The influence of modified zeolites as nucleating agents on crystallization behavior and mechanical properties of polypropylene

International Nuclear Information System (INIS)

Lv, Zhiping; Wang, Kunjun; Qiao, Zhihua; Wang, Wenjie

2010-01-01

Polypropylene (PP) composites with unmodified and modified zeolites were prepared by melt blending in single-screw extruder. The modified zeolites, diethoxy (distearoyl) silane (DDS)-zeolite 13X (DDS-13X) and diethoxy (distearoyl) silane-zeolite 5A (DDS-5A), were obtained by grafting diethoxy (distearoyl) silane onto zeolite 13X and 5A, respectively. The influence of the unmodified and modified zeolites as nucleating agents on properties of polypropylene was investigated with X-ray diffraction (XRD), differential scanning calorimetry (DSC), polarized light microscopy (PLM), Vicat softening temperature (VST) and mechanical properties test. The XRD results revealed that zeolite 13X and DDS-13X had a great influence on nucleation of PP compared to zeolite 5A and DDS-5A. The DSC results showed that the addition of small amount of modified zeolites lead to increase in crystallization temperature (T c ), initial crystallization temperature (T onset ) and crystallinity (X c ) of PP composites compared to unmodified zeolites, especially, DDS-13X was more effective than DDS-5A, and the highest crystallinity X c (50.48%) was observed in PP/0.3 wt.% DDS-13X, which was responsible to the higher tensile strength and flexural strength of PP/DDS-13X. The PP/DDS-5A, however, exhibited evident increase in flexural strength and a little change in tensile strength compared to pure PP. Moreover, as the addition amount of DDS-5A or DDS-13X up to 1 wt.%, the impact strength of both PP/DDS-5A and PP/DDS-13X reached 43 kJ/m 2 , which was about 2.8 times greater than that of the pure PP (11.3 kJ/m 2 ). These results were in good agreement with the spherulite morphology observed from PLM micrographs.

Chloride Diffusion and Acid Resistance of Concrete Containing Zeolite and Tuff as Partial Replacements of Cement and Sand.

Science.gov (United States)

Mohseni, Ehsan; Tang, Waiching; Cui, Hongzhi

2017-03-31

In this paper, the properties of concrete containing zeolite and tuff as partial replacements of cement and sand were studied. The compressive strength, water absorption, chloride ion diffusion and resistance to acid environments of concretes made with zeolite at proportions of 10% and 15% of binder and tuff at ratios of 5%, 10% and 15% of fine aggregate were investigated. The results showed that the compressive strength of samples with zeolite and tuff increased considerably. In general, the concrete strength increased with increasing tuff content, and the strength was further improved when cement was replaced by zeolite. According to the water absorption results, specimens with zeolite showed the lowest water absorption values. With the incorporation of tuff and zeolite, the chloride resistance of specimens was enhanced significantly. In terms of the water absorption and chloride diffusion results, the most favorable replacement of cement and sand was 10% zeolite and 15% tuff, respectively. However, the resistance to acid attack reduced due to the absorbing characteristic and calcareous nature of the tuff.

Preparation and Characterization of Zeolite Membrane for Bioethanol Purification

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Aprilina Purbasari

2013-06-01

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

Strength and deformability of hollow concrete blocks: correlation of block and cylindrical sample test results

OpenAIRE

Barbosa, C. S.; Hanai, J.B.

2009-01-01

This paper deals with correlations among mechanical properties of hollow blocks and those of concrete used to make them. Concrete hollow blocks and test samples were moulded with plastic consistency concrete, to assure the same material in all cases, in three diferente levels of strength (nominally 10 N/mm², 20 N/mm² and 30 N/mm²). The mechanical properties and structural behaviour in axial compression and tension tests were determined by standard tests in blocks and cylinders. Stress and str...

Lithium modified zeolite synthesis for conversion of biodiesel-derived glycerol to polyglycerol

Energy Technology Data Exchange (ETDEWEB)

Ayoub, Muhammad, E-mail: muhammad.ayoub@petronas.com.my [Department of Chemical Engineering, Universiti Teknologi PETRONAS, 31750, Tronoh, Perak, Malaysia and School of Chemical Engineering, Universiti Sains Malaysia, 43000, Pinang (Malaysia); Abdullah, Ahmad Zuhairi, E-mail: chzuhairi@usm.my [School of Chemical Engineering, Universiti Sains Malaysia, 43000, Pinang (Malaysia); Inayat, Abrar, E-mail: abrar.inayat@petronas.com.my [Department of Chemical Engineering, Universiti Teknologi PETRONAS, 31750, Tronoh, Perak (Malaysia)

2014-10-24

Basic zeolite has received significant attention in the catalysis community. These zeolites modified with alkaline are the potential replacement for existing zeolite catalysts due to its unique features with added advantages. The present paper covers the preparation of lithium modified zeolite Y (Li-ZeY) and its activity for solvent free conversion of biodiesel-derived glycerol to polyglycerol via etherification process. The modified zeolite was well characterized by X-ray diffraction (XRD), Scanning Electron Microscope (SEM) and Nitrogen Adsorption. The SEM images showed that there was no change in morphology of modified zeolite structure after lithium modification. XRD patterns showed that the structure of zeolite was sustained after lithium modification. The surface properties of parent and modified zeolite was also observed N{sub 2} adsortion-desorption technique and found some changes in surface area and pore size. In addition, the basic strength of prepared materials was measured by Hammet indicators and found that basic strength of Li-ZeY was highly improved. This modified zeolite was found highly thermal stable and active heterogamous basic catalyst for conversion of solvent free glycerol to polyglycerol. This reaction was conducted at different temperatures and 260 °C was found most active temperature for this process for reaction time from 6 to 12 h over this basic catalyst in the absence of solvent.

Development and evaluation of adsorption block of radiocesium

International Nuclear Information System (INIS)

Arakawa, Tsuyoshi; Yamanishi, Hirokuni; Ito, Tetsuo

2015-01-01

The removal of radioactive cesium from water solutions with some concrete blocks was investigated. When the concrete blocks were prepared by mixing zeolites, the ability of holding and transmitting water was greatly increased. The cesium ions were adsorbed to a certain extent in these concrete blocks. Moreover, when the mixtures of zeolite and metal ferrocyanide were used, the radioactive cesium could be highly removed. In particular, the residual rate of cobalt ferrocyanide was attained to 90% or above. (author)

Physical and mechanical properties of sand stabilized by cement and natural zeolite

Science.gov (United States)

Salamatpoor, Sina; Jafarian, Yaser; Hajiannia, Alborz

2018-05-01

Loose sands are prone to lose their shear strength when being subjected to static or cyclic loads. To this end, there exist several methods to improve the mechanical properties of sands, but the most crucial and viable approach is the one with the lowest harmful environmental impact both in production and recycling processes. In this regard, zeolite as a natural pozzolanic additive offers an eco-friendly improvement in strength parameters of cemented sandy soils. Thereby, in this study, a series of unconfined compressive strength (UCS) tests are conducted to evaluate the mechanical parameters of the zeolite-cemented sand. The results demonstrate a meaningful increase in the UCS of the treated sand samples for replacement of cement by zeolite at an optimum proportion of 40% in specimens with 14 and 28 days curing time. The effectiveness of the improvement process is demonstrated by the strength improvement ratio which was up to be 128% to 209% for the samples with 14 and 28 days curing time, respectively. With regard to the above results, zeolite can be introduced as a promising cement substitute in stabilization of sandy ground including backfills, roadbed, embankments, and other structural filling systems.

Optimum Compressive Strength of Hardened Sandcrete Building Blocks with Steel Chips

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Alohan Omoregie

2013-02-01

Full Text Available The recycling of steel chips into an environmentally friendly, responsive, and profitable commodity in the manufacturing and construction industries is a huge and difficult challenge. Several strategies designed for the management and processing of this waste in developed countries have been largely unsuccessful in developing countries mainly due to its capital-intensive nature. To this end, this investigation attempts to provide an alternative solution to the recycling of this material by maximizing its utility value in the building construction industry. This is to establish their influence on the compressive strength of sandcrete hollow blocks and solid cubes with the aim of specifying the range percent of steel chips for the sandcrete optimum compressive strength value. This is particularly important for developing countries in sub-Saharan Africa, and even Latin America where most sandcrete blocks exhibit compressive strengths far below standard requirements. Percentages of steel chips relative to the weight of cement were varied and blended with the sand in an attempt to improve the sand grading parameters. The steel chips variations were one, two, three, four, five, ten and fifteen percent respectively. It was confirmed that the grading parameters were improved and there were significant increases in the compressive strength of the blocks and cube samples. The greatest improvement was noticed at four percent steel chips and sand combination. Using the plotted profile, the margin of steel chips additions for the optimum compressive strength was also established. It is recommended that steel chip sandcrete blocks are suitable for both internal load bearing, and non-load bearing walls, in areas where they are not subjected to moisture ingress. However, for external walls, and in areas where they are liable to moisture attack after laying, the surfaces should be well rendered. Below ground level, the surfaces should be coated with a water

A Study of Compressive Strength Characteristics of Laterite Sand Hollow Blocks

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Abiodun Olanipekun

2007-01-01

Full Text Available This paper presents the results of experimental investigations carried out on partial replacement of sand with laterite as it affects the compressive strength of sandcrete hollow blocks. Two mix proportions (1:6 and 1:8 were used with laterite content varying between 0 and 50% at 10% intervals. Hand and machine compaction methods were used. Curing was done by sprinkling water on the specimens. The results showed that for each mix proportion and compaction method, the compressive strength decreases with increase in laterite content. Machine compacted hollow sandcrete blocks made from mix ratio 1:6 and with up to 10% laterite content is found suitable and hence recommended for building construction having attained a 28-day compressive strength of 2.07N/mm2 as required by the Nigerian Standards.

Alkali-activated fly ash-based geopolymers with zeolite or bentonite as additives

Energy Technology Data Exchange (ETDEWEB)

Hu, Mingyu; Zhu, Xiaomin; Long, Fumei [Nanchang University, Nanchang (China). College of Civil Engineering

2009-11-15

Geopolymers were synthesized by using fly ash as the main starting material, zeolite or bentonite as supplementary materials, and NaOH and CaO together as activator. An orthogonal array testing protocol was used to analyze the influence of the mix proportion on the properties of the geopolymers. The results indicate that the concentration of NaOH solution and the CaO content play an important role on the strength of the materials. Especially, with zeolite as additive, the fly ash-based geopolymer shows the highest strength and the best sulfate resistance. Infrared spectroscopy, X-ray, and SEM-EDX demonstrate that supplementary zeolite may involve the process of geopolymerization to form a stable zeolitic structure and improve the properties of the geopolymer. Bentonite simply acts as a filler to make the geopolymer more compact, but shows no improvement on the compositions and the microstructures of the geopolymer.

Changing of Sumatra backswamp peat properties by seawater and zeolite application

Science.gov (United States)

Sarifuddin; Nasution, Z.; Rauf, A.; Mulyanto, B.

2018-02-01

This research attempts to improve the properties of backswamp peatsoil originated from Asahan District, North Sumatra Indonesia by adding sea water and zeolite using factorial randomized block design with volume of sea water as first factor, consisting of without seawater, 500 ml, 1000 ml and 1500 ml and second factor are dosages of zeolite consisting of without zeolite, 100 g, 200 g each 10 kgs of wet peat soil. at green house in faculty of agriculture University of Sumatra Utara (USU) Medan, Indonesia. The result showed that the application of seawater decreased pH, C/N and Cation Exchange Capacity and increased of base saturation of peat soil. Adding of zeolite minerals can buffered the increasing of acidity and Electric Conductivity caused by sea water application. Interaction seawater + zeolite decreased of C/N and increased of percent of base saturation.

High ion-exchange properties of hybrid materials from X-type zeolite and ground glass powder

Science.gov (United States)

Taira, Nobuyuki; Yoshida, Kohei

2017-10-01

Zeolites are crystalline aluminosilicates with a homogeneous distribution of micropores with a superior cation-exchange capacity. Because they have especially excellent selective exchange properties, a considerable number of studies have been conducted on treating water containing radioisotopes using the zeolites. When using artificial zeolites, they have inferior sinterability; in addition, it is quite hard for them to remove from polluted liquid since these artificial zeolites are principally synthesized as a form of powder, which is a disadvantage. In this study, hybrid materials were prepared from X-type zeolite and waste glass powder. Their ion-removal effect and mechanical strength were investigated. The zeolite and waste glass were ground in an agate mortar in several ratios. 0.5 g of the mixture was pressure-molded into pellets having a diameter of 7 mm. These pellets were slowly heated at the speed of 240°C/h to 700°C and maintained at 700°C for 2 h. The removal rate of Sr2+ ions increased as the amount of X-type zeolite in the hybrid materials increased; the former increased up to 100% when the content of latter exceeded 50%. The mechanical strength increased by increasing the amount of glass in the hybrid materials. This is attributed to the fact that the glass powder acts as a binder that improves the densification and consequently the mechanical strength of the hybrid materials.

Strength and deformability of hollow concrete blocks: correlation of block and cylindrical sample test results

Directory of Open Access Journals (Sweden)

C. S. Barbosa

Full Text Available This paper deals with correlations among mechanical properties of hollow blocks and those of concrete used to make them. Concrete hollow blocks and test samples were moulded with plastic consistency concrete, to assure the same material in all cases, in three diferente levels of strength (nominally 10 N/mm², 20 N/mm² and 30 N/mm². The mechanical properties and structural behaviour in axial compression and tension tests were determined by standard tests in blocks and cylinders. Stress and strain analyses were made based on concrete’s modulus of elasticity obtained in the sample tests as well as on measured strain in the blocks’ face-shells and webs. A peculiar stress-strain analysis, based on the superposition of effects, provided an estimation of the block load capacity based on its deformations. In addition, a tentative method to preview the block deformability from the concrete mechanical properties is described and tested. This analysis is a part of a broader research that aims to support a detailed structural analysis of blocks, prisms and masonry constructions.

Compressive Strength Of Rice Husk Ash-Cement Sandcrete Blocks ...

African Journals Online (AJOL)

There is growing demand for alternative, low-cost building material in developing countries. The effect of partial substitution of ordinary Portland cement with Rice Husk Ash (RHA) on the compressive strength of hollow sandcrete block was investigated through laboratory experimental procedures. The specific gravity, initial ...

β-Zeolite modified by ethylenediamine for sorption of Th(IV)

Energy Technology Data Exchange (ETDEWEB)

Liu, Peng; Wu, Hanyu; Yuan, Ni; Yin, Zhuoxin; Pan, Duoqiang; Wu, Wangsuo [Lanzhou Univ. (China). Radiochemistry Lab.; Ministry of Education, Lanzhou (China). Key Lab. of Special Function Materials and Structure Design

2017-08-01

β-Zeolite-EDA was modified with ethylenediamine (EDA) after synthesized. The synthesized material was characterized and used for removal of Th(IV) from aqueous solutions. The influences of pH, ionic strength, contact time, temperature and humic acid (HA) on Th(IV) sorption onto synthesized β-zeolite-EDA was studied by batch technique. The dynamic process showed that the sorption of Th(IV) onto β-zeolite-EDA matched the pseudo-second-order kinetics model. The sorption of Th(IV) on β-zeolite-EDA was significantly dependent on pH values, the sorption percentage increased markedly at pH 3.5-4.5, and then maintained a steady state as pH values increased. Through simulating the sorption isotherms by Langmuir, Freundlich and Dubini-Radushkevich (D-R) models, it could be seen respectively that the sorption pattern of Th(IV) on β-zeolite-EDA was mainly controlled by surface complexation, and that the sorption processes was endothermic and spontaneous. The presence of HA increased Th(IV) sorption on β-zeolite-EDA.

Assessment of Structural Strength of Commercial Sandcrete Blocks in Kano State

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M. Mohammed

2014-12-01

Full Text Available This research was aimed at studying the strength properties of the commercial sandcrete blocks produced in Kano State. A total number of 250 block samples were randomly collected from five local government areas, fifty (50 from each of the local governments and cured for 3, 7, 14, 21 and 28 days. The blocks were subjected to various tests at wet and dry conditions as follow: wet compressive test, drying shrinkage, moisture movement and density all in accordance with established standards in the structural laboratory of Department of Civil Engineering, Ahmadu Bello University, Zaria, and the aggregates were subjected to sieve analysis and moisture content determination in the Geotechnical Laboratory of the department. The compressive strength was found to be between 0.25 N/mm2 and 0.92 N/mm2 which are far below the specified values (2.5 N/mm2 to 3.45N/mm2 respectively in the Nigerian Industrial Standard (NIS 87, 2000. It is concluded that the commercially produced sandcrete blocks in Kano State are of lower standard than expected. It is recommended that workshop should be organised periodically to enlighten the producers of sandcrete blocks. The importance of adhering to standard specifications should be emphasised and strict penalties be meted out to erring producers by the Nigerian Industrial Standard Organisation.

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

Energy Technology Data Exchange (ETDEWEB)

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

2017-06-15

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

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.

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...

Application of NKF-6 zeolite for the removal of U(VI) from aqueous solution

International Nuclear Information System (INIS)

Pengfei Zong; Hai Wang; Hui Pan; Yaolin Zhao; Chaohui He

2013-01-01

To better understand the application of NKF-6 zeolite as an adsorbent for the removal of U(VI) from radionuclides and heavy metal ions polluted water, herein, NKF-6 zeolite was employed to remove U(VI) at different experimental conditions. The influence of solid/liquid ratio, contact time, pH, ionic strength, humic substances and temperature on sorption of U(VI) to NKF-6 zeolite was investigated using batch technique under ambient conditions. The experimental results demonstrated that the sorption of U(VI) on NKF-6 zeolite was strongly dependent on pH. The sorption property of U(VI) was influenced by ionic strength at pH 7.0. The presence of fulvic acid or humic acid promoted the sorption of U(VI) on NKF-6 zeolite at low pH values while restrained the sorption at high pH values. The thermodynamic parameters (i.e., ΔS 0 , ΔH 0 , and ΔG 0 ) calculated from the temperature-dependent sorption isotherms demonstrated that the sorption process of U(VI) on NKF-6 zeolite was endothermic and spontaneous. At low pH values, the sorption of U(VI) was dominated by outer-sphere surface complexation and ion exchange with Na + /H + on NKF-6 zeolite surfaces, while inner-sphere surface complexation was the main sorption mechanism at high pH values. From the experimental results, one can conclude that NKF-6 zeolite can be used as a potential adsorbent for the preconcentration and solidification of U(VI) from large volumes of aqueous solutions. (author)

Zeolite studies. Aluminium phosphate zeolites

Energy Technology Data Exchange (ETDEWEB)

Haegh, G.S.; Blindheim, U.

1983-12-01

Alpo-zeolites (ALPO4-zeolites) have been synthesized by hydrothermal synthesis in an autoclave from alumina, tetralkylammonium hydroxide and phosphorus acid. Catalysis tests with hydrocarbons indicate that the compounds have good olefinisomerization activity and selectivity.

Shape-selective zeolite catalysis for bioplastics production

Science.gov (United States)

Dusselier, Michiel; Van Wouwe, Pieter; Dewaele, Annelies; Jacobs, Pierre A.; Sels, Bert F.

2015-07-01

Biodegradable and renewable polymers, such as polylactic acid, are benign alternatives for petrochemical-based plastics. Current production of polylactic acid via its key building block lactide, the cyclic dimer of lactic acid, is inefficient in terms of energy, time, and feedstock use. We present a direct zeolite-based catalytic process, which converts lactic acid into lactide. The shape-selective properties of zeolites are essential to attain record lactide yields, outperforming those of the current multistep process by avoiding both racemization and side-product formation. The highly productive process is strengthened by facile recovery and practical reactivation of the catalyst, which remains structurally fit during at least six consecutive reactions, and by the ease of solvent and side-product recycling.

Surfactant-modified zeolites as permeable barriers to organic and inorganic groundwater contaminants

International Nuclear Information System (INIS)

Bowman, R.S.; Sullivan, E.J.

1995-01-01

We have shown in laboratory experiments that natural zeolites treated with hexadecyltrimethylammonium (HDTMA) are effective sorbents for nonpolar organics, inorganic cations, and inorganic anions. Due to their low cost (∼$0.75/kg) and granular nature, HDTMA-zeolites appear ideal candidates for reactive, permeable subsurface barriers. The HDTMA-zeolites are stable over a wide range of pH (3-13), ionic strength (1 M Cs + or Ca 2+ ), and in organic solvents. Surfactant-modified zeolites sorb nonpolar organics (benzene, toluene, xylene, chlorinated aliphatics) via a partitioning mechanism, inorganic cations (Pb 2+ ) via ion exchange and surface complexation, and inorganic anions (CrO 4 2- , SeO 4 2- , SO 4 2- ) via surface precipitation.The goal of this work is to demonstrate the use of surfactant-modified zeolite as a permeable barrier to ground water contaminants

Syntheses, characterizations, and catalytic activities of mesostructured aluminophosphates with tailorable acidity assembled with various preformed zeolite nanoclusters

KAUST Repository

Suo, Hongri

2015-02-25

© 2015, Springer Science+Business Media New York. A series of ordered hexagonal mesoporous zeolites have been successfully synthesized by the assembly of various preformed aluminosilicates zeolite (MFI, FAU, BEA etc.) with surfactants (cetyltrimethylammonium chloride) under hydrothermal conditions. These unique samples were further characterized by X-ray diffraction, transmission electron microscopy, N2 adsorption, infrared spectroscopy. Characterization results showed that these samples contain primary and secondary structural building units of various zeolites, which may be responsible for their distinguished acidic strength, suggesting that the acidic strength of these mesoporous silicoaluminophosphates could be tailored and controlled. Furthermore, the prepared samples were catalytically active in the cracking of cumene.

Xenon capture on silver-loaded zeolites: characterization of very strong adsorption sites

International Nuclear Information System (INIS)

Daniel, Cecile; Elbaraoui, Adnane; Aguado, Sonia; Schuurman, Yves; Farrusseng, David; Springuel-Huet, Marie-Anne; Nossov, Andrei; Fontaine, Jean-Pierre; Topin, Sylvain; Taffary, Thomas; Deliere, Ludovic

2013-01-01

The number and strength of adsorption sites for Xe in silver-modified zeolites are estimated from isotherm measurements at various temperatures over a broad range of pressure (from 1 ppm to atmospheric pressure). Fully and partially exchanged silver zeolites were synthesized starting from Na-ZSM-5(25), Na-ZSM-5(40), Na-Beta, NaX, and NaY. We have discovered that silver-modified zeolites may present one or two distinct adsorption sites depending on the nature of the material and silver loadings. The strongest adsorption sites are characterized by isosteric heat of adsorption in the order of -40 to -50 kJ.mol -1 . For Pentasil-type zeolites, we observe a linear 2:1 correlation between the total amount of silver and the number of strong sites. The highest concentration of strong sites is found for fully silver exchanged ZSM-5 (5.7 * 10 -4 mol/g), which presents the largest silver content for Pentasil-type zeolite. The equilibrium constant of Ag-ZSM-5 at low pressure is about 50 times larger than that of AgX. Qualitative correlations were established between Xe adsorption isotherms and Xe NMR signals. We show that Xe NMR could be used as a quantitative method for the characterization of the strength and of the number of strong Xe adsorption sites on silver-exchanged zeolites. The numbers of strong adsorption sites responsible for the Xe adsorption at 10-1000 ppm can be determined by the length of the plateau observed at low Xe uptake. In practice, our findings give guidelines for the discovery and optimization of silver-loaded zeolites for the capture of Xe at ppm levels. It appears that the amount of silver is a key parameter. Silver-modified ZSM-5 shows adsorption capacities 2-3 orders of magnitude larger than currently applied adsorbents for atmospheric Xe capture. (authors)

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...

Hydrothermal conversion of FAU zeolite into RUT zeolite in TMAOH system

OpenAIRE

Jon, Hery; Takahashi, Shoutarou; Sasaki, Hitoshi; Oumi, Yasunori; Sano, Tsuneji

2008-01-01

The highly crystalline and pure RUT (RUB-10) zeolite could be obtained from the hydrothermal conversion of FAU zeolite used as a crystalline Si/Al source in tetramethylammonium hydroxide (TMAOH) media. As compared to amorphous silica/Al(OH)3 and amorphous silica/γ-Al2O3 sources, the crystallization rate for the formation of RUT zeolite was clearly faster when FAU zeolite was employed as the Si/Al source. Moreover, it was found that the hydrothermal conversion of FAU zeolite into RUT zeolite d...

A Hierarchically Micro-Meso-Macroporous Zeolite CaA for Methanol Conversion to Dimethyl Ether

Directory of Open Access Journals (Sweden)

Yan Wang

2016-11-01

Full Text Available A hierarchical zeolite CaA with microporous, mesoporous and macroporous structure was hydrothermally synthesized by a ”Bond-Blocking” method using organo-functionalized mesoporous silica (MS as a silica source. The characterization by XRD, SEM/TEM and N2 adsorption/desorption techniques showed that the prepared material had well-crystalline zeolite Linde Type A (LTA topological structure, microspherical particle morphologies, and hierarchically intracrystalline micro-meso-macropores structure. With the Bond-Blocking principle, the external surface area and macro-mesoporosity of the hierarchical zeolite CaA can be adjusted by varying the organo-functionalized degree of the mesoporous silica surface. Similarly, the distribution of the micro-meso-macroporous structure in the zeolite CaA can be controlled purposely. Compared with the conventional microporous zeolite CaA, the hierarchical zeolite CaA as a catalyst in the conversion of methanol to dimethyl ether (DME, exhibited complete DME selectivity and stable catalytic activity with high methanol conversion. The catalytic performances of the hierarchical zeolite CaA results clearly from the micro-meso-macroporous structure, improving diffusion properties, favoring the access to the active surface and avoiding secondary reactions (no hydrocarbon products were detected after 3 h of reaction.

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.

Adsorption characteristics of Cs"+ onto artificial zeolites synthesized from coal fly ash and diatomite

International Nuclear Information System (INIS)

Johan, Erni; Yoshida, Kohei; Itagaki, Yoshiteru; Aono, Hiromichi; Munthali, Moses Wazingwa; Matsue, Naoto

2015-01-01

The radioactive decontamination of water, soil and other materials requires cheap and effective adsorbents. Artificial zeolites synthesized from an industrial waste (coal fly ash: Na-P1 type zeolite) and a natural material (diatomite: mordenite type zeolite) have a high Cs"+ adsorptivity in the adsorption experiments using 0.1 g of the zeolite and 50 mL of up to 7.5 mM CsCl. The coexisting cation suppressed the Cs"+ adsorption onto the zeolites, and the effect of the suppression was in the order, K"+ > Na"+ > Ca"2"+ > Mg"2"+. A thermodynamic analysis proved that the Cs"+ adsorption onto the two zeolites was exothermic favoring a lower temperature. The artificial mordenite showed a greater Cs"+ adsorption strength, higher distribution coefficient and lower ΔG°, especially at low Cs"+ concentrations. Adsorption isotherm analysis by the Langmuir, Freundlich, Temkin and Dubinin-Radushkevich models showed a greater Cs"+ adsorption selectivity for the artificial mordenite even at a low pH. (author)

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.

Hydrogen radiolytic release from zeolite 4A/water systems under γ irradiations

International Nuclear Information System (INIS)

Frances, Laëtitia; Grivet, Manuel; Renault, Jean-Philippe; Groetz, Jean-Emmanuel; Ducret, Didier

2015-01-01

Although the radiolysis of bulk water is well known, some questions remain in the case of adsorbed or confined water, especially in the case of zeolites 4A, which are used to store tritiated water. An enhancement of the production of hydrogen is described in the literature for higher porous structures, but the phenomenon stays unexplained. We have studied the radiolysis of zeolites 4A containing different quantities of water under 137 Cs gamma radiation. We focused on the influence of the water loading ratio. The enhancement of hydrogen production compared with bulk water radiolysis has been attributed to the energy transfer from the zeolite to the water, and to the influence of the water structure organization in the zeolite. Both were observed separately, with a maximum efficiency for energy transfer at a loading ratio of about 13%, and a maximum impact of structuration of water at a loading ratio of about 4%. - Highlights: • We irradiated samples of zeolites 4A which contained different quantities of water. • We measured the quantity of hydrogen released. • Hydrogen radiolytic yields, present two maxima, for two water loading ratios. • Hydrogen release is enhanced by the strength of the zeolite/water interaction. • Hydrogen release is enhanced by the quantity of water interacting with the zeolite

Effect of zeolite on the nitrogen fertilizer efficiency in rice crop

International Nuclear Information System (INIS)

Villareal-Nunez, Jose Ezequiel; Barahona-Amores, Luis Alberto; Castillo-Ortiz, Ovidio Antonio

2015-01-01

The objective of this work was to evaluate the effect of zeolite on the efficiency of nitrogen fertilizer in rice crop. The experiment was conducted in Cacao, Tonosi, Los Santos, Panama, between August and December 2012 and 2013 under rainfed conditions. The rice variety used was IDIAP FL 106-11 with seeding density of 110 kg/ha in a medium- fertility vertic Fluvisol. This study consisted of five treatments with four replications, following a completely randomized block design using N rate of 80 kg/ha mixed with different percentages of zeolite (0; 15; 25; 35 and 45%). The isotopic technique 15 N 3% excess to determine the nitrogen fertilizer use efficiency (EUNF) was used. Each experimental unit consist of 15 m 2 with three micro-plots of 1 m 2 where 15 N-labeled urea was applied at different times of the crop cycle to determine EUNF in each application. Top grain yields were obtained with 80 kg N + 45% zeolite/ha and 80 kg N + 15% zeolite/ha. A 7% EUNF increase was achieved with the addition of natural zeolite. Small doses of 12 kg/ha (15%) of zeolite can improve EUNF; after subsequent experiments, it is recommended to reduce the amount of N applied in soils with similar soil and climatic conditions suitable for growing rice. (author) [es

Comparison of compressive strength of paving block with a mixture of Sinabung ash and paving block with a mixture of lime

Science.gov (United States)

Hastuty, I. P.; Sembiringand Nursyamsi, I. S.

2018-02-01

Paving block is one of the material used as the top layer of road structure besides asphalt and concrete paving block is usually made of mixed material such as Portland cement or other adhesive material, water, and aggregate. People nowadays prefer paving block compared to other pavement such as concrete or asphalt. Their interest toward the use of paving block increase because paving block is an eco-friendly construction which is very useful in helping soil water conservation, can be done faster, has easier installation and maintenance, has a variety of shades that increase the aesthetic value, also costs cheaper than the other. Preparation of the specimens with a mixture of Sinabung ash and a mixture of Sinabung ash and lime are implemented with a mixture ratio of cement : sand : stone ash is 1: 2 : 3. The mixture is used as a substitute material by reducing the percentage amount of the weight of the cement with the composition ratio variation based on the comparative volume category of the paving block aggregate, i.e. 0%, 5%, 10%, 15%, 20%, and 25%. The result of this research shows that the maximum compressive strength value is 42.27 Mpa, it was obtained from a mixture of 10% lime with curing time 28 days. The maximum compressive strength value which is obtained from the mixture of sinabung ash is 41.60 Mpa, it was obtained from a mixture of 15% sinabung ash. From the use of these two materials, paving blocks produced are classified as paving blocks quality A and B (350 - 400 Mpa) in accordance to specification from SNI 03-0691-1996.

Metal-Exchanged β Zeolites as Catalysts for the Conversion of Acetone to Hydrocarbons

Directory of Open Access Journals (Sweden)

Aurora J. Cruz-Cabeza

2012-01-01

Full Text Available Various metal-β zeolites have been synthesized under similar ion-exchange conditions. During the exchange process, the nature and acid strength of the used cations modified the composition and textural properties as well as the Brönsted and Lewis acidity of the final materials. Zeolites exchanged with divalent cations showed a clear decrease of their surface Brönsted acidity and an increase of their Lewis acidity. All materials were active as catalysts for the transformation of acetone into hydrocarbons. Although the protonic zeolite was the most active in the acetone conversion (96.8% conversion, the metal-exchanged zeolites showed varied selectivities towards different products of the reaction. In particular, we found the Cu-β to have a considerable selectivity towards the production of isobutene from acetone (over 31% yield compared to 7.5% of the protonic zeolite. We propose different reactions mechanisms in order to explain the final product distributions.

Immobilization of radioactive waste through cementation using Cuban zeolitic rock as additive

International Nuclear Information System (INIS)

Chales Suarez, G.; Castillo Gomez, R.

1997-01-01

The cementation of both simulated and real low level aqueous wastes using Cuban zeolite as additive is described. Mechanical characteristics and leach testing of the cemented waste forms has been studied. The results obtained have shown that the presence of zeolite in the cemented waste for reduces considerably the leach rates of Cs and Co and moreover, mechanical characteristics (set time and compressive strength) are better when compared with direct cementation of aqueous wastes. (author). 13 refs, 8 tabs

Preparation of zeolite-A/chitosan hybrid composites and their bioactivities and antimicrobial activities

International Nuclear Information System (INIS)

Yu, Liang; Gong, Jie; Zeng, Changfeng; Zhang, Lixiong

2013-01-01

Zeolite-A/chitosan hybrid composites with zeolite contents of 20–55 wt.% were prepared by in situ transformation of silica/chitosan mixtures in a sodium aluminate alkaline solution through impregnation–gelation–hydrothermal synthesis. The products were characterized by X-ray diffraction, diffuse reflectance infrared Fourier transform spectroscopy, scanning electron microscopy, thermogravimetric analysis, and mercury penetration porosimetry. Their in vitro bioactivities were examined using as-synthesized and Ca 2+ -exchanged hybrid composites in simulated body fluid (SBF) for hydroxyapatite (HAP) growth. Their antimicrobial activities for Escherichia coli (E. coli) in trypticase soy broth (TSB) were evaluated using Ag + -exchanged hybrid composites. The zeolite-A/chitosan hybrid composites could be prepared as various shapes, including cylinders, plates and thin films. They possessed macropores with pore sizes ranging from 100 to 300 μm and showed compressive mechanical strength as high as 3.2 MPa when the zeolite content was 35 wt.%. Fast growth on the Ca 2+ -exchanged hybrid composites was observed with the highest weight gain of 51.4% in 30 days. The 35 wt.% Ag + -exchanged hybrid composite showed the highest antimicrobial activity, which could reduce the 9 × 10 6 CFU mL −1 E. coli concentration to zero within 4 h of incubation time with the Ag + -exchanged hybrid composite amount of 0.4 g L −1 . The bioactivity and antimicrobial activity could be combined by ion-exchanging the composites first with Ca 2+ and then with Ag + . These zeolite-A/chitosan hybrid composites have potential applications on tissue engineering and antimicrobial food packaging. - Graphical abstract: Zeolite A/chitosan hybrid composites were prepared by in situ transformation of precursors in the chitosan matrix, which possess macroporous structures and exhibit superior bioactivity and antimicrobial activity and potential biomedical application. Highlights: • Zeolite A

Preparation of zeolite-A/chitosan hybrid composites and their bioactivities and antimicrobial activities

Energy Technology Data Exchange (ETDEWEB)

Yu, Liang; Gong, Jie [State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemistry and Chemical Engineering, Nanjing University of Technology, Nanjing 210009 (China); Zeng, Changfeng [College of Mechanic and Power Engineering, Nanjing University of Technology, Nanjing 210009 (China); Zhang, Lixiong, E-mail: lixiongzhang@yahoo.com [State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemistry and Chemical Engineering, Nanjing University of Technology, Nanjing 210009 (China)

2013-10-15

Zeolite-A/chitosan hybrid composites with zeolite contents of 20–55 wt.% were prepared by in situ transformation of silica/chitosan mixtures in a sodium aluminate alkaline solution through impregnation–gelation–hydrothermal synthesis. The products were characterized by X-ray diffraction, diffuse reflectance infrared Fourier transform spectroscopy, scanning electron microscopy, thermogravimetric analysis, and mercury penetration porosimetry. Their in vitro bioactivities were examined using as-synthesized and Ca{sup 2+}-exchanged hybrid composites in simulated body fluid (SBF) for hydroxyapatite (HAP) growth. Their antimicrobial activities for Escherichia coli (E. coli) in trypticase soy broth (TSB) were evaluated using Ag{sup +}-exchanged hybrid composites. The zeolite-A/chitosan hybrid composites could be prepared as various shapes, including cylinders, plates and thin films. They possessed macropores with pore sizes ranging from 100 to 300 μm and showed compressive mechanical strength as high as 3.2 MPa when the zeolite content was 35 wt.%. Fast growth on the Ca{sup 2+}-exchanged hybrid composites was observed with the highest weight gain of 51.4% in 30 days. The 35 wt.% Ag{sup +}-exchanged hybrid composite showed the highest antimicrobial activity, which could reduce the 9 × 10{sup 6} CFU mL{sup −1}E. coli concentration to zero within 4 h of incubation time with the Ag{sup +}-exchanged hybrid composite amount of 0.4 g L{sup −1}. The bioactivity and antimicrobial activity could be combined by ion-exchanging the composites first with Ca{sup 2+} and then with Ag{sup +}. These zeolite-A/chitosan hybrid composites have potential applications on tissue engineering and antimicrobial food packaging. - Graphical abstract: Zeolite A/chitosan hybrid composites were prepared by in situ transformation of precursors in the chitosan matrix, which possess macroporous structures and exhibit superior bioactivity and antimicrobial activity and potential biomedical

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

DEFF Research Database (Denmark)

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

2007-01-01

Recently, a new family of crystalline zeolitic materials was reported, the so-called mesoporous zeolite single crystals featuring individual zeolite single crystals with an additional noncrystalline mesopore system interconnected with the usual micropore system of the zeolite, resulting...... measurements. Additionally, the results of diffusion of n-hexadecane in conventional and mesoporous zeolites are presented. Isomerization and cracking of n-hexadecane was chosen as model test reaction for these materials. All results support that mesoporous zeolites are superior catalysts due to improved mass...... transport. Importantly, the mesoporous zeolites show significant improved resistance to poisoning by carbon formation....

Pemanfaatan zeolit sebagai bahan pengisi dalam pembuatan karet sponge untuk tatakan sepatu

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Herminiwati Herminiwati

2007-06-01

Full Text Available The purpose of this research was to study the effect of zeolite as filler in the preparation of sponge rubber for shoe insocks. During wearing period of shoes, unpleasant odor often smell for the result of sweat accumulation and their decomposition by microorganism. Besides as rubber filler, zeolit has odor adsorption function. The formula of rbber sponge could be as the following : crepe rubber 100 phr, paraffinic oil 20 phr, ZnO 10 phr, stearic acid 5 phr, MBTS 1 phr, TMTD 0.25 phr, anti-oxidant 1 phr and sulphur 2 phr. To obtain the best sponge rubber formula, some experiment was done by formulating variation of zeolite and blowing agent AZDM in the amount of 25, 50, 75 phr and 5, 10, 15 phr respectively. The vulcanization process was carried-out at temperature 140oC for minutes by compression moulding. The research showed that the best formula with high odor absorption was consist of zeolite 50 phr and blowing agent AZDM 5 phr. The sponge rubber had odor adsorption 93,47%, and the physical properties were as follow: tensile strength 2.018 N/mm2, elongation at break 251%, tear strength 1.029 N/mm2, density 0.717 g/cm3, and compression set 36.38%. Odor absorption was tested by using gas chromatography.

Synthesis of Zeolite NaA from Low Grade (High Impurities) Indonesian Natural Zeolite

OpenAIRE

Mustain, Asalil; Wibawa, Gede; Nais, Mukhammad Furoiddun; Falah, Miftakhul

2014-01-01

The zeolite NaA has been successfully synthesized from the low grade natural zeolite with high impurities. The synthesis method was started by mixing natural zeolite powder with NH4Cl aqueous solution in the reactor as pretreatment. The use of pretreatment was to reduce the impurities contents in the zeolite. The process was followed by alkaline fusion hydrothermal treatment to modify the framework structure of natural zeolite and reduce the SiO2/Al2O3 ratio. Finally, the synthesized zeolite ...

Catalytic performance of Metal‐Organic‐Frameworks vs. extra‐large pore zeolite UTL incondensation reactions

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Mariya eShamzhy

2013-08-01

Full Text Available Catalytic behavior of isomorphously substituted B‐, Al‐, Ga‐, and Fe‐containing extra‐large pore UTLzeolites was investigated in Knoevenagel condensation involving aldehydes, Pechmann condensationof 1‐naphthol with ethylacetoacetate, and Prins reaction of β‐pinene with formaldehyde andcompared with large‐pore aluminosilicate zeolite BEA and representative Metal‐Organic‐FrameworksCu3(BTC2 and Fe(BTC. The yield of the target product over the investigated catalysts in Knoevenagelcondensation increases in the following sequence: (AlBEA < (AlUTL < (GaUTL < (FeUTL < Fe(BTC <(BUTL < Cu3(BTC2 being mainly related to the improving selectivity with decreasing strength ofactive sites of the individual catalysts. The catalytic performance of Fe(BTC, containing the highestconcentration of Lewis acid sites of the appropriate strength is superior over large‐pore zeolite(AlBEA and B‐, Al‐, Ga‐, Fe‐substituted extra‐large pore zeolites UTL in Prins reaction of β‐pinene withformaldehyde and Pechmann condensation of 1‐naphthol with ethylacetoacetate.

CO{sub 2} adsorption in amine-grafted zeolite 13X

Energy Technology Data Exchange (ETDEWEB)

Bezerra, Diôgo P. [GPSA, Universidade Federal do Ceará (Brazil); Instituto Federal de Educação, Ciência e Tecnologia do Rio Grande do Norte, Campus Ipanguaçu, Rio Grande do Norte (Brazil); Silva, Francisco W.M. da; Moura, Pedro A.S. de; Sousa, Allyson G.S.; Vieira, Rodrigo S. [GPSA, Universidade Federal do Ceará (Brazil); Rodriguez-Castellon, Enrique [Departamento de Química Inorgánica, Facultad de Ciencias, Universidad de Málaga, 29071 Málaga (Spain); Azevedo, Diana C.S., E-mail: diana@gpsa.ufc.br [GPSA, Universidade Federal do Ceará (Brazil)

2014-09-30

Highlights: • CO{sub 2} adsorption mechanism in amine-grafted zeolite 13X was investigated. • The loaded amine tends to fill zeolite micropores and most of it is unaccessible to react with CO{sub 2}. • Part of loaded MEA binds covalently to the zeolitic structure and will not detach from the surface even at low pressures. • Chemisorption is likely to lead to CO{sub 2} higher uptakes upon a rise in temperature for solids with the highest amine load. - Abstract: The adsorption of CO{sub 2} on Zeolite 13X functionalized with amino groups was studied. Adsorbent functionalization was carried out by grafting with different loads of monoethanolamine (MEA). The adsorbents were characterized by N{sub 2} adsorption/desorption isotherms at 77 K, x-ray diffraction, TGA, in situ FTIR, XPS and adsorption microcalorimetry. CO{sub 2} isotherms were studied in a gravimetric device up to 10 bar at 298 and 348 K. It was found that increasing loads of amine to the adsorbent tend to reduce micropore volume of the resulting adsorbents by pore blocking with MEA. There is experimental evidence that part of the loaded MEA is effectively covalently bonded to the zeolitic structure, whereas there is also physisorbed excess MEA which will eventually be desorbed by raising the temperature beyond MEA boiling point. Heats of adsorption at nearly zero coverage indicate that some of the adsorbed CO{sub 2} reacts with available amino groups, which agrees with the finding that the adsorption capacity increases with increasing temperature for the modified zeolite with the highest MEA load.

Electron irradiation of zeolites

International Nuclear Information System (INIS)

Wang, S.X.; Wang, L.M.; Ewing, R.C.

1999-01-01

Three different zeolites (analcime, natrolite, and zeolite-Y) were irradiated with 200 keV and 400 keV electrons. All zeolites amorphized under a relatively low electron fluence. The transformation from the crystalline-to-amorphous state was continuous and homogeneous. The electron fluences for amorphization of the three zeolites at room temperature were: 7.0 x 10 19 e - /cm 2 (analcime), 1.8 x 10 20 e - /cm 2 (natrolite), and 3.4 x 10 20 e - /cm 2 (zeolite-Y). The different susceptibilities to amorphization are attributed to the different channel sizes in the structures which are the pathways for the release of water molecules and Na + . Natrolite formed bubbles under electron irradiation, even before complete amorphization. Analcime formed bubbles after amorphization. Zeolite-Y did not form bubbles under irradiation. The differences in bubble formation are attributed to the different channel sizes of the three zeolites. The amorphization dose was also measured at different temperatures. An inverse temperature dependence of amorphization dose was observed for all three zeolites: electron dose for amorphization decreased with increasing temperature. This unique temperature effect is attributed to the fact that zeolites are thermally unstable. A semi-empirical model was derived to describe the temperature effect of amorphization in these zeolites

Deposition of 60Co and 137Cs adsorbed on zeolite in matrices on the blast furnace slag

International Nuclear Information System (INIS)

Foeldesova, M.; Lukac, P.; Dillinger, P.

1995-01-01

The experimental data (leaching tests and compressive strength measurements) are presented for case the radionuclides from model water solution and radioactive waste water were uptake on natural and chemically modified granular zeolitic tuffite which show improved sorption ability and were subsequently incorporated into cement casts on blast furnace slags (BSF) basis. The all experiment were carried out with zeolite tuffite from Nizny Hrabovec, Slovak Republic. The natural zeolite was treated by the NaOH solution. The blends of individual components were casted into rectangular prism moulds (1 x 1 x 3 cm). The cast consisted invariably of 90% of BSF, 10% of fine zeolite and solution of water glass and to this basic mixture were added either 10 or 20% granular active, or non active zeolite during the mix formation, in excess to content of previous solid components. The water/cement ratio varied in interval 0.32-0.40. Model solutions labelled by cesium-137 or cobalt-60 have been used for sorption experiment and real waste water concentrate from NPP Jaslovske Bohunice as well. The real water consisted of cesium-134, cesium-137, cobalt-60, in borate and nitrate form. The radioactivity of dry cement casts was measured in 4π geometry. The leaching experiments were performed in three solutions: water (W), 0.03 M HCl (A) and 0.04 M NaOH (B). The mechanical properties of sample with non active granular zeolites and their corrosion characteristics as reflected by the bulk density changes. The experiments showed that leaching of radionuclides, which were sorbed from solution and radioactive waste water, in water and bases solution were negligible. Changes of radioactivity of casts, prepared from model solution, in acid solution, which were less than 5%. The mechanical strength of prepared composites is favourable and shows good compatibility of zeolitic additives with a basic matrix. Leaching experiments and mechanical strength are hopeful and show good retention of observed

Mechanical Property Of Zeolite-PVA Composite Mixture Irradiated By Gamma Ray Of Co-60

International Nuclear Information System (INIS)

Darsono; Danu, Sugiarto; Las, Tamzil

2000-01-01

Experiment on preparation of zeolite-polyvinyl alcohol composite for absorbance materials have been done by curring using Gamma γ-ray of Co-60. Zeolite with the particles size of 60 mesh was mixed with polyvinyl alcohol (PVA) at the concentration of the mixture were 6,9, and 12% by weight, than they were poured into glass tube (length = 100 mm; diameter = 10 mm) and irradiated at the doses of 10, 20, 30 dan 40 kGy with the dose rate of 7,5 kGy/ hr. Parameters observed were density, compressive strength, and hardness. Experimental results showed that polyvinyl alcohol in the mixture was significant effect to density and compressive strength, where as the irradiation dose was highly significant effect to compressive strength. The effect interaction between dose and polyvinyl alcohol concentration factors had significant effect to density or compressive strength. Almost all samples have pencil hardness of 4 - 5 H, for composite containing 6 % PVA, has pencil hardness of 2 - 3 H

Effect of precipitation conditions on the magnetic and sorption properties of zeolite-maghemite composites

International Nuclear Information System (INIS)

Matik, M.; Pechousek, J.; Zboril, R.; Sepelak, V.

2006-01-01

Natural zeolite (clinoptilolite) from Nizny Hrabovec (Slovakia) has been magnetically modified through maghemite (γ-Fe 2 O 3 ) nanoparticles by precipitation route at various reaction conditions. An effect of the precipitation temperature, weight ratio of Fe/zeolite and interaction time on the magnetic and surface properties of maghemite-zeolite composites was monitored by Moessbauer spectroscopy, TEM and BET surface area measurements. A decrease in reaction time and the Fe/zeolite ratio leads to smaller particles of γ-Fe 2 O 3 while lowering the precipitation temperature results in the larger crystallites. The reflection of the precipitation temperature being the key variable in the sorption properties of composites was tested with selected heavy metal ions. The sample prepared at highest temperature of 85 grad C reveals much higher maximum sorption capacity for Pb 2+ than commonly observed for magnetically modified natural zeolites. Good ability for sorption of anions was demonstrated with AsO 4 3- , which offers new applications of such modified zeolites. The sample with the best sorption properties was characterized by SEM, XRD, in-field Moessbauer spectroscopy and magnetic measurements. Following these data, maghemite nanoparticles form aggregates, which are sorbed on zeolite inhomogeneously with some free active surface of zeolite. The particles are about 15 nm in size and reveal the partial vacancies ordering as documented through the increased ratio of tetrahedral and octahedral positions being of 1/3. FC/ZFC curves confirm strongly interacting superparamagnetic particles with a blocking temperature of 230 K. (authors)

Increasing levels of zeolite and Yucca schidigera in diets for adult cats

Directory of Open Access Journals (Sweden)

Natália Charleaux Roque

2011-11-01

Full Text Available The effect of the additives Yucca schidigera (YSC and zeolite (clinoptilolite on digestibility, fecal texture and odor, blood parameters and urine pH of domesticated felines was evaluated. The experiment was conducted in a randomized block design, with twenty-one cats, in two periods, distributed in seven treatments: moist commercial feed (control; control + 125, 250 and 375 ppm YSC; and control + 0.5; 0.75 and 1.0 % zeolite. No differences were observed between the diets regarding apparent digestibility coefficients of nutrient, energy, urine pH or blood parameters. However, levels of 0.5 and 0.75% zeolite were effective both in reducing odor (R² = 96.39 and for fecal texture (R² = 99.63, showing a quadratic pattern for these variables. Levels of 125 and 375 ppm YSC were also efficient in reducing fecal odor; however they did not adjust to regression. Levels of 0.5% and 0.75% zeolite significantly reduce odor of feces and increase fecal texture when added to commercial feed for cats.

Effects of Calcined clay minerals and Silica fume on the compressive strength of concrete

Directory of Open Access Journals (Sweden)

Abolfazl Soltani

2017-05-01

Full Text Available Pozzolanic materials are well known as potential replacements for cement manufacturing in order to increase compressive strength and improve durability of concrete in different environments and leading to save energy particularly reducing global warming effect. The present study reveals the effect of calcined clay minerals as natural pozzolanic material, separately and in combination with and without silica fume. To achieve this aim, 15 mixed designs with a constant water to cementitious ratio of  0.38 is made. In six mixed designs only metakaolin, zeolite or silica fume  and in eight other designs metakaolin and silica fume or zeolite and silica fume have been combined. Mixes containing metakaolin or zeolite with ratio of 10 or 20 percent and silica fume with 7 or 10 percent show significant increasing in compressive strength and improving durability, being valuable replacement for cement (in percentages. In particular, the best practice is attributed to the age of 28 days for compressive strength the replacement of the composition is 10% zeolite with 7% of silica fume and for electrical resistance the replacement of the composition is 10% zeolite with 7% of silica fume.

Effect of Si/Al2 Ratio on 2-butanol Dehydration over HY Zeolite Catalysts

International Nuclear Information System (INIS)

Jung, Euna; Choi, Hyeonhee; Jeon, Jong-Ki

2015-01-01

Synthesis of butenes through dehydration of 2-butanol was investigated over HY zeolite catalysts. 2-Butanol dehydration reaction was carried out in a fixed bed catalytic reactor. 2-Butanol conversion was increased with increase of Si/Al 2 ratio of HY zeolite catalysts, which can be ascribed to increase of acid strength with increase of Si/Al 2 ratio. Selectivities to 1-butene, trans-2-butene, and cis-2-butene were not greatly influenced by the change of the Si/Al 2 ratio of HY zeolite. As a result, it was advantageous to use a HY zeolite catalyst with 60 Si/Al 2 ratio for maximizing the yield of 1-butene in the dehydration of 2-butanol. The optimal reaction temperature for maximizing the yield of 1-butene was 250 .deg. C over HY (60) catalyst

PHYSICAL, CHEMICAL AND STRUCTURAL EVOLUTIION OF ZEOLITE-CONTAINING WASTE FORMS PRODUCED FROM METAKAOLINITE AND CALCINED SODUIM BEARING WASTE (HLW AND/OR LLW)

International Nuclear Information System (INIS)

Grutzeck, Michael W.

2004-01-01

Zeolites are extremely versatile. They can adsorb liquids and gases and serve as cation exchange media. They occur in nature as well cemented deposits. The Romans used blocks of zeolitized tuff as a building material. Using zeolites for the management of radioactive waste is not new, but a process by which the zeolites can be made to act as a cementing agent is. Zeolitic materials are relatively easy to synthesize from a wide range of both natural and man-made precursors. The process under study is derived from a well known method in which metakaolin (thermally dehydroxylated kaolin a mixture of kaolinite and smaller amounts of quartz and mica that has been heated to ∼700 C) is mixed with sodium hydroxide (NaOH) and water and reacted in slurry form (for a day or two) at mildly elevated temperatures. The zeolites form as finely divided powders containing micrometer ((micro)m) sized crystals. However, if the process is changed slightly and just enough concentrated sodium hydroxide solution is added to the metakaolinite to make a thick paste and then the paste is cured under mild hydrothermal conditions (60-200 C), the mixture forms a concrete-like ceramic material made up of distinct crystalline tectosilicate minerals (zeolites and feldspathoids) imbedded in an X-ray amorphous hydrated sodium aluminosilicate matrix. Due to its vitreous character we have chosen to call this composite a ''hydroceramic''. Similar to zeolite powders, a hydroceramic is able to sequester cations in both lattice positions and within the channels and voids present in its tectosilicate framework structure. It can also accommodate a wide range of salt molecules (e.g., sodium nitrate) within these same openings thus rendering them insoluble. Due to its fine crystallite size and cementing character, the matrix develops significant physical strength. The obvious similarities between a hydroceramic waste form and a waste form based on solidified Portland cement grout are only superficial because

Conditioning sludge from chemical treatment for waste product Mo-99

International Nuclear Information System (INIS)

Harsono, D.; Zulfiyandi

1998-01-01

The testing for Ca-zeolite as additive in cementation process has been carried out. The experiment made cement block which weight radio of W/C 35%, S/C 75%, Ca-zeolite/C 1,5% and WL/C 20%. The quality of cement block was tested the compressive strength by Paul Weber apparatus and leaching test was tested with static method by demineralized water. The result of compressive strength is 22,64 N mm-2 and density is 1,81 g cm-3. This values was greater than the minimum standard by ISO 40. The leaching test was given undetectable activities, according to this investigation that those data show that Ca-zeolite can be use as additive material. (author)

Improved Catalysts for Heavy Oil Upgrading Based on Zeolite Y Nanoparticles Encapsulated Stable Nanoporous Host

Energy Technology Data Exchange (ETDEWEB)

Conrad Ingram; Mark Mitchell

2007-09-30

The objective of this project is to synthesize nanocrystals of highly acidic zeolite Y nanoclusters, encapsulate them within the channels of mesoporous (nanoporous) silicates or nanoporous organosilicates, and evaluate the 'zeolite Y/Nanoporous host' composites as catalysts for the upgrading of heavy petroleum feedstocks. In comparison to conventionally-used zeolite Y catalysts of micron size particles, the nanocrystals (< 100 nm particle size) which contain shorter path lengths, are expected to allow faster diffusion of large hydrocarbon substrates and the catalysis products within and out of the zeolite's channels and cages (<1 nm size). This is expected to significantly reduce deactivation of the catalyst and to prolong their period of reactivity. Encapsulating zeolite Y nanocrystals within the nanoporous materials is expected to protect its external surfaces and pore entrances from being blocked by large hydrocarbon substrates, since these substrates will initially be converted to small molecules by the nanoporous host (a catalyst in its own right). The project consisted of four major tasks as follows: (1) synthesis of the nanoparticles of zeolite Y (of various chemical compositions) using various techniques such as the addition of organic additives to conventional zeolite Y synthesis mixtures to suppress zeolite Y crystal growth; (2) synthesis of nanoporous silicate host materials of up to 30 nm pore diameter, using poly (alkylene oxide) copolymers which when removed will yield a mesoporous material; (3) synthesis of zeolite Y/Nanoporous Host composite materials as potential catalysts; and (4) evaluation of the catalyst for the upgrading of heavy petroleum feedstocks.

Synthesis of zeolite-zeolite (mfi-fau) composite catalysts for the isomerization of n-hexane

International Nuclear Information System (INIS)

Ghouri, A.S; Usman, M.R.

2017-01-01

In this research work, the aim is to produce a relatively novel zeolite-zeolite (MFI-FAU) composite catalyst having better potential of catalyzing isomerization of lighter hydrocarbons such as light naphtha, n-pentane, n-hexane, n-heptane and mixture thereof. A series of zeolite-zeolite (MFI-FAU) composite catalysts have been synthesized by incorporating previous practices and techniques. The catalytic performance of as-synthesized zeolite-zeolite (MFI-FAU) composite catalysts have been investigated by isomerizing 95% pure n-hexane in conventional fixed bed flow micro-reactor at temperature 200-240 ºC under atmospheric pressure. In order to explore chemical and physical features of zeolite-zeolite (MFI-FAU) composite catalysts, they are examined and characterized using powder X-ray diffraction (XRD), scanning electron microscopy (SEM) coupled with energy-dispersive X-ray spectrometry (EDX), N2 adsorption-desorption measurements (BET, BJH, t-plot measurements) and Fourier transform infrared (FTIR) spectroscopy equipped with attenuated total reflectance (ATR) arrangements. (author)

GREEN CHEMISTRY. Shape-selective zeolite catalysis for bioplastics production.

Science.gov (United States)

Dusselier, Michiel; Van Wouwe, Pieter; Dewaele, Annelies; Jacobs, Pierre A; Sels, Bert F

2015-07-03

Biodegradable and renewable polymers, such as polylactic acid, are benign alternatives for petrochemical-based plastics. Current production of polylactic acid via its key building block lactide, the cyclic dimer of lactic acid, is inefficient in terms of energy, time, and feedstock use. We present a direct zeolite-based catalytic process, which converts lactic acid into lactide. The shape-selective properties of zeolites are essential to attain record lactide yields, outperforming those of the current multistep process by avoiding both racemization and side-product formation. The highly productive process is strengthened by facile recovery and practical reactivation of the catalyst, which remains structurally fit during at least six consecutive reactions, and by the ease of solvent and side-product recycling. Copyright © 2015, American Association for the Advancement of Science.

Treatment options of low level liquid waste of ETP origin by synthetic zeolites

International Nuclear Information System (INIS)

Singh, I.J.; Jain, Savita; Sathi Sasidharan, N.; Deshingkar, D.S.

2001-08-01

Mixture of synthetic zeolites, AR1, 4A and 13X of Indian origin were tested in a single fixed bed column operation for the treatment of low level liquid waste received at Effluents Treatment Plant (ETP) Trombay, under dynamic conditions. The mixed bed of zeolites was highly effective in decontaminating thousands of bed volumes of waste stream from radio cesium, radio strontium and gross beta gamma activity. High volume reduction factors, upwards of 10,000 are available in this process compared to less than 100 available with chemical precipitation process, currently followed. Containment of entrapped activity in zeolite bed was studied by solidifying them in Portland cement matrix as stable waste form. Incorporation of minerals like vermiculite as minor additive for improving the leaching characteristics of the final waste form was evaluated. Zeolite incorporated cement blocks were subjected to leach tests in distilled water for over 200 days to assess the incremental and cumulative leach rates of individual activity components. Leachability index of radio cesium and strontium were computed, which indicated the suitability of the matrix for safe shallow land burial. (author)

The Strength Behaviour of Lime Stabilized Organic Clay Soil Modified by Catalyst Additeives

Directory of Open Access Journals (Sweden)

Khitam Abdulhussein Saeed

2016-12-01

Full Text Available The organic clay soil can be found in many large size reclaimed lands. These soils present enormously high settlement potential and low strength that needs to be improved by means of effective ground improvement techniques. One of the low cost techniques is to modify the soil with lime in-situ to make it suitable for construction and allow it to increase in strength by pozzolanic reactions between lime and clay minerals. Lime is known to be an effective stabilization material for clayey soil. Nevertheless, its effectiveness may be less with organic clay due to low effective strength properties. Thus, this study concerns the addition of catalyst i.e. zeolite which may improve the performance of lime stabilization to accelerate lime-organic clay reactions. The unconfined compressive test (UCT is conducted on remoulded samples (38mm x 80mm for 0, 7, 14 , 28, and 90 days of curing period. The addition of synthetic zeolite in lime-organic stabilized soil has increased the soil strength by 185% at 90 days curing period at the design mix of organic clay + 10% lime +10% zeolite. The higher value of UCS indicates that zeolite is an effective catalyst to enhance lime stabilization.

Effect of Si/Al{sub 2} Ratio on 2-butanol Dehydration over HY Zeolite Catalysts

Energy Technology Data Exchange (ETDEWEB)

Jung, Euna; Choi, Hyeonhee; Jeon, Jong-Ki [Kongju National University, Cheonan (Korea, Republic of)

2015-02-15

Synthesis of butenes through dehydration of 2-butanol was investigated over HY zeolite catalysts. 2-Butanol dehydration reaction was carried out in a fixed bed catalytic reactor. 2-Butanol conversion was increased with increase of Si/Al{sub 2} ratio of HY zeolite catalysts, which can be ascribed to increase of acid strength with increase of Si/Al{sub 2} ratio. Selectivities to 1-butene, trans-2-butene, and cis-2-butene were not greatly influenced by the change of the Si/Al{sub 2} ratio of HY zeolite. As a result, it was advantageous to use a HY zeolite catalyst with 60 Si/Al{sub 2} ratio for maximizing the yield of 1-butene in the dehydration of 2-butanol. The optimal reaction temperature for maximizing the yield of 1-butene was 250 .deg. C over HY (60) catalyst.

Phosphorus promotion and poisoning in zeolite-based materials: synthesis, characterisation and catalysis.

Science.gov (United States)

van der Bij, Hendrik E; Weckhuysen, Bert M

2015-10-21

Phosphorus and microporous aluminosilicates, better known as zeolites, have a unique but poorly understood relationship. For example, phosphatation of the industrially important zeolite H-ZSM-5 is a well-known, relatively inexpensive and seemingly straightforward post-synthetic modification applied by the chemical industry not only to alter its hydrothermal stability and acidity, but also to increase its selectivity towards light olefins in hydrocarbon catalysis. On the other hand, phosphorus poisoning of zeolite-based catalysts, which are used for removing nitrogen oxides from exhaust fuels, poses a problem for their use in diesel engine catalysts. Despite the wide impact of phosphorus-zeolite chemistry, the exact physicochemical processes that take place require a more profound understanding. This review article provides the reader with a comprehensive and state-of-the-art overview of the academic literature, from the first reports in the late 1970s until the most recent studies. In the first part an in-depth analysis is undertaken, which will reveal universal physicochemical and structural effects of phosphorus-zeolite chemistry on the framework structure, accessibility, and strength of acid sites. The second part discusses the hydrothermal stability of zeolites and clarifies the promotional role that phosphorus plays. The third part of the review paper links the structural and physicochemical effects of phosphorus on zeolite materials with their catalytic performance in a variety of catalytic processes, including alkylation of aromatics, catalytic cracking, methanol-to-hydrocarbon processing, dehydration of bioalcohol, and ammonia selective catalytic reduction (SCR) of NOx. Based on these insights, we discuss potential applications and important directions for further research.

Deposition of {sup 60}Co and {sup 137}Cs adsorbed on zeolite in matrices on the blast furnace slag

Energy Technology Data Exchange (ETDEWEB)

Foeldesova, M; Lukac, P; Dillinger, P [Slovak Technical Univ., Bratislava (Slovakia)

1996-12-31

The experimental data (leaching tests and compressive strength measurements) are presented for case the radionuclides from model water solution and radioactive waste water were uptake on natural and chemically modified granular zeolitic tuffite which show improved sorption ability and were subsequently incorporated into cement casts on blast furnace slags (BSF) basis. The all experiment were carried out with zeolite tuffite from Nizny Hrabovec, Slovak Republic. The natural zeolite was treated by the NaOH solution. The blends of individual components were casted into rectangular prism moulds (1x1x3 cm). The cast consisted invariably of 90% of BSF, 10% of fine zeolite and solution of water glass and to this basic mixture were added either 10 or 20% granular active, or non active zeolite during the mix formation, in excess to content of previous solid components. The water/cement ratio varied in interval 0.32-0.40. Model solutions labelled by cesium-137 or cobalt-60 have been used for sorption experiment and real waste water concentrate from NPP Jaslovske Bohunice as well. The real water consisted of cesium-134, cesium-137, cobalt-60, in borate and nitrate form. The radioactivity of dry cement casts was measured in 4{pi} geometry. The leaching experiments were performed in three solutions: water (W), 0.03 M HCl (A) and 0.04 M NaOH (B). The mechanical properties of sample with non active granular zeolites and their corrosion characteristics as reflected by the bulk density changes. The experiments showed that leaching of radionuclides, which were sorbed from solution and radioactive waste water, in water and bases solution were negligible. Changes of radioactivity of casts, prepared from model solution, in acid solution, which were less than 5%. The mechanical strength of prepared composites is favourable and shows good compatibility of zeolitic additives with a basic matrix. Leaching experiments and mechanical strength are hopeful and show good retention of observed

Method of producing zeolite encapsulated nanoparticles

DEFF Research Database (Denmark)

2015-01-01

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

Method for producing zeolites and zeotypes

DEFF Research Database (Denmark)

2015-01-01

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

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

International Nuclear Information System (INIS)

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

2016-01-01

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.

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.

Adsorption of tannic acid from aqueous solution onto surfactant-modified zeolite

Energy Technology Data Exchange (ETDEWEB)

Lin, Jianwei, E-mail: jwlin@shou.edu.cn [College of Marine Science, Shanghai Ocean University, No. 999 Hucheng Huan Road, Pudong District, Shanghai 201306 (China); Zhan, Yanhui; Zhu, Zhiliang [State Key Laboratory of Pollution Control and Resource Reuse, Tongji University, Shanghai 200092 (China); Xing, Yunqing [College of Marine Science, Shanghai Ocean University, No. 999 Hucheng Huan Road, Pudong District, Shanghai 201306 (China)

2011-10-15

Graphical abstract: Surfactant-modified zeolites (SMZs) with various loadings of cetylpyridinium bromide (CPB) were used as adsorbents to remove tannic acid (TA) from aqueous solution. Highlights: {yields} Surfactant modified zeolites (SMZs) have a good tannic acid (TA) adsorption capacity. {yields} Adsorption capacity for SMZ with bilayer was relatively high at solution pH 3.5-7.0. {yields} Adsorption was well described by pseudo-second-order kinetic model. {yields} Adsorption fitted well with Langmuir, Redlich-Peterson and Sips isotherm models. {yields} Coexisting Cu(II) in aqueous solution resulted in markedly enhanced TA adsorption. - Abstract: Surfactant-modified zeolites (SMZs) with various loadings of cetylpyridinium bromide (CPB) were used as adsorbents to remove tannic acid (TA) from aqueous solution. The TA adsorption efficiencies for natural zeolite and various SMZs were compared. SMZ presented higher TA adsorption efficiency than natural zeolite, and SMZ with higher loading amount of CPB exhibited higher TA adsorption efficiency. The adsorption of TA onto SMZ as a function of contact time, initial adsorbate concentration, temperature, ionic strength, coexisting Cu(II) and solution pH was investigated. The adsorbents before and after adsorption were characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), thermogravimetric analysis (TGA), and Fourier transform infrared (FT-IR) spectroscopy. The adsorption kinetics of TA onto SMZ with CPB bilayer coverage (SMZ-CBC) followed a pseudo-second-order model. The equilibrium adsorption data of TA onto SMZ-CBC were well represented by Langmuir, Redlich-Peterson and Sips isotherm models. The calculated thermodynamic parameters indicated that TA adsorption onto SMZ-CBC was spontaneous and exothermic. The TA adsorption capacity for SMZ-CBC slightly decreased with increasing ionic strength but significantly increased with increasing Cu(II) concentration. The TA adsorption

Oxygen-containing coke species in zeolite-catalyzed conversion of methanol to hydrocarbons

KAUST Repository

Liu, Zhaohui

2016-10-06

Zeolites are the most commonly used catalysts for methanol-to-hydrocarbon (MTH) conversion. Here, we identified two oxygen-containing compounds as coke species in zeolite catalysts after MTH reactions. We investigated the possible influences of the oxygen-containing compounds on coke formation, catalyst deactivation, product selectivity, and the induction period of the MTH reaction through a series of controlled experiments in which one of the identified compounds (2,3-dimethyl-2-cyclopenten-1-one) was co-fed with methanol over a zeolite H-ZSM-5 catalyst. Our results allow us to infer that once produced, the oxygen-containing compounds block the Brønsted acid sites by strong chemisorption and their rapid conversion to aromatics expedites the formation of coke and thus the deactivation of the catalyst. A minor effect of the production of such compounds during the MTH reaction is that the aromatic-based catalytic cycle can be slightly promoted to give higher selectivity to ethylene.

Zeolite function studied by neutron diffraction

International Nuclear Information System (INIS)

Newsam, J.M.

1988-01-01

Some recent figures relating to industrial uses of zeolites are summarized. Recent advances in the application of neutron diffraction to zeolite science are overviewed, with particular emphasis on powder diffraction (PND) results. Single crystal neutron diffraction studies of some 17 hydrated natural and synthetic zeolites have now appeared and they provide a consistent picture of zeolite-water interactions. Complete PND studies of hydrated synthetic ABW- and SOD-framework zeolites have also been reported. Other PND studies have explored the structural consequences of non-framework cation exchange, of framework modification by dealumination, and of framework cation substitution. Relatively simple zeolite-hydrocarbon sorbate complexes that have been studied include benzene in zeolite Y, and benzene and pyridine in zeolite L. Areas that are well poised for further development include further extensions to lower symmetry systems, the use of PND data for zeolite structure solution, studies at elevated temperatures and pressures, and further studies of zeolite sorbate complexes. (author) 68 refs., 7 figs

Removal of paraquat solution onto zeolite material

Science.gov (United States)

Sirival, Rujikarn; Patdhanagul, Nopbhasinthu; Preecharram, Sutthidech; Photharin, Somkuan

2018-04-01

The purpose of this research was to study the adsorption of paraquat herbicides onto zeolite Y materials by the batch method. Three adsorbents material: Zeolite-3, Zeolite-10, and Zeolite-100 were Si/Al ratio at 3.58, 8.57 and 154.37, respectively. The factors for adsorption of paraquat as follows, adsorption time, initial concentrations of paraquat, pH and adsorption isotherm were investigated. The results showed that zeolite-10 had higher adsorption capacity than zeolite-3 and zeolite-100. The appropriate conditions for adsorption were 24 h., Zeolite 0.1 g., Initial paraquat concentration 100 ppm at pH 6. The adsorption isotherm was found to correspond with Langmuir Isotherm and the maximum paraquat adsorption is 26.38 mg/g for zeolite-10, 21.41 mg/g and 9.60 mg/g for zeolite-3 and zeolite-100, respectively. The characterization of zeolite material with XRD, XRF and BET. Furthermore, the zeolite materials applied to remove other organic and inorganic wastewater.

ADSORPSI POLUTAN ION DIKROMAT MENGGUNAKAN ZEOLIT ALAM TERMODIFIKASI AMINA (Adsorption of Dichromate Ions Pollutant Using Ammine Modified-Natural Zeolites

Directory of Open Access Journals (Sweden)

Eko Sri Kunarti

2015-11-01

Full Text Available ABSTRAK Kromium (VI merupakan polutan logam berat berbahaya bagi kesehatan dan lingkungan oleh karena itu pengambilan ion Cr(VI dalam air penting dilakukan untuk mengatasi pencemaran lingkungan. Proses adsorpsi merupakan salah satu teknik sederhana yang dapat digunakan untuk pengambilan ion logam. Pada penelitian ini telah dilakukan kajian adsorpsi ion dikromat sebagai model limbah Cr(VI dalam air menggunakan adsorben zeolit alam termodifikasi amina. Penelitian diawali dengan preparasi adsorben zeolit alam termodifikasi amina. Preparasi dimulai dengan pencucian zeolit alam menggunakan akuades, kemudian refluks zeolit alam menggunakan HCl 3M. Zeolit hasil refluks selanjutnya dimodifikasi menggunakan garam ammonium kuarterner, N-cethyl-N,N,N-trimethylammonium bromide (CTAB dan amina primer, propilamin (PA. Zeolit alam (Z, zeolit teraktivasi asam (ZA dan zeolit hasil modifikasi amina selanjutnya digunakan sebagai adsorben untuk adsorpsi anion dikromat. Karakterisasi adsorben dilakukan dengan mengunakan metode spektroskopi infaramerah dan difraksi sinar-X, sedangkan jumlah anion dikromat yang teradsorpsi dianalisis dengan spektroskopi serapan atom. Hasil penelitian menunjukkan bahwa sampel zeolit mengandung mineral klinoptilolit, mordernit dan kuarsa. Struktur zeolit tidak mengalami kerusakan oleh perlakuan termal dan perlakuan kimia. Modifikasi zeolit meningkatkan efisiensi adsorpsi zeolit alam. Ion dikromat dapat teradsorpsi dengan lebih baik oleh zeolit termodifikasi amina daripada zeolit teraktivasi asam dan zeolit tanpa modifikasi, dengan kemampuan adsorpsi zeolit termodifikasi CTAB (CTAB-Z lebih besar daripada zeolit termodifikasi propilamin (PA-Z. Adsorpsi ion dikromat pada adsorben zeolit berlangsung baik dengan urutan CTAB-Z > PA-Z > ZA > Z, dengan kemampuan adsorpsi masing-masing sebesar 1,96; 1,74; 0,90 dan 0,48 mg/g. Adsorpsi anion dikromat oleh zeolit termodifikasi CTAB merupakan adsorpsi kimia (kemisorpsi dengan energi adsorpsi sebesar

Hydrothermally grown zeolite crystals

International Nuclear Information System (INIS)

Durrani, S.K.; Qureshi, A.H.; Hussain, M.A.; Qazi, N.K.

2009-01-01

The aluminium-deficient and ferrosilicate zeolite-type materials were synthesized by hydrothermal process at 150-170 degree C for various periods of time from the mixtures containing colloidal reactive silica, sodium aluminate, sodium hydroxide, iron nitrate and organic templates. Organic polycation templates were used as zeolite crystal shape modifiers to enhance relative growth rates. The template was almost completely removed from the zeolite specimens by calcination at 550 degree C for 8h in air. Simultaneous thermogravimetric (TG) and differential thermal analysis (DTA) was performed to study the removal of water molecules and the amount of organic template cations occluded inside the crystal pore of zeolite framework. The 12-13% weight loss in the range of (140-560 degree C) was associated with removal of the (C/sub 3/H/sub 7/)/sub 4/ N+ cation and water molecules. X-ray diffraction (XRD) analysis and scanning electron microscope (SEM) techniques were employed to study the structure, morphology and surface features of hydrothermally grown aluminium-deficient and ferrosilicate zeolite-type crystals. In order to elucidate the mode of zeolite crystallization the crystallinity and unit cell parameters of the materials were determined by XRD, which are the function of Al and Fe contents of zeolites. (author)

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

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

International Nuclear Information System (INIS)

Salim, Mashitah Mad; Malek, Nik Ahmad Nizam Nik

2016-01-01

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

Modeling and Optimization of Compressive Strength of Hollow Sandcrete Block with Rice Husk Ash Admixture

Directory of Open Access Journals (Sweden)

2016-11-01

Full Text Available The paper presents the report of an investigation into the model development and optimization of the compressive strength of 55/45 to 70/30 cement/Rice Husk Ash (RHA in hollow sandcrete block. The low cost and local availability potential of RHA, a pozzolanic material gasps for exploitation. The study applies the Scheffe\\'s optimization approach to obtain a mathematical model of the form f(xi1 ,xi2 ,xi3 xi4 , where x are proportions of the concrete components, viz: cement, RHA, sand and water. Scheffe\\'s i experimental design techniques are followed to mould various hollow block samples measuring 450mm x 225mm x 150mm and tested for 28 days strength. The task involved experimentation and design, applying the second order polynomial characterization process of the simplex lattice method. The model adequacy is checked using the control factors. Finally, a software is prepared to handle the design computation process to take the desired property of the mix, and generate the optimal mix ratios. Reversibly, any mix ratios can be desired and the attainable strength obtained.

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

International Nuclear Information System (INIS)

Motojima, K.; Kawamura, F.

1984-01-01

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

Use of Spent Zeolite Sorbents for the Preparation of Lightweight Aggregates Differing in Microstructure

Directory of Open Access Journals (Sweden)

Wojciech Franus

2017-02-01

Full Text Available Lightweight aggregates (LWAs made by sintering beidellitic clay deposits at high temperatures, with and without the addition of spent zeolitic sorbents (clinoptilolitic tuff and Na-P1 made from fly ash containing diesel oil, were investigated. Mineral composition of the aggregates determined by X-ray diffraction was highly uniformized in respect of the initial composition of the substrates. The microstructure of the LWAs, which were studied with a combination of mercury porosimetry, microtomography, nitrogen adsorption/desorption isotherms and scanning electron microscopy, was markedly modified by the spent zeolites, which diminished bulk densities, increased porosities and pore radii. The addition of zeolites decreased water absorption and the compressive strength of the LWAs. The spent Na-P1 had a greater effect on the LWAs’ structure than the clinoptilolite.

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.

Synthesis of 4A zeolites from kaolin for obtaining 5A zeolites through ionic exchange for adsorption of arsenic

International Nuclear Information System (INIS)

Resmini Melo, Carolina; Gracher Riella, Humberto; Cabral Kuhnen, Nivaldo; Angioletto, Elidio; Melo, Aline Resmini; Bernardin, Adriano Michael; Rocha, Marcio Roberto da; Silva, Luciano da

2012-01-01

Highlights: ► We synthesize 4A zeolite from kaolin by hydrothermal reaction with sodium hydroxide. ► The 4A zeolite synthesized underwent ion exchange with calcium ions, with different parameters, to obtain 5A zeolites. ► The best 4A zeolite obtained was used as adsorbent material for arsenic ions. ► The results showed that the 5A zeolite material obtained is a good adsorber of heavy ions. - Abstract: The synthesis of adsorbing zeolite materials requires fine control of the processing variables. There are distinct process variable settings for obtaining specific desired types of zeolites. The intent of this study was to obtain 4A zeolites from kaolin in order to obtain 5A zeolites through ionic exchange with the previously synthesized zeolite. This zeolite 5A was used as an adsorbent for arsenic ions. The results obtained were satisfactory.

Influence of zeolite pore structure on product selectivities for protolysis and hydride transfer reactions in the cracking of n-pentane.

Science.gov (United States)

Miyaji, Akimitsu; Iwase, Yasuyoshi; Nishitoba, Toshiki; Long, Nguyen Quang; Motokura, Ken; Baba, Toshihide

2015-02-21

The conversion of n-pentane was carried out to examine the effects of reaction conditions on changes in product selectivities at 823 K, using zeolites with 10- and 12-membered rings. We also investigated the influence of the pore structure of these zeolites on their catalytic activities for both protolysis and hydride transfer reactions. In the first half of this work, we examined the influence of acidic proton concentration and n-pentane pressure on the reaction rates for protolysis and hydride transfer reactions using ZSM-5 zeolites. The rates of hydride transfer reactions were more influenced by pentane pressure compared to protolysis reactions, and were proportional to the square of n-pentane pressure and the concentration of acidic protons. In the second half of this work, the influence of the zeolite pore structure on changes in product selectivities with n-pentane conversion and that on the rates of protolysis and the hydride transfer reactions were revealed using various zeolites with 10- and 12-membered rings. The catalytic activities of zeolites for the protolysis and hydride transfer reactions were influenced more by the spatial volume of the zeolite cavity than the acid strength of protons on the zeolite.

Pemberian Zeolit Dan Arang Sekam Pada Lahan Sawah Tercemar Limbah Pabrik Terhadap Pb Tanah Dan Tanaman Padi

OpenAIRE

Juliana, Ester; Sarifuddin, Sarifuddin; Jamilah, Jamilah

2015-01-01

This study aimed to determine the effect of zeolites and rice husk to soil Pb and growth and production of paddy rice. The research was conducted in the screen house at Faculty of Agriculture USU and soil analyzed at the Laboratory Institute for Agricultural Technology ( BPTP) Medan North Sumatra . This experiment using a factorial randomized block design with two factors , namely zeolite treatment consists of 3 levels: Z0 = 0 g / pot , Z1 = 12.5 g / pot , Z2 = 25 g / pot and rice Husk consis...

The effect of positioning cations on acidity and stability of the framework structure of Y zeolite

Science.gov (United States)

Deng, Changshun; Zhang, Junji; Dong, Lihui; Huang, Meina; Bin Li; Jin, Guangzhou; Gao, Junbin; Zhang, Feiyue; Fan, Minguang; Zhang, Luoming; Gong, Yanjun

2016-01-01

The investigation on the modification of NaY zeolite on LaHY and AEHY (AE refers Ca and Sr and the molar ratio of Ca and Sr is 1:1) zeolites was proformed by XRD, N2-physisorption (BET), XRF, XPS, NH3-TPD, Py-IR, hydrothermal stability, and catalytic cracking test. These results indicate that HY zeolite with ultra low content Na can be obtained from NaY zeolite through four exchange four calcination method. The positioning capability of La3+ in sodalite cage is much better than that of AE2+ and about 12 La3+ can be well coordinated in sodalite cages of one unit cell of Y zeolite. Appropriate acid amount and strength favor the formation of propylene and La3+ is more suitable for the catalytic cracking of cyclohexane than that of AE2+. Our results not only elaborate the variation of the strong and weak acid sites as well as the Brönsted and Lewis acid sites with the change of exchanged ion content but also explore the influence of hydrothermal aging of LaHY and AEHY zeolites and find the optimum ion exchange content for the most reserved acid sites. At last, the coordination state and stabilization of ion exchanged Y zeolites were discussed in detail. PMID:26987306

Quantification of hand function by power grip and pinch strength force measurements in ulnar nerve lesion simulated by ulnar nerve block.

Science.gov (United States)

Wachter, Nikolaus Johannes; Mentzel, Martin; Krischak, Gert D; Gülke, Joachim

2017-06-24

In the assessment of hand and upper limb function, grip strength is of the major importance. The measurement by dynamometers has been established. In this study, the effect of a simulated ulnar nerve lesion on different grip force measurements was evaluated. In 25 healthy volunteers, grip force measurement was done by the JAMAR dynamometer (Fabrication Enterprises Inc, Irvington, NY) for power grip and by a pinch strength dynamometer for tip pinch strength, tripod grip, and key pinch strength. A within-subject research design was used in this prospective study. Each subject served as the control by preinjection measurements of grip and pinch strength. Subsequent measurements after ulnar nerve block were used to examine within-subject change. In power grip, there was a significant reduction of maximum grip force of 26.9% with ulnar nerve block compared with grip force without block (P force could be confirmed. However, the assessment of other dimensions of hand strength as tip pinch, tripod pinch and key pinch had more relevance in demonstrating hand strength changes resulting from an distal ulnar nerve lesion. The measurement of tip pinch, tripod grip and key pinch can improve the follow-up in hand rehabilitation. II. Copyright © 2017 Hanley & Belfus. Published by Elsevier Inc. All rights reserved.

Synthesis of Foam-Shaped Nanoporous Zeolite Material: A Simple Template-Based Method

Science.gov (United States)

Saini, Vipin K.; Pires, Joao

2012-01-01

Nanoporous zeolite foam is an interesting crystalline material with an open-cell microcellular structure, similar to polyurethane foam (PUF). The aluminosilicate structure of this material has a large surface area, extended porosity, and mechanical strength. Owing to these properties, this material is suitable for industrial applications such as…

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.

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.

Thermal behavior of natural zeolites

International Nuclear Information System (INIS)

Bish, D.L.

1993-01-01

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

Krypton Adsorption on Zeolite-Templated Carbon and Anomalous Surface Thermodynamics.

Science.gov (United States)

Murialdo, Maxwell; Stadie, Nicholas P; Ahn, Channing C; Fultz, Brent

2015-07-28

Krypton adsorption was measured at eight temperatures between 253 and 433 K on a zeolite-templated carbon and two commercial carbons. The data were fitted using a generalized Langmuir isotherm model and thermodynamic properties were extracted. Differing from that on commercial carbons, krypton adsorption on the zeolite-templated carbon is accompanied by an increasing isosteric enthalpy of adsorption, rising by up to 1.4 kJ mol(-1) as a function of coverage. This increase is a result of enhanced adsorbate-adsorbate interactions promoted by the ordered, nanostructured surface of the adsorbent. An assessment of the strength and nature of these adsorbate-adsorbate interactions is made by comparing the measured isosteric enthalpies of adsorption (and other thermodynamic quantities) to fundamental metrics of intermolecular interactions of krypton and other common gases.

Spin probes of chemistry in zeolites

International Nuclear Information System (INIS)

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

1997-09-01

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

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. Copyright © 2015 Elsevier B.V. All rights reserved.

Separation of cesium and strontium with zeolites

Energy Technology Data Exchange (ETDEWEB)

Kanno, T; Hashimoto, H [Tohoku Univ., Sendai (Japan). Research Inst. of Mineral Dressing and Metallurgy

1976-06-01

The basic studies of separation of cesium and strontium were made with specimens of zeolite, which are synthetic zeolites A, X and Y; synthetic mordenite; natural mordenite; and clinoptilolite. Ammonium chloride was used as eluent, because it was considered to be a most appropriate eluent in alkaline chlorides. Cesium was easily eluted from the zeolites A and X by ammonium chloride solution, but it was difficult to elute from the synthetic mordenite, natural mordenite and clinoptilolite by ammonium chloride solution, but it was difficult to elute from the zeolites A and X. The zeolite Y is the only one zeolite among these zeolites from which both of cesium and strontium were easily eluted by ammonium chloride solution. Strontium could be separated from cesium with zeolites by formation of Sr-EDTA chelate at pH above 11. In this process, cesium was only exchanged in zeolite column, but strontium flow out from it.

Separation of cesium and strontium with zeolites

International Nuclear Information System (INIS)

Kanno, Takuji; Hashimoto, Hiroyuki

1976-01-01

The basic studies of separation of cesium and strontium were made with specimens of zeolite, which are synthetic zeolites A, X and Y; synthetic mordenite; natural mordenite; and clinoptilolite. Ammonium chloride was used as eluent, because it was considered to be a most appropriate eluent in alkaline chlorides. Cesium was easily eluted from the zeolites A and X by ammonium chloride solution, but it was difficult to elute from the synthetic mordenite, natural mordenite and clinoptilolite by ammonium chloride solution, but it was difficult to elute from the zeolites A and X. The zeolite Y is the only one zeolite among these zeolites from which both of cesium and strontium were easily eluted by ammonium chloride solution. Strontium could be separated from cesium with zeolites by formation of Sr-EDTA chelate at pH above 11. In this process, cesium was only exchanged in zeolite column, but strontium flow out from it. (auth.)

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

Processing of radioactive waste solution with zeolites. I. Thermal transformation of Na, Cs and Sr type zeolites

Energy Technology Data Exchange (ETDEWEB)

Kanno, T; Mimura, H; Kitamura, T [Tohoku Univ., Sendai (Japan). Research Inst. of Mineral Dressing and Metallurgy

1976-08-01

Thermal transformation of Na, Cs and Sr type zeolites were studied by means of differential thermal analysis (DTA), thermogravimetric analysis (TGA) and X-ray powder diffraction. Synthetic zeolites A, X and Y, synthetic mordenite (Zeolon) and natural mordenite were used in this study. Na type zeolites of A and X recrystallized to Nepheline (NaAlSiO/sub 4/) above 1,000/sup 0/C, but the structures of zeolite Y and mordenite collapsed above about 900/sup 0/C and did not recrystallize until 1,200/sup 0/C. Cs type zeolites of A and X recrystallized to pollucite (CsAlSi/sub 2/O/sub 6/) above 1,000/sup 0/C and Cs type of zeolite Y recrystallized to it above 1,100/sup 0/C, but the structure of mordenite collapsed above 1,000/sup 0/C and did not recrystallize until 1,200/sup 0/C. On Sr type zeolites, zeolite A and X recrystallized to strontium aluminosilicate (SrAl/sub 2/Si/sub 2/O/sub 8/) above 1,100/sup 0/C and zeolite Y recrystallized to it above 1,200/sup 0/C, but the structure of mordenite collapsed above 1,000/sup 0/C. The results described above were supported by microscopic observation and the measurement of density. If this solidifications by calcination of zeolites are further studied, new informations concerning the fixation of Cs and Sr will be obtained.

Removal of pyridine and quinoline by bio-zeolite composed of mixed degrading bacteria and modified zeolite

International Nuclear Information System (INIS)

Bai Yaohui; Sun Qinghua; Xing Rui; Wen Donghui; Tang Xiaoyan

2010-01-01

In the process of the biodegradation of pyridine and quinoline, ammonium is often generated because of the transformation of N from pyridine and quinoline. Zeolite has been proven to be an effective sorbent for the removal of the ammonium. The natural zeolite can be modified to be the macroporous carrier in the biological wastewater treatment process. In this study, a specific bio-zeolite composed of mixed bacteria (a pyridine-degrading bacterium and a quinoline-degrading bacterium) and modified zeolite was used for biodegradation and adsorption in two types of wastewater: sterile synthetic and coking wastewater. The experimental results indicated that pyridine and quinoline could be degraded simultaneously by the mixed bacteria. Furthermore, NH 4 + -N transformed from pyridine and quinoline could be removed by the modified zeolite. In addition, the bacterial community structures of the coking wastewater and the bio-zeolite were monitored by the amplicon length heterogeneity polymerase-chain reaction (LH-PCR) technique. Both LH-PCR results and scanning electron microscope (SEM) observations indicated that the microorganisms, including BW001 and BW003, could be easily attached on the surface of the modified zeolite and that the bio-zeolite could be used in the treatment of wastewater containing pyridine and/or quinoline.

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...

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

International Nuclear Information System (INIS)

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

2015-01-01

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

Carbon monoxide hydrogenation over ruthenium zeolites

Energy Technology Data Exchange (ETDEWEB)

Jacobs, P.A.; Nijs, H.H.; Verdonck, J.J.; Uytterhoeven, J.B.

1978-03-01

Ru zeolites are active and stable methanation catalysts. Under Fischer--Tropsch conditions they show a narrow product distribution. Further work is needed to assign this to a possible effect exerted by the zeolite cages. When the size of the Ru particles enclosed in the zeolite cages is increased, a lower methanation activity is found and a higher amount of C/sub 2/ and C/sub 3/ products are formed under Fischer--Tropsch conditions. This effect has not been reported until now on other supports. The less acidic zeolites act as promoters of the CO hydrogenation: under methanation conditions the activity is increased; under Fischer--Tropsch conditions, the selectivity is shifted toward higher hydrocarbons. This is explained by the particular zeolite property that electron deficient metal agglomerates seem to be formed on the acidic zeolites. With respect to kinetic behavior, relative activity of different metals, influence of reaction temperature on product distribution, the zeolite behaves in the same way a conventional alumina support. 4 figs., 4 tables.

Detergent zeolite filtration plant

OpenAIRE

Stanković Mirjana S.; Pezo Lato L.

2003-01-01

The IGPC Engineering Department designed basic projects for detergent zeolite filtration plant, using technology developed in the IGPC laboratories. Several projects were completed: technological, machine, electrical, automation. On the basis of these projects, a production plant with a capacity of 75,000 t/y was manufactured, at "Zeolite Mira", Mira (VE), Italy, in 1997, for increasing detergent zeolite production, from 50,000 to 100,000 t/y. The main goal was to increase the detergent zeoli...

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

OpenAIRE

Solanki, Parag; Gupta, Vikal; Kulshrestha, Ruchi

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.

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

Czech Academy of Sciences Publication Activity Database

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

2014-01-01

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

Retention of Cs on zeolite, bentonite and their mixtures

International Nuclear Information System (INIS)

Atun, G.

2002-01-01

The sorption behavior of cesium on zeolite and bentonite minerals and their mixtures was studied by means of a batch method and a tracer technique. All experiments were carried out in the presence of CsCl spiked with 137 Cs and NaCl as a supporting electrolyte in varying concentrations. The distribution coefficients (K D ) did not show significant differences at low Cs + loadings while they decreased in the high loading region. Freundlich and D-R isotherms were applied to the adsorption data of zeolite and bentonite. Adsorption capacities and mean energies calculated from D-R isotherm parameters decreased by increasing ionic strength on both minerals. The identification of the specific uptake sites was attempted on the basis of the Freundlich isotherm. Experimentally observed distribution coefficients of Cs on two mineral mixtures were smaller than theoretically calculated values, except at the highest NaCl concentration. (author)

Effect of different glasses in glass bonded zeolite

International Nuclear Information System (INIS)

Lewis, M.A.; Ackerman, J.P.; Verma, S.

1995-01-01

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

Design and fabrication of zeolite macro- and micromembranes

Science.gov (United States)

Chau, Lik Hang Joseph

2001-07-01

The chemical nature of the support surface influences zeolite nucleation, crystal growth and elm adhesion. It had been demonstrated that chemical modification of support surface can significantly alter the zeolite film and has a good potential for large-scale applications for zeolite membrane production. The incorporation of titanium and vanadium metal ions into the structural framework of MFI zeolite imparts the material with catalytic properties. The effects of silica and metal (i.e., Ti and V) content, template concentration and temperature on the zeolite membrane growth and morphology were investigated. Single-gas permeation experiments were conducted for noble gases (He and Ar), inorganic gases (H2, N2, SF6) and hydrocarbons (methane, n-C4, i-C4) to determine the separation performance of these membranes. Using a new fabrication method based on microelectronic fabrication and zeolite thin film technologies, complex microchannel geometry and network (supported zeolite films. The zeolite micropatterns were stable even after repeated thermal cycling between 303 K and 873 K for prolonged periods of time. This work also demonstrates that zeolites (i.e., Sil-1, ZSM-5 and TS-1) can be employed as catalyst, membrane or structural materials in miniature chemical devices. Traditional semiconductor fabrication technology was employed in micromachining the device architecture. Four strategies for the manufacture of zeolite catalytic microreactors were discussed: zeolite powder coating, uniform zeolite film growth, localized zeolite growth, and etching of zeolite-silicon composite film growth inhibitors. Silicalite-1 was also prepared as free-standing membrane for zeolite membrane microseparators.

Complex Reaction Environments and Competing Reaction Mechanisms in Zeolite Catalysis: Insights from Advanced Molecular Dynamics

NARCIS (Netherlands)

De Wispelaere, K.; Ensing, B.; Ghysels, A.; Meijer, E.J.; van Van Speybroeck, V.

2015-01-01

The methanol-to-olefin process is a showcase example of complex zeolite-catalyzed chemistry. At real operating conditions, many factors affect the reactivity, such as framework flexibility, adsorption of various guest molecules, and competitive reaction pathways. In this study, the strength of first

Strength characteristics of light weight concrete blocks using mineral admixtures

Science.gov (United States)

Bhuvaneshwari, P.; Priyadharshini, U.; Gurucharan, S.; Mithunram, B.

2017-07-01

This paper presents an experimental study to investigate the characteristics of light weight concrete blocks. Cement was partially replaced with mineral admixtures like Fly ash (FA), limestone powder waste (LPW), Rice husk ash (RHA), sugarcane fiber waste (SCW) and Chrysopogonzizanioides (CZ). The maximum replacement level achieved was 25% by weight of cement and sand. Total of 56 cubes (150 mm x 150 mm x150 mm) and 18 cylinders (100mmφ and 50mm depth) were cast. The specimens being (FA, RHA, SCW, LPW, CZ, (FA-RHA), (FA-LPW), (FA-CZ), (LPW-CZ), (FA-SCW), (RHA-SCW)).Among the different combination, FA,FA-SCW,CZ,FA-CZ showed enhanced strength and durability, apart from achieving less density.

Zeolite ZSM-57

International Nuclear Information System (INIS)

Valyocsik, E.W.; Page, N.M.; Chu, C.T.W.

1989-01-01

This patent describes a synthetic porous crystalline zeolite having a molar ratio of XO 2 ; Y 2 O 3 of at least 4. Wherein X represents silicon and/or germanium and Y represents aluminum, boron, chromium, iron and/or gallium. The porous crystalline zeolite having at least the X-ray diffraction lines as set forth in the text

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. Copyright © 2014 Elsevier B.V. All rights reserved.

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.

Ion-exchange properties of zeolite/glass hybrid materials

International Nuclear Information System (INIS)

Taira, Nobuyuki; Yoshida, Kohei; Fukushima, Takuya

2017-01-01

Hybrid materials were prepared from ground glass powder and various zeolites such as A-type, mordenite, X-type, and Y-type zeolites, and their ion removal effect was investigated. The hybrid materials of A-type, Y-type, and mordenite zeolites showed similar Sr"2"+ removal rates from aqueous solutions. The removal rate of Sr"2"+ ions increased as the amount of zeolite in the hybrid materials increased. Compared with other hybrid materials, the hybrid materials of X-type zeolite showed higher Sr"2"+ removal rates, especially for zeolite content greater than 25%. As the amount of X-type zeolite in the hybrid materials increased, the Sr"2"+ removal rate increased greatly, with a 100% removal rate when the content of X-type zeolite exceeded 62.5%. (author)

Introduction to zeolite theory and modelling

NARCIS (Netherlands)

Santen, van R.A.; Graaf, van de B.; Smit, B.; Bekkum, van H.

2001-01-01

A review. Some of the recent advances in zeolite theory and modeling are present. In particular the current status of computational chem. in Bronsted acid zeolite catalysis, mol. dynamics simulations of mols. adsorbed in zeolites, and novel Monte Carlo technique are discussed to simulate the

Relationship Between Selected Strength and Power Assessments to Peak and Average Velocity of the Drive Block in Offensive Line Play.

Science.gov (United States)

Jacobson, Bert H; Conchola, Eric C; Smith, Doug B; Akehi, Kazuma; Glass, Rob G

2016-08-01

Jacobson, BH, Conchola, EC, Smith, DB, Akehi, K, and Glass, RG. Relationship between selected strength and power assessments to peak and average velocity of the drive block in offensive line play. J Strength Cond Res 30(8): 2202-2205, 2016-Typical strength training for football includes the squat and power clean (PC) and routinely measured variables include 1 repetition maximum (1RM) squat and 1RM PC along with the vertical jump (VJ) for power. However, little research exists regarding the association between the strength exercises and velocity of an actual on-the-field performance. The purpose of this study was to investigate the relationship of peak velocity (PV) and average velocity (AV) of the offensive line drive block to 1RM squat, 1RM PC, the VJ, body mass (BM), and body composition. One repetition maximum assessments for the squat and PC were recorded along with VJ height, BM, and percent body fat. These data were correlated with PV and AV while performing the drive block. Peal velocity and AV were assessed using a Tendo Power and Speed Analyzer as the linemen fired, from a 3-point stance into a stationary blocking dummy. Pearson product analysis yielded significant (p ≤ 0.05) correlations between PV and AV and the VJ, the squat, and the PC. A significant inverse association was found for both PV and AV and body fat. These data help to confirm that the typical exercises recommended for American football linemen is positively associated with both PV and AV needed for the drive block effectiveness. It is recommended that these exercises remain the focus of a weight room protocol and that ancillary exercises be built around these exercises. Additionally, efforts to reduce body fat are recommended.

Shear bond strength of computer-aided design and computer-aided manufacturing feldspathic and nano resin ceramics blocks cemented with three different generations of resin cement.

Science.gov (United States)

Ab-Ghani, Zuryati; Jaafar, Wahyuni; Foo, Siew Fon; Ariffin, Zaihan; Mohamad, Dasmawati

2015-01-01

To evaluate the shear bond strength between the dentin substrate and computer-aided design and computer-aided manufacturing feldspathic ceramic and nano resin ceramics blocks cemented with resin cement. Sixty cuboidal blocks (5 mm × 5 mm × 5 mm) were fabricated in equal numbers from feldspathic ceramic CEREC(®) Blocs PC and nano resin ceramic Lava™ Ultimate, and randomly divided into six groups (n = 10). Each block was cemented to the dentin of 60 extracted human premolar using Variolink(®) II/Syntac Classic (multi-steps etch-and-rinse adhesive bonding), NX3 Nexus(®) (two-steps etch-and-rinse adhesive bonding) and RelyX™ U200 self-adhesive cement. All specimens were thermocycled, and shear bond strength testing was done using the universal testing machine at a crosshead speed of 1.0 mm/min. Data were analyzed using one-way ANOVA. Combination of CEREC(®) Blocs PC and Variolink(®) II showed the highest mean shear bond strength (8.71 Mpa), while the lowest of 2.06 Mpa were observed in Lava™ Ultimate and RelyX™ U200. There was no significant difference in the mean shear bond strength between different blocks. Variolink(®) II cement using multi-steps etch-and-rinse adhesive bonding provided a higher shear bond strength than the self-adhesive cement RelyX U200. The shear bond strength was not affected by the type of blocks used.

Producing zeolites from fly ash

International Nuclear Information System (INIS)

Rayalu, S.; Labhestwar, N.K.; Biniwale, R.B.; Udhoji, J.S.; Meshram, S.U.; Khanna, P.

1998-01-01

Fly ash has virtually become a menace of thermal power generation, leading to its devastating effects on the environment. Development of alternate methods of its disposal - especially those with recourse to recovery of valuable materials-has thus become imperative. This paper deals with the utilisation of fly ash for the production of high value-added products, viz., commercial grade zeolites. The physico-chemical and morphological characteristics of fly ash based Zeolite-A (FAZ-A) compares well with commercial Zeolite-A. High calcium binding capacity, appropriate particle/pore size and other detergency characteristics of FAZ-A brings forth its potential as a substitute for phosphatic detergent builder. The technology is extremely versatile, and other products like Zeolite-X, Zeolite-Y, sodalite and mordenite are also amenable for cost effective production with modifications in certain reaction parameters. Low temperature operations, ready availability of major raw materials, simplicity of process and recycling of unused reactants and process water are special features of the process. (author)

Human bile sorption by cancrinite-type zeolites

International Nuclear Information System (INIS)

Linares, Carlos F.; Colmenares, Maryi; Ocanto, Freddy; Valbuena, Oscar

2009-01-01

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

Properties of glass-bonded zeolite monoliths

International Nuclear Information System (INIS)

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

1994-01-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2008-11-15

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

Fabrication of 6FDA-durene membrane incorporated with zeolite T and aminosilane grafted zeolite T for CO2/CH4 separation

Science.gov (United States)

Jusoh, Norwahyu; Fong Yeong, Yin; Keong Lau, Kok; Shariff, Azmi Mohd

2017-08-01

In the present work, zeolite T and aminosilane grafted zeolite T are embedded into 6FDA-durene polyimide phase for the fabrication of mixed matrix membranes (MMMs). FESEM images demonstrated that the improvement of interfacial adhesion between zeolite and polymer phases in MMM loaded with aminosilane grafted zeolite T was not significant as compared to zeolite T/6FDA-durene MMM. From the gas permeation test, CO2/CH4 selectivity up to 26.4 was achieved using MMM containing aminosilane grafted zeolite T, while MMM loaded with ungrafted zeolite T showed CO2/CH4 selectivity of 19.1. In addition, MMM incorporated with aminosilane grafted zeolite T particles successfully lies on Robeson upper bound 2008, which makes it an attractive candidate for CO2/CH4 separation.

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

Energy Technology Data Exchange (ETDEWEB)

Alejandro, Serguei [Laboratorio de Tecnologías Limpias (F. Ingeniería), Universidad Católica de la Santísima Concepción, Alonso de Ribera 2850, Concepción (Chile); Núcleo de Energías Renovables (F. Ingeniería), Universidad Católica de Temuco, Rudecindo Ortega 02950, Temuco (Chile); Valdés, Héctor, E-mail: hvaldes@ucsc.cl [Laboratorio de Tecnologías Limpias (F. Ingeniería), Universidad Católica de la Santísima Concepción, Alonso de Ribera 2850, Concepción (Chile); Manéro, Marie-Hélène [Université de Toulouse (France); INPT, UPS (France); Laboratoire de Génie Chimique, 4, Allée Emile Monso, F–31030 Toulouse (France); CNRS (France); Laboratoire de Génie Chimique, F–31030 Toulouse (France); Zaror, Claudio A. [Departamento de Ingeniería Química (F. Ingeniería), Universidad de Concepción, Concepción, Correo 3, Casilla 160–C (Chile)

2014-06-01

Highlights: • Surface acidity of modified natural zeolite is related to its chemical reactivity. • Brønsted acid sites are associated to toluene adsorption. • Lewis acid sites could decompose ozone generating surface active oxygen species. • Infrared spectra evidence active atomic oxygen and oxidation by-product formation. • 2NH4Z1 sample shows the highest reactivity toward adsorbed toluene. - Abstract: In this study, the effect of zeolite chemical surface characteristics on the oxidative regeneration of toluene saturated-zeolite samples is investigated. A Chilean natural zeolite (53% clinoptilolite, 40% mordenite and 7% quartz) was chemically modified by acid treatment with hydrochloric acid and by ion-exchange with ammonium sulphate. Thermal pre-treatments at 623 and 823 K were applied and six zeolite samples with different chemical surface characteristics were generated. Chemical modification of natural zeolite followed by thermal out-gassing allows distinguishing the role of acidic surface sites on the regeneration of exhausted zeolites. An increase in Brønsted acid sites on zeolite surface is observed as a result of ammonium-exchange treatment followed by thermal treatment at 623 K, thus increasing the adsorption capacity toward toluene. High ozone consumption could be associated to a high content of Lewis acid sites, since these could decompose ozone into atomic active oxygen species. Then, surface oxidation reactions could take part among adsorbed toluene at Brønsted acid sites and surface atomic oxygen species, reducing the amount of adsorbed toluene after the regenerative oxidation with ozone. Experimental results show that the presence of adsorbed oxidation by-products has a negative impact on the recovery of zeolite adsorption capacity.

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

International Nuclear Information System (INIS)

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

2014-01-01

Highlights: • Surface acidity of modified natural zeolite is related to its chemical reactivity. • Brønsted acid sites are associated to toluene adsorption. • Lewis acid sites could decompose ozone generating surface active oxygen species. • Infrared spectra evidence active atomic oxygen and oxidation by-product formation. • 2NH4Z1 sample shows the highest reactivity toward adsorbed toluene. - Abstract: In this study, the effect of zeolite chemical surface characteristics on the oxidative regeneration of toluene saturated-zeolite samples is investigated. A Chilean natural zeolite (53% clinoptilolite, 40% mordenite and 7% quartz) was chemically modified by acid treatment with hydrochloric acid and by ion-exchange with ammonium sulphate. Thermal pre-treatments at 623 and 823 K were applied and six zeolite samples with different chemical surface characteristics were generated. Chemical modification of natural zeolite followed by thermal out-gassing allows distinguishing the role of acidic surface sites on the regeneration of exhausted zeolites. An increase in Brønsted acid sites on zeolite surface is observed as a result of ammonium-exchange treatment followed by thermal treatment at 623 K, thus increasing the adsorption capacity toward toluene. High ozone consumption could be associated to a high content of Lewis acid sites, since these could decompose ozone into atomic active oxygen species. Then, surface oxidation reactions could take part among adsorbed toluene at Brønsted acid sites and surface atomic oxygen species, reducing the amount of adsorbed toluene after the regenerative oxidation with ozone. Experimental results show that the presence of adsorbed oxidation by-products has a negative impact on the recovery of zeolite adsorption capacity

Sulfur removal from fuel using zeolites/polyimide mixed matrix membrane adsorbents

International Nuclear Information System (INIS)

Lin, Ligang; Wang, Andong; Dong, Meimei; Zhang, Yuzhong; He, Benqiao; Li, Hong

2012-01-01

Graphical abstract: Membrane adsorption process is proposed for sulfur removal. Three-dimensional network structure is key to fulfill adsorption function of MMMs, which adsorption/desorption behavior is markedly related with binding force with sulfur molecules. Highlights: ► Membrane adsorption process is proposed for sulfur removal. ► Three-dimensional network structure of MMMs is key to fulfill adsorption function. ► Adsorption/desorption behavior is markedly related with binding force. - Abstract: A novel membrane adsorption process was proposed for the sulfur removal from fuels. The mixed matrix membranes (MMMs) adsorbents composed of polyimide (PI) and various Y zeolites were prepared. By the detailed characterization of FT-IR, morphology, thermal and mechanical properties of MMMs adsorbents, combining the adsorption and desorption behavior research, the process–structure–function relationship was discussed. Field-emission scanning electron microscope (FESEM) images show that the functional particles are incorporated into the three-dimensional network structure. MMMs adsorbents with 40% of zeolites content possess better physical properties, which was confirmed by mechanical strength and thermo stability analysis. Influence factors including post-treatment, content of incorporated zeolites, adsorption time, temperature, initial sulfur concentration as well as sulfur species on the adsorption performance of MMMs adsorbents have been evaluated. At 4 wt.% zeolites content, adsorption capacity for NaY/PI, AgY/PI and CeY/PI MMMs adsorbents come to 2.0, 7.5 and 7.9 mg S/g, respectively. And the regeneration results suggest that the corresponding spent membranes can recover about 98%, 90% and 70% of the desulfurization capacity, respectively. The distinct adsorption and desorption behavior of MMMs adsorbents with various functional zeolites was markedly related with their various binding force and binding mode with sulfur compounds.

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.

Synthesis of zeolite membrane (Y / α-alumina)

International Nuclear Information System (INIS)

Araujo, Ana Paula; Silva, Valmir Jose da; Crispin, Alana Carolyne; Rodrigues, Meiry Glaucia F.; Menezes, Romualdo R.

2009-01-01

The general aim of this study was to develop materials of the type: Y zeolite (hydrothermal synthesis), ceramic support (forming of powder) and zeolite membrane (rubbing). The preparation of the Y zeolite was conducted in accordance with the hydrothermal synthesis method, the time of crystallization was one day. The ceramic support was prepared by means of the forming of powder technique and subsequently subjected to sintering at a temperature of 1400 deg C/1h. The zeolite membrane (Y/α- alumina) was prepared by secondary growth method (rubbing). These materials were characterized by XRD and SEM. Obtaining Y zeolite could be confirmed by X ray diffractograms. From the images obtained by SEM, it was possible to derive from analysis that the Y zeolite is composed of a homogeneous morphology, where the particles are crowded, with uniform size. The results obtained for the ceramic support (α-alumina) showed that it displays characteristics peaks of aluminum oxide. By using micrographs it was possible to observe a heterogeneous microstructure with a compact form, without cracks upon the layers. According to the XRD, for the method of secondary growth (rubbing), it was observed that the Y zeolite which had been synthesized on the ceramic support displayed a crystalline structure. The micrography of the zeolite membrane (Y/α-alumina) showed the formation of a layer of zeolite on the ceramic support. (author)

Characterization of Mexican zeolite minerals

International Nuclear Information System (INIS)

Jimenez C, M.J.

2005-01-01

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

The effect of heat treatment on the mechanical and structural properties of one-part geopolymer-zeolite composites

NARCIS (Netherlands)

Sturm, P.; Gluth, G.J.G.; Simon, S.; Brouwers, H.J.H.; Kühne, H.C.

2016-01-01

This contribution presents the results of structural and compressive strength investigations on cured and high-temperature treated silica-based one-part geopolymer-zeolite composites. The specimens were synthesized from two different silica sources, sodium aluminate and water. The phase content as

Zeolites as supports for transition-metal complexes

Energy Technology Data Exchange (ETDEWEB)

Le Van Mao, R

1979-01-01

The unique structural characteristics of the zeolites, including the presence of molecular-size cages and channels and of an internal electrostatic field, make them promising as supports for converting homogeneous to heterogeneous catalysts. The acidic sites on the zeolites may also contribute to catalysis of reactions, such as hydrocracking; may stabilize metal complexes in a highly disperse state; and may improve activity or selectivity. Recent studies on the synthesis of new types of zeolite-supported complexes of transition metals (TM), such as Co, Cu, Ag, Fe, Mo, Ru, Rh, Re, and Os, suggest the feasibility of the direct introduction of some TM complexes into the zeolitic cages during zeolite synthesis, especially during the crystallization phase. This method may considerably reduce the structural limitations associated with the incorporation of TM complexes into zeolites by conventional methods.

Acidity in zeolite catalysis

NARCIS (Netherlands)

Santen, van R.A.; Gauw, de F.J.M.M.; Corma, A.; Melo, F.; Mendioroz, S.; Fierro, J.L.G.

2000-01-01

A review with 21 refs. is provided on our current understanding of the activation of hydrocarbons by protonic zeolites. One has to distinguish the proton affinity of a zeolite, measured in an equil. expt., from proton activation that dets. a kinetic catalytic result. The proton affinity depends on

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.

Examination of zeolites by neutron reflection method

International Nuclear Information System (INIS)

Szegedi, S.; Varadi, M.; Boedy, Z.T.; Vas, L.

1991-01-01

Neutron reflection method has been used for the determination of zeolite content in minerals. The basis of this measurement is to observe the large difference between the water content of zeolite and that of other mineralic parts of the sample. The method suggested can be used in a zeolite mine for measuring the zeolite content continuously and controlling the quality of the end products. (author) 5 refs.; 3 figs.; 3 tabs

Biomineralization of hydroxyapatite in silver ion-exchanged nanocrystalline ZSM-5 zeolite using simulated body fluid.

Science.gov (United States)

Kaur, Balwinder; Srivastava, Rajendra; Satpati, Biswarup; Kondepudi, Kanthi Kiran; Bishnoi, Mahendra

2015-11-01

Silver ion-exchanged nanocrystalline zeolite (Ag-Nano-ZSM-5) and silver ion-exchanged conventional zeolite (Ag-ZSM-5) were synthesized. Zeolites were incubated in simulated body fluid at 310K for different time periods to grow hydroxyapatite in their matrixes. Significant large amount of hydroxyapatite was grown in Ag-Nano-ZSM-5 matrix after incubation in simulated body fluid when compared to Ag-ZSM-5. The resultant material was characterized using X-ray diffraction, N2-adsorption, scanning/transmission electron microscopy, energy dispersive X-ray, and inductively coupled plasma analysis. Mechanical properties such as compressive modulus, compressive strength, and strain at failure of the parent materials were evaluated. Biocompatibility assays suggested that Ag-Nano-ZSM-5 and hydroxyapatite grown in Ag-Nano-ZSM-5 were compatible and did not impose any toxicity to RAW 264.7 cells macrophase and Caco2 cells suggesting considerable potential for biomedical applications such as bone implants. Copyright © 2015 Elsevier B.V. All rights reserved.

Salt-occluded zeolite waste forms: Crystal structures and transformability

International Nuclear Information System (INIS)

Richardson, J.W. Jr.

1996-01-01

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

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.

Effects of heating on salt-occluded zeolite

International Nuclear Information System (INIS)

Lewis, M.A.; Hash, M.C.; Pereira, C.; Ackerman, J.P.

1996-01-01

The electrometallurgical treatment of spent nuclear fuel generates a waste stream of fission products in the electrolyte, LiCl-KCl eutectic salt. Argonne National Laboratory is developing a mineral waste form for this waste stream. The waste form consists of a composite formed by hot pressing salt-occluded zeolite and a glass binder. Pressing conditions must be judiciously chosen. For a given pressure, increasing temperatures and hold times give denser products but the zeolite is frequently converted to sodalite. Reducing the temperature or hold time leads to a porous zeolite composite. Therefore, conditions that affect the thermal stability of salt-occluded zeolite both with and without glass are being investigated in an ongoing study. The parameters varied in this stage of the work were heating time, temperature, salt loading, and glass content. The heat-treated samples were examined primarily by X-ray diffraction. Large variations were found in the rate at which salt-occluded zeolite converted to other phases such as nepheline, salt, and sodalite. The products depended on the initial salt loading. Heating times required for these transitions depended on the procedure and temperature used to prepare the salt-occluded zeolite. Mixtures of glass and zeolite reacted much faster than the pure salt-occluded zeolite and were almost always converted to sodalite

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.

Nuclear waste treatment using Iranian natural zeolites

International Nuclear Information System (INIS)

Kazemian, H.; Ghannadi Maraghe, M.

2001-01-01

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

New developments in zeolite science and technology

International Nuclear Information System (INIS)

Murakami, Y.

1986-01-01

The contributions in this volume introduce numerous new results and concepts. MAS-NMR has become a powerful tool in the structural analysis of zeolite, metallosilicate and aluminophosphate, enabling definition at the atomic level of the silicon and aluminum forming the zeolite framework. Detailed knowledge on the structure of natural zeolite has increased. Regarding synthesis, studies on the preparation of various metallosilicates, the role of various organic compounds at templates and the kinetics of crystallization and crystal growth are presented. Developments in zeolite catalysts focus not only on the solid-acid catalysts and the shape selective catalysts but on the bifunctional type catalysts as well. Catalyses by metallosilicates or silicoaluminophosphates are reported. Attempts to improve the catalytic performance by modification are presented. Effort is also being devoted to the analysis of adsorption state and diffusion in zeolites. Zeolite deposits of economic value are reported from several countries. (Auth.)

PENJERAPAN P-KHLOROFENOL DALAM AIR LIMBAH DENGAN ZEOLIT (Adsorption of p-Chlorophenol from Wastewater using Zeolite

Directory of Open Access Journals (Sweden)

Sarto Sarto

2007-07-01

Full Text Available ABSTRAK Penelitian ini bertujuan untuk mempelajari kemampuan zeolit untuk menjerap p-khlorofenol dari limbah cair secara batch, pada suhu 30 °C dan tekanan 1 atmosfer. Hasil penelitian menunjukkan bahwa proses penjerapan mengikuti persamaan Freundlich dan bersifat reversibel sebagian. Nisbah kinerja desorbsi dan penjerapan adalah antara 31,85 % dan 49,36 %. Kemampuan zeolit untuk menjerap p-khlorofenol meningkat dengan semakin rendahnya pH. pada nilai pH 3,92, berat zeolit 30 g, dan konsentrasi awal p-khlorofenol 97,302 mg/L. Adapun jumlah p-khlorofenol yang terjerap adalah sebesar 8,319 mg/L.   ABSTRACT The aim of this research is to study the characteristics of zeolit to adsorb p-chlorophenol from wastewater in a batch reactor at 30 oC and atmospheric conditions. The experimental results show that the adsorbtion process is partially reversible and fits with Freundlich Equation. The ratio of  desorption and adsortion performance is between 31.85 % and 49.36 %.  The performance of zeolit to adsorb p-chlorophenol increases with decreasing pH. At  pH about 3.92, using 30 g zeolit and 97.302 mg  p-chlorophenol/L. The concentration of adsorbed p-chlorophenol is about 8.319 mg/L.

Zeolitic materials with hierarchical porous structures.

Science.gov (United States)

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

2011-06-17

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

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,

Comparing gas separation performance between all known zeolites and their zeolitic imidazolate framework counterparts.

Science.gov (United States)

Gómez-Álvarez, Paula; Hamad, Said; Haranczyk, Maciej; Ruiz-Salvador, A Rabdel; Calero, Sofia

2016-01-07

To find optimal porous materials for adsorption-based separations is a challenging task due to the extremely large number of possible pore topologies and compositions. New porous material classes such as Metal Organic Frameworks (MOFs) are emerging, and hope to replace traditionally used materials such as zeolites. Computational screening offers relatively fast searching for candidate structures as well as side-by-side comparisons between material families. This work is pioneering at examining the families comprised by the experimentally known zeolites and their respective Zeolitic Imidazolate Framework (ZIF) counterparts in the context of a number of environmental and industrial separations involving carbon dioxide, nitrogen, methane, oxygen, and argon. Additionally, unlike related published work, here all the targeted structures have been previously relaxed through energy minimization. On the first level of characterization, we considered a detailed pore characterization, identifying 24 zeolites as promising candidates for gas separation based on adsorbate sizes. The second level involved interatomic potential-based calculations to assess the adsorption performance of the materials. We found no correlation in the values of heat of adsorption between zeolites and ZIFs sharing the same topology. A number of structures were identified as potential experimental targets for CO2/N2, and CO2/CH4 affinity-based separations.

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.

Exceptionally stable and hierarchically porous self-standing zeolite monolith based on a solution-mediated and solid-state transformation synergistic mechanism

Energy Technology Data Exchange (ETDEWEB)

Do, Manh Huy [Key Laboratory of Biomass Chemical Engineering of Ministry of Education, Zhejiang University, Hangzhou 310027, Zhejiang (China); College of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310027, Zhejiang (China); Institute of Chemical Technology, Vietnamese Academy of Science and Technology, 01 Mac Dinh Chi, District 1, Ho Chi Minh (Viet Nam); Cheng, Dang-guo, E-mail: dgcheng@zju.edu.cn [College of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310027, Zhejiang (China); Chen, Fengqiu [Key Laboratory of Biomass Chemical Engineering of Ministry of Education, Zhejiang University, Hangzhou 310027, Zhejiang (China); College of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310027, Zhejiang (China); Zhan, Xiaoli [College of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310027, Zhejiang (China)

2015-11-15

Although many strategies exist for fabricating hierarchical zeolite monolith, it is still challenging to synthesize pure hierarchical zeolite monolith with intracrystalline meso-/macropores and stability suitable for industrial application in a general and efficient process. Here we describe a simple quasi-solid gel crystallization route to prepare hierarchical self-standing ZSM-5 zeolite monolith via the use of Na{sup +} and OH{sup −} as counterions to modify the breaking and remaking of T–O–T (T = Si or Al) bonds. X-ray diffraction (XRD), scanning electron microcopy (SEM), transmission electron microscopy (TEM), laser scan confocal microscopy (LSCM), N{sub 2} adsorption–desorption, mercury porosimetry, solid-state nuclear magnetic resonance (NMR), and compression mechanical testing were applied to elucidate the structure and mechanical stability of the obtained monolith. The self-standing monolith is composed of self-interconnected meso-/macroporous MFI crystals with tunable intracrystalline meso-/macropores and possesses an unusually mechanical stability with a crushing strength of 5.01 MPa. Combined with controllable structure of the defect-free membrane layer on the monolith top, the self-standing zeolite monolith should widen their potential applications. - Highlights: • Hierarchical self-standing MFI zeolite monoliths were synthesized via a facile method. • Na{sup +} and OH{sup −} are used as counterions for breaking and remaking of T–O–T (T = Si or Al) bonds. • Hierarchical self-standing MFI zeolite monoliths result from zeolite crystal intergrowth. • Self-standing zeolite monolith has an excellent mechanical stability with tunable intracrystalline meso-/macropores.

Preparation of zeolite-A/chitosan hybrid composites and their bioactivities and antimicrobial activities.

Science.gov (United States)

Yu, Liang; Gong, Jie; Zeng, Changfeng; Zhang, Lixiong

2013-10-01

Zeolite-A/chitosan hybrid composites with zeolite contents of 20-55 wt.% were prepared by in situ transformation of silica/chitosan mixtures in a sodium aluminate alkaline solution through impregnation-gelation-hydrothermal synthesis. The products were characterized by X-ray diffraction, diffuse reflectance infrared Fourier transform spectroscopy, scanning electron microscopy, thermogravimetric analysis, and mercury penetration porosimetry. Their in vitro bioactivities were examined using as-synthesized and Ca(2+)-exchanged hybrid composites in simulated body fluid (SBF) for hydroxyapatite (HAP) growth. Their antimicrobial activities for Escherichia coli (E. coli) in trypticase soy broth (TSB) were evaluated using Ag(+)-exchanged hybrid composites. The zeolite-A/chitosan hybrid composites could be prepared as various shapes, including cylinders, plates and thin films. They possessed macropores with pore sizes ranging from 100 to 300 μm and showed compressive mechanical strength as high as 3.2 MPa when the zeolite content was 35 wt.%. Fast growth on the Ca(2+)-exchanged hybrid composites was observed with the highest weight gain of 51.4% in 30 days. The 35 wt.% Ag(+)-exchanged hybrid composite showed the highest antimicrobial activity, which could reduce the 9×10(6) CFU mL(-1)E. coli concentration to zero within 4h of incubation time with the Ag(+)-exchanged hybrid composite amount of 0.4 g L(-1). The bioactivity and antimicrobial activity could be combined by ion-exchanging the composites first with Ca(2+) and then with Ag(+). These zeolite-A/chitosan hybrid composites have potential applications on tissue engineering and antimicrobial food packaging. Copyright © 2013 Elsevier B.V. All rights reserved.

Methane emissions abatement by multi-ion-exchanged zeolite A prepared from both commercial-grade zeolite and coal fly ash.

Science.gov (United States)

Hui, K S; Chao, C Y H

2008-10-01

The performance of multimetal-(Cu, Cr, Zn, Ni, and Co)-ion-exchanged zeolite A prepared from both a commercial-grade sample and one produced from coal fly ash in methane emissions abatement was evaluated in this study. The ion-exchange process was used to load the metal ions in zeolite A samples. The methane conversion efficiency by the samples was studied under various parameters including the amount of metal loading (7.3-19.4 wt%), reaction temperature (25-500 degrees C), space velocity (8400-41 900 h(-1)), and methane concentration (0.5-3.2 vol %). At 500 degrees C, the original commercial-grade zeolite A catalyzed 3% of the methane only, whereas the addition of different percentages of metals in the sample enhanced the methane conversion efficiency by 40-85%. Greater methane conversion was observed by increasing the percentage of metals added to the zeolite even though the BET surface area of the zeolite consequently decreased. Higher percentage methane conversion over the multi-ion-exchanged samples was observed at lower space velocities indicating the importance of the mass diffusion of reactants and products in the zeolite. Compared to the multi-ion-exchanged zeolite A prepared from the commercial-grade zeolite, the one produced from coal fly ash demonstrated similar performances in methane emissions abatement, showing the potential use of this low cost recycled material in gaseous pollutant treatment.

Computational approach in zeolite science

NARCIS (Netherlands)

Pidko, E.A.; Santen, van R.A.; Chester, A.W.; Derouane, E.G.

2009-01-01

This chapter presents an overview of different computational methods and their application to various fields of zeolite chemistry. We will discuss static lattice methods based on interatomic potentials to predict zeolite structures and topologies, Monte Carlo simulations for the investigation of

Effects of Zeolite and Vermicompost on Changes of Zn Chemical Fractionation in a Polluted Soil

Directory of Open Access Journals (Sweden)

Mohsen Hamidpour

2017-02-01

Full Text Available Introduction: Soil contamination by heavy metals is a major concern throughout the world, due to persistence of metals in the environment and their toxicity and threat to all living organisms. Several strategies have been used to immobilize heavy metal ions in soils. Immobilization can be achieved by adding natural and synthetic amendments such as zeolites and organic materials. Because of large specific surface area, high cation exchange capacity (CEC, low cost and wide spread availability, zeolites are probably the most promising materials interacting with many heavy metal ions in contaminated soils and water. Organic amendments such as vermicompost contains a high proportion of humified organic matter (OM, may decrease the bioavailability of heavy metals in soil by adsorption and by forming stable complexes with surface functional groups, thus permitting the re-establishment of vegetation on contaminated sites. Recent studies showed that the co-application of zeolite and humic acids could be effective in reducing the available fraction of Pb in a garden polluted soil. Fractionation of heavy metals cations in amended polluted-soils is needed to predict elemental mobility in soil and phyto-availability to plants. Therefore, the objective of this study was to investigate the effects of co-application of zeolite and vermicompost on Zn redistribution in a contaminated soil. Material and Methods: A contaminated soil was collected from the top 20 cm in the vicinity of zinc mine in Zanjan province, western north of Iran. The soil sample was air-dried, passed through 2-mm sieve and stored at room temperature. The soil sample was thoroughly mixed to ensure uniformity. Sub-samples were then digested using the hot-block digestion procedure for total Zn concentration. The experiment was conducted under greenhouse condition. The polluted soil was put in polyethylene pots and mixed well vermicompost and zeolite at the rate of 0, 50 and 100 g kg-1 soil. The

Physical, Chemical and Structural Evolution of Zeolite-Containing Waste Forms Produced from Metakaolinite and Calcined Sodium Bearing Waste (HLW and/or LLW)

International Nuclear Information System (INIS)

Grutzeck, Michael W.

2005-01-01

Zeolites are extremely versatile. They can adsorb liquids and gases and serve as cation exchange media. They occur in nature as well cemented deposits. The ancient Romans used blocks of zeolitized tuff as a building material. Using zeolites for the management of radioactive waste is not a new idea, but a process by which the zeolites can be made to act as a cementing agent is. Zeolitic materials are relatively easy to synthesize from a wide range of both natural and man-made substances. The process under study is derived from a well known method in which metakaolin (an impure thermally dehydroxylated kaolinite heated to ∼700 C containing traces of quartz and mica) is mixed with sodium hydroxide (NaOH) and reacted in slurry form (for a day or two) at mildly elevated temperatures. The zeolites form as finely divided powders containing micrometer ((micro)m) sized crystals. However, if the process is changed slightly and only just enough concentrated sodium hydroxide solution is added to the metakaolinite to make a thick crumbly paste and then the paste is compacted and cured under mild hydrothermal conditions (60-200 C), the mixture will form a hard ceramic-like material containing distinct crystalline tectosilicate minerals (zeolites and feldspathoids) imbedded in an X-ray amorphous hydrated sodium aluminosilicate matrix. Due to its lack of porosity and vitreous appearance we have chosen to call this composite a ''hydroceramic''

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....

Effect of Adductor Canal Block Versus Femoral Nerve Block on Quadriceps Strength, Mobilization, and Pain After Total Knee Arthroplasty

DEFF Research Database (Denmark)

Grevstad, Jens Ulrik; Mathiesen, Ole; Valentiner, Laura Risted Staun

2015-01-01

strength. METHODS: We included 50 TKA patients with severe movement-related pain; defined as having visual analog scale pain score of greater than 60 mm during active flexion of the knee. The ACB group received an ACB with ropivacaine 0.2% 30 mL and a femoral nerve block (FNB) with 30 mL saline. The FNB...... group received an ACB with 30 mL saline and an FNB with ropivacaine 0.2% 30 mL. We compared the effect of the ACB versus FNB on maximum voluntary isometric contraction of the quadriceps muscle relative to a postoperative baseline value. Secondary end points were differences between groups in ability...

Vitrification of highly-loaded SDS zeolites

International Nuclear Information System (INIS)

Siemens, D.H.; Bryan, G.H.; Knowlton, D.E.; Knox, C.A.

1982-11-01

Pacific Northwest Laboratory (PNL) is demonstrating a vitrification system designed for immobilization of highly loaded SDS zeolites. The Zeolite Vitrification Demonstration Project (ZVDP) utilizes an in-can melting process. All steps of the process have been demonstrated, from receipt of the liners through characterization of the vitrified product. The system has been tested with both nonradioactive and radioactive zeolite material. Additional high-radioactivity demonstrations are scheduled to begin in FY-83. 5 figures, 4 tables

Chemical reactivity of cation-exchanged zeolites

OpenAIRE

Pidko, E.A.

2008-01-01

Zeolites modified with metal cations have been extensively studied during the last two decades because of their wide application in different technologically important fields such as catalysis, adsorption and gas separation. Contrary to the well-understood mechanisms of chemical reactions catalyzed by Brønsted acid sites in the hydrogen forms of zeolites, the nature of chemical reactivity, and related, the structure of the metal-containing ions in cation-exchanged zeolites remains the subject...

Antimicrobial properties of zeolite-X and zeolite-A ion-exchanged with silver, copper, and zinc against a broad range of microorganisms.

Science.gov (United States)

Demirci, Selami; Ustaoğlu, Zeynep; Yılmazer, Gonca Altın; Sahin, Fikrettin; Baç, Nurcan

2014-02-01

Zeolites are nanoporous alumina silicates composed of silicon, aluminum, and oxygen in a framework with cations, water within pores. Their cation contents can be exchanged with monovalent or divalent ions. In the present study, the antimicrobial (antibacterial, anticandidal, and antifungal) properties of zeolite type X and A, with different Al/Si ratio, ion exchanged with Ag(+), Zn(2+), and Cu(2+) ions were investigated individually. The study presents the synthesis and manufacture of four different zeolite types characterized by scanning electron microscopy and X-ray diffraction. The ion loading capacity of the zeolites was examined and compared with the antimicrobial characteristics against a broad range of microorganisms including bacteria, yeast, and mold. It was observed that Ag(+) ion-loaded zeolites exhibited more antibacterial activity with respect to other metal ion-embedded zeolite samples. The results clearly support that various synthetic zeolites can be ion exchanged with Ag(+), Zn(2+), and Cu(2+) ions to acquire antimicrobial properties or ion-releasing characteristics to provide prolonged or stronger activity. The current study suggested that zeolite formulations could be combined with various materials used in manufacturing medical devices, surfaces, textiles, or household items where antimicrobial properties are required.

Catalase-like activity studies of the manganese(II) adsorbed zeolites

Science.gov (United States)

Ćiçek, Ekrem; Dede, Bülent

2013-12-01

Preparation of manganese(II) adsorbed on zeolite 3A, 4A, 5A. AW-300, ammonium Y zeolite, organophilic, molecular sieve and catalase-like enzyme activity of manganese(II) adsorbed zeolites are reported herein. Firstly zeolites are activated at 873 K for two hours before contact manganese(II) ions. In order to observe amount of adsorption, filtration process applied for the solution. The pure zeolites and manganese(II) adsorbed zeolites were analysed by FT-IR. As a result according to the FT-IR spectra, the incorporation of manganese(II) cation into the zeolite structure causes changes in the spectra. These changes are expected particularly in the pseudolattice bands connected with the presence of alumino and silicooxygen tetrahedral rings in the zeolite structure. Furthermore, the catalytic activities of the Mn(II) adsorbed zeolites for the disproportionation of hydrogen peroxide were investigated in the presence of imidazole. The Mn(II) adsorbed zeolites display efficiency in the disproportion reactions of hydrogen peroxide, producing water and dioxygen in catalase-like activity.

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

Absorption behavior of iodine from molten salt mixture to zeolite

International Nuclear Information System (INIS)

Sugihara, Kei; Terai, Takayuki; Suzuki, Akihiro; Uozumi, Koichi; Tsukada, Takeshi; Koyama, Tadafumi

2011-01-01

Behavior of zeolite to absorb anion fission product (FP) elements in molten LiCl-KCl eutectic salt was studied using iodine. At first, zeolite-A was selected as the suitable type of zeolite among zeolite-A (powder), zeolite-X (powder and granule), and zeolite-Y (powder) through experiments to heat the zeolite together with LiCl-KCl-KI salt, respectively. As the next step, similar experiments to immerse zeolite-A in molten LiCl-KCl-KI salt containing various concentrations of iodine were performed. The affinity of iodine to zeolite was evaluated using the separation factor (SF) value, which is defined as [I/(I+Cl) mol ratio in zeolite after immersion]/[I/(I+Cl) mol ratio in salt after immersion]. Since the SF values ranged between 4.3 and 9.1, stronger affinity of iodine than chlorine to zeolite-A was revealed. Finally, influence of co-existing cation FPs was studied by similar absorption experiments in LiCl-KCl-KI salt containing CsCl, SrCl 2 , or NdCl 3 . The SF values were less than those obtained in the LiCl-KCl-KI salt and this can be ascribed to the sharing of inner space of zeolite cage among absorbed cations and anions. (author)

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

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.

ZEOLITIZATION OF SEWAGE SLUDGE ASH WITH A FUSION METHOD

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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.

Preparation of Synthetic Zeolites from Myanmar Clay Mineral

International Nuclear Information System (INIS)

Phyu Phyu Win

2004-04-01

Faujasite type zeolite X was successfully synthesized from Myanmar clay mineral kaolinite, by treating with sodium hydroxide at 820 C followed by dissolution in water and hydrothermal treatment. It was found that the solution of fused clay powder can be crystallized at 90C under ambient pressure to synthesize faujasite type zeolite X. The effects of aging time and the amount of water on the formation of the product phase and Si/ Al ratios of the resulting products were investigated. Most of the Si and Al components in kaolinite might be dissolved into an alkaline solution and reacted to form ring-like structures. Then it was effectively transformed into zeolite materials. The maximum relative crystallinity of faujasite zeolite obtained was found to be 100%. Zeolite P was found to be a competitive phase present in some resulting products during hydrothermal treatment. The cation exchange capacity of kaolinite is very low, but increased after a proper treatment. It was found that the prepared faujasite type zeolite X, zeolite P and hydrogen zeolite (HZ) can reduce the hardness, the alkalinity, the total dissolved solid and the dissolved iron of raw water in the batch wise operation of water treatment. Therefore, it can be used as the cation exchanged resin for water treatment

Strong white photoluminescence from annealed zeolites

International Nuclear Information System (INIS)

Bai, Zhenhua; Fujii, Minoru; Imakita, Kenji; Hayashi, Shinji

2014-01-01

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

Reaction mechanisms in zeolite catalysis

NARCIS (Netherlands)

Rozanska, X.; Santen, van R.A.; Auerbach, S.C.; Carrado, K.A.; Dutta, P.D.

2003-01-01

A review; described are the most basic mechanistic reaction steps that are induced by zeolite catalysts. Details on the zeolitic properties that are relevant to mol. reactivity are also provided. The theor. methods and models at hand to allow the investigation of these reaction steps and that have

Nondestructive evaluation of the oxidation and strength of the Fort Saint Vrain HTGR support block

International Nuclear Information System (INIS)

Tingey, G.L.; Posakony, G.J.; Morgan, W.C.; Prince, J.M.; Hill, R.W.; Lessor, D.L.

1982-04-01

Non-destructive detection of changes in the strength of graphite support structures in a HTGR appears to be feasible using sonic velocity measurements where access for through transmission is possible. Therefore, future HTGR designs should consider providing such access. Where access is not available, strength changes can be correlated with oxidation profiles in the support member. These oxidation profiles can be determined non-destructively by a combination of eddy current measurements to detect near surface oxidation and sonic backscattering measurements designed to determine oxidation in depth. The Fort Saint Vrain reactor provides an operating reactor to test the applicability of the eddy current and sonic backscattering techniques for determination of oxidation in a support block. Furthermore, such tests in Fort Saint Vrain will supply base line data which will be useful in assuring an adequate strength of the support structure for the lifetime of the reactor. Equipment is, therefore, being developed for tests to be conducted during the next major refueling of the reactor

Electrical conductivity of polyaniline/zeolite composites and synergetic interaction with CO

International Nuclear Information System (INIS)

Densakulprasert, Nataporn; Wannatong, Ladawan; Chotpattananont, Datchanee; Hiamtup, Piyanoot; Sirivat, Anuvat; Schwank, Johannes

2005-01-01

The effects of zeolite content, pore size and ion exchange capacity on electrical conductivity response to carbon monoxide (CO) of polyaniline/zeolite composites were investigated. Zeolite Y, 13X, and synthesized AlMCM41, all having the common cation Cu 2+ , were dry mixed with synthesized maleic acid (MA) doped polyaniline and compressed to form polyaniline (PANI)/zeolite pellet composites. The Y, 13X and AlMCM41 zeolite have the nominal pore sizes of 7, 10, 36 A, and the Cu 2+ exchange capacities of 0.161, 0.087, and 0.044 mol/g, respectively. With an addition of 13X zeolite to pristine polyaniline, the electrical conductivity sensitivity to CO/N 2 gas increases with zeolite content. For the effect of zeolite type, the highest electrical conductivity sensitivity is obtained with the 13X zeolite, followed by the Y zeolite, and the AlMCM41 zeolite, respectively. Poor sensitivity of zeolite AlMCM41 is probably due to its very large pore size and its lowest Cu 2+ exchange capacity. Y zeolite and 13X zeolite have comparable pore sizes but the latter has a greater pore free volume and a more favorable location distribution of the Cu 2+ ions within the pore. The temporal response time increases with the amount of zeolite in the composites but it is inversely related to the amount of ion exchange capacity

Structure–Property Relationships of Inorganically Surface-Modified Zeolite Molecular Sieves for Nanocomposite Membrane Fabrication

KAUST Repository

Lydon, Megan E.

2012-05-03

A multiscale experimental study of the structural, compositional, and morphological characteristics of aluminosilicate (LTA) and pure-silica (MFI) zeolite materials surface-modified with MgO xH y nanostructures is presented. These characteristics are correlated with the suitability of such materials in the fabrication of LTA/Matrimid mixed-matrix membranes (MMMs) for CO 2/CH 4 separations. The four functionalization methods studied in this work produce surface nanostructures that may appear superficially similar under SEM observation but in fact differ considerably in shape, size, surface coverage, surface area/roughness, degree of attachment to the zeolite surface, and degree of zeolite pore blocking. The evaluation of these characteristics by a combination of TEM, HRTEM, N 2 physisorption, multiscale compositional analysis (XPS, EDX, and ICP-AES elemental analysis), and diffraction (ED and XRD) allows improved understanding of the origin of disparate gas permeation properties observed in MMMs made with four types of surface-modified zeolite LTA materials, as well as a rational selection of the method expected to result in the best enhancement of the desired properties (in the present case, CO 2/CH 4 selectivity increase without sacrificing permeability). A method based on ion exchange of the LTA with Mg 2+, followed by base-induced precipitation and growth of MgO xH y nanostructures, deemed "ion exchange functionalization" here, offers modified particles with the best overall characteristics resulting in the most effective MMMs. LTA/Matrimid MMMs containing ion exchange functionalized particles had a considerably higher CO 2/CH 4 selectivity (∼40) than could be obtained with the other functionalization techniques (∼30), while maintaining a CO 2 permeability of ∼10 barrers. A parallel study on pure silica MFI surface nanostructures is also presented to compare and contrast with the zeolite LTA case. © 2012 American Chemical Society.

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

International Nuclear Information System (INIS)

Miura, Hidenori; Uozumi, Koichi

2009-01-01

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

Influence of zeolite structure on the activity and durability of Co-Pd-zeolite catalysts in the reduction of NOx with methane

International Nuclear Information System (INIS)

Pieterse, J.A.Z.; Van den Brink, R.W.; Booneveld, S.; De Bruijn, F.A.

2003-01-01

Selective catalytic reduction of NO with CH 4 was studied over ZSM-5, MOR, FER and BEA zeolite-based cobalt (Co) and palladium (Pd) catalysts in the presence of oxygen and water. As compared to other catalytic systems reported in literature for CH 4 -SCR in the presence of water, zeolite supported Co-Pd combination catalysts are very active and selective. The most active catalysts, based on MOR and ZSM-5, are characterised by well-dispersed Pd ions in the zeolite that activate methane. Wet ion exchange is a good method to achieve high dispersion of Pd provided that it is carried out in a competitive manner. The presence of cobalt (Co 3 O 4 , Co-oxo ions) boosts SCR activity by oxidising NO to NO 2 . The activity of the zeolite-based Co-Pd combination catalysts decreases with prolonged times on stream. The severity of the deactivation was found to be different for different zeolite topologies. The characterisation and evaluation of freshly calcined catalysts and spent catalysts show two things that occur during reaction: (1) zeolite solvated metal cations disappear in favour of (inactive) metal oxides and presumably larger metal entities, i.e. loss of dispersion; (2) loss of crystallinity affiliated with steam-dealumination and the concomitant formation of extra-framework aluminium (EFAL) in the presence of water. Both phenomena strongly depend on the (reaction) temperature. The deactivation of Co-Pd-zeolite resembles the deactivation of Pd-zeolite. Hence, future research could encompass the stabilisation of Pd (cations) in the zeolite pores by exploring additives other than cobalt. For this, detailed understanding on the siting of Pd in zeolites is important

Zeolite food supplementation reduces abundance of enterobacteria.

Science.gov (United States)

Prasai, Tanka P; Walsh, Kerry B; Bhattarai, Surya P; Midmore, David J; Van, Thi T H; Moore, Robert J; Stanley, Dragana

2017-01-01

According to the World Health Organisation, antibiotics are rapidly losing potency in every country of the world. Poultry are currently perceived as a major source of pathogens and antimicrobial resistance. There is an urgent need for new and natural ways to control pathogens in poultry and humans alike. Porous, cation rich, aluminosilicate minerals, zeolites can be used as a feed additive in poultry rations, demonstrating multiple productivity benefits. Next generation sequencing of the 16S rRNA marker gene was used to phylogenetically characterize the fecal microbiota and thus investigate the ability and dose dependency of zeolite in terms of anti-pathogenic effects. A natural zeolite was used as a feed additive in laying hens at 1, 2, and 4% w/w for a 23 week period. At the end of this period cloacal swabs were collected to sample faecal microbial communities. A significant reduction in carriage of bacteria within the phylum Proteobacteria, especially in members of the pathogen-rich family Enterobacteriaceae, was noted across all three concentrations of zeolite. Zeolite supplementation of feed resulted in a reduction in the carriage of a number of poultry pathogens without disturbing beneficial bacteria. This effect was, in some phylotypes, correlated with the zeolite concentration. This result is relevant to zeolite feeding in other animal production systems, and for human pathogenesis. Copyright © 2016 Elsevier GmbH. All rights reserved.

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%.

Natural zeolite reactivity towards ozone: The role of compensating cations

International Nuclear Information System (INIS)

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

2012-01-01

Highlights: ► Chemical and thermal treatment enhances catalytic activity of natural zeolite. ► Modified natural zeolite exhibits high stability after thermal treatment. ► Reducing the compensating cation content leads to an increase on ozone abatement. ► Surface active atomic oxygen was detected using the DRIFT technique. ► The highest reactivity toward ozone was performed by NH4Z3 zeolite sample. - Abstract: Among indoor pollutants, ozone is recognised to pose a threat to human health. Recently, low cost natural zeolites have been applied as alternative materials for ozone abatement. In this work, the effect of compensating cation content of natural zeolite on ozone removal is studied. A Chilean natural zeolite is used here as starting material. The amount of compensating cations in the zeolite framework was modified by ion exchange using an ammonium sulphate solution (0.1 mol L −1 ). Characterisation of natural and modified zeolites were performed by X-ray powder diffraction (XRD), nitrogen adsorption at 77 K, elemental analysis, X-ray fluorescence (XRF), thermogravimetric analysis coupled with mass spectroscopy (TGA-MS), and temperature-programmed desorption of ammonia (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.

Zeolitization at uranium ore manifestation

International Nuclear Information System (INIS)

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

1981-01-01

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

Hierarchical zeolites from class F coal fly ash

Science.gov (United States)

Chitta, Pallavi

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

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. Copyright © 2012 Elsevier B.V. All rights reserved.

Effect of SrO content on Zeolite Structure

Science.gov (United States)

Widiarti, N.; Sari, U. S.; Mahatmanti, F. W.; Harjito; Kurniawan, C.; Prasetyoko, D.; Suprapto

2018-04-01

The aims of current studies is to investigate the effect of strontium oxide content (SrO) on synthesized zeolite. Zeolite was synthesized from Tetraethyl orthosilicate (TEOS) as precursors of SiO2 and aluminum isopropoxide (AIP) precursors. The mixture was aged for 3 days and hydrothermally treated for 6 days. The SrO content was added by impregnation method. The products were then characterized using X-Ray Diffraction (XRD), Fourier Transform Infrared (FTIR), and Surface Area Analyzer (SAA). The diffractogram confirmed the formation of Faujasite-like zeolite. However, after the addition of SrO, the crystallinity of zeolite was deformed. The diffractograms shows the amorphous phase of zeolite were decrease as the SrO content is increase. The structural changes was also observed from FTIR spectra which shows the shifting and peak formation. The surface area analysis showed that the increasing loading of SrO/Zeolites reduced the catalyst surface area.

Zeolite and swine inoculum effect on poultry manure biomethanation

DEFF Research Database (Denmark)

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

2013-01-01

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

Zeolite and swine inoculum effect on poultry manure biomethanation

Science.gov (United States)

Kougias, P. G.; Fotidis, I. A.; Zaganas, I. D.; Kotsopoulos, T. A.; Martzopoulos, G. G.

2013-03-01

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

Three Mile Island zeolite vitirification demonstration program

International Nuclear Information System (INIS)

Siemens, D.H.; Knowlton, D.E.; Shupe, M.W.

1981-06-01

The cleanup of the high-activity-level water at Three Mile Island (TMI) provides an opportunity to further develop waste management technology. Approximately 790,000 gallons of high-activity-level water at TMI's Unit-2 Nuclear Power Station will be decontaminated at the site using the submerged demineralizer system (SDS). In the SDS process, the cesium and strontium in the water are sorbed onto zeolite that is contained within metal liners. The Department of Energy has asked the Pacific Northwest Laboratory (PNL) to take a portion of the zeolite from the SDS process and demonstrate, on a production scale, that this zeolite can be vitrified using the in-can melting process. This paper is a brief overview of the TMI zeolite vitrification program. The first section discusses the formulation of a glass suitable for immobilizing SDS zeolite. The following section describes a feed system that was developed to feed zeolite to the in-can melter. It also describes the in-can melting process and the government owned facilities in which the demonstrations will take place. Finally, the schedule for completing the program activities is outlined

Zeolites and Zeotypes for Oil and Gas Conversion

NARCIS (Netherlands)

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

2015-01-01

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

Splitting strength and abrasion resistance of concrete paving blocks as a function of dry bulk specific gravity and ultrasonic pulse velocity

Directory of Open Access Journals (Sweden)

Haktanir, T.

2005-06-01

Full Text Available Artificial Portland cement concrete paving blocks are widely used in many countries. These paving blocks come in a variety of designs with names such as "Interlocking" and "Italian Flower", and are manufactured with special machinery using rather high quality concrete having a compressive strength of about 50 MPa. Concrete blocks are employed instead of natural cobble stones for essentially economic reasons. The laboratoiy equipment required to measure paving block splitting strength and abrasion resistance, two of the chief properties to be tested in quality checks, is costly and the tests are time-consuming and labour-intensive. The present paper reports on a detailed experimental study performed to relate the splitting strength and abrasion resistance of concrete paving blocks to "dry bulk specific gravity" (DBSG and "ultrasonic pulse velocity" (UPV, respectively. Statistically significant regression equations describing the dependence of splitting strength on DBSG and abrasion resistance on UPV were obtained with data from random samples of material provided by seven different manufacturers.

RESUMEN Los bloques para pavimentos (adoquines elaborados con hormigón se utilizan habitualmente en numerosos países. Estos bloques de pavimentación se diseñan de diversas formas, como por ejemplo "Entrelazado " ("Interlocking " o "Flor Italiana " ("Italian Flower"; se fabrican con maquinaria especial y con frecuencia se utiliza hormigón de la más alta calidad, con resistencia a la compresión de alrededor de 50 MPa. La razón de utilizar bloques de hormigón en lugar de bloques de piedra natural es básicamente económica. Los equipos de laboratorio necesarios para medir la resistencia a la compresión y a la abrasión -dos de las propiedades más importantes para determinar la calidad de los bloques en estudio- son costosos y los ensayos requieren tiempo y mano de obra considerables. En el presente trabajo se exponen ensayos experimentales

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.

Sequestration and disposal of dissolved Cs+ using zeolite 13X

Science.gov (United States)

Park, M.; Park, J.; Jeong, H. Y.

2017-12-01

Low-to-intermediate level liquid radioactive wastes (LILLW) typically contain high levels of radioactive 137Cs. Due to the great radiational and thermal stability as well as the high selectivity, zeolite has been commonly utilized to sequester radioactive isotopes from nuclear wastewater effluents. In this study, an Al-rich synthetic zeolite 13X was evaluated for the sorption capacity of Cs+ as a function of pH (4.0-10.5), ionic strength (0.05 and 0.2 M), and initial Cs+ concentration (1×10-6-5×10-3 M). For safe disposal, Cs+-exchanged 13X was both thermally and hydrothermally treated under different temperature and pressure. Subsequently, the resultant materials were examined for the phase transition by X-ray diffraction (XRD) and the local coordination chemistry by X-ray absorption spectroscopy (XAS). Our experimental results will detail the Cs+ sorption behavior by 13X under varying solution compositions. Also, the structural changes of Cs+-exchanged 13X upon thermal and hydrothermal treatment will be delineated to assess the stability of Cs+ in the treated materials.

CoX zeolites and their exchange with deuterium

Energy Technology Data Exchange (ETDEWEB)

Novakova, J; Kubelkova, L; Jiru, P [Ceskoslovenska Akademie Ved, Prague. Ustav Fyzikalni Chemie

1976-04-01

An analysis of the gaseous phase using a mass spectrometer and analysis of the solid phase using an infrared spectrophotometer was made to investigate the deuterium exchange with hydrogen mostly bound in hydroxyl groups of zeolites CoX(21 and 47%) and NaX. It was found that with the increasing amount of cobalt ions the number of exchangeable hydrogens of the zeolite increases; the respective types of the hydrogen are discussed with respect to the particular dehydration temperatures. The rate of the D/sub 2/+OH exchange is substantially faster with the CoX than with the NaX zeolite, and exhibits a decrease with increasing dehydration. On the other hand, the rate of D/sub 2/+H/sub 2/ exchange without zeolite hydrogen incorporation, catalyzed by CoX zeolites, increases with increasing dehydration. The increased activation of gaseous hydrogen molecules is related to the presence in the zeolite of cobalt ions whose properties change during dehydration with the change in their environment. Hydroxyl groups of the CoX zeolites are not equivalent during the exchange; the hydroxyl hydrogens of the 3740 cm/sup -1/ band are exchanged more slowly than are the other hydrogens.

CoX zeolites and their exchange with deuterium

International Nuclear Information System (INIS)

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

1976-01-01

An analysis of the gaseous phase using a mass spectrometer and analysis of the solid phase using an infrared spectrophotometer was made to investigate the deuterium exchange with hydrogen mostly bound in hydroxyl groups of zeolites CoX(21 and 47%) and NaX. It was found that with the increasing amount of cobalt ions the number of exchangeable hydrogens of the zeolite increases; the respective types of the hydrogen are discussed with respect to the particular dehydration temperatures. The rate of the D 2 +OH exchange is substantially faster with the CoX than with the NaX zeolite, and exhibits a decrease with increasing dehydration. On the other hand, the rate of D 2 +H 2 exchange without zeolite hydrogen incorporation, catalyzed by CoX zeolites, increases with increasing dehydration. The increased activation of gaseous hydrogen molecules is related to the presence in the zeolite of cobalt ions whose properties change during dehydration with the change in their environment. Hydroxyl groups of the CoX zeolites are not equivalent during the exchange; the hydroxyl hydrogens of the 3740 cm -1 band are exchanged more slowly than are the other hydrogens. (author)

Dry method for recycling iodine-loaded silver zeolite

International Nuclear Information System (INIS)

Thomas, T.R.; Staples, B.A.; Murphy, L.P.

1978-01-01

Fission product iodine is removed from a waste gas stream and stored by passing the gas stream through a bed of silver-exchanged zeolite until the zeolite is loaded with iodine, passing dry hydrogen gas through the bed to remove the iodine and regenerate the bed, and passing the hydrogen stream containing the hydrogen iodide thus formed through a lead-exchanged zeolite which absorbs the radioactive iodine from the gas stream and permanently storing the lead-exchanged zeolite loaded with radioactive iodine

Suspending Zeolite Particles In Tanks

International Nuclear Information System (INIS)

Poirier, M.R.

1999-01-01

The Savannah River Site (SRS) is in the process of removing waste (sludge and salt cake) from million gallon waste tanks. The current practice for removing waste from the tanks is adding water, agitating the tanks with long shaft vertical centrifugal pumps, and pumping the sludge/salt solution from the tank to downstream treatment processes. This practice has left sludge heels (tilde 30,000 gallons) in the bottom of the tanks. SRS is evaluating shrouded axial impeller mixers for removing the sludge heels in the waste tanks. The authors conducted a test program to determine mixer requirements for suspending sludge heels using the shrouded axial impeller mixers. The tests were performed with zeolite in scaled tanks which have diameters of 1.5, 6.0, and 18.75 feet. The mixer speeds required to suspend zeolite particles were measured at each scale. The data were analyzed with various scaling methods to compare their ability to describe the suspension of insoluble solids with the mixers and to apply the data to a full-scale waste tank. The impact of changes in particle properties and operating parameters was also evaluated. The conclusions of the work are: Scaling of the suspension of fast settling zeolite particles was best described by the constant power per unit volume method. Increasing the zeolite particle concentration increased the required mixer power needed to suspend the particles. Decreasing the zeolite particle size from 0.7 mm 0.3 mm decreased the required mixer power needed to suspend the particles. Increasing the number of mixers in the tank decreased the required mixer power needed to suspend the particles. A velocity of 1.6 ft/sec two inches above the tank bottom is needed to suspend zeolite particles

Removal of strontium ions from solutions using granulated zeolites

International Nuclear Information System (INIS)

Bronic, J.; Subotic, B.

1992-01-01

The ion-exchange process on columns filled with granulated zeolites is determined by several physico-chemical parameters. The influence of these parameters (zeolite type, concentration of exchangeable ions in solution, temperature, flow rate, etc.) on the kinetics of ion-exchange process was studied by measuring the Sr 2+ ion concentration in solution before and after passing through a column filled with various granulated zeolites (zeolite 13X, zeolite A and synthetic mordenite). Using the experimental technique of radioactive labeling by 89 Sr, the distribution of Sr 2+ ions in column fillings were also determined. From the results obtained, the optimal conditions for the most efficient removal of strontium ions from solutions using granulated zeolites can be defined. (author) 24 refs.; 9 figs

Exchange of deuterium with hydrogen of zeolite catalyst surface

International Nuclear Information System (INIS)

Minachev, Kh.M.; Dmitriev, R.V.; Penchev, V.; Kanazirev, V.; Minchev, Kh.; Kasimov, Ch.K.; Bylgarska Akademiya na Naukite, Sofia. Inst. za Obshta i Organichna Khimiya; AN Azerbajdzhanskoj SSR, Baku. Inst. Neftekhimicheskikh Protsessov)

1981-01-01

Isotope heteromolecular exchange of hydrogen on the reduced nickel-containing zeolites takes places at the temperatures above 100 deg and it is controlled by activated hydrogen transfer from metal particles on the substrate surface. High-temperature redox treatment of nickel-containing zeolites results in the formation of large nickel crystallites on zeolite external faces. The rest part of nickel remains in zeolite pores and conditions a high promoting effect in the exchange reaction. Catalytic activity of reduced zeolites NiCaNaY in toluene disproportionation increases considerably only in the cases when nickel is introduced into zeolite by means of ion exchange. Close spatial location of nickel particles and OH groups promotes the procedure of both isotope exchange and disproportionation of toluene [ru

Minimum description length block finder, a method to identify haplotype blocks and to compare the strength of block boundaries.

Science.gov (United States)

Mannila, H; Koivisto, M; Perola, M; Varilo, T; Hennah, W; Ekelund, J; Lukk, M; Peltonen, L; Ukkonen, E

2003-07-01

We describe a new probabilistic method for finding haplotype blocks that is based on the use of the minimum description length (MDL) principle. We give a rigorous definition of the quality of a segmentation of a genomic region into blocks and describe a dynamic programming algorithm for finding the optimal segmentation with respect to this measure. We also describe a method for finding the probability of a block boundary for each pair of adjacent markers: this gives a tool for evaluating the significance of each block boundary. We have applied the method to the published data of Daly and colleagues. The results expose some problems that exist in the current methods for the evaluation of the significance of predicted block boundaries. Our method, MDL block finder, can be used to compare block borders in different sample sets, and we demonstrate this by applying the MDL-based method to define the block structure in chromosomes from population isolates.

Acid and redox activity of template-free Al-rich H-BEA* and Fe-BEA* zeolites

Czech Academy of Sciences Publication Activity Database

Sazama, Petr; Wichterlová, Blanka; Sklenák, Štěpán; Parvulescu, V. I.; Candu, N.; Sádovská, Galina; Dědeček, Jiří; Klein, Petr; Pashková, Veronika; Šťastný, Petr

2014-01-01

Roč. 318, OCT 2014 (2014), s. 22-33 ISSN 0021-9517 R&D Projects: GA ČR GAP106/11/0624; GA ČR(CZ) GA14-10251S; GA TA ČR TA01021377 Institutional support: RVO:61388955 Keywords : Acid strength * Alkylation of aromatics * Beta zeolite Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 6.921, year: 2014

Study on preparing the absorbent of potassium nickel hexacyanoferrate (II) loaded zeolite for removal of cesium from radioactive waste solutions and followed method for stable solidification of spent composites

International Nuclear Information System (INIS)

Pham Quynh Luong; Nguyen Hoang Lan; Nguyen Van Chinh; Nguyen Thu Trang; Vuong Huu Anh; Le Xuan Huu; Nguyen Thi Xuan; Le Van Duong

2017-01-01

The selective adsorption and stable immobilization of radioactive cesium, K-Ni-hexacyanoferrate (II) loaded zeolite (FC-zeolite) prepared by impregnation / precipitation method were studied. The uptake equilibrium of Cs + for composites FC-zeolite was attained within 8 h and estimated to be above 97% in Cs + 100 mg/l solution at pH 4-10. Maximum ion exchange capacity of Cs + ions (Q max ) for FC-zeoliteX was 112.5 and 69.7 mg/g in pure water and sea water, respectively. Those values for FC-zeolite A was 85.7 and 42.7 mg/g. Decontamination factor (DF) of FC-zeolite X for 134 Cs was 149.7 and 107.5 in pure water and sea water respectively. Study on synthesized zeolites (A and X) made of HUST was also conducted in similar manner. The values of Q max were 98.6 and 39.9 mg/g for zeolite A, and 69.5 and 20.8 mg/g for zeolite X in pure water and sea water, respectively. Decontamination factor (DF) of zeolite A and X for 134 Cs showed lower values. The spent CsFC-zeolite was solidificated in optimal experimental conditions: 5% Na 2 B 4 O 7 additives; calcination temperature at 900 o C for 2 h in air. Solid form was determined some of parameters: immobilization of Cs, compressive strength, volume reduction after calcination (%) and leaching rate of Cs + ions in deionization water. (author)

Structure modification of natural zeolite for waste removal application

Science.gov (United States)

Widayatno, W. B.

2018-03-01

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

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.

Ion exchange and hydrolysis reactions in zeolites

International Nuclear Information System (INIS)

Harjula, Risto.

1993-09-01

Among other uses, zeolites are efficient cation exchangers for aquatic pollution control. At present they they are mainly used in nuclear waste effluent treatment and in detergency. In the thesis, several ion exchange equilibria, important in these main fields of zeolite applications, were studied, with special emphasis on the formulation and calculation of the equilibria. The main interest was the development of thermodynamic formulations for the calculation of zeolite ion exchange equilibria in solutions of low or very low (trace) ion concentration, which are relevant for the removal of trace pollutants, such as radionuclides, from waste waters. Two groups of zeolite-cation systems were studied. First, binary Ca 2+ /Na + exchange in zeolites X and Y, which are of interest for detergency applications. Second, binary Cs + /Na + and Cs + /K + exchanges, and ternary Cs + /Na + /K + exchange in mordenite, which are important in nuclear waste effluent treatment. The thesis is based on five previous publications by author. (100 refs., 7 figs.)

Mechanism of nitric acid generation on Ag-X Zeolite

International Nuclear Information System (INIS)

Kanazawa, T.; Kishimoto, T.; Haseba, S.; Mitoh, Y.; Itoh, S.; Nakai, I.

1983-01-01

When Ag-X Zeolite is used for the removal of iodine from the off gas streams of nuclear facilities, it is possible that nitric acid is formed on Ag-X Zeolite from co-existing nitrogen dioxide and water vapor. If nitric acid is formed on the surface of Ag-X zeolite, Ag-X zeolite is damaged and is not able to operate for a long time. When Ag-X zeolite is used in NO 2 -O 2 -H 2 O mixture, the nitric acid generation reaction is varied, depending upon the reaction temperature, and concentration of NO 2 and H 2 O. At a temperature of more than 40 deg. C, however, only the surface reaction will be progressed on the zeolite surface. The generation of nitric acid solution on the zeolite can be forecasted through the relationship between the concentration of nitric acid solution, equilibrium vapor pressure of H 2 O, and equilibrium vapor pressure of HNO 3 . Concerning the surface reaction caused on the zeolite, the adsorption water reacts on NO 2 , and the resulting HNO 3 is adsorbed firmly by the zeolite, which is thought to interfere with the surface reaction for generation of the HNO 3 . When the adsorption bed is long, the time required for adsorbed HNO 3 to saturate is increased in proportion to the bed length

Synthesis and characterization of zeolite from coal fly ash

Science.gov (United States)

Liu, Yong; Luo, Qiong; Wang, Guodong; Li, Xianlong; Na, Ping

2018-05-01

Fly ash (FA) from coal-based thermal power plant was used to synthesize zeolite in NaOH solution with hydrothermal method in this work. Firstly, the effects of calcination and acid treatment on the removal of impurities in fly ash were studied. Then based on the pretreated FA, the effects of alkali concentration, reaction temperature and Si/Al ratio on the synthesis of zeolite were studied in detail. The mineralogy, morphology, thermal behavior, infrared spectrum and specific surface for the synthetic sample were investigated. The results indicated that calcination at 750 °C for 1.5 h can basically remove unburned carbon from FA, and 4 M hydrochloric acid treatment of calcined FA at 90 °C for 2 h will reduce the quality of about 34.3%wt, which are mainly iron, calcium and sulfur elements. The concentration of NaOH, reaction temperature and Si/Al ratio have important effect on the synthesis of zeolite. In this study, 0.5 M NaOH cannot obtain any zeolite. High temperature is beneficial to zeolite synthesis from FA, but easily lead to a variety of zeolites. The synthetic sample contains three kinds of zeolites such as zeolite P, sodalite and zeolite X, when the reaction conditions are 2 M NaOH and 120 °C for 24 h. In this research, quartz always exists in the synthetic sample, but will reduce with the increase of temperature. The synthetic zeolite has the specific surface area of about 42 m2 g‑1 and better thermal stability.

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)

Fracture properties of high-strength concrete obtained by direct modification of structure

Directory of Open Access Journals (Sweden)

Solodkyy Serhiy

2017-01-01

Full Text Available High-strength concrete is effectively used worldwide in the last three decades, but it is more brittle in comparison with normal strength concretes. Partial substitution of cement in concrete by active mineral additives and usage of chemical admixture of plasticizing and air-entraining action can considerably change their fracture properties. The obtained results show that the increase of the fracture properties is observed in concretes modified with chemical admixtures incorporating mineral additives such as zeolite and limestone due to consolidation of the concrete microstructure. Densification takes place as a result of limiting the amount of calcium hydroxide (CH due to its reaction with active silica included in the zeolite and the formation of larger amounts of hydrated calcium silicates of tobermorite type as well as calcium hydroaluminate and hydrocarboaluminate with the simultaneous adsorption modification of hydrated products by chemical admixtures.

Nafion/Zeolite nanocomposite membrane for high temperature PEMFCS

International Nuclear Information System (INIS)

Chen, Z.

2009-01-01

'Full text': The Nafion/Acid Functionalized Zeolite Beta (NAFB) nanocomposite membrane has been successfully prepared by the in situ hydrothermal crystallization method. Acid Functionalized Zeolite Beta (AFB) nanocrystals less than 20 nm were formed and embedded into the Nafion matrix. The physical-chemical properties of all membranes were investigated regarding their tensile strength, water uptake and thermogravimetric analyzer (TGA). The proton conductivity commercial Nafion membrane and the NAFB composite membrane were measured with different relative humidity (RH) at 80 and 120 o C. Compared with the commercial Nafion membrane, the NAFB composite membrane has much higher proton conductivity at 120 o C and reduced RH. The NAFB composite membrane and commercial Nafion membranes were also studied in an H 2 /O 2 PEMFC over a wide range of RH values from 25 to 100% at temperatures of 80 and 120 o C. The NAFB composite membrane showed a pronounced improvement over commercial Nafion membranes when operated at 120 o C and reduced RH. The high performance of the NAFB composite membranes at low RH was attributed to improved water retention due to the presence of absorbed water species within the pores and on the surface of AFB. NAFB composite membranes have the potential for use with high temperature PEMFC. (author)

Diagenetic Quartz Morphologies and Zeolite formation

DEFF Research Database (Denmark)

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

the Siri Canyon wells.  Volcanic lithoclasts are strongly altered and associated with diagenetic opal/ microquartz coatings and zeolite.  Zeolite crystals formed simultaneously with opal and prior to microquartz but dissolved with increased burial depth.  The dissolution of zeolite followed two steps...... in samples where no volcanic ash is demonstrated; it seems that a rapid supply of dissolved silica from dissolution of siliceous fossils was the main reason for the early co-precipitation of opal and zeolite. There are two important sources for Si: 1) Biogenic opal from diatoms or radiolarians, which...... are abundant in some of associated shales; and 2) volcanic ash. The dissolution of biogenic silica may result in a rapid release of silica thereby promoting the formation of diagenetic opal/microquartz, but there may be a limited release of Al. A limited release of Al may result in precipitation of Si...

Multi-elemental characterization of Cuban natural zeolites

International Nuclear Information System (INIS)

Rizo, O.D.; Peraza, E.F.H.

1997-01-01

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

Multi-elemental characterization of Cuban natural zeolites

International Nuclear Information System (INIS)

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

1996-01-01

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

Synthesis of uniform-sized zeolite from windshield waste

International Nuclear Information System (INIS)

Kim, Jae-Chan; Choi, Mingu; Song, Hee Jo; Park, Jung Eun; Yoon, Jin-Ho; Park, Kyung-Soo; Lee, Chan Gi; Kim, Dong-Wan

2015-01-01

We demonstrate the synthesis of A-type zeolite from mechanically milled windshield waste via acid treatment and a low-temperature hydrothermal method. As-received windshield cullet was crushed to a fine powder and impurities were removed by HNO 3 treatment. The resulting glass powder was used as the source material for the hydrothermal synthesis of A-type zeolite. Crystal structure, morphology, and elemental composition changes of the windshield waste were evaluated at each step of the process through scanning electron microscopy, X-ray diffraction, X-ray fluorescence spectrometry, etc. After a high-energy milling process, the glass had an average particle size of 520 nm; after acid treatment, its composition was over 94% silica. Zeolite was successfully synthesized in the A-type phase with a uniform cubic shape. - Highlights: • Environmental-friendly recycling of windshield waste for high valuable product of zeolite. • Synthesis of zeolite form windshield waste via a low-temperature hydrothermal process. • High-energy milling effect on the uniform cubic shape and high-purity A-type zeolite.

Zeolites with Continuously Tuneable Porosity**

Science.gov (United States)

Wheatley, Paul S; Chlubná-Eliášová, Pavla; Greer, Heather; Zhou, Wuzong; Seymour, Valerie R; Dawson, Daniel M; Ashbrook, Sharon E; Pinar, Ana B; McCusker, Lynne B; Opanasenko, Maksym; Čejka, Jiří; Morris, Russell E

2014-01-01

Zeolites are important materials whose utility in industry depends on the nature of their porous structure. Control over microporosity is therefore a vitally important target. Unfortunately, traditional methods for controlling porosity, in particular the use of organic structure-directing agents, are relatively coarse and provide almost no opportunity to tune the porosity as required. Here we show how zeolites with a continuously tuneable surface area and micropore volume over a wide range can be prepared. This means that a particular surface area or micropore volume can be precisely tuned. The range of porosity we can target covers the whole range of useful zeolite porosity: from small pores consisting of 8-rings all the way to extra-large pores consisting of 14-rings. PMID:25284344

Introduction to chemistry of crystalline zeolites and its applications

International Nuclear Information System (INIS)

Lobo Cabezas, Raul Francisco

2006-01-01

Establishes the zeolites as the most important group of solid acids and its relation to the contemporaneous chemical industry. It describes that zeolites are used in the following applications: refineries, chemicals/petrochemicals, environmental chemistry, separation of gas, adsorbent ia and ionic exchange in water purification in mineral processes, medicine and agricultural industry. Zeolites are defined as crystalline aluminium silicates with a compound structure of interconnected tetrahedrons. It mentions the key components in zeolites structure. It focuses that structural basic unity of the zeolite is the tetrahedron and compound structural unities are: cells and columns. Besides, it describes that pore system defines a lot of all its properties; but chemical composition affects them. Composition and properties of zeolites are established: adsorption, molecular sieves, acidity, selectivity, transition state in the hydrocarbon's chemistry. It concludes that the newer application of zeolite is in oxidations: Titanium-Silicate-1; production of propylene's oxide using peroxide of hydrogen as oxidizing. The catalysis is an active area of research, and the most popular areas are related to chemicals and the environment [es

The Immobilisation of Krom and Stronsium Waste Using Natural Fiber Reinforced Cement

International Nuclear Information System (INIS)

Susetyo Haria Putero; Nunung Prabaningrum; Widya Rosita

2007-01-01

Cementation of hazardous liquid waste is one of the methods to minimize its detrimental effect on the environmental quality and human health. This research purpose was to study the effect of natural fiber composition and temperature on quality of the cement block reinforced by coconut (Cocos nucifera) fiber and bamboo (Bambusa vulgaris) fiber. This research was pursued by adsorbing stronsium waste and krom using zeolite. Thirteen percent volume of zeolite was mixed with 0.3 of water/cement ratio. Composition of natural fiber was varied by 0.00v/o, 0.05v/o, 0.10v/o, 0.25v/o, 0.50v/o, 0.75v/o and 1.00v/o. The cement blocks produced were heated at 0℃, 50℃, 100℃, 150℃, 200℃ and 250℃ for 10 minutes and then determined their compressive strength and leaching rate. The optimum composition of natural fiber causing increasing of mechanical strength has been founded at 0.50% v/o of fiber. On that composition the axial force resistance of fiber is higher than the radial one. The hydration reaction completely works when cement block is heated until certain temperature that results in the increasing of its compressive strength. However, the compressive strength of cement block heated up to 250℃ is still beyond the standard. Based on its compressive strength, the bamboo (Bambusa vulgaris) fiber is more feasible than coconut (Cocos nucifera) fiber for reinforcing cement block. Heating just influences on the physics properties of cement block. But, the ability of block cement to immobilize a matter is affected by properties of matters. (author)

Environmental application of modified natural zeolites

International Nuclear Information System (INIS)

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

1998-01-01

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

Removal of cesium radioisotopes from solutions using granulated zeolites

International Nuclear Information System (INIS)

Bronic, J.; Subotic, B.

1991-01-01

The influence of type of zeolite and the flow rate of solution through the column on the removal efficiency of radioactive cesium ions from solution has been investigated. The analysis of the change in the concentration of cesium ions in the solutions and distribution of cesium ions in the column fillings (granulated zeolites), after passing the solutions through the columns filled with various granulated zeolites (zeolite 4A, zeolite 13X, synthetic mordenite) was performed. On the basis of the results of this study, the conditions for the most efficient removal of cesium ions from solutions have been discussed. (author) 35 refs.; 9 figs.; 1 tab

Catalytic Oxidation by Transition Metal Ions in Zeolites.

Science.gov (United States)

1984-09-28

exotic schemes were developed. It was previously demonstrated that MoCI5 may be reacted with a HYu (here Yu denotes a steam-stabilized or...34ultrastable" zeolite) to form a MoYu zeolite and HC1 which is removed from the system.1 In this study, MoYu zeolites have been prepared by reacting HYu with Mo

Ion exchange properties of zeolite-containing catalysts

Energy Technology Data Exchange (ETDEWEB)

Koval' chuk, L V; Takhtarova, G N; Topchieva, K V [Moskovskii Gosudarstvennyi Univ. (USSR). Kafedra Fizicheskoi Khimii

1975-03-01

In the paper the reaction of sodium ion exchange for ammonium cations, cations of calcium and lanthanum in the amorphous aluminium silicate Na/sub 0,856/(AlO/sub 2/)(SiO/sub 2/)/sub 9,831/, zeolite Na/sub 1/(AlO/sub 2/)(SiO/sub 2/)/sub 2,33/ and zeolite containing catalyst Na/sub 1,09/(AlO/sub 2/)(SiOsub(2))/sub 7,93/ were studied; exchange isotherms of sodium for ammonium, calcium and lanthanium are presented. Results received in the study indicate high selectivity of zeolite for calcium and lanthanum cations in comparison with amorphous aluminium silicate and also display electroselectivity effect. The highest separation coefficient takes place for lanthanum in the sodium exchange in zeolite.

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.

Adductor canal block versus femoral nerve block for analgesia after total knee arthroplasty

DEFF Research Database (Denmark)

Jaeger, Pia; Zaric, Dusanka; Fomsgaard, Jonna Storm

2013-01-01

Femoral nerve block (FNB), a commonly used postoperative pain treatment after total knee arthroplasty (TKA), reduces quadriceps muscle strength essential for mobilization. In contrast, adductor canal block (ACB) is predominately a sensory nerve block. We hypothesized that ACB preserves quadriceps...

Aluminum-rich mesoporous MFI - type zeolite single crystals

DEFF Research Database (Denmark)

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

2005-01-01

Zeolitcs are crystalline materials, which are widely used as solid acid catalysts and supports in many industrial processes. Recently, mesoporous MFI-type zeolite single crystals were synthesized by use of carbon particles as a mesopore template and sodium aluminate as the aluminum Source....... With this technique, only zeolites with relatively low Al contents were reported (Si/Al ratio about 100). In this work, the preparation of aluminum-rich mesoporous MFI-type zeolite single crystals (Si/Al similar to 16-50) using aluminum isopropoxide as the aluminum Source is reported for the first time. All samples...... are characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), ammonia temperature programmed desorption (NH3-TPD), and N-2 adsorption measurements. The obtained zeolites combine the high crystallinity and the characteristic micropores of zeolites with an intracrystalline mesopore system...

Pengaruh Kandungan Ca Pada Cao-zeolit Terhadap Kemampuan Adsorpsi Nitrogen

OpenAIRE

M Nasikin; Tania Surya Utami; Agustina TP Siahaan

2002-01-01

In industry, Ca zeolite is used as nitrogen selective adsorbent with the use of PSA (Pressure Swing Adsorption)/VSA (Vacuum Swing Adsorption) methods. Natural zeolite modified to be Cao-zeolite by ion exchange process using Ca(OH)2. Adsorption test was done on CaO-zeolite with different Ca concentration to understand how it's adsorption phenomena on oxygen and nitrogen. Adsorption test has been done for CaO-zeolite with Ca concentration = 0,682%, 0,849% and 1,244% to oxygen and nitrogen with ...

Natural Zeolite Sample and Investigation Its Use in Oil Bleaching Sector

Science.gov (United States)

Bilgin, Oyku

2017-12-01

In the sector of oil bleaching, the stored raw oil is subjected to physical and chemical methods such as degumming, neutralization, bleaching, deodorization and winterization. In the process of oil bleaching, the selection of correct bleaching earth in accordance with oil characteristics matters so much. Bleaching earth is an inorganic product used in removing impurities being available within the structures of vegetable, animal oil (sunflower, soya, corn, palm, tallow, rapeseed, fish oils…etc.) and fatty acids, mineral oils (glycerine, paraffin, mineral motor oils. etc.) with the adsorption process. The factors such as low cost of oil bleaching earth, low ratio of oil retaining, high bleaching capacity in spite of using them in small amounts, filter’s delayed blocking by the earth and non-increase of the free acidity of the oil should be taken into consideration. Bleaching earths are processed with some acids in order to widen their surface areas. During this process, a certain amount of acid is left within oil bleaching earths even if it is very little. These acids also increase oil’s acidity by oxidizing oil in the course of bleaching process. In this study, zeolite sample taken from Manisa -Demirci region was used. Following the processes of crushing and sieving, zeolite sample was subjected to chemical analyses according to their grain thickness, microscopic examination, the analyses of XRD and cation exchange capacity and their ore characteristics were determined. Afterwards, it was searched whether zeolite sample has oil bleaching ability or not or whether it can be used as oil bleaching earth or not.

Synthesis of Zeolite Nanomolecular Sieves of Different Si/Al Ratios

Directory of Open Access Journals (Sweden)

Pankaj Sharma

2015-01-01

Full Text Available Nanosized zeolite molecular sieves of different Si/Al ratios have been prepared using microwave hydrothermal reactor (MHR for their greater application in separation and catalytic science. The as-synthesized molecular sieves belong to four different type zeolite families: MFI (infinite and high silica, FAU (moderate silica, LTA (low silica and high alumina, and AFI (alumina rich and silica-free. The phase purity of molecular sieves has been assessed by X-ray diffraction (XRD analysis and morphological evaluation done by electron microscopy. Broad XRD peaks reveal that each zeolite molecular sieve sample is composed of nanocrystallites. Scanning electron microscopic images feature the notion that the incorporation of aluminum to MFI zeolite synthesis results in morphological change. The crystals of pure silica MFI zeolite (silicalite-1 have hexagon lump/disk-like shape, whereas MFI zeolite particles with Si/Al molar ratios 250 and 100 have distorted hexagonal lump/disk and pseudo spherical shapes, respectively. Furthermore, phase pure zeolite nanocrystals of octahedron (FAU, cubic (LTA, and rod (AFI shape have been synthesized. The average sizes of MFI, FAU, LTA, and AFI zeolite crystals are 250, 150, 50, and 3000 nm, respectively. Although the length of AFI zeolite rods is in micron scale, the thickness and width are of a few nanometers.

Characterization of UO22+ exchanged Y zeolite

International Nuclear Information System (INIS)

Olguin, M.T.; Bosch, P.; Bulbulian, S.; Duque, J.; Pomes, R.; Villafuerte-Castrejon, M.E.; Sansores, L.E.; Bosch, P.

1997-01-01

The present study discusses the incorporation of uranyl ion into Y-zeolite framework. The UO 2 2+ sorption was measured by neutron activation analyses. The Y-zeolite framework distorts in response to the cations present in the structure. Hence, depending on the amount and the location of the exchanged cations, the features of the X-ray diffraction pattern may vary. From the Rietveld analysis of these patterns, the positions occupied by the UO 2 2 + cations in the zeolite network were determined. (author)

Influencing the selectivity of zeolite Y for triglycine adsorption

NARCIS (Netherlands)

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

2007-01-01

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

Catalytic transformation of methyl benzenes over zeolite catalysts

KAUST Repository

Al-Khattaf, S.

2011-02-01

Catalytic transformation of three methyl benzenes (toluene, m-xylene, and 1,2,4-trimethyl benzene) has been investigated over ZSM-5, TNU-9, mordenite and SSZ-33 catalysts in a novel riser simulator at different operating conditions. Catalytic experiments were carried out in the temperature range of 300-400 °C to understand the transformation of these alkyl benzenes over large pore (mordenite and SSZ-33) in contrast to medium-pore (ZSM-5 and TNU-9) zeolite-based catalysts. The effect of reaction conditions on the isomerization to disproportionation product ratio, distribution of trimethylbenzene (TMB) isomers, and p-xylene/o-xylene ratios are reported. The sequence of reactivity of the three alkyl benzenes depends upon the pore structure of zeolites. The zeolite structure controls primarily the diffusion of reactants and products while the acidity of these zeolites is of a secondary importance. In the case of medium pore zeolites, the order of conversion was m-xylene > 1,2,4-TMB > toluene. Over large pore zeolites the order of reactivity was 1,2,4-TMB > m-xylene > toluene for SSZ-33 catalyst, and m-xylene ∼ 1,2,4-TMB > toluene over mordenite. Significant effect of pore size between ZSM-5 and TNU-9 was observed; although TNU-9 is also 3D 10-ring channel system, its slightly larger pores compared with ZSM-5 provide sufficient reaction space to behave like large-pore zeolites in transformation of aromatic hydrocarbons. We have also carried out kinetic studies for these reactions and activation energies for all three reactants over all zeolite catalysts under study have been calculated. © 2011 Elsevier B.V.

Crystallization and melting behavior of isotactic polypropylene composites filled by zeolite supported β-nucleator

International Nuclear Information System (INIS)

Jiang, Juan; Li, Gu; Tan, Nanshu; Ding, Qian; Mai, Kancheng

2012-01-01

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

PREPARASI DAN KARAKTERISASI ZEOLIT DARI ABU LAYANG BATUBARA SECARA ALKALI HIDROTERMAL

Directory of Open Access Journals (Sweden)

Jumaeri Jumaeri

2012-01-01

Full Text Available Preparasi zeolit dari abu layang batubara PLTU Suralaya secara alkali hidrotermal telah dilakukan. Preparasi dilakukan terhadap abu layang yang telah direfluks dengan HCl 1M dan tanpa refluks. Larutan NaOH dengan konsentrasi tertentu ( 1 ; 2 dan 3 M dicampur dengan abu layang batu bara dengan rasio 10 ml larutan tiap 1 gram abu layang, ke dalam tabung Teflon 100 ml dalam suatu autoclave stainless-steel. Autoclave kemudian dipanaskan pada temperature 80-16 oC selama tiga hari. Zeolit sintesis yang dihasilkan selanjutnya diuji secara kualitatif dengan menggunakan Spektroskopi Inframerah, dan Difraksi Sinar-X. Hasil penelitian menunjukkan bahwa aktivasi abu layang dengan proses alkali hidrotermal dapat menghasilkan material yang mempunyai struktur mirip zeolit (zeolit-like. Produk hidrotermal terdiri dari campuran zeolit (Zeolit P, Zeolit Y serta kristal sodalit dan mullit. Pada temperatur 160 oC, diperoleh zeolit dengan kristalinitas lebih tinggi dari pada 100 oC, baik melalui refluks atau tanpa refluks. Karakteristik zeolit yang terbentuk sangat ditentukan oleh kondisi proses, yang meliputi konsentrasi NaOH, waktu, dan temperatur.

Basic deposits of zeolites of the Republic of Tajikistan

International Nuclear Information System (INIS)

Normatov, I.Sh.; Mirsaidov, U.M.

2003-01-01

Natural zeolites increasingly using in the different fields of human economical activity. As a result of investigations of last years was determined that zeolites are the wide-spread rock forming minerals. In the Republic of Tajikistan zeolites was found out an the north of the Republic

The evolution of strength and crystalline phases for alkali-activated ground blast furnace slag and fly ash-based geopolymers

KAUST Repository

Oh, Jae Eun

2010-02-01

The increase in strength and evolution of crystalline phases in inorganic polymer cement, made by the alkali activation of slag, Class C and Class F fly ashes, was followed using compressive strength test and synchrotron X-ray diffraction. In order to increase the crystallinity of the product the reactions were carried out at 80 °C. We found that hydrotalcite formed in both the alkali-activated slag cements and the fly ash-based geopolymers. Hydroxycancrinite, one member of the ABC-6 family of zeolites, was found only in the fly ash geopolymers. Assuming that the predominantly amorphous geopolymer formed under ambient conditions relates to the crystalline phases found when the mixture is cured at high temperature, we propose that the structure of this zeolitic precursor formed in Na-based high alkaline environment can be regarded as a disordered form of the basic building unit of the ABC-6 group of zeolites which includes poly-types such as hydroxycancrinite, hydroxysodalite and chabazite-Na. © 2009 Elsevier Ltd.

The evolution of strength and crystalline phases for alkali-activated ground blast furnace slag and fly ash-based geopolymers

International Nuclear Information System (INIS)

Oh, Jae Eun; Monteiro, Paulo J.M.; Jun, Ssang Sun; Choi, Sejin; Clark, Simon M.

2010-01-01

The increase in strength and evolution of crystalline phases in inorganic polymer cement, made by the alkali activation of slag, Class C and Class F fly ashes, was followed using compressive strength test and synchrotron X-ray diffraction. In order to increase the crystallinity of the product the reactions were carried out at 80 deg. C. We found that hydrotalcite formed in both the alkali-activated slag cements and the fly ash-based geopolymers. Hydroxycancrinite, one member of the ABC-6 family of zeolites, was found only in the fly ash geopolymers. Assuming that the predominantly amorphous geopolymer formed under ambient conditions relates to the crystalline phases found when the mixture is cured at high temperature, we propose that the structure of this zeolitic precursor formed in Na-based high alkaline environment can be regarded as a disordered form of the basic building unit of the ABC-6 group of zeolites which includes poly-types such as hydroxycancrinite, hydroxysodalite and chabazite-Na.

Polyphosphates substitution for zeolite to in detergents

International Nuclear Information System (INIS)

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

1996-01-01

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

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

International Nuclear Information System (INIS)

Skvazyvaev, V.E.; Khvoshchev, S.S.; Zhdanov, S.P.

1975-01-01

Adsorption of air at low pressures on type E zeolites was studied as a function of their composition and dehydration regime. It was shown that zeolite CaE-T has a greatly increased sorption capacity for air at low pressures and that this is more than 3 times that of industrial zeolites currently used in vacuum technology. Mass-spectrometer studies were made of the gas phase over zeolites type E and A after adsorption of air at pressures from 10 -8 to 10 -5 mm Hg at liquid nitrogen temperatures under conditions approximating equilibrium. It was shown that zeolite CaE-T has a high adsorption capacity for Ar, O 2 , and H 2 . Adsorption of H 2 and Ar by zeolites of different structural types at low pressures was studied. It was shown that zeolite CaE-T has a significantly higher adsorption capacity for hydrogen and argon than all industrial zeolites

Fixing noble gas in zeolites

International Nuclear Information System (INIS)

Rocha Dorea, A.L. da.

1980-09-01

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

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.

Recent Advances on Bioethanol Dehydration using Zeolite Membrane

Science.gov (United States)

Makertihartha, I. G. B. N.; Dharmawijaya, P. T.; Wenten, I. G.

2017-07-01

Renewable energy has gained increasing attention throughout the world. Bioethanol has the potential to replace existing fossil fuel usage without much modification in existing facilities. Bioethanol which generally produced from fermentation route produces low ethanol concentration. However, fuel grade ethanol requires low water content to avoid engine stall. Dehydration process has been increasingly important in fuel grade ethanol production. Among all dehydration processes, pervaporation is considered as the most promising technology. Zeolite possesses high potential in pervaporation of bioethanol into fuel grade ethanol. Zeolite membrane can either remove organic (ethanol) from aqueous mixture or water from the mixture, depending on the framework used. Hydrophilic zeolite membrane, e.g. LTA, can easily remove water from the mixture leaving high ethanol concentration. On the other hand, hydrophobic zeolite membrane, e.g. silicate-1, can remove ethanol from aqueous solution. This review presents the concept of bioethanol dehydration using zeolite membrane. Special attention is given to the performance of selected pathway related to framework selection.

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

International Nuclear Information System (INIS)

Fungaro, D.A.; Borrely, S.I.

2010-01-01

Coal ash was used as starting material for zeolite synthesis by means of hydrothermal treatment. The surfactant-modified zeolite (SMZ) was prepared by adsorbing the cationic surfactant hexadecyltrimethylammonium bromide (HDTMA-Br) on the external surface of the zeolite from coal ash. The zeolite structure stability was monitored during the characterization of the materials by FTIR, XDR and SEM. The structural parameters of surfactant-modified zeolite are very close to that of corresponding non-modified zeolite which indicates that the crystalline nature of the zeolite remained intact after required chemical treatment with HDTMA-Br molecules and heating treatment for drying. The most intense peaks in the FTIR spectrum of HDTMA-Br were observed in SMZ spectrum confirming adsorption of surfactant on zeolites. (author)

Investigation of zeolites by solid state quadrapole NMR

International Nuclear Information System (INIS)

Janssen, R.

1990-01-01

The subject of this thesis is the NMR investigation of zeolites. The nature and properties of zeolites are discussed. Some of the basic priniples of NMR techniques on quadrupole nuclei are presented. A special technique, namely a two-dimensional nutation experiment is discussed in detail. The theory of the nutation experiment for quadrupole spin species with spin quantum number 3/2 as well as 5/2 is presented. For both spin spcies the theoretical spectra are compared with experimental results. It is also shown that the nutation expeirment can be performed with several pulse schemes. It is shown how phase-sensitive pure-absorption nutation spectra can be obtained and an NMR-probe is presented that is capable of performing NMR experiments at high (up to 500 degree C) temperatures. The two-dimensional nutation NMR technique has been applied to sodium cations in zeolite NaA. For this purpose a numbre of zeolite samples were prepared that contained different amounts of water. With the aid of nutation NMR the hydration of the zeolite can be studied and conclusions can be drawn about the symmetry of the surrounding of the sodium cations. With the aid of an extension of the nutation NMR experiment: Rotary Echo Nutation NMR, it is shown that in zeolite NaA, in various stages of hydration, the sodium cations or water molecules are mobile. Proof is given by means of high-temperature 23 Na-NMR that dehydrates zeolite NaA undergoes a phase transition at ca. 120 degree C. In a high-temperature NMR investigation of zeolite ZSM-5 it is shown that the sodium ions start to execute motions when the temperature is increased. (author). 198 refs.; 72 figs.; 6 tabs

Multicolor photoluminescence in ITQ-16 zeolite film

KAUST Repository

Chen, Yanli; Dong, Xinglong; Zhang, Zhenyu; Feng, Lai

2016-01-01

Exploring the native defects of zeolites is highly important for understanding the properties of zeolites, such as catalysis and optics. Here, ITQ-16 films were prepared via the secondary growth method in the presence of Ge atoms. Various intrinsic

Zeolites and clays behavior in presence of radioactive solutions

International Nuclear Information System (INIS)

Carrera Garcia, L.M.

1991-01-01

Natural aluminosilicates have found application as selective ion exchangers for radioactive cations, present in liquid wastes arising from nuclear facilities. Among severals cations and complex mixtures of them, Co is a common constituent of liquid radioactive wastes. Two types of zeolites (Y zeolite, and natural mexican erionite), and two types of clays (natural bentonite, and Al-expanded bentonite (Al-B) were used. Previous to the experiments, the zeolites and the natural bentonite were stabilized to their respective Na + form using 5N NaCl solution. 2Na + → 60 Co 2+ ion exchange kinetics in zeolites and clays was followed by gamma spectrometry using a NaCl-Co(NO 3 ) 2 isonormal solution (0.1N) labeled with 60 Co-Co(NO 3 ) 2 (100 μ Ci). Before and after experiments, the structural changes in the cristallinity of aluminosilicates were determined by X-ray diffraction. XRD analyzes show that the cristallinity of the aluminosilicates was not affected by ion exchange. After Co exchange the cell parameters were determined in all samples. The efficiency of zeolites, natual clays and expanded clays to remove cobalt ions from solutions depends on the ion echange capacity of the material. Results for long contacts time, 18 days, show that Co is more effectively removed by Y zeolite ( 4.07 wt %), followed by erionite (3.09 wt %), then bentonite ( 2.36 wt %) and finally expanded bentonite ( 0.70 wt %). In Y zeolite an unusual fast soportion uptake of 4.51 % wt Co was observed followed by a desorption process to 4.07 %. This effect is due to the different hydration degree of zeolites during the contact time between the zeolite and the 60 Co solution. In erionite the exchange is lower than in Y-zeolite, frist because the Si/Al ratio is higher for erionite than for Y-zeolite and second because K ions in erionite cannot be exchanged during the stabilization of erionite in 5N NaCl solution. The low exchange in expanded bentonite was expected because its cation exchange

Performance of zeolite scavenge column in Xe monitoring system

International Nuclear Information System (INIS)

Wang Qian; Wang Hongxia; Li Wei; Bian Zhishang

2010-01-01

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

Zeolites with continuously tuneable porosity

OpenAIRE

Wheatley, Paul S; Chlubná-Eliášová, Pavla; Greer, Heather; Zhou, Wuzong; Seymour, Valerie R; Dawson, Daniel M; Ashbrook, Sharon E; Pinar, Ana B; McCusker, Lynne B; Opanasenko, Maksym; Cejka, Jiří; Morris, Russell E

2014-01-01

Czech Science Foundation. Grant Number: P106/12/G015 Zeolites are important materials whose utility in industry depends on the nature of their porous structure. Control over microporosity is therefore a vitally important target. Unfortunately, traditional methods for controlling porosity, in particular the use of organic structure-directing agents, are relatively coarse and provide almost no opportunity to tune the porosity as required. Here we show how zeolites with a continuously tuneabl...

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.

Distribution of metal and adsorbed guest species in zeolites

International Nuclear Information System (INIS)

Chmelka, B.F.

1989-12-01

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

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.)

Impact of steel slag on the ammonium adsorption by zeolite and a new configuration of zeolite-steel slag substrate for constructed wetlands.

Science.gov (United States)

Shi, Pengbo; Jiang, Yingbo; Zhu, Hongtao; Sun, Dezhi

2017-07-01

The CaO dissolution from slag, as well as the effects of influencing parameters (i.e. pH and Ca 2+ concentration) on the ammonium adsorption onto zeolite, was systematically studied in this paper. Modeling results of Ca 2+ and OH - release from slag indicated that pseudo-second-order reaction had a better fitness than pseudo-first-order reaction. Changing pH value from 7 to 12 resulted in a drastic reduction of the ammonium adsorption capacity on zeolite, from the peak adsorption capacity at pH 7. High Ca 2+ concentration in solution also inhibited the adsorption of ammonium onto zeolite. There are two proposed mechanisms for steel slag inhibiting the ammonium adsorption capacity of zeolite. On the one hand, OH - released from steel slag can react with ammonium ions to produce the molecular form of ammonia (NH 3 ·H 2 O), which would cause the dissociation of NH 4 + from zeolite. On the other hand, Ca 2+ could replace the NH 4 + ions to adhere onto the surface of zeolite. An innovative substrate filling configuration with zeolite placed upstream of the steel slag was then proposed to eliminate the disadvantageous effects of steel slag. Experimental results showed that this novel filling configuration was superior to two other filling configurations in terms of ammonium removal.

Effect of Zeolite and Nitrogen Fertilizer Application under Water Deficit Stress Conditions on Agronomical and Physiological Traits of Rapeseed

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A. Ghiasvand Ghiasi

2014-08-01

Full Text Available In order to evaluation of zeolite and nitrogen fertilizer application effect on agronomic and physilogical traits of rapeseed (cv RGS003 under water deficit stress conditions, an experiment was conducted in factorial based on randomized complete block design with three replications during 2010 in Qazvin region, Iran. In the where, the two levels of irrigation factor as the normal irrigation (irrigation after 80 mm evaporation from class A pan as control and irrigation cease from stem elongation stage till end of growth, nitrogen factor was at three levels (0, 75 and 150 kg.ha-1 and zeolite factor (0 and 10tons per hectare were studied. Results showed that drought stress decreased evaluated traits such as silique per plant (41%, grain per silique (26%, 1000 seed weight (33%, grain yield (52.5%, oil percent (14%, RWC (31.5% and chlorophyll content (35%. Non-application of nitrogen had adverse effects on total traits and reduced them. However, zeolite application at water deficit stress conditions had positive and significant effect on total traits except of oil percent and chlorophyll content, specially improved grain yield and oil yield. Based on the results of this experiment, application of zeolite (10ton/ha-1 through storage and maintenance of water and nutrients, reduced the intensity and harmful effects of stress in plants and enhances crop yield.

Effects of Zeolite (Clinoptelolite on Performance Characteristics of

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A Hassan Abadim

2011-12-01

Full Text Available A 70-days experiment was conducted to investigate the effects of natural zeolite (clinoptelolite on the performance of commercial laying hens. 288 Hy-Line W36 strain laying hens (50 weeks old were allotted to 6 dietary treatments including basal diet as control and basal diet supplemented with 1, 2, 3, 4 and 5% zeolite that were fed ad -libitum throughout the experiment. Experimental diets for the 6 treatments were prepared to be iso-caloric and iso-nitrogenous. A completely randomized design with six treatments, eight replicates of six birds per replicate was used at this experiment. Daily feed intake (DFI, feed conversion ratio (FCR, egg production, egg weight, egg white quality, eggshell quality (thickness and percentage and body weight changes were measured during the experiment. Results of this experiment showed that DFI, FCR, egg production and egg abnormality were not significantly (P>0.05 affected by zeolite supplementation. Zeolite supplementation significantly increased egg weight, eggshell thickness and live body weight gain of the hens. Dietary zeolite significantly decreased haugh unit of the eggs. In conclusion, natural zeolite significantly improved egg weight and eggshell quality, decreased haugh unit and live weight gain, and had no significant effects on other parameters.

Synthesis and catalytic applications of combined zeolitic/mesoporous materials

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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.

Nanostructured Ag-zeolite Composites as Luminescence-based Humidity Sensors

Science.gov (United States)

Dieu, Bjorn; Roeffaers, Maarten B.J.; Hofkens, Johan

2016-01-01

Small silver clusters confined inside zeolite matrices have recently emerged as a novel type of highly luminescent materials. Their emission has high external quantum efficiencies (EQE) and spans the whole visible spectrum. It has been recently reported that the UV excited luminescence of partially Li-exchanged sodium Linde type A zeolites [LTA(Na)] containing luminescent silver clusters can be controlled by adjusting the water content of the zeolite. These samples showed a dynamic change in their emission color from blue to green and yellow upon an increase of the hydration level of the zeolite, showing the great potential that these materials can have as luminescence-based humidity sensors at the macro and micro scale. Here, we describe the detailed procedure to fabricate a humidity sensor prototype using silver-exchanged zeolite composites. The sensor is produced by suspending the luminescent Ag-zeolites in an aqueous solution of polyethylenimine (PEI) to subsequently deposit a film of the material onto a quartz plate. The coated plate is subjected to several hydration/dehydration cycles to show the functionality of the sensing film. PMID:27911397

Applications of natural zeolites on agriculture and food production.

Science.gov (United States)

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

2017-08-01

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

Application of positron annihilation to the characterization of zeolites

International Nuclear Information System (INIS)

Nakanishi, H.; Ujihira, Y.

1982-01-01

Positron annihilation lifetime and Doppler-broadening measurements were carried out for synthetic zeolite 13X, SK-40, NH 4 -X, and NH 4 -Y by varying the evacuation temperature in order to study the character of the zeolite cages. Four components of the positron annihilation, derived from the lifetime spectra, were interpreted from the results of the authors' measurements and other studies on zeolites. The o-Ps lifetimes in the cages became longer as the desorption of water molecules proceeded. It was found that some active groups in zeolites interacted with o-Ps and reduced the o-Ps lifetime after all the water molecules had detected. Bronsted acid in the zeolite acted not only as an oxidizer but also as an inhibitor of Ps formation. An attempt was made to estimate the amount of Bronsted acids by the positron lifetime technique. The longest lifetime of 50 ns indicates o-Ps annihilation in a pore with 60 A free diameter, which seems to exist irregularly in the faujasite zeolites. It was found that o-Ps was oxidized in this large cavity

Nonionic emulsion-mediated synthesis of zeolite beta

Indian Academy of Sciences (India)

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

Influence of Compacting Rate on the Properties of Compressed Earth Blocks

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Humphrey Danso

2016-01-01

Full Text Available Compaction of blocks contributes significantly to the strength properties of compressed earth blocks. This paper investigates the influence of compacting rates on the properties of compressed earth blocks. Experiments were conducted to determine the density, compressive strength, splitting tensile strength, and erosion properties of compressed earth blocks produced with different rates of compacting speed. The study concludes that although the low rate of compaction achieved slightly better performance characteristics, there is no statistically significant difference between the soil blocks produced with low compacting rate and high compacting rate. The study demonstrates that there is not much influence on the properties of compressed earth blocks produced with low and high compacting rates. It was further found that there are strong linear correlations between the compressive strength test and density, and density and the erosion. However, a weak linear correlation was found between tensile strength and compressive strength, and tensile strength and density.

Application of Zeolitic Additives in the Fluid Catalytic Cracking (FCC

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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.

Effect of alkali-treatment on the characteristics of natural zeolites with different compositions.

Science.gov (United States)

Ates, Ayten

2018-08-01

A series of natural zeolites with different compositions were modified by post-synthesis modification with sodium hydroxide (NaOH) solution. Natural and modified zeolites were characterized by XRD, SEM, nitrogen adsorption, FTIR, zeta potential and temperature programmed desorption of ammonia (NH 3 -TPD). The adsorption capacities of these samples were evaluated by the adsorption of manganese from aqueous solution. The treatment with NaOH led to a decrease in the surface area and microporosity of all natural zeolites as well as partly damage of the zeolite structure depending on zeolite composition. In addition, the amount of weak, medium and strong acid sites in the zeolites was changed significantly by NaOH treatment depending on zeolite composition. The NaOH treatment resulted in a four-fold improvement in adsorption capacity of natural zeolite originated from Bigadic and a twofold decrease in that of the natural zeolite originated from Manisa-Gordes. Although the improved adsorption capacity might be mainly due to modification of porosity in the zeolites and formation of hydroxysodalite, the reduced adsorption capacity of the zeolite might be mainly due to a significant deformation of the zeolite structure. The pseudo-second-order kinetic model for the adsorption of manganese on all natural and modified zeolites fits well. Copyright © 2018 Elsevier Inc. All rights reserved.

A database of new zeolite-like materials.

Science.gov (United States)

Pophale, Ramdas; Cheeseman, Phillip A; Deem, Michael W

2011-07-21

We here describe a database of computationally predicted zeolite-like materials. These crystals were discovered by a Monte Carlo search for zeolite-like materials. Positions of Si atoms as well as unit cell, space group, density, and number of crystallographically unique atoms were explored in the construction of this database. The database contains over 2.6 M unique structures. Roughly 15% of these are within +30 kJ mol(-1) Si of α-quartz, the band in which most of the known zeolites lie. These structures have topological, geometrical, and diffraction characteristics that are similar to those of known zeolites. The database is the result of refinement by two interatomic potentials that both satisfy the Pauli exclusion principle. The database has been deposited in the publicly available PCOD database and in www.hypotheticalzeolites.net/database/deem/. This journal is © the Owner Societies 2011

Comparison of the Effect of Continuous Femoral Nerve Block and Adductor Canal Block after Primary Total Knee Arthroplasty.

Science.gov (United States)

Seo, Seung Suk; Kim, Ok Gul; Seo, Jin Hyeok; Kim, Do Hoon; Kim, Youn Gu; Park, Beyoung Yun

2017-09-01

This study aimed to compare the effects of femoral nerve block and adductor canal block on postoperative pain, quadriceps strength, and walking ability after primary total knee arthroplasty. Between November 2014 and February 2015, 60 patients underwent primary total knee arthroplasty. Thirty patients received femoral nerve block and the other 30 received adductor canal block for postoperative pain control. Before spinal anesthesia, the patients received nerve block via a catheter (20 mL 0.75% ropivacaine was administered initially, followed by intermittent bolus injection of 10 mL 0.2% ropivacaine every 6 hours for 3 days). The catheters were maintained in the exact location of nerve block in 24 patients in the femoral nerve block group and in 19 patients in the adductor canal block group. Data collection was carried out from these 43 patients. To evaluate postoperative pain control, the numerical rating scale scores at rest and 45° flexion of the knee were recorded. To evaluate quadriceps strength, manual muscle testing was performed. Walking ability was assessed using the Timed Up and Go test. We also evaluated analgesic consumption and complications of peripheral nerve block. No significant intergroup difference was observed in the numerical rating scale scores at rest and 45° flexion of the knee on postoperative days 1, 2, 3, and 7. The adductor canal block group had significantly greater quadriceps strength than did the femoral nerve block group, as assessed by manual muscle testing on postoperative days 1, 2, and 3. The 2 groups showed no difference in walking ability on postoperative day 1, but on postoperative days 2, 3, walking ability was significantly better in the adductor canal block group than in the femoral nerve block group. No significant intergroup difference was observed in analgesic consumption. The groups showed no difference in postoperative pain control. Adductor canal block was superior to femoral nerve block in preserving quadriceps

EFFECT OF GRAIN SIZE AND ACTIVATION TIME OF ZEOLITE TO ADSORPTION AND DESORPTION OF NH4OH AND KCL AS MODEL OF FERTILIZER-ZEOLITE MIX

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Muhammad Prasantio Bimantio

2017-10-01

Full Text Available Zeolites can be used as adsorbent, ion exchange, catalyst, or catalyst carrier. Application of fertilizer use in the zeolite also be one of the interesting topic. Zeolites in a mixture of fertilizer can use to control the release of nutrients. The purpose of this research is to study the effect of grain size and time of the activation of zeolite to adsorption and desorption of NH4OH and KCl as modeling of ZA and KCl fertilizer, to obtain the value of adsorption rate constant (ka and desorption rate constant (kd. This research procedure include: the process of adsorption by adding zeolite with various size and time of activation into a sealed beaker glass and let the adsorption process occurs for 24 hours. After 24 hours, the solution was filtered, the zeolite then put in 100 ml of aquadest into a sealed beaker glass and let the desorption process happened for another 24 hours. Three samples with the largest difference solution concentrations looked for the value of the ka and kd. Zeolite configuration with the largest ka is trialed with fertilizer and compared with the value of ka obtained from modeling. The result for NH4OH adsorbate, -50+60 mesh 2 hours configuration zeolite give the largest ka. For KCl adsorbate, -30+40 mesh 4 hours configuration zeolite give the largest ka. The value between modeling and trials with fertilizers are not much different.

Nanodispersed Suspensions of Zeolite Catalysts for Converting Dimethyl Ether into Olefins

Science.gov (United States)

Kolesnichenko, N. V.; Yashina, O. V.; Ezhova, N. N.; Bondarenko, G. N.; Khadzhiev, S. N.

2018-01-01

Nanodispersed suspensions that are effective in DME conversion and stable in the reaction zone in a three-phase system (slurry reactor) are obtained from MFI zeolite commercial samples (TsVM, IK-17-1, and CBV) in liquid media via ultrasonic treatment (UST). It is found that the dispersion medium, in which ultrasound affects zeolite commercial sample, has a large influence on particle size in the suspension. UST in the aqueous medium produces zeolite nanoparticles smaller than 50 nm, while larger particles of MFI zeolite samples form in silicone or hydrocarbon oils. Spectral and adsorption data show that when zeolites undergo UST in an aqueous medium, the acid sites are redistributed on the zeolite surface and the specific surface area of the mesopores increases. Preliminary UST in aqueous media of zeolite commercial samples (TsVM, IK-17-1, and CBV) affects the catalytic properties of MFI zeolite nanodispersed suspensions. The selectivity of samples when paraffins and olefins form is largely due to superacid sites consisting of OH groups of hydroxonium ion H3O+.

Ion-exchange properties of cesium and strontium into zeolites from sodium salt solutions

International Nuclear Information System (INIS)

Kanno, Takuji; Hashimoto, Hiroyuki; Ohtani, Tozo.

1978-01-01

The ion-exchange properties of cesium and strontium into zeolite from sodium salt solution has been studied in zeolite A, zeolite X, zeolite Y, mordenite and clinoptilolite. The distribution of cesium into mordenite from about 1 -- 2 M sodium chloride and sodium hydroxide solutions is considerably larger than that into zeolite A. The distribution coefficient for 2 M solution of sodium salts was about 300. Therefore, the separation of cesium from sodium salt solution is possible by using mordenite. The distribution of strontium into zeolites form 1 -- 2 M solutions of sodium chloride and sodium nitrate were in the order of zeolite A>zeolite X>zeolite Y asymptoticaly equals mordenite. The distribution coefficient of 230 was obtained for 1 M solutions of sodium salts. The anion in solutions had no effect on the distribution of cesium and strontium into zeolite from sodium salt solution. (author)

Application of zeolite-based catalyst to hydrocracking of coal-derived liquids

Energy Technology Data Exchange (ETDEWEB)

Shimada, H.; Sato, T.; Yoshimura, Y.; Hinata, A.; Yoshitomi, S.; Castillo Mares, A.; Nishijima, A. (National Chemical Laboratory for Industry, Tsukuba (Japan))

1990-06-01

Y-zeolite supported catalysts were applied to the hydrocracking of coal-derived liquids. By the introduction of two-stage upgrading consisting of hydrotreating and hydrocracking, Wandoan coal-derived middle distillate was hydrocracked over Ni-Mo/Y-zeolite, producing a high gasoline fraction yield. Zeolite supported catalysts gave little hydrocracked compounds in the hydroprocessing of coal-derived heavy oils, even after hydrotreatment. The reaction inhibitors which seriously poison the active sites of zeolites were found to be small nitrogen-containing molecules. In the hydroprocessing of coal-derived heavy oils, zeolite supported catalysts were inferior to alumina supported catalysts. This is due to the high hydrocracking but low hydrogenation activity of zeolite supported catalysts. 22 refs., 5 figs., 11 tabs.

Zeolite from fly ash: synthesis and characterization

Indian Academy of Sciences (India)

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

Precipitation strengthened high strength, high conductivity Cu-Cr-Nb alloys produced by chill block melt spinning. Final Report Ph.D. Thesis

Science.gov (United States)

Ellis, David L.; Michal, Gary M.

1989-01-01

A series of Cu-based alloys containing 2 to 10 a/o Cr and 1 to 5 a/o Nb were produced by chill block melt spinning (CBMS). The melt spun ribbons were consolidated and hot rolled to sheet to produce a supersaturated Cu-Cr-Nb solid solution from which the high melting point intermetallic compound Cr2Nb could be precipitated to strengthen the Cu matrix. The results show that the materials possess electrical conductivities in excess of 90 percent that of pure Cu at 200 C and above. The strengths of the Cu-Cr-Nb alloys were much greater than Cu, Cu-0.6 Cr, NARloy-A, and NARloy-Z in the as-melt spun condition. The strengths of the consolidated materials were less than Cu-Cr and Cu-Cr-Zr below 500 C and 600 C respectively, but were significantly better above these temperatures. The strengths of the consolidated materials were greater than NARloy-Z, at all temperatures. The GLIDCOP possessed similar strength levels up to 750 C when the strength of the Cu-Cr-Nb alloys begins to degrade. The long term stability of the Cu-Cr-Nb alloys was measured by the microhardness of aged samples and the growth of precipitates. The microhardness measurements indicate that the alloys overage rapidly, but do not suffer much loss in strength between 10 and 100 hours which confirms the results of the electrical resistivity measurements taken during the aging of the alloys at 500 C. The loss in strength from peak strength levels is significant, but the strength remains exceptionally good. Transmission electron microscopy (TEM) of the as-melt spun samples revealed that Cr2Nb precipitates formed in the liquid Cu during the chill block melt spinning, indicating a very strong driving force for the formation of the precipitates. The TEM of the aged and consolidated materials indicates that the precipitates coarsen considerably, but remain in the submicron range.

Exfoliation of two-dimensional zeolites in liquid polybutadienes

KAUST Repository

Sabnis, Sanket; Tanna, Vijesh A.; Li, Chao; Zhu, Jiaxin; Vattipalli, Vivek; Nonnenmann, Stephen S.; Sheng, Guan; Lai, Zhiping; Winter, H. Henning; Fan, Wei

2017-01-01

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

Morpho-chemical characterization and surface properties of carcinogenic zeolite fibers

International Nuclear Information System (INIS)

Mattioli, Michele; Giordani, Matteo; Dogan, Meral; Cangiotti, Michela; Avella, Giuseppe; Giorgi, Rodorico; Dogan, A. Umran; Ottaviani, Maria Francesca

2016-01-01

Highlights: • Differently carcinogenic zeolite fibers were investigated combining physico-chemical methods. • For the first time, zeolite fibers were studied by means of the EPR technique using different spin probes. • The structural properties and the adsorption capability are function of different types and distributions of adsorption sites. • The interacting ability of erionite is higher than that of other fibrous zeolites. • The surface interacting properties may be related with the carcinogenicity of the zeolite fibers. - Abstract: Erionite belonging to the zeolite family is a human health-hazard, since it was demonstrated to be carcinogenic. Conversely, offretite family zeolites were suspected carcinogenic. Mineralogical, morphological, chemical, and surface characterizations were performed on two erionites (GF1, MD8) and one offretite (BV12) fibrous samples and, for comparison, one scolecite (SC1) sample. The specific surface area analysis indicated a larger availability of surface sites for the adsorption onto GF1, while SC1 shows the lowest one and the presence of large pores in the poorly fibrous zeolite aggregates. Selected spin probes revealed a high adsorption capacity of GF1 compared to the other zeolites, but the polar/charged interacting sites were well distributed, intercalated by less polar sites (Si–O–Si). MD8 surface is less homogeneous and the polar/charged sites are more interacting and closer to each other compared to GF1. The interacting ability of BV12 surface is much lower than that found for GF1 and MD8 and the probes are trapped in small pores into the fibrous aggregates. In comparison with the other zeolites, the non-carcinogenic SC1 shows a poor interacting ability and a lower surface polarity. These results helped to clarify the chemical properties and the surface interacting ability of these zeolite fibers which may be related to their carcinogenicity.

Kinetics and thermodynamic for sorption of arsenate by Lanthanum-exchanged zeolite

International Nuclear Information System (INIS)

Mohd Jelas Haron; Saiful Adli Masdan; Mohd Zobir Hussein; Zulkarnain Zainal; Anuar Kassim

2007-01-01

Zeolites are crystalline, hydrated aluminosilicate containing exchangeable alkaline and alkaline earth cations in their structural frameworks. Since zeolites have permanent negative charges on their surfaces, they have no affinity for anions. However recent studies have shown that modification of zeolites with certain surfactants or metal cations yield sorbents with a strong affinity for many anions. In this paper, modification of zeolites (zeolite A, X and ZSM5) were performed by exchange of naturally occurring cations with lanthanum ion that forms low solubility arsenate salt. The exchanged zeolites were used to sorb arsenate from aqueous solution. Among parameters investigated were effect of pH, arsenate initial concentrations, contact time and temperature. The maximum exchanged capacity of La (III) ion was obtained when using solution with initial pH of 4. Zeolite X gives the highest La (III) exchanged capacity compared to other zeolites. The results showed that As (V) sorption by La-zeolites occurred at about pH 6.5 and increased as pH increased and reaching maximum at equilibrium pH about 7.8. On the other hand, almost no arsenate sorption occurred on un exchanged zeolites. This indicates that La (III) ion on the exchanged zeolites is taking part on the As(V) sorption via surface precipitation. The results also showed that the sorption capacities increased with increasing initial As (V) concentrations. The sorption followed Langmuir model with maximum sorption capacities of 0.41, 0.21 and 0.19 mmol/g at 25 degree Celsius for La exchanged zeolite X (La-ZX), La exchanged zeolite ZSM5 (La-ZSM) and La exchanged zeolite A (La-ZA), respectively. The amounts of sorption of As (V) by La exchanged zeolite increased as temperature increased from 25 to 70 degree Celsius indicating that the process is endothermic. The free energy changes ( ΔG degree) for the sorption at 25 degree Celsius were -10.25, -9.65 and -8.49 kJ/ mol for La-ZX, La-ZSM and La-ZA, respectively. The

Cure kinetics and mechanical interfacial characteristics of zeolite/DGEBA composites

International Nuclear Information System (INIS)

Park, Soo Jin; Kim, Young Mi; Shin, Jae Sup

2003-01-01

In this work, the zeolite/diglycidylether of bisphenol A(DGEBA) systems were investigated in terms of the cure kinetics and mechanical interfacial properties of the composites. The 4, 4-Diamino Diphenyl Methane(DDM) was used as a curing agent for epoxy. Two types of zeolite(PZ) were prepared with 15 and 35 wt% KOH treatments(15-BZ and 35-BZ, respectively) for 24 h, and their surface characteristics were studied by X-ray Photoelectron Spectroscopy (XPS) and X-Ray Diffraction (XRD). Cure kinetics of the composites were examined in the context of Differential Scanning Calorimetry(DSC), and mechanical interfacial properties were investigated in critical stress intensity factor(K IC ) and critical strain energy release rate(G IC ). In the results of XPS and XRD, sodium ion(Na) of zeolite was exchanged for potassium ion(K), resulting from the treatment of KOH. Also, Si 2p /A1 2p composition ratios of the treated zeolite were increased, which could be attributed to the weakening of A1-O bond in framework. Cure activation energy(E a ) of 15-BZ composites was decreased, whereas K IC and G IC were increased, compared with those of the pure zeolite/DGEBA composites. It was probably accounted that the acidity of zeolite was increased by surface treatments and the cure reaction between zeolite and epoxy was influenced on the increased acidity of zeolite

Reduction volume of radioactive wastes using natural zeolite

International Nuclear Information System (INIS)

Endro Kismolo; Nurimaniwathy; Vemi Ridantami

2013-01-01

The aim of this experience was to know of the characteristics of zeolite as the sorbent for reduction volume of liquid waste with the Pb contaminant contain. The experiment was done by sorption method a batch performed by using zeolite from Gedangsari Gunung Kidul with the grain size (-60+80) mesh, (-80+100) mesh dan (-100+120) mesh which was activated by (NH 4 ) CI and NH 4 N0 3 1.0 M. Weight of sorbent was added was variated from 5.0 to 40.0 %, and variation of silica sand to added from 0.5 to 2.5 % of weight sorbent. Stirring speed was varied from 30 to 180 rpm and the stirring time of 10 to 120 minutes, and filtrates from filtering process to analyzed by Absorption Analysis Spectrophotometry utilities. From the experience can be achieved of data that the best sorption to obtained at the condition of zeolite on (-80+100) mesh, sorbent added of 25 %, stirring speed of 120 rpm, time of stirring of 90 minutes, and the setting time of 120 minutes. At this condition to obtained sorption efficiency are 64.162 % for natural zeolite, 7.034 % for zeolite be activated with NH 4 N0 3 and 77.414 % for zeolite be activated with NH 4 Cl 1.0 M. (author)

Catalytic conversion of ethanol on H-Y zeolite

Directory of Open Access Journals (Sweden)

Čegar Nedeljko

2005-01-01

Full Text Available The catalytic activity of the H-form of synthetic zeolite NaY was examined in this study. The catalytic activity was determined according to the rate of ethanol conversion in a gas phase in the static system. In the conversion of ethanol on synthetic NaY zeolite at 585, 595, and 610 K, on which the reaction develops at an optimal rate, ethene and diethyl ether are evolved in approximately the same quantity. After transforming the NaY zeolite into the H-form, its catalytic activity was extremely increases so, the reaction develops at a significantly lower temperature with a very large increase in the reaction rate. The distribution of the products also changes, so that at lower temperatures diethyl ether is elvolved in most cases, and the development of ethene is favored at higher ones, and after a certain period of time there is almost complete conversion of ethanol into ethene. The increase in catalytic activity, as well as the change of selectivity of conversion of ethanol on the H-form of zeolite, is the result of removing Na+ cations in the NaY zeolite, so that more acidic catalyst is obtained which contains a number of acidic catalytically active centers, as well as a more powerful one compared to the original NaY zeolite.

Inhibition of palm oil oxidation by zeolite nanocrystals.

Science.gov (United States)

Tan, Kok-Hou; Awala, Hussein; Mukti, Rino R; Wong, Ka-Lun; Rigaud, Baptiste; Ling, Tau Chuan; Aleksandrov, Hristiyan A; Koleva, Iskra Z; Vayssilov, Georgi N; Mintova, Svetlana; Ng, Eng-Poh

2015-05-13

The efficiency of zeolite X nanocrystals (FAU-type framework structure) containing different extra-framework cations (Li(+), Na(+), K(+), and Ca(2+)) in slowing the thermal oxidation of palm oil is reported. The oxidation study of palm oil is conducted in the presence of zeolite nanocrystals (0.5 wt %) at 150 °C. Several characterization techniques such as visual analysis, colorimetry, rheometry, total acid number (TAN), FT-IR spectroscopy, (1)H NMR spectroscopy, and Karl Fischer analyses are applied to follow the oxidative evolution of the oil. It was found that zeolite nanocrystals decelerate the oxidation of palm oil through stabilization of hydroperoxides, which are the primary oxidation product, and concurrently via adsorption of the secondary oxidation products (alcohols, aldehydes, ketones, carboxylic acids, and esters). In addition to the experimental results, periodic density functional theory (DFT) calculations are performed to elucidate further the oxidation process of the palm oil in the presence of zeolite nanocrystals. The DFT calculations show that the metal complexes formed with peroxides are more stable than the complexes with alkenes with the same ions. The peroxides captured in the zeolite X nanocrystals consequently decelerate further oxidation toward formation of acids. Unlike the monovalent alkali metal cations in the zeolite X nanocrystals (K(+), Na(+), and Li(+)), Ca(2+) reduced the acidity of the oil by neutralizing the acidic carboxylate compounds to COO(-)(Ca(2+))1/2 species.

Mixing of zeolite powders and molten salt

International Nuclear Information System (INIS)

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

1996-01-01

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

Detergent zeolite complex "Alusil", Zvornik

OpenAIRE

Stanković Mirjana S.; Pezo Lato L.

2003-01-01

The IGPC Engineering Department designed the basis technological and machine projects for a detergent zeolite complex, on the basis of which a pilot plant with an initial capacity of 5,000 t/y was constructed in 1983 within Birač-Zvornik production complex. Additional projects were done afterwards and the starting capacity increased to 200,000 t/y in 1988. This plant became the biggest producer of detergent zeolite in the world. These projects were manufactured on the basis of specific techno...

Preliminary study of zeolite-pva composite application in removal of SR-90

International Nuclear Information System (INIS)

Las, Thamzil; Zamroni, Huzen; Sugiarto; Darsono

1998-01-01

Zeolite-PAN composite was prepared by contacting the purified Bayah and Lampung zeolites with poly-vinyl alcohol binder and cured by using Gamma-ray of Co-60 at various doses, i.e., 10, 20, 30 dan 40 kGray with dose rates 7.5 kGy/hour. Zeolite-PAN composites were treated with solution containing Sr-90 up to 5 days and the Sr sorption was measured by Liquid Scintillation Counter for determination of their sorption efficiencies. The result obtained that, zeolite-PAN composites were shown high sorption efficiencies on the composites zeolite-PVA which was formulated from 20% zeolite, irradiated by 40 kGy and obtained the sorption efficiency of 94% with the Kd values similar to the purified zeolites. (author)

PHYSICAL, CHEMICAL AND STRUCTURAL EVOLUTIION OF ZEOLITE-CONTAINING WASTE FORMS PRODUCED FROM METAKAOLINITE AND CALCINED SODUIM BEARING WASTE (HLW AND/OR LLW)

International Nuclear Information System (INIS)

Grutzeck, Michael W.

2003-01-01

Zeolites can adsorb liquids and gases, take part in catalytic reactions and serve as cation exchange media. They are commercially available as finely divided powders. Using zeolites to manage radioactive waste is not new, but a process by which zeolites can be made to act both as a host phase and a cementing agent is. It is notable that zeolites occur in nature as well consolidated/cemented deposits. The Romans used blocks of Neapolitan zeolitized tuff as a building material and some of these buildings are still standing. Zeolites are easy to synthesize from a wide range of both natural and man-made precursor materials. The method of making a ''hydroceramic'' is derived from a process in which metakaolinite (thermally dehydroxylated kaolinite) is slurried with a dilute sodium hydroxide (NaOH) solution and then reacted for hours to days at mildly elevated temperatures (60-200 C). The zeolites that form in solution are finely divided powders containing micrometer sized crystals. However, if the process is changed and only enough concentrated sodium hydroxide solution (e.g. 12 M) is added to the metakaolinite to give the mixture a putty-like consistency and the mixture is then cured under similar conditions, the mixture becomes a very hard ceramic-like material containing distinct tectosilicate crystallites (zeolites and feldspathoids) imbedded in an X-ray amorphous sodium aluminosilicate hydrate matrix. Due to the material's vitreous character, the composite has been called a hydroceramic. Similar to zeolite/feldspathoid powders, a hydroceramic is able to sequester cations and a wide range of salt molecules (e.g., nitrate, nitrite and sulfate) in lattice positions and within structural channels and voids thus rendering them ''insoluble'' and making them an ideal contingency waste form for solidifying radioactive waste. The obvious similarities between a hydroceramic waste form and a waste form based on solidified Portland-cement grout are superficial because their

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.

Exploitation of Unique Properties of Zeolites in the Development of Gas Sensors

Directory of Open Access Journals (Sweden)

Prabir K. Dutta

2012-04-01

Full Text Available The unique properties of microporous zeolites, including ion-exchange properties, adsorption, molecular sieving, catalysis, conductivity have been exploited in improving the performance of gas sensors. Zeolites have been employed as physical and chemical filters to improve the sensitivity and selectivity of gas sensors. In addition, direct interaction of gas molecules with the extraframework cations in the nanoconfined space of zeolites has been explored as a basis for developing new impedance-type gas/vapor sensors. In this review, we summarize how these properties of zeolites have been used to develop new sensing paradigms. There is a considerable breadth of transduction processes that have been used for zeolite incorporated sensors, including frequency measurements, optical and the entire gamut of electrochemical measurements. It is clear from the published literature that zeolites provide a route to enhance sensor performance, and it is expected that commercial manifestation of some of the approaches discussed here will take place. The future of zeolite-based sensors will continue to exploit its unique properties and use of other microporous frameworks, including metal organic frameworks. Zeolite composites with electronic materials, including metals will lead to new paradigms in sensing. Use of nano-sized zeolite crystals and zeolite membranes will enhance sensor properties and make possible new routes of miniaturized sensors.

Thermal Analysis of Lampung Zeolite as Ion Cesium Replacement

International Nuclear Information System (INIS)

Aslina-Br-Ginting; Dian-Anggraini; Arif-Nugroho

2007-01-01

Zeolite have the cation can move freely and as exchangeable partly or totally with other cations. Therefore, it can serve the purpose of ion exchanger very selectively to ion cesium which is present in fuel waste. In this research analysis of pore surface area, radius pore, and adsorption have been done. After the characters of Lampung zeolite is known and then analysis of cation exchange capacity (CEC) toward ion 137 Cs is conducted, analysis of Lampung zeolite adsorption to ion 137 Cs in waste of fissile product and in research waste is subsequently done. Result of analysis show Lampung zeolite has surface area of 10,0478 m 2 , specific surface area of 47,0841 m 2 /g, pore radius of 19,3020 o A and adsorption of 24,500 cc/g. For application as a ion exchange, Lampung zeolite can adsorb ion 137 Cs reaching maximum at concentration of CsCl 0,5 N with the contact time 1 day and the optimum KTK value is 0,8360 m eq/g. While Lampung zeolite is able to adsorb 86,4 % ion Cs in waste of fission product. (author)

The Effect of Zeolite on Aggregate Stability Indices

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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

Dealuminization treatment effect of krypton gas adsorption on zeolite

International Nuclear Information System (INIS)

Shin, J. M.; Shin, S. W.; Park, J. J.; Lee, H. H.; Yang, M. S.

2003-01-01

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

Regeneration of zeolite catalysts of isobutane alkylation with butenes

Energy Technology Data Exchange (ETDEWEB)

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

1986-12-10

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

Desulfurization of the exhaust gas with zeolite synthesized from diatomaceous earth

Energy Technology Data Exchange (ETDEWEB)

Miyamoto, M

1975-07-01

Both A type and X type zeolites were prepared from diatomaceous earth and tested for use in flue gas desulfurization. Several diatomaceous earths of known chemical compositions were mixed to obtain a desired molar ratio of silicates, whose maturation was achieved in two steps; room temperature maturation and reflux maturation by heating. If the second maturation was carried out for more than 12 hr, the X type zeolite formation was low. At the best conditions, 80% pure zeolite could be prepared for both types according to their x-ray diffraction spectra. The synthesized x type zeolite adsorbed sulfur dioxide more efficiently than A type zeolite. When a simulated flue gas containing 680 to 840 ppM sulfur dioxide was passed at a flow rate of 9.0 Nl/min through a 250 g zeolite column, the column breaking time (time required for the SO/sub 2/ concentration of the column effluent to reach 10% of the initial SO/sub 2/ concentration) was 5.3 hr, while that for the commercial zeolite and activated carbon was 6.8 hr and 8.0 hr, respectively. If the flue gas contained more than 1% moisture, the adsorbed water reacted with SO/sub 2/ and the zeolite crystal tended to break down. The use of zeolite for flue gas desulfurization was more costly than the use of activated carbon.

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

Science.gov (United States)

Anis, Shaheen Fatima; Hashaikeh, Raed

2018-02-01

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

The Effect of Zeolite Composition and Grain Size on Gas Sensing Properties of SnO2/Zeolite Sensor

Directory of Open Access Journals (Sweden)

Yanhui Sun

2018-01-01

Full Text Available In order to improve the sensing properties of tin dioxide gas sensor, four kinds of different SiO2/Al2O3 ratio, different particle size of MFI type zeolites (ZSM-5 were coated on the SnO2 to prepared zeolite modified gas sensors, and the gas sensing properties were tested. The measurement results showed that the response values of ZSM-5 zeolite (SiO2/Al2O3 = 70, grain size 300 nm coated SnO2 gas sensors to formaldehyde vapor were increased, and the response to acetone decreased compared with that of SnO2 gas sensor, indicating an improved selectivity property. The other three ZSM-5 zeolites with SiO2/Al2O3 70, 150 and 470, respectively, and grain sizes all around 1 μm coated SnO2 sensors did not show much difference with SnO2 sensor for the response properties to both formaldehyde and acetone. The sensing mechanism of ZSM-5 modified sensors was briefly analyzed.

Fluorescence labelling as tool for zeolite particle tracking in nanoremediation approaches

International Nuclear Information System (INIS)

Gillies, Glenn; Mackenzie, Katrin; Kopinke, Frank-Dieter; Georgi, Anett

2016-01-01

Colloidal Fe-zeolites such as Fe-BEA-35 are currently under study as new adsorbent and catalyst materials for in-situ chemical oxidation with H_2O_2. As for nanoremediation in general, the availability of suitable particle detection methods is a requirement for successful process development and particle tracing. Detection and distinguishing between natural colloids and introduced particles with a similar composition are a challenge. By means of fluorescence labelling, a highly specific detection option for Fe-BEA-35 was developed. ‘Ship-in-a-bottle’ synthesis of fluorescein within the zeolite pores, which was applied for the first time for a BEA type zeolite, provides a product with stable and non-extractable fluorescence. When the fluorescent labelled zeolite is added at a concentration of 1 wt.% referring to the total zeolite mass, a very low detection limit of 1 mg/L of total zeolite is obtained. Compared to commonly applied turbidity measurements, detection via fluorescence labelling is much more specific and sensitive. Fluorescence is only marginally affected by carboxymethyl cellulose, which is frequently applied as stabilizer in application suspensions but will be depleted upon contact with H_2O_2. Transport properties of fluorescent labelled and non-labelled Fe-zeolite particles are in agreement as determined in a column study with quartz sand and synthetic groundwater (classified as very hard). - Highlights: • Fluorescent BEA zeolite was prepared for first time by ‘ship-in-a-bottle’ synthesis. • Fluorescein synthesized inside zeolite channels is stable and non-extractable. • Detection limit of Fe-zeolite particles in suspension with 1 wt.% fluorescent zeolite is 1 mg/L. • Transport properties of fluorescent and Fe-loaded BEA particles are identical.

The potential of Saudi Arabian natural zeolites in energy recovery technologies

International Nuclear Information System (INIS)

Nizami, A.S.; Ouda, O.K.M.; Rehan, M.; El-Maghraby, A.M.O.; Gardy, J.; Hassanpour, A.; Kumar, S.; Ismail, I.M.I.

2016-01-01

Energy consumption in KSA (kingdom of Saudi Arabia) is growing rapidly due to economic development with raised levels of population, urbanization and living standards. Fossil fuels are currently solely used to meet the energy requirements. The KSA government have planned to double its energy generating capacity (upto 120 GW (gigawatts)) by 2032. About half of the electricity capacity of this targeted energy will come from renewable resources such as nuclear, wind, solar, WTE (waste-to-energy) etc. Natural zeolites are found abundantly in KSA at Jabal Shamah occurrence near Jeddah city, whose characteristics have never been investigated in energy related applications. This research aims to study the physical and chemical characteristics of natural zeolite in KSA and to review its potential utilization in selected WTE technologies and solar energy. The standard zeolite group of alumina–silicate minerals were found with the presence of other elements such as Na, Mg and K etc. A highly crystalline structure and thermal stability of natural zeolites together with unique ion exchange, adsorption properties, high surface area and porosity make them suitable in energy applications such as WTE and solar energy as an additive or catalyst. A simple solid–gas absorption system for storing solar energy in natural zeolites will be a cheap alternative method for KSA. In AD (anaerobic digestion), the dual characteristics of natural zeolite like Mordenite will increase the CH_4 production of OFMSW (organic fraction of municipal solid waste). Further investigations are recommended to study the technical, economical, and environmental feasibility of natural zeolite utilization in WTE technologies in KSA. - Highlights: • A highly crystalline structure is found in natural zeolites. • Natural zeolites will store solar energy in solid–gas absorption system. • The composites of natural zeolites will produce more liquid fuel like gasoline. • The natural zeolite will increase

CO hydrogenation on zeolite-supported Ru: Effect of neutralizing cations

International Nuclear Information System (INIS)

Oukaci, R.; Wu, J.C.S.; Goodwin, J.G. Jr.

1986-01-01

Previous results for zeolite-supported Ru prepared by ion exchange suggested a possible effect of the nature and concentration of the neutralizing cations in the zeolite on the catalytic properties of the metal. However, the interpretation of these results was complicated by the fact that a series of zeolites with different Si/Al ratios was used. The present study was undertaken to investigate systematically the influence of the nature of alkali neutralizing cations on CO hydrogenation over ion-exchanged Y-zeolite-supported ruthenium catalysts

Utilization of Natural Zeolite from Ponorogo and Purworejo for Naphthol Substance Adsorption

Science.gov (United States)

Imandiani, Sundus; Indira, Christine; Johan, Anthony; Budiyono

2018-02-01

Indonesia has many zeolite producing areas yet untapped. Researchers developed the utilization of natural zeolites useful for the adsorption of naphthol dyes commonly found in batik waste. In this study researchers used natural zeolites from Purworejo and Ponorogo that are activated using hydrochloric acid that is used for adsorption. The purpose of this research is to know the effect of natural zeolite activation from Ponorogo and Purworejo on the effectiveness of adsorption of naphthol dyes widely used in batik industry. Natural zeolite was activated using HCl concentration of 1.3N; 1.8N; 3.2N; and 3.9N for 60 minutes. The methods are preparation of natural zeolite from Purworejo and Ponorogo, dealumination using hydrochloric acid, adsorption process of naphthol dyes using activated zeolite, and test of adsorption result with uv-vis spectrophotometry. The test results showed that the higher HCl concentration will increase adsorption capacity. This can be known from the concentration of naphthol dye which decreased both using natural zeolite Ponorogo and Purworejo. While the effectiveness of adsorption shows natural zeolite Purworejo has a greater adsorption capacity than Ponorogo with optimum conditions of dealumination using concentration HCl 3,9N.

Minimum Description Length Block Finder, a Method to Identify Haplotype Blocks and to Compare the Strength of Block Boundaries

OpenAIRE

Mannila, H.; Koivisto, M.; Perola, M.; Varilo, T.; Hennah, W.; Ekelund, J.; Lukk, M.; Peltonen, L.; Ukkonen, E.

2003-01-01

We describe a new probabilistic method for finding haplotype blocks that is based on the use of the minimum description length (MDL) principle. We give a rigorous definition of the quality of a segmentation of a genomic region into blocks and describe a dynamic programming algorithm for finding the optimal segmentation with respect to this measure. We also describe a method for finding the probability of a block boundary for each pair of adjacent markers: this gives a tool for evaluating the ...

Generalized synthesis of mesoporous shells on zeolite crystals

KAUST Repository

Han, Yu; Pitukmanorom, Pemakorn; Zhao, L. J.; Ying, Jackie

2010-01-01

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

Application of multi-block methods in cement production

DEFF Research Database (Denmark)

Svinning, K.; Høskuldsson, Agnar

2008-01-01

distribution and the two last blocks the superficial microstructure analysed by differential thermo gravimetric analysis. The multi-block method is used to identify the role of each part. The score vectors of each block can be analysed separately or together with score vectors of other blocks. Stepwise......Compressive strength at 1 day of Portland cement as a function of the microstructure of cement was statistically modelled by application of multi-block regression method. The observation X-matrix was partitioned into four blocks, the first block representing the mineralogy, the second particle size...... regression is used to find minimum number of variables of each block. The multi-block method proved useful in determining the modelling strength of each data block and finding minimum number of variables within each data block....

Synthesis of Zeolite Materials for Noble Gas Separation

International Nuclear Information System (INIS)

Achey, R.; Rivera, O.; Wellons, M.; Hunter, D.

2017-01-01

Microporous zeolite adsorbent materials are widely used as a medium for separating gases. Adsorbent gas separation systems can run at ambient temperature and require minimal pressure to flow the input gas stream across the adsorbent bed. This allows for low energy consumption relative to other types of separation systems. Specific zeolites also have a high capacity and selectivity for the gases of interest, leading to compact and efficient separation systems. These characteristics are particularly advantageous for the application of signatures detection for non-proliferation, which often requires portable systems with low power draw. Savannah River National Laboratory currently is the leader in using zeolites for noble gas sampling for non-proliferation detection platforms. However, there is a constant customer need for improved sampling capabilities. Development of improved zeolite materials will lead to improved sampling technology. Microwave-assisted and conventional hydrothermal synthesis have been used to make a variety of zeolites tailored for noble gas separation. Materials characterization data collected in this project has been used to help guide the synthesis of improved zeolite materials. Candidate materials have been down-selected based on highest available surface area, maximum overall capacity for gas adsorption and highest selectivity. The creation of improved adsorbent materials initiated in this project will lead to development of more compact, efficient and effective noble gas collectors and concentrators. The work performed in this project will be used as a foundation for funding proposals for further material development as well as possible industrial applications.

Synthesis of Zeolite Materials for Noble Gas Separation

Energy Technology Data Exchange (ETDEWEB)

Achey, R. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Rivera, O. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Wellons, M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Hunter, D. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2017-10-02

Microporous zeolite adsorbent materials are widely used as a medium for separating gases. Adsorbent gas separation systems can run at ambient temperature and require minimal pressure to flow the input gas stream across the adsorbent bed. This allows for low energy consumption relative to other types of separation systems. Specific zeolites also have a high capacity and selectivity for the gases of interest, leading to compact and efficient separation systems. These characteristics are particularly advantageous for the application of signatures detection for non-proliferation, which often requires portable systems with low power draw. Savannah River National Laboratory currently is the leader in using zeolites for noble gas sampling for non-proliferation detection platforms. However, there is a constant customer need for improved sampling capabilities. Development of improved zeolite materials will lead to improved sampling technology. Microwave-assisted and conventional hydrothermal synthesis have been used to make a variety of zeolites tailored for noble gas separation. Materials characterization data collected in this project has been used to help guide the synthesis of improved zeolite materials. Candidate materials have been down-selected based on highest available surface area, maximum overall capacity for gas adsorption and highest selectivity. The creation of improved adsorbent materials initiated in this project will lead to development of more compact, efficient and effective noble gas collectors and concentrators. The work performed in this project will be used as a foundation for funding proposals for further material development as well as possible industrial applications.

Micro-shear bond strength of different resin cements to ceramic/glass-polymer CAD-CAM block materials.

Science.gov (United States)

Cekic-Nagas, Isil; Ergun, Gulfem; Egilmez, Ferhan; Vallittu, Pekka Kalevi; Lassila, Lippo Veli Juhana

2016-10-01

The aim of this study was to evaluate the effects of hydrofluoric acid treatment on bond strength of resin cements to three different types of ceramic/glass containing CAD-CAM block composite materials. CAD-CAM block materials of polymer infiltrated (Vita Enamic), resin nanoceramic (Lava Ultimate) and nanoceramic (Cerasmart) with a thickness of 1.5mm were randomly divided into two groups according to the surface treatment performed. In Group 1, specimens were wet-ground with silicon carbide abrasive papers up to no. 1000. In Group 2, 9.6% hydrofluoric acid gel was applied to ceramics. Three different resin cements (RelyX, Variolink Esthetic and G-CEM LinkAce) were applied to the tubes in 1.2-mm thick increments and light-cured for 40s using LED light curing unit. Half of the specimens (n=10) were submitted to thermal cycling (5000 cycles, 5-55°C). The strength measurements were accomplished with a universal testing machine (Lloyd Instruments) at a cross-head speed of 0.5mm/min until the failure occurs. Failure modes were examined using a stereomicroscope and scanning electron microscope. The data were analyzed with multivariate analysis of variance (MANOVA) and Tukey's post hoc tests (α=0.05). There were significant differences between ceramics and resin cements (pceramics (pceramic/glass-polymer materials might promote the bonding capacity of these systems. Copyright © 2016 Japan Prosthodontic Society. Published by Elsevier Ltd. All rights reserved.

Characterization of gallium-containing zeolites for catalytic applications

Energy Technology Data Exchange (ETDEWEB)

Garcia Sanchez, M.

2003-12-08

The present study considers the synthesis, characterization, and catalytic evaluation of extra-framework gallium-containing zeolites. We focus on modification of zeolites by chemical vapor deposition of trimethylgallium on HZSM-5 and Mordenite zeolites. Chapter 2 is dedicated to the chemisorption and stability of TMG on HZSM-5 and HMOR zeolites. The effect of silylation is also addressed. Some theoretical calculations are also shown in this study to support part of the experimental results. In Chapter 3, the effect of oxidation and reduction treatments on these catalysts is investigated by FTIR, ICP and multinuclei NMR. In Chapter 4, the oxidation state and Ga coordination obtained during and after thermal treatment with H2 and O2 is analysed by X-ray adsorption spectroscopy (XANES and EXAFS) and IR analysis of CO adsorption. These results allow a better understanding of the catalytic behaviour of Ga-containing zeolites catalyst. Chapter 5 consists of two parts: one discusses the H2 activation over Ga/HZSM5 and Ga/MOR catalysts by H2/D2 isotopic exchange reaction, and the second part deals with the aromatization of n-heptane over the same catalysts.

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.

PREPARATION, CHARACTERIZATIONS AND MODIFICATION OF Ni-Pd/NATURAL ZEOLITE CATALYSTS

Directory of Open Access Journals (Sweden)

Wega Trisunaryanti

2010-06-01

Full Text Available Preparation, and modification of Ni-Pd/natural zeolite as well as their characterizations had been carried out. The aim of this research for the fututure is to prepare the best characters catalyst for the conversion of waste plastics fraction to gasoline fraction (C5-C12 hydrocarbons. The preparation of catalysts was performed by reacting a natural zeolite with the precursor of Ni(NO32. 9H2O and PdCl2 in an ammonia solution (25%. The modifications were performed by varying the rasio of Ni/Pd loaded to the zeolite, whereas the Pd was previously loaded and total metal content was 1 wt.% based on the zeolite. The characterization of catalysts included determination of acidity gravimetrically by adsorption of ammonia or pyridine vapour  base method, metal content by Atomic Adsorption Spectrophotometer (AAS and X-ray Fluoresence (XRF and crystallinity by X-ray Diffraction (XRD. The treatment of catalysts using Etilene Diamine Tetra Acetic acid  (EDTA was performed to study the metal distribution on the outer or inner surface of the zeolite. The characterization results showed that the loading of metals to the zeolite increased its acidity and decreased its spesific surface area, however, did not defect its crystallnity.  The metals loaded on the zeolite were distributed inside the pore and at outer surface of the zeolite. For all catalyst samples, the acidities determined using ammonia were higher than those of pyridine, and the acidities determined before the EDTA treatment was lower than those after the treatment.  Metal contents of the zeolite before the EDTA treatment were higher than those after the treatment. The EDTA treatment enhanced the crystallinity of the sampel. The relationship between the metal rasio towards the acidity of the catalyst samples were in variation. Catalyst samples produced in this research have good characters, thus promisingly can be used for conversion process of waste plastics to gasoline fraction.    Keywords

Zeolite Vitrification Demonstration Program nonradioactive-process operations summary

International Nuclear Information System (INIS)

Bryan, G.H.; Knox, C.A.; Goles, R.G.; Ethridge, L.J.; Siemens, D.H.

1982-09-01

The Submerged Demineralizer System is a process developed to decontaminate high-activity level water at Three Mile Island by sorbing the activity (primarily Cs and Sr) onto beds of zeolite. Pacific Northwest Laboratory's Zeolite Vitrification Demonstration Program has the responsibility of demonstrating the full-scale vitrification of this zeolite material. The first phase of this program has been to develop a glass formulation and demonstrate the vitrification process with the use of nonradioactive materials. During this phase, four full-scale nonradioactive demonstration runs were completed. The same zeolite mixture being used in the SDS system was loaded with nonradioactive isotopes of Cs and Sr, dried, blended with glass-forming chemicals and fed to a canister in an in-can melter furnace. During each run, the gaseous effluents were sampled. After each run, glass samples were removed and analyzed

Zeolite-catalyzed biomass conversion to fuels and chemicals

DEFF Research Database (Denmark)

Taarning, Esben; Osmundsen, Christian Mårup; Yang, Xiaobo

2011-01-01

Heterogeneous catalysts have been a central element in the efficient conversion of fossil resources to fuels and chemicals, but their role in biomass utilization is more ambiguous. Zeolites constitute a promising class of heterogeneous catalysts and developments in recent years have demonstrated...... their potential to find broad use in the conversion of biomass. In this perspective we review and discuss the developments that have taken place in the field of biomass conversion using zeolites. Emphasis is put on the conversion of lignocellulosic material to fuels using conventional zeolites as well...

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...

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...

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 ...

High-strength beryllium block

International Nuclear Information System (INIS)

Pinto, N.P.; Keith, G.H.

1977-01-01

Beryllium billets hot isopressed using fine powder of high purity have exceptionally attractive properties; average tensile ultimate, 0.2% offset yield strength and elongation are 590 MPa, 430 MPa and 4.0% respectively. Properties are attributed to the fine grain size (about 4.0 μm average diameter) and the relatively low levels of BeO present as fine, well-dispersed particles. Dynamic properties, e.g., fracture toughness, are similar to those of standard grade, high-purity beryllium. The modulus of beryllium is retained to very high stress levels, and the microyield stress or precision elastic limit is higher than for other grades, including instrument grades. Limited data for billets made from normal-purity fine powders show similar room temperature properties. (author)

Microwave preparation of Li-zeolite directly from alumatrane and silatrane

International Nuclear Information System (INIS)

Sathupunya, Mathavee; Gulari, Erdogan; Wongkasemjit, Sujitra

2004-01-01

Li-zeolites were successfully synthesized in a one-step sol-gel process and microwave technique using silatrane and alumatrane as precursors and lithium hydroxide as the hydrolytic agent. Many types of Li-zeolites were obtained by controlling synthesis parameters. Perfect crystalline zeolite, EDI type zeolite, was obtained at 90 deg. C after heating for 60 min while ABW type zeolite was produced after heating for 300 min at 110 deg. C. With increasing temperature, a higher packing density product was generated. Changing Si/Al loading ratio highly influenced the morphology of the synthesized product. With increasing Al loading, more irregular morphology products were obtained. Changing Li 2 O/SiO 2 ratio, led to changes in the unit cell structure and crystal morphology. Lowering the Li 2 O/SiO 2 ratio to one produced FAU type zeolite at 110 deg. C for 240 min. The thermal stability of EDI and ABW were very low while that of FAU was higher which might come from the effect of low ring strain construction of FAU

Nanosized zeolites as a perspective material for conductometric biosensors creation

Science.gov (United States)

Kucherenko, Ivan; Soldatkin, Oleksandr; Kasap, Berna Ozansoy; Kirdeciler, Salih Kaan; Kurc, Burcu Akata; Jaffrezic-Renault, Nicole; Soldatkin, Alexei; Lagarde, Florence; Dzyadevych, Sergei

2015-05-01

In this work, the method of enzyme adsorption on different zeolites and mesoporous silica spheres (MSS) was investigated for the creation of conductometric biosensors. The conductometric transducers consisted of gold interdigitated electrodes were placed on the ceramic support. The transducers were modified with zeolites and MSS, and then the enzymes were adsorbed on the transducer surface. Different methods of zeolite attachment to the transducer surface were used; drop coating with heating to 200°C turned out to be the best one. Nanozeolites beta and L, zeolite L, MSS, and silicalite-1 (80 to 450 nm) were tested as the adsorbents for enzyme urease. The biosensors with all tested particles except zeolite L had good analytical characteristics. Silicalite-1 (450 nm) was also used for adsorption of glucose oxidase, acetylcholinesterase, and butyrylcholinesterase. The glucose and acetylcholine biosensors were successfully created, whereas butyrylcholinesterase was not adsorbed on silicalite-1. The enzyme adsorption on zeolites and MSS is simple, quick, well reproducible, does not require use of toxic compounds, and therefore can be recommended for the development of biosensors when these advantages are especially important.

Selective synthesis of FAU-type zeolites

Science.gov (United States)

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

2018-05-01

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

Adsorption methods for hydrogen isotope storage on zeolite sieves

International Nuclear Information System (INIS)

Cristescu, Ioana; Cristescu, Ion; Vasut, Felicia; Brad, Sebastian; Lazar, Alin

2001-01-01

Adsorption molecular sieves and activated carbon were used for hydrogen isotopes. The adsorption process proceeds at liquid nitrogen and liquid hydrogen temperatures. The synthetic zeolites have similar properties as natural zeolites, but they have a regular pore structure and affinity for molecules of different size with defined shapes. Experimental results obtained at liquid nitrogen and liquid hydrogen temperatures evidenced the efficient behavior of the activated carbon and zeolite sieves for hydrogen isotope temporary storage. (authors)

Cupric natural zeolites as microbic ides

International Nuclear Information System (INIS)

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

2009-01-01

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

ADSORPTION MALACHITE GREEN ON NATURAL ZEOLITE

Directory of Open Access Journals (Sweden)

Eko Ariyanto

2012-02-01

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

Detergent zeolite complex "Ceosil", Tallinn, Estonia

OpenAIRE

Stanković Mirjana S.; Pezo Lato L.

2003-01-01

The IGPC Engineering Department, together with the "Birac", Zvornik Engineering Department designed basic projects for detergent zeolite production, using waste flotation sand and hydrates. Several projects were completed: technological, machine, electrical, automation. On the basis of these projects, production plant in Tallinn, Estonia was constructed, with a capacity of 100,000 t/y from 1989. to 1993. This plant became the biggest producer of detergent zeolite in the world.Several goals we...

PHOTODEGRADATION OF ALIZARIN S DYE USING TiO2-ZEOLITE AND UV RADIATION

Directory of Open Access Journals (Sweden)

Karna Wijaya

2010-06-01

Full Text Available An investigation of Alizarin S photodegradation using TiO2-zeolite and UV radiation was performed. TiO2-zeolite was prepared by dispersing oligocations of titanium into suspension of zeolite. The suspension was stirred and then filtered to separate the solid phase from the filtrate. the solid phase was calcined by microwave oven at 800 Watt for 5 minutes to convert the oligocations into its oxide forms. The calcined product and unmodified zeolite were characterized using x-ray diffractometry, FT-IR spectrophotometry, X-ray fluorescence and gas sorption analysis methods to determine their physicochemical properties. Photocatalytic activity of TiO2-zeolite was tested on Alizarin S solution using following method: 50 mg of zeolite was dispersed into 25 mL of 10-4 M Alizarin S. The dispersion was irradiated using 365 nm UV light at room temperature on various irradiation times, i.e. 10, 20, 30, 40 and 60 minutes. At certain irradiation time, the dispersion was filtered and the filtrate was then analyzed its concentration using UV-Vis spectrophotometry method. Characterization results exhibited that the formation of TiO2 on internal as well as external surfaces of zeolite could not be detected  with x-ray diffractometry and FT-IR spectrophotometry, however determination of titanium using x-ray fluorescence analysis on the calcined product showed that the concentration of titanium was much higher than zeolite (0.22% on zeolite and 12.08% on TiO2-zeolite. Gas sorption analysis result indicated that the the calcination  resulted in the increase of specific surface area (16,31 m2/g on zeolite and 100.96 m2/g on TiO2-zeolite as well as total pore volume of calcined product (13.34 mL/Å/g on zeolite and 57.54 mL/Å/g on TiO2-zeolite. The result of photocatalytic activitiy study showed that ca 99 % of Alizarin S was degraded by TiO2-zeolite after UV irradiation for 60 min.   Keywords: TiO2-zeolite, photocatalytic, Alizarin S.

Cr(VI) retention and transport through Fe(III)-coated natural zeolite

Energy Technology Data Exchange (ETDEWEB)

Du, Gaoxiang [School of Materials Science and Technology, China University of Geosciences, Beijing 100083 (China); Li, Zhaohui, E-mail: li@uwp.edu [School of Materials Science and Technology, China University of Geosciences, Beijing 100083 (China); Geosciences Department, University of Wisconsin-Parkside, Kenosha, WI 53144 (United States); Department of Earth Sciences, National Cheng Kung University, 1 University Road, Tainan 70101, Taiwan (China); Liao, Libing [School of Materials Science and Technology, China University of Geosciences, Beijing 100083 (China); Hanson, Renee; Leick, Samantha; Hoeppner, Nicole [Geosciences Department, University of Wisconsin-Parkside, Kenosha, WI 53144 (United States); Jiang, Wei-Teh [Department of Earth Sciences, National Cheng Kung University, 1 University Road, Tainan 70101, Taiwan (China)

2012-06-30

Graphical abstract: Breakthrough curves of Cr(VI) from columns packed with raw zeolite (a) and Fe(III)-zeolite (b). The solid line in (b) is the HYDRUS-1D fit to the observed data with adsorption term only, while the dashed line in (b) includes a reduction term in the HYDRUS-1D fit. Highlights: Black-Right-Pointing-Pointer Zeolite modified with Fe(III) could be used for adsorption and retention of Cr(VI). Black-Right-Pointing-Pointer The Fe present on zeolite was in an amorphous Fe(OH){sub 3} form. Black-Right-Pointing-Pointer A Cr(VI) adsorption capacity of 82 mg/kg was found on Fe(III)-zeolite. Black-Right-Pointing-Pointer A Cr(VI) retardation factor of 3 or 5 was determined from column and batch studies. - Abstract: Cr(VI) is a group A chemical based on the weight of evidence of carcinogenicity. Its transport and retention in soils and groundwater have been studied extensively. Zeolite is a major component in deposits originated from volcanic ash and tuff after alteration. In this study, zeolite aggregates with the particle size of 1.4-2.4 mm were preloaded with Fe(III). The influence of present Fe(III) on Cr(VI) retention by and transport through zeolite was studied under batch and column experiments. The added Fe(III) resulted in an enhanced Cr(VI) retention by the zeolite with a capacity of 82 mg/kg. The Cr(VI) adsorption on Fe(III)-zeolite followed a pseudo-second order kinetically and the Freundlich adsorption isotherm thermodynamically. Fitting the column experimental data to HYDRUS-1D resulted in a retardation factor of 3 in comparison to 5 calculated from batch tests at an initial Cr(VI) concentration of 3 mg/L. The results from this study showed that enhanced adsorption and retention of Cr(VI) may happen in soils derived from volcanic ash and tuff that contains significant amounts of zeolite with extensive Fe(III) coating.

Zeolite from fly ash: synthesis and characterization

Indian Academy of Sciences (India)

Unknown

to attempt making zeolite from fly ash (Höller and Wir- sching 1985; Henmi ... thermal treatment method to synthesize low silica NaX- type zeolite from .... catalytic applications. Mixture of ... amount of Fe2O3 and the oxides of Mg, Ca, P, Ti etc. The chemical ..... This work is partly supported by the Ministry of Human. Resource ...

Picosecond infrared activation of methanol in acid zeolites

NARCIS (Netherlands)

Bonn, Miacha; van Santen, Rutger A.; Lercher, J.A.; Kleyn, Aart W.; Bakker, H.J.; Bakker, Huib J.

1997-01-01

Highly porous, crystalline zeolite catalysts are used industrially to catalyze the conversion of methanol to gasoline. We have performed a picosecond spectroscopic study providing insights into both the structure and the dynamics of methanol adsorbed to acid zeolites. We reveal the adsorption

Defluorination of drinking water using surfactant modified zeolites ...

African Journals Online (AJOL)

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

Calcining natural zeolites to improve their effect on cementitious mixture workability

International Nuclear Information System (INIS)

Seraj, Saamiya; Ferron, Raissa D.; Juenger, Maria C.G.

2016-01-01

Despite the benefits to long-term concrete durability, the use of natural zeolites as supplementary cementitious materials (SCMs) is uncommon due to their high water demand. The motivation of the research presented here was to better understand how the physical and chemical characteristics of natural zeolites influenced the workability of cementitious mixtures and whether those properties could be modified through calcination to mitigate the high water demand of natural zeolites. In this research, three different natural zeolites were characterized in their original and calcined states using x-ray diffraction (XRD) and Brunauer–Emmett–Teller (BET) surface area measurements. Rheology experiments were then conducted on cementitious pastes containing these natural zeolites, in their original and calcined states, to assess mixture viscosity and yield stress. Results showed that calcination destabilized the structure of the natural zeolites and reduced their surface area, which led to an improvement in mixture viscosity and yield stress.

Fly ash based zeolitic pigments for application in anticorrosive paints

International Nuclear Information System (INIS)

Shaw, Ruchi; Tiwari, Sangeeta

2016-01-01

The purpose of this work is to evaluate the utilization of waste fly ash in anticorrosive paints. Zeolite NaY was synthesized from waste fly ash and subsequently modified by exchanging its nominal cation Na + with Mg 2+ and Ca 2+ ions. The metal ion exchanged zeolite was then used as anticorrosive zeolitic pigments in paints. The prepared zeolite NaY was characterized using X-Ray diffraction technique and Scanning electron microscopy. The size, shape and density of the prepared fly ash based pigments were determined by various techniques. The paints were prepared by using fly ash based zeolitic pigments in epoxy resin and the percentages of pigments used in paints were 2% and 5%. These paints were applied to the mild steel panels and the anticorrosive properties of the pigments were assessed by the electrochemical spectroscopy technique (EIS).

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 biogas samples were used, and no significant effects due to biogas impurities (e.g. humidity, dust, moisture, etc.) were observed. Thermal and vacuum regenerations were also optimized and confirmed to be possible, without significant variations in efficiency. Hence, natural zeolites from tuffs may successfully be used in a pressure/vacuum swing adsorption process.

Synthesis of Zeolite-X from Bottom Ash for H2 Adsorption

Science.gov (United States)

Kurniawan, R. Y.; Romadiansyah, T. Q.; Tsamarah, A. D.; Widiastuti, N.

2018-01-01

Zeolite-X was synthesized from bottom ash power plant waste using fusion method on air atmosphere. The fused product dissolved in demineralized water and aluminate solution was added to adjust the SiO2/Al2O3 molar ratio gel prior hydrothermal process. The synthesis results were characterized using X-Ray Diffraction (XRD), Scanning Electron Microscope (SEM), and Fourier Transform Infrared (FTIR). The results showed that the zeolite-X has a high crystallinity with octahedral particle. The pure-form zeolite-X then was characterized and tested for H2 gas adsorption by gravimetric method to determine the H2 gas adsorption capacity of zeolite-X from bottom ash and it was compared to synthetic zeolite-X.

Influence of zeolite nanofillers on properties of polymeric materials

OpenAIRE

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

2012-01-01

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

Study of the ortho-positron annihilation process in zeolite Y

International Nuclear Information System (INIS)

Alvarado D, M. E.

2010-01-01

For several years a great interest has existed for the study of the natural and synthetic zeolites due to its properties. The porosity, one of their main characteristics allows that these materials are used as molecular sieves, catalysts, gases drying, etc. In order to investigating the porosity and other zeolite properties one carries out the study of the process of positron annihilation lifetime spectroscopy (Pals). This is a technique that provides information about the size and the pores form since is highly sensitive to the free volume and the superficial area of those porous materials as the zeolites. The study began with the elaboration of zeolite Y tablets in a hydraulic press where different pressures (from 0 to 1.26 GPa) and masses (70, 80 and 100 mg) were proven to obtain the estimate porosity of each tablet. A graph was elaborated and the effect of the mass and pressure with regard to the zeolite porosity was analyzed. Later on, the powder and tablets of 70 mg were characterized by means of X-ray diffraction (the glass size, interplanar distance, length and the volume of the unitary cell); scanning electron microscopy (the particles size and morphology); thermo gravimetric analysis (dehydration temperature and the stability up to 700 C) and the Brunauer Emmett Teller method (specific area). After the zeolite Y tablets characterization was carried out the positron annihilation process by means of Pals where its free volume of zeolite Y was analyzed, which includes to the structural cavities and the interparticle volume. The powdered zeolite was analyzed to different experimental conditions (preparation of the sample and the Pals equipment) to obtain the optimal conditions (a window with a time of 400 ns and a enlarged energy window) of analysis. On the other hand, the tablets were analyzed under optimal conditions to obtain the four components of time and intensity (τ, Ι), result of the different ways of positrons annihilation in the zeolite. These

Densification of salt-occluded zeolite a powders to a leach-resistant monolith

International Nuclear Information System (INIS)

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

1993-01-01

Pyrochemical processing of spent fuel from the Integral Fast Reactor (IFR) yields a salt waste of LiCl-KCl that contains approximately 6 wt% fission products, primarily as CsCl and SrCl 2 . Past work has shown that zeolite A will preferentially sorb cesium and strontium and will encapsulate the salt waste in a leach-resistant, radiation-resistant aluminosilicate matrix. However, a method is sill needed to convert the salt-occluded zeolite powders into a form suitable for geologic disposal. We are thus investigating a method that forms bonded zeolite by hot pressing a mixture of glass frit and salt-occluded zeolite powders at 990 K (717 degree C) and 28 MPa. The leach resistance of the bonded zeolite was measured in static leach tests run for 28 days in 363 K (90 degree C) deionized water. Normalized release rates of all elements in the bonded zeolite were low, 2 d. Thus, the bonded zeolite may be a suitable waste form for IFR salt waste

Theoretical determination of proton affinity differences in zeolites

NARCIS (Netherlands)

Kramer, G.J.; Santen, van R.A.

1993-01-01

An important factor in zeolite catalysis is the proton affinity, i.e., the energy required to remove a proton from the zeolite lattice. Differences in proton affinity are expected to influence the catalytic activity of acid sites, making the catalytically active sites inhomogeneous (within one

Dietary effects of Ca-zeolite supplementation on some blood and ...

African Journals Online (AJOL)

smyo

to the Al, Si, Zn, Na or K concentrations of zeolite, because these minerals have been ... The SiO2, Al2O3, H2O related to loss on ignition, and CaO are the essential ...... The effect of interaction between narasin and nicarbazin with zeolite ... Protective role of zeolite on short- and long-term lead toxicity in the teleost fish.

Studi Hubungan Struktur Mikro dan Keaktifan Zeolit Alam Akibat Proses Pengasaman

Directory of Open Access Journals (Sweden)

Made Cuaca Vahindra Suriawan

2012-11-01

Full Text Available Natural zeolite is known as metal pollutant adsorbent in industrial waste treatment. As initial study for utilization ofnatural zeolite from Indonesia for metal pollutants adsorbent in liquid waste, then the physical properties should berecognized first. Activation is the first step in order to the natural zeolite able to adsorb the metal pollutants in the waste.One method to activate is by applying acid solution such as sulfuric acid (H2SO4 to activate the natural zeolite. The purposeof this research is to observe the change on microstructure of natural zeolite obtained from the mining at Tasikmalaya, WestJava, Indonesia due to chemical activated, to be compared to one without chemical activation. The variation of concentrationof H2SO4 namely: 2 4 , 6, 8, and 10 % , with 30 minutes soaking time , in a room temperatur. The microstructure then isobserved by using optical microscope following standard for ceramography. The change in microstructure then is analyzedand studied to be related with the ability of natural zeolite in adsorb the metal pollutant. The level activity of the zeolite canbe recognized by measuring its porosity.

Stability of krypton fixed in zeolite-3A and -5A

International Nuclear Information System (INIS)

Matsuoka, Shingo; Nakamura, Hirone; Tamura, Takaaki; Takano, Takemi; Ito, Yasuo; Sugawara, Ichiro.

1986-01-01

The fixation operation was carried out at 450 ∼ 650 deg C, 1,000 atm for 24 h. The amount of fixed Kr was measured using thermal neutron activation analysis. For zeolite-3A the amount of Kr fixed decreased from 20 to 5 w/o as the fixation temperature rose. In the case of zeolite-5A, Kr fixation was observed at 550 deg C and above, and the amount increased to 15 w/o as the temperature rose to 650 deg C. The diffusion coefficient of Kr in the zeolite was determined from the result of heating tests. The value obtained was substituted in a diffusion equation, enabling us to predict the Kr release behavior at any temperature in a dry atmosphere. Both the samples of zeolite-3A fixed below 525 deg C and of zeolite-5A below 625 deg C showed an intensive Kr release in water that would not be expected from the release behavior under dry conditions. However, such unexpected release was not observed in either sample fixed above these respective temperatures. This could be accounted for by the fact that zeolite cations move easily when zeolite is moisturized. (author)

Synthesis of type A zeolite from calcinated kaolin

International Nuclear Information System (INIS)

Rodrigues, E.C.; Neves, R.F.; Souza, J.A.S.; Moraes, C.G.; Macedo, E.N.

2011-01-01

The mineral production has caused great concern in environmental and industrial scenario due to the effects caused to the environment. The industries of processing kaolin for paper are important economically for the state of Para, but produce huge quantities of tailings, which depend on large areas to be stocked. This material is rich in silico-aluminates can be recycled and used as raw material for other industries. The objective is to synthesize zeolite A at different temperatures of calcination and synthesis. The starting materials and synthesis of zeolite A have been identified and characterized through analysis of X-ray diffraction (DRX) and scanning electron microscopy (MEV). The synthesis process of zeolite A, using as source of silica and the aluminum metakaolin, which was calcined at temperatures of 700 ° C and 800 ° C for 2 hours of landing in a burning furnace type muffle. Observed in relation to the calcination of kaolin as the main phase, the metakaolin. This is just a removal of water from its structure, so we opted for the lower temperature, less energy consumption. The synthesis process of zeolite A, produced good results for the formation of zeolites type A, which were characterized with high purities. (author)

Processing of radioactive waste solution with zeolites, (4)

International Nuclear Information System (INIS)

Mimura, Hitoshi; Kanno, Takuji

1978-01-01

Volatilization of Cs from Cs type zeolites and calcined zeolites were studied at high temperature. Synthetic zeolites A, X, Y, synthetic mordenite (Zeolon), natural mordenite and clinoptilolite saturated with Cs were used in this study. Volatilized Cs from CsX was largest in quantity and from cs type natural zeolites smallest. Volatilization of Cs was observed at about 800 0 C and increased as the calcining temperature rose. Volatilized Cs from CsA was smallest in synthetic zeolites. CsA recrystallized to nepheline and pollucite with the ratio of about 1 : 1 above 1,000 0 C and it seemed that the volatilization of Cs from pollucite was suppressed with the nepheline phase surrounded them. The rate of volatilization was very fast within the initial 10 min and very slow after 60 min except for CsX. This behavior suggested that the rate was very fast before structural transformation. The mean volatilization rate of Cs in 3 hr from calcined CsX (pollucite) was 1.1 x 10 -4 mg/cm 2 .min and the others were 10 -5 -- 10 -6 mg/cm 2 .min. The amount of volatilized Cs in Ar flow was decreased 20 -- 90% of that in air flow. Volatilized species was identified with Cs 2 O by mass spectrometry. (auth.)

Uranium,Radium and Iron Absorption from Liquid Waste Uranium Ore Processing by Zeolite

International Nuclear Information System (INIS)

Wismawati, T; Sorot sudiro, A; Herjati, T

1998-01-01

The aim of this work is to determine zeolites sorption capacity and the distribution coefficient of uranium, radium, and iron in zeolite-liquid waste system. Mineralogical composition of zeolite used in the experiment has been determine by examining the thin sections of zeolite grains under a microscope. Zeolite has ben activated by the dilute sulfuric acid or sodium hydroxide solution. The results show that the use of 0.25 N sodium hydroxide solution could be optimizing the zeolite for uranium and iron ions sorption and that of 0.1 N sulfuric acid solution is for radium sorption. The re-activation process has been carried out in three hours. Under such a condition, the sorption efficiency of zeolite to those ions have been known to be 45.85% for uranium, 96.63 % for iron and 87.80 % for radium. The distribution coefficients of uranium, radium and iron ion in zeolite-liquid waste system have been calculated 0.85, 7.02, and 28.65 ml/g respectively

Characterization of natural and modified zeolites using ion beam analysis techniques

Energy Technology Data Exchange (ETDEWEB)

Andrade, E. [Instituto de Fisica, Departamento de Fisica Experimental, Universidad Nacional Autonoma de Mexico, Apdo. Postal 20-364, 01000 (Mexico)], E-mail: andrade@fisica.unam.mx; Solis, C. [Instituto de Fisica, Departamento de Fisica Experimental, Universidad Nacional Autonoma de Mexico, Apdo. Postal 20-364, 01000 (Mexico); Aceves, J.M.; Miranda, R. [Facultad de Estudios Superiores Cuautitlan Itzcalli, Departamento de Quimica, Universidad Nacional Autonoma de Mexico, 1 de Mayo S/N, Cuatitlan Itzcalli, Edo. de Mexico, C.P. 74540 (Mexico); Cruz, J. [Instituto de Fisica, Departamento de Fisica Experimental, Universidad Nacional Autonoma de Mexico, Apdo. Postal 20-364, 01000 (Mexico); Rocha, M.F. [Escuela Superior de Ingenieria Mecanica y Electrica, Instituto Politecnico Nacional, U.P. ' Adolfo Lopez Mateos' , Zacatenco, Del. Gustavo A. Madero, Mexico D.F. 07738 (Mexico); Zavala, E.P. [Instituto de Fisica, Departamento de Fisica Experimental, Universidad Nacional Autonoma de Mexico, Apdo. Postal 20-364, 01000 (Mexico)

2008-05-15

Zeolites are very important materials in catalytic and industrial processes. Natural, modified and synthetic zeolites have a wide range of uses because of their good adsorption, ion exchange capacity and catalytic properties. Mexico is an import source of natural zeolites, however their utilization in the natural form is limited due to the presence of trace metallic impurities. For example, metals such as vanadium and chromium inhibit the elimination of sulfur in hydrocarbons. Therefore, it is important to know the precise composition of the zeolite material. In this work, we report the elemental characterization of zeolites using various IBA techniques. {sup 3}He{sup +} and {sup 2}H{sup +} beams were used to measure the major element concentrations (Si, Al, O, C) by RBS and NRA. PIXE and SEM-EDS were used to measure the total trace element content (V, Cr, Fe, Ni, Cu, Zn, Rb, Sr, Zr, Pb, etc). Additionally, XRD was used to study the zeolite crystal structure.

PEMANFAATAN ZEOLIT DARI ABU SEKAM PADI DENGAN AKTIVASI ASAM UNTUK PENURUNAN KESADAHAN AIR

Directory of Open Access Journals (Sweden)

VH Putranto

2016-04-01

Full Text Available 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 Inframerah (FTIR dan Difraksi Sinar-X (XRD kemudian dimanfaatkan untuk menurunkan kadar ion logam Ca2+ dan Mg2+ penyebab kesadahan air dengan variasi waktu kontak (0, 20, 30, 40, 50, 60, 90, dan 120 menit dilanjutkan variasi massa zeolit sintetis (0,05; 0,1; 0,125; 0,25; serta 0,5 gram per volume air sumur 25 ml. Hasil uji komposisi kimia dengan Fluoresensi Sinar-X menunjukkan abu sekam padi yang telah diaktivasi memiliki kadar silika (SiO2 yang lebih tinggi yakni mencapai 95,83%. Hasil penelitian menunjukkan bahwa zeolit sintetis yang dihasilkan merupakan zeolit tipe NaY (zeolite like dengan kristal cancrinite sebagai fasa dominan. Adsorbsi optimum ion logam Ca2+ dan Mg2+ dalam air sumur oleh zeolit hasil sintesis terjadi pada waktu 60 menit dengan penyerapan optimum sebesar 94,71% Ca2+ dan 84,55% Mg2+ serta pada massa adsorben optimum 0,125 gram dengan penyerapan optimum sebesar 93,02% Ca2+ dan 83,78% Mg2+.Activation using a strong acid in zeolite synthesis is known can enhance the ability of zeolite as adsorbent. This study aims to utilize rice husk ash as a source of silica, which is activated with 2 M HCl in zeolite synthesis hydrothermally and apply the zeolite to reduce the level of hardness in well water. The activation process is performed by using HCl 2 M solution. Zeolite product is analyzed qualitatively using infrared spectrometer (FTIR and X-ray Diffraction (XRD and then used to reduce the levels of metal ions Ca2+ and Mg2+ which cause water hardness

Antibacterial properties of Ag-exchanged Philippine natural zeolite-chitosan composites

Science.gov (United States)

Taaca, Kathrina Lois M.; Olegario, Eleanor M.; Vasquez, Magdaleno R.

2017-12-01

Zeolites are microporous minerals composed of silicon, aluminum and oxygen. These aluminosilicates consist of tetrahedral units which produce open framework structures to generate a system of pores and cavities of molecular dimensions. Zeolites are naturally abundant and can be mined in most parts of the world. In this study, natural zeolites (NaZ) which are locally-sourced here in the Philippines were investigated to determine its properties. An ion-exchange process was utilized, using the zeolite to silver (Ag) solution ratio of 1:20 (w/v), to incorporate Ag into the zeolite framework. Characterizations such as XRD, AAS, and Agar diffusion assay were used to evaluate the properties of the synthesized Ag-exchanged zeolites (AgZ). X-ray diffraction revealed that both NaZ and AgZ have peaks mostly corresponding to the clinoptilolite structure, with some trace peaks of the mordenite and quartz. Absorption spectroscopy revealed that the ion exchange process added about 0.61188g of silver into the zeolite structure. This Ag content was seen to be enough to make the AgZ sample exhibit an antibacterial effect where clearing zones against E. coli and S. aureus were observed in the agar diffusion assay, respectively. The AgZ sample was also tested as ceramic filler to a polymer matrix-chitosan. The diffusion assay revealed presence of antibacterial activity to the polymer composite with AgZ fillers. These results indicate that the Philippine natural zeolite, incorporated with metals such as Ag, can be used as an antibacterial agent and can be developed as a ceramic filler to improve the antibacterial property of composite materials for biomedical application.

Langmuir and Freundlich Isotherm Adsorption Equations for Chromium (VI) Waste Adsorption by Zeolite

International Nuclear Information System (INIS)

Murni Handayani; Eko Sulistiyono

2009-01-01

The research of chromium (VI) waste adsorption by zeolite has done. Wastes which are produced by Industries, both radioactive waste and heavy metal waste need done more processing so that they are not endanger environment and human health. Zeolite has very well-ordered crystal form with cavity each other to way entirely so that cause surface wide of zeolite become very big and very good as adsorbents. This research intends to know appropriate isotherm adsorption method to determine maximum capacity of zeolite to chromium (VI) waste. The equations which used in adsorption process are Langmuir and Freundlich isotherm Adsorption equations. The instrument was used in adsorption process by using Atomic Adsorption Spectroscopy (AAS). The experiment result showed that the biggest mass of chromium (VI) metal ion which was absorb by zeolite in 20 ppm concentration was 7.71 mg/gram zeolite. Adsorption process of Chromium (VI) waste by zeolite followed Langmuir and Freundlich isotherm equations with R 2 >0,9 . Appropriate equation to determine maximum adsorption capacity of zeolite for chromium (VI) waste adsorption is Langmuir equation. The maximum adsorption capacity of zeolite is 52.25 mg/gram. (author)

Environmental applications of natural zeolitic materials based on their ion-exchange properties

International Nuclear Information System (INIS)

Colella, C.

1998-01-01

Natural zeolites, such as clinoptilolite, chabazite, phillipsite and mordenite, exhibit good selectivities for some water pollutants, e.g., Cs + , NH 4 + and Pb 2+ . Zeolite-rich tuffs may be therefore utilized for removing the above and other cations from wastewaters before discharge. Continuous processes with fixed beds are usually employed for water purification, such as those in service in the U.S.A for ammonium removal from municipal sewage. Direct action of the ion exchanger is needed when the pollutant must be removed from soil and trapped in the zeolite framework. Discontinuous processes (addition of zeolite to the waste solution) are also possible, provided the polluted zeolitic sludge is stabilized-solidified in a cement matrix matrix before disposal. Removal of radionuclides from nuclear power plant waters with natural zeolites is discussed

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.

Magnetic zeolites a and p synthesized from kaolin: synthesis and characterization

Energy Technology Data Exchange (ETDEWEB)

Bessa, R.A.; Oliveira, C.P.; Nascimento, R.F.; Bohn, F.; Loiola, A.R. [Universidade Federal do Ceara (UFCE), CE (Brazil)

2016-07-01

Full text: Zeolites are hydrated aluminosilicates of open chain, formed by silica and alumina tetrahedral structures linked by common oxygen atoms, generating interconnected pores and cages with molecular dimensions and well defined sizes that limit matter transference between internal surface and application medium. They can be found naturally or synthesized using different aluminum and silicon sources that may modify the produced zeolite. Their industrial application has grown enormously over the last century. However, a big issue that still remains is the difficulty in retrieving zeolite powders when used in aqueous media. This work reports the use of kaolin as an alternative raw material for zeolite syntheses by means of hydrothermal route and subsequent preparation of magnetic composites through magnetite impregnation. The syntheses of two different zeolites were carried out by mixing appropriate amounts of metakaolin (kaolin previously calcined at 600 deg C for 2 h), sodium metasilicate and sodium hydroxide solution, aged for 18 h and heated at 100 °C for 4-48 h. After these processes, the final materials were washed several times with distilled water, filtered and dried at 80 deg C for 12 h. Magnetic composites were prepared by impregnating the zeolites with of Fe3O4 nanoparticles (NP) synthesized by the partial oxidation and precipitation of Fe2+ ions. The obtained materials were characterized by X-ray diffraction, scanning electron microscopy, FTIR spectroscopy and magnetization measurements. The results of XRD and FTIR provide evidence of the success in the synthesis of both zeolites A and P as well as Fe3O4. Subsequently, composites were formed by mixtures of zeolite A + NP and zeolite P + NP. The existence of secondary crystalline phases was also confirmed. However, it did not interfered significantly in the results as these phases appear as minor amounts and are most likely residues from the clay used as the main silica and alumina sources. Scanning

Catalytic Cracking of Used Palm Oil using Composite Zeolite

International Nuclear Information System (INIS)

Chang, W.H.; Tye, C.T.

2013-01-01

The rapid expansion of human society implies greater energy demand and environmental issues. In face of depletion energy resources, research is being carried out widely in order to convert the plant oil into biofuel. In this research, the production of liquid biofuels via catalytic cracking of used palm oil in the presence of composite zeolite was studied. The performance of composite zeolite of different properties in the reaction has been evaluated. The catalytic cracking reactions were carried out in a batch reactor at reaction temperature of 350 degree Celsius for an hour. In the present study, adjusting the ratio of meso porous coating to microporous zeolite and magnesium loading on composite zeolite catalyst were found to be able to increase the gasoline fraction and overall conversion of the reaction. (author)

Directing factors affecting the synthesis of a MFI-type zeolite

Energy Technology Data Exchange (ETDEWEB)

Vinaches, P.; Pergher, S.B.C. [Universidade Federal de Rio Grande do Norte (UFRN), RN (Brazil); Lopes, C.W. [Institute of Chemical Technology, Mumbai (India); Gomez-Hortiguela, L. [Instituto de Catalisis y Petroleoquimica, Madrid (Spain); Finger, P.H.; Silva, B.A. da; Dallago, R.M.; Mignoni, M.L. [Universidade Regional Integrada do Alto Uruguai e das Missoes (URI), Erechim, RS (Brazil)

2016-07-01

Full text: Zeolites are crystalline tectosilicates constituted by (TO4) tetrahedra connected through the oxygens of their vertices. The importance of these materials is that their properties differ, due to their variable compositions and structures, leading to the possibility of applying them into different industries, for example, as catalyst in petroleum industry or sensors in quality control. One of the big questions in this area is about the understanding of the chemistry that directs to one or another type of zeolite. Another important question is the search of new zeolitic structures for new applications. One approach to answer both is the study of the structure-directing agents, which are inorganic or organic molecules used in the synthesis of zeolites. New and already-used molecules have been studied within different synthesis conditions and different techniques, as characterization or computational studies. And several attempts of rationalization were and, still, will be performed. In this research, an imidazolium-based compound was studied in hydrothermal zeolite synthesis as organic structure-directing agent (OSDA). The products were obtained with Si/Al or Si/(Al+Zn) compositions, proved by ICP data. X-ray diffractograms showed two different zeolitic types: MFI and TON. It was observed that when Zn was present in the synthesis gel, pure MFI phases were able to appear. But in his absence, the products were all mixtures of MFI and TON zeolites. It was also possible to distinguish both phases by SEM micrographs, as MFI had brick-like shape and TON appeared as needles. The obtained zeolites were stable until 900°C minimum, as tested by a TG/DTG/DSC experiment. To prove that the chosen OSDA directed these structures, a CHN analysis was performed, resulting in integrity of the molecules inside the zeolitic pores and cavities. Finally, a rationale about the location and conformation of the OSDA was needed to understand these experimental results. So, it was

Directing factors affecting the synthesis of a MFI-type zeolite

International Nuclear Information System (INIS)

Vinaches, P.; Pergher, S.B.C.; Lopes, C.W.; Gomez-Hortiguela, L.; Finger, P.H.; Silva, B.A. da; Dallago, R.M.; Mignoni, M.L.

2016-01-01

Full text: Zeolites are crystalline tectosilicates constituted by (TO4) tetrahedra connected through the oxygens of their vertices. The importance of these materials is that their properties differ, due to their variable compositions and structures, leading to the possibility of applying them into different industries, for example, as catalyst in petroleum industry or sensors in quality control. One of the big questions in this area is about the understanding of the chemistry that directs to one or another type of zeolite. Another important question is the search of new zeolitic structures for new applications. One approach to answer both is the study of the structure-directing agents, which are inorganic or organic molecules used in the synthesis of zeolites. New and already-used molecules have been studied within different synthesis conditions and different techniques, as characterization or computational studies. And several attempts of rationalization were and, still, will be performed. In this research, an imidazolium-based compound was studied in hydrothermal zeolite synthesis as organic structure-directing agent (OSDA). The products were obtained with Si/Al or Si/(Al+Zn) compositions, proved by ICP data. X-ray diffractograms showed two different zeolitic types: MFI and TON. It was observed that when Zn was present in the synthesis gel, pure MFI phases were able to appear. But in his absence, the products were all mixtures of MFI and TON zeolites. It was also possible to distinguish both phases by SEM micrographs, as MFI had brick-like shape and TON appeared as needles. The obtained zeolites were stable until 900°C minimum, as tested by a TG/DTG/DSC experiment. To prove that the chosen OSDA directed these structures, a CHN analysis was performed, resulting in integrity of the molecules inside the zeolitic pores and cavities. Finally, a rationale about the location and conformation of the OSDA was needed to understand these experimental results. So, it was

Thermophysical properties of novel zeolite materials for sorption cycles

KAUST Repository

Thu, Kyaw; Kim, Youngdeuk; Xi, Baojuan; Ismail, Azhar Bin; Ng, K. C.

2013-01-01

his article discusses the thermophysical properties of zeolite-based adsorbents. Three types of zeolite (Z-01, Z-02 and Z-05) with different chemical compositions developed by Mitsubishi Plastics, Inc. are analyzed for possible applications

Multicomponent liquid ion exchange with chabazite zeolites

International Nuclear Information System (INIS)

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

ZEOLITE PERFORMANCE AS AN ANION EXCHANGER FOR ARSENIC SEQUESTRATION IN WATER

Science.gov (United States)

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

Using zeolites for fixation and long-term storage of krypton

International Nuclear Information System (INIS)

Pirogova, G.N.; Voronin, Yu.V.; Pribylov, A.A.; Serpinskii, V.V.; Mirskii, Ya.V.; Almazova, B.B.; Golitsina, V.V.

1993-01-01

It is known that large quantities of 85 Kr are liberated during the operation of nuclear power plants and, in particular, during the processing of nuclear fuel. At the present time, there are several methods of its fixation (accumulation), viz., storage in high-pressure gas balloons, adsorption, plasma-aided implantation into metals, introduction into clathrate compounds, and obtaining kryptonates. Encapsulation in zeolites is one of the most promising methods. The merits of this method include safety during storage, a favorable volume-to-mass ratio, the possibility of separating krypton from a mixture of different gases, and purity of the encapsulated gas. The encapsulation technique has been developed quite recently. Several recent reports established the possibility of encapsulating krypton in the 3A-type zeolites. However, most of the investigators observed leakage during the storage of the zeolite-gas system and complete liberation of krypton from the zeolite during prolonged storage. This paper deals with a study of the encapsulation process of krypton in the zeolites obtained by cation exchange from NaA. The experimental specimens were characterized by the degree of exchange of sodium into potassium and cesium. It is known that the introduction of cesium into the structure (body) of a zeolite reduces the size of the window of entrance. All the synthesized specimens were used in their granulated form. The aim of this study was to develop zeolite specimens for carrying out long-term storage of krypton

IR and TPD studies of the interaction of alkenes with Cu + sites in CuNaY and CuNaX zeolites of various Cu content. The heterogeneity of Cu + sites

Science.gov (United States)

Datka, J.; Kukulska-Zajaç, E.; Kozyra, P.

2006-08-01

Cu + ions in zeolites activate organic molecules containing π electrons by π back donation, which results in a distinct weakening of multiple bonds. In this study, we followed the activation of alkenes (ethene and propene) by Cu + ions in CuY and CuX zeolites of various Cu content. We also studied the strength of bonding of alkenes to Cu + ions. IR studies have shown that there are two kinds of Cu + sites of various electron donor properties. We suppose that they could be attributed to the presence of Cu + ions of various number of oxygen atoms surrounding the cation. IR studies have shown that Cu ions introduced into Y and X zeolites in the first-order (at low Cu content) form Cu + ions of stronger electron donor properties (i.e. activate alkenes to larger extend) than Cu ions introduced in the next order (at higher Cu content). IR and TPD studies of alkenes desorption evidenced that Cu + ions of stronger electron donor properties bond alkenes stronger than less electron donor ones. It suggests that π back donation has more important contribution to the strength of bonding alkenes to cation than π donation.

An innovative zinc oxide-coated zeolite adsorbent for removal of humic acid

Energy Technology Data Exchange (ETDEWEB)

Wang, Lingling, E-mail: lasier_wang@hotmail.com [College of Chemical Engineering and Materials, Quanzhou Normal University, Quanzhou 362000, Fujian (China); Environmental Engineering and Science Program, 705 Engineering Research Center, University of Cincinnati, Cincinnati, OH 45221-0012 (United States); Han, Changseok [ORISE Post-doctoral Fellow, The U.S. Environmental Protection Agency, ORD, NRMRL, STD, CPB, 26 W. Martin Luther King Jr. Drive, Cincinnati, OH 45268 (United States); Nadagouda, Mallikarjuna N. [The U.S. Environmental Protection Agency, ORD, NRMRL, WSWRD, WQMB, 26 W. Martin Luther King Jr. Drive, Cincinnati, OH 45268 (United States); Dionysiou, Dionysios D., E-mail: dionysios.d.dionysiou@uc.edu [Environmental Engineering and Science Program, 705 Engineering Research Center, University of Cincinnati, Cincinnati, OH 45221-0012 (United States); Nireas-International Water Research Centre, School of Engineering, University of Cyprus, PO Box 20537, 1678, Nicosia (Cyprus)

2016-08-05

Highlights: • An innovative adsorbent was successfully synthesized to remove humic acid. • The adsorbent possessed high adsorption capacity for humic acid. • The adsorption capacity remarkably increased after an acid modification. • The adsorption capacity was proportional to the amount of ZnO coated on zeolite. • Electrostatic interactions are a major factor at the first stage of the process. - Abstract: Zinc oxide (ZnO)-coated zeolite adsorbents were developed by both nitric acid modification and Zn(NO{sub 3}){sub 2}·6H{sub 2}O functionalization of zeolite 4A. The developed adsorbents were used for the removal of humic acid (HA) from aqueous solutions. The synthesized materials were characterized by porosimetry analysis, scanning electron microscopy, X-Ray diffraction analysis, and high resolution transmission electron microscopy. The maximum adsorption capacity of the adsorbents at 21 ± 1 °C was about 60 mgC g{sup −1}. The results showed that the positive charge density of ZnO-coated zeolite adsorbents was proportional to the amount of ZnO coated on zeolite and thus, ZnO-coated zeolite adsorbents exhibited a greater affinity for negatively charged ions. Furthermore, the adsorption capacity of ZnO-coated zeolite adsorbents increased markedly after acid modification. Adsorption experiments demonstrated ZnO-coated zeolite adsorbents possessed high adsorption capacity to remove HA from aqueous solutions mainly due to strong electrostatic interactions between negative functional groups of HA and the positive charges of ZnO-coated zeolite adsorbents.

An innovative zinc oxide-coated zeolite adsorbent for removal of humic acid

International Nuclear Information System (INIS)

Wang, Lingling; Han, Changseok; Nadagouda, Mallikarjuna N.; Dionysiou, Dionysios D.

2016-01-01

Highlights: • An innovative adsorbent was successfully synthesized to remove humic acid. • The adsorbent possessed high adsorption capacity for humic acid. • The adsorption capacity remarkably increased after an acid modification. • The adsorption capacity was proportional to the amount of ZnO coated on zeolite. • Electrostatic interactions are a major factor at the first stage of the process. - Abstract: Zinc oxide (ZnO)-coated zeolite adsorbents were developed by both nitric acid modification and Zn(NO_3)_2·6H_2O functionalization of zeolite 4A. The developed adsorbents were used for the removal of humic acid (HA) from aqueous solutions. The synthesized materials were characterized by porosimetry analysis, scanning electron microscopy, X-Ray diffraction analysis, and high resolution transmission electron microscopy. The maximum adsorption capacity of the adsorbents at 21 ± 1 °C was about 60 mgC g"−"1. The results showed that the positive charge density of ZnO-coated zeolite adsorbents was proportional to the amount of ZnO coated on zeolite and thus, ZnO-coated zeolite adsorbents exhibited a greater affinity for negatively charged ions. Furthermore, the adsorption capacity of ZnO-coated zeolite adsorbents increased markedly after acid modification. Adsorption experiments demonstrated ZnO-coated zeolite adsorbents possessed high adsorption capacity to remove HA from aqueous solutions mainly due to strong electrostatic interactions between negative functional groups of HA and the positive charges of ZnO-coated zeolite adsorbents.

Evaluation of the rheological behavior of asphaltic binder modified with zeolite material

Energy Technology Data Exchange (ETDEWEB)

Silveira, E.M. da; Sant' ana, Hosiberto B.; Soares, Sandra A.; Soares, Jorge B. [Federal University of Ceara, Fortaleza, CE (Brazil)

2008-07-01

Several new processes have been developed to reduce mixing and compaction temperatures of hot mix asphalt without sacrificing the quality of the resulting pavement. One of these processes utilizes the zeolite, a crystalline hydrated aluminum silicate. A laboratory study was conducted to determine the applicability of zeolite to improve the rheological and chemical behavior of an asphaltic binder. The synthetic asphaltic binder was produced with different zeolite contents (0,1; 0.3; and 0.5% w/w) by wet process. The rheological and chemical behavior was verified by Dynamic Shear Rheometer and Infrared Spectroscopy, respectively. The zeolite's chemical composition and morphology was studied by Dispersive X-ray Spectroscopy (EDX). Additionally, the scanning electron microscope (SEM) was utilized to establish the zeolite elemental composition. The results showed that investigated zeolite was classified as a sodium aluminum silicate and it was able to modify the rheological properties of the neat asphalt binder. The G*/sin{delta} parameter was affected by the zeolite presence, indicating better performance for the binders with zeolite. The results show that synthetic binders can partly replicate the rheological properties of conventional AB. Comparable complex modulus values was obtained. No significant difference was found in viscoelastic response, given by the phase angles as a function of both temperature and frequency. (author)

Metal doped green zeolites for water treatment a sustainable remediation model

International Nuclear Information System (INIS)

Tabassum, N.; Rafique, U.

2016-01-01

The synthesis of zeolites from refused materials presents a greener model for environmental remediation. The present study offers a novel procedure to synthesize not only the basic framework but also Vanadium modified polymeric zeolites. The spent polythene bags, lunch boxes, and packaging are used as raw material for synthesis of zeolites. Characterization through EDX showed incorporation of vanadium is more than 35%, exhibiting FTIR frequencies in the range 601-995cm-1. Thermogravimetric (TG) analysis revealed a stabilizing effect of zeolites on addition of dopant upto 320 degree C as determined by higher residue percentage (> 98%). Vanadium doped synthesized zeolites (MP1, MP2, MP3) were applied in batch adsorption experiments for in-situ (synthetic metal salt solution) and ex-situ (industrial effluents) removal of metals (Pb, Cr, and Cd). Adsorption results indicated the successful metal removal of more than 90% in the sequence Pb > Cd > Cr. The sequence follows, higher is the ionic radius of the metal cation, more is the adsorption on zeolites. Application of adsorption isotherms demonstrated fitness of Freundlich and Temkin models, whereas pseudo first order kinetics depicts metal removal. The study concludes that synthesized zeolites are suitable candidates with improvised green economy for industrial sector to treat effectively industrial discharges. (author)

Effect of cation nature of zeolite on carbon replicas and their electrochemical capacitance

International Nuclear Information System (INIS)

Zhou, Jin; Li, Wen; Zhang, Zhongshen; Wu, Xiaozhong; Xing, Wei; Zhuo, Shuping

2013-01-01

Graphical abstract: Cation nature of zeolite influences the porosity, surface chemical properties of carbon replicas of zeolite, resulting in different electrochemical capacitance. Highlights: ► The porosity of carbon replica strongly depends on zeolite's effective pore size. ► The surface chemical properties influence by the cation nature of zeolite. ► The N-doping introduces large pseudo-capacitance. ► The HYC800 carbon showed a high capacitance of up to 312 F g −1 in 1 M H 2 SO 4 . ► The prepared carbons show good durability of galvanostatic cycle. -- Abstract: N-doped carbon replicas of zeolite Y are prepared, and the effect of cation nature of zeolite (H + or Na + ) on the carbon replicas is studied. The morphology, structure and surface properties of the carbon materials are investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), N 2 adsorption, X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FT-IR). The pore regularity, pore parameter and surface chemical properties of the carbons may strongly depend on the cation nature of the zeolite Y. The carbon replicas of zeolite HY (H-form of zeolite Y) possesses higher pore regularity and much larger surface area than those of zeolite NaY (Na-form of zeolite Y), while the latter carbons seem to possess higher carbonization degrees. Electrochemical measurements show a large faradaic capacitance related to the N- or O-containing groups for the prepared carbons. Owing to the large specific surface area, high pore regularity and heteroatom-doping, the HYC800 sample derived from zeolite HY presents very high gravimetric capacitance, up to 312.4 F g −1 in H 2 SO 4 electrolyte, and this carbon can operate at 1.2 V with good retention ratio in the range of 0.25 to 10 A g −1

Synthesis of zeolite from coal fly ashes with different silica-alumina composition

Energy Technology Data Exchange (ETDEWEB)

Miki Inada; Yukari Eguchi; Naoya Enomoto; Junichi Hojo [Kyushu University, Fukuoka (Japan). Department of Chemistry and Biochemistry, Graduate School of Engineering

2005-02-01

Coal fly ashes can be converted into zeolites by hydrothermal alkaline treatment. This study focuses on the effect of Si/Al molar ratio of the fly ash source on the type of formed zeolite, which also is affected by the alkaline condition. The fly ashes were mixed with an aqueous NaOH solution and hydrothermally treated at about 100{degree}C. Zeolite Na-P1 and/or hydroxy-sodalite appeared after the treatment. Zeolite Na-P1 predominantly formed from silica-rich fly ash at a low-NaOH concentration. The cation exchange capacity of the product with a large content of zeolite Na-P1 reached a value of 300 meq/100 g. The type of the product was controlled by addition of aerosil silica or alumina. It was found that silica addition effectively enhances the formation of zeolite Na-P1, even at a high-NaOH concentration. These results were discussed on the basis of a formation mechanism of zeolite from coal fly ash through dissolution-precipitation process. 10 refs., 6 figs., 1 tab.

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.

Sorption of 60 Co in natural zeolite (clinoptilolite)

International Nuclear Information System (INIS)

Hernandez B, E.

1996-01-01

A Mexican zeolite (clinoptilolite) from Taxco, Guerrero, was partially stabilized with sodium cations. Radioactive Cobalt ( 60 Co) was used to study the Co 2+ sorption in the stabilized zeolite (Na + ). It was found that sorption in general does not favour the diffusion of cobalt between framework, it explains because of it is a natural zeolite and its composition heterogeneous decrease its exchange capacity by the generated competence to the existence other type of exchange ions. The cobalt retention reached the highest level, around 0.408 m eq Co 2+ /g in the Na-Clinoptilolite. The crystallinity of the aluminosilicates was maintained during experiments, it was verified by XRD patterns. (Author)

The Use of Zeolit and Activated Carbon on Packing System of Corydoras aenus

Directory of Open Access Journals (Sweden)

E. Supriyono

2007-07-01

Full Text Available Problem frequently found by Indonesian exporter in sending ornamental fish including Corydoras aenus to overseas is the low survival rate that caused by decrease in water quality during transportation.  Suitable and efficient packing technology is very needed to send live fish for long time transportation.  Two third of packing plastic volume was filled by oxygen, and Corydoras aenus 20 fish/pack.  Packing plastic was placed into styrofoam and ice was added to maintain at low temperature.  Zeolit and activated carbon was cover up by cloth and then placed into the pack.  Dosage treatment of zeolit and activated carbon was 20 gram zeolit, 15 gram zeolit and 5 gram activated carbon, 10 gram zeolit and 10 gram activated carbon, 5 gram zeolit and 15 gram activated carbon, 20 gram activated carbon, and no added zeolit and no activated carbon as control.  Fish condition was observed every 6 hours, while water quality measurement was performed every 24 hours for 120 hours.  The results of study showed that adding 20 gram zeolit without activated carbon in closed packing system of Corydoras aenus in 20oC could maintained in lower concentration of total nitrogen ammonia and unionized ammonia (NH3, reached of 7.83±0.13 mg/l and 0.046±0.003 mg/l, respectively.  The level of total nitrogen ammonia and unionized ammonia were relatively lower compared to mix of zeolit and activated carbon, and only activated carbon.  Survival rate of fish by this treatment was 100%, higher than other treatment (85-95%. Keywords: zeolit, activated carbon, packing, Corydoras   ABSTRAK Permasalahan yang sering dihadapi oleh para eksportir Indonesia dalam pengiriman ikan hias termasuk Corydoras aenus ke luar negeri adalah rendahnya survival rate diantaranya disebabkan oleh kualitas air yang memburuk selama pengangkutan. Teknologi pengepakan yang tepat dan efisien sangat dibutuhkan dalam rangka pengiriman ikan hidup untuk tempat tujuan yang membutuhkan waktu lama

Zeolit Sintetis Terfungsionalisasi 3-(Trimetoksisilil-1-Propantiol sebagai Adsorben Kation Cu(II dan Biru Metilena

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Sri Sugiarti

2017-05-01

Full Text Available The more commonly used method for making synthetic zeolite from kaolin is hydrothermal method. This research tested a sol-gel method in processing synthetic zeolit  using kaolin as the basic ingrediant. The synthetic  zeolite  derived from the sol-gel method was then characterized using X-ray Difractometer and Scanning Electron Microscope, which found resulting products zeolite-A, zeolite Y and sodalite. The adsorption ability of the synthetic zeolites was tested using Cu(II and methylene blue.  Functionalization of the synthetic zeolites by 3-(trimetoksisilil-1-propantiol was  done to increase adsorption capacity. Zeolite A modified by 3-(trimetoksisilil-1-propantiol  had the greater capacity to adsorb methylene blue at 30.11 mg/g. The adsorption isotherms of all the synthetic zeolites approached the Langmuir form. The adsorption energy off all synthetic zeolites approached the chemical adsorption.DOI: http://dx.doi.org/10.15408/jkv.v0i0.5144

The Separation Of The Uranium On The Liquid Radioactive Wastes By Using Zeolites

International Nuclear Information System (INIS)

Budiyono, ME; Peornomo, Herry; S, Djoko

2000-01-01

The experimental investigation on the separation of uranium of liquid radioactive wastes by using zeolite has been carried out. The aims of this investigation was to separate uranium and to determine the solid content of the liquid radioactive waste. This investigation was carried out because zeolite could be used as a good sorption material. The investigation parameters were the number of zeolites, the pH of wastes and the grain size of zeolites. The number of zeolites was varied from 10-100 g, the waste pH was varied from 1-12 and the grain size of zeolites was varied from 20/40-100/200 mesh, each parameters to included in the waste. The conclusion that could be drawn from this investigation were that the best result of the 80 g zeolites used, pH was 9, and the grain size of zeolites was 60/80 mesh, the solid content was 119,46 g/l and efficiency of separation was 81,74 %. As a rule, the solid content in the evaporator process should be about 200-300 g/l

Penggunaan Zeolit Sebagai Media Penyaring Pada Pengolahan Air LimbahDomestik

Directory of Open Access Journals (Sweden)

Yanto Yanto

2011-02-01

Full Text Available Sand filter is frequentlyused to treat contaminated water. Channel filter system is a modification of sand filter where the channel is shaped thus the land requirement could be minimized, water is flowed horizontallyfrom intial tank to finaltank through sand filter. Employing the channel filter to treat domestic wastewateris capable of reducing E. Coli up to 98.14%, increasing DO up to 27% and decreasing BOD5 up to 27%. Unfortunately, the final content of E.Coli after treatment process completed is still unacceptable for drinking water. Several options are available to improve the performance of the channel filter system. One of the promising alternativesis modifying the filter medium. Zeolite is natural material that has been utilized to improvewater quality based on several parameters such as Fe, Mn, organic materials, CO and others. Application of zeolite to diminish E. Coli is a challenge. This paper will investigate the effectiveness of zeolite to lower E. Coli contained in domestic wastewater . Zeolite was added to sand filter where thefraction of zeolite is about 5%. Two kind of zeolite-sand combination was implemented that is arranged and mixed zeolite-sand. Wastewater containing E.Coli was then put in the initial tank. Through the hole createdin the tank, wastewater then flowed passing through the combined zeolite-sand filter and accumulated in the final tank. Both E. Coli from initial and final tank was measured to compute treatment efficiency. The result showsE. Coli decreases up to99.99%, BOD5and DO decrease more than 71% and 66% respectively. It can be concluded that 5% addition ofzeolite is able to improve treatment efficiency ofsand filter.

Natural zeolites: characteristic, properties and uses

International Nuclear Information System (INIS)

Bosch, P.; Bulbulian, S.; Olguin, M. T.

2011-01-01

The zeolites are a crystalline aluminium silicates family of volcanic origin. It characterizes them a porous structure, nano metric, regular and homogeneous. Therefore, they turn out to be excellent molecular sieves besides exchangers of ions. This last property it has been extremely exploited, in order to retain the radioactive ions of the contaminated waters in the accident of Three Mile Island (USA), of Chernobyl (Russia) and Fukushima Daiichi (Japan). Nevertheless, the use of the zeolites goes but there ... these they can work as much as nutritional supplement for chickens and pigs, as well as for to retain odors or to separate gases. The construction industry has welcomed this mineral, when either using it as quarry or additive in the called pozzolanic cements. In this book the authors explain the zeolites formation in the nature, their structure and the main uses of these minerals that some authors have baptized as the magic rocks. (Author)

Adsorption methods for hydrogen isotope storage on zeolitic sieves

International Nuclear Information System (INIS)

Cristescu, Ioana; Cristescu, Ion; Vasut, F.; Brad, S.; Lazar, A.

2001-01-01

For hydrogen isotope separation, adsorption molecular sieves and active carbon were used. Adsorption process proceeds at liquid nitrogen and liquid hydrogen temperatures. Commercial zeolites have the same proprieties with natural zeolites, but they have a regular pore structure. They also have affinity for molecules of different size with defined shapes. Experimental results obtained at liquid nitrogen temperature (77.4 K) and liquid hydrogen revealed the efficient behaviour of the active carbon and zeolitic sieves for hydrogen isotopes temporary storage. We study adsorption of the synthetic zeolites in a wide range of temperatures and pressures and we used the molecular sieves 4A, 5A and active carbon. The 4A and 5A zeolites have a tridimensional structure with 11.4 A diameter. When the hydration water is eliminated, the material keeps a porous structure. The porous volume represents 45% from the zeolite mass for 4A and 5A sieves. The activation temperature of the zeolite and the carbon is very important for obtaining a high adsorption capacity. If the temperature used for activation is low, the structural water will be not eliminated and the adsorption capacity will be low. The excessive temperature will destroy the porous structure. The adsorption capacity for the hydrogen isotopes was calculated with the relation: A = V ads /m (cm 3 /g). The adsorption capacity and efficiency for the adsorbent materials, are given. Physical adsorption process of the hydrogen isotopes was carried out at liquid nitrogen temperature. The flux gas used in the adsorption system is composed of dry deuterium and protium. This mixture is cooled in liquid nitrogen and then is passed to the adsorbent getter at the same temperature (77.4 K). The gas flux in the adsorbent getter is 5 and 72 l/h (which correspond to 0.008 and 0.134 discharge velocity, respectively). (authors)

Adsorption of aqueous Zn(II) species on synthetic zeolites

International Nuclear Information System (INIS)

Badillo-Almaraz, Veronica; Trocellier, Patrick; Davila-Rangel, Ignacio

2003-01-01

To supply a good quality drinkable water tends to become a strategic task in both developed and under development countries in the world due to the number of potential contamination sources. One of the major problems is derived from the presence of heavy toxic metals like zinc or lead resulting from industrial activities. Zeolites are known as very efficient mineral substrates for fixing aqueous ionic species through their wide range of channels present in the crystalline structure and due to their strong surface reactivity. MicroPIXE coupled with microRBS (3.05 MeV 4 He + ions) have been used to quantify the incorporation of zinc within two commercial zeolites containing alkali elements (zeolite X and clinoptilolite) in the concentration range of: 0.0002-0.05 M at neutral pH. At the beginning of the interaction between zeolite and Zn(II) solution, the adsorption process exhibits a direct proportionality between the content of zinc fixed on the mineral substrate and the aqueous concentration up to 0.01 M. Beyond this point a saturation effect seems to occur, indicating the strong decrease of available adsorption sites. Sodium or potassium ions are probably exchanged with Zn(II) ions during this process. The compared behaviour of the two zeolites is then discussed in terms of kinetic effects based on ionic radius values. A co-adsorption test carried on with a 50-50% Zn(II) 0.001 M-Pb(II) 0.001 M solution shows that lead does not occupy the same sites as zinc because the content of zinc fixed on the zeolite sample exactly corresponds to the result obtained with a pure 0.001 M Zn(II) solution. All these data clearly showed that zeolite surface reactivity is greatly influenced by the mineral cage-like structure and particularly the presence of pockets, spaces and channels

Hot isostatic pressing of glass-zeolite composites

International Nuclear Information System (INIS)

Hash, M.C.; Pereira, C.; Lewis, M.A.

1996-01-01

Glass-zeolite waste forms are being developed for immobilizing the chloride waste salt generated from the electrometallurgical treatment of spent fuel. Glass-zeolite composites with high densities were made using hot isostatic pressing (HIP) techniques. Processing parameters were investigated to yield desirable structural ceramic properties such as mechanical, chemical, and thermal stability. Limits for these parameters were determined by differential thermal and thermogravimetric analysis. The resulting ceramic properties such as bulk density, open or apparent porosity, and leach resistance were determined. In addition, phase equilibria and particle-size distribution were observed by optical light and electron microscopy. Pre-HIP processing techniques were also studied to ensure intimate mixing of the glass and zeolite powders. Particle size distributions resulting from dry blending procedure are appropriate for needed flow and packing characteristics

Risk assessment for the transportation of radioactive zeolite liners

International Nuclear Information System (INIS)

1982-01-01

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

Microtensile Bond Strength of CAD/CAM Resin Blocks to Dual-Cure Adhesive Cement: The Effect of Different Sandblasting Procedures.

Science.gov (United States)

Tekçe, Neslihan; Tuncer, Safa; Demirci, Mustafa; Kara, Dilan; Baydemir, Canan

2018-02-11

To investigate the effect of sandblasting powder particles on microtensile bond strength (μTBS) of dual-cure adhesive cement to CAD/CAM blocks. CAD/CAM blocks (Cerasmart, VITA, and LAVA) were cut in slabs and divided into groups: group 1, no sandblasting; group 2, sandblasted with 27-μm Al 2 O 3 ; group 3, sandblasted with 30-μm CoJet; group 4, sandblasted with 50-μm Al 2 O 3 . After sandblasting, all specimens were silanized and luted using dual-cure adhesive cement (G-CEM LinkForce). After 24 hours, bonded specimens were cut into 1 ± 0.2 mm 2 sticks, and μTBS values were obtained (N = 30). Additionally, 132 CAD/CAM block sections were prepared for surface roughness testing and scanning electron microscopy (SEM) evaluations. Results were analyzed using Kruskal-Wallis One-way ANOVA and Dunn's Post Hoc Test (p 0.05). For LAVA, μTBS values of specimens that were sandblasted with 50-μm Al 2 O 3 powder were significantly higher than 30-μm-SiO 2 and 27-μm Al 2 O 3 (p CAD/CAM blocks for Cerasmart and VITA, although the results changed significantly for LAVA. The ideal bond protocol for CAD/CAM blocks is specific to the material used. © 2018 by the American College of Prosthodontists.

Effect of Annealing Temperature on Broad Luminescence of Silver-Exchanged Zeolites Y and A

Science.gov (United States)

Gui, Sa Chu Rong; Lin, H.; Bao, W.; Wang, W.

2018-05-01

The annealing temperature dependence of luminescence properties of silver (Ag)-exchanged zeolites Y and A was studied. It was found that the absorbance and excitation/emission bands are strongly affected by the thermal treatments. With increase in annealing temperature, the absorbance of Ag in zeolite Y increases at first and then decreases. However, the position of the excitation/emission band in zeolite Y was found to be insensitive to the annealing temperature. In contrast, the excitation/emission bands in zeolite A are particularly sensitive to the annealing temperature. The difference of such temperature dependence in zeolites Y and A may be due to the different microporous structure of the two minerals. Moreover, the fact that this dependence is not observed in Ag-exchanged zeolite Y is likely to be due to the difficulty in dehydration of zeolite Y in air or due to the weak Ag+-Ag+ interaction in zeolite Y.

Epitaxially Grown Layered MFI–Bulk MFI Hybrid Zeolitic Materials

KAUST Repository

Kim, Wun-gwi; Zhang, Xueyi; Lee, Jong Suk; Tsapatsis, Michael; Nair, Sankar

2012-01-01

The synthesis of hybrid zeolitic materials with complex micropore-mesopore structures and morphologies is an expanding area of recent interest for a number of applications. Here we report a new type of hybrid zeolite material, composed of a layered

Modifikasi Zeolit Dengan Tembaga (Cu) Dan Uji Sifat Katalitiknya Pada Reaksi Esterifikasi

OpenAIRE

Arjek, Orien Claudia Handayani; Fatimah, Is

2017-01-01

Zeolite modification with Cu has been conducted. Material modification is done by impregnating Cu through a zeolite powder reflux process with CuSO4.5H2O solution so that theoretical Cu concentration is 5% followed by oxidation and reduction of solids. Material characterization was performed by x-ray diffraction analysis (XRD), Fourier Transform Infra-Red (FTIR) and acidity testing of Cu/Zeolite catalyst.The results showed that the crystallinity level of Cu/Zeolite did not change significantl...

Zeolitic catalytic conversion of alcohols to hydrocarbons

Science.gov (United States)

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

2018-04-10

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

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.

Molecular interactions of alcohols with zeolite BEA and MOR frameworks.

Science.gov (United States)

Stückenschneider, Kai; Merz, Juliane; Schembecker, Gerhard

2013-12-01

Zeolites can adsorb small organic molecules such as alcohols from a fermentation broth. Also in the zeolite-catalyzed conversion of alcohols to biofuels, biochemicals, or gasoline, adsorption is the first step. Several studies have investigated the adsorption of alcohols in different zeolites experimentally, but computational investigations in this field have mostly been restricted to zeolite MFI. In this study, the adsorption of C1-C4 alcohols in BEA and MOR was investigated using density functional theory (DFT). Calculated adsorption geometries and the corresponding energies of the designed cluster models were comparable to periodic calculations, and the adsorption energies were in the same range as the corresponding computational and experimental values reported in the literature for zeolite MFI. Thus, BEA and MOR may be good adsorption materials for alcohols in the field of downstream processing and catalysis. Aside from the DFT calculations, adsorption isotherms were determined experimentally in this study from aqueous solutions. For BEA, the adsorption of significant amounts of alcohol from aqueous solution was observed experimentally. In contrast, MOR was loaded with only a very small amount of alcohol. Although differences were found between the affinities obtained from gas-phase DFT calculations and those observed experimentally in aqueous solution, the computational data presented here represent molecular level information on the geometries and energies of C1-C4 alcohols adsorbed in zeolites BEA and MOR. This knowledge should prove very useful in the design of zeolite materials intended for use in adsorption and catalytic processes, as it allows adsorption behavior to be predicted via judiciously designed computational models.

Effects of ultrasonic treatment on zeolite NaA synthesized from by-product silica.

Science.gov (United States)

Vaičiukynienė, Danutė; Kantautas, Aras; Vaitkevičius, Vitoldas; Jakevičius, Leonas; Rudžionis, Žymantas; Paškevičius, Mantas

2015-11-01

The synthesis of zeolite NaA from silica by-product was carried out in the presence of 20 kHz ultrasound at room temperature. Zeolites obtained in this type of synthesis were compared to zeolites obtained by performing conventional static syntheses under similar conditions. The sonication effects on zeolite NaA synthesis were characterized by phase identification, crystallinity etc. The effects of different parameters such as crystallization time and initial materials preparation methods on the crystallinity and morphology of the synthesized zeolites were investigated. The final products were characterized by XRD and FT-IR. It was possible to obtain crystalline zeolite NaA from by-product silica in the presence of ultrasound. Copyright © 2015 Elsevier B.V. All rights reserved.

Measurement of cation exchange capacity (CEC) on natural zeolite by percolation method

Science.gov (United States)

Wiyantoko, Bayu; Rahmah, Nafisa

2017-12-01

The cation exchange capacity (CEC)measurement has been carried out in natural zeolite by percolation method. The natural zeolite samples used for cation exchange capacity measurement were activated beforehand with physical activation and chemical activation. The physically activated zeolite was done by calcination process at 600 °C for 4 hours. The natural zeolite was activated chemically by using sodium hydroxide by refluxing process at 60-80 °C for 3 hours. In summary, cation exchange capacity (CEC) determination was performed by percolation, distillation and titration processes. Based on the measurement that has been done, the exchange rate results from physical activated and chemical activated of natural zeolite were 181.90cmol (+)/kg and 901.49cmol (+)/kg respectively.

Beyond Creation of Mesoporosity: The Advantages of Polymer-Based Dual-Function Templates for Fabricating Hierarchical Zeolites

KAUST Repository

Tian, Qiwei

2016-02-05

Direct synthesis of hierarchical zeolites currently relies on the use of surfactant-based templates to produce mesoporosity by the random stacking of 2D zeolite sheets or the agglomeration of tiny zeolite grains. The benefits of using nonsurfactant polymers as dual-function templates in the fabrication of hierarchical zeolites are demonstrated. First, the minimal intermolecular interactions of nonsurfactant polymers impose little interference on the crystallization of zeolites, favoring the formation of 3D continuous zeolite frameworks with a long-range order. Second, the mutual interpenetration of the polymer and the zeolite networks renders disordered but highly interconnected mesopores in zeolite crystals. These two factors allow for the synthesis of single-crystalline, mesoporous zeolites of varied compositions and framework types. A representative example, hierarchial aluminosilicate (meso-ZSM-5), has been carefully characterized. It has a unique branched fibrous structure, and far outperforms bulk aluminosilicate (ZSM-5) as a catalyst in two model reactions: conversion of methanol to aromatics and catalytic cracking of canola oil. Third, extra functional groups in the polymer template can be utilized to incorporate desired functionalities into hierarchical zeolites. Last and most importantly, polymer-based templates permit heterogeneous nucleation and growth of mesoporous zeolites on existing surfaces, forming a continuous zeolitic layer. In a proof-of-concept experiment, unprecedented core-shell-structured hierarchical zeolites are synthesized by coating mesoporous zeolites on the surfaces of bulk zeolites. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Removal of cesium and strontium from low active waste solutions by zeolites

International Nuclear Information System (INIS)

Jain, Savita; Ramaswamy, M.; Theyyunni, T.K.

1994-01-01

Ion exchange, crystallographic and thermal characteristics of sodium, cesium and strontium forms of locally available synthetic zeolites have been investigated. X-ray and differential thermal analyses have confirmed that the synthetic materials AR1 and 4A belonged to the mordenite and A type families of zeolites respectively. Equilibrium uptake of cesium and strontium ions by sodium forms of zeolite was studied as a function of time, pH and sodium concentration. It was found that the rate of sorption by AR1 was higher than that by 4A. In regard to pH, distribution of nuclides on zeolites was found to pass through maxima at a pH value of around 9. Sodium ion interfered with the sorption of cesium and strontium by zeolites. However, at sodium concentration ≤ 0.01 M, distribution coefficient values for these nuclides were sufficiently high to merit consideration of these zeolites for low level waste treatment. Lab-scale column runs using 5 ml beds of materials showed that the zeolites AR1 and 4A were very effective in removing cesium and strontium nuclides respectively from large volumes (a decontamination factor of 50 for a throughput of 6000 bed volumes) of actual low level waste solutions. Thus, the zeolite system has a potential future for large scale application in the treatment of low level wastes. (author). 6 refs., 5 figs., 6 tabs

ZEOLITE: "THE MAGIC STONE"; MAIN NUTRITIONAL, ENVIRONMENTAL, EXPERIMENTAL AND CLINICAL FIELDS OF APPLICATION.

Science.gov (United States)

Laurino, Carmen; Palmieri, Beniamino

2015-08-01

zeolites (clinoptilolites) are a family of alluminosilicates and cations clustered to form macro aggregates by small individual cavities. In the medical area they are involved in detoxification mechanisms capturing ions and molecules into their holes. Actually, we classify about 140 types of natural and 150 synthetic zeolites, for specific and selective use. Clinoptilolite is a natural zeolite and it is the most widespread compound in the medical market. this review analyzes the main fields of zeolite utilization. we searched Pubmed/Medline using the terms "zeolite" and "clinoptilolite". in zoothechnology and veterinary medicine zeolite improves the pets' fitness, removes radioactive elements, aflatoxines and poisons. Zeolite displays also antioxidant, whitening, hemostatic and anti-diarrhoic properties, projected in human care. However very scanty clinical studies have been run up to now in immunodeficiency, oncology after chemotherapy and radiotherapy as adjuvants. further clinical investigations are urgently required after this review article publication which updates the state of the art. Copyright AULA MEDICA EDICIONES 2014. Published by AULA MEDICA. All rights reserved.

Thermal expansion of ceramic samples containing natural zeolite

Science.gov (United States)

Sunitrová, Ivana; Trník, Anton

2017-07-01

In this study the thermal expansion of ceramic samples made from natural zeolite is investigated. Samples are prepared from the two most commonly used materials in ceramic industry (kaolin and illite). The first material is Sedlec kaolin from Czech Republic, which contains more than 90 mass% of mineral kaolinite. The second one is an illitic clay from Tokaj area in Hungary, which contains about 80 mass% of mineral illite. Varying amount of the clay (0 % - 50 %) by a natural zeolite from Nižný Hrabovec (Slovak Republic), containing clinoptilolite as major mineral phase is replaced. The measurements are performed on cylindrical samples with a diameter 14 mm and a length about 35 mm by a horizontal push - rod dilatometer. Samples made from pure kaolin, illite and zeolite are also subjected to this analysis. The temperature regime consists from linear heating rate of 5 °C/min from 30 °C to 1100 °C. The results show that the relative shrinkage of ceramic samples increases with amount of zeolite in samples.

Modification of Natural Zeolite with Fe(III) and Its Application as Adsorbent Chloride and Carbonate ions

Science.gov (United States)

Suhartana; Sukmasari, Emmanuella; Azmiyawati, Choiril

2018-04-01

The aim of the research is to natural zeolite with Fe(III) using anion exchange process to improve the anion exchange capacity. Natural zeolite was activated using HNO3 1 N and then mixed with FeCl3 solution and refluxed followed by oven and calcination at a temperature of 550°C. The influence of Fe(III) to zeolite was characterized by FTIR while presence of Fe in zeolite characterized by AAS. Zeolite and Zeolite-Fe adsorption capacity of chloride and carbonate anions were determined through adsorption test by variation of pH and contact time. In advanced, and then to determining the Fe adsorbed concentration at Zeolite using UV-Vis spectrophotometer. FTIR analysis result showed that the addition of Fe does not affect the zeolite’s structure but change the intensity of the zeolite spectra. The Fe concentration in Zeolite-Fe of 714 mg L-1, indicate that Fe was present in the zeolite. Both Zeolite and Zeolite-Fe adsorbtion results showed that optimum pH of Chloride anion is 2, with adsorption capacity 2,33 x 10-3 gg-1 and optimum contact time is 8 minutes. While Zeolite and Zeolite-Fe adsorbtion results showed that optimum pH of Carbonate anion is 5, with adsorption capacity 5,31 x 10-3 gg-1 and optimum contact time is 8 minutes.

Catalytic Fast Pyrolysis of Kraft Lignin over Hierarchical HZSM-5 and Hβ Zeolites

Directory of Open Access Journals (Sweden)

Yadong Bi

2018-02-01

Full Text Available The hierarchical HZSM-5 and Hβ zeolites were prepared by alkaline post-treatment methods adopting Na2CO3, TMAOH/NaOH mixture, and NaOH as desilication sources, respectively. More mesopores are produced over two kinds of zeolites, while the micropores portion is well preserved. The mesopores formed in hierarchical Hβ zeolites were directly related to the basicity of the alkaline solution, indicating that Hβ zeolite is more sensitive to the alkaline post-treatment. The hierarchical HZSM-5 and Hβ zeolites are more active than the parent one for catalytic fast pyrolysis (CFP of Kraft lignin. Hierarchical zeolites retained the function of acid catalysis, while additionally creating larger mesopores to ensure the entry of bulkier reactant molecules. The increase of the condensable volatiles yield can be attributed to the improvement of the mass transfer performance, which correlates well with the change of mesoporous surface area. In particular, the condensable volatiles yield for the optimized hierarchical Hβ reached approximately two times that of the parent Hβ zeolites. In contrast to the parent HZSM-5, the optimized hierarchical HZSM-5 zeolite significantly reduced the selectivity of oxygenates from 27.2% to 3.3%.

Zeolite and zeotype-catalysed transformations of biofuranic compounds

DEFF Research Database (Denmark)

Li, Hu; Yang, Song; Riisager, Anders

2016-01-01

,5-furandicarboxylic acid can be obtained from hexoses and pentoses via selective dehydration and subsequent etherification, hydrogenation, oxidation reactions, which show great potential for industrial applications to replace petroleum-based chemicals and fuels. Zeolite and zeotype micro- and mesoporous materials...... with tuneable acidity, good thermal stability and shape-selectivity have recently emerged as promising solid catalysts, exhibiting superior catalytic performance to other heterogeneous catalysts. This review focuses on the synthesis of biomass-derived furanic compounds catalysed by zeolitic materials, firstly...... introducing zeolite-catalysed hydrolysis of di-, oligo- and polysaccharides and isomerization reactions of monomeric sugars. Subsequently, the catalytic dehydration reactions of hexoses and pentoses to obtain HMF and furfural are reported. Particularly, a variety of reaction pathways towards upgrading...

Methanol conversion to lower olefins over RHO type zeolite

KAUST Repository

Masih, Dilshad; Imai, Hiroyuki; Yokoi, Toshiyuki; Kondo, Junkonomura; Tatsumi, Takashi

2013-01-01

Eight-membered ring small-pore zeolite of RHO-type topology has been synthesized, characterized and tested for methanol-to-olefin (MTO) reaction. The zeolite was hydrothermally crystallized from the gel with Si/Al ratio of 5.0. It showed a high BET

Enhanced catalytic oxidation by hierarchically structured TS-1 zeolite

NARCIS (Netherlands)

Xin, H.; Zhao, Jiao; Zhao, J.; Xu, S.; Li, Junping; Zhang, Weiping; Guo, X.; Hensen, E.J.M.; Yang, Q.; Li, Can

2010-01-01

A TS-1 zeolite with a disordered network of mesopores penetrating the microporous crystalline zeolite framework was successfully synthesized by a one-pot carbon hard-templating synthesis approach. Besides conventional methods to characterize the mesoporosity, the use of variable-temperature 129Xe

Zeolites - a high resolution electron microscopy study

International Nuclear Information System (INIS)

Alfredsson, V.

1994-10-01

High resolution transmission electron microscopy (HRTEM) has been used to investigate a number of zeolites (EMT, FAU, LTL, MFI and MOR) and a member of the mesoporous M41S family. The electron optical artefact, manifested as a dark spot in the projected centre of the large zeolite channels, caused by insufficient transfer of certain reflections in the objective lens has been explained. The artefact severely hinders observation of materials confined in the zeolite channels and cavities. It is shown how to circumvent the artefact problem and how to image confined materials in spite of disturbance caused by the artefact. Image processing by means of a Wiener filter has been applied for removal of the artefact. The detailed surface structure of FAU has been investigated. Comparison of experimental micrographs with images simulated using different surface models indicates that the surface can be terminated in different ways depending on synthesis methods. The dealuminated form of FAU (USY) is covered by an amorphous region. Platinum incorporated in FAU has a preponderance to aggregate in the (111) twin planes, probably due to a local difference in cage structure with more spacious cages. It is shown that platinum is intra-zeolitic as opposed to being located on the external surface of the zeolite crystal. This could be deduced from tomography of ultra-thin sections among observations. HRTEM studies of the mesoporous MCM-41 show that the pores have a hexagonal shape and also supports the mechanistic model proposed which involves a cooperative formation of a mesophase including the silicate species as well as the surfactant. 66 refs, 24 figs

Characterization of Mexican zeolite minerals; Caracterizacion de minerales zeoliticos mexicanos

Energy Technology Data Exchange (ETDEWEB)

Jimenez C, M.J

2005-07-01

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

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

Removal of excess nutrients by Australian zeolite during anaerobic digestion of swine manure.

Science.gov (United States)

Wijesinghe, D Thushari N; Dassanayake, Kithsiri B; Scales, Peter; Sommer, Sven G; Chen, Deli

2018-03-21

The objective of this study was to investigate the feasibility of using natural and NaCl-treated Australian zeolites to simultaneously remove excess nutrients from anaerobically digested swine manure. Ion adsorption and desorption properties of Australian zeolite during the anaerobic digestion of swine manure were investigated. Two experiments were conducted: the first was an adsorption experiment with multi-component solutions that corresponded with the ionic composition of swine manure digestates. The second experiment determined the effects of zeolite dose rates during anaerobic digestion of swine manure on the removal of N, P and K from solution. Adsorption isotherms confirmed selectivity for K + over NH 4 + by Australian natural and sodium zeolites. Therefore, NH 4 + removal was considerably reduced when there was simultaneous K + uptake. Natural zeolite desorbed more Ca 2+ during K + and NH 4 + adsorption than sodium zeolite. The ion exchange reaction was independent of the presence of P. P removal was very dependent on the pH of the medium. Natural Australian zeolite was shown to be a potential sorbent for the removal of NH 4 + , K + and P during the anaerobic digestion of swine manure. However, the application of high concentrations of zeolite at higher pH values (> 7.5) might not be appropriate for anaerobic digestion, because zeolite desorbed more Ca 2+ ions into the solution at the higher doses of zeolite and then availability of P for microbial growth might be reduced as a result of PO 4 3- precipitation with Ca 2+ at the higher pH.

Optimization for zeolite regeneration and nitrogen removal performance of a hypochlorite-chloride regenerant.

Science.gov (United States)

Zhang, Wei; Zhou, Zhen; An, Ying; Du, Silu; Ruan, Danian; Zhao, Chengyue; Ren, Ning; Tian, Xiaoce

2017-07-01

Simultaneous zeolites regeneration and nitrogen removal were investigated by using a mixed solution of NaClO and NaCl (NaClO-NaCl solution), and effects of the regenerant on ammonium removal performance and textural properties of zeolites were analyzed by long-term adsorption and regeneration operations. Mixed NaClO-NaCl solution removed more NH 4 + exchanged on zeolites and converted more of them to nitrogen than using NaClO or NaCl solution alone. Response surface methodological analysis indicated that molar ratio of hypochlorite and nitrogen (ClO - /N), NaCl concentration and pH value all had significant effects on zeolites regeneration and NH 4 + conversion to nitrogen, and the optimum condition was obtained at ClO - /N of 1.75, NaCl concentration of 20 g/L and pH of 10.0. Zeolites regenerated by mixed NaClO-NaCl solution showed higher ammonium adsorption rate and lower capacity than unused zeolites. Zeolites and the regeneration solution were both effective even after 20 cycles of use. Composition and morphological analysis revealed that the main mineral species and surface morphology of zeolites before and after NaClO-NaCl regeneration were unchanged. Textural analysis indicated that NaClO-NaCl regeneration leads to an increased surface area of zeolites, especially the microporosity. The results indicated that NaClO-NaCl regeneration is an attractive method to achieve sustainable removal of nitrogen from wastewater through zeolite. Copyright © 2017 Elsevier Ltd. All rights reserved.

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.

Zeolite - a possible substitute of silica gel in spectrophotometric determination of uranium?

International Nuclear Information System (INIS)

Foeldesova, M; Dillinger, P.

2006-01-01

Zeolites sorption abilities differ from the ones of the silica gel, which is normally used for uranium determination by spectrophotometric method. The difference is obvious mainly in the case of zeolites chemically modified with 1 or 2 mol/L NaOH solution. Absorbances measured using these zeolites on an radioactive water samples were 4 to 4.2 times bigger than the ones with silica gel. This avoids a use of one universal calibration curve for experimental data evaluation. Within delivered experimental data only a calibration curve for silica gel was provided. Its application to zeolites caused substantial misinterpretation of the results. Calculational construction of individual calibration curves made at this work shaw, that zeolites have a potential to replace the silica gel. This possibility is necessary to confirm by more experiments. Better sorption abilities of the modified zeolites would be utilized to reduce the lower limit for uranium determination by spectrophotometric method. (authors)

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

Directory of Open Access Journals (Sweden)

Ivančica Kovaček

2009-10-01

Full Text Available Activated natural zeolite clinoptilolite is microporous hydrated aluminosilicates crystals with well-defined structures containing AlO4 and SiO4 tetrahedral linked through the common oxygen atoms. It is to point out that zeolites act as strong adsorbents and ion-exchangers but having many other useful properties. Due to its cationexchange ability, zeolites have catalytic properties and, for that, multiple uses in medicine and industry, agriculture, water purification and detergents. Zeolites are nontoxic substance, excellent for UVR and microbes protection, for proteins and small molecules such as glucose adsorption. In this paper its positive effect on the metabolism of living organisms and its anticancerogenic, antiviral, antimetastatic and antioxidant effect. The activity of natural zeolite as natural immunostimulator was presented as well as its help in healing wounds. Therefore, the present paper is an attempt to modify cotton (by mercerization and polyester (by alkaline hydrolysis fabrics for summer clothing with addition of natural zeolite nanoparticles for achieving UV and antibacterial protective textiles

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

International Nuclear Information System (INIS)

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

2001-01-01

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

Potential and challenges of zeolite chemistry in the catalytic conversion of biomass.

Science.gov (United States)

Ennaert, Thijs; Van Aelst, Joost; Dijkmans, Jan; De Clercq, Rik; Schutyser, Wouter; Dusselier, Michiel; Verboekend, Danny; Sels, Bert F

2016-02-07

Increasing demand for sustainable chemicals and fuels has pushed academia and industry to search for alternative feedstocks replacing crude oil in traditional refineries. As a result, an immense academic attention has focused on the valorisation of biomass (components) and derived intermediates to generate valuable platform chemicals and fuels. Zeolite catalysis plays a distinct role in many of these biomass conversion routes. This contribution emphasizes the progress and potential in zeolite catalysed biomass conversions and relates these to concepts established in existing petrochemical processes. The application of zeolites, equipped with a variety of active sites, in Brønsted acid, Lewis acid, or multifunctional catalysed reactions is discussed and generalised to provide a comprehensive overview. In addition, the feedstock shift from crude oil to biomass involves new challenges in developing fields, like mesoporosity and pore interconnectivity of zeolites and stability of zeolites in liquid phase. Finally, the future challenges and perspectives of zeolites in the processing of biomass conversion are discussed.

Selective adsorption of thiophene and 1-benzothiophene on metal-ion-exchanged zeolites in organic medium.

Science.gov (United States)

Xue, Mei; Chitrakar, Ramesh; Sakane, Kohji; Hirotsu, Takahiro; Ooi, Kenta; Yoshimura, Yuji; Feng, Qi; Sumida, Naoto

2005-05-15

Adsorption of the organic sulfur compounds thiophene (TP) and 1-benzothiophene (1-BTP) in an organic model solution of hydrodesulfurizated gasoline (heptane with 1 wt% toluene and 0.156 mM (5 ppmw as sulfur) TP or 1-BTP) was studied by a batch method at 80 degrees C using metal-ion-exchanged Y-zeolites. Although NaY-zeolite or its acid-treated material rarely adsorbed the organic sulfur compounds, NaY-zeolites exchanged with Ag+, Cu2+, and Ce3+ ions and NH(4)Y-zeolites exchanged with Ce3+ ions showed markedly high adsorptive capacities for TP and 1-BTP. The sulfur uptake increased in the order CuY-zeolite(Na)(Na) for both the organic sulfur compounds. The adsorption isotherms for TP and 1-BTP followed the Langmuir's relationship and the saturation capacities by CeY-zeolite(Na) were calculated as 0.022 and 0.033 mmol/g, respectively. The mole ratios of TP/Ce and 1-BTP/Ce were 0.031 and 0.047, respectively. CeY-zeolite(NH4) which was prepared from NH4Y-zeolite showed less uptake of TP and 1-BTP than CeY-zeolite(Na), probably due to its lower cerium content.

XAFS Study on TiO2 Photocatalyst Loaded on Zeolite Synthesized from Steel Slag

International Nuclear Information System (INIS)

Kuwahara, Yasutaka; Ohmichi, Tetsutaro; Mori, Kosuke; Katayama, Iwao; Yamashita, Hiromi

2007-01-01

The convenient route for the synthesis of Y-zeolites by utilizing steel slag as a material source was developed. Through hydrothermal treatment, well-crystallized Y-zeolite was obtained. We also synthesized TiO2-loaded Y-zeolites by an impregnation method. The structure of titanium oxide species highly dispersed on the zeolite, which couldn't be detected by XRD patterns, was investigated by XAFS analysis. Photocatalytic activity for decomposition of 2-propanol in liquid phase was found to be enhanced by the hydrophobic surface property of zeolite. It has been demonstrated that the zeolite synthesized from steel slag would be applicable as a promising support of TiO2 photocatalyst

PENINGKATAN KECEPATAN PROSES PENGERINGAN KARAGINAN MENGGUNAKAN PENGERING ADSORPSI DENGAN ZEOLIT

Directory of Open Access Journals (Sweden)

Mohamad Djaeni

2012-07-01

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

Immobilization technology for krypton in amorphous zeolite

International Nuclear Information System (INIS)

Takusagawa, Atsushi; Ishiyama, Keiichi

1989-01-01

Radioactive krypton recovered from the offgas of a reprocessing plant requires long-term storage on the order of 100 years. Immobilization technology for krypton into amorphous zeolite 5A is considered one of the best methods for long-term storage. In this report, conditions for immobilization treatment and stability of amorphous zeolite 5A loaded krypton against heat, radiation and water are discussed, and a treatment system using this technology is described. (author)

Zeolite and wollastonite synthesis from rice hull ash

International Nuclear Information System (INIS)

Fernandes, Alberto de Andrade

2006-01-01

Rice hull ash (RHA) is a industry scrap rich in amorphous silica. A simple and low-energy cost method for the extraction of this silica was researched. A low level of impurity and high reactivity material was produced, which is appropriate for the synthesis of zeolites and wollastonite (CaSiO 3 ). The synthetic zeolites has not similar structures in nature, and they have been more and more valued in the market due to their purity and efficiency in specific applications like ion exchange, molecular sieve and catalysis areas. High purity wollastonite has many applications in manufacturing and agriculture. The mineral wollastonite can be formed in nature in different ways; it is generally accepted two forming processes, both encompassing limestone metamorphism (heat and pressure). In this work, a new process for the synthesis of zeolites and wollastonite from RHA colloidal silica was developed. Moreover, the process is aimed at lower energy costs, fewer stages and fewer reactants consume. In this work, zeolite A used in detergent and zeolite ZSM-5, employed in the petrochemical industry due to its high selectivity in catalytic reactions and its high thermo and acid stability, were synthesized. The first step of the wollastonite synthesis was studied, with the purpose of obtaining calcium hydrosilicate. Eleven different hydrosilicates occur in the system Ca(OH) 2 -SiO 2 -H 2 O, in the second step it was annealed to form the wollastonite phase. (author)

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

Directory of Open Access Journals (Sweden)

Stephanie Reuss

2018-01-01

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

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

Science.gov (United States)

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

2018-01-21

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

The remediation of the lead-polluted garden soil by natural zeolite.

Science.gov (United States)

Li, Hua; Shi, Wei-yu; Shao, Hong-bo; Shao, Ming-an

2009-09-30

The current study investigated the remediation effect of lead-polluted garden soil by natural zeolite in terms of soil properties, Pb fraction of sequential extraction in soil and distribution of Pb in different parts of rape. Natural zeolite was added to artificially polluted garden soil to immobilize and limit the uptake of lead by rape through changing soil physical and chemical properties in the pot experiment under greenhouse conditions. Results indicated that the addition of natural zeolite could increase soil pH, CEC, content of soil organic matter and promote formation of soil aggregate. The application of zeolite decreased the available fraction of Pb in the garden soil by adjusting soil pH rather than CEC, and restrained the Pb uptake by rape. Data obtained suggested that the application of a dose of zeolite was adequate (>or=10 g kg(-1)) to reduce soluble lead significantly, even if lead pollution is severe in garden soil (>or=1000 mg kg(-1)). An appropriate dose of zeolite (20 g kg(-1)) could reduce the Pb concentration in the edible part (shoots) of rape up to 30% of Pb in the seriously polluted soil (2000 mg kg(-1)).

Recent Advances in the Mechanistic Studies of Alkylaromatic Conversions over Zeolite Catalysts

International Nuclear Information System (INIS)

Min, Hyung-Ki; Hong, Suk Bong

2013-01-01

The transformation of alkylaromatic hydrocarbons using zeolite catalysts play big part in the current petrochemical industry. Here we review recent advances in the understanding of the reaction mechanisms of various alkylaromatic conversions with respect to the structural and physicochemical properties of zeolite catalysts employed. Indeed, the shape-selective nature of zeolite catalysts determines the type of reaction intermediates and hence the prevailing reaction mechanism together with the product distribution. The prospect of zeolite catalysis in the development of more efficient petrochemical processes is also described

Inoculum and zeolite synergistic effect on anaerobic digestion of poultry manure

DEFF Research Database (Denmark)

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

2014-01-01

zeolite dosages on the mesophilic AD of poultry manure inoculated with a non-acclimatised to ammonia inoculum (dairy manure) was investigated. Additionally, a comparative analysis was performed between the data extracted from this study and the results of a previous study which has been conducted under...... the same experimental conditions but with the use of ammonia acclimatised inoculum (swine manure). At 5 and 10 g zeolite L−1, the methane yield of poultry manure was 43.4% and 80.3% higher compared with the experimental set without zeolite addition. However, the ammonia non-acclimatised inoculum...... was not efficient in digesting poultry manure even in the presence of 10 g zeolite L−1, due to low methane production (only 39%) compared to the maximum theoretical yield. Finally, ammonia acclimatised inoculum and zeolite have demonstrated a possible “synergistic effect” which led to a more efficient AD of poultry...

Dissolution of Iron During Biochemical Leaching of Natural Zeolite

Directory of Open Access Journals (Sweden)

Lengauer C.

2004-12-01

Full Text Available Natural zeolite, including clinoptilolite, often contains iron and manganese which decrease the whiteness of this sharp angular material.The biological treatment of zeolite enables its use as an substitute for tripolyphosphates in wash powders which have to comply with strict requirements as far as whiteness is concerned and rounded off grain content. Insoluble Fe3+ and Mn4+ in the zeolite could be reduced to soluble Fe2+ and Mn2+ by silicate bacteria of Bacillus spp. These metals were efficiently removed from zeolite as documented by Fe2O3 decrease (from 1.37% to 1.08% and MnO decrease (from 0.022% to 0.005% after bioleaching. The whiteness of zeolite was increased by 8%. The leaching effect, observed by scanning electron microscopy, caused also a chamfer of the edges of sharp angular grains. Despite the enrichment by fine-grained fraction, the decrease of the surface area of clinoptilolite grains from the value 24.94 m2/g to value 22.53 m2/g was observed. This fact confirms the activity of bacteria of Bacillus genus in the edge corrosion of mineral grains.Removal of iron and manganese as well as of sharp edges together with the whiteness increase would provide a product suitable for industrial applications.

Bendable Zeolite Membranes: Synthesis and Improved Gas Separation Performance.

Science.gov (United States)

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

2015-06-23

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

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

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Tatana Supinkova

2017-07-01

Full Text Available Zeolites are stable microporous aluminosilicates with numerous applications in chemical technology such as separation of species and catalytic transformations. Our study is focused on a weakly explored zeolite SSZ-16 with pore constrictions defined by 8-membered oxygen rings. Key results are the preparation of Et6-diquat-5 dication used as a structure directing agent (SDA and finding the optimum synthesis conditions with respect to zeolite phase purity. Stability of SDA was examined in conditions similar to those of autoclave synthesis (concentration, pH, temperature. Moreover, the content and location of SDA species in zeolite phase and conditions of SDA decomposition were investigated.

Adductor Canal Block With 10 mL Versus 30 mL Local Anesthetics and Quadriceps Strength

DEFF Research Database (Denmark)

Jæger, Pia; Koscielniak-Nielsen, Zbigniew J; Hilsted, Karen Lisa

2015-01-01

weakness. METHODS: We performed a paired, blinded, randomized trial including healthy men. All subjects received bilateral ACBs with ropivacaine 0.1%; 10 mL in 1 leg and 30 mL in the other leg. The primary outcome was the difference in number of subjects with quadriceps strength reduced by more than 25...... of the predefined time points or in sensory block. The only statistically significant difference between volumes was found in the 30-Second Chair Stand Test at 2 hours (P = 0.02), but this difference had disappeared at 4 hours (P = 0.06). CONCLUSIONS: Varying the volume of ropivacaine 0.1% used for ACB between 10...

Synthesis and Characterization of High Aluminum Zeolite X from Technical Grade Materials

Directory of Open Access Journals (Sweden)

Seyed Kamal Masoudian

2013-06-01

Full Text Available Zeolites are widely used as ion exchangers, adsorbents, separation materials and catalyst due to their well-tailored and highly-reproducible structures; therefore, the synthesis of zeolite from low grade resources can be interested. In the present work, high aluminum zeolite X was prepared from mixing technical grade sodium aluminate and sodium silicate solutions at temperatures between 70°C and 100°C. The synthesized zeolite X was characterized by SEM and X-ray methods according to ASTM standard procedures. The results showed that aging of the synthesis medium at the room temperature considerably increased the selectivity of zeolite X formation. On the other hand, high temperature of reaction mixture during crystallization formed zeolite A in the product; therefore, it decreased the purity of zeolite X. In addition, it was found that increasing H2O/Na2O and decreasing Na2O/SiO2 molar ratios in the reaction mixture resulted product with higher purity. © 2013 BCREC UNDIP. All rights reservedReceived: 7th January 2013; Revised: 7th April 2013; Accepted: 19th April 2013[How to Cite: Masoudian, S. K., Sadighi, S., Abbasi, A. (2013. Synthesis and Characterization of High Alu-minum Zeolite X from Technical Grade Materials. Bulletin of Chemical Reaction Engineering & Catalysis, 8 (1: 54-60. (doi:10.9767/bcrec.8.1.4321.54-60][Permalink/DOI: http://dx.doi.org/10.9767/bcrec.8.1.4321.54-60] | View in  |

Immobilization of krypton-85 in zeolite 5A and porous glass

International Nuclear Information System (INIS)

Christensen, A.B.; DelDebbio, J.A.; Knecht, D.A.; Tanner, J.E.; Cossel, S.C.

1981-12-01

This report demonstrates the technical and economic feasibility for immobilizing krypton-85 by high pressure/high temperature encapsulation in zeolite 5A or thirsty Vyco porous glass. Data are presented to show how process conditions affect the encapsulation and how to compact the zeolite beads with glass frit or other additives to form a fused mass with low dispersibility potential. Krypton specific loadings of 30 and 50 m 3 STP gas per m 3 solid are readily achieved at 100 MPa in porous glass at 900 0 C and zeolite 5A at 700 0 C. Krypton is encapsulated by a sintering process where the porous glass and zeolite 5A voids are sealed. With zeolite 5A, the initial water concentration has a catalytic effect on the sintering, resulting in a transition from crystalline zeolite 5A to an amorphous aluminosilicate. Krypton leakage experiments are used to predict leakage rates from glass or zeolite of less than 0.03% and 0.3% for 10-y storage at 300 and 400 0 C, respectively. Heating the loaded zeolite at 600 to 700 0 C for 4 h removes 0.1% of the total krypton which is loosely held and reduces the subsequent leakage rates at 300 to 400 0 C. Zeolite 5A is chosen as the preferred material to immobilize krypton-85. A preconceptual design and cost estimate is given for a facility to encapsulate 110% of the krypton production of a 2000 metric ton of heavy metal per year reprocessing plant, or 230 m 3 of gas containing 19 MCi of krypton-85. A hot isostatic press (HIP) with an isolated work zone of 8 or 16 L capacity is required to operate for 600 or 300 cycles per year, respectively. Existing HIP technology uses work zones from 1 to 3500 L capacity at similar production rates. A preliminary safety evaluation shows that an incredible worst case accident could be contained and the maximum off-site dose would be well below accident protective action guidance levels

Adsorption of CO2 in FAU zeolites: Effect of zeolite composition

Czech Academy of Sciences Publication Activity Database

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

2014-01-01

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

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...... materials were all prepared by hydrothermal crystallization of gels adsorbed on carbon matrices which were subsequently removed by combustion. The procedures presented here resulted in mesoporous zeolite and zeotypes materials with MFI, MEL, BEA, AFI and CHA framework structures. All samples were...... 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...

Hydrogen Adsorption in Zeolite Studied with Sievert and Thermogravimetric Methods

International Nuclear Information System (INIS)

Lesnicenoks, P; Sivars, A; Grinberga, L; Kleperis, J

2012-01-01

Natural clinoptilolite (mixture from clinoptilolite, quartz and muscovite) is activated with palladium and tested for hydrogen adsorption capability at temperatures RT - 200°C. Thermogravimetric and volumetric methods showed that zeolite activated with palladium (1.25%wt) shows markedly high hydrogen adsorption capacity - up to 3 wt%. Lower amount of adsorbed hydrogen (∼1.5 wt%) was found for raw zeolite and activated with higher amount of palladium sample. Hypothesis is proposed that the heating of zeolite in argon atmosphere forms and activates the pore structure in zeolite material, where hydrogen encapsulation (trapping) is believed to occur when cooling down to room temperature. An effect of catalyst (Pd) on hydrogen sorption capability is explained by spillover phenomena were less-porous fractions of natural clinoptilolite sample (quartz and muscovite) are involved.

Obtaining zeolite Y synthesized by hydrothermal treatment assisted by microwave

International Nuclear Information System (INIS)

Simoes, A.N.; Simoes, V.N.; Neiva, L.S.; Rodrigues, M.G.F.; Gama, L.; Oliveira, J. B.L.

2011-01-01

n search of new catalysts several man-made structures have been developed. The use of zeolites in catalysis is applied due to its ability to associate activity, selectivity and stability, the main conditions to have an effective catalyst. Thus, studies have been done on the hydrothermal synthesis of zeolites by microwave assisted, since the use of microwave radiation offers several advantages over conventional heating. In this context, this work aims to synthesis and characterization of zeolite Y via hydrothermal treatment in a microwave oven. The sample obtained was characterized by XRD, BET and SEM. XRD results showed the formation of zeolite Y in just 60 minutes. The sample showed high value of surface area, the latter being of 476.2 m² / g. The particles are agglomerated, but with a narrow distribution of size. (author)

New ion-exchanged zeolite derivatives: antifungal and antimycotoxin properties against Aspergillus flavus and aflatoxin B1

Science.gov (United States)

Savi, Geovana D.; Cardoso, Willian A.; Furtado, Bianca G.; Bortolotto, Tiago; Da Agostin, Luciana O. V.; Nones, Janaína; Torres Zanoni, Elton; Montedo, Oscar R. K.; Angioletto, Elidio

2017-08-01

Zeolites are microporous crystalline hydrated aluminosilicates with absorbent and catalytic properties. This material can be used in many applications in stored-pest management such as: pesticide and fertilizer carriers, animal feed additives, mycotoxin binders and food packaging materials. Herein, four 4A zeolite forms were prepared by ion-exchange and their antifungal effect against Aspergillus flavus was highlighted. Additionally, the antimycotoxin activity and the aflatoxin B1 (AFB1) adsorption capacity of these zeolites as well as their toxic effects on Artemia sp. were investigated. The ion-exchanged zeolites with Li+ and Cu2+ showed the best antifungal activity against A. flavus, including effects on conidia germination and hyphae morphological alterations. Regarding to antimycotoxin activity, all zeolite samples efficiently inhibited the AFB1 production by A. flavus. However, the ion-exchanged zeolites exhibited better results than the 4A zeolite. On the other hand, the AFB1 adsorption capacity was only observed by the 4A zeolite and zeolite-Li+. Lastly, our data showed that all zeolites samples used at effective concentrations for antifungal and antimycotoxin assays (2 mg ml-1) showed no toxic effects towards Artemia sp. Results suggest that some these ion-exchanged zeolites have great potential as an effective fungicide and antimycotoxin agent for agricultural and food safety applications.

Pore Topology Effects in Positron Annihilation Spectroscopy of Zeolites.

Science.gov (United States)

Zubiaga, Asier; Warringham, Robbie; Mitchell, Sharon; Gerchow, Lars; Cooke, David; Crivelli, Paolo; Pérez-Ramírez, Javier

2017-03-03

Positron annihilation spectroscopy (PAS) is a powerful method to study the size and connectivity of pores in zeolites. The lifetime of positronium within the host material is commonly described by the Tao-Eldrup model. However, one of its largest limitations arises from the simple geometries considered for the shape of the pores, which cannot describe accurately the complex topologies in zeolites. Here, an atomic model that combines the Tao potential with the crystallographic structure is introduced to calculate the distribution and lifetime of Ps intrinsic to a given framework. A parametrization of the model is undertaken for a set of widely applied zeolite framework types (*BEA, FAU, FER, MFI, MOR, UTL), before extending the model to all known structures. The results are compared to structural and topological descriptors, and to the Tao-Eldrup model adapted for zeolites, demonstrating the intricate dependence of the lifetime on the pore architecture. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Thermal change and ion exchange properties of zeolite L with cesium and strontium

International Nuclear Information System (INIS)

Mimura, Hitoshi; Akiba, Kenichi

1986-01-01

Thermal change and ion exchange properties of Cs and Sr have been studied for zeolite L. The zeolite structure is stable below 900 deg C and converts to the amorphous phase above 1000 deg C. The cesium form of zeolite L recrystallized to pollucite (CsAlSi 2 O 6 ) by calcination at 1400 deg C for 1 h or under hydrothermal condition (300 deg C, 290 atm, 24 h). Hydrogen-form zeolites were prepared by the acid treatment in 10 -2 ∼ 10 -1 M HNO 3 solutions or thermal decomposition of NH 4 form zeolites at 460 ∼ 500 deg C. The distribution of Cs and Sr was dependent on equilibrium pH and the distribution coefficient (K d ) was about 10 4 (ml/g) at pH 5 ∼ 7. The exchange capacity of Cs and Sr was 0.89 (meq./g zeolite) and exchanging ratio was 68 % at D sites in main channel. These cations in zeolite were completely eluted with 10 -1 M HNO 3 solution. (author)

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

Science.gov (United States)

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

2018-03-01

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

Characteristics of Heavy Metals Adsorption Cu, Pb and Cd Using Synthetics Zeolite Zsm-5

OpenAIRE

Priyadi,; Iskandar,; Suwardi,; Mukti, Rino Rakhmata

2015-01-01

It is generally known that zeolite has potential for heavy metal adsorption. The objectives of this study were to synthesize and characterize zeolite ZSM-5 and to figure out the adsorption capacity of zeolite ZSM-5 for heavy metals of Cu2+, Pb2+ and Cd2+. Characterization of zeolite ZSM-5 included some variables i.e. crystal structure (XRD), morphology (SEM), specific surface area and total pore volume (N2 physisorption). Adsorption capacity of zeolite ZSM-5 was analysed using a batch system...

From metal-organic squares to porous zeolite-like supramolecular assemblies

KAUST Repository

Wang, Shuang; Zhao, Tingting; Li, Guanghua; Wojtas, Łukasz; Huo, Qisheng; Eddaoudi, Mohamed; Liu, Yunling

2010-01-01

We report the synthesis, structure, and characterization of two novel porous zeolite-like supramolecular assemblies, ZSA-1 and ZSA-2, having zeolite gis and rho topologies, respectively. The two compounds were assembled from functional metal