZ-13 and Cu/SAPO-34 were about one third of the rate per mole of Cu on Cu/ZSM-5. Based on the apparent lack of correlation of rate with the presence of Cu(I), we propose that the reaction occurs via a redox cycle of Cu(I) and Cu(II). Cu(I) was not found in in situSCR experiments on Cu/Zeolites under the same conditions, demonstrating a possible pitfall of in situ measurements. A Cu/SiO₂ catalyst, reduced in H₂ at 300 °C, was also used to demonstrate the reactor's operando capabilities using a bending magnet beamline. Analysis of the EXAFS data showed the Cu/SiO₂ catalyst to be in a partially reduced Cu metal–Cu(I) state. In addition to improvements in data quality, the reactors are superior in temperature, stability, strength and ease of use compared to previously proposed borosilicate glass, polyimide tubing, beryllium and capillary reactors. The solid carbon tubes are non-porous, machinable, can be operated at high pressure (tested at 25 bar), are inert, have high material purity and high X-ray transmittance.

  13. Low absorption vitreous carbon reactors for operando XAS: a case study on Cu/Zeolites for selective catalytic reduction of NO(x) by NH3.

    Science.gov (United States)

    Kispersky, Vincent F; Kropf, A Jeremy; Ribeiro, Fabio H; Miller, Jeffrey T

    2012-02-21

    We describe the use of vitreous carbon as an improved reactor material for an operando X-ray absorption spectroscopy (XAS) plug-flow reactor. These tubes significantly broaden the operating range for operando experiments. Using selective catalytic reduction (SCR) of NO(x) by NH(3) on Cu/Zeolites (SSZ-13, SAPO-34 and ZSM-5) as an example reaction, we illustrate the high-quality XAS data achievable with these reactors. The operando experiments showed that in Standard SCR conditions of 300 ppm NO, 300 ppm NH(3), 5% O(2), 5% H(2)O, 5% CO(2) and balance He at 200 °C, the Cu was a mixture of Cu(I) and Cu(II) oxidation states. XANES and EXAFS fitting found the percent of Cu(I) to be 15%, 45% and 65% for SSZ-13, SAPO-34 and ZSM-5, respectively. For Standard SCR, the catalytic rates per mole of Cu for Cu/SSZ-13 and Cu/SAPO-34 were about one third of the rate per mole of Cu on Cu/ZSM-5. Based on the apparent lack of correlation of rate with the presence of Cu(I), we propose that the reaction occurs via a redox cycle of Cu(I) and Cu(II). Cu(I) was not found in in situ SCR experiments on Cu/Zeolites under the same conditions, demonstrating a possible pitfall of in situ measurements. A Cu/SiO(2) catalyst, reduced in H(2) at 300 °C, was also used to demonstrate the reactor's operando capabilities using a bending magnet beamline. Analysis of the EXAFS data showed the Cu/SiO(2) catalyst to be in a partially reduced Cu metal-Cu(I) state. In addition to improvements in data quality, the reactors are superior in temperature, stability, strength and ease of use compared to previously proposed borosilicate glass, polyimide tubing, beryllium and capillary reactors. The solid carbon tubes are non-porous, machinable, can be operated at high pressure (tested at 25 bar), are inert, have high material purity and high X-ray transmittance.

  14. Are Some Fungal Volatile Organic Compounds (VOCs) Mycotoxins?

    Science.gov (United States)

    Bennett, Joan W; Inamdar, Arati A

    2015-09-22

    Volatile organic compounds (VOCs) are carbon-compounds that easily evaporate at room temperature. Toxins are biologically produced poisons; mycotoxins are those toxins produced by microscopic fungi. All fungi emit blends of VOCs; the qualitative and quantitative composition of these volatile blends varies with the species of fungus and the environmental situation in which the fungus is grown. These fungal VOCs, produced as mixtures of alcohols, aldehydes, acids, ethers, esters, ketones, terpenes, thiols and their derivatives, are responsible for the characteristic moldy odors associated with damp indoor spaces. There is increasing experimental evidence that some of these VOCs have toxic properties. Laboratory tests in mammalian tissue culture and Drosophila melanogaster have shown that many single VOCs, as well as mixtures of VOCs emitted by growing fungi, have toxic effects. This paper describes the pros and cons of categorizing toxigenic fungal VOCs as mycotoxins, uses genomic data to expand on the definition of mycotoxin, and summarizes some of the linguistic and other conventions that can create barriers to communication between the scientists who study VOCs and those who study toxins. We propose that "volatoxin" might be a useful term to describe biogenic volatile compounds with toxigenic properties.

  15. Are Some Fungal Volatile Organic Compounds (VOCs Mycotoxins?

    Directory of Open Access Journals (Sweden)

    Joan W. Bennett

    2015-09-01

    Full Text Available Volatile organic compounds (VOCs are carbon-compounds that easily evaporate at room temperature. Toxins are biologically produced poisons; mycotoxins are those toxins produced by microscopic fungi. All fungi emit blends of VOCs; the qualitative and quantitative composition of these volatile blends varies with the species of fungus and the environmental situation in which the fungus is grown. These fungal VOCs, produced as mixtures of alcohols, aldehydes, acids, ethers, esters, ketones, terpenes, thiols and their derivatives, are responsible for the characteristic moldy odors associated with damp indoor spaces. There is increasing experimental evidence that some of these VOCs have toxic properties. Laboratory tests in mammalian tissue culture and Drosophila melanogaster have shown that many single VOCs, as well as mixtures of VOCs emitted by growing fungi, have toxic effects. This paper describes the pros and cons of categorizing toxigenic fungal VOCs as mycotoxins, uses genomic data to expand on the definition of mycotoxin, and summarizes some of the linguistic and other conventions that can create barriers to communication between the scientists who study VOCs and those who study toxins. We propose that “volatoxin” might be a useful term to describe biogenic volatile compounds with toxigenic properties.

  16. Self-assembly sandwiches of reduced graphene oxide layers with zeolitic-imidazolate-frameworks-derived mesoporous carbons as polysulfides reservoirs for lithium-sulfur batteries

    Science.gov (United States)

    Tan, Yingbin; Jia, Zhiqing; Lou, Peili; Cui, Zhonghui; Guo, Xiangxin

    2017-02-01

    Confinement of sulfur and alleviation of the polysulfides dissolution are the key issues for development of high-performance lithium-sulfur (Li-S) batteries. Here, we report self-assembly sandwiches composed of zeolitic-imidazolate-frameworks (ZIF-8)-derived mesoporous carbons (ZIF-8(C)) in between reduced graphene oxide (rGO) layers, which are filled with sulfurs inside and coated with poly(3, 4-ethylenedioxythiophene) (PEDOT) outside (noted as P@rGO/ZIF-8(C)). During the synthesis process, the rGO layers stabilize the structure of ZIF-8 nanocrystals to obtain large specific surface area and high electric conductivity of mesoporous materials (rGO/ZIF-8(C)), ensuring accommodation of a large amount of sulfur and the efficient utilization of the confined sulfur. The mesoporous rGO/ZIF-8(C), PEDOT and N-doping provide physical absorption and chemical binding to the polysulfides during cycles. Consequently, the Li-S batteries with the composite cathodes exhibit the high capacity of 1308 mAh g-1 and 865 mAh g-1 at 0.2 C and 1 C, respectively, and a very low capacity fading of 0.03% per cycle after 500 reversible cycles at 1 C rate. The results indicate that the P@rGO/ZIF-8(C)-S composite cathode may offer a feasible strategy for construction of sulfur cathodes for high-performance Li-S batteries.

  17. Feasibility Study of Reducing the Total Dissolved Solids (TDS from Contaminated Water in Radish Plant (Raphanus Sativus Using Nano Activated Carbon and Zeolite

    Directory of Open Access Journals (Sweden)

    S. Hassanpour Aslani

    2013-06-01

    Full Text Available Applying Nanoporous Materials is an appropriate method for improving chemical quality of the water due to high surface area, internal porous structure (porosity, high absorption capability of harmful gases and liquids, and capability of reactivating the surface. Therefore, actions were carried out in order to investigate the effect of Activated carbon and Zeolite on reducing the total dissolved solids in water to perform experiment in a randomized complete block design with four treatments and three replications in greenhouse. Results indicated that there are significant differences among various treatments of water in terms of change in the concentrations of chemical elements in water. Subsequently, we measured some traits in plant samples in order to evaluate the reaction of the radish plant related to changes in water quality resulting from use of these absorbers. Other characteristics did not show remarkable differences with the control sample based on the results of variance analysis related to plant samples with the exception of shoot’s chloride.

  18. 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.

  19. 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

  20. Dejima VOC dan rangaku

    Directory of Open Access Journals (Sweden)

    Bambang Wibawarta

    2008-10-01

    Full Text Available Japan and the Netherlands have maintained a special relationship for about 300years since the adoption of the National Seclusion policy, the so-called sakoku bythe Tokugawa shogunate (1603-1867. The Dutch began trading with Japan andengaging with Japanese society in 1600, when a Dutch ship, De Liefde, arrived inKyushu. The Tokugawa government measures regarding foreign policy includedregulations on foreign access to Japan and a prohibition on Japanese goingabroad. Between the middle of the seventeenth to the early nineteenth century,Japan was characterized by a stable political pattern in which representativesof the VOC (Dutch East India Company, were the only Europeans with a rightto trade in Japan. In the course of this period, the Japanese evaluation of theDutch changed from regarding them as commercial agents to seeing them asimporters of European knowledge. This paper is especially concerned with theinfluence of the so-called ‘Dutch Studies’ (rangaku on the early modernizationof Japan, especially with regard to medicine and the natural sciences. Thisresearch examines the development of rangaku and the trading between Japanand VOC at Dejima.

  1. Zeolites and Usage Areas

    Directory of Open Access Journals (Sweden)

    Jale Gülen

    2012-06-01

    Full Text Available Zeolites are formed via several reactions from the minerals that consist of aluminium and silica. Zeolites, which have a growing significance in recent days are one of important industrial raw materials. As well as being used as a catalyst, theirability to do ion exchange and adsorption make them even more valuable. Zeolites are used in several industries such as energy, agriculture and animal husbandry, mining and metallurgy, construction, detergent, paper, etc. In this study, the definiton, formation and usage areas of zeolites are explained.

  2. Measurement of VOCs in vehicle exhaust by extractive FTIR spectroscopy

    Science.gov (United States)

    Lechner, Bernhard; Paar, H.; Sturm, Peter J.

    2001-02-01

    12 The detection of benzene and other organic compounds in vehicle exhaust by FT-IR-spectroscopy is seriously limited by the strong interference of carbon dioxide and the rather weak absorption coefficient of the gases. Therefore, a measurement device was developed which separates the components of interest (mostly VOCs) from carbon dioxide, water and nitric oxide. In addition the VOCs have to be pre- concentrated. To avoid condensation of VOCs the measurements have to take place at higher temperatures. The vehicle exhaust was led through an activated charcoal tube where the organic compounds were adsorbed. Afterwards, the charcoal tube was heated in a furnace, the VOCs were desorbed thermically and were carried by (heated) nitrogen into a gas cell with a path-length of 10 m where the concentration of the different species was measured. With the help of this measurement device a lot of VOC- components like benzene, toluene, and xylene were detected successfully. Measurements were performed on an engine test bed and a chassis dynamometer for heavy duty vehicles. The detection limit of most of the VOCs was about 2 to 3 ppb for a sampling time of 20 min. Calibration measurements showed an accuracy of 15%.

  3. On speciation of VOC localization

    Science.gov (United States)

    Chen, S.; Chang, J.; Wang, J.

    2011-12-01

    Most of the gas-phase chemical mechanisms successfully used in gas-phase atmospheric chemical processes, such as CBM-Z, RADM2 or SAPRC-07, treat hundreds of VOC as lumped organic species by their chemical characteristics. Most of the model results are compared with total VOC observations, and it is not appropriate to compare lumped VOC simulations to observations even if there are separate VOC observations like Photochemical Assessment Monitoring Stations (PAMS). While the PAMS Air Quality Model (PAMS-AQM) is developed, separate organic species observed by PAMS without a doubt can be directly compared with model simulations. From the past case study (Chen et al., 2010), it shows a major and very significant finding in that detailed emissions of VOC in the existing emissions database are often in error in Taiwan or other countries due to the fact that the annual VOC emissions are classified into hundreds of species-specific emissions by using the speciation factors following the protocol of the U.S. EPA (AP-42). Based on all PAMS observations from 2006-2007, four base cases with well comparable meteorological simulations were selected for the unified correction for all sources in Taiwan. After the PAMS species emissions are modified, the diurnal patterns and simulation-observation correlation for most of the PAMS species are improved, and the concentration levels are more comparable with those of observations. More expanded case studies also revealed necessary corrections for the PAMS species emissions. Sensitivity analyses for lumped organic species with modified PAMS species emissions are also conducted. After modified PAMS emissions are added into lumped VOC emissions, there is an increase of only 10% of totally VOC emissions. While the sources of the lumped VOC emissions are changed, ozone formation shows no significant change with modified lumped VOC emissions. This helps to support the argument that for ozone simulation, the lumped VOC processes balance out

  4. Potential and actual uses of zeolites in crop protection.

    Science.gov (United States)

    De Smedt, Caroline; Someus, Edward; Spanoghe, Pieter

    2015-10-01

    In this review, it is demonstrated that zeolites have a potential to be used as crop protection agents. Similarly to kaolin, zeolites can be applied as particle films against pests and diseases. Their honeycomb framework, together with their carbon dioxide sorption capacity and their heat stress reduction capacity, makes them suitable as a leaf coating product. Furthermore, their water sorption capacity and their smaller particle sizes make them effective against fungal diseases and insect pests. Finally, these properties also ensure that zeolites can act as carriers of different active substances, which makes it possible to use zeolites for slow-release applications. Based on the literature, a general overview is provided of the different basic properties of zeolites as promising products in crop protection.

  5. Use of Natural Zeolite to Upgrade Activated Sludge Process

    Directory of Open Access Journals (Sweden)

    Hanife Büyükgüngör

    2003-01-01

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

  6. The Fate and Transport of the SiO2 Nanoparticles in a Granular Activated Carbon Bed and Their Impact on the Removal of VOCs

    Science.gov (United States)

    Adsorption isotherm, adsorption kinetics and column breakthrough experiments evaluating trichloroethylene (TCE) adsorption onto granular activated carbon (GAC) were conducted in the presence and absence of silica nanoparticles (SiO2 NPs). Zeta potential of the SiO

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

    DEFF Research Database (Denmark)

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

    2005-01-01

    . 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......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...

  8. 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...... 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...

  9. Diagram of Zeolite Crystals

    Science.gov (United States)

    2003-01-01

    The Center for Advanced Microgravity Materials Processing (CAMMP) in Cambridge, MA, a NASA-sponsored Commercial Space Center, is working to improve zeolite materials for storing hydrogen fuel. CAMMP is also applying zeolites to detergents, optical cables, gas and vapor detection for environmental monitoring and control, and chemical production techniques that significantly reduce by-products that are hazardous to the environment. Depicted here is one of the many here complex geometric shapes which make them highly absorbent. Zeolite experiments have also been conducted aboard the International Space Station

  10. Computer simulation study of in-zeolites templated carbon replicas: structural and adsorption properties for hydrogen storage application; simulation numerique de repliques de zeolithes en carbone: structures et proprietes d'adsorption en vue d'une application au stockage d'hydrogene

    Energy Technology Data Exchange (ETDEWEB)

    Roussel, T

    2007-05-15

    Hydrogen storage is the key issue to envisage this gas for instance as an energy vector in the field of transportation. Porous carbons are materials that are considered as possible candidates. We have studied well-controlled microporous carbon nano-structures, carbonaceous replicas of meso-porous ordered silica materials and zeolites. We realized numerically (using Grand Canonical Monte Carlo Simulations, GCMC) the atomic nano-structures of the carbon replication of four zeolites: AlPO{sub 4}-5, silicalite-1, and Faujasite (FAU and EMT). The faujasite replicas allow nano-casting of a new form of carbon crystalline solid made of tetrahedrally or hexagonally interconnected single wall nano-tubes. The pore size networks are nano-metric giving these materials optimized hydrogen molecular storage capacities (for pure carbon phases). However, we demonstrate that these new carbon forms are not interesting for room temperature efficient storage compared to the void space of a classical gas cylinder. We showed that doping with an alkaline element, such as lithium, one could store the same quantities at 350 bar compared to a classical tank at 700 bar. This result is a possible route to achieve interesting performances for on-board docking systems for instance. (author)

  11. Composite zeolite membranes

    Science.gov (United States)

    Nenoff, Tina M.; Thoma, Steven G.; Ashley, Carol S.; Reed, Scott T.

    2002-01-01

    A new class of composite zeolite membranes and synthesis techniques therefor has been invented. These membranes are essentially defect-free, and exhibit large levels of transmembrane flux and of chemical and isotopic selectivity.

  12. 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 research...... topic. Until now, the main reason for developing hierarchical zeolites has been to achieve heterogeneous catalysts with improved performance but this particular facet has not yet been reviewed in detail. Thus, the present paper summaries and categorizes the catalytic studies utilizing hierarchical...... zeolites that have been reported hitherto. Prototypical examples from some of the different categories of catalytic reactions that have been studied using hierarchical zeolite catalysts are highlighted. This clearly illustrates the different ways that improved performance can be achieved with this family...

  13. 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.

  14. Cu2+ coordinated graphitic carbon nitride (Cu-g-C3N4) nanosheets from melamine for the liquid phase hydroxylation of benzene and VOCs

    Science.gov (United States)

    Muniandy, Lingeswarran; Adam, Farook; Mohamed, Abdul Rahman; Iqbal, Anwar; Rahman, Nur Ruzaina Abdul

    2017-03-01

    Copper modified graphitic carbon nitride nanosheets (Cu-g-C3N4) was synthesized and used in the hydroxylation of benzene under mild conditions with hydrogen peroxide as a "green" oxidant. The presence of copper ions (Cu2+) was confirmed from the XPS, EDX and also the hydrogen TPR analyses. The catalyst shows excellent activity, resulting in 74.1% conversion of benzene with phenol as the major product (97.5%) and only p-benzoquinone as the by-product. The catalyst's selectivity towards phenol did not exhibit significant change even after being reused for several cycles. The catalyst was also used for the oxidation of several other organic compounds with interesting results.

  15. Rapid synthesis of beta zeolites

    Science.gov (United States)

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

    2015-08-18

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

  16. 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.

  17. Characteristic study on volatile organic compounds optical fiber sensor with zeolite thin film-coated spherical end

    Science.gov (United States)

    Wu, Binqing; Zhao, Chunliu; Kang, Juan; Wang, Dongning

    2017-03-01

    In this paper, characteristic of volatile organic compounds (VOCs) optical fiber sensor with zeolite thin film-coated spherical end were investigated detailedly. The zeolite film and spherical end constituted an arc-shaped inline Fabry-Perot (F-P) cavity, and VOCs were measured by monitoring the wavelength shift of F-P interference which induced by the VOCs molecule adsorption of the zeolite film. The responses of the optical fiber sensor for monitoring isopropanol and formaldehyde were observed and especially observing the response of the optical fiber sensor in the mixed VOCs state. Experimental results show that the sensitivities of the optical fiber sensor for monitoring isopropanol and formaldehyde are 281.9 pm/ppm and 4.99 pm/ppm, respectively. The optical fiber sensor is more suitable for isopropanol measurement than formaldehyde. In the mixed VOCs state, the characteristic of the optical fiber sensor for isopropanol measurement is slightly changed when the air chamber is mixed with low concentration of formaldehyde, but the optical fiber sensor is still effective for isopropanol measurement.

  18. Fabrication of a gas sensor array with micro-wells for VOCs gas sensing based on polymer/carbon nanotube thin films

    Science.gov (United States)

    Xie, Guangzhong; Xie, Tao; Zhu, Tao; Jiang, Yadong; Tai, Huiling

    2014-08-01

    In this paper, gas sensor array with micro-well was designed and prepared by Micro Electro-Mechanical Systems (MEMS) technology. The micro-well and interdigital electrodes of sensor array were prepared using photolithography process, reactive ion etching (RIE) process, wet etching and conventional vacuum evaporation. In the manufacture process of the gas sensor array, KOH wet etching process was mainly discussed. The optimum etching processing parameters were as follows: 30 wt% KOH solution at 80 °C, a cooling back-flow device and a magnetic stirrer. The multi-walled carbon nanotubes (MWCNTs)-polyethyleneoxide (PEO) and MWNTs-Polyvinylpyrrolidone (PVP) composite films were utilized as sensitive layers to test gas-sensing properties. Response performances of MWCNTs- PEO and MWNTs-PVP composite films to toluene vapor and methanol vapor at room temperature were investigated. The results revealed that the sensor array showed a larger sensitivity to toluene vapor than to methanol vapor. In addition, the sensing mechanisms were studied as well.

  19. Composting domestic sewage sludge with natural zeolites in a rotary drum reactor.

    Science.gov (United States)

    Villaseñor, J; Rodríguez, L; Fernández, F J

    2011-01-01

    This work aimed the influence of zeolites addition on a sludge-straw composting process using a pilot-scale rotary drum reactor. The type and concentration of three commercial natural zeolites were considered: a mordenite and two clinoptilolites (Klinolith and Zeocat). Mordenite caused the greatest carbon removal (58%), while the clinoptilolites halved losses of ammonium. All zeolites removed 100% of Ni, Cr, Pb, and significant amounts (more than 60%) of Cu, Zn and Hg. Zeocat displayed the greatest retention of ammonium and metals, and retention efficiencies increased as Zeocat concentration increased. The addition of 10% Zeocat produced compost compliant with Spanish regulations. Zeolites were separated from the final compost, and leaching studies suggested that zeolites leachates contained very low metals concentrations (zeolites could be separated from the compost prior to application. The different options have been discussed.

  20. Selective treatment of VOC-polluted industrial air using an hybrid adsorption-ozonization process; Traitement selectif de l'air industriel pollue en COV par un procede hybride adsorption-ozonation

    Energy Technology Data Exchange (ETDEWEB)

    Manero, M.H. [Toulouse-3 Univ., Lab. d' Ingenierie des Procedes de L' Environnement, INSA de Toulouse, 31 (France); Monneyron, P. [Bordeaux-1 Univ., Lab. Transfert, Ecoulement, Fluides, Energetiques (TREFLE), UMR 8508, 33 - Talence (France)

    2005-09-01

    This article describes an hybrid process combining the adsorption on zeolites and the oxidation by ozone at ambient temperature and pressure in a single reactor for the selective treatment of volatile organic compounds (VOCs). After several cycles of operation, the zeolite capacity is maintained and not altered by the ozonization. The analysis of the output gases shows the absence of ozone and only traces of oxidation products meaning that the oxidation of the organic molecules is complete. The oxygen statuses show that the ozone introduced in the system is totally used to oxide VOCs. The industrial scale feasibility of the method requires further studies. (J.S.)

  1. Synthesis of A type zeolite from rice husk ash; Momigarabai kara no A gata zeolite no gosei

    Energy Technology Data Exchange (ETDEWEB)

    Inoue, K. [Kyushu National Industrial Research Institute, Saga (Japan); Hara, N. [Kagoshima Prefectural Industrial Technology Center, Kagoshima (Japan)

    1995-09-01

    Attempts have been made on synthesizing A-type zeolite from rice husk ash made from burning under different conditions. The rice husk ash (comprising SiO2 at 90 and odd percent) was obtained by heating the rice husk to remove volatile constituents, burning at 350{degree}C to reduce carbon content, and further burning at 400 to 900{degree}C. Soda aluminate and caustic soda were used as additional materials for zeolite. Zeolite was synthesized by so mixing the raw materials that predetermined composition is achieved, adding seed crystals, and heating at 90{degree}C. The result may be summarized as follows: raising the burning temperature reduces the carbon content and increases whiteness of the rice husk ash; dissolution velocity of rice husk ash into NaOH aqueous solution was measured to evaluate the reactivity of the ash (the higher the more preferable); raised burning temperature causes transfer from amorphous state to crystalline state, reducing the dissolution velocity; the lower the burning temperature, the higher the A-type zeolite production rate becomes; whiteness in zeolite is insufficient; preparing water glass from rice husk ash and synthesizing zeolite therefrom achieves high whiteness and high production rate. 6 refs., 4 figs., 2 tabs.

  2. 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.

  3. 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.

  4. 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.

  5. Advances in nanosized zeolites

    Science.gov (United States)

    Mintova, Svetlana; Gilson, Jean-Pierre; Valtchev, Valentin

    2013-07-01

    This review highlights recent developments in the synthesis of nanosized zeolites. The strategies available for their preparation (organic-template assisted, organic-template free, and alternative procedures) are discussed. Major breakthroughs achieved by the so-called zeolite crystal engineering and encompass items such as mastering and using the physicochemical properties of the precursor synthesis gel/suspension, optimizing the use of silicon and aluminium precursor sources, the rational use of organic templates and structure-directing inorganic cations, and careful adjustment of synthesis conditions (temperature, pressure, time, heating processes from conventional to microwave and sonication) are addressed. An on-going broad and deep fundamental understanding of the crystallization process, explaining the influence of all variables of this complex set of reactions, underpins an even more rational design of nanosized zeolites with exceptional properties. Finally, the advantages and limitations of these methods are addressed with particular attention to their industrial prospects and utilization in existing and advanced applications.

  6. Pollution characteristic of VOCs of ambient air in winter and spring in Shijiazhuang City

    Directory of Open Access Journals (Sweden)

    Qing CHANG

    2015-06-01

    Full Text Available In order to further explore the pollution characteristics of volatile organic compounds in ambient air in winter and spring in Shijiazhuang City, the pollution characteristics of 62 volatile organic compounds (VOCs, monthly and quarterly variation, the correlation between VOCs and PM2.5, and the main sources of VOCs are investigated by using EPA TO-15 method. It shows that 40 organic compounds of the 64 VOCs have been quantitatively determined in winter and spring in the city, which are mainly acetone, benzene, carbon tetrachloride, dichloromethane, toluene, ethyl acetate, etc.. In the no-quantitatively determined components, higher ethanol, butyl acetate, butane etc. are detected. The VOCs concentration has positive correlation with the PM2.5 concentration during haze days.

  7. Dimethyl carbonate synthesis via basic zeolite catalyzed transesterification%钾盐修饰KX分子筛催化酯交换反应合成碳酸二甲酯

    Institute of Scientific and Technical Information of China (English)

    赵天生; 李永昕; 陈兴权; 韩怡卓; 孙予罕

    2001-01-01

    Potassium salt modified KX zeolite has been investigated as base catalyst for the synthesis of dimethyl carbonate (DMC)via transesterification. The activity of the catalyst varies with both the type of potassium salt and the preparation of KX. KOH/KX and K2CO3/KX result in the highest conversion of propylene carbonate and yield of dimethyl carbonate. The basicity originates mainly from thermal reaction of potassium salt with the surface of KX by analyzing XRD, FTIR and TPD characterization. The base site correspondent to formic acid TPD peaks above 678 K is considered to be highly active towards the transesterification.%考察了钾盐修饰的KX分子筛作为固体碱对碳酸丙烯酯和甲醇酯交换反应合成碳酸二甲酯的催化性能.结果表明,催化活性随着负载钾盐的种类的不同而变化,KOH/KX和K2CO3/KX给出了高的碳酸丙烯酯转化率和碳酸二甲酯产率.XRD,FTIR和TPD表征表明,催化剂的碱性主要来源于钾盐与KX表面的反应,相应于678 K以上催化刘的甲酸TPD峰对应的碱性位是酯交换反应的活性位.

  8. 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.

  9. Zeolites and Catalysis

    Science.gov (United States)

    1999-12-15

    Handbook of Heterogeneous Catalysis ,Vol. als: State of the Art 1994, Studies in Surface Science and 5, Wiley-VCH, Weinheim, 1997, p. 2329. Catalysis, Vol...Weitkamp (Eds.), in Zeolite and Microporous Materials, Studies in Surface Handbook of Heterogeneous Catalysis , Vol. 4, Wiley-VCH, Science and Catalysis

  10. 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...

  11. 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.

  12. Synthesis of Modified β-Zeolite Under Microwave Irradiation and Its Use on Etherification

    Institute of Scientific and Technical Information of China (English)

    Ma Jun; Wang Haiyan; Hu Tingfang; Tian Yanwen; Zhou Tong; Qin Zhiwei

    2004-01-01

    β -zeolite was synthesized by using tetraethyl ammonium hydroxide as the template reagent and microwave radiation as the heat source. The effect of the sol composition and the radiation temperature on zeolite crystallinity was investigated. The zeolite was tested and compared with the commercial product, which was produced by conventional hydrothermal synthesis method. ,The physico-chemical properties of the synthesized samples, the specific surface area of the samples synthesized under microwave irradiation and pore volume measured by X-ray diffraction apparatus, were better than the conventional samples. The etherification experiment on FCC light naphtha in the presence of transition metals modified H β -zeolite, which was synthesized firstly under microwave irradiation, was studied in a fixed-bed reactor. The effect of catalyst preparation conditions on its activity, stability and the effect of reaction temperature, methanol/tertiary-carbon olefin molar ratio and liquid hourly space velocity on the etherification reaction were discussed. The experimental results showed that the different metals modified H β -zeolite had different etherification performances. And the conversion of tertiary carbon-olefins of the molybdenum modified H β zeolite, which was loaded at a concentration of 3 percents, was higher than that on 6.0 percent of H β zeolite. The modified H β zeolite catalysts possessed favorable prospects for its higher stability.

  13. Anthropogenic VOC speciation in emission inventories: a method for improvement and evaluation

    Science.gov (United States)

    von Schneidemesser, E.; D'angiola, A.; Granier, C.; Monks, P. S.; Law, K.

    2011-12-01

    Volatile organic compounds (VOCs) are important precursor compounds for the formation of ozone and other secondary organic aerosols. Anthropogenic sources of VOCs are dominated by industrial usage and transportation sources, the latter being extremely important in urban areas. Megacities and large urban conglomerations are emission hot spots that exert disproportionately large adverse health effects on the population and surrounding environment, owing to their high population density and concentrated emission sources. Exceedances of ozone air quality standards are a problem in many urban areas. Improvements in the modelling of ozone precursors would benefit our understanding of the impact of changes in emissions and the effect of future legislation on air quality. As many VOCs are extremely reactive in the atmosphere and have high ozone forming potential, improved speciation of VOCs in models could lead to better predictions of ozone levels and secondary organic aerosol formation. Previously, VOC and carbon monoxide (CO) data from urban areas around the world were compared. Significant differences in VOC concentrations were observed, however, when normalized to CO, the VOC-CO ratios were similar for many locations and over time, even as emission reductions were implemented. The largest variation was found in the lighter alkanes due to the use of alternative transportation fuels in various world regions. These ratios were grouped by region and used to develop a new speciation for surface emissions of VOCs, by applying the regional observed VOC-CO ratios to the CO emissions for the urban areas. Urban areas were defined as 150 inhabitants per km2 or greater. Model simulations were performed using the MOZART-4 chemistry transport model to assess the improved speciation of the VOC emissions. The model outputs were compared to urban observational data where available. The impact of the new speciation of the distribution of CO, OH and ozone at the global scale will be

  14. [Evaluation and selection of VOCs treatment technologies in packaging and printing industry].

    Science.gov (United States)

    Wang, Hai-Lin; Wang, Jun-Hui; Zhu, Chun-Lei; Nie, Lei; Hao, Zheng-Ping

    2014-07-01

    Volatile organic compounds (VOCs) play an important role in urban air pollution. Activities of industries including the packaging and printing industries are regarded as the major sources. How to select the suitable treating techniques is the major problem for emission control. In this article, based on the VOCs emission characteristics of the packaging and printing industry and the existing treatment technologies, using the analytic hierarchy process (AHP) model, an evaluation system for VOCs selection was established and all the technologies used for treatment were assessed. It showed that the priority selection was in the following order: Carbon Fiber Adsorption-Desorption > Granular Carbon Adsorption-Desorption > Thermal Combustion > Regenerative Combustion > Catalytic combustion > Rotary adsorption-concentration and combustion > Granular Carbon adsorption-concentration and combustion. Carbon Fiber Adsorption-Desorption was selected as the best available technology due to its highest weight among those technologies.

  15. The Effect of Zeolite on Aggregate Stability Indices

    Directory of Open Access Journals (Sweden)

    F. Sohrab

    2016-02-01

    Full Text Available Introduction: Soil structural stability affects the profitability and sustainability of agricultural systems. Particle size distribution (PSD and aggregate stability are the important characteristics of soil. Aggregate stability has a significant impact on the development of the root system, water and carbon cycle and soil resistance against soil erosion. Soil aggregate stability, defined as the ability of the aggregates to remain intact when subject to a given stress, is an important soil property that affects the movement and storage of water, aeration, erosion, biological activity and growth of crops. Dry soil aggregate stability (Mean Weight Diameter (MWD, Geometric Mean Diameter (GMD and Wet Aggregate Stability (WAS are important indices for evaluating soil aggregate stability.To improve soil physical properties, including modifying aggregate, using various additives (organic, inorganic and chemicals, zeolites are among what has been studied.According to traditional definition, zeolites are hydratealuminosilicates of alkaline and alkaline-earth minerals. Their structure is made up of a framework of[SiO4]−4 and [AlO4]−5 tetrahedron linked to each other's cornersby sharing oxygen atoms. The substitution of Si+4 by Al+3 intetrahedral sites results inmore negative charges and a high cation exchange capacity.Zeolites, as natural cation exchangers, are suitable substitutes to remove toxic cations. Among the natural zeolites,Clinoptilolite seems to be the most efficient ion exchanger and ion-selective material forremoving and stabilizing heavy metals.Due to theexisting insufficient technical information on the effects of using different levels of zeolite on physical properties of different types of soils in Iran, the aim of this research was to assess the effects of two different types of zeolite (Clinoptilolite natural zeolite, Z4, and Synthetic zeolite, A4 on aggregate stability indicesof soil. Materials and Methods: In this study at first

  16. Discovery of optimal zeolites for challenging separations and chemical transformations using predictive materials modeling

    Science.gov (United States)

    Bai, Peng; Jeon, Mi Young; Ren, Limin; Knight, Chris; Deem, Michael W.; Tsapatsis, Michael; Siepmann, J. Ilja

    2015-01-01

    Zeolites play numerous important roles in modern petroleum refineries and have the potential to advance the production of fuels and chemical feedstocks from renewable resources. The performance of a zeolite as separation medium and catalyst depends on its framework structure. To date, 213 framework types have been synthesized and >330,000 thermodynamically accessible zeolite structures have been predicted. Hence, identification of optimal zeolites for a given application from the large pool of candidate structures is attractive for accelerating the pace of materials discovery. Here we identify, through a large-scale, multi-step computational screening process, promising zeolite structures for two energy-related applications: the purification of ethanol from fermentation broths and the hydroisomerization of alkanes with 18-30 carbon atoms encountered in petroleum refining. These results demonstrate that predictive modelling and data-driven science can now be applied to solve some of the most challenging separation problems involving highly non-ideal mixtures and highly articulated compounds.

  17. 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.

  18. Granulated zeolite plant "Alusil", Zvornik

    Directory of Open Access Journals (Sweden)

    Stanković Mirjana S.

    2003-01-01

    Full Text Available The IGPC's Engineering Department designed basic technological and machine projects for a granulated zeolite production plant, on the basis of which a pilot plant with an initial capacity of 5,000 t/y was constructed in 1984, within Birač - Zvornik production complex. The technology in these projects was developed in the laboratories of the IGPC.Several goals were realized by designing a granulated zeolite production plant. This technology is one of the newest state of the art high tech technologies. The product meets all quality demands, as well as environmental regulations, by which granulated zeolite production for various uses was developed. The granulated zeolite production process is fully automatized, and the product has uniform quality. There is no waste material in granulated zeolite production, because all products with unsatisfactory quality are returned to the process. The production process can be controlled manually, which is necessary during start - up, and repairs.

  19. Understanding the dissolution of zeolites.

    Science.gov (United States)

    Hartman, Ryan L; Fogler, H Scott

    2007-05-08

    Scientific knowledge of how zeolites, a unique classification of microporous aluminosilicates, undergo dissolution in aqueous hydrochloric acid solutions is limited. Understanding the dissolution of zeolites is fundamental to a number of processes occurring in nature and throughout industry. To better understand the dissolution process, experiments were carried out establishing that the Si-to-Al ratio controls zeolite framework dissolution, by which the selective removal of aluminum constrains the removal of silicon. Stoichiometric dissolution is observed for Type 4A zeolite in HCl where the Si-to-Al ratio is equal to 1.0. Framework silicon dissolves completely during Type 4A dissolution and is followed by silicate precipitation. However, for the zeolite analcime which has a Si-to-Al ratio of 2.0 dissolves non-stoichiometrically as the selective removal of aluminum results in partially dissolved silicate particles followed by silicate precipitation. In Type Y zeolite, exhibiting a Si-to-Al ratio of 3.0, there is insufficient aluminum to weaken the structure and cause silicon to dissolve in HCl. Thus, little or no precipitation is observed, and amorphous undissolvable silicate particles remain intact. The initial dissolution rates of Type Y and 4A zeolites demonstrate that dissolution is constrained by the number of available reaction sites, and a selective removal rate parameter is applied to delineate the mechanism of particle dissolution by demonstrating the kinetic influence of the Si-to-Al ratio. Zeolite framework models are constructed and used to undergird the basic dissolution mechanism. The framework models, scanning electron micrographs of partially dissolved crystals, and experimentally measured dissolution rates all demonstrate that a zeolite's Si-to-Al framework ratio plays a universal role in the dissolution mechanism, independent of framework type. Consequently, the unique mechanism of zeolite dissolution has general implications on how petroleum

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

    Directory of Open Access Journals (Sweden)

    Fitriyah Fitriyah

    2016-07-01

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

  1. 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.

  2. 688 AMBIENT VOLATILE ORGANIC COMPOUNDS (VOCS ...

    African Journals Online (AJOL)

    Osondu

    The VOCs were classified thus: aromatics 41%, halogenated 42%, esters 3%, ketones 8%, ... and Industrial emission were identified as sources of VOCs in the studied industrial area with ... canisters, or by dynamic or diffusive adsorption .... The GC/FID was standardized and ... with CS2 was prepared from stock standard in.

  3. DEVELOPING A NO-VOC WOOD TOPCOAT

    Science.gov (United States)

    The paper reports an evaluation of a new low-VOC (volatile organic compound) wood coating technology, its performance characteristics, and its application and emissions testing. The low-VOC wood coating selected for the project was a two-component, water-based epoxy coating. Poly...

  4. In situ infrared molecular detection using palladium-containing zeolite films.

    Science.gov (United States)

    Thomas, Sébastien; Bazin, Philippe; Lakiss, Louwanda; de Waele, Vincent; Mintova, Svetlana

    2011-12-06

    In situ IR detection of carbon monoxide in the presence of hydrocarbons (methanol and pentane) using Pd-containing zeolite thin films is reported. The thin films are prepared by spin coating deposition of nanosized LTL and BEA type zeolites suspensions; the palladium clusters are introduced in the nanosized zeolites by ion exchange followed by γ radiolysis of the coating suspensions. The Pd-containing zeolite films with a thickness of 200 nm are exposed to a single gas (either CO or hydrocarbons) or gas mixtures in the presence of water (100 ppm), and the IR spectra are collected continuously at 25, 75, and 100 °C. The fast recognition of very low concentrations of CO (2-100 ppm) in the presence of highly concentrated vapors of methanol or pentane (400-4000 ppm) with the Pd-containing zeolite films is demonstrated. The detection of CO and hydrocarbons is instant, which is a function of the low thickness of the films, small size of the individual zeolite crystals, and regular size and high stability of the Pd clusters in the zeolite films. The heat of adsorption for all experiments is similar (15 kJ.mol(-1)), which is explained with weak interactions between the carbon monoxide and palladium clusters in the zeolite films at temperatures below 100 °C. The nanosized zeolites with homogeneously distributed Pd clusters deposited in thin films demonstrate high molecular recognition capacity toward low concentrations of carbon monoxide under real environmental conditions, i.e., in the presence of water and hydrocarbons.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2013-01-29

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

  6. T2VOC user`s guide

    Energy Technology Data Exchange (ETDEWEB)

    Falta, R.W. [Clemson Univ., Clemson, SC (United States). Dept. of Earth Sciences; Pruess, K.; Finsterle, S. [Lawrence Berkeley Lab., CA (United States); Battistelli, A. [AQUATER S.p.A., San Lorenzo in Campo, (Italy)

    1995-03-01

    T2VOC is a numerical simulator for three-phase, three-component, non-isothermal flow of water, air, and a volatile organic compound (VOC) in multidimensional heterogeneous porous media. Developed at the Lawrence Berkeley Laboratory, T2VOC is an extension of the TOUGH2 general-purpose simulation program. This report is a self-contained guide to application of T2VOC to subsurface contamination problems involving nonaqueous phase liquids (NAPLs). It gives a technical description of the T2VOC code, including a discussion of the physical processes modeled, and the mathematical and numerical methods used. Detailed instructions for preparing input data are presented along with several illustrative sample problems.

  7. Properties and applications of zeolites.

    Science.gov (United States)

    Rhodes, Christopher J

    2010-01-01

    Zeolites are aluminosilicate solids bearing a negatively charged honeycomb framework of micropores into which molecules may be adsorbed for environmental decontamination, and to catalyse chemical reactions. They are central to green-chemistry since the necessity for organic solvents is minimised. Proton-exchanged (H) zeolites are extensively employed in the petrochemical industry for cracking crude oil fractions into fuels and chemical feedstocks for other industrial processes. Due to their ability to perform cation-exchange, in which the cations that are originally present to counterbalance the framework negative charge may be exchanged out of the zeolite by cations present in aqueous solution, zeolites are useful as industrial water-softeners, in the removal of radioactive Cs+ and Sr2+ cations from liquid nuclear waste and in the removal of toxic heavy metal cations from groundwaters and run-off waters. Surfactant-modified zeolites (SMZ) find particular application in the co-removal of both toxic anions and organic pollutants. Toxic anions such as arsenite, arsenate, chromate, cyanide and radioactive iodide can also be removed by adsorption into zeolites that have been previously loaded with co-precipitating metal cations such as Ag+ and Pb2+ which form practically insoluble complexes that are contained within the zeolite matrix.

  8. [Effect of Nano Zeolite on Chemical Fractions of Cd in Soil and Its Uptake by Cabbage].

    Science.gov (United States)

    Xiong, Shi-juan; Xu, Wei-hong; Xie, Wen-wen; Chen, Rong; Chen, Yong-qin; Chi, Sun-lin; Chen, Xu- gen; Zhang, Jin-zhong; Xiong, Zhi-ting; Wang, Zheng-yin; Xie, De-ti

    2015-12-01

    Incubation experiments were carried out to investigate the influence of different nano zeolite (NZ) and ordinary zeolite (OZ) levels(0, 5, 10 and 20 g · kg⁻¹) on the change trends in fraction distribution coefficient (FDC) of Cd when exposed to different Cadmium (Cd) levels (1, 5, 10 and 15 mg · kg⁻¹), and pot experiments were carried out to investigate their influence on soil Cd fraction and Cd uptake by cabbage. The results in incubation experiments showed that the application of nano zeolite as well as ordinary zeolite effectively decreased the FDC of exchangeable Cd and increased the FDC of Fe-Mn oxide fraction. The FDC of soil Cd from 0 d to 28 d was deceased at first, then increased and tended to be stable, and finally increased. At the end of incubation, the FDC of soil exchangeable Cd decreased from 72.0%-88.0% to 30.0%-66.4%. Exchangeable fraction Cd was the most dominant Cd fraction in soil during the whole incubation. The results in pot experiment indicated that the application of nano zeolite and ordinary zeolite decreased the concentration and FDC of soil exchangeable Cd, and concurrently the concentration and FDC of Cd in carbonate, Fe-Mn oxide, organic matter and residual fraction were increased. The lowest EX-Cd was observed in the treatment with high dose of nano zeolite (20 g · kg⁻¹). The FDC of exchangeable Cd showed significant negative relationship with the soil pH (P zeolite when exposed to 5 mg · kg⁻¹ 1 and Cd, respectively; FDC of exchangeable Cd decreased by 16.3%-47.7% and 16.2%-46.7%; Cd concentration in each tissues of cabbage decreased by 1.0%-75.0% and 3.8%-53.2%, respectively. Moreover, the reduction effect of nano zeolite on soil and plant Cd was better than that of ordinary zeolite. The growth of cabbage was stimulated by low and medium zeolite doses (≤ 10 g · kg⁻¹), while inhibited by high zeolite doses (20 g · kg⁻¹). Compared to ordinary zeolite, the biomass of Chinese cabbage was significantly increased

  9. DFT investigations of the reaction mechanism of diethyl carbonate synthesis catalyzed by Cu(I)/β or Pd(II)/β zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Shen, Yongli [Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Wang, Shengping, E-mail: spwang@tju.edu.cn [Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Huang, Shouying [Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Li, Zhong [Key Laboratory of Coal Science and Technology of Ministry of Education, Taiyuan University of Technology, Taiyuan 030024, Shanxi (China); Ma, Xinbin [Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China)

    2014-07-01

    Density functional theory (DFT) calculations are used to investigate the oxidative carbonylation of ethanol occurring on Cu(I)/β or Pd(II)/β. The thermochemistry and activation energy for all elementary steps involved in the formation of diethyl carbonate are presented. Upon calculation, we identify that the mechanisms for the formation of surface O atom are varying on different catalysts. Ethanol can react with the surface O atom to produce (C{sub 2}H{sub 5}O)(OH)-M/β (M = Cu{sup +}, Pd{sup 2+}) species. And this intermediate can further react with carbon monoxide or ethanol to give monoethyl carbonate or di-ethoxied species ((C{sub 2}H{sub 5}O){sub 2}-M/β). Diethyl carbonate can form via two distinct reaction pathways: (I) ethanol reacts with monoethyl carbonate or (II) carbon monoxide inserts into di-ethoxide species. Upon calculation, we confirmed that both reaction pathways for the formation of DEC are accessible on Cu(I)/β catalyst, whereas only Path II is achievable on Pd(II)/β catalyst.

  10. DFT investigations of the reaction mechanism of diethyl carbonate synthesis catalyzed by Cu(I)/β or Pd(II)/β zeolites

    Science.gov (United States)

    Shen, Yongli; Wang, Shengping; Huang, Shouying; Li, Zhong; Ma, Xinbin

    2014-07-01

    Density functional theory (DFT) calculations are used to investigate the oxidative carbonylation of ethanol occurring on Cu(I)/β or Pd(II)/β. The thermochemistry and activation energy for all elementary steps involved in the formation of diethyl carbonate are presented. Upon calculation, we identify that the mechanisms for the formation of surface O atom are varying on different catalysts. Ethanol can react with the surface O atom to produce (C2H5O)(OH)-M/β (M = Cu+, Pd2+) species. And this intermediate can further react with carbon monoxide or ethanol to give monoethyl carbonate or di-ethoxied species ((C2H5O)2-M/β). Diethyl carbonate can form via two distinct reaction pathways: (I) ethanol reacts with monoethyl carbonate or (II) carbon monoxide inserts into di-ethoxide species. Upon calculation, we confirmed that both reaction pathways for the formation of DEC are accessible on Cu(I)/β catalyst, whereas only Path II is achievable on Pd(II)/β catalyst.

  11. Effect of the formation of secondary pores in zeolite ZSM-5 on the properties of molybdenum-zeolite catalysts for methane aromatization

    Science.gov (United States)

    Kucherov, A. V.

    2014-03-01

    A study is performed of 4% Mo/ZSM-5 (30) catalysts for methane aromatization prepared by solid-phase synthesis with mechanical mixing of a zeolite with MoO3 followed by calcination at 550°C. Zeolite etched with sodium hydroxide solutions and dealuminated with aluminum nitrate solutions is used as a support. Catalytic studies of the catalysts are conducted. The effect of treating the initial zeolite on the properties of catalysts in methane aromatization is determined. The effect subsequently treating a zeolite support has on the acid sites of a catalyst is confirmed by means of temperature-programmed reduction and the temperature-programmed desorption of NH3. The formation of molybdenum ions in the +5 oxidation state during catalysis and the presence of graphitized carbon deposits on a spent catalyst's surface are confirmed by EPR and temperature-programmed oxidation.

  12. Photoelectron Imaging of OXIDE.VOC Clusters

    Science.gov (United States)

    Patros, Kellyn M.; Mann, Jennifer; Chick Jarrold, Caroline

    2016-06-01

    Perturbations of the bare O2- and O4- electronic structure arising from VOC (VOC = hexane, isoprene, benzene and benzene.D6) interactions are investigated using anion photoelectron imaging at 2.33 and 3.49 eV photon energies. Trends observed from comparing features in the spectra include VOC-identity-dependent electron affinities of the VOC complexes relative to the bare oxide clusters, due to enhance stability in the anion complex relative to the neutral. Autodetachment is observed in all O4-.VOC spectra and only isoprene with O2-. In addition, the intensities of transitions to states correlated with the singlet states of O2 neutral via detachment from the O2-.VOC anion complexes show dramatic VOC-identity variations. Most notably, benzene as a complex partner significantly enhances these transitions relative to O2- and O2-.hexane. A less significant enhancement is also observed in the O2-.isoprene complex. This enhancement may be due to the presence of low-lying triplet states in the complex partners.

  13. Preparation of zeolite covered cellulose fibers

    Energy Technology Data Exchange (ETDEWEB)

    Mintova, S.; Valtchev, V. [Institute of Applied Mineralogy, Sofia (Bulgaria)

    1995-12-01

    Membrane separation has proved to be an important technology in chemical industry. That is why the design of different type of zeolite containing membranes has received much attention during the last decade. Zeolite containing filters and membranes were prepared by embedding zeolite crystals with adhesive substances in the cellulose matrix. This communication discussed the preparation of zeolite containing cellulose materials by in situ crystallization. Discussed axe: (1) the effect of the vegetal fiber structure and chemical composition (2) the effect of the type of the zeolite coating; (3) the effect of the mechanical and chemical treatment of the fibers on the process of the fiber zeolite coating.

  14. Hot topic: prevention of parturient paresis and subclinical hypocalcemia in dairy cows by zeolite A administration in the dry period

    DEFF Research Database (Denmark)

    Thilsing-Hansen, T; Jørgensen, R J; Thilsing, Trine

    2001-01-01

    To test the effects of a zeolite feed supplement on parturient calcium status and milk fever, two groups of dry cows were treated with either 1 kg of zeolite/d or none for 4 wk prepartum. At calving and d 1 and 2 after calving all cows were given 250 g of calcium carbonate as a drench, and a bloo...... taken, none of the zeolite-treated cows contracted milk fever or experienced subclinical hypocalcemia.......To test the effects of a zeolite feed supplement on parturient calcium status and milk fever, two groups of dry cows were treated with either 1 kg of zeolite/d or none for 4 wk prepartum. At calving and d 1 and 2 after calving all cows were given 250 g of calcium carbonate as a drench, and a blood...... sample was taken. Serum calcium analysis revealed a greater calcium concentration in zeolite-treated cows. While three control cows contracted milk fever, necessitating intravenous calcium therapy, and six out of eight control cows experienced serum calcium levels below 2 mmol/L in one or more samples...

  15. EVALUATION OF LOW-VOC LATEX PAINTS

    Science.gov (United States)

    The paper gives results of an evaluation of four commercially available low-VOC (volatile organic compound) latex paints as substitutes for conventional latex paints by assessing both their emission characteristics and their performance as coatings. Bulk analysis indicated that ...

  16. Locating industrial VOC sources with aircraft observations.

    Science.gov (United States)

    Toscano, P; Gioli, B; Dugheri, S; Salvini, A; Matese, A; Bonacchi, A; Zaldei, A; Cupelli, V; Miglietta, F

    2011-05-01

    Observation and characterization of environmental pollution, focussing on Volatile Organic Compounds (VOCs), in a high-risk industrial area, are particularly important in order to provide indications on a safe level of exposure, indicate eventual priorities and advise on policy interventions. The aim of this study is to use the Solid Phase Micro Extraction (SPME) method to measure VOCs, directly coupled with atmospheric measurements taken on a small aircraft environmental platform, to evaluate and locate the presence of VOC emission sources in the Marghera industrial area. Lab analysis of collected SPME fibres and subsequent analysis of mass spectrum and chromatograms in Scan Mode allowed the detection of a wide range of VOCs. The combination of this information during the monitoring campaign allowed a model (Gaussian Plume) to be implemented that estimates the localization of emission sources on the ground.

  17. Hydrothermal alteration and zeolitization of the Fohberg phonolite, Kaiserstuhl Volcanic Complex, Germany

    Science.gov (United States)

    Weisenberger, Tobias Björn; Spürgin, Simon; Lahaye, Yann

    2014-11-01

    The subvolcanic Fohberg phonolite (Kaiserstuhl Volcanic Complex, Germany) is an economic zeolite deposit, formed by hydrothermal alteration of primary magmatic minerals. It is mined due to the high (>40 wt%) zeolite content, which accounts for the remarkable zeolitic physicochemical properties of the ground rock. New mineralogical and geochemical studies are carried out (a) to evaluate the manifestation of hydrothermal alteration, and (b) to constrain the physical and chemical properties of the fluids, which promoted hydrothermal replacement. The alkaline intrusion is characterized by the primary mineralogy: feldspathoid minerals, K-feldspar, aegirine-augite, wollastonite, and andradite. The rare-earth elements-phase götzenite is formed during the late-stage magmatic crystallization. Fluid-induced re-equilibration of feldspathoid minerals and wollastonite caused breakdown to a set of secondary phases. Feldspathoid minerals are totally replaced by various zeolite species, calcite, and barite. Wollastonite breakdown results in the formation of various zeolites, calcite, pectolite, sepiolite, and quartz. Zeolites are formed during subsolidus hydrothermal alteration (values indicate a local origin of the elements necessary for secondary mineral formation from primary igneous phases. In addition, fractures cut the intrusive body, which contain zeolites, followed by calcite and a variety of other silicates, carbonates, and sulfates as younger generations. Stable isotope analysis of late-fracture calcite indicates very late circulation of meteoric fluids and mobilization of organic matter from surrounding sedimentary units.

  18. [Effects of Phosphate and Zeolite on the Transformation of Cd Speciation in Soil].

    Science.gov (United States)

    Wang, Xiu-li; Liang, Cheng-hua; Ma, Zi-hui; Han, Yue

    2015-04-01

    The test simulated exogenous Cd contaminated soil indoors, and studied separate application of potassium dihydrogen phosphate, diammonium hydrogen phosphate and zeolite, and combined application of zeolite and dipotassium hydrogen phosphate, zeolite and diammonium hydrogen phosphate, as well as the effect on the morphological changes of Cd contaminated soil. The results showed that soil exchangeable Cd contents were reduced in different degrees after the application of different modifiers, and the carbonate bound and Fe-Mn oxide bound, organic bound and residual Cd contents increased. By comparison, the separate application of potassium dihydrogen phosphate, diammonium hydrogen phosphate and zeolite, and the combined application of zeolite and dipotassium hydrogen phosphate, zeolite and diammonium hydrogen phosphate respectively reduced the soil available Cd contents at 25.2% -51.7%, 21.6% - 46.8%, 6.4% - 23.2%, 38.6% - 61.4%, and 34.1% - 56.4%. All treatments could increase the soil available phosphorus contents, making the soil available phosphorus contents negatively correlated with the available Cd contents significantly, with the correlation coefficient r = - 0.902 6, and the soil pH values had a negative correlation with the available Cd content during the treatments. Therefore, it could be known that the changes of soil available phosphorus contents were the major factor in reducing the availability of soil cadmium under the conditions of the application of phosphate and natural zeolite.

  19. Fire Performance of Plywood Treated with Ammonium Polyphosphate and 4A Zeolite

    Directory of Open Access Journals (Sweden)

    Mingzhi Wang

    2014-07-01

    Full Text Available Plywood samples treated with ammonium polyphosphate (APP and 4A zeolite were prepared to investigate the effect of zeolite on wood’s burning behavior using a cone calorimeter under a heat flux of 35 kW/m2. Results showed that APP decreased the heat release rate (HRR, total heat release (THR, and mass loss rate (MLR of treated plywood. However, APP significantly increased the total smoke release (TSR and carbon monoxide (CO yield. The addition of 4A zeolite reduced the HRR, peak HRR, and THR of the plywood treated with only APP. The second HRR peak in a typical plywood curve diminished with the addition of as little as 2% 4A zeolite. The average specific extinction area (ASEA and CO yield decreased significantly with the presence of zeolite in the APP. The ignition time did not change significantly and the TSR increased when zeolite was present. Thus, a suitable amount of 4A zeolite works synergistically with APP in promoting flame retardancy in flame retardant plywood.

  20. Low VOC Barrier Coating for Industrial Maintenance

    Science.gov (United States)

    2012-09-01

    Technology Certification Program HAP Hazardous Air Pollutant HW hazardous waste LVBC low VOC barrier coating MEK methyl ethyl ketone MIL-DTL...peeling, blistering , tape adhesion, pull-off adhesion, film thickness, and LVBC/ZVT patch test adhesion testing in an acceptable or better manner...significant reductions in the amount of hazardous waste generated by the Navy. The ZVT technology contains less than 5 g/l of VOC and the resulting

  1. 预积炭对FER分子筛催化正丁烯骨架异构反应性能的影响%Effect of carbon pre-deposition on FER zeolite catalyzed reaction of n-butenes skeletal isomerization

    Institute of Scientific and Technical Information of China (English)

    范丹丹; 周峰; 于绍先; 马会霞; 乔凯

    2016-01-01

    A series of FER zeolites with different amount of pre-deposited carbon were prepared by pretreatment at high temperature using mixture of 1-butene and N2. The effect of pre-coking on the catalytic performances of FER zeolite in the skeletal isomerization ofn-butenes into isobutene were studied. TG-DTA results indicated that there were two kinds of carbon deposits,i.e. CarbonLT (mass loss at low temperature) and CarbonHT (mass loss at high temperature). The amount of CarbonLT increased linearly with the extension of pre-coking time,while the amount of CarbonHTremained constant after being treated for one hour. The amount of CarbonLT had closely related to the initial isobutene selectivity and the CarbonLT might deposit on the active sites where propylene and ethylene were produced.%采用1-丁烯和N2混合气对FER分子筛进行高温预积炭处理,得到一系列具有不同预积炭量的FER分子筛。对预积炭的FER分子筛进行表征,研究预积炭行为对其催化正丁烯骨架异构制异丁烯反应性能的影响。热重表征结果表明,预沉积在FER分子筛上的积炭有两种,即CarbonLT(低温失重峰)和CarbonHT(高温失重峰)。CarbonLT含量随预积炭处理时间增加而呈线性增加的趋势,而CarbonHT含量在预积炭处理1h后就基本保持不变。CarbonLT 量与初始异丁烯选择性具有较好的相关性,CarbonLT 可能沉积在诱发生成丙烯和乙烯的副反应活性中心上。

  2. 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.

  3. Associations of indoor carbon dioxide concentrations, VOCS, environmental susceptibilities with mucous membrane and lower respiratory sick building syndrome symptoms in the BASE study: Analyses of the 100 building dataset

    Energy Technology Data Exchange (ETDEWEB)

    Apte, M.G.; Erdmann, C.A.

    2002-10-01

    Using the 100 office-building Building Assessment Survey and Evaluation (BASE) Study dataset, we performed multivariate logistic regression analyses to quantify the associations between indoor minus outdoor CO{sub 2} (dCO{sub 2}) concentrations and mucous membrane (MM) and lower respiratory system (Lresp) Sick Building Syndrome (SBS) symptoms, adjusting for age, sex, smoking status, presence of carpet in workspace, thermal exposure, relative humidity, and a marker for entrained automobile exhaust. Using principal components analysis we identified a number of possible sources of 73 measured volatile organic compounds in the office buildings, and assessed the impact of these VOCs on the probability of presenting the SBS symptoms. Additionally we included analysis adjusting for the risks for predisposition of having SBS symptoms associated with the allergic, asthmatic, and environmentally sensitive subpopulations within the office buildings. Adjusted odds ratios (ORs) for statistically significant, dose-dependant associations (p<0.05) for dry eyes, sore throat, nose/sinus congestion, and wheeze symptoms with 100-ppm increases in dCO{sub 2} ranged from 1.1 to 1.2. These results suggest that increases in the ventilation rates per person among typical office buildings will, on average significantly reduce the prevalence of several SBS symptoms, up to 80%, even when these buildings meet the existing ASHRAE ventilation standards for office buildings. VOC sources were observed to play an role in direct association with mucous membrane and lower respiratory irritation, and possibly to be indirectly involved in indoor chemical reactions with ozone that produce irritating compounds associated with SBS symptoms. O-xylene, possibly emitted from furniture coatings was associated with shortness of breath (OR at the maximum concentration = 8, p < 0.05). The environmental sensitivities of a large subset of the office building population add to the overall risk of SBS symptoms (ORs

  4. Optimization of an Innovative Biofiltration System as a VOC Control Technology for Aircraft Painting Facilities

    Science.gov (United States)

    2004-04-20

    Cladosporium resinae (ATCC 34066), Cladosporium sphaerospermum (ATCC 200384), Exophiala lecanii-corni (CBS 102400), Mucor rouxii (ATCC 44260), and...degrade all VOCs tested except for styrene under the conditions imposed. Cladosporium resinae was able to degrade both organic acids, all of the ketones...2002). Cladosporium Cladosporium Exophiala Mucor Phanerochaete resinae sphaerospermum lecanii-corni rouxii chrysosporium No carbon source Glucose

  5. Simulation of Water Gas Shift Zeolite Membrane Reactor

    Science.gov (United States)

    Makertiharta, I. G. B. N.; Rizki, Z.; Zunita, Megawati; Dharmawijaya, P. T.

    2017-07-01

    The search of alternative energy sources keeps growing from time to time. Various alternatives have been introduced to reduce the use of fossil fuel, including hydrogen. Many pathways can be used to produce hydrogen. Among all of those, the Water Gas Shift (WGS) reaction is the most common pathway to produce high purity hydrogen. The WGS technique faces a downstream processing challenge due to the removal hydrogen from the product stream itself since it contains a mixture of hydrogen, carbon dioxide and also the excess reactants. An integrated process using zeolite membrane reactor has been introduced to improve the performance of the process by selectively separate the hydrogen whilst boosting the conversion. Furthermore, the zeolite membrane reactor can be further improved via optimizing the process condition. This paper discusses the simulation of Zeolite Membrane Water Gas Shift Reactor (ZMWGSR) with variation of process condition to achieve an optimum performance. The simulation can be simulated into two consecutive mechanisms, the reaction prior to the permeation of gases through the zeolite membrane. This paper is focused on the optimization of the process parameters (e.g. temperature, initial concentration) and also membrane properties (e.g. pore size) to achieve an optimum product specification (concentration, purity).

  6. 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.

  7. Simulation of methane adsorption on A-zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Woestyn, A.M.; Mentasty, L. [Departamento de Quimic, Universidad Nacional de San Luis-CONICET, Chacabuco y Pedernera, 5700 San Luis (Argentina); Riccardo, J.L.; Zgrablich, G. [Departamento de Fisica, Universidad Nacional de San Luis-CONICET, Chacabuco y Pedernera, 5700 San Luis (Argentina)

    1996-07-01

    A Monte Carlo simulation has been performed to study adsorption of CH{sub 4} on zeolites and the result are here presented for NaA and CaNaA zeolites. The adsorption isotherms of CH{sub 4} and the radial distribution of the adsorbed molecules have been obtained at four different temperatures in the pressure range 0 to 5 Mpa. The potential energy of adsorption has been calculated and the energy profile of a CH{sub 4} molecule along different axes in the zeolite cavity are discussed. High density storage of natural gas is essential for the efficient use of this gas as an alternative transportation fuel. One of the promising storage technologies is the adsorbed natural gas (ANG), in which the gas is adsorbed on highly microporous solids like zeolites or actived carbons. Structural as well as chemical properties of the porous adsorbents influence strongly the adsorption phenomenon, therefore, both experimental as theorical investigation are still necessary to select better solids for specific applications. {copyright} {ital 1996 American Institute of Physics.}

  8. Catalytic pyrolysis using UZM-44 aluminosilicate zeolite

    Science.gov (United States)

    Nicholas, Christopher P; Boldingh, Edwin P

    2013-12-17

    A new family of aluminosilicate zeolites designated UZM-44 has been synthesized. These zeolites are represented by the empirical formula Na.sub.nM.sub.m.sup.k+T.sub.tAl.sub.1-xE.sub.xSi.sub.yO.sub.z where "n" is the mole ratio of Na to (Al+E), M represents a metal or metals from zinc, Group 1, Group 2, Group 3 and or the lanthanide series of the periodic table, "m" is the mole ratio of M to (Al+E), "k" is the average charge of the metal or metals M, T is the organic structure directing agent or agents, and E is a framework element such as gallium. The process involves contacting a carbonaceous biomass feedstock with UZM-44 at pyrolysis conditions to produce pyrolysis gases comprising hydrocarbons. The catalyst catalyzes a deoxygenation reaction converting oxygenated hydrocarbons into hydrocarbons and removing the oxygen as carbon oxides and water. A portion of the pyrolysis gases is condensed to produce low oxygen biomass-derived pyrolysis oil.

  9. Metal immobilization in soils using synthetic zeolites

    NARCIS (Netherlands)

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

    2002-01-01

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

  10. Metal immobilization in soils using synthetic zeolites

    NARCIS (Netherlands)

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

    2002-01-01

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

  11. Removal of Arsenic(V) from Aqueous Solutions by Lanthanum-loaded Zeolite

    Institute of Scientific and Technical Information of China (English)

    PU Hongping; HUANG Jiangbo; JIANG Zhe

    2008-01-01

    A new adsorption process for the removal of As(V) ion from aqueous solutions is studied in this paper using lanthanum-loaded zeolite. The removal efficiency of different adsorbents, activated alumina and activated carbon are obtained in the study for comparison. The results show that lanthanum-loaded zeolite is an effective adsorbent for the removal of As(V) from aqueous solutions.Then, the pH effect and regeneration of modified zeolite on the As(V) removing efficiency are also assessed. It functions with a wide range of pH (2-8). After adsorption, zeolite adsorbed with As(V) ions can be regenerated successfully with 1 M NaOH. Based on the data obtained, an adsorption mechanism and the possible complex structure are tentatively presented. Compare to other adsorbents, easy availability of this adsorbent, excellent adsorption capacity, wide optimum pH range, and regeneration are expected to be utilized in practical operations.

  12. Color and shade parameters of ultramarine zeolitic pigments synthesized from kaolin waste

    Energy Technology Data Exchange (ETDEWEB)

    Menezes, Raquel Aranha de; Paz, Simone Patricia Aranha da; Angelica, Romulo Simoes; Neves, Roberto de Freitas; Pergher, Sibele Berenice Castella, E-mail: raquel_arn@hotmail.com [Universidade Federal do Para (UFPA), Belem, PA (Brazil). Inst. de Geociencias. Grupo de Mineralogia e Geoquimica Aplicada

    2014-08-15

    Ultramarine pigments were successful synthesized from zeolite A obtained from kaolin waste. This waste has been used as an excellent source of silicon and aluminum for zeolite synthesis because of its high kaolinite concentrations and low contents of other accessory minerals. The cost is naturally less than the industrialized product. Color additives (Sulfur and Sodium Carbonate) were mixed with different proportions of zeolite A and further calcined for 5 h at 500 °C. They were characterized by XRD and XRF in addition to visual classification by color and shade. These products show colors from blue to green at different shades, both influenced by the amount of additives and cooling rate after calcination. Thus, a different quantity of the same additives in the same zeolitic matrix provides an increase in the color intensity. Cooling rate after calcination induces the color change which is substantially important in the pigments production. (author)

  13. POCP for individual VOC under European conditions

    Energy Technology Data Exchange (ETDEWEB)

    Altenstedt, J.; Pleijel, K.

    1998-09-01

    Ground level ozone has been recognised as one of the most important environmental threats on the regional scale in Europe. Ozone is today considered to be harmful to human health already at the relatively low concentrations present in southern Scandinavia. The fact that ozone has the potential to damage vegetation at these concentrations is already well known. Ozone also gives rise to degradation of materials and is one of the gases which adds to the greenhouse effect. Ground level ozone is formed from nitrogen oxides (NO{sub x}) and volatile organic compounds (VOC) in the presence of sunlight. The only way to reduce ozone is therefore to reduce the emissions of the precursors. Ranking individual VOC by their ozone formation potential can make emission reductions more environmentally efficient and save time and money. POCP values give a ranking of the ozone formation ability of an individual VOC relative to other VOC. A critical analysis of the POCP concept has been performed which shows that the background emissions of NO{sub x} and VOC affect the POCP values to a large extent. Based on the critical analysis, five scenarios with different background emissions of NO{sub x} and VOC were selected for calculation of POCP values. These scenarios were chosen because they reflect the variation in POCP values which arise in different environments within Europe. The range thus indicates POCP values which are intended to be applicable within Europe. POCP values for 83 different VOC are presented in the form of ranges in this report. 42 refs, 13 figs, 3 tabs

  14. Zeolites for nitrosamine and pharmaceutical removal from demineralised and surface water: Mechanisms and efficacy

    KAUST Repository

    De Ridder, David J.

    2012-03-01

    Zeolites with a high Si/Al ratio can be used as selective adsorbents in water treatment, targeting organic micropollutants which are removed poorly with activated carbon. Due to size exclusion, many Natural Organic Matter (NOM) components cannot access the pores, thus limiting adsorption competition between organic micropollutant and NOM. Furthermore, zeolite channel diameters are close to molecule diameters, which results in strong van der Waals interaction. MOR200 and ZSM5, the two most hydrophobic zeolites, showed the highest removal of neutral nitrosamines in demineralised water, with higher efficacy than activated carbon. DAY and MOR30, which were relatively hydrophilic zeolites, did not show appreciable removal of any of the nitrosamines. When nitrosamines were adsorbed from surface water, there was no influence of competition with, or pore blockage by, NOM components on nitrosamine removal for ZSM5 zeolite, in contrast to activated carbon. Repulsion of negatively charged pharmaceuticals was significant for ZSM5, which had a Si/Al ratio of 80. MOR200 had a Si/Al ratio of 200, indicating a lower Al content than ZSM5 and, as such, a lower negative surface charge. Charge effects were not observed for MOR200. A relationship was found between the Stokes diameter of the pharmaceuticals and nitrosamines, and their removal by ZSM5 and MOR200, indicating that a "close fit" adsorption mechanism is more likely than hydrophobic interaction in these zeolites. Due to their selective nature, adsorption on zeolites should only be considered as an additional treatment step to existing processes, dedicated for the removal of specific organic micropollutants. Less specific treatment techniques, such as activated carbon filtration, are still required to ensure a broad barrier for organic micropollutants in water treatment. © 2012 Elsevier B.V. All rights reserved.

  15. Preparation of a Titania/X-Zeolite/Porous Glass Composite Photocatalyst Using Hydrothermal and Drop Coating Processes

    Directory of Open Access Journals (Sweden)

    Atsuo Yasumori

    2015-01-01

    Full Text Available Combinations of TiO2 photocatalysts and various adsorbents have been widely studied for the adsorption and photocatalytic decomposition of gaseous pollutants such as volatile organic compounds (VOCs. Herein, a TiO2-zeolite-porous glass composite was prepared using melt-quenching and partial sintering, hydrothermal treatment, and drop coating for preparation of the porous glass support and X-zeolite and their combination with TiO2, respectively. The obtained composite comprised anatase phase TiO2, X-zeolite, and the porous glass support, which were combined at the micro to nanometer scales. The composite had a relatively high specific surface area of approximately 25 m2/g and exhibited a good adsorption capacity for 2-propanol. These data indicated that utilization of this particular phase-separated glass as the support was appropriate for the formation of the bulk photocatalyst-adsorbent composite. Importantly, the photocatalytic decomposition of adsorbed 2-propanol proceeded under UV light irradiation. The 2-propanol was oxidized to acetone and then trapped by the X-zeolite rather than being released to the atmosphere. Consequently, it was demonstrated that the micrometer-scaled combination of TiO2 and zeolite in the bulk form is very useful for achieving both the removal of gaseous organic pollutants and decreasing the emission of harmful intermediates.

  16. Gas-phase adsorption in dealuminated natural clinoptilolite and liquid-phase adsorption in commercial DAY zeolite and modified ammonium Y zeolite

    Science.gov (United States)

    Costa Hernandez, Alba Nydia

    The adsorption of Carbon Dioxide (CO2) is a very important tool for the material characterization. On the other hand, in separation and recovery technology, the adsorption of the CO2 is important to reduce the concentration of this gas considered as one of the greenhouse gases. Natural zeolites, particularly clinoptilolite, are widely applied to eliminate some pollutants from the environment. One of the goals of this research is to study the structure, composition and morphology of one natural clinoptilolite dealuminated with ammonium hexafluorosilicate (AHFi) and with orthophosphoric acid (H3PO4). Each modified sample was characterized using X-ray Diffraction (XRD), Carbon Dioxide adsorption at 0° C, Thermogravimetric Analysis (TGA), and Scanning Electron Microscopy with Energy Dispersive X-Ray Analysis (SEM-EDAX). In addition, the surface chemistry of the modified clinoptilolites was analyzed with Diffuse Reflectance Fourier Transform Infrared Spectroscopy (DRIFTS). The adsorption measurements were also used to study of the interaction of CO2 molecule within the adsorption space of these modified clinoptilolites. It was concluded that one of the modified clinoptilolites, (CSW-HFSi-0.1M), showed a great quality as adsorbent and as catalytic comparable to commercial synthetic zeolites. As far as we know, the modification of clinoptilolite with HFSi to improve their adsorption properties had not been previously attempted. In the second part of this dissertation, the dynamic adsorption of three isomers of nitrophenols using as adsorbent a commercial DAY zeolite was investigated. Also, the dynamic adsorption of methanol in a less hydrophobic zeolite, Ammonium Y Zeolite was investigated. The obtained breakthrough curves showed that the commercial DAY zeolite could be a suitable adsorbent to the liquid-phase adsorption of the phenolic compounds. Notwithstanding the modified ammonium Y zeolite had a low Si/Al ratio (less hydrophobic) than commercial DAY zeolite; this

  17. Locating industrial VOC sources with aircraft observations

    Energy Technology Data Exchange (ETDEWEB)

    Toscano, P., E-mail: p.toscano@ibimet.cnr.it [Institute for Biometeorology (IBIMET - CNR), Via G. Caproni 8, 50145 Firenze (Italy); Gioli, B. [Institute for Biometeorology (IBIMET - CNR), Via G. Caproni 8, 50145 Firenze (Italy); Dugheri, S. [Careggi Hospital-University of Florence, Occupational Health Division, Largo Palagi 1, 50100 Florence (Italy); Salvini, A. [Department of Organic Chemistry, University of Florence, Via della Lastruccia 13, 50019 Sesto Fiorentino, Florence (Italy); Matese, A. [Institute for Biometeorology (IBIMET - CNR), Via G. Caproni 8, 50145 Firenze (Italy); Bonacchi, A. [Careggi Hospital-University of Florence, Occupational Health Division, Largo Palagi 1, 50100 Florence (Italy); Zaldei, A. [Institute for Biometeorology (IBIMET - CNR), Via G. Caproni 8, 50145 Firenze (Italy); Cupelli, V. [Careggi Hospital-University of Florence, Occupational Health Division, Largo Palagi 1, 50100 Florence (Italy); Miglietta, F. [Institute for Biometeorology (IBIMET - CNR), Via G. Caproni 8, 50145 Firenze (Italy); Fondazione Edmund Mach, Via Mach 1, San Michele all' Adige, Trento (Italy)

    2011-05-15

    Observation and characterization of environmental pollution, focussing on Volatile Organic Compounds (VOCs), in a high-risk industrial area, are particularly important in order to provide indications on a safe level of exposure, indicate eventual priorities and advise on policy interventions. The aim of this study is to use the Solid Phase Micro Extraction (SPME) method to measure VOCs, directly coupled with atmospheric measurements taken on a small aircraft environmental platform, to evaluate and locate the presence of VOC emission sources in the Marghera industrial area. Lab analysis of collected SPME fibres and subsequent analysis of mass spectrum and chromatograms in Scan Mode allowed the detection of a wide range of VOCs. The combination of this information during the monitoring campaign allowed a model (Gaussian Plume) to be implemented that estimates the localization of emission sources on the ground. - Highlights: > Flight plan aimed at sampling industrial area at various altitudes and locations. > SPME sampling strategy was based on plume detection by means of CO{sub 2}. > Concentrations obtained were lower than the limit values or below the detection limit. > Scan mode highlighted presence of {gamma}-butyrolactone (GBL) compound. > Gaussian dispersion modelling was used to estimate GBL source location and strength. - An integrated strategy based on atmospheric aircraft observations and dispersion modelling was developed, aimed at estimating spatial location and strength of VOC point source emissions in industrial areas.

  18. 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.

  19. 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.

  20. Assessment of Exposure to VOCs among Pregnant Women in the National Children’s Study

    Directory of Open Access Journals (Sweden)

    Elizabeth Barksdale Boyle

    2016-03-01

    Full Text Available Epidemiologic studies can measure exposure to volatile organic compounds (VOCs using environmental samples, biomarkers, questionnaires, or observations. These different exposure assessment approaches each have advantages and disadvantages; thus, evaluating relationships is an important consideration. In the National Children’s Vanguard Study from 2009 to 2010, participants completed questionnaires and data collectors observed VOC exposure sources and collected urine samples from 488 third trimester pregnant women at in-person study visits. From urine, we simultaneously quantified 28 VOC metabolites of exposure to acrolein, acrylamide, acrylonitrile, benzene, 1-bromopropane, 1,3-butadiene, carbon disulfide, crotonaldehyde, cyanide, N,N-dimethylformamide, ethylbenzene, ethylene oxide, propylene oxide, styrene, tetrachloroethylene, toluene, trichloroethylene, vinyl chloride, and xylene exposures using ultra high performance liquid chromatography coupled with an electrospray ionization tandem mass spectrometry (UPLC-ESI/MSMS method. Urinary thiocyanate was measured using an ion chromatography coupled with an electrospray ionization tandem mass spectrometry method (IC-ESI/MSMS. We modeled the relationship between urinary VOC metabolite concentrations and sources of VOC exposure. Sources of exposure were assessed by participant report via questionnaire (use of air fresheners, aerosols, paint or varnish, organic solvents, and passive/active smoking and by observations by a trained data collector (presence of scented products in homes. We found several significant (p < 0.01 relationships between the urinary metabolites of VOCs and sources of VOC exposure. Smoking was positively associated with metabolites of the tobacco constituents acrolein, acrylamide, acrylonitrile, 1,3-butadiene, crotonaldehyde, cyanide, ethylene oxide, N,N-dimethylformamide, propylene oxide, styrene, and xylene. Study location was negatively associated with the toluene metabolite

  1. Assessment of Exposure to VOCs among Pregnant Women in the National Children’s Study

    Science.gov (United States)

    Boyle, Elizabeth Barksdale; Viet, Susan M.; Wright, David J.; Merrill, Lori S.; Alwis, K. Udeni; Blount, Benjamin C.; Mortensen, Mary E.; Moye, John; Dellarco, Michael

    2016-01-01

    Epidemiologic studies can measure exposure to volatile organic compounds (VOCs) using environmental samples, biomarkers, questionnaires, or observations. These different exposure assessment approaches each have advantages and disadvantages; thus, evaluating relationships is an important consideration. In the National Children’s Vanguard Study from 2009 to 2010, participants completed questionnaires and data collectors observed VOC exposure sources and collected urine samples from 488 third trimester pregnant women at in-person study visits. From urine, we simultaneously quantified 28 VOC metabolites of exposure to acrolein, acrylamide, acrylonitrile, benzene, 1-bromopropane, 1,3-butadiene, carbon disulfide, crotonaldehyde, cyanide, N,N-dimethylformamide, ethylbenzene, ethylene oxide, propylene oxide, styrene, tetrachloroethylene, toluene, trichloroethylene, vinyl chloride, and xylene exposures using ultra high performance liquid chromatography coupled with an electrospray ionization tandem mass spectrometry (UPLC-ESI/MSMS) method. Urinary thiocyanate was measured using an ion chromatography coupled with an electrospray ionization tandem mass spectrometry method (IC-ESI/MSMS). We modeled the relationship between urinary VOC metabolite concentrations and sources of VOC exposure. Sources of exposure were assessed by participant report via questionnaire (use of air fresheners, aerosols, paint or varnish, organic solvents, and passive/active smoking) and by observations by a trained data collector (presence of scented products in homes). We found several significant (p < 0.01) relationships between the urinary metabolites of VOCs and sources of VOC exposure. Smoking was positively associated with metabolites of the tobacco constituents acrolein, acrylamide, acrylonitrile, 1,3-butadiene, crotonaldehyde, cyanide, ethylene oxide, N,N-dimethylformamide, propylene oxide, styrene, and xylene. Study location was negatively associated with the toluene metabolite N

  2. Airborne VOC measurements on board the Zeppelin NT during the PEGASOS campaigns in 2012 deploying the improvement Fast-GC-MSD system

    Energy Technology Data Exchange (ETDEWEB)

    Jaeger, Julia Elisabeth

    2014-04-01

    Volatile organic compounds (VOCs) comprise a large number of different species, estimated to 10{sup 4}-10{sup 6}. They are emitted on the Earth's surface from a variety of biogenic and anthropogenic sources. VOCs are removed by multiple pathways from the atmosphere, by oxidation and finally by dry or wet deposition. Most primary emitted VOCs are non-polar and therefore have a low solubility in water. Oxidation facilitates efficient VOC removal by wet deposition. In the atmosphere the main photochemical VOC oxidation agent is the OH radical. As a consequence the polarity of the VOCs is increased and they can be removed faster. The oxidation of VOCs proceeds in several steps until the VOCs are deposited or are eventually oxidized to carbon dioxide. A downside of the VOCs oxidation process lies in the production of significant amounts ozone if nitrogen oxide is present which is a serious health hazard. Most of the VOC oxidation takes place in lower part of the atmosphere between the altitudes of 100 to 1000 m, which is only sparsely analyzed. Therefore, fast VOCs measurements by GC-MSD on board the Zeppelin NT offered new important insights in the distribution of VOCs. The measurements were performed within the PEAGSOS campaigns in the Netherlands and in Italy in 2012. For the implementation of the GC-MSD system (HCG) on board the Zeppelin it was reconstructed to enhance its performance and to meet aviation requirements. The system was optimized to measure VOCs ranging from C4 to C10 as well as oxygenated VOCs (OVOCs) with a detection limit below 10 ppt. The analyzed VOCs for both parts of the campaigns showed low mean concentration below 5 ppb for all VOCs. Especially, the mixing ratios of the primary emitted VOCs were very low with mean values lower than 200 ppt. Higher concentrations could be observed for the OVOCs with mean concentrations up to 5 ppb. The most abundant OVOCs apart from formaldehyde were methanol, ethanol, acetone and acetaldehyde.

  3. Reducing VOC Press Emission from OSB Manufacturing

    Energy Technology Data Exchange (ETDEWEB)

    Dr. Gary D. McGinnis; Laura S. WIlliams; Amy E. Monte; Jagdish Rughani: Brett A. Niemi; Thomas M. Flicker

    2001-12-31

    Current regulations require industry to meet air emission standards with regard to particulates, volatile organic compounds (VOCs), hazardous air pollutants (HAPs) and other gases. One of many industries that will be affected by the new regulations is the wood composites industry. This industry generates VOCs, HAPs, and particulates mainly during the drying and pressing of wood. Current air treatment technologies for the industry are expensive to install and operate. As regulations become more stringent, treatment technologies will need to become more efficient and cost effective. The overall objective of this study is to evaluate the use of process conditions and chemical additives to reduce VOC/HAPs in air emitted from presses and dryers during the production of oriented strand board.

  4. 陶粒-沸石-活性炭组合填料生物滤池的研究%Research on Ceramic-zeolite-active Carbon Combined Medium Biological Aerated Filter

    Institute of Scientific and Technical Information of China (English)

    张尊举; 董春艳

    2013-01-01

    采用陶粒、沸石、活性炭填料合理组合作为曝气生物滤池的填料对高校生活污水进行处理。研究了组合填料生物滤池生物膜的培养,不同水力负荷、容积负荷和气水比对污水处理效率的影响,以及该生物滤池对生活污水的处理效果。结果表明,采用组合填料生物滤池,接种挂膜培养周期为25 d,在水力负荷为2.5 m3/(m2·h),气水比3.5:1,组合填料生物滤池出水COD、 BOD5、 SS、 NH3-N和色度平均值达到《城市污水再生利用城市杂用水水质》GB/T 18920-2002水质要求。%As a filter medium, Ceramic, zeolite, activated carbon were combined to use for biological aerated filter in the treatment of campus domestic wastewater. The study focused on the start rule of the combined medium biological aerated filter. Meanwhile, different hydraulic load, load capacity and water ratio on the sewage treatment effect, and the treatment effect of biological aerated filter for domestic wastewater were studied. The results show that, the time needed for the start-up and film formation of combined medium biological aerated filter about 25 d. When the hydraulic load was 2.5 m3/(m2·h) , the water ratio was 3.5:1, combined medium biological aerated filter becomes more reasonable and suitable, achieving good results in practical operation. the average values of COD、 BOD5、 SS、 NH3-N and Chrominance reached the Standards for The reuse of urban recycling water-water quality standard for urban miscellaneous water consumption GB/T 18920-2002.

  5. Metal immobilization in soils using synthetic zeolites.

    Science.gov (United States)

    Oste, Leonard A; Lexmond, Theo M; Van Riemsdijk, Willem H

    2002-01-01

    In situ immobilization of heavy metals in contaminated soils is a technique to improve soil quality. Synthetic zeolites are potentially useful additives to bind heavy metals. This study selected the most effective zeolite in cadmium and zinc binding out of six synthetic zeolites (mordenite-type, faujasite-type, zeolite X, zeolite P, and two zeolites A) and one natural zeolite (clinoptilolite). Zeolite A appeared to have the highest binding capacity between pH 5 and 6.5 and was stable above pH 5.5. The second objective of this study was to investigate the effects of zeolite addition on the dissolved organic matter (DOM) concentration. Since zeolites increase soil pH and bind Ca, their application might lead to dispersion of organic matter. In a batch experiment, the DOM concentration increased by a factor of 5 when the pH increased from 6 to 8 as a result of zeolite A addition. A strong increase in DOM was also found in the leachate of soil columns, particularly in the beginning of the experiment. This resulted in higher metal leaching caused by metal-DOM complexes. In contrast, the free ionic concentration of Cd and Zn strongly decreased after the addition of zeolites, which might explain the reduction in metal uptake observed in plant growth experiments. Pretreatment of zeolites with acid (to prevent a pH increase) or Ca (to coagulate organic matter) suppressed the dispersion of organic matter, but also decreased the metal binding capacity of the zeolites due to competition of protons or Ca.

  6. VOC methods and levels in Spain

    Energy Technology Data Exchange (ETDEWEB)

    Bomboi, M.T. [Area de Contaminacion Atmosferica, Instituto de Salud Carlos III, Majadahonda (Spain)

    2004-07-01

    Ozone precursors began to be studied in the eighties in Spain, in order to know their levels and composition in areas, which had high concentrations of other atmospheric polluting agents. At the end of the eighties, VOC were incorporated into the air quality networks in urban areas in order to anticipate at the derived amendments of the entrance into force on the Directive 92/72/CEE of 1992 on air pollution by ozone. At the same time, field campaigns for VOC toxics were started in specific industrial areas and the zones with high traffic. More recently, the air quality networks have been orientated to non-urban areas, to cover the knowledge of VOC in semi-urban and rural areas. On the other hand, the role of the biogenic emissions and the role that their chemical and photochemical products play in atmospheric chemistry was becoming important in the nineties. Therefore some research projects, e.g. 'Biogenic Emissions in the Mediterranean Area (BEMA)', were developed in order to understand the vegetation emissions in the Mediterranean area in relation to anthropogenic compounds and to get information on their participation in tropospheric ozone formation. VOC have been sampled at European Monitoring and Evaluation Programme (EMEP) sites since 1999, based on recommendations from the EMEP Workshop on Measurements of Hydrocarbons/VOC in Lindau 1989. Collection of light hydrocarbons started in 1999, whereas measurements of carbonyls have just started in 2003. In this work, the most important sampling and analysis techniques to determine ozone precursors and to control VOC are shown, as well as the main results obtained in projects, networks and measurement campaigns performed with these methods.

  7. Silica deactivation of bead VOC catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Libanati, C.; Pereira, C.J. [Research Division, W. R. Grace and Co., Columbia, MD (United States); Ullenius, D.A. [Grace TEC Systems, De Pere, WI (United States)

    1998-01-15

    Catalytic oxidation is a key technology for controlling the emissions of Volatile Organic Compounds (VOCs) from industrial plants. The present paper examines the deactivation by silica of bead VOC catalysts in a flexographic printing application. Post mortem analyses of field-aged catalysts suggest that organosilicon compounds contained in the printing ink diffuse into the catalyst and deposit as silica particles in the micropores. Laboratory activity evaluation of aged catalysts suggests that silica deposition is non-selective and that silica masks the noble metal active site

  8. 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

  9. Quantitative determination of volatile organic compounds (VOC) in milk by multiple dynamic headspace extraction and GC-MS.

    Science.gov (United States)

    Ciccioli, Paolo; Brancaleoni, Enzo; Frattoni, Massimiliano; Fedele, Vincenzo; Claps, Salvatore; Signorelli, Federica

    2004-01-01

    A method for the accurate determination of volatile organic compounds (VOC) in milk samples has been developed and tested. It combines multiple dynamic headspace extraction with GC-MS. Absolute amounts of VOC in the liquid phase are obtained by determining the first order kinetic dependence of the stepwise extraction of the analytes and internal standards from the liquid matrix. Compounds released from milk were collected on a train of traps filled with different solid sorbents to cover all components having a number of carbon atoms ranging from 4 to 15. They were analysed by GC-MS after thermal desorption of VOC from the collecting traps. Quantification of VOC in milk was performed using deuterated compounds as internal standards. The method was used to follow seasonal variations of monoterpenes in goat milk and to detect the impact of air pollution on the quality of milk.

  10. Antimicrobial Effect of Metal Ions Substitution to HAp, Zeolite

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Y. J.; Kim, S. B.; Cho, S. B; Cho, K. J.; Lee, T. H. [Pai Chai University, Taejeon (Korea); Kim, T. N. [Korea Institute of Geoscience and Mineral Resources, Taejeon (Korea)

    2001-02-01

    Generally, hydroxyapatite(HAp), zeolite, carbon molecular sieve, activated carbon and alumina are used as heavy metal ions adsorption materials. Among those adsorption materials, HAp which has good positive ion-exchange ability with metal ion, and zeolite are utilized in wastewater treatment. Most of water pollutions are caused by hazardous heavy metals ions as well as bacteria in waste water. In this study, a adsorption materials (HAp and zeolite) are ion-exchanged with a well known antimicrobial metal ions, such as Ag{sup +}, Cu{sup 2+}, and Zn{sup 2+}, in order to give a adsorption of heavy metal ions and a killing effects of bacteria. The antimicrobial effects of adsorption materials are observed using by E. Coli. The results show that there is a complete antimicrobial effect in the adsorption materials with Ag{sup +} at the concentration of 1x10{sup -4}cell/ml of E. Coli until 24 hours. However, there is not good antimicrobial effects in the adsorption materials with Cu{sup 2+} and Zn{sup 2+} substitution. Feng et. al. showed the denaturation effects of silver ions which induces the condensed DNA molecules and losing their replication abilities. (author). 13 refs., 6 figs., 2 tabs.

  11. The investigation of phenol removal from aqueous solutions by zeolites as solid adsorbents.

    Science.gov (United States)

    Damjanović, Ljiljana; Rakić, Vesna; Rac, Vladislav; Stošić, Dušan; Auroux, Aline

    2010-12-15

    This work reports results on phenol adsorption from aqueous solutions on synthetic BEA (β) and MFI (ZSM-5) zeolites, studied by heat-flow microcalorimetry. For the sake of comparison, the adsorption was performed on activated carbon, a solid customarily used for removal of phenol from water. The obtained values of heats evolved during phenol adsorption indicate the heterogeneity of active sites present on the investigated systems for the adsorption of phenol. In addition, the amounts of adsorbed pollutant were determined and presented in the form of adsorption isotherms, which were interpreted using Langmuir, Freundlich, Dubinin-Astakov and Sips' equations. The latter was found to express high level of agreement with experimental data. The results obtained in this work reveal that the adsorption of phenol on zeolites depends on both Si/Al ratio and on the pore size. Hydrophobic zeolites that possess higher contents of Si show higher affinities for phenol adsorption. Among investigated zeolites, zeolite β possesses the highest capacity for adsorption of phenol. The possibility of regeneration of used adsorbents was investigated by thermal desorption technique. It has been shown that in the case of β zeolite the majority of adsorbed phenol is easily released in the low temperature region.

  12. THE OPTIMIZATION OF PRODUCTION ZEOLITE Y CATALYST FROM RHA BY RESPONSE SURFACE METHODOLOGY

    Directory of Open Access Journals (Sweden)

    Didi Dwi Anggoro

    2012-02-01

    Full Text Available Rice husk is the milling byproduct of rice and is a major waste product of the agriculture industry. Amorphous silica, commonly referred to as rice husk ash, was extracted from rice husk by acid leaching, pyrolysis, and carbon-removing processes. These properties make the ash a valuable raw material for many industries.  This paper is study of synthesized of zeolite Y from rice husk ash. Zeolite Y synthesis is used for petroleum industry as expensive catalyst. Rice husk was calcined at temperature 700oC for two hours using furnace to produce pure silica. The composition of synthesized of zeolite Y from rice husk was 2.24 Na2O:Al2O3:8SiO2:112 H2O. The gel solution was mixed at room temperature for 24 hours using autoclave. Then, the gel solution was heated with variable temperature and time crystallization. The product zeolite synthesis Y was filtered and washed with distilled water until pH lower than ten, than dried at oven. This product was analyzed with X-Ray Diffraction (XRD. From XRD analyze result indicated that from rice husk ash can produced zeolite synthesis Y which high crystallization degree. The optimum conditions for synthesis of zeolite Y from rice husk ash are temperature at 100oC for 48 hours, silicate at 20%, and aluminate at 10%.

  13. Structural simulation of natural zeolites; Simulacion estructural de zeolitas naturales

    Energy Technology Data Exchange (ETDEWEB)

    Sanchez P, E.; Carrera G, L.M. [Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, 11801 Mexico D.F. (Mexico)

    1997-07-01

    The application of X-ray diffraction (XRD) in the study of crystalline structures of the natural and modified zeolites allows the identification, lattice parameter determination and the crystallinity grade of the sample of interest. Until two decades ago, simulation methods of X-ray diffraction patterns were developed with which was possible to do reliable determinations of their crystalline structure. In this work it is presented the first stage of the crystalline structure simulation of zeolitic material from Etla, Oaxaca which has been studied for using it in the steam production industry and purification of industrial water. So that the natural material was modified for increasing its sodium contents and this material in its turn was put in contact with aqueous solutions of Na, Mg and Ca carbonates. All the simulations were done with the Lazy-Pulverix method. The considered phase was clinoptilolite. It was done the comparison with three clinoptilolite reported in the literature. (Author)

  14. Martian zeolites as a source of atmospheric methane

    CERN Document Server

    Mousis, Olivier; Bellat, Jean-Pierre; Schmidt, Frédéric; Bouley, Sylvain; Chassefière, Eric; Sautter, Violaine; Quesnel, Yoann; Picaud, Sylvain; Lectez, Sébastien

    2016-01-01

    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 $\\sim$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 curr...

  15. UTILITY OF ZEOLITES IN HAZARDOUS METAL REMOVAL FROM WATER

    Science.gov (United States)

    Zeolites are well known for their ion exchange, adsorption and acid catalysis properties. Different inorganic pollutants have been removed from water at room temperature by using synthetic zeolites. Zeolite Faujasite Y has been used to remove inorganic pollutants including arseni...

  16. VOC transport in vented drums containing simulated waste sludge

    Energy Technology Data Exchange (ETDEWEB)

    Liekhus, K.J.; Gresham, G.L.; Rae, C.; Connolly, M.J.

    1994-02-01

    A model is developed to estimate the volatile organic compound (VOC) concentration in the headspace of the innermost layer of confinement in a lab-scale vented waste drum containing simulated waste sludge. The VOC transport model estimates the concentration using the measured VOC concentration beneath the drum lid and model parameters defined or estimated from process knowledge of drum contents and waste drum configuration. Model parameters include the VOC diffusion characteristic across the filter vent, VOC diffusivity in air, size of opening in the drum liner lid, the type and number of layers of polymer bags surrounding the waste, VOC permeability across the polymer, and the permeable surface area of the polymer bags. Comparison of model and experimental results indicates that the model can accurately estimate VOC concentration in the headspace of the innermost layer of confinement. The model may be useful in estimating the VOC concentration in actual waste drums.

  17. World Calibration Center for VOC (WCC-VOC), a new Facility for the WMO-GAW-Programme

    Science.gov (United States)

    Rappenglueck, B.-

    2002-12-01

    Volatile organic compounds (VOC) are recognized to be important precursors of tropospheric ozone as well as other oxidants and organic aerosols. In order to design effective control measures for the reduction of photooxidants, photochemical processes have to be understood and the sources of the precursors known. Reliable and representative measurements of VOCs are necessary to describe the anthropogenic and biogenic sources, to follow the photochemical degradation of VOCs in the troposphere. Measurement of VOCs is of key importance for the understanding of tropospheric chemistry. Tropospheric VOCs have been one of the recommended measurements to be made within the GAW programme. The purpose will be to monitor their atmospheric abundance, to characterize the various compounds with regard to anthropogenic and biogenic sources and to evaluate their role in the tropospheric ozone formation process. An international WMO/GAW panel of experts for VOC measurements developed the rational and objectives for this GAW activity and recommended the configuration and required activities of the WCC-VOC. In reflection of the complexity of VOC measurements and the current status of measurement technology, a "staged" approach was adopted. Stage 1 measurements: C2-C9 hydrocarbons, including alkanes, alkenes, alkynes, dienes and monocyclics. (The WCC-VOC operates currently under this mode). Stage 2 measurements: C10-C14 hydrocarbons, including higher homologs of the Stage 1 set as well as biogenic hydrocarbon compounds. Stage 3 measurements: Oxygenated VOCs, including alcohols, carbonyls, carboxylic acids. The Quality Assurance/Science Activity Centre (QA/SAC) Germany currently has established the World Calibration Centre for VOC (WCC-VOC). The WCC-VOC has operated in the research mode und has become operational recently. From now on, the WCC-VOC conducts one round-robin calibration audit per year at all global stations that measure VOCs and assists other stations in setting up VOC

  18. GEIGER BRICKEL BENEFITS FROM LOW -VOC COATINGS

    Science.gov (United States)

    Midwest Research Institute, under a cooperative agreement with the U.S. Environmental Protection Agency (EPA), conducted a study to identify wood furniture manufacturing facilities that had converted to low-volatile organic compound (VOC)/hazardous air pollutant (HAP) wood furnit...

  19. Tailored zeolites for the removal of metal oxyanions: overcoming intrinsic limitations of zeolites.

    Science.gov (United States)

    Figueiredo, Hugo; Quintelas, Cristina

    2014-06-15

    This review aims to present a global view of the efforts conducted to convert zeolites into efficient supports for the removal of heavy metal oxyanions. Despite lacking affinity for these species, due to inherent charge repulsion between zeolite framework and anionic species, zeolites have still received considerable attention from the scientific community, since their versatility allowed tailoring them to answer specific requirements. Different processes for the removal and recovery of toxic metals based on zeolites have been presented. These processes resort to modification of the zeolite surface to allow direct adsorption of oxyanions, or by combination with reducing agents for oxyanions that allow ion-exchange with the converted species by the zeolite itself. In order to testify zeolite versatility, as well as covering the wide array of physicochemical constraints that oxyanions offer, chromium and arsenic oxyanions were selected as model compounds for a review of treatment/remediation strategies, based on zeolite modification.

  20. 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...

  1. Experimental proof for resonant diffusion of normal alkanes in LTL and ZSM-12 zeolites

    CERN Document Server

    Yoo, K; Smirniotis, P G

    2015-01-01

    The intra-crystalline diffusion of normal alkanes in LTL and ZSM-12 zeolite was experimentally studied via gravimetric measurements performed at different temperatures. A periodic dependence of the diffusion coefficient on the number of carbon atoms in alkane was detected, which is an experimental proof for resonant diffusion. The present observations were described on the base of the existing theory of the resonant diffusion and several important parameters of the alkane-zeolite interaction and zeolite vibrations were obtained. In the considered temperature region the diffusion coefficient follows the Arrhenius law with periodic dependences of the pre-exponential factor and activation energy on the number of carbon atoms in alkanes. A compensation effect of simultaneous increases of the pre-exponential factor and the activation energy was also established.

  2. Synthesis of Zeolite from Fly Ash and Removal of Heavy Metal Ions from Newly Synthesized Zeolite

    Directory of Open Access Journals (Sweden)

    Parag Solanki

    2010-01-01

    Full Text Available Coal fly ash was used to synthesize X-type zeolite by alkali fusion followed by hydrothermal treatment. Characteristics of the various Fly ash samples were carried out. Coal proximate analysis was done. Batch experiment was carried out for the adsorption of some heavy metal ions on to synthesized Zeolite. The cost of synthesized zeolite was estimated to be almost one-fifth of that of commercial 13X zeolite available in the market.

  3. Synthesis of Zeolite from Fly Ash and Removal of Heavy Metal Ions from Newly Synthesized Zeolite

    OpenAIRE

    Parag Solanki; Vikal Gupta; Ruchi Kulshrestha

    2010-01-01

    Coal fly ash was used to synthesize X-type zeolite by alkali fusion followed by hydrothermal treatment. Characteristics of the various Fly ash samples were carried out. Coal proximate analysis was done. Batch experiment was carried out for the adsorption of some heavy metal ions on to synthesized Zeolite. The cost of synthesized zeolite was estimated to be almost one-fifth of that of commercial 13X zeolite available in the market.

  4. VOCs Speciation From Steam Boiler Stacks of Industries Located in Naucalpan

    Science.gov (United States)

    Mejia, G. M.; Tejeda, D. D.; Bremauntz, M. P.; Valdez, A.; Montufar, P. C.; Martinez, M. A.; Sierra, M. J.; Gonzalez, C. A.

    2007-05-01

    Results of VOCs speciation from industrial steam boiler stacks located in Naucalpan are presented and discussed. This municipality is located north of the Metropolitan Zone of the Valley of Mexico (MZVM). Speciation of VOCs is important to generate information about sources of pollution, to update emission inventories, to study the dynamics of pollutants in the atmosphere, and to estimate possible risks of population exposure. This information is valuable for decision making on air pollution control strategies. Samples from 35 steam boilers form industries burning Diesel, LPG, or CNG were taken using the US-EPA Method 18. Selected samples from the use of different fuels were analyzed using gas chromatography and flame ionization detection (GC-FID) according to US-EPA protocol TO-14. The VOCs analyzed included alkanes of 9 carbons or less, alkenes of 7 carbons or less and aromatics (families of benzene). The results show consistency on the VOCs detected on Diesel samples. The main compounds found were 1- Butene+iButylene, m/p-Xylene, Ethane, Propene, Propane, Acetylene, 2Me-1Butene, and Toluene. The average concentrations of these compounds were in the range of 130 to 385 ppbC. The results of LPG samples did not show a definite pattern of VOCs, although light components predominate and, in some samples, Toluene and Xylene. These last components were not expected for industries reporting the use of LPG, perhaps due to the use of a combination of fuels and mistakes in the reports of fuel used at the time of sampling. The analysis of CNG samples show predominance of light VOCs, in the range of 90 to 300 ppbC. As in the case of LPG, some aromatics showed high concentrations in some samples analyzed perhaps due to the use of different fuels in the boiler. The results of this study are the first results of VOCs speciation obtained form exhaust gases from stacks of Mexican industries. The data reported are valuable to analyze emission inventories of VOCs and to better

  5. Zeolite based microconcentrators for volatile organic compounds sensing at trace-level: fabrication and performance

    Science.gov (United States)

    Almazán, Fernando; Pellejero, Ismael; Morales, Alberto; Urbiztondo, Miguel A.; Sesé, Javier; Pina, M. Pilar; Santamaría, Jesús

    2016-08-01

    A novel 6-step microfabrication process is proposed in this work to prepare microfluidic devices with integrated zeolite layers. In particular, microfabricated preconcentrators designed for volatile organic compounds (VOC) sensing applications are fully described. The main novelty of this work is the integration of the pure siliceous MFI type zeolite (silicalite-1) polycrystalline layer, i.e. 4.0  ±  0.5 μm thick, as active phase, within the microfabrication process just before the anodic bonding step. Following this new procedure, Si microdevices with an excellent distribution of the adsorbent material, integrated resistive heaters and Pyrex caps have been obtained. Firstly, the microconcentrator performance has been assessed by means of the normal hexane breakthrough curves as a function of sampling and desorption flowrates, temperature and micropreconcentrator design. In a step further, the best preconcentrator device has been tested in combination with downstream Si based microcantilevers deployed as VOC detectors. Thus, a preliminar evaluation of the improvement on detection sensitivity by silicalite-1 based microconcentrators is presented.

  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. 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.

  8. 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.

  9. Mesoporosity--a new dimension for zeolites.

    Science.gov (United States)

    Möller, Karin; Bein, Thomas

    2013-05-07

    Frameworks of precisely defined pores with diameters matching the size of small molecules endow crystalline zeolites with valuable size- and shape-selectivity. Being important selective adsorbers and separators, zeolites are also indispensable as solid acids in size-selective catalysis. However, despite being extremely beneficial, micropores impose restrictions on the mass transport of reactants, especially when bulky molecules are involved. The prospect to boost the catalytic power of zeolites and to extend their applications into new areas has prompted numerous efforts to synthesize mesoporous zeolitic materials that combine diffusional pathways on two different size scales. Our tutorial review will introduce the reader to this exciting recent development in zeolite science. We will give a general overview of the diverse strategies on how to implement a secondary pore system in zeolites. We will distinguish top-down from bottom-up and template-assisted from 'template-free' procedures. Advantages and limitations of the different methods will also be addressed.

  10. Diagenetic Quartz Morphologies and Zeolite formation

    DEFF Research Database (Denmark)

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

    ; the core of the zeolite crystals appears to have been more unstable than the rim and dissolved first.  Later the entire crystal dissolved and left an impression of the euhedral zeolite crystal in the microquartz coating.  Such openings in the microquartz coating are nucleation points for macroquartz.  Thus......, the precipitation of zeolite may later facilitate further quartz cementation, which might otherwise be retarded by the presence of disordered microquartz. The silica activity of pore fluids can influence zeolite precipitation.  Although zeolite formation is clearly related to volcanic ash, zeolite has also formed...... are abundant in some of associated shales; and 2) volcanic ash. The dissolution of biogenic silica may result in a rapid release of silica thereby promoting the formation of diagenetic opal/microquartz, but there may be a limited release of Al. A limited release of Al may result in precipitation of Si...

  11. Zeolite formation from coal fly ash and heavy metal ion removal characteristics of thus-obtained Zeolite X in multi-metal systems.

    Science.gov (United States)

    Jha, Vinay Kumar; Nagae, Masahiro; Matsuda, Motohide; Miyake, Michihiro

    2009-06-01

    Zeolitic materials have been prepared from coal fly ash as well as from a SiO(2)-Al(2)O(3) system upon NaOH fusion treatment, followed by subsequent hydrothermal processing at various NaOH concentrations and reaction times. During the preparation process, the starting material initially decomposed to an amorphous form, and the nucleation process of the zeolite began. The carbon content of the starting material influenced the formation of the zeolite by providing an active surface for nucleation. Zeolite A (Na-A) was transformed into zeolite X (Na-X) with increasing NaOH concentration and reaction time. The adsorption isotherms of the obtained Na-X based on the characteristics required to remove heavy ions such as Ni(2+), Cu(2+), Cd(2+) and Pb(2+) were examined in multi-metal systems. Thus obtained experimental data suggests that the Langmuir and Freundlich models are more accurate compared to the Dubinin-Kaganer-Radushkevich (DKR) model. However, the sorption energy obtained from the DKR model was helpful in elucidating the mechanism of the sorption process. Further, in going from a single- to multi-metal system, the degree of fitting for the Freundlich model compared with the Langmuir model was favored due to its basic assumption of a heterogeneity factor. The Extended-Langmuir model may be used in multi-metal systems, but gives a lower value for equilibrium sorption compared with the Langmuir model.

  12. CHARACTERIZATION OF LOW-VOC LATEX PAINTS: VOLATILE ORGANIC COMPOUND CONTENT, VOC AND ALDEHYDE EMISSIONS, AND PAINT PERFORMANCE

    Science.gov (United States)

    The report gives results of laboratory tests to evaluate commercially available latex paints advertised as "low-odor," "low-VOC (volatile organic compound)," or "no-VOC." Measurements were performed to quantify the total content of VOCs in the paints...

  13. Arid sites stakeholder participation in evaluating innovative technologies: VOC-Arid Site Integrated Demonstration

    Energy Technology Data Exchange (ETDEWEB)

    Peterson, T.S.; McCabe, G.H.; Brockbank, B.R. [and others

    1995-05-01

    Developing and deploying innovative environmental cleanup technologies is an important goal for the U.S. Department of Energy (DOE), which faces challenging remediation problems at contaminated sites throughout the United States. Achieving meaningful, constructive stakeholder involvement in cleanup programs, with the aim of ultimate acceptance of remediation decisions, is critical to meeting those challenges. DOE`s Office of Technology Development sponsors research and demonstration of new technologies, including, in the past, the Volatile Organic Compounds Arid Site Integrated Demonstration (VOC-Arid ID), hosted at the Hanford Site in Washington State. The purpose of the VOC-Arid ID has been to develop and demonstrate new technologies for remediating carbon tetrachloride and other VOC contamination in soils and ground water. In October 1994 the VOC-Arid ID became a part of the Contaminant Plume Containment and Remediation Focus Area (Plume Focus Area). The VOC Arid ID`s purpose of involving stakeholders in evaluating innovative technologies will now be carried on in the Plume Focus Area in cooperation with Site Technology Coordination Groups and Site Specific Advisory Boards. DOE`s goal is to demonstrate promising technologies once and deploy those that are successful across the DOE complex. Achieving that goal requires that the technologies be acceptable to the groups and individuals with a stake in DOE facility cleanup. Such stakeholders include groups and individuals with an interest in cleanup, including regulatory agencies, Native American tribes, environmental and civic interest groups, public officials, environmental technology users, and private citizens. This report documents the results of the stakeholder involvement program, which is an integral part of the VOC-Arid ID.

  14. Zeolites in poultry and swine production

    Directory of Open Access Journals (Sweden)

    Aline Félix Schneider

    Full Text Available ABSTRACT: Zeolites are minerals that have intriguing properties such as water absorption, ion adsorption and cation exchange capacity. There are approximately 80 species of natural zeolites recognized and hundreds of artificial zeolites, which have been researched in several fields. Due to their chemical characteristics, zeolites have great potential for use in animal production, especially in poultry and swine farms, as food additives, litter amendment and treatment of residues, with direct and indirect effects on performance, yield and quality of carcass, ambience of farm sheds and reduction of environmental pollution.

  15. Peculiarities in aromatization mechanism of low-molecular aliphatic compounds over high-silica zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Isagulyants, G.V.; Gitis, K.M.; Dubinskij, Yu.G.; Timokhov, A.G.; Kornyshev, V.N. (AN SSSR, Moscow. Inst. Organicheskoj Khimii)

    1984-01-01

    By means of /sup 14/C labelled compounds, transformations of methanol, lower olefins and piperylene over high-silica zeolites the data on the mechanism of carbon sceleton growth in the course of olefins production from methanol and aromatic piperylene hydrocarbons are obtained. Compound transformations have been studied at the pulse microcatalytic installation with radiochromatographic analysis of products.

  16. Unconventional, highly selective CO2 adsorption in zeolite SSZ-13.

    Science.gov (United States)

    Hudson, Matthew R; Queen, Wendy L; Mason, Jarad A; Fickel, Dustin W; Lobo, Raul F; Brown, Craig M

    2012-02-01

    Low-pressure adsorption of carbon dioxide and nitrogen was studied in both acidic and copper-exchanged forms of SSZ-13, a zeolite containing an 8-ring window. Under ideal conditions for industrial separations of CO(2) from N(2), the ideal adsorbed solution theory selectivity is >70 in each compound. For low gas coverage, the isosteric heat of adsorption for CO(2) was found to be 33.1 and 34.0 kJ/mol for Cu- and H-SSZ-13, respectively. From in situ neutron powder diffraction measurements, we ascribe the CO(2) over N(2) selectivity to differences in binding sites for the two gases, where the primary CO(2) binding site is located in the center of the 8-membered-ring pore window. This CO(2) binding mode, which has important implications for use of zeolites in separations, has not been observed before and is rationalized and discussed relative to the high selectivity for CO(2) over N(2) in SSZ-13 and other zeolites containing 8-ring windows.

  17. Mesopore quality determines the lifetime of hierarchically structured zeolite catalysts

    Science.gov (United States)

    Milina, Maria; Mitchell, Sharon; Crivelli, Paolo; Cooke, David; Pérez-Ramírez, Javier

    2014-05-01

    Deactivation due to coking limits the lifetime of zeolite catalysts in the production of chemicals and fuels. Superior performance can be achieved through hierarchically structuring the zeolite porosity, yet no relation has been established between the mesopore architecture and the catalyst lifetime. Here we introduce a top-down demetallation strategy to locate mesopores in different regions of MFI-type crystals with identical bulk porous and acidic properties. In contrast, well-established bottom-up strategies as carbon templating and seed silanization fail to yield materials with matching characteristics. Advanced characterization tools capable of accurately discriminating the mesopore size, distribution and connectivity are applied to corroborate the concept of mesopore quality. Positron annihilation lifetime spectroscopy proves powerful to quantify the global connectivity of the intracrystalline pore network, which, as demonstrated in the conversions of methanol or of propanal to hydrocarbons, is closely linked to the lifetime of zeolite catalysts. The findings emphasize the need to aptly tailor hierarchical materials for maximal catalytic advantage.

  18. [VOCs tax policy on China's economy development].

    Science.gov (United States)

    Liu, Chang-Xin; Wang, Yu-Fei; Wang, Hai-Lin; Hao, Zheng-Ping; Wang, Zheng

    2011-12-01

    In this paper, environmental tax was designed to control volatile organic compounds (VOCs) emissions. Computable general equilibrium (CGE) model was used to explore the impacts of environmental tax (in forms of indirect tax) on the macro-economy development at both national and sector levels. Different levels of tax were simulated to find out the proper tax rate. It is found out that imposing environmental tax on high emission sectors can cause the emission decreased immediately and can lead to negative impacts on macro-economy indicators, such as GDP (gross domestic products), total investment, total product and the whole consumption etc. However, only the government income increased. In addition, the higher the tax rate is, the more pollutants can be reduced and the worse economic effects can be caused. Consequently, it is suggested that, the main controlling policies of VOCs abatement should be mandatory orders, and low environmental tax can be implemented as a supplementary.

  19. Zeolites Remove Sulfur From Fuels

    Science.gov (United States)

    Voecks, Gerald E.; Sharma, Pramod K.

    1991-01-01

    Zeolites remove substantial amounts of sulfur compounds from diesel fuel under relatively mild conditions - atmospheric pressure below 300 degrees C. Extracts up to 60 percent of sulfur content of high-sulfur fuel. Applicable to petroleum refineries, natural-gas processors, electric powerplants, and chemical-processing plants. Method simpler and uses considerably lower pressure than current industrial method, hydro-desulfurization. Yields cleaner emissions from combustion of petroleum fuels, and protects catalysts from poisoning by sulfur.

  20. Catalytic pyrolysis using UZM-39 aluminosilicate zeolite

    Science.gov (United States)

    Nicholas, Christpher P; Boldingh, Edwin P

    2013-12-17

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

  1. 长江三角洲地区基于喷涂工艺的溶剂源 VOCs 排放特征%Process-based Emission Characteristics of Volatile Organic Compounds(VOCs) from Paint Industry in the Yangtze River Delta, China

    Institute of Scientific and Technical Information of China (English)

    莫梓伟; 牛贺; 陆思华; 邵敏; 勾斌

    2015-01-01

    了解挥发性有机物(volatile organic compounds,VOCs)的溶剂源排放特征是制定长江三角洲地区 PM2.5和臭氧防控策略的关键.本研究通过罐采样-GC-MS/ FID 测定了长江三角洲地区重点喷涂行业(集装箱喷涂、造船喷涂、木器喷涂和汽车喷涂业)的 VOCs 排放特征.结果表明,长江三角洲地区喷涂行业排放的主要 VOCs 组分为甲苯、二甲苯、乙苯等芳香烃类物质,三者之和占总 VOCs 的质量分数为79%~99%.生产工艺的不同对 VOCs 的排放组成影响并不大,废气处理装置中活性炭吸附对 VOCs 的组成并无明显影响,而催化燃烧的处理过程会使 VOCs 的排放组成产生显著变化,乙烯排放明显增大,同时也使得催化燃烧处理最大增量反应活性(maximum increment reactivity,MIR)值高于活性炭吸附处理后的 MIR 值,说明不同的处理措施的使用将影响 VOCs 对臭氧的生成作用.%Understanding the volatile organic compounds (VOCs) emission characteristics from solvent usage industry is essential to reduce PM2. 5 and O3 in Yangtze River Delta region. In this work, VOCs source characteristics of ship container, shipbuilding, wood, and automobile painting industry were measured using canister-GC-MS/ FID analysis system. The results showed that VOCs emitted from these industrial sectors were mainly aromatics, such as toluene, xylene, and ethylbenzene, accounting for 79% - 99% of total VOCs. The VOCs treatment facilities of activated carbon adsorption had little impact on changing the composition patterns of VOCs, while catalytic combustion treatments produced more alkenes. The combustion treatment of VOCs changed the maximum increment reactivity (MIR) of the VOCs emissions, and was thus very likely to change the ozone formation potentials.

  2. Inlfuence of the Alkali Treatment of HZSM-5 Zeolite on Catalytic Performance of PtSn-Based Catalyst for Propane Dehydrogenation

    Institute of Scientific and Technical Information of China (English)

    Huang Li; Zhou Shijian; Zhou Yuming; Zhang Yiwei; Xu Jun; Wang Li

    2013-01-01

    The porous material ATZ with micro-mesopore hierarchical porosity was prepared by alkali treatment of parent HZSM-5 zeolite and applied for propane dehydrogenation. The zeolite samples were characterized by XRD, N2-physisorption, and NH3-TPD analysis. The results showed that the alkali treatment can modify the physicochemical prop-erties of HZSM-5 zeolite. In this case, the porous material ATZ showed larger external surface area with less acid sites as compared to the HZSM-5 zeolite. It was found out that the alkali treatment of HZSM-5 zeolite could promote the catalytic performance of PtSn/ATZ catalyst. The possible reason was ascribed to the low acidity of ATZ. Furthermore, the presence of mesopores could reduce the carbon deposits on the metallic surface, which was also favorable for the dehydrogenation reaction.

  3. Transferable force-field for modelling of CO2, N2, O2 and Ar in all silica and Na+ exchanged zeolites

    Science.gov (United States)

    Vujić, Bojan; Lyubartsev, Alexander P.

    2016-05-01

    In this work we propose a new force field for modelling of adsorption of CO2, N2, O2 and Ar in all silica and Na+ exchanged Si-Al zeolites. The force field has a standard molecular-mechanical functional form with electrostatic and Lennard-Jones interactions satisfying Lorentz-Berthelot mixing rules and thus has a potential for further extension in terms of new molecular types. The parameters for the zeolite framework atom types are optimized by an iterative procedure minimizing the difference with experimental adsorption data for a number of different zeolite structures and Si:Al ratios. The new force field shows a good agreement with available experimental data including those not used in the optimization procedure, and which also shows a reasonable transferability within different zeolite topologies. We suggest a potential usage in screening of different zeolite structures for carbon capture and storage process, and more generally, for separation of other gases.

  4. New insights into alkylammonium-functionalized clinoptilolite and Na-P1 zeolite: Structural and textural features

    Science.gov (United States)

    Muir, Barbara; Matusik, Jakub; Bajda, Tomasz

    2016-01-01

    The area of zeolites' application could be expanded by utilizing their surfaces. Zeolites are frequently modified to increase their hydrophobicity and to generate the negative charge of the surface. The main objective of the study was to investigate and compare the features of natural clinoptilolite and synthetic zeolite Na-P1 modified by selected surfactants involving quaternary ammonium salts. The FTIR study indicates that with increasing carbon chain length in the surfactant attached to the zeolites surface the molecules adopt a more disordered structure. FTIR was also used to determine the efficiency of surface modification. Thermal analysis revealed that the presence of surfactant results in additional exothermic effects associated with the breaking of electrostatic bonds between zeolites and surfactants. The mass losses are in line with ECEC and CHN data. The textural study indicates that the synthetic zeolite Na-P1 has better sorption properties than natural clinoptilolite. The modification process always reduces the SBET and porosity of the material. With an increasing carbon chain length of surfactants all the texture parameters decrease.

  5. THE OPTIMIZATION OF PRODUCTION ZEOLITE Y CATALYST FROM RHA BY RESPONSE SURFACE METHODOLOGY

    OpenAIRE

    Didi Dwi Anggoro; Aprilina Purbasari

    2012-01-01

    Rice husk is the milling byproduct of rice and is a major waste product of the agriculture industry. Amorphous silica, commonly referred to as rice husk ash, was extracted from rice husk by acid leaching, pyrolysis, and carbon-removing processes. These properties make the ash a valuable raw material for many industries.  This paper is study of synthesized of zeolite Y from rice husk ash. Zeolite Y synthesis is used for petroleum industry as expensive catalyst. Rice husk was calcined at t...

  6. REMOVAL OF VOCs FROM THE AQUEOUS SOLUTIONS BY PERVAPORATION USING A FILLING-TYPE MEMBRANE

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    IntroductionThe major contaminants in industrial wastewaterand groundwater are volatile organic comPOunds(VOCs), particularly chlorinated and aromatichydrocarbons. Conventional technologies such as airstripping and activated carbon treatment do not alwaysprovide a complete and economical solution for someof these wastewater applications. Since no furtherseparation of the pollutant from the gaseous,liquid orsolid medium is not required, pervaporation has beendemonstrated as a POtentially attractive process f...

  7. Investigation of the behavior of VOCs in ground water across fine- and coarse-grained geological contacts using a medium-scale physical model

    Energy Technology Data Exchange (ETDEWEB)

    Hoffman, F.; Chiarappa, M.L.

    1998-03-01

    One of the serious impediments to the remediation of ground water contaminated with volatile organic compounds (VOCs) is that the VOCs are retarded with respect to the movement of the ground water. Although the processes that result in VOC retardation are poorly understood, we have developed a conceptual model that includes several retarding mechanisms. These include adsorption to inorganic surfaces, absorption to organic carbon, and diffusion into areas of immobile waters. This project was designed to evaluate the relative contributions of these mechanisms; by improving our understanding, we hope to inspire new remediation technologies or approaches. Our project consisted of a series of column experiments designed to measure the retardation, in different geological media, of four common ground water VOCs (chloroform, carbon tetrachloride, trichloroethylene, and tetrachloroethylene) which have differing physical and chemical characteristics. It also included a series of diffusion parameters that constrain the model, we compared the data from these experiments to the output of a computational model.

  8. Effect of heat waves on VOC emissions from vegetation and urban air quality

    Science.gov (United States)

    Churkina, G.; Kuik, F.; Lauer, A.; Bonn, B.; Butler, T. M.

    2015-12-01

    Programs to plant millions of trees in cities around the world aim at the reduction of summer temperatures, increase carbon storage, storm water control, provision of space for recreation, as well as poverty alleviation. Although these multiple benefits speak positively for urban greening programs, the programs do not take into account how close human and natural systems are coupled in urban areas. Elevated temperatures together with anthropogenic emissions of air and water pollutants distinguish the urban system. Urban and sub-urban vegetation responds to ambient changes and reacts with pollutants. Neglecting this coupling may lead to unforeseen drawbacks of urban greening programs. The potential for emissions of volatile organic compounds (VOC) from vegetation combined with anthropogenic emissions to produce ozone has long been recognized. This potential increases under rising temperatures. Here we investigate how heat waves affect emissions of VOC from urban vegetation and corresponding ground-level ozone. In this study we use Weather Research and Forecasting Model with coupled atmospheric chemistry (WRF-CHEM) to quantify these feedbacks in Berlin, Germany during the 2006 heat wave. VOC emissions from vegetation are simulated with MEGAN 2.0 coupled with WRF-CHEM. Our preliminary results indicate that contribution of VOCs from vegetation to ozone formation may increase by more than twofold during the heat wave period. We highlight the importance of the vegetation for urban areas under changing climate and discuss associated tradeoffs.

  9. Exfoliation of two-dimensional zeolites in liquid polybutadienes

    KAUST Repository

    Sabnis, Sanket

    2017-06-16

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

  10. UTILITY OF ZEOLITES IN ARSENIC REMOVAL FROM WATER

    Science.gov (United States)

    Zeolites are well known for their ion exchange and adsorption properties. So far the cation exchanger properties of zeolites have been extensively studied and utilized. The anion exchanger properties of zeolites are less studied. Zeolite Faujasite Y has been used to remove arseni...

  11. 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.

  12. 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.

  13. Catalytic oxidation of volatile organic compounds (VOCs) - A review

    Science.gov (United States)

    Kamal, Muhammad Shahzad; Razzak, Shaikh A.; Hossain, Mohammad M.

    2016-09-01

    Emission of volatile organic compounds (VOCs) is one of the major contributors to air pollution. The main sources of VOCs are petroleum refineries, fuel combustions, chemical industries, decomposition in the biosphere and biomass, pharmaceutical plants, automobile industries, textile manufacturers, solvents processes, cleaning products, printing presses, insulating materials, office supplies, printers etc. The most common VOCs are halogenated compounds, aldehydes, alcohols, ketones, aromatic compounds, and ethers. High concentrations of these VOCs can cause irritations, nausea, dizziness, and headaches. Some VOCs are also carcinogenic for both humans and animals. Therefore, it is crucial to minimize the emission of VOCs. Among the available technologies, the catalytic oxidation of VOCs is the most popular because of its versatility of handling a range of organic emissions under mild operating conditions. Due to that fact, there are numerous research initiatives focused on developing advanced technologies for the catalytic destruction of VOCs. This review discusses recent developments in catalytic systems for the destruction of VOCs. Review also describes various VOCs and their sources of emission, mechanisms of catalytic destruction, the causes of catalyst deactivation, and catalyst regeneration methods.

  14. The Zeolite Deposit of Hekimhan in the Malatya Basin

    Science.gov (United States)

    Önal, Mehmet; Depci, Tolga; Ceylan, Cigdem; Kizilkaya, Nilgun

    2016-10-01

    Zeolite deposits in the Malatya Basin which is formed of the Yüksekova Group were investigated in the present study. The zeolites were occurred in the two layers: the lower zeolite layer and the upper zeolite layer of the Sankiz Formation of Campanian-Maastrichtian age within the flysch like sediments at Hekimhan in the northern part of the Malatya Basin. Characterization studies of the zeolite samples were done by XRF, XRD and SEM images and the results showed that the main structures of the zeolites were clinoptilolite-(Cs), heulandite and calcite and the geological occurrences of zeolite is in marine environments.

  15. An electrode with Ni(II) loaded analcime zeolite catalyst for the electrooxidation of methanol

    Institute of Scientific and Technical Information of China (English)

    Seyed Naser Azizi; Shahram Ghasemi; Neda Salek Gilani

    2014-01-01

    There is a high overvoltage in the oxidation of methanol in fuel cells, and so modified electrodes are used to decrease it. A modified electrode that used Ni(II) loaded analcime zeolite to catalyze the electrooxidation of methanol in alkaline solution was proposed. Analcime zeolite was synthesized by hydrothermal synthesis, and Ni(II) ions were incorporated into the analcime structure, which was then mixed with carbon paste to prepare modified electrode. The electrocatalytic oxidation of methanol on the surface of the modified electrode in alkaline solution was investigated by cyclic voltammetry and chronoamperometry. The effects of the scan rate of the potential, concentration of methanol, and amount of zeolite were investigated. The rate constant for the catalytic reaction of methanol was 6 × 103 cm3 mol-1 s-1 from measurements using chronoamperometry. The proposed electrode significantly improved the electron transfer rate and decreased the overpotential for methanol oxidation.

  16. Characterizing the chemical evolution of air masses via multi-platform measurements of volatile organic compounds (VOCs) during CalNEX: Composition, OH reactivity, and potential SOA formation

    Science.gov (United States)

    Gilman, J. B.; Kuster, W. C.; Bon, D.; Warneke, C.; Lerner, B. M.; Williams, E. J.; Holloway, J. S.; Pollack, I. B.; Ryerson, T. B.; Atlas, E. L.; Blake, D. R.; Herndon, S. C.; Zahniser, M. S.; Vlasenko, A. L.; Li, S.; Alvarez, S. L.; Rappenglueck, B.; Flynn, J. H.; Grossberg, N.; Lefer, B. L.; De Gouw, J. A.

    2011-12-01

    Volatile organic compounds (VOCs) are critical components in the photochemical production of ozone (O3) and secondary organic aerosol (SOA). During the CalNex 2010 field campaign, an extensive set of VOCs were measured at the Pasadena ground site, and aboard the NOAA WP-3D aircraft and the WHOI Research Vessel Atlantis. The measurements from each platform provide a unique perspective into the emissions, transport, and atmospheric processing of VOCs within the South Coast Air Basin (SoCAB). The observed enhancement ratios of the hydrocarbons measured on all three platforms are in good agreement and are generally well correlated with carbon monoxide (CO), indicating the prevalence of on-road VOC emission sources throughout the SoCAB. Offshore measurements aboard the ship and aircraft are used to characterize the air mass composition as a function of the land/sea-breeze effect. VOC ratios and other trace gases are used to identify air masses containing relatively fresh emissions that were often associated with offshore flow and re-circulated continental air associated with onshore flow conditions. With the prevailing southwesterly airflow pattern in the LAB throughout the daytime, the Pasadena ground site effectively functions as a receptor site and is used to characterize primary VOC emissions from downtown Los Angeles and to identify the corresponding secondary oxidation products. The chemical evolution of air masses as a function of the time of day is investigated in order to determine the relative impacts of primary emissions vs. secondary VOC products on OH reactivity and potential SOA formation. The reactivity of VOCs with the hydroxyl radical (OH) at the Pasadena site was dominated by the light hydrocarbons, isoprene, and oxygenated VOCs including aldehydes (secondary products) and alcohols (primary anthropogenic emissions). Toluene and benzaldehyde, both of which are associated with primary anthropogenic emissions, are the predominant VOC precursors to the

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

    Science.gov (United States)

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

    2015-03-01

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

  18. Ultraviolet and radical oxidation of airborne VOC`s. Technical report

    Energy Technology Data Exchange (ETDEWEB)

    Heinsohn, R.J.; Spaeder, T.A.; Albano, M.T.; Schmelzle, J.P.; Fetter, R.O.

    1994-03-18

    Airborne VOC`s reactions initiated by UV radiation at selected wavelengths from 185 to 308 nm have been studied. A simplified chemical kinetic mechanism is proposed incorporating photolysis and radical reactions. The concentration of HCHO and CH{sub 3}OH were predicted as a function of time, radiation wavelength, actinic flux and initial ozone concentration. The gas velocity and HCHO concentration were predicted in a gas stream flowing over a UV bulb. Experiments were conducted in which ethanol vapor and air were irradiated by low-pressure mercury bulbs. Ethanol disappeared in an overall first-order manner and an intermediate species, believed to be acetaldehyde, appeared and then disappeared.

  19. Nitric oxide adsorbed on zeolites: EPR studies.

    Science.gov (United States)

    Yahiro, Hidenori; Lund, Anders; Shiotani, Masaru

    2004-05-01

    CW-EPR studies of NO adsorbed on sodium ion-exchanged zeolites were focused on the geometrical structure of NO monoradical and (NO)2 biradical formed on zeolites. The EPR spectrum of NO monoradical adsorbed on zeolite can be characterized by the three different g-tensor components and the resolved y-component hyperfine coupling with the 14N nucleus. Among the g-tensor components, the value of g(zz) is very sensitive to the local environment of zeolite and becomes a measure of the electrostatic field in zeolite. The temperature dependence of the g-tensor demonstrated the presence of two states of the Na-NO adduct, in rigid and rotational states. The EPR spectra of NO adsorbed on alkaline metal ion-exchanged zeolite and their temperature dependency are essentially the same as that on sodium ion-exchanged zeolite. On the other hand, for NO adsorbed on copper ion-exchanged zeolite it is known that the magnetic interaction between NO molecule and paramagnetic copper ion are observable in the spectra recorded at low temperature. The signals assigned to (NO)2 biradical were detected for EPR spectrum of NO adsorbed on Na-LTA. CW-EPR spectra as well as their theoretical calculation suggested that the two NO molecules are aligned along their N-O bond axes. A new procedure for automatical EPR simulation is described which makes it possible to analyze EPR spectrum easily. In the last part of this paper, some instances when other nitrogen oxides were used as a probe molecule to characterize the zeolite structure, chemical properties of zeolites, and dynamics of small molecules were described on the basis of selected literature data reported recently.

  20. 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.

  1. Performance of the JULES land surface model for UK Biogenic VOC emissions

    Science.gov (United States)

    Hayman, Garry; Comyn-Platt, Edward; Vieno, Massimo; Langford, Ben

    2017-04-01

    Emissions of biogenic non-methane volatile organic compounds (NMVOCs) are important for air quality and tropospheric composition. Through their contribution to the production of tropospheric ozone and secondary organic aerosol (SOA), biogenic VOCs indirectly contribute to climate forcing and climate feedbacks [1]. Biogenic VOCs encompass a wide range of compounds and are produced by plants for growth, development, reproduction, defence and communication [2]. There are both biological and physico-chemical controls on emissions [3]. Only a few of the many biogenic VOCs are of wider interest and only two or three (isoprene and the monoterpenes, α- and β-pinene) are represented in chemical transport models. We use the Joint UK Land Environment Simulator (JULES), the UK community land surface model, to estimate biogenic VOC emission fluxes. JULES is a process-based model that describes the water, energy and carbon balances and includes temperature, moisture and carbon stores [4, 5]. JULES currently provides emission fluxes of the 4 largest groups of biogenic VOCs: isoprene, terpenes, methanol and acetone. The JULES isoprene scheme uses gross primary productivity (GPP), leaf internal carbon and the leaf temperature as a proxy for the electron requirement for isoprene synthesis [6]. In this study, we compare JULES biogenic VOC emission estimates of isoprene and terepenes with (a) flux measurements made at selected sites in the UK and Europe and (b) gridded estimates for the UK from the EMEP/EMEP4UK atmospheric chemical transport model [7, 8], using site-specific or EMEP4UK driving meteorological data, respectively. We compare the UK-scale emission estimates with literature estimates. We generally find good agreement in the comparisons but the estimates are sensitive to the choice of the base or reference emission potentials. References (1) Unger, 2014: Geophys. Res. Lett., 41, 8563, doi:10.1002/2014GL061616; (2) Laothawornkitkul et al., 2009: New Phytol., 183, 27, doi

  2. Pulsed Corona Discharges and Their Applications in Toxic VOCs Abatement

    Institute of Scientific and Technical Information of China (English)

    MuhammadArifMalik; SalmanAkbarMalik

    1999-01-01

    plasma processes are among the emerging technologies for volatile organic compounds (VOCs) sbatoment. Both thermal plasmas and non-equil[brimn plasmas (cold plasmas) are being developed for VOCs clesnup. Particularly, pulsed corona discharges offer several edvantages over conventional VOCs abatement tochniqvee, To optimize the existing technology and to developit further, there is need to understand the mechanlsms involved in plasma chemical reacticms, Furthermore, it is strongly desirable to be able to predict the behavior of new VOCs in non-equillbrlum plasma enviromuent from the data known for a few representative oompounds, Pulsed corona discharge technique is introduced here with dtafion of refevant literature, Fundamental principfes,useful for predicting the VOCs' decomposition behavior, have been worked out from the published literature. Latest developments in the area, targeted to minimize the enersy losses, improve the VOCs destruction efficiency and reduce the generation of unwanted organic and inorganic by-products, are presented.

  3. Outdoor, indoor, and personal exposure to VOCs in children.

    Science.gov (United States)

    Adgate, John L; Church, Timothy R; Ryan, Andrew D; Ramachandran, Gurumurthy; Fredrickson, Ann L; Stock, Thomas H; Morandi, Maria T; Sexton, Ken

    2004-10-01

    We measured volatile organic compound (VOC) exposures in multiple locations for a diverse population of children who attended two inner-city schools in Minneapolis, Minnesota. Fifteen common VOCs were measured at four locations: outdoors (O), indoors at school (S), indoors at home (H), and in personal samples (P). Concentrations of most VOCs followed the general pattern O approximately equal to S long-term health risks from children's exposure to these compounds.

  4. Eddy covariance VOC emission and deposition fluxes above grassland using PTR-TOF

    Directory of Open Access Journals (Sweden)

    T. M. Ruuskanen

    2010-09-01

    Full Text Available Eddy covariance (EC is the preferable technique for flux measurements since it is the only direct flux determination method. It requires a continuum of high time resolution measurements (e.g. 5–20 Hz. For volatile organic compounds (VOC soft ionization via proton transfer reaction has proven to be a quantitative method for real time mass spectrometry; here we use a proton transfer reaction time of flight mass spectrometer (PTR-TOF for 10 Hz EC measurements of full mass spectra up to m/z 315. The mass resolution of the PTR-TOF enabled the identification of chemical formulas and separation of oxygenated and hydrocarbon species exhibiting the same nominal mass. We determined 481 ion mass peaks from ambient air concentration above a managed, temperate mountain grassland in Neustift, Stubai Valley, Austria. During harvesting we found significant fluxes of 18 compounds distributed over 43 ions, including protonated parent compounds, as well as their isotopes and fragments and VOC-H+-water clusters. The dominant BVOC fluxes were methanol, acetaldehyde, ethanol, hexenal and other C6 leaf wound compounds, acetone, acetic acid, monoterpenes and sequiterpenes.

    The smallest reliable fluxes we determined were less than 0.1 nmol m−2 s−1, as in the case of sesquiterpene emissions from freshly cut grass. Terpenoids, including mono- and sesquiterpenes, were also deposited to the grassland before and after the harvesting. During cutting, total VOC emission fluxes up to 200 nmol C m−2 s−1 were measured. Methanol emissions accounted for half of the emissions of oxygenated VOCs and a third of the carbon of all measured VOC emissions during harvesting.

  5. Remove volatile organic compounds (VOCs) with membrane separation techniques

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Membrane separation, a new technology for removing VOCs including pervaporation, vapor permeation, membrane contactor, and membrane bioreactor was presented. Comparing with traditional techniques, these special techniques are an efficient and energy-saving technology. Vapor permeation can be applied to recovery of organic solvents from exhaust streams. Membrane contactor could be used for removing or recovering VOCs from air or wastewater. Pervaporation and vapor permeation are viable methods for removing VOCs from wastewater to yield a VOC concentrate which could either be destroyed by conventional means, or be recycled for reuse.

  6. Use of mass spectrometric methods for field screening of VOC`s

    Energy Technology Data Exchange (ETDEWEB)

    Evans, J.C.

    1994-11-01

    While mass spectrometric (MS) methods of chemical analysis, particularly gas chromatography-mass spectrometry (GC/MS), have been the mainstay of environmental organic analytical techniques in the laboratory through the use of EPA and other standard methods, field implementation is relatively rare. Instrumentation and methods now exist for utilizing MS and GC/MS techniques in the field for analysis of VOC`s in gas phase, aqueous, and soil media. Examples of field investigations utilizing HP 5971A and Viking SpectraTrak systems for analysis of VOC`s in all three media will be presented. Mass spectral methods were found to offer significant advantages in terms of speed of analysis and reliability of compound identification over field gas chromatography (GC) methods while preserving adequate levels of detection sensitivity. The soil method in particular provides a method for rapid in-field analysis of methanol preserved samples thus minimizing the problem of volatiles loss which typically occurs with routine use of the EPA methods and remote analysis. The high cost of MS instrumentation remains a major obstacle to more widespread use.

  7. Preliminary insights into the chemical composition and emissions of urban VOCs in the East Mediterranean

    Science.gov (United States)

    Sauvage, S.; Borbon, A.; Afif, C.; Bechara, J.; Leonardis, T.; Fronval, I.; Waked, A.; Brioude, J.; Locoge, N.

    2011-12-01

    The Mediterranean region is an area where polluted air masses coming from Eastern and Central Europe increase air pollution, particularly during stagnation periods, together with intense solar radiation. It was demonstrated that the eastern coast of the Mediterranean Sea suffers from this kind of phenomena. Favorable weather conditions, remote sources, high urban and biogenic emissions lead to the formation of secondary pollutants (ozone and secondary organic aerosols, SOA), which may have significant impacts on health and climate. However, data are sparse in this region. The ECOCEM (Emission and Chemistry of Organic Carbon in the East Mediterranean - Beirut) project aims to improve our understanding of air pollution in this area by studying the composition of the gaseous and particulate phases in Beirut (Lebanon). Beirut is located on the eastern border of the Mediterranean basin. The goal of the project, which is taking place over two intensive field campaigns (July 2011 and February 2012), is to provide valuable observations on the composition and the temporal evolution of organics (summer versus winter),to identify and quantify the relative importance of sources of volatile organic compounds (VOCs) and aerosols (SOA) and to study the role of VOCs in the first oxidation steps of SOA formation. For that purpose, a large suite of primary and secondary VOCs (>60) were measured during the summertime campaign (July 2nd to July 17th 2011) at one suburban site in Beirut. Techniques encompass off-line sampling on carbonaceous sorbent tubes (2-hour time resolution) and liquid coil scrubbing (1-hour time resolution), an on-line GCFID (1-hour time resolution) and a PTR-MS (4-min time resolution). We will discuss here the atmospheric composition of VOCs in relation with their emissions. In particular, these data provide useful constraints to evaluate the first temporally and spatially resolved national emission inventory that was built for the year 2010. Preliminary results

  8. Zeolites on Mars: Prospects for Remote Sensing

    Science.gov (United States)

    Gaffney, E. S.; Singer, R. B.; Kunkle, T. D.

    1985-01-01

    The Martian surface composition measured by Viking can be represented by several combinations of minerals incorporating major fractions of zeolites known to occur in altered mafic rocks and polar soils on Earth. The abundant occurrence of zeolites on Mars is consistent with what is known about both the physical and chemical environment of that planet. The laboratory reflectance spectra (0.65 to 2.55 microns) of a number of relatively pure zeolite minerals and some naturally occurring zeolite-clay soils were measured. All of the spectra measured are dominated by strong absorption near 1.4 and 1.9 microns and a steep reflectance drop longward of about 2.2 microns, all of which are due to abundant H2O. Weaker water overtone bands are also apparent, and in most cases there is spectral evidence for minor Fe(3+). In these features the zeolite spectra are similar to spectra of smectite clays which have abundant interlayer water. The most diagnostic difference between clay and zeolite spectra is the total absence in the zeolites of the weak structural OH absorption.

  9. N-C isotopic investigation of a zeolite-amended agricultural field

    Science.gov (United States)

    Ferretti, Giacomo; Natali, Claudio; Faccini, Barbara; Di Giuseppe, Dario; Bianchini, Gianluca; Coltorti, Massimo

    2016-04-01

    In this study, a C and N isotopic investigation in the soil-plant system of the ZeoLIFE project experimental field have been carried out. Since many years, natural and NH4-enriched zeolites have been used as soil amendant in agricultural context in order to reduce N losses, increase NUE (Nitrogen Use Efficiency) and crop yield. Nevertheless up to now there are no studies that, using the stable isotopes approach, highlighted the interaction between zeolites and plants in agricultural systems. The main aims of this study is to verify if natural zeolites amendment can enhance chemical fertilization efficiency and if N transfer from NH4-enriched zeolites to plants really occurs. Plants grown following traditional cultivation methods (with no zeolite addition) and plants grown on soils amended with natural and NH4-enriched zeolites (the latter obtained after mixing with pig-slurry with a very high 15N) were compared for two cultivation cycles (maize and wheat). As widely known, plants grown under conventional farming systems (use of chemical fertilizers as urea) and plants grown under organic farming can be discriminated by the isotopic signatures of plant tissues. For both years the main results of the study reveals that plants grown on plots amended with natural zeolites generally have their nitrogen isotopic signature more similar to that of the chemical fertilizers employed during the cultivation with respect to the plants cultivated in the non-amended plot. This suggests an enhanced N uptake by the plant from this specific N source with respect to the non-amended plot. On the other hand, plants grown on NH4-enriched zeolites registered a higher 15N, approaching the pig-slurry isotopic signature, confirming that this material can constitute an N pool for plants at least for two cultivation cycles. The distinct agricultural practices seem to be reflected in the plant physiology as recorded by the carbon discrimination factor (13C) which generally increases

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

    DEFF Research Database (Denmark)

    2015-01-01

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

  11. Removal of VOCs from air stream with corrugated sheet as adsorbent

    Directory of Open Access Journals (Sweden)

    Rabia Arshad

    2016-10-01

    Full Text Available A large proportional of volatile organic compounds (VOCs are released into the environment from various industrial processes. The current study elucidates an application of a simple adsorption phenomenon for removal of three main types of VOCs, i.e., benzene, xylene and toluene, from an air stream. Two kinds of adsorbents namely acid digested adsorbent and activated carbon are prepared to assess the removal efficiency of each adsorbent in the indoor workplace environment. The results illustrate that the adsorbents prepared from corrugated sheets were remarkably effective for the removal of each pollutant type. Nevertheless, activated carbon showed high potential of adsorbing the targeted VOC compared to the acid digested adsorbent. The uptake by the adsorbents was in the following order: benzene > xylene > toluene. Moreover, maximum adsorption of benzene, toluene and xylene occurred at 20 °C and 1.5 cm/s for both adsorbents whereas minimum success was attained at 30 °C and 1.0 cm/s. However, adsorption pattern are found to be similar for each of the the three aromatic hydrocarbons. It is concluded that the corrugated sheets waste can be a considered as a successful and cost-effective solution towards effective removal of targeted pollutants in the air stream.

  12. HYDROGEN AND VOC RETENTION IN WASTE BOXES

    Energy Technology Data Exchange (ETDEWEB)

    PACE ME; MARUSICH RM

    2008-11-21

    The Hanford Waste Management Project Master Documented Safety Analysis (MDSA) (HNF-14741, 2003) identifies derived safety controls to prevent or mitigate the risks of a single-container deflagration during operations requiring moving, venting or opening transuranic (TRU)-waste containers. The issue is whether these safety controls are necessary for operations involving TRU-waste boxes that are being retrieved from burial at the Hanford Site. This paper investigates the potential for a deflagration hazard within these boxes and whether safety controls identified for drum deflagration hazards should be applied to operations involving these boxes. The study evaluates the accumulation of hydrogen and VOCs within the waste box and the transport of these gases and vapors out of the waste box. To perform the analysis, there were numerous and major assumptions made regarding the generation rate and the transport pathway dimensions and their number. Since there is little actual data with regards to these assumptions, analyses of three potential configurations were performed to obtain some indication of the bounds of the issue (the concentration of hydrogen or flammable VOCs within a waste box). A brief description of each of the three cases along with the results of the analysis is summarized.

  13. 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.

  14. Analysis of Sidestream Smoke VOCs and Characterization of their Odor Profiles by VOC Preconcentrator-GC-O Techniques

    Directory of Open Access Journals (Sweden)

    Higashi N

    2014-12-01

    Full Text Available Various techniques have been employed in the analysis of volatile organic compounds (VOCs. However, these techniques are insufficient for the precise analysis of tobacco smoke VOCs because of the complexity of the operating system, system instability, or poor sensitivity. To overcome these problems, a combined system of VOC preconcentrator, gas chromatograph, and olfactometer has been developed. The performance of this new system was evaluated in the analysis of VOCs in tobacco smoke and applied to the odor profiling of sidestream smoke (SSS that has not been sufficiently investigated in the past.

  15. Fabrication a composite electrode based on MWCNT/Zeolite for potentiometric determination of Cr3+

    Directory of Open Access Journals (Sweden)

    Zahra Heidari

    2016-03-01

    Full Text Available A nanocomposite based on carbon paste electrode fabricated, by using zeolite as ion carrier .Functional multi-wall carbon nanotube was used for improvement of electrode response. The optimal composition of CPE was built from 65% graphite powder, 20 wt% paraffin oil, 5% ion carrier (zeolite, 10% MWCNTs. Electrode showed Nernstian response 19.88 (±0.2mVdecade−1 in the measuring range 10−7–10−2 mol L−1 and showed detection limit of 6.3×10-7 M. The sensor was successfully used for potentiometric titration Cr3+ with EDTA. The carbon paste electrode showed fast response time, good selectivity and applicable in the wide pH range of 3 -10.

  16. 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.

  17. A Novel Wireless Wearable Volatile Organic Compound (VOC Monitoring Device with Disposable Sensors

    Directory of Open Access Journals (Sweden)

    Yue Deng

    2016-12-01

    Full Text Available A novel portable wireless volatile organic compound (VOC monitoring device with disposable sensors is presented. The device is miniaturized, light, easy-to-use, and cost-effective. Different field tests have been carried out to identify the operational, analytical, and functional performance of the device and its sensors. The device was compared to a commercial photo-ionization detector, gas chromatography-mass spectrometry, and carbon monoxide detector. In addition, environmental operational conditions, such as barometric change, temperature change and wind conditions were also tested to evaluate the device performance. The multiple comparisons and tests indicate that the proposed VOC device is adequate to characterize personal exposure in many real-world scenarios and is applicable for personal daily use.

  18. Modified EL model to correlate the adsorption equilibrium of binary VOCs gases on activated carbon%用修正的E-L模型描述二元VOCs气体在活性炭上的吸附平衡

    Institute of Scientific and Technical Information of China (English)

    曹利; 黄学敏; 宋文斌; 马广大

    2011-01-01

    The binary adsorption equilibrium of different VOCs gases was studied.Results show that for the binary adsorption systems,as of toluene-benzene,toluene-ethyl acetate,toluene-acetone,acetone-ethyl acetate and benzene-acetone,displacement phenomena take place in the adsorption processes.With the increase of adsorbed amount of high boiling point components in adsorber,the low boiling point components desorb more easily,and displacements from high boiling point components to low boiling point components occur,with the breakthrough curves of components displaced having peaks.But for the benzene-ethyl acetate,there is no clear displacement effect because of their close boiling point.Associating the adsorption amount of activated carbon to adsorbate with affinity coefficient,the modified E-L model was proposed to predict VOCs binary adsorption equilibrium by introducing depression factor.The values of prediction by the modified E-L equation for amount of single component and the total in binary system show good agreement with the experimental results,with average errors about 9.6% and 6.2%,respectively.%对不同VOCs气体二元吸附平衡进行了研究。结果表明,对于甲苯-苯、甲苯-乙酸乙酯、甲苯-丙酮、丙酮-乙酸乙酯及苯-丙酮二元吸附体系,吸附过程存在置换现象,即随着高沸点组分在床层内吸附量的逐渐增加,相对挥发性大的低沸点组分更易脱附,出现高沸点组分置换低沸点组分的现象,表现为被置换组分的穿透曲线上出现峰值;但对于苯-乙酸乙酯二元体系,由于沸点相近,吸附过程没有明显的置换现象。将活性炭对吸附质吸附量的大小与亲和系数相关联,通过引入抑制因子建立了修正的E-L模型,该模型对不同VOCs二元体系平衡吸附量的预测值与实验值吻合较好,其对二元体系中单组分和总吸附量预测的平均误差分别为9.6%和6.2%。

  19. High performance nano-titania photocatalytic paper composite. Part I: Experimental design study for TiO{sub 2} composite sheet using a natural zeolite microparticle system and its photocatalytic property

    Energy Technology Data Exchange (ETDEWEB)

    Ko, Seonghyuk, E-mail: sko@ncat.ed [Department of Paper Engineering, Chemical Engineering and Imaging, Western Michigan University, Kalamazoo, MI 49008 (United States); Pekarovic, Jan; Fleming, Paul D. [Department of Paper Engineering, Chemical Engineering and Imaging, Western Michigan University, Kalamazoo, MI 49008 (United States); Ari-Gur, Pnina [Department of Mechanical and Aeronautical Engineering, Western Michigan University, Kalamazoo, MI 49008 (United States)

    2010-01-25

    Nanosized titanium dioxide (TiO{sub 2}) photocatalytic papers were successfully prepared using a natural zeolite microparticle retention aid in papermaking. Applying a factorial experimental design, natural zeolite has been demonstrated to be the most significant and interactive factor for increasing the TiO{sub 2} retention rate in paper stock. The photocatalysis of as-prepared sheets was evaluated with toluene as one of the representative volatile organic compounds (VOCs). Under UV irradiation, it was shown to be effective in removing gaseous toluene by photodecomposition, assisted by adsorption. It was revealed that natural zeolite plays an important role in both increasing retention rate of TiO{sub 2} nanoparticles and enhancing photocatalytic efficiency of the paper. The photocatalytic paper can be potentially applied for environmental purification.

  20. NEW SOIL VOC SAMPLERS: EN CORE AND ACCU CORE SAMPLING/STORAGE DEVICES FOR VOC ANALYSIS

    Energy Technology Data Exchange (ETDEWEB)

    Susan S. Sorini; John F. Schabron; Joseph F. Rovani Jr

    2006-06-01

    Soil sampling and storage practices for volatile organic analysis must be designed to minimize loss of volatile organic compounds (VOCs) from samples. The En Core{reg_sign} sampler is designed to collect and store soil samples in a manner that minimizes loss of contaminants due to volatilization and/or biodegradation. An ASTM International (ASTM) standard practice, D 6418, Standard Practice for Using the Disposable En Core Sampler for Sampling and Storing Soil for Volatile Organic Analysis, describes use of the En Core sampler to collect and store a soil sample of approximately 5 grams or 25 grams for volatile organic analysis and specifies sample storage in the En Core sampler at 4 {+-} 2 C for up to 48 hours; -7 to -21 C for up to 14 days; or 4 {+-} 2 C for up to 48 hours followed by storage at -7 to -21 C for up to five days. This report discusses activities performed during the past year to promote and continue acceptance of the En Core samplers based on their performance to store soil samples for VOC analysis. The En Core sampler is designed to collect soil samples for VOC analysis at the soil surface. To date, a sampling tool for collecting and storing subsurface soil samples for VOC analysis is not available. Development of a subsurface VOC sampling/storage device was initiated in 1999. This device, which is called the Accu Core{trademark} sampler, is designed so that a soil sample can be collected below the surface using a dual-tube penetrometer and transported to the laboratory for analysis in the same container. Laboratory testing of the current Accu Core design shows that the device holds low-level concentrations of VOCs in soil samples during 48-hour storage at 4 {+-} 2 C and that the device is ready for field evaluation to generate additional performance data. This report discusses a field validation exercise that was attempted in Pennsylvania in 2004 and activities being performed to plan and conduct a field validation study in 2006. A draft ASTM

  1. SUBSTRATE EFFECTS ON VOC EMISSIONS FROM A LATEX PAINT

    Science.gov (United States)

    The effects of two substrates -- a stainless steel plate and a gypsum board -- on the volatile organic compound (VOC) emissions from a latex paint were evaluated by environmental chamber tests. It was found that the amount of VOCs emitted from the painted stainless steel was 2 to...

  2. FORMULATING ULTRA-LOW-VOC WOOD FURNITURE COATINGS

    Science.gov (United States)

    The article discusses the formulation of ultra-low volatile organic compound (VOC) wood furniture coatings. The annual U.S. market for wood coatings is about 240, 000 cu m (63 million gal). In this basis, between 57 and 91 million kg (125 and 200 million lb) of VOCs are emitted i...

  3. Direct measurement of VOC diffusivities in tree tissues

    DEFF Research Database (Denmark)

    Baduru, K.K.; Trapp, Stefan; Burken, Joel G.

    2008-01-01

    fundamental terminal fate processes for VOCs that have been translocated from contaminated soil or groundwater, and diffusion constitutes the mass transfer mechanism to the plant−atmosphere interface. Therefore, VOC diffusion through woody plant tissues, that is, xylem, has a direct impact on contaminant fate...

  4. Removal of petroleum aromatic hydrocarbons by surfactant-modified natural zeolite: the effect of surfactant

    Energy Technology Data Exchange (ETDEWEB)

    Torabian, Ali; Seifi, Laleh; Bidhendi, Gholamreza Nabi; Azimi, Ali Akbar [Faculty of the Environment, University of Tehran (Iran); Kazemian, Hossein [SPAG Zeolite R and D Group, Technology Incubation Centre, Science and Technology Park of Tehran University, Tehran (Iran); Department of Chemical and Biochemical Engineering, University of Western Ontario, London, Ontario (Canada); Ghadiri, Seid Kamal [Department of Environmental Health Engineering, School of Public Health and Institute of Public Health Research, Tehran University of Medical Sciences, Tehran (Iran)

    2010-01-15

    Monoaromatic hydrocarbons including benzene, toluene, ethylbenzene and xylene isomers (BTEX) are a very important category of water pollutants. These volatile compounds are very hazardous because of their fast migration in soil and water bodies and their acute and chronic toxicities when inhaled or ingested, especially benzene which is a known carcinogenic molecule. In this study, a natural zeolite (i. e., clinoptilolite-rich tuffs) was modified by two cationic surfactants (i. e., hexadecyltrimethyl ammonium chloride (HDTMA-Cl), and N-cetylpyridinium bromide (CPB)). The prepared adsorbents were then characterized, and their adsorptive capabilities for BTEX examined at different experimental conditions. The results of adsorption tests at 24 h revealed that the adsorption capacity of the modified zeolites improved by increasing the surfactant loading (i. e., less than the critical micelle concentration (CMC), to higher than the CMC), which caused an increase in sorption capacity from 60 to 70% for HDTMA-modified samples, and from 47 to 99% for CPB-modified zeolite. Adsorption kinetic tests showed the optimum contact time was 48 h with an average BTEX removal of 90 and 93% for HDTMA-modified and CPB-modified zeolite, respectively. Results showed that by increasing of pH from 3 to 11, the sorption capacity of the adsorbent decreased markedly from 97 to 75%. Analyzing the influence of temperature showed that the adsorption efficiency of adsorbents for benzene reduced from 93% at 20 C to 10% at 4 C. However, the influence of temperature on other compounds was not remarkable. Overall, CPB-modified zeolite exhibited higher selectivity toward BTEX compounds at optimum experimental conditions. Although commercial powder activated carbon (PAC) showed a higher capacity for all BTEX compounds and faster adsorption kinetics, the adsorption capacity of the CPB-modified zeolite at optimized conditions was competitive with PAC results. (Abstract Copyright [2010], Wiley Periodicals

  5. The Effect of zeolite addition on viability of paddy straw mushroom spawn

    Directory of Open Access Journals (Sweden)

    DJUMHAWAN RATMAN PERMANA

    2007-01-01

    Full Text Available The objective of this research was to increase the viability of the paddy straw mushroom spawn by adding natural stone on the media’s composition for the paddy straw mushroom spawn. Mycelium of the paddy straw mushroom was take from the pure development of the paddy straw mushroom which was planted on the various treatment for media e.i. 100% cotton media and rice bran + 0% zeolite (A, 75% cotton media and rice bran + 25% zeolite (B, 50% cotton media and rice bran + 50% zeolite (C, 25% cotton and rice bran + 75% zeolite (D, 0% cotton media and rice bran + 100% rice bran (E. Each treatment was observed for the length of mycelium, the concentration of reduced sugar, total carbon and water content, spawn media weight, pH and temperature. Results demonstrated that there is a positive effect of zeolite added to the paddy straw mushroom media. The zeolite able to adsorbed nutrient through its pores, so the mycelium of the paddy straw mushroom able to use the nutrient gradually and equally appropriate with its growth. Therefore the viability of the paddy straw mushroom is increase. Result showed that the B is the best viability in the Potetos Dectrose Agar (PDA media, that has viability power up to 50 days after inoculation and the temperature are 29,6 0C, then followed by treatment C, D, A and E, each has viability power up to 42; 38; 34; 22 days after inoculation and the maximum length of each mycelium are 17.5; 9.2; 0.9; 0.5 cm, but in the treatment D being contaminated by Aspergillus sp.

  6. 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.

  7. Enriched natural zeolites – mineral fertilizer

    Directory of Open Access Journals (Sweden)

    Rybárová Lucia

    2001-12-01

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

  8. Factors affecting drug adsorption on beta zeolites.

    Science.gov (United States)

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

    2013-05-01

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

  9. MnS clusters in natural zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Iacomi, Felicia; Vasile, Aurelia; Polychroniadis, E.K

    2003-08-15

    FTIR, ESR, optical absorption, photoconductivity, and luminescence measurements are used to evidence the nature of MnS clusters, synthesized by treating the Mn{sup 2+} forms of natural zeolites with Na{sub 2}S.

  10. Synthesis of LTA zeolite for bacterial adhesion

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-07-01

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

  11. 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.

  12. ADSORPTION MALACHITE GREEN ON NATURAL ZEOLITE

    OpenAIRE

    Eko Ariyanto

    2012-01-01

    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.

  13. Zeolitic catalytic conversion of alochols to hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

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

    2017-01-03

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

  14. 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...

  15. Hydrogen sulphide, odor, and VOC air emission control systems for heavy oil storage, transport, and processing operations

    Energy Technology Data Exchange (ETDEWEB)

    Tandon, H.P. [APC Technologies, Inc. (Canada)

    2011-07-01

    In the heavy oil industry, companies have to control their air emissions in compliance with regulatory and process improvement objectives. The industry therefore operates air emission control systems to eliminate odor complaints, reduce personnel exposure to H2S and remove BTEX and VOC emissions. This paper studies different cases of companies which have chosen to use a fixed activated carbon adsorption unit. The study was conducted on three cases of heavy oil industries which installed the CarbonPure adsorption system and describes their objectives, processes, emissions, technology options and performances. Results showed an elimination of odor complaints, a reduction of personnel exposure to harmful air contaminants and a reduction of VOC concentrations in a reliable, low maintenance and economic manner. This study presents the greater benefits of the CarbonPure adsorption system combined with an ultra high efficiency unit over those of other adsorption systems.

  16. Nieuwsgaring in Batavia tijdens de VOC

    Directory of Open Access Journals (Sweden)

    Adrienne Zuiderweg

    2010-12-01

    Full Text Available  The board members of the Dutch East India Company (1602-1795, the Heren Zeventien, promulgated various decrees in which they forbade to bring out information regarding their colonies in the Dutch East Indies and Batavia in letters, manuscripts and printed matter. But in Batavia some inventive Company servants and even staff members got around these regulations, as did some printers in Holland. They published newspapers like Bataviase Nouvelles and Vendu-Nieuws, and also the specialized journal Verhandelingen van het Bataviaasch Genootschap. The initiators of this journal joined hands with the Dutch world of learning and its journals. This article provides an overview of early journalism in the Dutch East Indies and thus contributes to the reconstruction of the literary and cultural climate in Batavia at the time of the VOC.

  17. 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.

  18. Enhancing the Porosity of Mesoporous Carbon-Templated ZSM-5 by Desilication

    DEFF Research Database (Denmark)

    Holm, Martin Spangsberg; Egeblad, Kresten; Vennestrøm, Peter Nicolai Ravnborg

    2008-01-01

    A tunable desilication protocol applied on a mesoporous ZSM-5 zeolite synthesized by carbon-templating is reported. The strategy enables a systematic manufacture of zeolite catalysts with moderate to very high mesoporosities. Coupling carbon-templating and desilication thus allow for more than...

  19. The zeolite deposits of Greece

    Science.gov (United States)

    Stamatakis, M.G.; Hall, A.; Hein, J.R.

    1996-01-01

    Zeolites are present in altered pyroclastic rocks at many localities in Greece, and large deposits of potential economic interest are present in three areas: (1) the Evros region of the province of Thrace in the north-eastern part of the Greek mainland; (2) the islands of Kimolos and Poliegos in the western Aegean; and (3) the island of Samos in the eastern Aegean Sea. The deposits in Thrace are of Eocene-Oligocene age and are rich in heulandite and/or clinoptilolite. Those of Kimolos and Poliegos are mainly Quaternary and are rich in mordenite. Those of Samos are Miocene, and are rich in clinoptilolite and/or analcime. The deposits in Thrace are believed to have formed in an open hydrological system by the action of meteoric water, and those of the western Aegean islands in a similar way but under conditions of high heat flow, whereas the deposits in Samos were formed in a saline-alkaline lake.

  20. 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.

  1. Zeolite formation from coal fly ash and heavy metal ion removal characteristics of thus-obtained Zeolite X in multi-metal systems

    Energy Technology Data Exchange (ETDEWEB)

    Jha, V.K.; Nagae, M.; Matsuda, M.; Miyake, M. [Okayama University, Okayama (Japan). Dept. of Material & Energy Science

    2009-06-15

    Zeolitic materials have been prepared from coal fly ash as well as from a SiO{sub 2}-Al{sub 2}O{sub 3} system upon NaOH fusion treatment, followed by subsequent hydrothermal processing at various NaOH concentrations and reaction times. During the preparation process, the starting material initially decomposed to an amorphous form, and the nucleation process of the zeolite began. The carbon content of the starting material influenced the formation of the zeolite by providing an active surface for nucleation. Zeolite A (Na-A) was transformed into zeolite X (Na-X) with increasing NaOH concentration and reaction time. The adsorption isotherms of the obtained Na-X based on the characteristics required to remove heavy ions such as Ni{sup 2+}, Cu{sup 2+}, Cd{sup 2+} and Pb{sup 2+} were examined in multi-metal systems. Thus obtained experimental data suggests that the Langmuir and Freundlich models are more accurate compared to the Dubinin-Kaganer-Radushkevich (DKR) model. However, the sorption energy obtained from the DKR model was helpful in elucidating the mechanism of the sorption process. Further, in going from a single- to multi-metal system, the degree of fitting for the Freundlich model compared with the Langmuir model was favored due to its basic assumption of a heterogeneity factor. The Extended-Langmuir model may be used in multi-metal systems, but gives a lower value for equilibrium sorption compared with the Langmuir model.

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

    Energy Technology Data Exchange (ETDEWEB)

    Robert Lee; Liangxiong Li

    2008-03-31

    Desalination of brines produced from oil and gas fields is an attractive option for providing potable water in arid regions. Recent field-testing of subsurface sequestration of carbon dioxide for climate management purposes provides new motivation for optimizing efficacy of oilfield brine desalination: as subsurface reservoirs become used for storing CO{sub 2}, the displaced brines must be managed somehow. However, oilfield brine desalination is not economical at this time because of high costs of synthesizing membranes and the need for sophisticated pretreatments to reduce initial high TDS and to prevent serious fouling of membranes. In addition to these barriers, oil/gas field brines typically contain high concentrations of multivalent counter cations (eg. Ca{sup 2+} and SO{sub 4}{sup 2-}) that can reduce efficacy of reverse osmosis (RO). Development of inorganic membranes with typical characteristics of high strength and stability provide a valuable option to clean produced water for beneficial uses. Zeolite membranes have a well-defined subnanometer pore structure and extreme chemical and mechanical stability, thus showing promising applicability in produced water purification. For example, the MFI-type zeolite membranes with uniform pore size of {approx}0.56 nm can separate ions from aqueous solution through a mechanism of size exclusion and electrostatic repulsion (Donnan exclusion). Such a combination allows zeolite membranes to be unique in separation of both organics and electrolytes from aqueous solutions by a reverse osmosis process, which is of great interest for difficult separations, such as oil-containing produced water purification. The objectives of the project 'Treating Coalbed Natural Gas Produced Water for Beneficial Use by MFI Zeolite Membranes' are: (1) to conduct extensive fundamental investigations and understand the mechanism of the RO process on zeolite membranes and factors determining the membrane performance, (2) to improve

  3. Measurements of VOCs in Mexico City during the MILAGRO Campaign

    Science.gov (United States)

    Baker, A. K.; Beyersdorf, A. J.; Blake, N. J.; Meinardi, S.; Atlas, E.; Rowland, F.; Blake, D. R.

    2006-12-01

    During March of 2006 we participated in MILAGRO (Megacities Initiative: Local and Global Research Observations), a multi-platform campaign to measure pollutants in and in outflow from the Mexico City metropolitan area. As part of MILAGRO we collected whole air canister samples at two Mexico City ground sites: the Instituto Mexicano del Petroleo, located in the city, northeast of the center, and the Universidad Technologica de Tecamac, a suburban site approximately 50 km northeast of the city center. Samples were also collected in various other locations throughout Mexico City. Over 300 whole air samples were collected and analyzed for a wide range of volatile organic compounds (VOCs) including methane, carbon monoxide, nonmethane hydrocarbons (NMHCs) and halocarbons. Propane was the most abundant NMHC at both the urban and suburban locations, with mixing ratios frequently in excess of 10 parts per billion at both locations. This is likely the result of the widespread use of liquefied petroleum gas (LPG) of which propane is the major component. For most species, median mixing ratios at the urban sites were significantly greater than at the suburban site. Here we compare results from both urban and suburban locations and also examine the influence of transport on the composition of outflow from Mexico City.

  4. Adsorption-electro-desorption treatment of air polluted by VOCs; Traitement de l'air charge en COV par adsorption-electrodesorption

    Energy Technology Data Exchange (ETDEWEB)

    Subrenat, A.; Le Cloirec, P. [Ecole des Mines de Nantes 44 (France)

    2004-10-01

    Volatile organic compounds (VOCs) are pollutants involved in the greenhouse effect. Their abatement is today seriously controlled when they are produced by industrial classified facilities. This paper presents a air treatment system based on the adsorption by activated carbon tissues. The filters are regenerated by electrical heating. The physico-chemical and electrical properties of activated carbon tissues are presented first with their adsorption properties with respect to VOCs. Then the design of a specific adsorber is described: adsorption filters, pressure drops and air flow, implementation and efficiency. Finally, the efficiency results obtained on a real-scale industrial plant are presented. (J.S.)

  5. Effects of Chemical Fertilizer, Algea Compost and Zeolite on Green Bean Yield

    Directory of Open Access Journals (Sweden)

    Aysun Türkmen

    2017-03-01

    Full Text Available The present study used chemical fertilizer, brown algae compost and zeolite carried out in the field of Giresun Hazelnut Research Center between May-November 2014 in pots according to randomized blog design as three replicate each. Treatment groups were consist of eight different combinations as follow; G1-Control, G2-Zeolite, G3-Compost, G4-Chemical Fertilizer, G5-Zeolite+Compost, G6-Zeolite+Chemical Fertilizer, G7-Compost+ Chemical Fertilizer, G8-Compost+Zeolite+ Chemical Fertilizer. The brown algae (Cystoseira sp. were used as compost material. These combinations were applied to green beans (Phaseolus vulgaris. The green beans were seeded by hand to arrange planting depth of 5-6 cm and 20 seeds/m2. Except control group, each treatment was added fertilizers as 50 g zeolite, 50 g compost, and 25 g chemical according to treatment design. Half of the chemical fertilizers were added at seeding time and the rest after two weeks. Collected soil samples were analyzed right after harvest, the greatest values of treatment groups were determined as; Carbon% G1: 5.08, nitrogen G3: 0.09 ppm, sodium G5: 139 ppm, potassium G6 and G8: 5 ppm, magnesium G2: 1865 ppm, calcium G6: 8.33 ppm, manganese G2: 359 ppm, iron G6 : 16070 ppm, cobalt G6 and G7: 7.91 ppm, copper G2: 17.5 ppm, zinc G8: 28.0 ppm, selenium G7: 4.17 ppm, cadmium G5: 0.08 ppm, lead G4: 5.31 ppm. The greatest harvest value as g/m2 was obtained from zeolite only group G2 with 273 while the lowest was obtained from Compost only group G3 with 113 g/m2, obviously showing the effectiveness of zeolite only application moreover, also thinking that better results may get if the present study run for longer period.

  6. New observations of VOC emissions and concentrations in, above, and around the Central Valley of California

    Science.gov (United States)

    Goldstein, A. H.; Fares, S.; Gentner, D. R.; Park, J.; Weber, R.; Ormeno, E.; Holzinger, R.; Misztal, P. K.; Karl, T. R.; Guenther, A. B.; Fischer, M. L.; Harley, R. A.; Karlik, J. F.

    2011-12-01

    in-situ GC included more than 200 anthropogenic and biogenic VOCs with a wide range of volatilities (up to 17 carbon atoms in size) and various functional groups (e.g. aldehydes, ketones, alcohols, halogens, sulfur, & nitrogen). Finally, in 2011 vertical profiles of VOC were made at 5 heights on a communication tower at Walnut Grove (~20 miles south of Sacramento) from 30' to 1550' by PTRMS. Results from all of these studies combined provide a novel overview of the distribution of VOC emissions and concentrations in, around, and above the Central Valley of California.

  7. Seasonal variability and source apportionment of volatile organic compounds (VOCs) in the Paris megacity (France)

    Science.gov (United States)

    Baudic, Alexia; Gros, Valérie; Sauvage, Stéphane; Locoge, Nadine; Sanchez, Olivier; Sarda-Estève, Roland; Kalogridis, Cerise; Petit, Jean-Eudes; Bonnaire, Nicolas; Baisnée, Dominique; Favez, Olivier; Albinet, Alexandre; Sciare, Jean; Bonsang, Bernard

    2016-09-01

    Within the framework of air quality studies at the megacity scale, highly time-resolved volatile organic compound (C2-C8) measurements were performed in downtown Paris (urban background sites) from January to November 2010. This unique dataset included non-methane hydrocarbons (NMHCs) and aromatic/oxygenated species (OVOCs) measured by a GC-FID (gas chromatograph with a flame ionization detector) and a PTR-MS (proton transfer reaction - mass spectrometer), respectively. This study presents the seasonal variability of atmospheric VOCs being monitored in the French megacity and their various associated emission sources. Clear seasonal and diurnal patterns differed from one VOC to another as the result of their different origins and the influence of environmental parameters (solar radiation, temperature). Source apportionment (SA) was comprehensively conducted using a multivariate mathematical receptor modeling. The United States Environmental Protection Agency's positive matrix factorization tool (US EPA, PMF) was used to apportion and quantify ambient VOC concentrations into six different sources. The modeled source profiles were identified from near-field observations (measurements from three distinct emission sources: inside a highway tunnel, at a fireplace and from a domestic gas flue, hence with a specific focus on road traffic, wood-burning activities and natural gas emissions) and hydrocarbon profiles reported in the literature. The reconstructed VOC sources were cross validated using independent tracers such as inorganic gases (NO, NO2, CO), black carbon (BC) and meteorological data (temperature). The largest contributors to the predicted VOC concentrations were traffic-related activities (including motor vehicle exhaust, 15 % of the total mass on the annual average, and evaporative sources, 10 %), with the remaining emissions from natural gas and background (23 %), solvent use (20 %), wood-burning (18 %) and a biogenic source (15 %). An important finding of

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

    Science.gov (United States)

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

    2011-08-01

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

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

    African Journals Online (AJOL)

    Journal of Science and Technology (Ghana) ... by employing surfactant modified zeolites (SMZ) synthesized using locallyavailable kaolin material as precursor. ... The SEM showed the zeolite NaLSX crystals to be octahedrally shaped.

  10. VOCs and odors: key factors in selecting `green` building materials?

    Energy Technology Data Exchange (ETDEWEB)

    Coombs, C. [Steven Winter Associates Inc., Norwalk, CT and Washington DC (United States)

    1998-12-01

    The current state of knowledge available for selecting building materials on the basis of emissions of volatile organic compounds (VOCs) and odors is reviewed. The significance of VOCs and odors in building materials is related to their role in influencing indoor air quality. As far as toxicity is concerned, many of the VOCs detected in indoor air are relatively inert when considered singly. They are not however, unimportant because in actual fact they are invariably found in mixtures some of which can be toxic. Although knowledge of VOCs is incomplete, it is important to specify ozone-resistant polymeric building products, i.e. those that are chemically stable and inert to oxidation. In addition to VOCs, attention should also be focused on semi-volatile organic compounds (SVOCs) since they are even more persistent than VOCs and tend to offgas for prolonged periods of time. Similarly, it is reasonable to specify low-odor materials. Inclusion of issues related to complex indoor chemistry, less volatile emissions, in addition to VOCs and odor, should in time result in expanded choices of building materials that promote indoor air quality. 16 refs.,2 tabs.

  11. Application of Zeolitic Additives in the Fluid Catalytic Cracking (FCC

    Directory of Open Access Journals (Sweden)

    A. Nemati Kharat

    2013-06-01

    Full Text Available Current article describes application of zeolites in fluid catalytic cracking (FCC. The use of several zeolitic additives for the production light olefins and reduction of pollutants is described. Application of zeolites as fluid catalytic cracking (FCC catalysts and additives due to the presence of active acid sites in the zeolite framework  increase the formation of desired cracking products (i.e., olefin and branched products  in the FCC unit.

  12. Efficiency of catalytic processes for the reduction of CO and VOC emissions from wood combustion in domestic fireplaces

    Energy Technology Data Exchange (ETDEWEB)

    Ozil, Fabien; Tschamber, V.; Trouve, G. [Universite de haute Alsace - Laboratoire Gestion des Risques Environnement, 25 rue de Chemnitz, 68200 Mulhouse (France); Haas, Frederic (FONDIS SA, ZI Vieux Thann, 68801 Thann Cedex France)

    2009-09-15

    Pollutant characterization of domestic fireplaces, according to two paces of functioning (normal and low-charge phase) was performed. Two catalysts supported on cordierite or metal were placed in the exhaust of two domestic fireplaces (old and new generation) in order to reduce gaseous pollutants. Active phase of catalysts is composed of noble metals (Pd, Pt) and cerium. Methane was the dominant compound of the released Volatile Organic Compounds (VOC, 80% b. v.). Products resulting from incomplete combustion (CO and other VOC) did not represent more than 6% of the initial carbon content in wood. Lower concentration of CO in the exhaust was obtained with the new generation fireplace as compared to the older one with mean concentrations of CO normalized for 13% oxygen b.v. equal to 0.12% and 0.3%, respectively. Emission of VOC is also drastically reduced for new generation fireplace. The presence of a catalyst induced a decrease of the CO and VOC emission factors during ignition and low-charge phases by factors ranging from 65% to 70%. The abatement of VOC for the old generation fireplace was better in the presence of metal as compared to cordierite, with efficiency values of 65% and 30%, respectively. The new fireplace was the one on which the addition of the cleanup implements had most impact. Besides the introduction of a catalyst, a heating system of the fume was set up below the catalyst. This heating system allowed a faster activation of the catalyst, particularly during ignition and low-charge phases. Best abatements were obtained with the heated metallic support with values close to 80% and 94% for VOC and CO respectively. (author)

  13. Functionalized Cellulose: PET Polymer Fibers with Zeolites for Detoxification Against Nerve Agents%Functionalized Cellulose:PET Polymer Fibers with Zeolites for Detoxification Against Nerve Agents

    Institute of Scientific and Technical Information of China (English)

    Agarwal Satya R; Sundarrajan Subramanian; Ramakrishna Seeram

    2012-01-01

    Presently activated carbon is used as an adsorptive material for chemical and biological warfare agents.It possess excellent surface properties such as large surface area,fire-resistance and plenty availability,but has disadvantages such as its heavy weight,low breathability (after adsorption of moisture) and disposal.In this paper,we propose to utilize novel electrospun polymeric nanostructures having zeolites as catalyst materials.In this respective,the electrospun polymer nanofibers would serve as the best possible substitutes to activated carbon based protective clothing applications.This is the first in the literature that reports the integration of these types of catalysts with nanofiberous membranes.Electrospinning of cellulose/polyethylene terephthalate (PET) blend nanofibers has been carried out.Zeolite catalysts (Linde Type A and Mordenite) for the detoxification of nerve agent stimulant-paraoxon,were prepared due to their relative simplicity of synthesis.The catalysts were then coated onto nanofiber membranes and their morphology was confirmed using SEM.This is the first report on the coating of nanofibers with zeolites and their successful demonstration against nerve agent stimulant.The UV absorption spectra clearly show the detoxification ability of the functionalized fibers and their potential to be used in textiles for protection and decontamination.

  14. Hydrothermal conversion of FAU zeolite into LEV zeolite in the presence of non-calcined seed crystals

    Science.gov (United States)

    Yashiki, Ayako; Honda, Koutaro; Fujimoto, Ayumi; Shibata, Shohei; Ide, Yusuke; Sadakane, Masahiro; Sano, Tsuneji

    2011-06-01

    Hydrothermal conversion of Faujasite-type (FAU) zeolite into Levynite (LEV) zeolite without the use of an organic structure-directing agent (OSDA) was successfully achieved in the presence of non-calcined seed crystals. The interzeolite conversion depended strongly upon the alkalinity (OH -/SiO 2) of the starting gel, the Si/Al ratio of the starting FAU zeolite and the type of alkaline metal employed. Successful conversion of FAU zeolites into pure LEV zeolite was achieved only for FAU zeolites with Si/Al ratios in the range of 19-26, under highly alkaline conditions (OH -/SiO 2=0.6) by using NaOH as an alkali source. Although the yield of LEV zeolite prepared by this method was lower (18-26%) than that of the conventional hydrothermal synthesis with the use of SDA, the obtained LEV zeolite exhibited a unique core/shell structure.

  15. Thermodynamic selectivity of functional agents on zeolite for sodium dodecyl sulfate sequestration.

    Science.gov (United States)

    Leng, Ling; Wang, Jian; Qiu, Xianxiu; Zhao, Yanxiang; Yip, Yuk-Wang; Law, Ga-Lai; Shih, Kaimin; Zhou, Zhengyuan; Lee, Po-Heng

    2016-11-15

    This study proposes a thermodynamic approach to effectively select functional agents onto zeolite for sodium dodecyl sulfate (SDS) sequestration in greywater reuse. We combine isothermal titration calorimetry (ITC) and quantum chemistry simulation (QCS) to identify the interactions between SDS and agents at the molecular level. Three potential agents, cetyl trimethyl ammonium bromide (CTAB), N,N,N-trimethyltetradecan-1-aminium bromide (C14TAB), and 14-hydroxy-N,N,N-trimethyltetradecan-1-aminium bromide (C14HTAB), differ in carbon chain length and hydrophilic groups. The ITC titration of SDS with CTAB released the highest heat, followed by those with C14TAB and C14HTAB, as was the same trend for the amounts of SDS adsorbed by the respective functionalized-zeolites. Results suggest that the favorable SDS sorption occurred at the bilayer CTAB-zeolite is driven by enthalpy as similar as the SDS…CTAB interaction found, regardless of the contribution from electrostatic and/or hydrophobic behaviors, while the declined sorption is entropy-driven via the predominant hydrophobic interaction onto the monolayer CTAB-zeolite. The data presented here interpret the nature of molecularly thermodynamic quantities and enable the manipulation of sorption capacity optimization.

  16. Oxidation of H2 and CO over ion-exchanged X and Y zeolites.

    Science.gov (United States)

    Lahr, Daniel G; Li, Junhui; Davis, Robert J

    2007-03-21

    Zeolites X and Y exchanged with Group IA cations were synthesized by aqueous ion exchange of NaX and NaY and used as catalysts in the oxidation of H2 and CO at temperatures ranging from 473 to 573 K. The CsX zeolite was the most active material of the series for both reactions whereas HX was the least active. Moreover, the oxidation of CO in H2 was very selective (approximately 80%) over the alkali-metal exchanged materials. Isotopic transient analysis of CO oxidation during steady-state reaction at 573 K was used to evaluate the coverage of reactive carbon-containing intermediates that lead to product as well as the pseudo-first-order rate constant of the reaction. A factor of 4 enhancement in activity achieved by exchanging Cs for Na was attributed to a higher coverage of reactive intermediates in CsX because the pseudo-first-order rate constant was nearly same for the two materials (approximately 0.7 s(-1)). The number of reactive intermediates on both materials was orders of magnitude below the number of alkali metal cations in the zeolites but was similar to the number of impurity Fe atoms in the samples. Because the trend in Fe impurity loading was the same as that for oxidation activity, a role of transition metal impurities in zeolite oxidation catalysis is suggested.

  17. Effect of pretreatment conditions on the catalytic properties of zeolites in phenol arylalkylation with styrene

    Energy Technology Data Exchange (ETDEWEB)

    Kolesnichenko, N.V.; Romanovskii, B.V.; Kurashev, M.V.

    1980-04-01

    The effect of pretreatment conditions on the catalytic properties of zeolites in phenol arylalkylation with styrene was studied in a flow microreactor at 250/sup 0/C, 1 atm, 4:1 phenol/styrene, and 2.6 sec contact time. Samples of the zeolite-containing AShNTs-3 catalyst (a Soviet commercial grade) in the ammonia form calcined at 300/sup 0/C in flowing helium contained mainly protic acid sites and rapidly lost their catalytic activity. The same catalyst calcined in air at 500/sup 0/C contained mainly aprotic sites and its activity increased with time. Air calcination at 400/sup 0/C gave catalysts which contained similar concentrations of both protic and aprotic sites and showed stable activities and selectivities for the major products, i.e., 4- and 2-((GAMMA)-methylbenzyl)-phenol. The properties of a NH/sub 4/Y zeolite were less affected by thermal pretreatment. The commercial zeolite catalysts AShNTs-3 and Tseokar-2 (unexchanged with ammonia) were strongly promoted by steam and deactivated by carbon dioxide continuously added to the reaction zone. Both effects were reversible.

  18. Hollow Alveolus-Like Nanovesicle Assembly with Metal-Encapsulated Hollow Zeolite Nanocrystals.

    Science.gov (United States)

    Dai, Chengyi; Zhang, Anfeng; Liu, Min; Gu, Lin; Guo, Xinwen; Song, Chunshan

    2016-08-23

    Inspired by the vesicular structure of alveolus which has a porous nanovesicle structure facilitating the transport of oxygen and carbon dioxide, we designed a hollow nanovesicle assembly with metal-encapsulated hollow zeolite that would enhance diffusion of reactants/products and inhibit sintering and leaching of active metals. This zeolitic nanovesicle has been successfully synthesized by a strategy which involves a one-pot hydrothermal synthesis of hollow assembly of metal-containing solid zeolite crystals without a structural template and a selective desilication-recrystallization accompanied by leaching-hydrolysis to convert the metal-containing solid crystals into metal-encapsulated hollow crystals. We demonstrate the strategy in synthesizing a hollow nanovesicle assembly of Fe2O3-encapsulated hollow crystals of ZSM-5 zeolite. This material possesses a microporous (0.4-0.6 nm) wall of hollow crystals and a mesoporous (5-17 nm) shell of nanovesicle with macropores (about 350 nm) in the core. This hierarchical structure enables excellent Fe2O3 dispersion (3-4 nm) and resistance to sintering even at 800 °C; facilitates the transport of reactant/products; and exhibits superior activity and resistance to leaching in phenol degradation. Hollow nanovesicle assembly of Fe-Pt bimetal-encapsulated hollow ZSM-5 crystals was also prepared.

  19. Cation exchange properties of zeolites in hyper alkaline aqueous media.

    Science.gov (United States)

    Van Tendeloo, Leen; de Blochouse, Benny; Dom, Dirk; Vancluysen, Jacqueline; Snellings, Ruben; Martens, Johan A; Kirschhock, Christine E A; Maes, André; Breynaert, Eric

    2015-02-03

    Construction of multibarrier concrete based waste disposal sites and management of alkaline mine drainage water requires cation exchangers combining excellent sorption properties with a high stability and predictable performance in hyper alkaline media. Though highly selective organic cation exchange resins have been developed for most pollutants, they can serve as a growth medium for bacterial proliferation, impairing their long-term stability and introducing unpredictable parameters into the evolution of the system. Zeolites represent a family of inorganic cation exchangers, which naturally occur in hyper alkaline conditions and cannot serve as an electron donor or carbon source for microbial proliferation. Despite their successful application as industrial cation exchangers under near neutral conditions, their performance in hyper alkaline, saline water remains highly undocumented. Using Cs(+) as a benchmark element, this study aims to assess the long-term cation exchange performance of zeolites in concrete derived aqueous solutions. Comparison of their exchange properties in alkaline media with data obtained in near neutral solutions demonstrated that the cation exchange selectivity remains unaffected by the increased hydroxyl concentration; the cation exchange capacity did however show an unexpected increase in hyper alkaline media.

  20. Effect of VOC emissions from vegetation on urban air quality during hot periods

    Science.gov (United States)

    Churkina, Galina; Kuik, Friderike; Bonn, Boris; Lauer, Axel; Grote, Ruediger; Butler, Tim

    2016-04-01

    Programs to plant millions of trees in cities around the world aim at the reduction of summer temperatures, increase of carbon storage, storm water control, and recreational space, as well as at poverty alleviation. These urban greening programs, however, do not take into account how closely human and natural systems are coupled in urban areas. Compared with the surroundings of cities, elevated temperatures together with high anthropogenic emissions of air and water pollutants are quite typical in urban systems. Urban and sub-urban vegetation respond to changes in meteorology and air quality and can react to pollutants. Neglecting this coupling may lead to unforeseen negative effects on air quality resulting from urban greening programs. The potential of emissions of volatile organic compounds (VOC) from vegetation combined with anthropogenic emissions of air pollutants to produce ozone has long been recognized. This ozone formation potential increases under rising temperatures. Here we investigate how emissions of VOC from urban vegetation affect corresponding ground-level ozone and PM10 concentrations in summer and especially during heat wave periods. We use the Weather Research and Forecasting Model with coupled atmospheric chemistry (WRF-CHEM) to quantify these feedbacks in the Berlin-Brandenburg region, Germany during the two summers of 2006 (heat wave) and 2014 (reference period). VOC emissions from vegetation are calculated by MEGAN 2.0 coupled online with WRF-CHEM. Our preliminary results indicate that the contribution of VOCs from vegetation to ozone formation may increase by more than twofold during heat wave periods. We highlight the importance of the vegetation for urban areas in the context of a changing climate and discuss potential tradeoffs of urban greening programs.

  1. VOC Composition of Air Masses Transported from Asia to the U.S. West Coast

    Science.gov (United States)

    de Gouw, J.; Warneke, C.; Kuster, B.; Parrish, D.; Holloway, J.; Huebler, G.; Fehsenfeld, F.

    2002-12-01

    Airborne measurements of volatile organic compounds (VOCs) were performed using a proton-transfer-reaction mass spectrometer (PTR-MS) operated onboard a NOAA WP-3 aircraft during the Intercontinental Transport and Chemical Transformation (ITCT) experiment in 2002. Enhancements of acetone (CH3COCH3), methanol (CH3OH), acetonitrile (CH3CN) and in some cases benzene were observed in air masses that were impacted by outflow from Asia. The enhancement ratios with respect to carbon monoxide are compared to emission factors for fossil fuel combustion and biomass burning, which gives some insight into the sources responsible for the pollution. The observed mixing ratios for acetone, methanol and in particular acetonitrile were generally reduced in the marine boundary layer, suggesting the presence of an ocean uptake sink. The ocean uptake of acetonitrile was found to be particularly efficient in a zone with upwelling water off of the U.S. west coast. Reduced mixing ratios of acetone and methanol were observed in a stratospheric intrusion. This observation gives some information about the lifetime of these VOCs in the stratosphere. Enhanced concentrations of aromatic hydrocarbons were observed in air masses that were impacted by urban sources in California. The ratio between the concentrations of benzene, toluene and higher aromatics indicated the degree of photochemical oxidation. PTR-MS only gives information about the mass of the ions produced by proton-transfer reactions between H3O+ and VOCs in the instrument. The identification of VOCs was confirmed by coupling a gas-chromatographic (GC) column to the instrument and post-flight GC-PTR-MS analyses of canister samples collected during the flights.

  2. VOC and HAP recovery using ionic liquids

    Energy Technology Data Exchange (ETDEWEB)

    Michael R. Milota : Kaichang Li

    2007-05-29

    During the manufacture of wood composites, paper, and to a lesser extent, lumber, large amounts of volatile organic compounds (VOCs) such as terpenes, formaldehyde, and methanol are emitted to air. Some of these compounds are hazardous air pollutants (HAPs). The air pollutants produced in the forest products industry are difficult to manage because the concentrations are very low. Presently, regenerative thermal oxidizers (RTOs and RCOs) are commonly used for the destruction of VOCs and HAPs. RTOs consume large amounts of natural gas to heat air and moisture. The combustion of natural gas generates increased CO2 and NOx, which have negative implications for global warming and air quality. The aforementioned problems are addressed by an absorption system containing a room-temperature ionic liquid (RTIL) as an absorbent. RTILs are salts, but are in liquid states at room temperature. RTILs, an emerging technology, are receiving much attention as replacements for organic solvents in industrial processes with significant cost and environmental benefits. Some of these processes include organic synthesis, extraction, and metal deposition. RTILs would be excellent absorbents for exhausts from wood products facilities because of their unique properties: no measurable vapor pressure, high solubility of wide range of organic compounds, thermal stability to 200°C (almost 400°F), and immisciblity with water. Room temperature ionic liquids were tested as possible absorbents. Four were imidizolium-based and were eight phosphonium-based. The imidizolium-based ionic liquids proved to be unstable at the conditions tested and in the presence of water. The phosphonium-based ionic liquids were stable. Most were good absorbents; however, cleaning the contaminates from the ionic liquids was problematic. This was overcome with a higher temperature (120°C) than originally proposed and a very low pressure (1 kPa. Absorption trials were conducted with tetradecy

  3. Using one waste to tackle another: Preparation of a CO{sub 2} capture material zeolite X from laterite residue and bauxite

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Liying [School of Materials and Metallurgy, Northeastern University, Shenyang 110004 (China); Du, Tao, E-mail: dutao0106@gmail.com [School of Materials and Metallurgy, Northeastern University, Shenyang 110004 (China); Li, Gang [School of Mechanical and Chemical Engineering, The University of Western Australia, Crawley, WA 6009 (Australia); Yang, Fan; Che, Shuai [School of Materials and Metallurgy, Northeastern University, Shenyang 110004 (China)

    2014-08-15

    Highlights: • Valuable zeolite X has been synthesized from laterite residue and bauxite. • High product purity has been achieved by optimizing the process conditions. • Prepared zeolite X shows comparable gas adsorption properties to commercial ones. • Prepared zeolite X can be used for carbon capture by vacuum swing adsorption. - Abstract: In this work, zeolite X, a benchmark adsorbent for carbon capture, has been successfully prepared from low cost waste minerals namely laterite residue and bauxite using alkali fusion process followed by hydrothermal treatment. The structure and morphology of the as-synthesized zeolite X were verified and characterized with a range of experimental techniques such as X-ray diffraction, scanning electronic microscopy and infrared spectroscopy. The surface area and (N{sub 2} and CO{sub 2}) gas adsorption isotherms of this product were found comparable to that of commercial ones, demonstrating the effectiveness of synthesizing zeolite X from laterite and bauxite. Further improvement of the product purity was also accomplished by optimizing the process conditions.

  4. Zeolites and Zeotypes for Oil and Gas Conversion

    NARCIS (Netherlands)

    Vogt, Eelco T C; Whiting, Gareth T.; Dutta Chowdhury, Abhishek; Weckhuysen, Bert M.|info:eu-repo/dai/nl/285484397

    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

  5. 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

  6. 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

  7. 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

  8. 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.

  9. Adsorption of neopentane on HNaY-FAU zeolite studied by IR spectroscopy

    Science.gov (United States)

    Kiricsi, I.; Tasi, Gy.; Förster, H.; Fejes, P.

    1994-01-01

    Adsorption of neopentane on HNaY-FAU zeolite was studied by IR spectroscopy. At beam temperature neopentane already shows a weak interaction with Brønsted acidic sites. At high temperatures, irreversible consumption of both Brønsted and Lewis sites is observed. According to the results of quantum chemical calculations a proton attack on the central carbon of neopentane seems to be favoured.

  10. 1 - Aromatization of n-hexane and natural gasoline over ZSM-5 zeolite, 2- Wet catalytic oxidation of phenol on fixed bed of active carbon; 1 - Aromatisation de n-hexane et d'essence sur zeolithe ZSM-5, 2 - Oxydation catalytique en voie humide du phenol sur charbon actif

    Energy Technology Data Exchange (ETDEWEB)

    Suwanprasop, S.

    2005-04-15

    I - The production of aromatic hydrocarbons from n-hexane and natural gasoline over Pd loaded ZSM-5 zeolite in a tubular reactor was achieved under the suitable conditions at 400 deg. C, and 0.4 ml/min reactant feeding rate, employing ZSM-5 (0.5% Pd content) as a catalyst. Under these conditions, n-hexane and natural gasoline conversions were found to be 99.7% and 94.3%, respectively (with respective aromatic selectivity of 92.3% and 92.6%). II - Wet catalytic air oxidation of phenol over a commercial active carbon was studied in a three phase fixed bed reactor under mild temperature and oxygen partial pressure. Exit phenol concentration, COD, and intermediates were analysed. Oxidation of phenol was significantly improved when increasing operating temperature, oxygen partial pressure, and liquid space time, while up or down flow modes had only marginal effect. A complete model involving intrinsic kinetics and all mass transfer limitations gave convenient reactor simulation. (author)

  11. Processing of Radioactive Waste Solution with Zeolites (I) : Thermal-Transformations of Na, Cs and Sr Forms of Zeolites

    OpenAIRE

    Mimura, Hitoshi; KANNO, Takuji

    1980-01-01

    Thermal-transformations of several kinds of zeolites have been studied by means of differential thermal analysis (DTA), thermo-gravimetric analysis (TGA) and X-ray powder diffraction. Some synthetic zeolites (A, X, Y, mordenite), natural mordenite and clinoptilolite were used. Sodium forms of A and X zeolites recrystallized above 1000℃ to nepheline (NaAlSiO_4) , whereas the structure of zeolite Y, synthetic and natural mordenites, and clinoptilolite collapsed above around 900℃ and did not rec...

  12. Stable carbon isotope ratios of ambient aromatic volatile organic compounds

    Science.gov (United States)

    Kornilova, Anna; Huang, Lin; Saccon, Marina; Rudolph, Jochen

    2016-09-01

    Measurements of mixing ratios and stable carbon isotope ratios of aromatic volatile organic compounds (VOC) in the atmosphere were made in Toronto (Canada) in 2009 and 2010. Consistent with the kinetic isotope effect for reactions of aromatic VOC with the OH radical the observed stable carbon isotope ratios are on average significantly heavier than the isotope ratios of their emissions. The change of carbon isotope ratio between emission and observation is used to determine the extent of photochemical processing (photochemical age, ∫ [OH]dt) of the different VOC. It is found that ∫ [OH]dt of different VOC depends strongly on the VOC reactivity. This demonstrates that for this set of observations the assumption of a uniform ∫ [OH]dt for VOC with different reactivity is not justified and that the observed values for ∫ [OH]dt are the result of mixing of VOC from air masses with different values for ∫ [OH]dt. Based on comparison between carbon isotope ratios and VOC concentration ratios it is also found that the varying influence of sources with different VOC emission ratios has a larger impact on VOC concentration ratios than photochemical processing. It is concluded that for this data set the use of VOC concentration ratios to determine ∫ [OH]dt would result in values for ∫ [OH]dt inconsistent with carbon isotope ratios and that the concept of a uniform ∫ [OH]dt for an air mass has to be replaced by the concept of individual values of an average ∫ [OH]dt for VOC with different reactivity.

  13. Transport properties of zeolite Na-X-Nafion membranes: effect of zeolite loadings and particle size

    Energy Technology Data Exchange (ETDEWEB)

    Lavorgna, M. [Institute of Composite and Biomedical Materials, National Research Council, Portici (Italy); Sansone, L.; Scherillo, G. [Department of Materials and Production, University of Napoli Federico II, Napoli (Italy); Gu, R.; Baker, A.P. [Department of Materials Science and Engineering, HIT Graduate School, Xili, Shenzhen (China)

    2011-12-15

    Na-X zeolites particles, synthesized in two size ranges, namely 200-300 nm and 30-100 nm, were used to prepare Nafion/Na-X zeolite composite membranes by recast method. The physical, chemical, and morphological properties of the zeolite powders and composite membranes were examined by XRD, N{sub 2} adsorption isotherms, FTIR, SEM, and SAXS analysis. Furthermore, the effect of zeolite particles size and loadings (i.e., 5 and 10% w/w) on the water, methanol, and proton transport properties was investigated. It has been found that the size of the Na-X zeolite particles plays a key role in the proton and methanol transport behavior since it rules the zeolite hydrophilic behavior, the morphology of polymer-filler interphase, and also the nature of water established in the composite membrane. The results show that the membranes loaded with a 5% w/w of submicron-sized Na-X zeolite exhibit a proton conductivity and selectivity significantly higher than Nafion. In particular the proton conductivity at 120 C is around eight times and the selectivity at 25 C is around 40% higher than those exhibited by recast Nafion. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

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

    Science.gov (United States)

    Nowicki, Janusz; Mokrzycki, Łukasz; Sulikowski, Bogdan

    2015-04-08

    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.

  15. 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.

  16. 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.

  17. Controlling chemistry with cations: photochemistry within zeolites.

    Science.gov (United States)

    Ramamurthy, V; Shailaja, J; Kaanumalle, Lakshmi S; Sunoj, R B; Chandrasekhar, J

    2003-08-21

    The alkali ions present in the supercages of zeolites X and Y interact with included guest molecules through quadrupolar (cation-pi), and dipolar (cation-carbonyl) interactions. The presence of such interactions can be inferred through solid-state NMR spectra of the guest molecules. Alkali ions, as illustrated in this article, can be exploited to control the photochemical and photophysical behaviors of the guest molecules. For example, molecules that rarely phosphoresce can be induced to do so within heavy cation-exchanged zeolites. The nature (electronic configuration) of the lowest triplet state of carbonyl compounds can be altered with the help of light alkali metal ions. This state switch (n pi*-pi pi*) helps to bring out reactivity that normally remains dormant. Selectivity obtained during the singlet oxygen oxidation of olefins within zeolites illustrates the remarkable control that can be exerted on photoreactions with the help of a confined medium that also has active sites. The reaction cavities of zeolites, like enzymes, are not only well-defined and confined, but also have active sites that closely guide the reactant molecule from start to finish. The examples provided here illustrate that zeolites are far more useful than simple shape-selective catalysts.

  18. 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.

  19. Assessment of the reduction methods used to develop chemical schemes: building of a new chemical scheme for VOC oxidation suited to three-dimensional multiscale HOx-NOx-VOC chemistry simulations

    Directory of Open Access Journals (Sweden)

    S. Szopa

    2005-01-01

    Full Text Available The objective of this work was to develop and assess an automatic procedure to generate reduced chemical schemes for the atmospheric photooxidation of volatile organic carbon (VOC compounds. The procedure is based on (i the development of a tool for writing the fully explicit schemes for VOC oxidation (see companion paper Aumont et al., 2005, (ii the application of several commonly used reduction methods to the fully explicit scheme, and (iii the assessment of resulting errors based on direct comparison between the reduced and full schemes. The reference scheme included seventy emitted VOCs chosen to be representative of both anthropogenic and biogenic emissions, and their atmospheric degradation chemistry required more than two million reactions among 350000 species. Three methods were applied to reduce the size of the reference chemical scheme: (i use of operators, based on the redundancy of the reaction sequences involved in the VOC oxidation, (ii grouping of primary species having similar reactivities into surrogate species and (iii grouping of some secondary products into surrogate species. The number of species in the final reduced scheme is 147, this being small enough for practical inclusion in current three-dimensional models. Comparisons between the fully explicit and reduced schemes, carried out with a box model for several typical tropospheric conditions, showed that the reduced chemical scheme accurately predicts ozone concentrations and some other aspects of oxidant chemistry for both polluted and clean tropospheric conditions.

  20. 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.

  1. Adsorption of benzene, cyclohexane and hexane on ordered mesoporous carbon.

    Science.gov (United States)

    Wang, Gang; Dou, Baojuan; Zhang, Zhongshen; Wang, Junhui; Liu, Haier; Hao, Zhengping

    2015-04-01

    Ordered mesoporous carbon (OMC) with high specific surface area and large pore volume was synthesized and tested for use as an adsorbent for volatile organic compound (VOC) disposal. Benzene, cyclohexane and hexane were selected as typical adsorbates due to their different molecular sizes and extensive utilization in industrial processes. In spite of their structural differences, high adsorption amounts were achieved for all three adsorbates, as the pore size of OMC is large enough for the access of these VOCs. In addition, the unusual bimodal-like pore size distribution gives the adsorbates a higher diffusion rate compared with conventional adsorbents such as activated carbon and carbon molecular sieve. Kinetic analysis suggests that the adsorption barriers mainly originated from the difficulty of VOC vapor molecules entering the pore channels of adsorbents. Therefore, its superior adsorption ability toward VOCs, together with a high diffusion rate, makes the ordered mesoporous carbon a promising potential adsorbent for VOC disposal.

  2. Towards a sustainable manufacture of hierarchical zeolites.

    Science.gov (United States)

    Verboekend, Danny; Pérez-Ramírez, Javier

    2014-03-01

    Hierarchical zeolites have been established as a superior type of aluminosilicate catalysts compared to their conventional (purely microporous) counterparts. An impressive array of bottom-up and top-down approaches has been developed during the last decade to design and subsequently exploit these exciting materials catalytically. However, the sustainability of the developed synthetic methods has rarely been addressed. This paper highlights important criteria to ensure the ecological and economic viability of the manufacture of hierarchical zeolites. Moreover, by using base leaching as a promising case study, we verify a variety of approaches to increase reactor productivity, recycle waste streams, prevent the combustion of organic compounds, and minimize separation efforts. By reducing their synthetic footprint, hierarchical zeolites are positioned as an integral part of sustainable chemistry. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-02-01

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

  4. Natural zeolite reactivity towards ozone: the role of compensating cations.

    Science.gov (United States)

    Valdés, Héctor; Alejandro, Serguei; Zaror, Claudio A

    2012-08-15

    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 77K, elemental analysis, X-ray fluorescence (XRF), thermogravimetric analysis coupled with mass spectroscopy (TGA-MS), and temperature-programmed desorption of ammonia (NH(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.

  5. Adsorption of CO2 by alginate immobilized zeolite beads

    Science.gov (United States)

    Suratman, A.; Kunarti, E. S.; Aprilita, N. H.; Pamurtya, I. C.

    2017-03-01

    Immobilized zeolit in alginate beads for adsorption of CO2 was developed. Alginate immobilized zeolit beads was generated by dropping the mixture of Na-alginate and zeolite solution into Ca2+ solution. The adsorption efficacy such as the influence of contact time, mass of zeolite, flowrate of CO2, and mass of adsorbent was evaluated. The adsorption of CO2 onto alginate immobilized zeolit beads was investigated by performing both equilibrium and kinetic batch test. Bead was characterized by FTIR and SEM. Alginate immobilized zeolit beads demonstrated significantly higher sorption efficacy compared to plain alginate beads and zeolite with 0.25 mmol CO2 adsorbed /g adsorbent. Optimum condition was achieved with mass composition of alginate:zeolite (3:1), flowrate 50 mL/min for 20 minutes. The alginate immobilized zeolit beads showed that adsorption of CO2 followed Freundlich isotherm and pseudo second order kinetic model. Adsorption of CO2 onto alginate immobilized zeolite beads is a physisorption with adsorption energy of 6.37 kJ/mol. This results indicates that the alginate immobilized zeolit beads can be used as promising adsorbents for CO2.

  6. 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.

  7. 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.

  8. 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

  9. 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%.

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

    Science.gov (United States)

    Campen, Adam

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

  11. 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.

  12. Synergistic effect of UV pretreated Fe-ZSM-5 catalysts for heterogeneous catalytic complete oxidation of VOC: A technology development for sustainable use.

    Science.gov (United States)

    Aziz, Abdul; Kim, Kwang Soo

    2017-10-15

    In this work, the performance of benzene, toluene, ethylbenzene, and xylene (BTEX) removal and degradation from gas, air streams on UV pretreated Fe-ZSM-5 in a batch reactor at room temperature were studied. The Fe-ZSM-5 zeolite catalyst was prepared by hydrothermal reaction method. The influence of UV pre-irradiation time on the removal of BTEX were assessed by varying the time, ranging from 15min to 60smin. Then, sustainability of the activation of the catalyst resulted by UV pretreatment was studied by the four-cycle experiment with one time UV irradiation and after each cycle irradiation followed by BTEX removal after every cycle respectively. The results of BTEX removal depicted that 30min of UV pretreatment was sufficient for complete organics removal. The UV pretreatment effect on the catalytic oxidation and the stability of the catalyst were studied by modern instrumental techniques. The novelty of the process was the sustainable reuse of catalyst with persistent VOC removal, which works on the -adsorption-oxidation-regeneration-adsorption- cycle, which was confirmed by the characterization studies of the catalyst after four runs. The results revealed that the change in the structure, stability, morphology, and removal efficiency of the catalyst during the experiments was negligible. The VOC degradation mechanism studies showed that the oxidation occurs due to the formation of free radicals as well as hydroxyl ions, so named it heterogeneous photo-Fenton oxidation. The residual materials analysis showed the complete mineralization of VOC except small amount of acetone as oxidation product. Lastly, the kinetics of the VOC removal was studied. Copyright © 2017 Elsevier B.V. All rights reserved.

  13. A Novel Methodology to Evaluate Health Impacts Caused by VOC Exposures Using Real-Time VOC and Holter Monitors

    Directory of Open Access Journals (Sweden)

    Hiroaki Kumano

    2010-11-01

    Full Text Available While various volatile organic compounds (VOCs are known to show neurotoxic effects, the detailed mechanisms of the action of VOCs on the autonomic nervous system are not fully understood, partially because objective and quantitative measures to indicate neural abnormalities are still under development. Nevertheless, heart rate variability (HRV has been recently proposed as an indicative measure of the autonomic effects. In this study, we used HRV as an indicative measure of the autonomic effrects to relate their values to the personal concentrations of VOCs measured by a real-time VOC monitor. The measurements were conducted for 24 hours on seven healthy subjects under usual daily life conditions. The results showed HF powers were significantly decreased for six subjects when the changes of total volatile organic compound (TVOC concentrations were large, indicating a suppression of parasympathetic nervous activity induced by the exposure to VOCs. The present study indicated these real-time monitoring was useful to characterize the trends of VOC exposures and their effects on autonomic nervous system.

  14. 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

  15. A High Performance Biofilter for VOC Emission Control.

    Science.gov (United States)

    Wu, G; Conti, B; Leroux, A; Brzezinski, R; Viel, G; Heitz, M

    1999-02-01

    Biofiltration is a cleaning technique for waste air contaminated with some organic compounds. The advantages of the conventional biofilter over other biological systems are a high-superficial area best suited for the treatment of some compounds with poor water solubility, ease of operation, and low operating costs. It has crucial disadvantages, however; for example, it is not suitable to treat waste gases with high VOC concentrations and it has poor control of reaction conditions. To improve on these problems and to build a high-performance biofilter, three structured peat media and two trickling systems have been introduced in this study. The influences of media size and composition have been investigated experimentally. Peat bead blended with 30% (w/w) certain mineral material with a good binding capacity has advantages over other packing materials, for example, suitable size to prevent blockage due to microbial growth, strong buffering capacity to neutralize acidic substances in the system, and a pH range of 7.0-7.2 suitable for the growth of bacteria. Dropwise trickling system offers an effective measure to easily control the moisture content of the bed and the reaction conditions (pH, nutrient) and to partially remove excess biomass produced during the metabolic processes of microorganisms. The influence of nutrient supplementation has also been investigated in this study, which has revealed that the biological system was in a condition of nutrient limitation instead of carbon limitation. The biofilters built in our laboratory were used to treat waste gas contaminated with toluene in a concentration range of 1 to 3.2 g/m(3) and at the specific gas flow rate of 24 to120 m(3)/m(2).hr. Under the conditions employed, a high elimination capacity (135 g/m(3).hr) was obtained in the biofilter packed with peat beads (blended with 30% of the mineral material), and no blockage problem was observed in an experimental period of 2-3 months.

  16. 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.

  17. 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.

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

    Directory of Open Access Journals (Sweden)

    Is Fatimah

    2010-06-01

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

  19. Experimental study of uranium(6+) sorption of the zeolite mineral clinoptilolite

    Energy Technology Data Exchange (ETDEWEB)

    Pabalan, R.T.; Prikryl, J.D.; Muller, P.M.; Dietrich, T.B. [Southwest Research Institute, San Antonio, TX (United States)

    1993-12-31

    Experiments on the sorption of uranium(6+) on clinoptilolite from solutions in equilibrium with atmospheric CO{sub 2}(g) were conducted to understand the fundamental controls on uranium sorption on zeolite minerals, including the effects of pH, aqueous uranium speciation, and uranium concentration in solution. The results indicate that uranium(6+) species are strongly sorbed on the zeolite mineral clinoptilolite at near-neutral pH. The amount of uranium sorbed is strongly dependent on pH and, to some extent, on the total concentration of uranium. Uranium sorption on clinoptilolite is important in the pH range where UO{sub 2}(OH){sub 2}{degrees}(aq) is the predominant uranium aqueous species, whereas sorption is inhibited at pH`s where carbonate- and hydroxy-carbonate-complexes are the primary uranyl species. Surface adsorption appears to be the main sorption mechanism, although at pH<4 the results suggest ion exchange may occur between the UO{sub 2}{sup 2+} ions in solution and the cations in the intracrystalline cation exchange sites of clinoptilolite. The effectiveness of zeolite-rich horizons underneath Yucca Mountain, Nevada, as barriers to actinide transport through sorption processes will depend strongly on groundwater chemistry. Reliable predictions of radionuclide transport through these horizons will need to properly account for changes in solution chemistry.

  20. Accurate fit and thermochemical analysis of the adsorption isotherms of methane in zeolite 13X

    Energy Technology Data Exchange (ETDEWEB)

    Llano-Restrepo, M. [University of Valle, Valle (Colombia). School of Chemical Engineering

    2010-07-01

    The recovery of methane from landfill gases and coal mines has become of the utmost importance because methane has a global-climate warming potential much higher than that of carbon dioxide. Zeolite 13X is widely used for the separation of methane and carbon dioxide from such sources. Accurate fits of the adsorption isotherms of methane in zeolite 13X are required for the rigorous simulation of that separation. In this work, a generalized statistical thermodynamic adsorption (GSTA) model has been used to obtain a very accurate correlation of a published set of adsorption isotherms of methane in zeolite 13X that were measured from 120 K to 273 K over the pressure range 0.07 Pa to 12.2 MPa. In contrast, none of five traditional adsorption models was capable of fitting these isotherms. A thermochemical interpretation of the correlation is provided and predictions for the isosteric heat of adsorption are made, which turn out to be in excellent agreement with the available experimental data.

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

    Energy Technology Data Exchange (ETDEWEB)

    Anstett, M.

    1996-11-25

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

  2. 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.

  3. 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.

  4. 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…

  5. MERCURY SEPARATION FROM POLLUTANT WATER USING ZEOLITES

    Science.gov (United States)

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

  6. ARSENIC SEPARATION FROM WATER USING ZEOLITES

    Science.gov (United States)

    Arsenic is known to be a hazardous contaminant in drinking water. The presence of arsenic in water supplies has been linked to arsenical dermatosis and skin cancer . Zeolites are well known for their ion exchange capacities. In the present work, the potential use of a variety of ...

  7. Framework Al zoning in zeolite ECR-1.

    Science.gov (United States)

    Shin, Jiho; Ahn, Nak Ho; Cho, Sung June; Ren, Limin; Xiao, Feng-Shou; Hong, Suk Bong

    2014-02-25

    Rietveld analyses of the synchrotron X-ray diffraction data for various cation forms of zeolite ECR-1 have demonstrated framework Al zoning, which parallels the alternation of Al-rich maz and Al-poor mor layers. This can be further supported by notable differences in the average bond valence of its 10 crystallographically distinct tetrahedral sites.

  8. Diagenetic Quartz Morphologies and Zeolite formation

    DEFF Research Database (Denmark)

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

    -rich clinoptolite, or zeolite may not precipitate at all.  The dissolution of volcanic lithoclasts may also release a high rate of Al, resulting in abundant formation of Al-rich clinoptilolite.  If both sources interact, a compositional variation may occur with time.  The compositional variation may result...

  9. Selective Production of Aromatics from 2-Octanol on Zinc Ion-Exchanged MFI Zeolite Catalysts

    Directory of Open Access Journals (Sweden)

    Masakazu Iwamoto

    2015-12-01

    Full Text Available The aromatization of 2-octanol derived from castor oil as a byproduct in the formation of sebacic acid was investigated on various zeolite catalysts. Zn ion-exchanged MFI (ZSM-5 zeolites with small silica/alumina ratios and zinc contents of 0.5 to 2.0 wt. % were determined to exhibit good and stable activity for the reaction at 623 to 823 K. The yield of aromatics was 62% at 773 K and the space velocity 350 to 1400 h−1. The temperature and contact time dependences of the product distributions indicated the reaction pathways of 2-octanol→dehydration to 2-octene→decomposition to C5 and C3 compounds→further decomposition to small alkanes and alkenes→aromatization with dehydrogenation. Alcohols with carbon numbers of 5 to 8 exhibited similar distributions of products compared to 2-octanol, while corresponding carbonyl compounds demonstrated different reactivity.

  10. Identifying Optimal Zeolitic Sorbents for Sweetening of Highly Sour Natural Gas.

    Science.gov (United States)

    Shah, Mansi S; Tsapatsis, Michael; Siepmann, J Ilja

    2016-05-10

    Raw natural gas is a complex mixture comprising methane, ethane, other hydrocarbons, hydrogen sulfide, carbon dioxide, nitrogen, and water. For sour gas fields, selective and energy-efficient removal of H2 S is one of the crucial challenges facing the natural-gas industry. Separation using nanoporous materials, such as zeolites, can be an alternative to energy-intensive amine-based absorption processes. Herein, the adsorption of binary H2 S/CH4 and H2 S/C2 H6 mixtures in the all-silica forms of 386 zeolitic frameworks is investigated using Monte Carlo simulations. Adsorption of a five-component mixture is utilized to evaluate the performance of the 16 most promising materials under close-to-real conditions. It is found that depending on the fractions of CH4 , C2 H6 , and CO2 , different sorbents allow for optimal H2 S removal and hydrocarbon recovery.

  11. Zeolite Nanoparticles for Selective Sorption of Plasma Proteins.

    Science.gov (United States)

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

    2015-11-30

    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.

  12. Energetics of sodium-calcium exchanged zeolite A.

    Science.gov (United States)

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

    2015-05-07

    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.

  13. Enhanced chromium adsorption capacity via plasma modification of natural zeolites

    Science.gov (United States)

    Cagomoc, Charisse Marie D.; Vasquez, Magdaleno R., Jr.

    2017-01-01

    Natural zeolites such as mordenite are excellent adsorbents for heavy metals. To enhance the adsorption capacity of zeolite, sodium-exchanged samples were irradiated with 13.56 MHz capacitively coupled radio frequency (RF) argon gas discharge. Hexavalent chromium [Cr(VI)] was used as the test heavy metal. Pristine and plasma-treated zeolite samples were soaked in 50 mg/L Cr solution and the amount of adsorbed Cr(VI) on the zeolites was calculated at predetermined time intervals. Compared with untreated zeolite samples, initial Cr(VI) uptake was 70% higher for plasma-treated zeolite granules (50 W 30 min) after 1 h of soaking. After 24 h, all plasma-treated zeolites showed increased Cr(VI) uptake. For a 2- to 4-month period, Cr(VI) uptake increased about 130% compared with untreated zeolite granules. X-ray diffraction analyses between untreated and treated zeolite samples revealed no major difference in terms of its crystal structure. However, for plasma-treated samples, an increase in the number of surface defects was observed from scanning electron microscopy images. This increase in the number of surface defects induced by plasma exposure played a crucial role in increasing the number of active sorption sites on the zeolite surface.

  14. 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.

  15. UTILITY OF ZEOLITES IN REMOVAL OF INORGANIC AND ORGANIC WATER POLLUTANTS

    Science.gov (United States)

    Zeolites are well known for their ion exchange, adsorption and acid catalysis properties. Different inorganic and organic pollutants have been removed from water at room temperature using various zeolites. Synthetic zeolite Faujasite Y has been used to remove inorganic pollutants...

  16. Survey of Modified Clinoptilolite Zeolite and Cooper Oxide Nanoparticles-Containing Modified Clinoptilolite Efficiency for Polluted Air BTX Removal

    Directory of Open Access Journals (Sweden)

    Ruhollah Rostami

    2012-04-01

    zeolite, but It cause promote more catalytic effect of zeolite in the decomposition process of contaminants by breaking the molecules of pollutants and their further degradation progress is done for conversion to carbon dioxide /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso-para-margin:0cm; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:Arial; mso-bidi-theme-font:minor-bidi;}

  17. TO PURGE OR NOT TO PURGE? VOC CONCENTRATION ...

    Science.gov (United States)

    Soil vapor surveys are commonly used as a screening technique to delineate volatile organic compound (VOC) contaminant plumes and provide information for soil sampling plans. Traditionally, three purge volumes of vapor are removed before a sample is collected. One facet of this study was to evaluate the VOC concentrations lost during purging and explore the potential implications of those losses. The vapor data was compared to collocated soil data to determine if any correlation existed between the VOC concentrations. Two different methods for soil vapor collection were compared: 1) active/micro-volume; and 2) active/macro-volume. The active/micro-volume vapor sample had total line purge volume of 1.25 mL and the active/macro-volume vapor sample had a total line purge volume of 15 mL. Six line purge volumes were collected for each vapor sampling technique, with the fourth purge volume representing the traditional sample used for site screening data. Each sample was collected by gas tight syringe and transferred to a thermal de sorption tube for sorption, transport, and analysis. Following the removal of the soil vapor samples, collocated soil samples were taken. For both active vapor sampling techniques, the VOC concentrations in the first three purge volumes exceeded the VOC concentrations in the last three purge volumes. This implies that the general rule of removal of three purge volumes prior to taking a sample for analysis could lead to underestimating the

  18. 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.

  19. Synthesis, loading control and preliminary tests of 2,4,6-triphenylpyrylium supported onto Y-zeolite as solar photocatalyst

    Energy Technology Data Exchange (ETDEWEB)

    Amat, Ana M.; Arques, Antonio; Vercher, Rosa F. [Departamento de Ingeniera Textil y Papelera, Escuela Politecnica Superior de Alcoy, Universidad Politecnica de Valencia, Paseo Viaducto 1, 03801 Alcoy (Spain); Bossmann, Stefan H.; Braun, Andre M. [Lehrstuhl fuer Umweltmesstechnik, Engler-Bunte-Institut, Universitaet Karlsruhe, 76128 Karlsruhe (Germany); Miranda, Miguel A. [Departamento de Quimica, Instituto de Tecnologia Quiica UPV-CSIC, Universidad Politecnica de Valencia, 46071 Valencia (Spain)

    2005-04-15

    A heterogeneous photocatalyst has been obtained by hosting the 2,4,6-triphenylpyrylium cation inside the supercages of Y-zeolite. Preparation of the new material has been achieved by means of a formal ion exchange in aqueous medium. Nevertheless, the mechanism is more complex, as bulky 2,4,6-triphenylpyrylium cation is unable to diffuse through the channels of Y-zeolite. The following steps are involved: (a) hydrolytic opening of the pyrylium ion to give a linear diketone; (b) diffusion of the diketone through the channels to reach the supercages; and (c) thermal recyclization under dehydrating conditions. Elemental analysis of the new material was consistent with the pyrylium cation located inside the zeolite. No sulfur was found in the loaded zeolite, indicating that hydrogensulfate is no longer the counter-ion of pyrylium. Accordingly, the stoichiometric amount of Na{sup +} was found in the filtered waters recovered after the synthesis. Besides, the IR spectrum of the dry material was coincident with that of 2,4,6-triphenylpyrylium, while the spectrum of a less thoroughly dried sample showed, together with the absorption bands corresponding to pyrylium, other bands assignable to the diketone. Zeolite loading can be controlled in the range of 3-15% of organic carbon. The performance of the new material as a solar photocatalyst for oxidative pollutant degradation was checked using four cinnamic acid derivatives as target compounds. Aqueous solutions (250mL) of these model pollutants (0.001M) were irradiated by solar light in the presence of different amounts of solid photocatalyst. Oxidation was efficiently achieved as analysed by HPLC and followed in all cases a pseudo first order kinetics. The most satisfactory results were obtained using 1g/L of Y-zeolite containing 6% of 2,4,6-triphenylpyrylium cation.

  20. Synthesis strategies in the search for hierarchical zeolites.

    Science.gov (United States)

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

    2013-05-07

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

  1. 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.

  2. Conversion of rice husk ash to zeolite beta.

    Science.gov (United States)

    Prasetyoko, Didik; Ramli, Zainab; Endud, Salasiah; Hamdan, Halimaton; Sulikowski, Bogdan

    2006-01-01

    White rice husk ash (RHA), an agriculture waste containing crystalline tridymite and alpha-cristobalite, was used as a silica source for zeolite Beta synthesis. The crystallization of zeolite Beta from RHA at 150 degrees C in the presence of tetraethylammonium hydroxide was monitored by XRD, FTIR and (29)Si MAS NMR techniques. It was found that zeolite Beta started to form after 12h and the complete crystallization of zeolite Beta phase was achieved after 2d. XRD, (29)Si MAS NMR and solid yield studies indicate that the transformation mechanism of silica present in RHA to zeolite Beta involves dissolution of the ash, formation of an amorphous aluminosilicate after 6h of crystallization, followed by dissolution in the mother liquor and final transformation to pure zeolite Beta crystals.

  3. Arabidopsis thaliana as Bioindicator of Fungal VOCs in Indoor Air

    Science.gov (United States)

    Hung, Richard; Yin, Guohua; Klich, Maren A.; Grimm, Casey; Bennett, Joan W.

    2016-01-01

    In this paper, we demonstrate the ability of Arabidopsis thaliana to detect different mixtures of volatile organic compounds (VOCs) emitted by the common indoor fungus, Aspergillus versicolor, and demonstrate the potential usage of the plant as a bioindicator to monitor fungal VOCs in indoor air. We evaluated the volatile production of Aspergillus versicolor strains SRRC 108 (NRRL 3449) and SRRC 2559 (ATCC 32662) grown on nutrient rich fungal medium, and grown under conditions to mimic the substrate encountered in the built environment where fungi would typically grow indoors (moist wallboard and ceiling tiles). Using headspace solid phase microextraction/gas chromatography-mass spectrometry, we analyzed VOC profiles of the two strains. The most abundant compound produced by both strains on all three media was 1-octen-3-ol. Strain SRRC 2559 made several terpenes not detected from strain SRRC 108. Using a split-plate bioassay, we grew Arabidopsis thaliana in a shared atmosphere with VOCs from the two strains of Aspergillus versicolor grown on yeast extract sucrose medium. The VOCs emitted by SRRC 2559 had an adverse impact on seed germination and plant growth. Chemical standards of individual VOCs from the Aspergillus versicolor mixture (2-methyl-1-butanol, 3-methyl-1-butanol, 1-octen-3-ol, limonene, and β-farnesene), and β-caryophyllene were tested one by one in seed germination and vegetative plant growth assays. The most inhibitory compound to both seed germination and plant growth was 1-octen-3-ol. Our data suggest that Arabidopsis is a useful model for monitoring indoor air quality as it is sensitive to naturally emitted fungal volatile mixtures as well as to chemical standards of individual compounds, and it exhibits relatively quick concentration- and duration-dependent responses.

  4. Distributions of personal VOC exposures: a population-based analysis.

    Science.gov (United States)

    Jia, Chunrong; D'Souza, Jennifer; Batterman, Stuart

    2008-10-01

    Information regarding the distribution of volatile organic compound (VOC) concentrations and exposures is scarce, and there have been few, if any, studies using population-based samples from which representative estimates can be derived. This study characterizes distributions of personal exposures to ten different VOCs in the U.S. measured in the 1999--2000 National Health and Nutrition Examination Survey (NHANES). Personal VOC exposures were collected for 669 individuals over 2-3 days, and measurements were weighted to derive national-level statistics. Four common exposure sources were identified using factor analyses: gasoline vapor and vehicle exhaust, methyl tert-butyl ether (MBTE) as a gasoline additive, tap water disinfection products, and household cleaning products. Benzene, toluene, ethyl benzene, xylenes chloroform, and tetrachloroethene were fit to log-normal distributions with reasonably good agreement to observations. 1,4-Dichlorobenzene and trichloroethene were fit to Pareto distributions, and MTBE to Weibull distribution, but agreement was poor. However, distributions that attempt to match all of the VOC exposure data can lead to incorrect conclusions regarding the level and frequency of the higher exposures. Maximum Gumbel distributions gave generally good fits to extrema, however, they could not fully represent the highest exposures of the NHANES measurements. The analysis suggests that complete models for the distribution of VOC exposures require an approach that combines standard and extreme value distributions, and that carefully identifies outliers. This is the first study to provide national-level and representative statistics regarding the VOC exposures, and its results have important implications for risk assessment and probabilistic analyses.

  5. 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.

  6. 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.

  7. Violations of L\\"owensteins rule in zeolites

    OpenAIRE

    Fletcher, Rachel E.; Ling, Sanliang; Slater, Ben

    2016-01-01

    Zeolites, microporous aluminosilicates, are amongst the most widely used catalysts in the petrochemical industry. Zeolite catalytic functionality is coupled to the distribution of tetrahedral alumina (AlO4-) and associated counter-cations throughout the aluminosilicate framework, yet little is definitively known about the factors that govern framework aluminium arrangement. It is generally accepted that all zeolites obey Lowensteins rule of aluminium avoidance and that Al-O-Al linkages are fo...

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

    Science.gov (United States)

    Sacco, Albert, Jr.

    1991-01-01

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

  9. Zeólitas hierarquicamente estruturadas Hierarchically structured zeolites

    Directory of Open Access Journals (Sweden)

    Saulo de Tarso Figueiredo Grecco

    2013-01-01

    Full Text Available This review presents the main characteristics and properties of microporous (zeolites and ordered mesoporous materials, focusing on structural aspects and preparation. In addition, their use as heterogeneous catalysts are also discussed, with emphasis on their advantages and disadvantages. Due to difficulty in application of zeolites in the conversion of bulky molecules, the most relevant strategies of synthesis for the preparation of zeolitic materials with hierarchical pore structure was also analyzed, which allow this limitation to be overcome.

  10. Volatile organic compound (VOC) emissions during malting and beer manufacture

    Science.gov (United States)

    Gibson, Nigel B.; Costigan, Gavin T.; Swannell, Richard P. J.; Woodfield, Michael J.

    Estimates have been made of the amounts of volatile organic compounds (VOCs) released during different stages of beer manufacture. The estimates are based on recent measurements and plant specification data supplied by manufacturers. Data were obtained for three main manufacturing processes (malting, wort processing and fermentation) for three commercial beer types. Some data on the speciation of emitted compounds have been obtained. Based on these measurements, an estimate of the total unabated VOC emission. from the U.K. brewing industry was calculated as 3.5 kta -1, over 95% of which was generated during barley malting. This value does not include any correction for air pollution control.

  11. 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

  12. Activities of aluminum forms of zeolites and zeolite-containing aluminosilicates in phenol arylalkylation by styrene

    Energy Technology Data Exchange (ETDEWEB)

    Kurashev, M.V.; Kolesnichenko, N.V.; Romanovskii, B.V.; Lokshin, B.V.

    1979-03-01

    The activities of aluminum forms of zeolites and zeolite-containing aluminosilicates in phenol arylalkylation by styrene were studied in a flow microreactor at 250/sup 0/C, 1 atm, 4:1 phenol-styrene, and 2.6 sec contact time. The aluminum-exchanged forms of a NaY zeolite and a zeolite-containing amorphous aluminosilicate (the Soviet commercial AShNTs-3 grade) were prepared by the K. M. Wang technique and some of the samples were pretreated by phenol at 250/sup 0/C and 2 atm for two hours. The AShNTs-3 and Al/AShNTs-3 catalysts showed maximum steady-state activities in terms of over-all styrene conversion (67.6 and 46.7Vertical Bar3<, respectively) and the combined yield of 2- and 4-(..cap alpha..-methylbenzyl)phenols (64.1 and 32.2Vertical Bar3<, respectively). The AlNaY zeolite rapidly and irreversibly deactivated, and pure amorphous aluminosilicate (AAS) showed relatively low activity. The pretreatment with phenol improved the activities of the aluiminum forms and increased the ortho-to-para isomer ratio of the alkylate from 2.74 to 4.33 for Al/AShNTs-3 and from 2.37 to 4.00 for AAS, probably because of the formation of active surface aluminum phenolate structures, but deteriorated the catalytic properties of AShNTs-3.

  13. 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.

  14. 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

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

    Science.gov (United States)

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

    2017-07-01

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

  16. 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.

  17. Zeolite Crystal Growth in Microgravity and on Earth

    Science.gov (United States)

    2003-01-01

    The Center for Advanced Microgravity Materials Processing (CAMMP), a NASA-sponsored Research Partnership Center, is working to improve zeolite materials for storing hydrogen fuel. CAMMP is also applying zeolites to detergents, optical cables, gas and vapor detection for environmental monitoring and control, and chemical production techniques that significantly reduce by-products that are hazardous to the environment. Shown here are zeolite crystals (top) grown in a ground control experiment and grown in microgravity on the USML-2 mission (bottom). Zeolite experiments have also been conducted aboard the International Space Station.

  18. 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.

  19. ZEOLITIZATION OF SEWAGE SLUDGE ASH WITH A FUSION METHOD

    Directory of Open Access Journals (Sweden)

    Jolanta Latosińska

    2016-11-01

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

  20. Zeolites are effective ROS-scavengers in vitro.

    Science.gov (United States)

    Pellegrino, Perrine; Mallet, Bernard; Delliaux, Stéphane; Jammes, Yves; Guieu, Regis; Schäf, Oliver

    2011-07-08

    We report on the use of zeolites to limit the effects of reactive oxygen species (ROS) on human albumin under in vitro conditions. Zeolites of different structure type, channel size, channel polarity, and charge-compensating cation were screened for the elimination of ROS, notably HO(·), resulting from the Fenton reaction. A test based on ischemia-modified albumin (IMA) was used as a marker to monitor the activity of HO(·) after co-exposure of human serum to these zeolites. Two commercial zeolites, faujasite (FAU 13×, channel opening 0.74×0.74 nm with Na(+) as charge-compensating cation) and ferrierite (FER, channel opening 0.54×0.42 nm with H(+) as charge-compensating cation), were found to reduce IMA formation by more than 65% due to removal of HO(·) relative to reference values. It was established that partial ion exchange of the zeolites' respective charge-compensating cation vs. Fe(3+) implicated in the Fenton reaction plays a major role in HO(·) deactivation process. Moreover, our results show that no saturation of the respective zeolite active sites occurred. This is possible only when ROS are actively converted to water molecules within the zeolite void system, which generates H(+) ion transport. Because zeolites cannot be administered in blood, their use in medicine should be limited to extra corporeal circuits. Zeolites could be of use during cardiopulmonary bypass or hemodialysis procedures.

  1. Mineral resource of the month: natural and synthetic zeolites

    Science.gov (United States)

    Virta, Robert L.

    2008-01-01

    Volcanic rocks containing natural zeolites — hydrated aluminosilicate minerals that contain alkaline and alkaline-earth metals — have been mined worldwide for more than 1,000 years for use as cements and building stone. For centuries, people thought natural zeolites occurred only in small amounts inside cavities of volcanic rock. But in the 1950s and early 1960s, large zeolite deposits were discovered in volcanic tuffs in the western United States and in marine tuffs in Italy and Japan. And since then, similar deposits have been found around the world, from Hungary to Cuba to New Zealand. The discovery of these larger deposits made commercial mining of natural zeolite possible.

  2. 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 zeolites from tuffs may successfully be used in a pressure/vacuum swing adsorption process.

  3. 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.

  4. 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.

  5. Preparation of zeolite ANA crystal from zeolite Y by in situ solid phase iso-structure transformation.

    Science.gov (United States)

    Wang, Yi; Li, Xuguang; Xue, Zhiyuan; Dai, Linsen; Xie, Songhai; Li, Quanzhi

    2010-05-06

    A new method has been explored to synthesize zeolite ANA crystals with regular icositetrahedron in aqueous media via transformation of zeolite Y under the conditions of low temperature, short reaction time, and without organic template. The products are perfect, almost 100% crystals. The samples prepared at different crystallization stages are measured by XRD, TEM, and SEM to investigate the transformation mechanism from zeolite Y to zeolite ANA. It has been demonstrated for the first time that the mechanism of forming a zeolite ANA polycrystal with sphere or shell morphologies is the in situ solid phase iso-structure transformation (Is-SPIST) of zeolite Y. The Is-SPIST mechanism is also supported by the results of steam-induced crystallization experiments and other assistant means, including the same Si/Al ratio, the same weight, the same particle size, and the same morphology before and after transformation of zeolite Y to zeolite ANA. It is also observed that a spherical or shell ANA polycrystal is constructed via the reconstruction from its exterior to interior, to form an ANA single crystal with a solid or hollow icositetrahedron. The main driving force of the reconstruction is considered to be the grain boundary energy existing between polycrystalline grains. This process also obeys the mechanism of in situ solid phase reconstruction (Is-SPR). Furthermore, the size and morphology of the zeolite ANA single crystal can be modified by surfactants.

  6. Electrical Response of PEDOT-PSS/FAU Zeolite Composites toward SO2: Controlling the Adsorption Properties of FAU Zeolite

    Science.gov (United States)

    Chanthaanont, Pojjawan; Sirivat, Anuvat

    2012-02-01

    In our work, we propose to combine a conductive polymer, Poly(3,4-ethylenedioxythiophene) doped with poly(styrene sulfonic acid) (PEDOT-PSS), with FAU zeolites to investigate the potential of the composites for use as SO2 sensing materials.Composites with PEDOT-PSS as a matrix containing faujasite zeolites of various cation types (divalent transition metal ions: Fe^2+, Co^2+, Ni^2+ and Cu^2+), were fabricated to investigate the effect of the cation type of the faujasite zeolites on the electrical conductivity response when exposed to SO2. The composite was tested through repeated sensing and recovery processes to investigate the reversibility and reproducibility. During the recovery process, the electrical conductivity of the composites were recovered, which proves that the sensing characteristics are repeatable. Responses and the interaction mechanism of the conductive polymer/zeolite composites were investigated. The composite with 20% (v/v) of zeolite content gives the highest sensitivity. The electrical conductivity responses of PEDOT-PSS/Zeolite composites can be altered due to the available adsorption sites for gas molecules. The addition of zeolites to the pristine PEDOT-PSS improved the electrical conductivity sensitivity of the composites by enhancing the interaction between PEDOT-PSS and SO2. The type of cation in the zeolite pores effected the sensitivity of the composites, depending on the acidity of the ion-exchanged zeolites.

  7. Low VOC drying of lumber and wood panel products. Progress report No. 8

    Energy Technology Data Exchange (ETDEWEB)

    Su, W.; Yan, H.; Hooda, U.; Wild, M.P.; Banerjee, S. [Inst. of Paper Science and Technology, Atlanta, GA (United States); Shmulsky, R.; Thompson, A.; Ingram, L.; Conners, T. [Mississippi State Univ., MS (United States)

    1998-07-01

    This study was initiated by an Institute of Paper Science and Technology finding that heating softwood in a low-headspace environment removed much of the VOCs without removing the water. This offered the possibility of removing VOCs from wet wood, capturing them as a product, and then drying the VOC-depleted wood conventionally with little or no VOC controls. Two means of low-headspace heating were explored: steam and radiofrequency (RF). It was found in the previous year, that while both steam and RF were able to drive out VOCs, steam was impracticably slow for lumber. Hence the effect of RF or microwave on wood was the principal focus of the work reported here. Finally, in order to understand the mechanism of VOC release, the transport of the VOCs in wood was studied, together with the seasonal effects that influence VOC concentration in trees.

  8. Zeolites as possible biofortifiers in Maitake cultivation

    Directory of Open Access Journals (Sweden)

    Vunduk Jovana

    2014-01-01

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

  9. 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...

  10. Adsorption of Xe in zeolite MCM-22

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Adsorption of xenon in zeolite MCM-22, a zeo lite containing two separate pore systems, has been investigated in detail by variable temperature (VT) 129Xe NMR spectroscopy. NMR results suggest that Xe atoms are preferentially adsorbed in the supercages of the zeolite at low Xe pressure (less than a few atmosphere), while Xe atoms can penetrate into the two-dimensional sinusoidal channels at high Xe pressure. Exchange of xenon at the different adsorption sites in the same supercage, i.e. xenon atoms in the two pockets and those in the central part of the supercage, was confirmed at 145 K by two-dimensional (2D) 129Xe NMR exchange spectroscopy. The time scale for the exchange is about several milliseconds.

  11. Biodegradation of Spilled Diesel Fuel in Agricultural Soil: Effect of Humates, Zeolite, and Bioaugmentation

    Directory of Open Access Journals (Sweden)

    Pavel Kuráň

    2014-01-01

    Full Text Available Possible enhancement of biodegradation of petroleum hydrocarbons in agricultural soil after tank truck accident (~5000 mg/kg dry soil initial concentration by bioaugmentation of diesel degrading Pseudomonas fluorescens strain and addition of abiotic additives (humates, zeolite was studied in a 9-month pot experiment. The biodegradation process was followed by means of analytical parameters (hydrocarbon index expressed as content of C10–C40 aliphatic hydrocarbons, ratio pristane/C17, and total organic carbon content and characterization of soil microbial community (content of phospholipid fatty acids (PLFA as an indicator of living microbial biomass, respiration, and dehydrogenase activity. The concentration of petroleum hydrocarbons (C10–C40 was successfully reduced by ~60% in all 15 experiment variants. The bioaugmentation resulted in faster hydrocarbon elimination. On the contrary, the addition of humates and zeolite caused only a negligible increase in the degradation rate. These factors, however, affected significantly the amount of PLFA. The humates caused significantly faster increase of the total PLFA suggesting improvement of the soil microenvironment. Zeolite caused significantly slower increase of the total PLFA; nevertheless it aided in homogenization of the soil. Comparison of microbial activities and total PLFA revealed that only a small fraction of autochthonous microbes took part in the biodegradation which confirms that bioaugmentation was the most important treatment.

  12. Mechanisms of CPB Modified Zeolite on Mercury Adsorption in Simulated Wastewater.

    Science.gov (United States)

    Liu, Jiang; Huang, Hui; Huang, Rong; Zhang, Jinzhong; Hao, Shuoshuo; Shen, Yuanyuan; Chen, Hong

    2016-06-01

    A systematic study was carried out to analyze the effects of mercury(II) adsorption by surface modified zeolite (SMZ) and adsorption mechanism. Cetylpyridinium bromide (CPB) was used to prepare SMZ. The characterization methods by means of powder X-ray diffraction (XRD), Fourier transform infrared (FT-IR), scanning electron microscope (SEM) showed that both the surface and internal zeolite were covered with CPB molecules, but the main binding sites were surface. Results showed that the organic carbon and cation exchange capacity of the SMZ were 7.76 times and 4.22 times higher than those of natural zeolite (NZ), respectively. Zeta potentials before and after modification were measured at -7.80 mV and -30.27 mV, respectively. Moreover, the saturation adsorptive capacity of SMZ was 16.35 times higher than NZ in mercury-containing wastewater. The possible mechanisms of mercury elimination were surface adsorption, hydrophobic interaction, ion exchange, electricity neutralization. The adsorption process was affected little by competitive ions.

  13. Experimental investigation on the optimal performance of Zeolite-water adsorption chiller

    KAUST Repository

    Myat, Aung

    2013-02-01

    This paper presents the performance testing of Zeolite adsorption cooling system driven by low grade waste heat source extracted from prime mover\\'s exhaust, power plant\\'s exhaust and the solar energy. The adsorbent FAM Z01 is used as an adsorbent in the adsorption chiller facility. Owing to its large equilibrium pore volume, it has the high affinity for the water vapor adsorbate. The key advantages of the Zeolite adsorption cooling system are: (i) it has no moving parts rendering less maintenance, (ii) the energy efficient means of cooling by the adsorption process with a low temperature heat source, (iii) the use of vapor pipes are replaced by self actuating vapor valves rendering smaller footprint area and (iv) it is environmental friendly with low carbon footprint. The experimental investigations were carried out for Zeolite adsorption chiller at different key operating conditions namely (i) heat source temperature, (ii) the cycle time and (iii) the heat recovery time. It is investigated that performance of coefficient (COP) of this system could be as high as 0.48 while the waste heat source temperature is applicable as low as 55 °C. © 2012.

  14. Consequences of Confinement in Zeolite Acid Catalysis

    OpenAIRE

    Gounder, Rajamani Pachayappan

    2011-01-01

    The catalytic consequences of confinement within zeolite voids were examined for several elimination (alkane cracking and dehydrogenation, alkene cracking, alkanol dehydration) and addition (alkene hydrogenation, alkylation and oligomerization) reactions catalyzed by Brønsted solid acids. These reactions are mediated by cationic transition states that are confined within voids of molecular dimensions (0.4-1.3 nm) and proceed at rates that reflect the Gibbs free energies of late ion-pairs at t...

  15. 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.

  16. VocVille - A Casual Social Game for Learning Vocabulary

    OpenAIRE

    Jensen, Michel

    2012-01-01

    The document introduces VocVille, a causal online game for learning vocabularies. This application is created for the author's diploma thesis of his career as a Computervisualist (computer vision) for the University of Koblenz-Landau, which he terminated as an exchange student at the University of Cádiz, in which he developed this diploma thesis.

  17. Assessment of Industrial VOC Gas-Scrubber Performance

    Energy Technology Data Exchange (ETDEWEB)

    Saito, H

    2004-02-13

    Gas scrubbers for air-pollution control of volatile organic compounds (VOC) cover a wide range of technologies. In this review, we have attempted to evaluate the single-pass scrubber destruction and removal efficiencies (DREs) for a range of gas-scrubber technologies. We have focused primarily on typical industrial DREs for the various technologies, typical problems, and any DRE-related experiential information available. The very limited literature citations found suggest significant differences between actual versus design performance in some technologies. The potentially significant role of maintenance in maintaining DREs was also investigated for those technologies. An in-depth portrayal of the entire gas scrubbing industry is elusive. Available literature sources suggest significant differences between actual versus design performance in some technologies. Lack of scrubber system maintenance can contribute to even larger variances. ''Typical'' industrial single-pass performance of commonly used VOC gas scrubbers generally ranged from {approx}80 to 99%. Imperfect solid and/or liquid particulates capture (possibly as low as 95% despite design for 99+% capture efficiency) can also lead to VOC releases. Changing the VOC composition in the gas stream without modifying scrubber equipment or operating conditions could also lead to significant deterioration in attainable destruction and removal efficiencies.

  18. EVALUATION OF SINK EFFECTS ON VOCS FROM A LATEX PAINT

    Science.gov (United States)

    The sink strength of two common indoor materials, a carpet and a gypsum board, was evaluated by environmental chamber tests with four volatile organic compounds (VOCs): propylene glycol, ethylene glycol, 2-(2-butoxyethoxy)ethanol (BEE), and texanol. These oxygenated compounds rep...

  19. CASE STUDIES: LOW-VOC/HAP WOOD FURNITURE COATINGS

    Science.gov (United States)

    The report gives results of a study in which wood furniture manufacturing facilities were identified that had converted at least one of their primary coating steps to low-volatile organic compound (VOC)/hazardous Air pollutant (HAP) wood furniture coatings: high-solids, water...

  20. RESEARCH AND PRODUCT DEVELOPMENT OF LOW-VOC WOOD COATINGS

    Science.gov (United States)

    The report discusses a project, cofunded by the South Coast Air Quality Management District (SCAQMD) and the U.S. EPA, to develop a new, low volatile organic compound (VOC) wood coating. Traditional wood furniture coating technologies contain organic solvents which become air pol...

  1. Solid-phase microextraction and the human fecal VOC metabolome.

    Directory of Open Access Journals (Sweden)

    Emma Dixon

    Full Text Available The diagnostic potential and health implications of volatile organic compounds (VOCs present in human feces has begun to receive considerable attention. Headspace solid-phase microextraction (SPME has greatly facilitated the isolation and analysis of VOCs from human feces. Pioneering human fecal VOC metabolomic investigations have utilized a single SPME fiber type for analyte extraction and analysis. However, we hypothesized that the multifarious nature of metabolites present in human feces dictates the use of several diverse SPME fiber coatings for more comprehensive metabolomic coverage. We report here an evaluation of eight different commercially available SPME fibers, in combination with both GC-MS and GC-FID, and identify the 50/30 µm CAR-DVB-PDMS, 85 µm CAR-PDMS, 65 µm DVB-PDMS, 7 µm PDMS, and 60 µm PEG SPME fibers as a minimal set of fibers appropriate for human fecal VOC metabolomics, collectively isolating approximately 90% of the total metabolites obtained when using all eight fibers. We also evaluate the effect of extraction duration on metabolite isolation and illustrate that ex vivo enteric microbial fermentation has no effect on metabolite composition during prolonged extractions if the SPME is performed as described herein.

  2. DEVELOPMENT OF AEROBIC BIOFILTER DESIGN CRITERIA FOR TREATING VOCS

    Science.gov (United States)

    This paper reports preliminary results on the use of trickle bed biofilters with monolithic ceramic channelized microbial support structures for the treatment of VOCs typical of landfill leachate stripping. Toluene was used for the purpose of characterizing the trickle bed biofi...

  3. Accuracy of seven vapour intrusion algorithms for VOC in groundwater

    Energy Technology Data Exchange (ETDEWEB)

    Provoost, Jeroen; Bronders, Jan; Seuntjens, Piet [Flemish Inst. for Technological Research (VITO), Mol (Belgium); Reijnders, Lucas [Dept. of Science, Open Univ. Netherlands (OU NL), Heerlen (Netherlands); Swartjes, Frank; Lijzen, Johannes [National Inst. for Public Health and the Environment (RIVM), Bilthoven (Netherlands)

    2009-02-15

    During the last decade, soil contamination with volatile organic contaminants (VOC) received special attention because of their potential to cause indoor air problems. Moreover, research has shown that people spend 64% to 94% of there time indoors; therefore, the indoor air quality is of a primary importance for exposure to VOC. Human health risks to VOC-in cases of soil contamination-are often dominated by the exposure route 'inhalation of indoor air'. Exposure is often a result of vapour transport from the soil or groundwater to the indoor air of the building. Within human health risk assessments, a variety of algorithms are available that calculate transfer of soil gas to the indoor air. These algorithms suffer from a relatively high uncertainty due to a lack of representation of spatial and temporal variability. For such an application, these algorithms need to be further verified empirically against field observations so that they can be sufficiently reliable for regulatory purposes. This paper presents the accuracy for seven algorithms by using observed and predicted soil and indoor air concentrations from three sites, where the groundwater had been contaminated with aromatic and chlorinated VOC. (orig.)

  4. DEVELOPMENT OF AEROBIC BIOFILTER DESIGN CRITERIA FOR TREATING VOCS

    Science.gov (United States)

    This paper reports preliminary results on the use of trickle bed biofilters with monolithic ceramic channelized microbial support structures for the treatment of VOCs typical of landfill leachate stripping. Toluene was used for the purpose of characterizing the trickle bed biofi...

  5. Accuracy of seven vapour intrusion algorithms for VOC in groundwater

    NARCIS (Netherlands)

    Provoost, J.; Reijnders, L.; Swartjes, F.; Bronders, J.; Seuntjens, P.; Lijzen, J.

    2009-01-01

    Background, aim and scope: During the last decade, soil contamination with volatile organic contaminants (VOC) received special attention because of their potential to cause indoor air problems. Moreover, research has shown that people spend 64% to 94% of there time indoors; therefore, the indoor ai

  6. VOC signatures from North American oil and gas sources (Invited)

    Science.gov (United States)

    Simpson, I. J.; Marrero, J.; Blake, N. J.; Barletta, B.; Hartt, G.; Meinardi, S.; Schroeder, J.; Apel, E. C.; Hornbrook, R. S.; Blake, D. R.

    2013-12-01

    Between 2008 and 2013 UC Irvine has used its whole air sampling (WAS) technique to investigate VOC source signatures from a range of oil and gas sources in North America, including five separate field campaigns at the Alberta oil sands (1 airborne, 4 ground-based); the 2010 Deepwater Horizon oil spill (airborne and ship-based); the 2012 airborne Deep Convective Clouds and Chemistry Project (DC3) mission over oil and gas wells in Colorado, Texas and Oklahoma; and the 2013 ground-based Barnett Shale Campaign in Texas. Each campaign has characterized more than 80 individual C1-C10 VOCs including alkanes, alkenes and aromatics. For example, oil sands are an extra-heavy, unconventional crude oil that is blended with diluent in order to flow, and upgraded into synthetic crude oil. The VOC signature at the oil sands mining and upgrading facilities is alkane-rich, and the fuel gas associated with these operations has an i-butane/n-butane ratio similar to that of liquefied petroleum gas (LPG). In addition to light alkanes, enhanced levels of benzene were observed over US oil and natural gas wells during DC3, likely because of its use in hydrofracking fluid. A series of VOC emission ratios from North American petrochemical sources will be presented and compared, including oil sands, conventional oil and hydrofracking operations.

  7. Periodic modeling of zeolite Ti-LTA

    Science.gov (United States)

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

    2017-08-01

    We have proposed a combination of density functional theory calculations and interatomic potential-based simulations to study the structural, electronic, and mechanical properties of pure-silica zeolite Linde Type A (LTA), as well as two titanium-doped compositions. The energetics of the titanium distribution within the zeolite framework suggest that the inclusion of a second titanium atom with configurations Ti-(Si0)-Ti, Ti-(Si1)-Ti, and Ti-(Si2)-Ti is more energetically favorable than the mono-substitution. Infra-red spectra have been simulated for the pure-silica LTA, the single titanium substitution, and the configurations Ti-(Si0)-Ti and Ti-(Si2)-Ti, comparing against experimental benchmarks where available. The energetics of the direct dissociation of water on these Lewis acid sites indicate that this process is only favored when two titanium atoms form a two-membered ring (2MR) sharing two hydroxy groups, Ti-(OH2)-Ti, which suggests that the presence of water may tune the distribution of titanium atoms within the framework of zeolite LTA. The electronic analysis indicates charge transfer from H2O to the Lewis acid site and hybridization of their electronic states.

  8. 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.

  9. Lead removal and recovery from battery wastewaters by natural zeolite clinoptilolite

    Energy Technology Data Exchange (ETDEWEB)

    Petruzzelli, D.; Pagano, M.; Tiravanti, G. [National Research Council, Bari (Italy). Ist. di Ricerca sulle Acque; Passino, R. [National Research Council, Rome (Italy). Ist. di Ricerca sulle Acque

    1999-05-01

    Technical feasibility of an ion exchange process for removal and recovery of lead present in battery manufacturing wastewaters is demonstrated. In absence of aluminium and ferric species, lead is quantitatively removed and recovered ({approx}90%) from the neutralized wastewaters after elution on the natural zeolite clinoptilolite. Control of pH to 5.5--6 is necessary to minimize degradation of the exchanger material. Throughput volumes exceeding 2,700 bed volumes (BV) (flowrate: F{sub exh} = 10 BV/h) is obtained, when the initial Pb concentration is 4 mg/L, with the metal leakage steadily below the maximum allowable concentration (MAC < 0.2 mgPb/L) set by the EU for discharge in rivers, lakes, coastal seawater. Regeneration of the zeolite is carried out by controlled elution of limited amounts of 1M NaCl, pH 4.5 (40BV, F{sub reg} = 5 BV/h) to minimize in situ precipitation of metals and preserve the zeolite from degradation. From spent regeneration eluate /lead is recovered to the battery manufacturing operations. This latter operation is carried-out by precipitation in the form of hydroxycerussite (basic lead carbonate) or electrolysis as pure metal. In this way the environmental impact is minimized after waste disposal (no hazardous waste formation) and, at the same time, raw materials are recovered to the productive lines of origin (environmental protection and resource conservation). The exhausted mother liquors from lead precipitation operation are recycled to the subsequent zeolite regeneration step, after back-up of the initial regenerant concentration and solution pH.

  10. Thermodynamic selectivity of functional agents on zeolite for sodium dodecyl sulfate sequestration

    Energy Technology Data Exchange (ETDEWEB)

    Leng, Ling; Wang, Jian [Department of Civil and Environmental Engineering, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong SAR (China); Qiu, Xianxiu; Zhao, Yanxiang; Yip, Yuk-Wang; Law, Ga-Lai [Department of Applied Biology and Chemical Technology, State Key Laboratory of Chirosciences, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong SAR (China); Shih, Kaimin; Zhou, Zhengyuan [Department of Civil Engineering, The University of Hong Kong, Pokfulam Road, Hong Kong, Hong Kong SAR (China); Lee, Po-Heng, E-mail: poheng76@gmail.com [Department of Civil and Environmental Engineering, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong SAR (China)

    2016-11-15

    Highlights: • A thermodynamic approach to select a functional agent for adsorbent is proposed. • ITC and QCS were used to interpret the interaction between adsorbate and agent. • The interaction identifies the adsorption mechanism and performance. • This approach enables the manipulation of adsorption capacity optimization. - Abstract: This study proposes a thermodynamic approach to effectively select functional agents onto zeolite for sodium dodecyl sulfate (SDS) sequestration in greywater reuse. We combine isothermal titration calorimetry (ITC) and quantum chemistry simulation (QCS) to identify the interactions between SDS and agents at the molecular level. Three potential agents, cetyl trimethyl ammonium bromide (CTAB), N,N,N-trimethyltetradecan-1-aminium bromide (C{sub 14}TAB), and 14-hydroxy-N,N,N-trimethyltetradecan-1-aminium bromide (C{sub 14}HTAB), differ in carbon chain length and hydrophilic groups. The ITC titration of SDS with CTAB released the highest heat, followed by those with C{sub 14}TAB and C{sub 14}HTAB, as was the same trend for the amounts of SDS adsorbed by the respective functionalized-zeolites. Results suggest that the favorable SDS sorption occurred at the bilayer CTAB-zeolite is driven by enthalpy as similar as the SDS…CTAB interaction found, regardless of the contribution from electrostatic and/or hydrophobic behaviors, while the declined sorption is entropy-driven via the predominant hydrophobic interaction onto the monolayer CTAB-zeolite. The data presented here interpret the nature of molecularly thermodynamic quantities and enable the manipulation of sorption capacity optimization.

  11. Increasing competitiveness of wine producers in strategic alliances VOC

    Directory of Open Access Journals (Sweden)

    Martin Prokeš

    2012-01-01

    Full Text Available The paper describes the main reasons for the formation of new regional association of wineries, based on a different origin for wines in the wine region of Moravia in the southeast part of the Czech Republic. This research aim is to create a plan for new development of such strategic alliances on the basis of results of localization factors. There coefficient of localization is used for identification of cluster. Results are compared with already operating on associations for the appellation in Austria DAC. They were traced changes in consumer preferences in the Czech wine market. Consumers are placing more emphasis on the selection of wine on its descent from a particular area, growing community and the individual grower. This paper specifically introduces new associations for appellation system VOC. This alliance is described in the context of the establishment, operation, development and expansion, respectively the possibility of involvement of additional organizations suppliers and research institutions. The application of the results of research was a plan for the establishment of new alliance VOC Modré Hory, where are associated 30 wine producers of wine in 5 villages around the center Velké Pavlovice. Based on the experience of newly emerging VOC system of appellations was setting up a plan of formation association with the proposed methodological approach. Open cooperation between associations VOC appellation and other entities involving suppliers, customers, research institutions and universities has the possibility of creating an institutionalized wine cluster. The plan to create a wine cluster was proposed to establish cooperation between the newly emerging associations of VOC at three sub-regions of South Moravia, in order to achieve competitive advantage.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-03-01

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

  13. Ozone production and its sensitivity to NOx and VOCs: results from the DISCOVER-AQ field experiment, Houston 2013

    Science.gov (United States)

    Mazzuca, Gina M.; Ren, Xinrong; Loughner, Christopher P.; Estes, Mark; Crawford, James H.; Pickering, Kenneth E.; Weinheimer, Andrew J.; Dickerson, Russell R.

    2016-11-01

    An observation-constrained box model based on the Carbon Bond mechanism, version 5 (CB05), was used to study photochemical processes along the NASA P-3B flight track and spirals over eight surface sites during the September 2013 Houston, Texas deployment of the NASA Deriving Information on Surface Conditions from COlumn and VERtically Resolved Observations Relevant to Air Quality (DISCOVER-AQ) campaign. Data from this campaign provided an opportunity to examine and improve our understanding of atmospheric photochemical oxidation processes related to the formation of secondary air pollutants such as ozone (O3). O3 production and its sensitivity to NOx and volatile organic compounds (VOCs) were calculated at different locations and times of day. Ozone production efficiency (OPE), defined as the ratio of the ozone production rate to the NOx oxidation rate, was calculated using the observations and the simulation results of the box and Community Multiscale Air Quality (CMAQ) models. Correlations of these results with other parameters, such as radical sources and NOx mixing ratio, were also evaluated. It was generally found that O3 production tends to be more VOC-sensitive in the morning along with high ozone production rates, suggesting that control of VOCs may be an effective way to control O3 in Houston. In the afternoon, O3 production was found to be mainly NOx-sensitive with some exceptions. O3 production near major emissions sources such as Deer Park was mostly VOC-sensitive for the entire day, other urban areas near Moody Tower and Channelview were VOC-sensitive or in the transition regime, and areas farther from downtown Houston such as Smith Point and Conroe were mostly NOx-sensitive for the entire day. It was also found that the control of NOx emissions has reduced O3 concentrations over Houston but has led to larger OPE values. The results from this work strengthen our understanding of O3 production; they indicate that controlling NOx emissions will provide

  14. 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.

  15. Volatile organic compound emissions in relation to plant carbon fixation and the terrestrial carbon budget

    NARCIS (Netherlands)

    Kesselmeier, J.; Ciccioli, P.; Kuhn, U.; Stefani, P.; Biesenthal, T.; Rottenberger, S.; Wolf, A.; Vitullo, M.; Valentini, R.; Nobre, A.; Kabat, P.; Andreae, M.O.

    2002-01-01

    A substantial amount of carbon is emitted by terrestrial vegetation as biogenic volatile organic compounds (VOC), which contributes to the oxidative capacity of the atmosphere, to particle production and to the carbon cycle. With regard to the carbon budget of the terrestrial biosphere, a release of

  16. Zeolites in Eocene basaltic pillow lavas of the Siletz River Volcanics, Central Coast Range, Oregon.

    Science.gov (United States)

    Keith, T.E.C.; Staples, L.W.

    1985-01-01

    Zeolites and associated minerals occur in a tholeiitic basaltic pillow lava sequence. Although the zeolite assemblages are similar to those found in other major zeolite occurrences in basaltic pillow lavas, regional zoning of the zeolite assemblages is not apparent. The formation of the different assemblages is discussed.-D.F.B.

  17. Alkaline cations directing the transformation of FAU zeolites into five different framework types.

    Science.gov (United States)

    Van Tendeloo, Leen; Gobechiya, Elena; Breynaert, Eric; Martens, Johan A; Kirschhock, Christine E A

    2013-12-28

    Exposure of faujasite zeolites to different alkali hydroxide solutions readily yields zeolites with ABW, CHA, MER and ANA topologies. In NaOH faujasite persisted. Aside from new opportunities for zeolite synthesis, this reveals that a suitable aluminosilicate connectivity in the source material significantly facilitates zeolite crystallization.

  18. 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...

  19. 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.

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

    Science.gov (United States)

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

    2011-09-15

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

  1. 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

  2. Oxidation of cyclohexane catalyzed by metal-ion-exchanged zeolites.

    Science.gov (United States)

    Sökmen, Ilkay; Sevin, Fatma

    2003-08-01

    The ion-exchange rates and capacities of the zeolite NaY for the Cu(II), Co(II), and Pb(II) metal ions were investigated. Ion-exchange equilibria were achieved in approximately 72 h for all the metal ions. The maximum ion exchange of metal ions into the zeolite was found to be 120 mg Pb(II), 110 mg Cu(II), and 100 mg Co(II) per gram of zeolite NaY. It is observed that the exchange capacity of a zeolite varies with the exchanged metal ion and the amount of metal ions exchanged into zeolite decreases in the sequence Pb(II) > Cu(II) > Co(II). Application of the metal-ion-exchanged zeolites in oxidation of cyclohexane in liquid phase with visible light was examined and it is observed that the order of reactivity of the zeolites for the conversion of cyclohexane to cyclohexanone and cyclohexanol is CuY > CoY > PbY. It is found that conversion increases by increase of the empty active sites of a zeolite and the formation of cyclohexanol is favored initially, but the cyclohexanol is subsequently converted to cyclohexanone.

  3. 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 ...

  4. Antibacterial activity of heavy metal-loaded natural zeolite.

    Science.gov (United States)

    Hrenovic, Jasna; Milenkovic, Jelena; Ivankovic, Tomislav; Rajic, Nevenka

    2012-01-30

    The antibacterial activity of natural zeolitized tuffs containing 2.60wt.% Cu(2+), 1.47 Zn(2+) or 0.52 Ni(2+) were tested. Antibacterial activities of the zeolites against Escherichia coli and Staphylococcus aureus were tested after 1h and 24h of exposure to 1g of the zeolite in 100mL of three different media, namely Luria Bertani, synthetic wastewater and secondary effluent wastewater. The antibacterial activities of the zeolites in Luria Bertani medium were significantly lower than those in the other media and negatively correlated with the chemical oxygen demand of the media. The Ni-loaded zeolite showed high leaching of Ni(2+) (3.44-9.13wt.% of the Ni(2+) loaded) and weak antibacterial activity in the effluent water. Since Cu-loaded zeolite did not leach Cu(2+) and the leaching of Zn(2+) from Zn-loaded zeolite was low (1.07-1.61wt.% of the Zn(2+) loaded), the strong antibacterial activity classified the Cu- and Zn-loaded zeolite as promising antibacterial materials for disinfection of secondary effluent water.

  5. 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 ...... as conversion of sugars using Lewis acidic zeolites to produce useful chemicals....

  6. Zeolites in the Pine Ridge Indian Reservation, South Dakota

    Science.gov (United States)

    Raymond, William H.; Bush, Alfred L.; Gude, Arthur J.

    1982-01-01

    Zeolites of possible commercial value occur in the Brule Formation of Oligocene age and the Sharps Formation (Harksen, 1961) of Miocene age which crop out in a wide area in the northern part of the Pine Ridge Indian Reservation. The thickness of the zeolite-bearing Interval and the extent of areas within the Interval which contain significant amounts of zeolites are far greater than was expected prior to this investigation. The shape of the zeolite-bearing Interval is tabular and the dimensions of Its exposure are roughly 10 ml x 200 mi x 150 ft (16 km x 160 km x 45 m) thick. Within the study area, there are tracts in which the zeolite resource potential is significant (see pl. 2). This report is intended to inform the Oglala Sioux Tribe of some of the most promising zeolite occurrences. Initial steps can then be taken by the Tribe toward possible development of the resources, should they wish to do so. The data contained herein identify areas of high zeolite potential, but are not adequate to establish economic value for the deposits. If development is recommended by the tribal government, we suggest that the tribal government contact companies involved in research and production of natural zeolites and provide them with the data in this report.

  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

  8. Silanization-Based Zeolite Crystallization: Participation Degree and Pathway.

    Science.gov (United States)

    Yan, Yueer; Azhati, Arepati; Guo, Xiao; Zhang, Yahong; Tang, Yi

    2015-08-17

    A clear and deep understanding of zeolite crystallization with the addition of organosilane is desirable for the reasonable design and preparation of hierarchical zeolites. Herein, the effects of different organosilanes on zeolite crystallization were systematically studied. It was found that organosilane plays the role of an inhibitor in the silanization-based zeolite preparation, and this inhibition effect was determined by its participation degree. An organosilane with a high participation degree can result in the prolongation of nucleation and growth periods of zeolite as well as the variation of product properties. More importantly, a dynamic participation pathway of organosilane is proposed, that is, the growth of zeolite is accompanied by the continuous removal of organosilane, leading to an increase of product crystallinity as well as the decrease of mesoporosity. This study gives a new insight into the role that organosilane plays in zeolite crystallization, which will help to direct the rational selection of organosilane and design of crystallization condition for the optimal synthesis of hierarchical zeolites.

  9. Adsorption, Diffusion and Reaction Studies of Hydrocarbons on Zeolite Catalysts

    NARCIS (Netherlands)

    Donk, Sander van

    2002-01-01

    Zeolites are crystalline microporous materials that are widely applied as catalysts in industries like oil refining, basic petrochemistry and fine chemistry. The major benefit of the use of zeolites as catalysts lies in their unique microporous structures. However, in some cases the presence of micr

  10. 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

  11. defluorination of drinking water using surfactant modified zeolites

    African Journals Online (AJOL)

    PUBLICATIONS1

    The unmodified zeolite NaLSX was incapable of adsorbing fluoride ions but the surfactant modified zeolite ... high fluoride (> 10 mg F-/day) over a prolonged period (i.e. 10 to 20 years) ... attracted to positively charged ions therefore there was ...

  12. 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

  13. 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

  14. 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.

  15. 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.

  16. 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).

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

    Energy Technology Data Exchange (ETDEWEB)

    Shaw, Ruchi, E-mail: shawruchi1@gmail.com; Tiwari, Sangeeta, E-mail: stiwari2@amity.edu [Amity Institute of Applied Sciences, Amity University, Noida, Uttar Pradesh-201301 (India)

    2016-04-13

    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{sup +} with Mg{sup 2+} and Ca{sup 2+} ions. The metal ion exchanged zeolite was then used as anticorrosive zeolitic pigments in paints. The prepared zeolite NaY was characterized using X-Ray diffraction technique and Scanning electron microscopy. The size, shape and density of the prepared fly ash based pigments were determined by various techniques. The paints were prepared by using fly ash based zeolitic pigments in epoxy resin and the percentages of pigments used in paints were 2% and 5%. These paints were applied to the mild steel panels and the anticorrosive properties of the pigments were assessed by the electrochemical spectroscopy technique (EIS).

  18. Microwave-Assisted Solvent-Free Synthesis of Zeolitic Imidazolate Framework-67

    Directory of Open Access Journals (Sweden)

    Heng Zhang

    2016-01-01

    Full Text Available A microporous metal-organic framework (MOF, cobalt-based zeolitic imidazolate framework-67 (ZIF-67, was synthesized by the combination of solvent-free hand-mill and microwave irradiation, without any organic solvent and within 30 minutes. The hand-milling process can mix the reactants well by the virtue of high moisture/water absorption capacity of reactants. In addition, the outstanding electromagnetic wave absorption capability of cobalt leads to efficient conversion to MOF structures before carbonization. The obtained ZIF-67 possesses high surface area and micropore volume.

  19. Personal exposures and microenvironment concentrations of PM 2.5, VOC, NO 2 and CO in Oxford, UK

    Science.gov (United States)

    Lai, H. K.; Kendall, M.; Ferrier, H.; Lindup, I.; Alm, S.; Hänninen, O.; Jantunen, M.; Mathys, P.; Colvile, R.; Ashmore, M. R.; Cullinan, P.; Nieuwenhuijsen, M. J.

    Between 1998 and 2000 in Oxford, UK, simultaneous personal exposures and microenvironmental measurements (home indoor, home outdoor and work indoor) to fine particulate matters PM 2.5, volatile organic compounds (VOC), nitrogen dioxide (NO 2) and carbon monoxide (CO) were carried out once per person among 50 adults over a 48-h period. Thirty-seven elements in PM 2.5 and 30 different VOCs were analysed. Questionnaires were distributed to record their time-activity patterns and exposure-related information. Results showed that participants spent more time (89.5%) in all indoors than in other microenvironments. Geometric mean (GM) of personal and home indoor levels of PM 2.5, 14 elements (aluminium, arsenic, bromine, calcium, copper, iron, gallium, potassium, sodium, phosphorus, lead, selenium, silicon, titanium), total VOC (TVOC) and 8 individual compounds (nonane, decane, undecane, trimethylbenzene, toluene, benzaldehyde, alpha-pinene and d-limonene) were over 20% higher than their GM outdoor levels. Those of NO 2, 5 aromatic VOCs (benzene, o-xylene, ethylbenzene, propylbenzene, m, p-xylene) and 5 other elements (chlorine, magnesium, manganese, sulphur, zinc) were close to their GM outdoor levels. For PM 2.5 and TVOC, personal exposures and residential indoor levels (in GM) were about 2 times higher among the tobacco-smoke exposed group compared to the non-smoke exposed group, suggesting that smoking is an important determinant of these exposures. Determinants for CO were visualised by real-time monitoring, and we showed that the peak levels of personal exposure to CO were associated with smoking, cooking and transportation activities. Moderate to good correlations were only found between the personal exposures and residential indoor levels for both PM 2.5 ( r=0.60, pp=0.003).

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

    DEFF Research Database (Denmark)

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

    2017-01-01

    −Y by thermolysis. Stages II and III may instead be performed using commercially available zeolites, Na−Y and NH4−Y, respectively, which shifts the learning objectives to structural characterization of zeolites. The characterization of the product and intermediate materials gives the students a practical insight...

  1. 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.

  2. Synthesis and Characterization of Zeolite Na-Y and Its Conversion to the Solid Acid Zeolite H-Y

    Science.gov (United States)

    Warner, Terence E.; Klokker, Mads Galsgaard; Nielsen, Ulla Gro

    2017-01-01

    Zeolite Y has an iconic crystal structure, but more importantly, the hydrogen modification zeolite H-Y is the classic example of a solid acid which is used extensively as a catalyst in the oil industry. This metastable compound cannot be synthesized directly, which creates an opportunity to discuss various preparative strategies with the students,…

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

    DEFF Research Database (Denmark)

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

    2017-01-01

    Zeolite Y has an iconic crystal structure, but more importantly, the hydrogen modification zeolite H−Y is the classic example of a solid acid which is used extensively as a catalyst in the oil industry. This metastable compound cannot be synthesized directly, which creates an opportunity to discu...

  4. Removal of metal contaminants and radionuclides with natural zeolites - competitive sorption and effects of zeolite modifications

    Energy Technology Data Exchange (ETDEWEB)

    Reddy, K.V.; Prakash, A. [The Univ. of Western Ontario, Dept. of Chemical and Biochemical Engineering, London, ON (Canada); Vijayan, S. [Atomic Energy of Canada Limited, Chalk River, ON (Canada)

    2011-07-01

    Metal contaminants including radionuclides found in wastewaters must be reduced to acceptable levels before discharging the wastewater into receiving waters. These cations can accumulate in aquatic organisms causing toxicity and death, hence strict regulatory limits for their allowable discharge levels have been established over the years. This has also prompted the development of cost effective technologies that will permit the efficient removal of contaminants, while concentrating the contaminants in a form suitable for immobilization, storage and disposal. Removal requirements can be met by some inorganic zeolites, which can be natural or synthetic. The zeolites have a strong affinity for transition metal cations, and their cage-like structures offer large internal and external surface areas for ion exchange and adsorption. In view of these considerations, investigations with two low-cost natural zeolites (clinoptilolite and chabazite) were started, with the objective of developing a cost effective technology for column operations. Sorption tests of Cs{sup +}, Sr{sup 2+} and Cu{sup 2+} ions on chabazite and clinoptilolite were carried out using batch experiments in 125 mL vessels under various test conditions. Competitive sorption was studied in mixed cation solutions containing the commonly occurring non-toxic cations Ca{sup 2+} and Na{sup +}. The presence of these non-toxic cations inhibits removal of the targeted cations. Additional pretreatments and modifications of the 'as received' sorbent particles were also investigated, which are important in multiple cation systems, to enhance removal selectivity for the target contaminant cations. Sorption tests with chabazite and clinoptilolite showed that these two natural zeolites can be effectively used to remove cesium, strontium and copper ions from aqueous solutions. The performance can be controlled by maintaining the zeolite to waste volume ratio. The contaminant removal performance of chabazite was

  5. Efficiency of basalt zeolite and Cuban zeolite to adsorb ammonia released from poultry litter.

    Science.gov (United States)

    Nuernberg, Giselle B; Moreira, Marcelo A; Ernani, Paulo R; Almeida, Jaime A; Maciel, Tais M

    2016-12-01

    Confined poultry production is an important livestock activity, which generates large amounts of waste associated with the potential for environmental pollution and ammonia (NH3) emissions. The release of ammonia negatively affects poultry production and decreases the N content of wastes that could be used as soil fertilizers. The objective of this study was to evaluate a low-cost, simple and rapid method to simulate ammonia emissions from poultry litter as well as to quantify the reduction in the ammonia emissions to the environment employing two adsorbent zeolites, a commercial Cuban zeolite (CZ) and a ground basalt Brazilian rock containing zeolite (BZ). The experiments were conducted in a laboratory, in 2012-2013. The zeolites were characterized by X-ray diffraction (XRD), X-ray fluorescence spectrometry (XRF), physical adsorption of N2 (BET) and scanning electron microscopy (SEM). Ammonia released from poultry litter and its simulation from NH4OH solution presented similar capture rates of 7.99 × 10(-5) and 7.35 × 10(-5) mg/h, respectively. Both zeolites contain SiO2 and Al2O3 as major constituents, with contents of 84% and 12% in the CZ, and 51% and 12% in the BZ, respectively, besides heulandite groups. Their BET surface areas were 89.4 and 11.3 m(2) g(-1), respectively, and the two zeolites had similar surface morphologies. The zeolites successfully adsorbed the ammonia released, but CZ was more efficient than BZ, since to capture all of the ammonia 5 g of CZ and 20 g of BZ were required. This difference is due to higher values for the superficial area, porosity, CEC and acid site strength of CZ relatively to BZ. The proposed methodology was shown to be an efficient method to simulate and quantify the ammonia released from poultry litter. Copyright © 2016 Elsevier Ltd. All rights reserved.

  6. PEMANFAATAN ZEOLIT DARI ABU SEKAM PADI DENGAN AKTIVASI ASAM UNTUK PENURUNAN KESADAHAN AIR

    OpenAIRE

    VH Putranto; E Kusumastuti; Jumaeri Jumaeri

    2016-01-01

    Aktivasi menggunakan asam kuat dalam sintesis zeolit dikenal dapat meningkatkan kemampuan zeolit sebagai adsorben. Penelitian ini bertujuan untuk memanfaatkan abu sekam padi sebagai sumber silika yang diaktivasi dengan HCl 2 M pada sintesis zeolit secara hidrotermal dan memanfaatkan zeolit hasil sintesis untuk menurunkan tingkat kesadahan air sumur. Proses aktivasi dilakukan dengan menggunakan larutan HCl 2 M. Zeolit hasil sintesis diuji secara kualitatif menggunakan Spektrofotometer Inframer...

  7. 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...

  8. Modeling unsteady-state VOC transport in simulated waste drums. Revision 1

    Energy Technology Data Exchange (ETDEWEB)

    Liekhus, K.J.; Gresham, G.L.; Peterson, E.S.; Rae, C.; Hotz, N.J.; Connolly, M.J.

    1994-01-01

    This report is a revision of an EG&G Idaho informal report originally titled Modeling VOC Transport in Simulated Waste Drums. A volatile organic compound (VOC) transport model has been developed to describe unsteady-state VOC permeation and diffusion within a waste drum. Model equations account for three primary mechanisms for VOC transport from a void volume within the drum. These mechanisms are VOC permeation across a polymer boundary, VOC diffusion across an opening in a volume boundary, and VOC solubilization in a polymer boundary. A series of lab-scale experiments was performed in which the VOC concentration was measured in simulated waste drums under different conditions. A lab-scale simulated waste drum consisted of a sized-down 55-gal metal drum containing a modified rigid polyethylene drum liner. Four polyethylene bags were sealed inside a large polyethylene bag, supported by a wire cage, and placed inside the drum liner. The small bags were filled with VOC-air gas mixture and the VOC concentration was measured throughout the drum over a period of time. Test variables included the type of VOC-air gas mixtures introduced into the small bags, the small bag closure type, and the presence or absence of a variable external heat source. Model results were calculated for those trials where the permeability had been measured.

  9. PARAMETRIC EVALUATION OF VOC CONVERSION VIA CATALYTIC INCINERATION

    Directory of Open Access Journals (Sweden)

    Kaskantzis Neto G.

    1997-01-01

    Full Text Available Abstract - A pilot-scale catalytic incineration system was used to investigate the effectiveness of catalytic incineration as a means of reducing volatile organic compound (VOC air pollutants. The objectives of the study were: 1 to investigate the effects of operating and design variables on the reduction efficiency of VOCs; and 2 to evaluate reduction efficiencies for specific compounds in different chemical classes. The study results verified that the following factors affect the catalyst performance: inlet temperature, space velocity, compound type, and compound inlet concentration. Tests showed that reduction efficiencies exceeding 98% were possible, given sufficiently high inlet gas temperatures for the following classes of compounds: alcohols, acetates, ketones, hydrocarbons, and aromatics

  10. Modeling the uncertainty of several VOC and its impact on simulated VOC and ozone in Houston, Texas

    Science.gov (United States)

    Pan, Shuai; Choi, Yunsoo; Roy, Anirban; Li, Xiangshang; Jeon, Wonbae; Souri, Amir Hossein

    2015-11-01

    A WRF-SMOKE-CMAQ modeling system was used to study Volatile Organic Compound (VOC) emissions and their impact on surface VOC and ozone concentrations in southeast Texas during September 2013. The model was evaluated against the ground-level Automated Gas Chromatograph (Auto-GC) measurement data from the Texas Commission on Environmental Quality (TCEQ). The comparisons indicated that the model over-predicted benzene, ethylene, toluene and xylene, while under-predicting isoprene and ethane. The mean biases between simulated and observed values of each VOC species showed clear daytime, nighttime, weekday and weekend variations. Adjusting the VOC emissions using simulated/observed ratios improved model performance of each VOC species, especially mitigating the mean bias substantially. Simulated monthly mean ozone showed a minor change: a 0.4 ppb or 1.2% increase; while a change of more than 5 ppb was seen in hourly ozone data on high ozone days, this change moved model predictions closer to observations. The CMAQ model run with the adjusted emissions better reproduced the variability in the National Aeronautics and Space Administration (NASA)'s Ozone Monitoring Instrument (OMI) formaldehyde (HCHO) columns. The adjusted model scenario also slightly better reproduced the aircraft HCHO concentrations from NASA's DISCOVER-AQ campaign conducted during the simulation episode period; Correlation, Mean Bias and RMSE improved from 0.34, 1.38 ppb and 2.15 ppb to 0.38, 1.33 ppb and 2.08 ppb respectively. A process analysis conducted for both industrial/urban and rural areas suggested that chemistry was the main process contributing to ozone production in both areas, while the impact of chemistry was smaller in rural areas than in industrial and urban areas. For both areas, the positive chemistry contribution increased in the sensitivity simulation largely due to the increase in emissions. Nudging VOC emissions to match the observed concentrations shifted the ozone hotspots

  11. Aromatic VOCs global influence in the ozone production

    Science.gov (United States)

    Cabrera-Perez, David; Pozzer, Andrea

    2016-04-01

    Aromatic hydrocarbons are a subgroup of Volatile Organic Compounds (VOCs) of special interest in the atmosphere of urban and semi-urban areas. Aromatics form a high fraction of VOCs, are highly reactive and upon oxidation they are an important source of ozone. These group of VOCs are released to the atmosphere by processes related to biomass burning and fossil fuel consumption, while they are removed from the atmosphere primarily by OH reaction and by dry deposition. In addition, a branch of aromatics (ortho-nitrophenols) produce HONO upon photolysis, which is responsible of certain amount of the OH recycling. Despite their importance in the atmosphere in anthropogenic polluted areas, the influence of aromatics in the ozone production remains largely unknown. This is of particular relevance, being ozone a pollutant with severe side effects on air quality, health and climate. In this work the atmospheric impacts at global scale of the most emitted aromatic VOCs in the gas phase (benzene, toluene, xylenes, ethylbenzene, styrene, phenol, benzaldehyde and trimethylbenzenes) are analysed and assessed. Specifically, the impact on ozone due to aromatic oxidation is estimated, as this is of great interest in large urban areas and can be helpful for developing air pollution control strategies. Further targets are the quantification of the NOx loss and the OH recycling due to aromatic oxidation. In order to investigate these processes, two simulations were performed with the numerical chemistry and climate simulation ECHAM/MESSy Atmospheric Chemistry (EMAC) model. The simulations compare two cases, one with ozone concentrations when aromatics are present or the second one when they are missing. Finally, model simulated ozone is compared against a global set of observations in order to better constrain the model accuracy.

  12. Ensurdecimento vocálico em Zo’é

    Directory of Open Access Journals (Sweden)

    Ana Suelly Arruda Câmara Cabral

    2012-11-01

    Full Text Available Neste trabalho apresentamos uma descrição do fenômeno deensurdecimento vocálico na língua Zo’é (Tupi-Guarani. Sãoapresentadas ainda hipóteses acerca das restrições sincrônicas ativasno condicionamento deste fenômeno, além de uma hipótese acercada origem histórica do mesmo.

  13. Determination of VOC emission rates and compositions for offset printing.

    Science.gov (United States)

    Wadden, R A; Scheff, P A; Franke, J E; Conroy, L M; Keil, C B

    1995-07-01

    The release rates of volatile organic compounds (VOC) as fugitive emissions from offset printing are difficult to quantify, and the compositions are usually not known. Tests were conducted at three offset printing shops that varied in size and by process. In each case, the building shell served as the test "enclosure," and air flow and concentration measurements were made at each air entry and exit point. Emission rates and VOC composition were determined during production for (1) a small shop containing three sheetfed presses and two spirit duplicators (36,700 sheets, 47,240 envelopes and letterheads), (2) a medium-size industrial in-house shop with two webfed and three sheetfed presses, and one spirit duplicator (315,130 total sheets), and (3) one print room of a large commercial concern containing three webfed, heatset operations (1.16 x 10(6) ft) served by catalytic air pollution control devices. Each test consisted of 12 one-hour periods over two days. Air samples were collected simultaneously during each period at 7-14 specified locations within each space. The samples were analyzed by gas chromatography (GC) for total VOC and for 13-19 individual organics. Samples of solvents used at each shop were also analyzed by GC. Average VOC emission rates were 4.7-6.1 kg/day for the small sheetfed printing shop, 0.4-0.9 kg/day for the industrial shop, and 79-82 kg/day for the commercial print room. Emission compositions were similar and included benzene, toluene, xylenes, ethylbenzene, and hexane. Comparison of the emission rates with mass balance estimates based on solvent usage and composition were quite consistent.(ABSTRACT TRUNCATED AT 250 WORDS)

  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. A novel processing of carbon nanotubes grown on molecular sieve coated porous ceramics

    Science.gov (United States)

    Mazumder, Sangram; Sarkar, Naboneeta; Park, Jung Gyu; Zhao, Wei; Kim, Sukyoung; Kim, Ik Jin

    2015-08-01

    The present study focuses on the growth of carbon nanotubes (CNTs) on Fe-containing zeolites coated porous ceramics by implementing three different and independent techniques, successively. Direct foaming-derived porous ceramics were subjected to hydrothermal reaction for on-site growth of NaA zeolites within it. The porous ceramics-zeolite composite was subjected to ion-exchange reaction to obtain the catalyst for CNT synthesis. Multi-walled CNTs (MWCNTs) were grown by catalytic chemical vapour deposition (CCVD) process using acetylene as carbon source. Microstructural, thermogravimetric and spectroscopic analyses showed distinctive differences in terms of hollow structural feature, yield and crystallinity of the MWCNTs with different reaction temperatures.

  17. 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.

  18. Biofiltration for control of volatile organic compounds (VOCS)

    Energy Technology Data Exchange (ETDEWEB)

    Bishop, D.F. [Environmental Protection Agency, Cincinnati, OH (United States); Govind, R. [Univ. of Cincinnati, OH (United States)

    1995-10-01

    Air biofiltration is a promising technology for control of air emissions of biodegradable volatile organic compounds (VOCs). In conjunction with vacuum extraction of soils or air stripping of ground water, it can be used to mineralize VOCs removed from contaminated soil or groundwater. The literature describes three major biological systems for treating contaminated air bioscrubbers, biotrickling filters and biofilters. Filter media can be classified as: bioactive fine or irregular particulates, such as soil, peat, compost or mixtures of these materials; pelletized, which are randomly packed in a bed; and structured, such as monoliths with defined or variable passage size and geometry. The media can be made of sorbing and non-absorbing materials. Non-bioactive pelletized and structured media require recycled solutions of nutrients and buffer for efficient microbial activity and are thus called biotrickling filters. Extensive work has been conducted to improve biofiltration by EPA`s Risk Reduction Engineering Laboratory and the University of Cincinnati in biofilters using pelletized and structured media and improved operational approaches. Representative VOCs in these studies included compounds with a range of aqueous solubilities and octanol-water partition coefficients. The compounds include iso-pentane, toluene, methylene chloride, trichloroethylene (TCE), ethyl benzene, chlorobenzene and perchloroethylene (PCE) and alpha ({alpha}-) pinene. Comparative studies were conducted with peat/compost biofilters using isopentane and {alpha}-pinene. Control studies were also conducted to investigate adsorption/desorption of contaminants on various media using mercuric chloride solution to insure the absence of bioactivity.

  19. Light dependency of VOC emissions from selected Mediterranean plant species

    Science.gov (United States)

    Owen, S. M.; Harley, P.; Guenther, A.; Hewitt, C. N.

    The light, temperature and stomatal conductance dependencies of volatile organic compound (VOC) emissions from ten plant species commonly found in the Mediterranean region were studied using a fully controlled leaf cuvette in the laboratory. At standard conditions of temperature and light (30°C and 1000 μmol m -2 s -1 PAR), low emitting species ( Arbutus unedo, Pinus halepensis, Cistus incanus, Cistus salvifolius, Rosmarinus officinalis and Thymus vulgaris) emitted between 0.1 and 5.0 μg (C) (total VOCs) g -1 dw h -1, a medium emitter ( Pinus pinea) emitted between 5 and 10 μg (C) g -1 dw h -1 and high emitters ( Cistus monspeliensis, Lavendula stoechas and Quercus sp.) emitted more than 10 μg (C) g -1 dw h -1. VOC emissions from all of the plant species investigated showed some degree of light dependency, which was distinguishable from temperature dependency. Emissions of all compounds from Quercus sp. were light dependent. Ocimene was one of several monoterpene compounds emitted by P. pinea and was strongly correlated to light. Only a fraction of monoterpene emissions from C. incanus exhibited apparent weak light dependency but emissions from this plant species were strongly correlated to temperature. Data presented here are consistent with past studies, which show that emissions are independent of stomatal conductance. These results may allow more accurate predictions of monoterpene emission fluxes from the Mediterranean region to be made.

  20. A demonstration of biofiltration for VOC removal in petrochemical industries.

    Science.gov (United States)

    Zhao, Lan; Huang, Shaobin; Wei, Zongmin

    2014-05-01

    A biotrickling filter demo has been set up in a petrochemical factory in Sinopec Group for about 10 months with a maximum inlet gas flow rate of 3000 m3 h(-1). The purpose of this project is to assess the ability of the biotrickling filter to remove hardly biodegradable VOCs such as benzene, toluene and xylene which are recalcitrant and poorly water soluble and commonly found in petrochemical factories. Light-weight hollow ceramic balls (Φ 5-8 cm) were used as the packing media treated with large amounts of circulating water (2.4 m3 m(-2) h(-1)) added with bacterial species. The controlled empty bed retention time (EBRT) of 240 s is a key parameter for reaching a removal efficiency of 95% for benzene, toluene, xylene, and 90% for total hydrocarbons. The demo has been successfully adopted and practically applied in waste air treatments in many petrochemical industries for about two years. The net inlet concentrations of benzene, toluene and xylene were varied from 0.5 to 3 g m(-3). The biofiltration process is highly efficient for the removal of hydrophobic and recalcitrant VOCs with various concentrations from the petrochemical factories. The SEM analysis of the bacterial community in the BTF during VOC removal showed that Pseudomonas putida and Klebsiella sp. phylum were dominant and shutdown periods could play a role in forming the community structural differences and leading to the changes of removal efficiencies.

  1. A mass transfer model for VOC emission from silage

    Science.gov (United States)

    Hafner, Sasha D.; Montes, Felipe; Rotz, C. Alan

    2012-07-01

    Silage has been shown to be an important source of emissions of volatile organic compounds (VOCs), which contribute to the formation of ground-level ozone. Measurements have shown that environmental conditions and silage properties strongly influence emission rates, making it difficult to assess the contribution of silage in VOC emission inventories. In this work, we present an analytical convection-diffusion-dispersion model for predicting emission of VOCs from silage. It was necessary to incorporate empirical relationships from wind tunnel trials for the response of mass transfer parameters to surface air velocity and silage porosity. The resulting model was able to accurately predict the effect of temperature on ethanol emission in wind tunnel trials, but it over-predicted alcohol and aldehyde emission measured using a mass balance approach from corn silage samples outdoors and within barns. Mass balance results confirmed that emission is related to gas-phase porosity, but the response to air speed was not clear, which was contrary to wind tunnel results. Mass balance results indicate that alcohol emission from loose silage on farms may approach 50% of the initial mass over six hours, while relative losses of acetaldehyde will be greater.

  2. 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...... and its density was found to be slightly less than that of the densest ZIF phase, ZIF-zni. The mechanism of the phase transition involves a cooperative rotation of imidazolate linkers resulting in isotropic framework contraction and pore space minimization. DFT calculations established the energy...

  3. Hydrogen storage in Chabazite zeolite frameworks.

    Science.gov (United States)

    Regli, Laura; Zecchina, Adriano; Vitillo, Jenny G; Cocina, Donato; Spoto, Giuseppe; Lamberti, Carlo; Lillerud, Karl P; Olsbye, Unni; Bordiga, Silvia

    2005-09-07

    We have recently highlighted that H-SSZ-13, a highly siliceous zeolite (Si/Al = 11.6) with a chabazitic framework, is the most efficient zeolitic material for hydrogen storage [A. Zecchina, S. Bordiga, J. G. Vitillo, G. Ricchiardi, C. Lamberti, G. Spoto, M. Bjørgen and K. P. Lillerud, J. Am. Chem. Soc., 2005, 127, 6361]. The aim of this new study is thus to clarify both the role played by the acidic strength and by the density of the polarizing centers hosted in the same framework topology in the increase of the adsorptive capabilities of the chabazitic materials towards H2. To achieve this goal, the volumetric experiments of H2 uptake (performed at 77 K) and the transmission IR experiment of H2 adsorption at 15 K have been performed on H-SSZ-13, H-SAPO-34 (the isostructural silico-aluminophosphate material with the same Brønsted site density) and H-CHA (the standard chabazite zeolite: Si/Al = 2.1) materials. We have found that a H2 uptake improvement has been obtained by increasing the acidic strength of the Brønsted sites (moving from H-SAPO-34 to H-SSZ-13). Conversely, the important increase of the Brønsted sites density (moving from H-SSZ-13 to H-CHA) has played a negative role. This unexpected behavior has been explained as follows. The additional Brønsted sites are in mutual interaction via H-bonds inside the small cages of the chabazitic framework and for most of them the energetic cost needed to displace the adjacent OH ligand is higher than the adsorption enthalpy of the OH...H2 adduct. From our work it can be concluded that proton exchanged chabazitic frameworks represent, among zeolites, the most efficient materials for hydrogen storage. We have shown that a proper balance between available space (volume accessible to hydrogen), high contact surface, and specific interaction with strong and isolated polarizing centers are the necessary characteristics requested to design better materials for molecular H2 storage.

  4. H{sub 2} storage in microporous materials: a comparison between zeolites and Mos

    Energy Technology Data Exchange (ETDEWEB)

    Ricchiardi, G.; Regli, L.; Vitillo, J. G.; Cocina, D.; Bordiga, S.; Lamberti, C.; Spoto, G.; Zecchina, A.; Bjorgen, M.; Lillerud, K. P.

    2005-07-01

    One of the main concerns about a hydrogen-based energy economy is the efficient storage and transport of this highly flammable gas. Many strategies have been followed or suggested in recent years to solve this problem. The most important ones are: 1) storage in metals and alloys; 2) storage in complex hydrides (alanates, borides); 3) storage by trapping in clathrates (ice and others); 4) storage in microporous materials (carbons, zeolitic materials, metal-organic frameworks, polymers). [1, 2] In this work we have focused our attention on microporous materials, where the crucial point is the strength of the interaction between the molecular hydrogen and the internal surfaces of micropores and/ or of cages of entrapping materials. It is known from fundamental studies that H2 strongly interacts with ions in the gas but that the presence of counterions decreases the interaction energy substantially. The most prominent class of microporous materials, which contains isolated and exposed cations, are zeolites and zeotypes: ideal systems to investigate the interaction of H2 with both dispersive and electrostatic forces [3]. So, even if they are not sufficiently light to represent the final solution to H2 storage, the availability of a large variety of frameworks and chemical compositions combined with low cost and superior mechanical and thermal stabilities increases the interest in these materials. In this work we have studied in detail, by means of volumetric and spectroscopic measurements, zeolites with CHA topology (as they are characterized by a strong acidity and by a big surface area). H-SSZ-13 zeolite, characterized by a low Al content (Si/Al = 11), has shown the best properties in hydrogen storage in respect to all the other zeolites and zeotypes with different compositions and topologies [4]. The results have been compared with those obtained for MOF-5 [5], a well known Metal-Organic Framework, indicated as a very good material for molecular hydrogen storage [6

  5. Preparation, Processing, and Characterization of Oriented Polycrystalline Zeolite and Aluminophosphate Membranes

    Science.gov (United States)

    Stoeger, Jared Andrew

    Since the advent of zeolite membranes, speculation on their industrial applicability has been closely monitored, although widespread commercialization has been hampered by limitations in fabrication and post-synthesis processing. Economical, energy-efficient technology breakthroughs require an evaluation of a range of material candidates which show robustness and reliability. Straightforward manufacturing techniques should be devised to generate thousands of square meters of membrane area; however, this demands control of structural characteristics on the scale of nanometers. As described in this dissertation, the path forward will be forged by exploiting the intrinsic crystalline properties of zeolites or aluminophosphates for the next advancement in membrane technology. A facile method is described for the preparation of silicalite-1 (MFI zeolite type) membranes using the secondary growth technique on symmetric porous stainless steel tubes. Activation through rapid thermal processing (RTP), a lamp-based heat-treatment process used as a critical fabrication step in silicon integrated circuit manufacturing, is proven to reduce the density of non-zeolitic transport pathways which are detrimental to high-resolution molecular sieving. RTP-treated membranes are shown to have enhanced performance in the binary separation of vapor-phase isomers (p-/o-xylene), gas-phase isomers (n-/i-butane), and alcohol/water when compared to membranes activated at a much slower heating rate but otherwise similarly-prepared. The performance is discussed in the context of the market potential for industrially-attractive separations: the recovery of p-xylene from an isomeric mixture or alcohol biofuels from aqueous post-fermentation streams. Hydrothermal growth techniques for the preparation and characterization of continuous aluminophosphate (AFI zeolite type) membranes with a preferential crystallographic alignment on porous alpha-Al2O3 disc supports are demonstrated. A mechanism is

  6. 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

  7. 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.

  8. Zeolite Crystal Growth (ZCG) Flight on USML-2

    Science.gov (United States)

    Sacco, Albert, Jr.; Bac, Nurcan; Warzywoda, Juliusz; Guray, Ipek; Marceau, Michelle; Sacco, Teran L.; Whalen, Leah M.

    1997-01-01

    The extensive use of zeolites and their impact on the world's economy has resulted in many efforts to characterize their structure, and improve the knowledge base for nucleation and growth of these crystals. The zeolite crystal growth (ZCG) experiment on USML-2 aimed to enhance the understanding of nucleation and growth of zeolite crystals, while attempting to provide a means of controlling the defect concentration in microgravity. Zeolites A, X, Beta, and Silicalite were grown during the 16 day - USML-2 mission. The solutions where the nucleation event was controlled yielded larger and more uniform crystals of better morphology and purity than their terrestrial/control counterparts. The external surfaces of zeolite A, X, and Silicalite crystals grown in microgravity were smoother (lower surface roughness) than their terrestrial controls. Catalytic studies with zeolite Beta indicate that crystals grown in space exhibit a lower number of Lewis acid sites located in micropores. This suggests fewer structural defects for crystals grown in microgravity. Transmission electron micrographs (TEM) of zeolite Beta crystals also show that crystals grown in microgravity were free of line defects while terrestrial/controls had substantial defects.

  9. 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.)

  10. Synthesis of zeolite phases from combustion by-products

    Energy Technology Data Exchange (ETDEWEB)

    Pimraksa, K.; Chindaprasirt, P.; Setthaya, N. [Chiang Mai University, Chiang Mai (Thailand). Dept. of Industrial Chemistry

    2010-12-15

    Synthesis of zeolites from combustion by-products, including fly ash, bottom ash and rice husk ash, was studied. A molar ratio of SiO{sub 2}/Al2O{sub 3} of 1.5 was used for the syntheses. Refluxing and hydrothermal methods were also used for synthesis for comparison. The reaction temperatures of refluxing and hydrothermal methods were 100{sup o}C and 130{sup o}C, respectively. Sodalite, phillipsite-K, and zeolite P1 with analcime were obtained when fly ash, bottom ash and rice husk ash were used as starting materials, respectively. With rice husk ash as a starting material, zeolite P1 was produced. This result had advantages over previous studies as there was no prior activation required for the synthesis. The concentrations and types of alkaline used in the synthesis also determined the zeolite type. The different zeolites obtained from three systems were measured for specific surface area and pore size by using BET and Hg-porosimetry, respectively. Ammonium exchange capacities of the synthesised powders containing zeolites, sodalite, zeolite P1 and phillipsite-K were 38.5, 65.0 and 154.7 meq 100 g{sup 1}, respectively.

  11. Synthesis of zeolite phases from combustion by-products.

    Science.gov (United States)

    Pimraksa, Kedsarin; Chindaprasirt, Prinya; Setthaya, Naruemon

    2010-12-01

    Synthesis of zeolites from combustion by-products, including fly ash, bottom ash and rice husk ash, was studied. A molar ratio of SiO2/Al2O3 of 1.5 was used for the syntheses. Refluxing and hydrothermal methods were also used for synthesis for comparison. The reaction temperatures of refluxing and hydrothermal methods were 100 degrees C and 130 degrees C, respectively. Sodalite, phillipsite-K, and zeolite P1 with analcime were obtained when fly ash, bottom ash and rice husk ash were used as starting materials, respectively. With rice husk ash as a starting material, zeolite P1 was produced. This result had advantages over previous studies as there was no prior activation required for the synthesis. The concentrations and types of alkaline used in the synthesis also determined the zeolite type. The different zeolites obtained from three systems were measured for specific surface area and pore size by using BET and Hg-porosimetry, respectively. Ammonium exchange capacities of the synthesised powders containing zeolites, sodalite, zeolite P1 and phillipsite-K were 38.5, 65.0 and 154.7 meq 100 g(-1), respectively.

  12. Experiments in the EMRP project KEY-VOCs: Adsorption/desorption effects of VOCs in different tubing materials and preparation and analysis of a zero gas

    Science.gov (United States)

    Englert, Jennifer; Claude, Anja; Kubistin, Dagmar; Tensing, Erasmus; Michl, Katja; Plass-Duelmer, Christian

    2017-04-01

    Atmospheric chemistry and composition are influenced by volatile organic compounds (VOCs) emitted from natural and anthropogenic sources. Due to their toxicity and their crucial role in ozone and aerosol formation VOCs impact air quality and climate change and high quality observations are demanded. The European Metrology Research Programme (EMRP) project KEY-VOCs has targeted the improvement of VOC measurement capabilities with the focus on VOCs relevant for indoor air as well as for air quality and climate monitoring programmes. One major uncertainty is the influence of surface effects of the measurement devices. By developing a test system the adsorption/desorption effects of certain VOCs can be systematically examined. Different tubing materials e.g. stainless steel and PFA were analysed with the oxygenated VOC methanol and results of these experiments will be presented. In air quality monitoring very low levels of VOCs have to be measured. Purified air or nitrogen is widely used as a zero gas to characterize measurement systems and procedures as well as for instrument calibration. A high quality zero gas is an important contributor to the quality of the measurements and generally achieved by using state-of-the-art purification technologies. The efficiency of several air purifiers was assessed and the results have been analysed.

  13. 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

  14. Primary VOC emissions from Commercial Aircraft Jet Engines

    Science.gov (United States)

    Kilic, Dogushan; Huang, Rujin; Slowik, Jay; Brem, Benjamin; Durdina, Lukas; Rindlisbacher, Theo; Baltensperger, Urs; Prevot, Andre

    2014-05-01

    Air traffic is growing continuously [1]. The increasing number of airplanes leads to an increase of aviation emissions giving rise to environmental concerns globally by high altitude emissions and, locally on air quality at the ground level [2]. The overall impact of aviation emissions on the environment is likely to increase when the growing air transportation trend [2] is considered. The Aviation Particle Regulatory Instrumentation Demonstration Experiment (APRIDE)-5 campaign took place at Zurich Airport in 2013. In this campaign, aircraft exhaust is sampled during engine acceptance tests after engine overhaul at the facilities of SR Technics. Direct sampling from the engine core is made possible due to the unique fixed installation of a retractable sampling probe and the use of a standardized sampling system designed for the new particulate matter regulation in development for aircraft engines. Many of the gas-phase aircraft emissions, e.g. CO2, NOX, CO, SO2, hydrocarbons, and volatile organic compounds (VOC) were detected by the instruments in use. This study, part of the APRIDE-5 campaign, focuses on the primary VOC emissions in order to produce emission factors of VOC species for varying engine operating conditions which are the surrogates for the flight cycles. Previously, aircraft plumes were sampled in order to quantify VOCs by a proton transfer reaction quadrupole mass spectrometer (PTR-MS) [3]. This earlier study provided a preliminary knowledge on the emission of species such as methanol, acetaldehyde, acetone, benzene and toluene by varying engine thrust levels. The new setup was (i) designed to sample from the diluted engine exhaust and the new tool and (ii) used a high resolution time of flight PTR-MS with higher accuracy for many new species, therefore providing a more detailed and accurate inventory. We will present the emission factors for species that were quantified previously, as well as for many additional VOCs detected during the campaign

  15. Volatile organic compound (VOC) determination in working atmospheres; Determinacion de compuestos organicos volatiles (VOC) en ambiente laboral

    Energy Technology Data Exchange (ETDEWEB)

    Blass A, Georgina; Panama T, Luz A; Corrales C, Deyanira [Instituto de Investigaciones Electricas, Cuernavaca, Morelos (Mexico)

    2003-07-01

    The present work describes, in a synthesized way, the implementation and application of procedures based on the normativity related to the subject of the volatile organic compounds (Volatile Organic Compounds VOC), that allow to sample, quantify and evaluate the present contamination in the working atmosphere of a refinery due to the fugitive emissions of VOC and other substances. In accordance with the corresponding normativity, more than 189 organic compounds denominated dangerous air polluting agents (Hazardous Air Pollutants, HAP) can be found in a working atmosphere, but they are the 11 main HAP that can be found in a refinery. In the present article the work made for the sampling and quantification of 5 of the 11 dangerous polluting agents of the air: benzene, toluene, xylene, iso-octane and naphthalene. [Spanish] El presente trabajo describe, de manera sintetizada, la implementacion y aplicacion de procedimientos basados en la normatividad relacionada al tema de los compuestos organicos volatiles (Volatil Organic Compounds, VOC), que permiten muestrear, cuantificar y evaluar la contaminacion presente en el ambiente laboral de una refineria debido a las emisiones fugitivas de VOC y otras sustancias. De acuerdo con la normatividad correspondiente, mas de 189 compuestos organicos denominados contaminantes peligrosos del aire (Hazardous Air Pollutants, HAP), pueden ser encontrados en un ambiente laboral, pero son 11 los principales HAP que pueden ser hallados en una refineria. En el presente articulo se informa el trabajo realizado para el muestreo y cuantificacion de 5 de los 11 contaminantes peligrosos del aire: benceno, tolueno, xileno, iso-octano y naftaleno.

  16. Volatile Organic Compound (VOC Removal by Vapor Permeation at Low VOC Concentrations: Laboratory Scale Results and Modeling for Scale Up

    Directory of Open Access Journals (Sweden)

    Philippe Moulin

    2011-03-01

    Full Text Available Petroleum transformation industries have applied membrane processes for solvent and hydrocarbon recovery as an economic alternative to reduce their emissions and reuse evaporated components. Separation of the volatile organic compounds (VOCs (toluene-propylene-butadiene from air was performed using a poly dimethyl siloxane (PDMS/α-alumina membrane. The experimental set-up followed the constant pressure/variable flow set-up and was operated at ~21 °C. The membrane is held in a stainless steel module and has a separation area of 55 × 10−4 m². Feed stream was set to atmospheric pressure and permeate side to vacuum between 3 and 5 mbar. To determine the performance of the module, the removed fraction of VOC was analyzed by Gas Chromatography/Flame Ionization Detector (GC/FID. The separation of the binary, ternary and quaternary hydrocarbon mixtures from air was performed at different flow rates and more especially at low concentrations. The permeate flux, permeance, enrichment factor, separation efficiency and the recovery extent of the membrane were determined as a function of these operating conditions. The permeability coefficients and the permeate flux through the composite PDMS-alumina membrane follow the order given by the Hildebrand parameter: toluene > 1,3-butadiene > propylene. The simulated data for the binary VOC/air mixtures showed fairly good agreement with the experimental results in the case of 1,3-butadiene and propylene. The discrepancies observed for toluene permeation could be minimized by taking into account the effects of the porous support and an influence of the concentration polarization. Finally, the installation of a 0.02 m2 membrane module would reduce 95% of the VOC content introduced at real concentration conditions used in the oil industry.

  17. Volatile Organic Compound (VOC) Removal by Vapor Permeation at Low VOC Concentrations: Laboratory Scale Results and Modeling for Scale Up.

    Science.gov (United States)

    Rebollar-Perez, Georgette; Carretier, Emilie; Lesage, Nicolas; Moulin, Philippe

    2011-03-03

    Petroleum transformation industries have applied membrane processes for solvent and hydrocarbon recovery as an economic alternative to reduce their emissions and reuse evaporated components. Separation of the volatile organic compounds (VOCs) (toluene-propylene-butadiene) from air was performed using a poly dimethyl siloxane (PDMS)/α-alumina membrane. The experimental set-up followed the constant pressure/variable flow set-up and was operated at ~21 °C. The membrane is held in a stainless steel module and has a separation area of 55 × 10-4 m². Feed stream was set to atmospheric pressure and permeate side to vacuum between 3 and 5 mbar. To determine the performance of the module, the removed fraction of VOC was analyzed by Gas Chromatography/Flame Ionization Detector (GC/FID). The separation of the binary, ternary and quaternary hydrocarbon mixtures from air was performed at different flow rates and more especially at low concentrations. The permeate flux, permeance, enrichment factor, separation efficiency and the recovery extent of the membrane were determined as a function of these operating conditions. The permeability coefficients and the permeate flux through the composite PDMS-alumina membrane follow the order given by the Hildebrand parameter: toluene > 1,3-butadiene > propylene. The simulated data for the binary VOC/air mixtures showed fairly good agreement with the experimental results in the case of 1,3-butadiene and propylene. The discrepancies observed for toluene permeation could be minimized by taking into account the effects of the porous support and an influence of the concentration polarization. Finally, the installation of a 0.02 m2 membrane module would reduce 95% of the VOC content introduced at real concentration conditions used in the oil industry.

  18. Hierarchical porous structured zeolite composite for removal of ionic contaminants from waste streams and effective encapsulation of hazardous waste.

    Science.gov (United States)

    Al-Jubouri, Sama M; Curry, Nicholas A; Holmes, Stuart M

    2016-12-15

    A hierarchical structured composite made from clinoptilolite supported on date stones carbon is synthesized using two techniques. The composites are manufactured by fixing a natural zeolite (clinoptilolite) to the porous surface of date stones carbon or by direct hydrothermal synthesis on to the surface to provide a supported high surface area ion-exchange material for metal ion removal from aqueous streams. The fixing of the clinoptilolite is achieved using sucrose and citric acid as a binder. The composites and pure clinoptilolite were compared to test the efficacy for the removal of Sr(2+) ions from an aqueous phase. The encapsulation of the Sr(2+) using either vitrification or a geo-polymer addition was tested to ensure that the hazardous waste can be made safe for disposal. The hierarchical structured composites were shown to achieve a higher ion exchange capacity per gram of zeolite than the pure clinoptilolite (65mg/g for the pure natural clinoptilolite and 72mg/g for the pure synthesized clinoptilolite) with the synthesized composite (160mg/g) having higher capacity than the natural clinoptilolite composite (95mg/g). The rate at which the equilibria were established followed the same trend showing the composite structure facilitates diffusion to the ion-exchange sites in the zeolite.

  19. Oxidation of Bioethanol using Zeolite-Encapsulated Gold Nanoparticles

    DEFF Research Database (Denmark)

    Mielby, Jerrik Jørgen; Abildstrøm, Jacob Oskar; Wang, Feng

    2014-01-01

    With the ongoing developments in biomass conversion, the oxidation of bioethanol to acetaldehyde may become a favorable and green alternative to the preparation from ethylene. Here, a simple and effective method to encapsulate gold nanoparticles in zeolite silicalite‐1 is reported and their high...... zeolite crystals comprise a broad range of mesopores and contain up to several hundred gold nanoparticles with a diameter of 2–3 nm that are distributed inside the zeolites rather than on the outer surface. The encapsulated nanoparticles have good stability and result in 50 % conversion of ethanol with 98...

  20. Oxidation of Bioethanol using Zeolite-Encapsulated Gold Nanoparticles

    DEFF Research Database (Denmark)

    Mielby, Jerrik Jørgen; Abildstrøm, Jacob Oskar; Wang, Feng

    2014-01-01

    With the ongoing developments in biomass conversion, the oxidation of bioethanol to acetaldehyde may become a favorable and green alternative to the preparation from ethylene. Here, a simple and effective method to encapsulate gold nanoparticles in zeolite silicalite-1 is reported and their high...... zeolite crystals comprise a broad range of mesopores and contain up to several hundred gold nanoparticles with a diameter of 2-3nm that are distributed inside the zeolites rather than on the outer surface. The encapsulated nanoparticles have good stability and result in 50% conversion of ethanol with 98...