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Sample records for direct denitration calciner

  1. Screw calciner mechanical direct denitration process for plutonium nitrate to oxide conversion

    International Nuclear Information System (INIS)

    Souply, K.R.; Sperry, W.E.

    1977-01-01

    This report describes a screw calciner direct-denitration process for converting plutonium nitrate to plutonium oxide. The information should be used when making comparisons of alternative plutonium nitrate-to-oxide conversion processes or as a basis for further detailed studies. The report contains process flow sheets with a material balance; a process description; and a discussion of the process including history, advantages and disadvantages, and additional research required

  2. Activity Based Startup Plan for Prototype Vertical Denitration Calciner

    International Nuclear Information System (INIS)

    SUTTER, C.S.

    1999-01-01

    Testing activation on the Prototype Vertical Denitration Calciner at PFP were suspended in January 1997 due to the hold on fissile material handling in the facility. The restart of testing activities will require a review through an activity based startup process based upon Integrated Safety Management (ISM) principles to verify readiness. The Activity Based Startup Plan for the Prototype vertical Denitration Calciner has been developed for this process

  3. Restart plan for the prototype vertical denitration calciner

    International Nuclear Information System (INIS)

    SUTTER, C.S.

    1999-01-01

    Testing activities on the Prototype Vertical Denitration Calciner at PFP were suspended in January 1997 due to the hold on fissile material handling in the facility. The Restart Plan will govern the transition of the test program from the completion of the activity based startup review; through equipment checkout and surrogate material runs; to resumption of the testing program and transition to unrestricted testing

  4. Restart plan for the prototype vertical denitration calciner

    Energy Technology Data Exchange (ETDEWEB)

    SUTTER, C.S.

    1999-09-01

    Testing activities on the Prototype Vertical Denitration Calciner at PFP were suspended in January 1997 due to the hold on fissile material handling in the facility. The Restart Plan will govern the transition of the test program from the completion of the activity based startup review; through equipment checkout and surrogate material runs; to resumption of the testing program and transition to unrestricted testing.

  5. CSER 95-005: PFP vertical denitration calciner

    International Nuclear Information System (INIS)

    Geiger, J.L.

    1995-01-01

    The Vertical Denitrating Calciner system will stabilize certain unique solutions containing fissile salts by removing the water and nitrate ion to produce a more easily stored powder. This end is achieved by high-firing the solution in the calciner. The resultant calcine is distinguished by particles which are larger and denser than those produced by the more conventional oxalate precipitation process. This criticality safety evaluation report examines criticality safety for the denitration system, installed in glovebox 188-1 at PFP. The examination shows that, due to the incorporation of standard criticality safety design techniques, the glovebox can be maintained subcritical with minimal reliance on administrative controls. The examination also shows that, ignoring the necessary administrative controls can make a criticality possible in glovebox 188-1. Section 3.0 of this report lists the necessary administrative controls

  6. Restart Plan for the Prototype Vertical Denitration Calciner [SD Coversheet has Incorrect Document Number

    Energy Technology Data Exchange (ETDEWEB)

    SUTTER, C.S.

    1999-07-26

    Testing activities on the Prototype Vertical Denitration Calciner at PFP were suspended in January 1997 due to the hold on fissile material handling in the facility. The Restart Plan will govern the transition of the test program from the completion of the activity based startup review; through equipment checkout and surrogate material runs; to resumption of the testing program and transition to unrestricted testing.

  7. Feasibility investigation of a denitration/conversion equipment concept (2)

    International Nuclear Information System (INIS)

    Tanimoto, Ryoji; Yoshimura, Tadahiro; Hoshino, Yasushi; Munekata, Hideki; Tamaki, Yoshihisa

    2004-02-01

    In this investigation, ceramics denitration containers with ball valve units were manufactured and preliminary tests of microwave denitration, calcination and reduction were carried out in last fiscal year. In this fiscal year, a small scale denitration/conversion apparatus with turntable system was designed and manufactured, then a series of microwave denitration/conversion tests was conducted. Feasibility of the denitration/conversion apparatus with turntable system was evaluated by checking powder properties and soundness of apparatus through the series of tests. The summary of the results are as follows; (1) By the series of microwave denitration, calcination, and reduction tests using small scale denitration/conversion apparatus with turntable system manufactured, it is confirmed that there are no critical problem in the apparatus. (2) Checking the power properties after grinding, it is confirmed that the powder is equivalent of one obtained by conventional microwave denitration/conversion facility. (3) Reduced powder was grinded and pressed to several pellets, then sintered. It was confirmed that high density pellet fuel can be obtained. (4) Studying the test results from the viewpoint of feasibility of denitration/conversion facility with turntable system, the R and D issues were made clear. (author)

  8. Technical evaluation of the direct denitration process to obtain ceramic-grade UO2 powders using microwaves

    International Nuclear Information System (INIS)

    Lorenzo, Viviana J.; Marchi, Daniel E.; Menghini, Jorge E.

    1999-01-01

    The direct denitration process to obtain ceramic-grade UO 2 powders using microwaves has been studied and developed at laboratory scale. Conditions were given to obtain powders apt for fuel pellets fabrication within the required specifications, where mechanical treatments before pressing are not necessary. This work describes the equipment used in the process, evaluates the necessary supply and waste generation and describes the characteristics of the product obtained, as well as the conditions for its fabrication. Results show that this method allows to reduce the volume of liquid wastes generated due to their partial re-utilization, simplifying their final disposal treatment, which, in addition to their operational advantages, make this method attractive from the economical point of view. (author)

  9. Pilot-scale demonstration of the modified direct denitration process to prepare uranium oxide for fuel fabrication evaluation

    International Nuclear Information System (INIS)

    Kitts, F.G.

    1994-04-01

    The Uranium-Atomic Vapor Laser Isotope Separation (U-AVLIS) Program has the objective of developing a cost-competitive enrichment process that will ultimately replace the gaseous diffusion process used in the United States. Current nuclear fuel fabricators are set up to process only the UF 6 product from gaseous diffusion enrichment. Enriched uranium-iron alloy from the U-AVLIS separator system must be chemically converted into an oxide form acceptable to these fabricators to make fuel pellets that meet American Society for Testing and Materials (ASTM) and utility company specifications. A critical step in this conversion is the modified direct denitration (MDD) that has been selected and presented in the AVLIS Conceptual Design for converting purified uranyl nitrate to UO 3 to be shipped to fabricators for making UO 2 pellets for power reactor fuel. This report describes the MDD process, the equipment used, and the experimental work done to demonstrate the conversion of AVLIS product to ceramic-grade UO 3 suitable for making reactor-grade fuel pellets

  10. Study on the mechanism of a manganese-based catalyst for catalytic NOX flue gas denitration

    Science.gov (United States)

    Zhang, Lei; Wen, Xin; Lei, Zhang; Gao, Long; Sha, Xiangling; Ma, Zhenhua; He, Huibin; Wang, Yusu; Jia, Yang; Li, Yonghui

    2018-04-01

    Manganese-based bimetallic catalysts were prepared with self-made pyrolysis coke as carrier and its denitration performance of low-temperature SCR (selective catalyst reduction) was studied. The effects of different metal species, calcination temperature, calcination time and the metal load quantity on the denitration performance of the catalyst were studied by orthogonal test. The denitration mechanism of the catalyst was analyzed by XRD (X-ray diffraction), SEM (scanning electron microscope), BET test and transient test. The experiments show that: * The denitration efficiency of Mn-based bimetallic catalysts mainly relates to the metal type, the metal load quantity and the catalyst adjuvant type. * The optimal catalyst preparation conditions are as follows: the load quantity of monometallic MnO2 is 10%, calcined at 300°C for 4h, and then loaded with 8% CeO2, calcined at 350°Cfor 3h. * The denitration mechanism of manganese-based bimetallic oxide catalysts is stated as: NH3 is firstly adsorbed by B acid center Mn-OH which nears Mn4+==O to form NH4+, NH4+ was then attacked by the gas phase NO to form N2, H2O and Mn3+-OH. Finally, Mn3+-OH was oxidized by O2 to regenerate Mn4+.

  11. Formulation Efforts for Direct Vitrification of INEEL Blend Calcine Waste Simulate: Fiscal Year 2000

    Energy Technology Data Exchange (ETDEWEB)

    Crum, Jarrod V.; Vienna, John D.; Peeler, David K.; Reamer, I. A.

    2001-03-30

    This report documents the results of glass formulation efforts for Idaho National Engineering and Environmental Laboratory (INEEL) high level waste (HWL) calcine. Two waste compositions were used during testing. Testing started by using the Run 78 calcine composition and switched to simulated Blend calcine composition when it became available. The goal of the glass formulation efforts was to develop a frit composition that will accept higher waste loading that satisfies the glass processing and product acceptance constraints. 1. Melting temperature of 1125 ? 25?C 2. Viscosity between 2 and 10 Pa?s at the melting temperature 3. Liquidus temperature at least 100?C below the melting temperature 4. Normalized release of B, Li and Na each below 1 g/m2 (per ASTM C 1285-97) Glass formulation efforts tested several frit compositions with variable waste loadings of Run 78 calcine waste simulant. Frit 107 was selected as the primary candidate for processing since it met all process and performance criteria up to 45 mass% waste loading. When the simulated Blend calcine waste composition became available Frits 107 and 108 compositions were retested and again Frit 107 remained the primary candidate. However, both frits suffered a decrease in waste loading when switching from the Run 78 calcine to simulated Blend calcine waste composition. This was due to increase concentrations of both F and Al2O3 along with a decrease in CaO and Na2O in the simulate Blend calcine waste all of which have strong impacts on the glass properties that limit waste loading of this type of waste.

  12. Synthesis and characterization of ZSM-5 and calcined kaolin evaluation using the content of structure-directing

    International Nuclear Information System (INIS)

    Rodrigues, J.J.; Silva, V.J. da; Rodrigues, M.G.F.

    2012-01-01

    This study aims to evaluate the effect of the structure-directing content, tetrapropylammonium bromide, on the structural and morphological characteristics of ZSM-5 zeolite obtained using calcined kaolin as silicon and aluminum. The samples were characterized by XRD, EDX, SEM and Physics Adsorption N 2 . Trough X ray diffraction patterns was possible to observed the formation of the structure of ZSM-5 with intense peaks and well-defined characteristic of crystalline. The micrographs showed that the samples consist of agglomerates and/or aggregates of particles characteristic of the MFI structure typical of ZSM-5 zeolite. And through the adsorption-desorption isotherms physical N2 was possible to observe that the samples show hysteresis type I typical of microporous materials with specific surface areas of 218 and 222 m 2 /g. Therefore, the use of calcined kaolin to obtain ZSM-5 zeolite was effective. (author)

  13. Thermal denitration and mineralization of waste constituents

    Energy Technology Data Exchange (ETDEWEB)

    Nenni, J.A.; Boardman, R.D.

    1997-08-01

    In order to produce a quality grout from LLW using hydraulic cements, proper conditioning of the waste is essential for complete cement curing. Several technologies were investigated as options for conditions. Since the LLW is dilute, removal of all, or most, of the water will significantly reduce the final waste volume. Neutralization of the LLW is also desirable since acidic liquids to not allow cement to cure properly. The nitrate compounds are very soluble and easily leached from solid waste forms; therefore, denitration is desirable. Thermal and chemical denitration technologies have the advantages of water removal, neutralization, and denitration. The inclusion of additives during thermal treatment were investigated as a method of forming insoluable waste conditions.

  14. Thermal denitration and mineralization of waste constituents

    International Nuclear Information System (INIS)

    Nenni, J.A.; Boardman, R.D.

    1997-01-01

    In order to produce a quality grout from LLW using hydraulic cements, proper conditioning of the waste is essential for complete cement curing. Several technologies were investigated as options for conditions. Since the LLW is dilute, removal of all, or most, of the water will significantly reduce the final waste volume. Neutralization of the LLW is also desirable since acidic liquids to not allow cement to cure properly. The nitrate compounds are very soluble and easily leached from solid waste forms; therefore, denitration is desirable. Thermal and chemical denitration technologies have the advantages of water removal, neutralization, and denitration. The inclusion of additives during thermal treatment were investigated as a method of forming insoluable waste conditions

  15. Chemical denitration of aqueous nitrate solutions

    International Nuclear Information System (INIS)

    Burrill, K.A.

    1987-11-01

    The Plant for Active Waste Liquids (PAWL) at CRNL will immobilize in glass the fission products in waste from Mo-99 production. The nitrate ions in the waste can be destroyed by heating, but also by chemical reaction with formic acid (HCOOH). Since chemical denitration has several advantages over thermal denitration it was studied in the course of vitrification process development. Two free radical mechanisms are examined here to explain kinetic data on chemical denitration of nitric acid solutions with formic acid. One mechanism is applicable at > 1 mol/L HNO 3 and involves the formate radical (HCOO . ). The second mechanism holds at 3 and involves the hyponitrous radical (HNO . ). Mass balances for various species were written based on the law of mass action applied to the equations describing the reaction mechanism. Analytical and numerical solutions were obtained and compared. Literature data on batch denitration were used to determine some of the rate constants while others were set arbitrarily. Observed stoichiometry and trends in reactant concentrations are predicted accurately for batch data. There are no literature data to compare with the prediction of negligible induction time

  16. Spray calcination of nuclear wastes

    International Nuclear Information System (INIS)

    Bonner, W.F.; Blair, H.T.; Romero, L.S.

    1976-01-01

    The spray calciner is a relatively simple machine; operation is simple and is easily automated. Startup and shutdown can be performed in less than an hour. A wide variety of waste compositions and concentrations can be calcined under easily maintainable conditions. Spray calcination of all commercial fuel reprocessor high-level liquid wastes and mixed high and intermediate-level wastes have been demonstrated. Wastes have been calcined containing over 2M sodium. Thus waste generated during plant startup and shutdown can be blended with normal waste and calcined. Spray calcination of ILLW has also been demonstrated. A remotely replaceable atomizing nozzle has been developed for use in plant scale equipment. The 6 mm (0.25 inch) orifice and ceramic tip offer freedom from plugging and erosion thus nozzle replacement should be required only after several months operation. Calciner capacity of over 75 l/h (20 gal/h) has been demonstrated in pilot scale equipment. Sintered stainless steel filters are effective in deentraining over 99.9 percent of the solids that result from calcining the feedstock. Since such a small amount of radionuclides escape the calciner the volume of recycle required from the effluent treatment system is very small. The noncondensable off-gas volume is also low, less than 0.5 m 3 /min (15 scfm) for a liquid feedrate of 75 l/hr (20 gal/hr). Calcine holdup in the calciner is less than 1 kg, thus the liquid feedrate is directly relatable to calcine flowrate. The calcine produced is very fine and reactive. Successful remote operation and maintenance of a heated wall spray calciner has been demonstrated while processing actual high-level waste. During these operations radionuclide volatilization from the calciner was acceptably low. 8 figures

  17. Formulation Efforts for Direct Vitrification of INEEL Blend Calcine Waste Simulate: Fiscal Year 2000

    International Nuclear Information System (INIS)

    Crum, Jarrod V; Vienna, John D; Peeler, David K

    2001-01-01

    The TFA uses a systematic process for developing its annual program that draws from the tanks science and technology development needs expressed by the five DOE tank waste sites. TFA's annual program development process is iterative and involves the following steps: Collection of site needs; Needs analysis; Development of technical responses and initial prioritization; Refinement of the program for the next fiscal year; Formulation of the Corporate Review Budget (CRB); Preparation of Program Execution Guidance (PEG) for the next FY Revision of the Multiyear Program Plan (MYPP). This document describes the outcomes of the first phase of this process, from collection of site needs to the initial prioritization of technical activities. The TFA received site needs in October- December 2000. A total of 170 site needs were received, an increase of 30 over the previous year. The needs were analyzed and integrated, where appropriate. Sixty-six distinct technical responses were drafted and prioritized. In addition, seven strategic tasks were approved to compete for available funding in FY 2002 and FY 2003. Draft technical responses were prepared and provided to the TFA Site Representatives and the TFA User Steering Group (USG) for their review and comment. These responses were discussed at a March 15, 2001, meeting where the TFA Management Team established the priority listing in preparation for input to the DOE Office of Science and Technology (OST) budget process. At the time of publication of this document, the TFA continues to finalize technical responses as directed by the TFA Management Team and clarify the intended work scopes for FY 2002 and FY 2003

  18. The denitration of simulated fast reactor highly active liquor waste

    International Nuclear Information System (INIS)

    Saum, C.J.; Ford, L.H.; Platts, N.

    1981-11-01

    Vitrification of the highly active arisings from PFR fuel reprocessing is proposed as the optimum long-term solution to the disposal problem. During vitrification ruthenium volatilises as the tetroxide. Evidence is presented which indicates that a substantial reduction in volatility can be effected by denitration of the liquid feed by treatment with formic acid. The kinetics and stoichiometry of the reactions involved in denitration are examined and empirical rate equations developed. The predictions of the empirical rate equation have been confirmed using a one-tenth scale continuous denitrator, thus giving confidence for the design of full-scale units. (author)

  19. Influence of calcination temperature on the morphology and energy storage properties of cobalt oxide nanostructures directly grown over carbon cloth substrates

    KAUST Repository

    Baby, Rakhi Raghavan

    2013-09-23

    Nanostructured and mesoporous cobalt oxide (Co3O4) nanowire in flower-like arrangements have been directly grown over flexible carbon cloth collectors using solvothermal synthesis for supercapacitor applications. Changes in the morphology and porosity of the nanowire assemblies have been induced by manipulating the calcination temperature (200–300 °C) of the one-dimensional (1-D) structures, resulting in significant impact on their surface area and pseudocapacitive properties. As the calcination temperature increases from 200 to 250 °C, the flower morphology gradually modifies to the point where the electrolyte could access almost all the nanowires over the entire sample volume, resulting in an increase in specific capacitance from 334 to 605 Fg−1, depending on the nanowire electrode morphology. The 300 °C calcination results in the breakdown of the mesoporous morphology and decreases the efficiency of electrolyte diffusion, resulting in a drop in pseudocapacitance after 300 °C. A peak energy density of 44 Wh kg−1 has been obtained at a power density of 20 kW kg−1 for the 250 °C calcined sample.

  20. Physical, Chemical and Structural Evolution of Zeolite - Containing Waste Forms Produced from Metakaolinite and Calcined HLW

    Energy Technology Data Exchange (ETDEWEB)

    Grutzeck, Michael

    2005-06-01

    During the seventh year of the current grant (DE-FG02-05ER63966) we completed an exhaustive study of cold calcination and began work on the development of tank fill materials to fill empty tanks and control residuals. Cold calcination of low and high NOx low activity waste (LAW) SRS Tank 44 and Hanford AN-107 simulants, respectively with metallic Al + Si powders was evaluated. It was found that a combination of Al and Si powders could be used as reducing agents to reduce the nitrate and nitrite content of both low and high NOx LAW to low enough levels to allow the LAW to be solidified directly by mixing it with metakaolin and allowing it to cure at 90 C. During room temperature reactions, NOx was reduced and nitrogen was emitted as N2 or NH3. This was an important finding because now one can pretreat LAW at ambient temperatures which provides a low-temperature alternative to thermal calcination. The significant advantage of using Al and Si metals for denitration/denitrition of the LAW is the fact that the supernate could potentially be treated in situ in the waste tanks themselves. Tank fill materials based upon a hydroceramic binder have been formulated from mixtures of metakaolinite, Class F fly ash and Class C flue gas desulphurization (FGD) ash mixed with various concentrations of NaOH solution. These harden over a period of hours or days depending on composition. A systematic study of properties of the tank fill materials (leachability) and ability to adsorb and hold residuals is under way.

  1. Description and starting of the VERA denitration plant

    International Nuclear Information System (INIS)

    Kartes, H.; Koschorke, H.; Kaufmann, F.

    1977-05-01

    In the beginning of 1976 a plant for denitration of high and medium level fission product solutions has been set in inactive operation in the Karlsruhe Nuclear Research Center. The plant and its several components are presented. The operation and the start-up are described in detail. Also the methods of measurement important for controlling the process are explained. The procedure for denitration of medium level waste with a molarity of 1.5 is described in detail. In this connection a discussion of possible failures is included. (orig.) [de

  2. Calcination of liquid radioactive wastes. Part II

    International Nuclear Information System (INIS)

    Ditl, P.; Jecmen, J.; Napravnik, J.; Neumann, L.

    1983-01-01

    An attempt is made to design a universal modular system of machine equipment for processing wastes of different composition. First-stage concentration of radioactive wastes is assumed to 200 - 500 kg/m 3 which is solved by the inclusion in the system of a single-stage circulation evaporator. Another equipment is the intermittently operating charging reactor with a high-speed stirrer for denitration or other chemical treatment. The types of mixers and the geometrical configuration of the system are described in detail. Also described is the equipment for water evaporation from the chemically treated solution. Several types of equipment have been designed for calcination. The most suitable is the equipment using the principle of a film evaporator. Several solutions are described which comprise the basis for the horizontal calciner for processing 10 l of active wastes per hour with several variants of sealings and heating systems. The performance tests of the equipment were successful in active and non-active operation. (M.D.)

  3. Simulation of Calcite Calcination

    Directory of Open Access Journals (Sweden)

    A. G. Коzhevnikov

    2006-01-01

    Full Text Available Mathematical modeling and experimental investigation results of heat transfer in the case of calcite calcinations in regenerative shaft furnaces are given in the paper. Influence of heating gas temperature, calcined material fragment size and desired final product output on the duration of calcite calcination has been studied. It has been shown that with the given percentage of final product output and permissible changes in heating gas temperature in the furnace it is the fraction size of the calcined material that greatly determines such parameter as a process duration.

  4. Application of microwaves in the denitration of nitric solutions of uranium and/or plutonium

    International Nuclear Information System (INIS)

    Quesada, C.A.; Adelfang, P.

    1990-01-01

    A method for the conversion of nitric solutions of uranium and/or plutonium that would be an alternative more economic and operatively simpler than the conventional processes is the direct denitration by means of microwaves and vacuum application. This conversion method has the following technical advantages: a) the process is simple, which allows a stable operation; b) neither the addition of chemical reagents nor the dilution of the starting solution are required, thereby the volume of residual liquids is small as compared with other processes; c) one fraction of the evaporation residues is nitric acid which can be reused. The development (on laboratory scale) of this conversion process was initiated. In this first stage, a description of the employed equipment is presented. An example of one of the evaporation and denitration batches and obtained products are fully described. The operative experience leads to deduce that the equipment is satisfactory, due to the following characteristics: 1) it permits an easy manipulation within the glove boxes; 2) the projections, coming out from the reactor, are retained completely; 3) the microwaves oven and the vacuum pump are effectively protected from the corrosive vapors. It is concluded that the employed experimental device is adequate to obtain the necessary materials for the reduction, pressing and sinterability studies. This equipment is adopted for the integral development of sintered pellets fabrication process. (Author) [es

  5. Application of NO Reduction Dynamical Model in SNCR Denitration System Based on Biomass

    Directory of Open Access Journals (Sweden)

    Feng Ran

    2016-06-01

    Full Text Available In recent years, studies on denitration by applying biomass reburning method has drawn the attention of many researchers due to the characteristics of low sulfur and nitrogen content, high volatile, high ash focal activity, zero CO2 net emissions, etc. Based on Chemkin software and selective non-catalytic reduction (SNCR denitration chemical kinetic model, this paper conducted SNCR denitration chemical kinetic modeling. And the results showed that: with the increase of residence time, under the different initial concentration of NO, SNCR denitration efficiency tends to stabilize after the first increase. Moreover, the higher the initial concentration of NO, the longer the residence time which is required to achieve the greatest denitration efficiency. With the increase of ammonia nitrogen ratio, SNCR denitration efficiency increases step by step. When the normalized stoichiometric ratio (NSR is greater than 1.5, the denitration efficiency is at a basic stable state. Under the same conditions, simulation results of the SNCR results agree well with the test results. Therefore, it can be concluded that carrying out the SNCR denitration chemical dynamics simulation using Chemkin software can provide a reference for tests and mechanism researches on SNCR, biomass reburning and advanced reburning denitration.

  6. [Infrared spectral analysis for calcined borax].

    Science.gov (United States)

    Zhao, Cui; Ren, Li-Li; Wang, Dong; Zhou, Ping; Zhang, Qian; Wang, Bo-Tao

    2011-08-01

    To valuate the quality of calcined borax which is sold in the market, 18 samples of calcined borax were studied using the Fourier transform infrared, and samples with different water content were selected and analyzed. Then, the results of analysis were used to evaluate the quality of calcined borax. Results show that the infrared spectra of calcined borax include OH vibration, BO3(-3) vibration and BO4(5-) vibration absorption bands. The position and width of OH vibration absorption band depend on the level of water content, and the more the water content, the wider the absorption band. The number of BO3(3-) vibration and BO4(5-) vibration bands also depend on the level of water content, and the more the water content, and the stronger the hydrogen bond and the lower the symmetry of B atoms, the more the number of infrared absorption peaks. It was concluded that because the quality of calcined borax has direct correlation with water content, the infrared spectroscopy is an express and objective approach to quality analysis and evaluation of calcined borax.

  7. Characterization of the precipitates formed during the denitration of simulated HRLW

    International Nuclear Information System (INIS)

    Music, S.; Ristic, M.; Popovic, S.

    1989-01-01

    The denitration of several chemical compositions of simulated highly radioactive liquid waste (HRLW) was performed using formic acid as reducing agent. Precipitates formed during the denitration of simulated HRLW were analyzed using x-ray diffraction and 57 Fe Moessbauer spectroscopy. Goethite and amorphous fractions were the principal phases in these precipitates. It was found that the chemical composition of HRLW and the experimental conditions of denitration had more influence on the crystal formation and the particle size than on the phase composition of the precipitates. (author) 27 refs.; 6 figs.; 6 tabs

  8. DENITRATION OF WASTEWATER GENERATED BY NITROSATION OF ORGANIC COMPOUNDS

    Directory of Open Access Journals (Sweden)

    BORIS M. LASKIN

    2017-12-01

    Full Text Available Subject of the article was to study the method aimed at denitration of liquid wastes that appear during the nitrosation of organic compounds. Liquid waste represents an aqueous solution of sodium sulfate with sodium nitrate and nitrite as admixtures. The method involves addition of sulfuric acid to the wastes followed by drying and thermal treatment of a salt mixture at temperature above 150 °C. Experimental study revealed that sodium nitrite fully decomposes in the solution during the drying resulting in formation of sodium sulfate, nitrogen oxide, and nitrogen dioxide. Solid-phase interaction of sodium hydrogen sulfate and sodium nitrate was investigated by combined DSC-TG technique in the temperature range 100 - 270 °C. The mixture of salts was obtained by drying the aqueous solution. It was shown that the reaction rate is defined by the removal rate of vapors formed nitric acid.

  9. Operating experience and development of fluidized-bed denitrators for UNH at Tokai Reprocessing Plant

    International Nuclear Information System (INIS)

    Sasaki, Minoru; Nakamichi, Hideya; Takeda, Seiichiro; Kubota, Kanya; Katoh, Shuji

    1983-01-01

    The fluidized bed denitrator for uranyl nitrate hexahydrate (UNH) at Tokai reprocessing plant has been operated since 1976. About 170 tons of spent fuel have been reprocessed, and the denitrator has encountered numerous operational problems during the period. This report deals with these technical problems and the associated countermeasures taken, including the dismantling and reconstruction of equipment and the improvement of operating method. The major problems encountered were as follows: (1) the crystallization of UNH on the UNH feeding line, (2) spray nozzle clogging and candle filter clogging, (3) particle growth, (4) plugging of the drawing-out line by nozzle caking, and (5) slugging in fluidized-bed denitration. The total quantity and quality of UO 3 products obtained so far at the plant are also briefly described together with some future R and D programs such as the improvement of UO 3 reactivity and the automation of denitrators. (Aoki, K.)

  10. The flashcal process for the fabrication of fuel-metal oxides using the whiteshell roto-spray calciner

    International Nuclear Information System (INIS)

    Sridhar, T.S.

    1988-01-01

    A one-step, continuous, thermochemical calcination process, called the FLASHCAL (Flash Calcination) process has been developed for the production of single- and mixed-oxide powders of fuel metals (uranium, thorium and plutonium) from the respective nitrate solutions using the Whiteshell Roto-Spray Calciner (RSC). The metal-nitrate feed solution, either by itself or mixed with a suitable chemical reactant or additive, is converted to its oxide powder in the RSC at temperatures between 300 and 600 0 C. Rapid denitration takes place in the calciner, yielding the metal-oxide powders while simultaneously destroying any excess chemical additive and reaction by-products. In the production of precursor oxide powders suitable for fuel fabrication, the FLASHCAL process has advantages over batch calcination and other processes that involve precipitation and filtration steps because fewer processing and handling operations are needed. Results obtained with thorium nitrate and uranium nitrate-thorium nitrate mixtures indicate that some measure of control over the size distribution and morphology of the oxide product powders is possible in this process with the proper selection of chemical additive, as well as the operating parameters of the calciner

  11. Dissolution Kinetics of Alumina Calcine

    Energy Technology Data Exchange (ETDEWEB)

    Batcheller, Thomas Aquinas

    2001-09-01

    Dissolution kinetics of alumina type non-radioactive calcine was investigated as part of ongoing research that addresses permanent disposal of Idaho High Level Waste (HLW). Calcine waste was produced from the processing of nuclear fuel at the Idaho Nuclear Technology and Engineering Center (INTEC). Acidic radioactive raffinates were solidified at ~500°C in a fluidized bed reactor to form the dry granular calcine material. Several Waste Management alternatives for the calcine are presented in the Idaho High Level Waste Draft EIS. The Separations Alternative addresses the processing of the calcine so that the HLW is ready for removal to a national geological repository by the year 2035. Calcine dissolution is the key front-end unit operation for the separations alternative.

  12. Investigation on Calcination Behaviors of Coal Gangue by Fluidized Calcination in Comparison with Static Calcination

    Directory of Open Access Journals (Sweden)

    Shuai Yuan

    2017-02-01

    Full Text Available In order to comprehensively utilize coal gangue, we present fluidized calcination as a new thermal technology for activating coal gangue and systematical study was conducted in comparison with static calcination. The calcined products obtained by different calcination methods under various temperatures were characterized by the means of X-ray diffraction (XRD, thermal gravimetry-differential scanning calorimeter (TG-DSC, Fourier transform-infrared spectroscopy (FT-IR and scanning electron microscope-energy dispersive spectrometer (SEM-EDS. Chemical and physical characteristics such as aluminium leaching rate, chemical oxygen demand and whiteness of calcined products were also investigated. The results show that aluminium leaching rate could reach to the maximal value 74.42% at 500 °C by fluidized calcination, while the maximal value of 66.33% could be reached at 600 °C by static calcination. Products by fluidized calcination obtained higher whiteness and lower chemical oxygen demand (COD under the same calcination temperature. The well-crystallized kaolinite transform to amorphous meta-kaolinite under 600 °C and mullite presence under 1000 °C according to phase transformation, chemical bond variation and microstructure evolution analysis. Fluidized calcination was more efficiently for combustion of carbon/organic matter and dehydroxylation of kaolinite, which might applied in coal gangue industry in future.

  13. Study on denitration technology of coal char reduction method

    Directory of Open Access Journals (Sweden)

    Wenjie FU

    2016-06-01

    Full Text Available In order to more effectively control NO emissions in coal-fired flue gas, the denitration reaction is carried out with simulated industrial boiler flue gas in a fixed bed reactor. The influence of char types, reaction conditions, the composition of flue gas and other factors on the conversion rate of NO are discussed. The result shows that the industrial semi-coke is the most suitable experimental coal in the three coals studied, and the industrial semi-coke particle size of 0.6 ~ 10 mm is relatively suitable; The conversion rate of NO increases gradually with the increase of temperature, and when the reaction temperature is 700 ℃ and the space velocity is 10 000 h-1, the conversion rate of NO can reach 99%; the conversion rate of NO decreases gradually as airspeed increases, but the airspeed change has no effect on the conversion rate of NO at 700 ℃; under anaerobic conditions,the change of NO concentration has no effect on the conversion rate of NO; at the same temperature, NO conversion rate is higher at the presence of oxygen compared with that at anaerobic situation, and the conversion rate of NO is the highest when O2 concentration is 4%; under aerobic conditions, the concentration change of SO2 and CO2 has no effect on the conversion rate of NO.

  14. Research on the conversion of highly enriched uranium (HEU) nitrate by using the microwave denitration

    International Nuclear Information System (INIS)

    Bao Weimin; Song Chongli

    1998-08-01

    In order to simplify the denitration process by microwave heating, the uranyl nitrate is firstly denitrated and converted into UO 3 . The produced UO 3 was then further heated in the microwave field to transfer UO 3 to U 3 O 8 and to form a single product of U 3 O 8 . When the phase transfer from UO 3 to U 3 O 8 occurs, the temperature of the product increases 200∼300 degree C in two minutes. The phase-transfer temperature can be controlled by the input power of microwave. High quality U 3 O 8 can be obtained at a denitration temperature about 500 degree C. It contains no residual NO x and has a specific surface area great than 3 m 2 /g. The denitration temperature is measured with an IR-thermometer and checked with an optic fiber thermometer. The working curve and process parameter were studied in a microwave denitration unit for high enriched uranyl nitrate solution (90 g(U)/L, 4 mol/L HNO 3 and 1.2 L per batch)

  15. Denitration of glycerol trinitrate by resting cells and cell extracts of Bacillus thuringiensis/cereus and Enterobacter agglomerans.

    Science.gov (United States)

    Meng, M; Sun, W Q; Geelhaar, L A; Kumar, G; Patel, A R; Payne, G F; Speedie, M K; Stacy, J R

    1995-07-01

    A number of microorganisms were selected from soil and sediment samples which were known to have been previously exposed to nitrate ester contaminants. The two most effective bacteria for transforming glycerol trinitrate (GTN) were identified as Bacillus thuringiensis/cereus and Enterobacter agglomerans. For both isolates, denitration activities were expressed constitutively and GTN was not required for induction. Dialysis of cell extracts from both isolates did not affect denitration, which indicates that dissociable and depletable cofactors are not required for denitration. With thin-layer chromatography and high-performance liquid chromatography, the denitration pathway for both isolates was shown to be a sequential denitration of GTN to glycerol dinitrate isomers, glycerol mononitrate isomers, and ultimately to glycerol. GTN was observed to be completely converted to glycerol during a long-term incubation of cell extracts.

  16. Dynamic simulation in the process of pressurized denitration based on oxy-fuel combustion

    Science.gov (United States)

    Huang, Qiang; Zhou, Dong

    2018-02-01

    Oxy-fuel combustion is considered as one of the most promising technologies for capturing CO2 from coal-fired power plants. It will greatly reduce the cost of gas purification if we remove NOx in the process of compression, which is the characteristic of oxy-combustion. In this paper, simulation of denitration process of oxy-fuel combustion flue gas was realized by the Aspen Plus software, systematically analyzed the effect of temperature, pressure, initial concentration of O2 and NO in the denitration process. Results show that the increasing of pressure, initial concentration of O2, initial concentration of NO and the decrease of temperature are all beneficial to the denitration process.

  17. SPRAY CALCINATION REACTOR

    Science.gov (United States)

    Johnson, B.M.

    1963-08-20

    A spray calcination reactor for calcining reprocessin- g waste solutions is described. Coaxial within the outer shell of the reactor is a shorter inner shell having heated walls and with open regions above and below. When the solution is sprayed into the irner shell droplets are entrained by a current of gas that moves downwardly within the inner shell and upwardly between it and the outer shell, and while thus being circulated the droplets are calcined to solids, whlch drop to the bottom without being deposited on the walls. (AEC) H03 H0233412 The average molecular weights of four diallyl phthalate polymer samples extruded from the experimental rheometer were redetermined using the vapor phase osmometer. An amine curing agent is required for obtaining suitable silver- filled epoxy-bonded conductive adhesives. When the curing agent was modified with a 47% polyurethane resin, its effectiveness was hampered. Neither silver nor nickel filler impart a high electrical conductivity to Adiprenebased adhesives. Silver filler was found to perform well in Dow-Corning A-4000 adhesive. Two cascaded hot-wire columns are being used to remove heavy gaseous impurities from methane. This purified gas is being enriched in the concentric tube unit to approximately 20% carbon-13. Studies to count low-level krypton-85 in xenon are continuing. The parameters of the counting technique are being determined. The bismuth isotopes produced in bismuth irradiated for polonium production are being determined. Preliminary data indicate the presence of bismuth207 and bismuth-210m. The light bismuth isotopes are probably produced by (n,xn) reactions bismuth-209. The separation of uranium-234 from plutonium-238 solutions was demonstrated. The bulk of the plutonium is removed by anion exchange, and the remainder is extracted from the uranium by solvent extraction techniques. About 99% of the plutonium can be removed in each thenoyltrifluoroacetone extraction. The viscosity, liquid density, and

  18. Study of the calcination temperature in samples of calcium phosphate synthesized by the method of direct way; Estudo da temperatura de calcinacao em amostras de fosfatos de calcio sintetizadas pelo metodo de via direta

    Energy Technology Data Exchange (ETDEWEB)

    Lima, M.G.; Santos, P.T.A.; Costa, A.C.F.M, E-mail: patyquimica@hotmail.com [Universidade Federal de Campina Grande (DEMA/UFCG), PB (Brazil). Unidade Academica de Engenharia de Materiais

    2012-07-01

    The use of phosphates in bioceramics have attracted the interest of many researchers, especially when it is in the Ca / P = 1.67, which allows the obtention of the hydroxyapatite. This work aims to investigate different calcination temperatures on the structural and morphological characteristics of samples of calcium phosphates synthesized by the method of direct way, aiming for hydroxyapatite as a major phase. For this purpose, we used the calcium hydroxide and phosphoric acid in the Ca / P = 1.67. The samples were calcined at temperatures of 600, 700, 800, 900, 1000, 1100, 1200 and 1350°C/2h, and characterized by XRD, FTIR and Size Distribution. The XRD showed that 600-800°C, the major phase is the tricalcium phosphate, 900-1100°C, there is a phase calcium pyrophosphate. And at 1200 and 1350 ° C, there is a phase monetite. The infrared spectrum showed the characteristic vibrations of calcium phosphates in all conditions studied. It was observed from the results of FTIR presence of bands of the P-OH group and HPO{sub 4}{sup 2-}, PO{sub 4}{sup 3}, for all temperatures studied. The highest average size of agglomerates of 108.05 mM was observed for the temperature of 1100 ° C. (author)

  19. Calcination/dissolution residue treatment

    International Nuclear Information System (INIS)

    Knight, R.C.; Creed, R.F.; Patello, G.K.; Hollenberg, G.W.; Buehler, M.F.; O'Rourke, S.M.; Visnapuu, A.; McLaughlin, D.F.

    1994-09-01

    Currently, high-level wastes are stored underground in steel-lined tanks at the Hanford site. Current plans call for the chemical pretreatment of these wastes before their immobilization in stable glass waste forms. One candidate pretreatment approach, calcination/dissolution, performs an alkaline fusion of the waste and creates a high-level/low-level partition based on the aqueous solubilities of the components of the product calcine. Literature and laboratory studies were conducted with the goal of finding a residue treatment technology that would decrease the quantity of high-level waste glass required following calcination/dissolution waste processing. Four elements, Fe, Ni, Bi, and U, postulated to be present in the high-level residue fraction were identified as being key to the quantity of high-level glass formed. Laboratory tests of the candidate technologies with simulant high-level residues showed reductive roasting followed by carbonyl volatilization to be successful in removing Fe, Ni, and Bi. Subsequent bench-scale tests on residues from calcination/dissolution processing of genuine Hanford Site tank waste showed Fe was separated with radioelement decontamination factors of 70 to 1,000 times with respect to total alpha activity. Thermodynamic analyses of the calcination of five typical Hanford Site tank waste compositions also were performed. The analyses showed sodium hydroxide to be the sole molten component in the waste calcine and emphasized the requirement for waste blending if fluid calcines are to be achieved. Other calcine phases identified in the thermodynamic analysis indicate the significant thermal reconstitution accomplished in calcination

  20. Ultrasonic effect on RuO2 nanostructures prepared by direct calcination of two new Ru(II)-organic supramolecular polymers.

    Science.gov (United States)

    Jin, Chang; Bigdeli, Fahime; Jin, Zhi-Min; Xie, Yong-Rong; Hu, Mao-Lin; Morsali, Ali

    2017-11-01

    Two novel Ru(II) complexes [(η 6 -p-cymene)RuCl(L1)]PF 6 (R1) and [(η 6 -C 6 H 6 )RuCl(L1)]PF 6 (R3) with ligand (E)-4-(methylthio)-N-((quinolin-2-yl)methylene)benzenamine (L1), were synthesized and investigated using elemental analysis, IR, 1 H NMR, 13 C NMR spectroscopy and X-ray crystallography. Complexes R1 and R3 have coordination environments with formulated (η 6 -p-cymene)Ru(N 2 Cl) and (η 6 -C 6 H 6 )Ru(N 2 Cl) respectively. The thermal stabilities of compounds R1 and R3 were studied by thermal gravimetric (TG) and differential scanning calorimetry (DSC). The binding of the complexes R1 and R3 to calf thymus DNA (CT DNA) was investigated by using electronic absorption spectra, fluorescence and redox behavior studies. Such experimental data showed that there are interactions between complexes and CT-DNA and the nature of this binding is electrostatic interaction type. Calcination of ultrasonic treated R1 and R3 results in the formation of nanoparticles of RuO 2 . The nanoparticles were characterized by IR spectroscopy and X-ray diffraction (XRD). Also size and morphology of nanoparticles were investigated by scanning electron microscopy (SEM). Copyright © 2017 Elsevier B.V. All rights reserved.

  1. Alternative calcination development status report

    International Nuclear Information System (INIS)

    Boardman, R.D.

    1997-12-01

    The Programmatic Spent Nuclear Fuel and (INEEL) Environmental Restoration and Waste Management Programs Environmental Impact Statement Record of Decision, dated June 1, 1995, specifies that high-level waste stored in the underground tanks at the ICPP continue to be calcined while other options to treat the waste are studied. Therefore, the High-Level Waste Program has funded a program to develop new flowsheets to increase the liquid waste processing rate. Simultaneously, a radionuclide separation process, as well as other options, are also being developed, which will be compared to the calcination treatment option. Two alternatives emerged as viable candidates; (1) elevated temperature calcination (also referred to as high temperature calcination), and (2) sugar-additive calcination. Both alternatives were determined to be viable through testing performed in a lab-scale calcination mockup. Subsequently, 10-cm Calciner Pilot Plant scoping tests were successfully completed for both flowsheets. The results were compared to the standard 500 C, high-ANN flow sheet (baseline flowsheet). The product and effluent streams were characterized to help elucidate the process chemistry and to investigate potential environmental permitting issues. Several supplementary tests were conducted to gain a better understanding of fine-particles generation, calcine hydration, scrub foaming, feed makeup procedures, sugar/organic elimination, and safety-related issues. Many of the experiments are only considered to be scoping tests, and follow-up experiments will be required to establish a more definitive understanding of the flowsheets. However, the combined results support the general conclusion that flowsheet improvements for the NWCF are technically viable

  2. Progress on flue gas desulfurization and denitration with electron beam irradiation in CAEP

    International Nuclear Information System (INIS)

    Ren Min; Wang Baojian; Yang Ruizhuang; Huang Wenfeng; He Xiaohai; Mao Benjiang

    2005-01-01

    The first pilot plant with electron beam irradiation for desulfurization and denitration of flue gas in China and the experimental results based on the pilot plant are briefly introduced in this paper. The FGD (flue gas desulfurization) demonstration installation designed by CAEP (China Academy of Engineering Physics) in Beijing Jingfeng Thermal Powe Co., Ltd. is recommended. (author)

  3. Characteristics of a continuous denitration by formic acid - electrolytic trimming of residual acid with accompanying the precipitation of metal ions

    International Nuclear Information System (INIS)

    Kim, G. W.; Kim, S. H.; Lim, J. G.; Lee, I. H.

    2003-01-01

    This work has studied the characteristics of destruction of nitric acid and precipitation of several metal ions in a continuous denitration process combining a denitration by formic acid and a residual acid-electrolytic trimming system. The metal ions of Zr, Mo, Fe, and Nd did not affect the electrodes at the step of electrolytic trimming of the residual acid after denitration by formic acid. The Mo ion in electrolytic solution enhanced the generation of nitrite ion during the electrolytic reaction. The mole ratio of formic acid to nitric acid fed into the continuous denitration reactor using formic acid affected much the final acidity, the precipitation yields of metal ions, the precipitate morphology. At the ratio of 1.65, the process had the lowest final acidity of less than 0.1 M, and the precipitation yields of Zr and Mo reached 95% and 83%, respectively as the highest values

  4. Conditioning of HLW-calcines

    International Nuclear Information System (INIS)

    Kofler, O.; Neuman, W.

    1977-12-01

    PyC-coating of simulated HLW-calcines from a fluidized bed calciner was studied. As the wellknown properties of PyC layers meet the demands, which were made in HTR fuel production, for the similar problems a suitable protection of granules by such coating is expected. To avoid volatilization of radioactive components the coating temperature should not exceed 1300 K in regard of the thermal stability of granules, too. Therefore, acetylene was used as coating gas. The obtained low efficiency caused a great content of hydrocarbons and soot in the off gas. Since disturbing effects by deposition of its can occur, a device was designed for burning off these substances. Ceramographical and microoptical controls were performed on each layer. Density and thickness were determined (p approximately 1,88 g/cm 3 , d 140 μ) and leaching behaviour and mechanical strength were tested, too. The obtained results showed an excellent stability of waste products conditioned by PyC-coating, but you have to consider the suitable temperature range is limited and, therefore, calcines have to be heatresistant up to 1220 K. (author)

  5. Mathematical modeling of an in-line low-NOx calciner

    DEFF Research Database (Denmark)

    Iliuta, Ion; Dam-Johansen, Kim; Jensen, Lars Skaarup

    2002-01-01

    is very important. A heterogeneous, dynamic mathematical model for an in-line low-NOx calciner based on non-isothermal diffusion reaction models for char combustion and limestone calcination has been developed. The importance of the rate at which preheated combustion air was mixed into the main flow...... transport limitation is significant for the endothermic limestone calcination. The rate at which preheated combustion air is mixed into the main flow directly influences the coal combustion rate, and thereby through the rate of heat release from combustion, it also influences the calcination rate...

  6. Summary of Waste Calcination at INTEC

    Energy Technology Data Exchange (ETDEWEB)

    O' Brien, Barry Henry; Newby, Bill Joe

    2000-10-01

    Fluidized-bed calcination at the Idaho Nuclear Technologies and Engineering Center (INTEC, formally called the Idaho Chemical Processing Plant) has been used to solidify acidic metal nitrate fuel reprocessing and incidental wastes wastes since 1961. A summary of waste calcination in full-scale and pilot plant calciners has been compiled for future reference. It contains feed compositions and operating conditions for all the processing campaigns for the original Waste Calcining Facility (WCF), the New Waste Calcining Facility (NWCF) started up in 1982, and numerous small scale pilot plant tests for various feed types. This summary provides a historical record of calcination at INTEC, and will be useful for evaluating calcinability of future wastes.

  7. Kinetic Study of Calcination of Jakura Limestone Using Power Rate ...

    African Journals Online (AJOL)

    The calcination of Jakura limestone was also found to be first order reaction with respect to CaCO3 concentration having average regression coefficient of 0.99. The temperature dependent terms were found using Arrhenius law and it was observed that the reaction temperature has a direct effect on the rate of reaction.

  8. Volatilities of ruthenium, iodine, and technetium on calcining fission product nitrate wastes

    International Nuclear Information System (INIS)

    Rimshaw, S.J.; Case, F.N.

    1980-01-01

    Various high-level nitrate wastes were subjected to formic acid denitration. Formic acid reacts with the nitrate anion to yield noncondensable, inert gases according to the following equation: 4 HCOOH + 2 HNO 3 → N 2 O + 4 CO 2 + 5 H 2 O. These gases can be scrubbed free of 106 Ru, 131 I, and 99 Tc radioactivities prior to elimination from the plant by passage through HEPA filters. The formation of deleterious NO/sub x/ is avoided. Moreover, formic acid reduces ruthenium to a lower valence state with a sharp reduction in RuO 4 volatility during subsequent calcination of the pretreated waste. It is shown that a minimum of 3% of RuO 4 in an off-gas stream reacts with Davison silica gel (Grade 40) to give a fine RuO 2 aerosol having a particle size of 0.5 μ. This RuO 2 aerosol passes through water or weak acid scrub solutions but is trapped by a caustic scrub solution. Iodine volatilizes almost completely on calcining an acidic waste, and the iodine volatility increases with increasing calcination temperature. On calcining an alkaline sodium nitrate waste the iodine volatility is about an order of magnitude lower, with a relatively low iodine volatility of 0.39% at a calcination temperature of 250 0 C and a moderate volatility of 9.5% at 600 0 C. Volatilities of 99 Tc were generally 0 C. Data are presented to indicate that 99 Tc concentrates in the alkaline sodium nitrate supernatant waste, with approx. 10 mg 99 Tc being associated with each curie of 137 Cs present in the waste. It is shown that lutidine (2,4 dimethyl-pyridine) extracts Tc(VII) quantitatively from alkaline supernatant wastes. The distribution coefficient (K/sub D/) for Tc(VII) going into the organic phase in the above system is 102 for a simulated West Valley waste and 191 for a simulated Savannah River Plant (SRP) waste

  9. Process Design Concepts for Stabilization of High Level Waste Calcine

    Energy Technology Data Exchange (ETDEWEB)

    T. R. Thomas; A. K. Herbst

    2005-06-01

    The current baseline assumption is that packaging ¡§as is¡¨ and direct disposal of high level waste (HLW) calcine in a Monitored Geologic Repository will be allowed. The fall back position is to develop a stabilized waste form for the HLW calcine, that will meet repository waste acceptance criteria currently in place, in case regulatory initiatives are unsuccessful. A decision between direct disposal or a stabilization alternative is anticipated by June 2006. The purposes of this Engineering Design File (EDF) are to provide a pre-conceptual design on three low temperature processes under development for stabilization of high level waste calcine (i.e., the grout, hydroceramic grout, and iron phosphate ceramic processes) and to support a down selection among the three candidates. The key assumptions for the pre-conceptual design assessment are that a) a waste treatment plant would operate over eight years for 200 days a year, b) a design processing rate of 3.67 m3/day or 4670 kg/day of HLW calcine would be needed, and c) the performance of waste form would remove the HLW calcine from the hazardous waste category, and d) the waste form loadings would range from about 21-25 wt% calcine. The conclusions of this EDF study are that: (a) To date, the grout formulation appears to be the best candidate stabilizer among the three being tested for HLW calcine and appears to be the easiest to mix, pour, and cure. (b) Only minor differences would exist between the process steps of the grout and hydroceramic grout stabilization processes. If temperature control of the mixer at about 80„aC is required, it would add a major level of complexity to the iron phosphate stabilization process. (c) It is too early in the development program to determine which stabilizer will produce the minimum amount of stabilized waste form for the entire HLW inventory, but the volume is assumed to be within the range of 12,250 to 14,470 m3. (d) The stacked vessel height of the hot process vessels

  10. Experimental and modeling study of flash calcination of kaolinite rich clay particles in a gas suspension calciner

    DEFF Research Database (Denmark)

    Gebremariam, Abraham Teklay; Yin, Chungen; Rosendahl, Lasse

    2015-01-01

    gas suspension calciner, with the aim to derive useful guidelines on smart calcination for obtaining products of the best pozzolanic properties. Calcination tests are performed in the calciner under six different operation conditions. The raw feed and the calcined clay samples are all characterized...

  11. Proposed Atomic Energy of Canada Ltd. 99Mo waste calcination process

    International Nuclear Information System (INIS)

    Ramey, D.W.; Haas, P.A.; Malkemus, D.W.; McGinnis, C.P.; Meyers, E.S.; Patton, B.D.; Birdwell, J.F.; Jubin, R.T.; Coltharp, K.A.

    1994-10-01

    Atomic Energy of Canada Limited (AECL), at its Chalk River Laboratory, generates from 3000 to 5000 L/year of high-level fissile waste solution from the production of 99 Mo. In this Mo process, highly enriched uranium (93 wt % 235 U, total uranium basis) contained in uranium-aluminum alloy target rods is irradiated to produce the 99 Mo product. The targets are removed from the reactor and dissolved in a mercury nitrate-catalyzed reaction with nitric acid. The 99 Mo product is then recovered by passing the solution through an alumina (Al 2 O 3 ) column. During discussions with personnel from the Oak Ridge National Laboratory (ORNL) on September 10, 1992, the ORNL-developed technology formerly applied to the solidification of aqueous uranium waste (Consolidated Edison Uranium Solidification Program or CEUSP) was judged potentially applicable to the AECL 99 Mo waste. Under a Work-for-Others contract (no. ERD-92-1132), which began May 24, 1993, ORNL was tasked to determine the feasibility of applying the CEUSP (or a similar) calcination process to solidify AECL's 99 Mo waste for > 30 years of safe dry storage. This study was to provide sufficient detailed information on the applicability of a CEUSP-type waste solidification process to allow AECL to select the process which best suited its needs. As with the CEUSP process, evaporation of the waste and a simultaneously partial destruction of acid by reaction with formaldehyde followed by in situ waste can thermal denitration waste was chosen as the best means of solidification. Unlike the CEUSP material, the 99 Mo waste has a considerable number of problem volatile and semivolatile constituents which must be recovered in the off-gas treatment system. Mercury removal before calcination was seen as the best option

  12. XANES analysis of dried and calcined bones

    Energy Technology Data Exchange (ETDEWEB)

    Rajendran, Jayapradhi [Materials Science and Engineering Department, University of Texas at Arlington (United States); Gialanella, Stefano [Materials Science and Industrial Technology Department, University of Trento (Italy); Aswath, Pranesh B., E-mail: aswath@uta.edu [Materials Science and Engineering Department, University of Texas at Arlington (United States)

    2013-10-15

    The structure of dried and calcined bones from chicken, bovine, deer, pig, sheep and chamois was examined using X-ray Absorption Near Edge Structure (XANES) spectroscopy. The oxygen K-edge absorption edge indicates that the surface of dried bone has a larger proportion of carbonate than the interior that is made up of phosphates. The phosphorus L and K edge clearly indicate that pyrophosphates, α-tricalcium phosphate (α-TCP) and hydrogen phosphates of Ca do not exist in either the dried bone or calcined bone and phosphorus exists as either β-tricalcium phosphate (β-TCP) or hydroxyapatite, both in the dried and calcined conditions. The Ca K-edge analysis indicates that β-TCP is the likely form of phosphate in both the dried and calcined conditions. - Highlights: • For the first time bones of five different species of vertebrates have been compared in both the dried and calcined states. • O, P and Ca edges detail the local coordination of these atoms in dried and calcined bone. • O K-edge shows that the surface of bone has more CO{sub 3} while the interior has more PO{sub 4}. • P and Ca edges eliminate the presence of pyrophosphates and confirmed the presence of HA and β-TCP. • The stability of these phosphates on calcination has been examined using XANES.

  13. Calcined solids storage facility closure study

    Energy Technology Data Exchange (ETDEWEB)

    Dahlmeir, M.M.; Tuott, L.C.; Spaulding, B.C. [and others

    1998-02-01

    The disposal of radioactive wastes now stored at the Idaho National Engineering and Environmental Laboratory is currently mandated under a {open_quotes}Settlement Agreement{close_quotes} (or {open_quotes}Batt Agreement{close_quotes}) between the Department of Energy and the State of Idaho. Under this agreement, all high-level waste must be treated as necessary to meet the disposal criteria and disposed of or made road ready to ship from the INEEL by 2035. In order to comply with this agreement, all calcined waste produced in the New Waste Calcining Facility and stored in the Calcined Solids Facility must be treated and disposed of by 2035. Several treatment options for the calcined waste have been studied in support of the High-Level Waste Environmental Impact Statement. Two treatment methods studied, referred to as the TRU Waste Separations Options, involve the separation of the high-level waste (calcine) into TRU waste and low-level waste (Class A or Class C). Following treatment, the TRU waste would be sent to the Waste Isolation Pilot Plant (WIPP) for final storage. It has been proposed that the low-level waste be disposed of in the Tank Farm Facility and/or the Calcined Solids Storage Facility following Resource Conservation and Recovery Act closure. In order to use the seven Bin Sets making up the Calcined Solids Storage Facility as a low-level waste landfill, the facility must first be closed to Resource Conservation and Recovery Act (RCRA) standards. This study identifies and discusses two basic methods available to close the Calcined Solids Storage Facility under the RCRA - Risk-Based Clean Closure and Closure to Landfill Standards. In addition to the closure methods, the regulatory requirements and issues associated with turning the Calcined Solids Storage Facility into an NRC low-level waste landfill or filling the bin voids with clean grout are discussed.

  14. Calcined solids storage facility closure study

    International Nuclear Information System (INIS)

    Dahlmeir, M.M.; Tuott, L.C.; Spaulding, B.C.

    1998-02-01

    The disposal of radioactive wastes now stored at the Idaho National Engineering and Environmental Laboratory is currently mandated under a open-quotes Settlement Agreementclose quotes (or open-quotes Batt Agreementclose quotes) between the Department of Energy and the State of Idaho. Under this agreement, all high-level waste must be treated as necessary to meet the disposal criteria and disposed of or made road ready to ship from the INEEL by 2035. In order to comply with this agreement, all calcined waste produced in the New Waste Calcining Facility and stored in the Calcined Solids Facility must be treated and disposed of by 2035. Several treatment options for the calcined waste have been studied in support of the High-Level Waste Environmental Impact Statement. Two treatment methods studied, referred to as the TRU Waste Separations Options, involve the separation of the high-level waste (calcine) into TRU waste and low-level waste (Class A or Class C). Following treatment, the TRU waste would be sent to the Waste Isolation Pilot Plant (WIPP) for final storage. It has been proposed that the low-level waste be disposed of in the Tank Farm Facility and/or the Calcined Solids Storage Facility following Resource Conservation and Recovery Act closure. In order to use the seven Bin Sets making up the Calcined Solids Storage Facility as a low-level waste landfill, the facility must first be closed to Resource Conservation and Recovery Act (RCRA) standards. This study identifies and discusses two basic methods available to close the Calcined Solids Storage Facility under the RCRA - Risk-Based Clean Closure and Closure to Landfill Standards. In addition to the closure methods, the regulatory requirements and issues associated with turning the Calcined Solids Storage Facility into an NRC low-level waste landfill or filling the bin voids with clean grout are discussed

  15. Criticality safety analysis of a calciner exit chute

    International Nuclear Information System (INIS)

    Haught, C.F.; Basoglu, B.; Brewer, R.W.; Hollenback, D.F.; Wilkinson, A.D.; Dodds, H.L.

    1994-01-01

    Calcination of uranyl nitrate into uranium oxide is part of normal operations of some enrichment plants. Typically, a calciner discharges uranium oxide powder (U 3 O 8 ) into an exit chute that directs the powder into a receiving can located in a glove box. One possible scenario for a criticality accident is the exit chute becoming blocked with powder near its discharge. The blockage restricts the flow of powder causing the exit chute to become filled with the powder. If blockage does occur, the height of the powder could reach a level that would not be safe from a criticality point of view. In this analysis, the subcritical height limit is examined for 98% enriched U 3 O 8 in the exit chute with full water reflection and optimal water moderation. The height limit for ensuring criticality safety during such an accumulation is 28.2 cm above the top of the discharge pipe at the bottom of the chute. Chute design variations are also evaluated with full water reflection and optimal water moderation. Subcritical configurations for the exit chute variation are developed, but the configurations are not safe when combined with the calciner. To ensure criticality safety, modifications must be made to the calciner tube or safety measures must be implemented if these designs are to be utilized with 98% enriched material. A geometrically safe configuration for the exit chute is developed for a blockage of 20% enriched powder with full water reflection and optimal water moderation, and this configuration is safe when combined with the existing calciner

  16. Denitration of medium level liquid radioactive wastes by catalytic destruction of nitrogen oxides

    International Nuclear Information System (INIS)

    Donato, A.; Ricci, G.

    1984-01-01

    The catalytic abatement by means of NH 3 of the NOsub(x) produced in the radwaste conditioning has been studied. With reference to the gas produced in a bituminization plant, the thermodynamics and the chemistry of the NOsub(x) catalytic reduction to nitrogen and H 2 O have been evaluated. The following operational parameters have been experimentally studied: the catalyst bed temperature; the gas residence time; the vapour concentration; the NOsub(x) concentration; the gas velocity; the catalyst grain size distribution; the catalyst time-life. Abatement yields of the order of 99,5% have been obtained following experimental conditions must be selected. In the case of a bituminization plant, a NOsub(x) catalytic reactor, if installed between the evaporator denitrator and the condenser, could reduce to less than 1/100 the volume of the NaNO 3 secondary wastes produced by the gas scrubbing

  17. A Summary of Properties Used to Evaluate INEEL Calcine Disposal in the Yucca Mountain Repository

    International Nuclear Information System (INIS)

    Dahl, C.A.

    2003-01-01

    To support evaluations of the direct disposal of Idaho National Engineering and Environmental Laboratory calcines to the repository at Yucca Mountain, an evaluation of the performance of the calcine in the repository environment must be performed. This type of evaluation demonstrates, through computer modeling and analysis, the impact the calcine would have on the ability of the repository to perform its function of containment of materials during the repository lifetime. This report discusses parameters that were used in the scoping evaluation conducted in FY 2003. It provides nominal values for the parameters, with explanation of the source of the values, and how the values were modified for use in repository analysis activities

  18. New Waste Calcining Facility (NWCF) Waste Streams

    International Nuclear Information System (INIS)

    K. E. Archibald

    1999-01-01

    This report addresses the issues of conducting debris treatment in the New Waste Calcine Facility (NWCF) decontamination area and the methods currently being used to decontaminate material at the NWCF

  19. Bin Set 1 Calcine Retrieval Feasibility Study

    Energy Technology Data Exchange (ETDEWEB)

    R. D. Adams; S. M. Berry; K. J. Galloway; T. A. Langenwalter; D. A. Lopez; C. M. Noakes; H. K. Peterson; M. I. Pope; R. J. Turk

    1999-10-01

    At the Department of Energy's Idaho Nuclear Technology and Engineering Center, as an interim waste management measure, both mixed high-level liquid waste and sodium bearing waste have been solidified by a calculation process and are stored in the Calcine Solids Storage Facilities. This calcined product will eventually be treated to allow final disposal in a national geologic repository. The Calcine Solids Storage Facilities comprise seven ''bit sets.'' Bin Set 1, the first to be constructed, was completed in 1959, and has been in service since 1963. It is the only bin set that does not meet current safe-shutdown earthquake seismic criteria. In addition, it is the only bin set that lacks built-in features to aid in calcine retrieval. One option to alleviate the seismic compliance issue is to transport the calcine from Bin Set 1 to another bin set which has the required capacity and which is seismically qualified. This report studies the feasibility of retrieving the calcine from Bi n Set 1 and transporting it into Bin Set 6 which is located approximately 650 feet away. Because Bin Set 1 was not designed for calcine retrieval, and because of the high radiation levels and potential contamination spread from the calcined material, this is a challenging engineering task. This report presents preconceptual design studies for remotely-operated, low-density, pneumatic vacuum retrieval and transport systems and equipment that are based on past work performed by the Raytheon Engineers and Constructors architectural engineering firm. The designs presented are considered feasible; however, future development work will be needed in several areas during the subsequent conceptual design phase.

  20. Bin Set 1 Calcine Retrieval Feasibility Study

    International Nuclear Information System (INIS)

    Adams, R.D.; Berry, S.M.; Galloway, K.J.; Langenwalter, T.A.; Lopez, D.A.; Noakes, C.M.; Peterson, H.K.; Pope, M.I.; Turk, R.J.

    1999-01-01

    At the Department of Energy's Idaho Nuclear Technology and Engineering Center, as an interim waste management measure, both mixed high-level liquid waste and sodium bearing waste have been solidified by a calculation process and are stored in the Calcine Solids Storage Facilities. This calcined product will eventually be treated to allow final disposal in a national geologic repository. The Calcine Solids Storage Facilities comprise seven ''bit sets.'' Bin Set 1, the first to be constructed, was completed in 1959, and has been in service since 1963. It is the only bin set that does not meet current safe-shutdown earthquake seismic criteria. In addition, it is the only bin set that lacks built-in features to aid in calcine retrieval. One option to alleviate the seismic compliance issue is to transport the calcine from Bin Set 1 to another bin set which has the required capacity and which is seismically qualified. This report studies the feasibility of retrieving the calcine from Bi n Set 1 and transporting it into Bin Set 6 which is located approximately 650 feet away. Because Bin Set 1 was not designed for calcine retrieval, and because of the high radiation levels and potential contamination spread from the calcined material, this is a challenging engineering task. This report presents preconceptual design studies for remotely-operated, low-density, pneumatic vacuum retrieval and transport systems and equipment that are based on past work performed by the Raytheon Engineers and Constructors architectural engineering firm. The designs presented are considered feasible; however, future development work will be needed in several areas during the subsequent conceptual design phase

  1. Stop Smoking—Tube-In-Tube Helical System for Flameless Calcination of Minerals

    Directory of Open Access Journals (Sweden)

    Nils Haneklaus

    2017-11-01

    Full Text Available Mineral calcination worldwide accounts for some 5–10% of all anthropogenic carbon dioxide (CO2 emissions per year. Roughly half of the CO2 released results from burning fossil fuels for heat generation, while the other half is a product of the calcination reaction itself. Traditionally, the fuel combustion process and the calcination reaction take place together to enhance heat transfer. Systems have been proposed that separate fuel combustion and calcination to allow for the sequestration of pure CO2 from the calcination reaction for later storage/use and capture of the combustion gases. This work presents a new tube-in-tube helical system for the calcination of minerals that can use different heat transfer fluids (HTFs, employed or foreseen in concentrated solar power (CSP plants. The system is labeled ‘flameless’ since the HTF can be heated by other means than burning fossil fuels. If CSP or high-temperature nuclear reactors are used, direct CO2 emissions can be divided in half. The technical feasibility of the system has been accessed with a brief parametric study here. The results suggest that the introduced system is technically feasible given the parameters (total heat transfer coefficients, mass- and volume flows, outer tube friction factors, and –Nusselt numbers that are examined. Further experimental work will be required to better understand the performance of the tube-in-tube helical system for the flameless calcination of minerals.

  2. Experimental results: Pilot plant calcine dissolution and liquid feed stability

    International Nuclear Information System (INIS)

    Herbst, R.S.; Fryer, D.S.; Brewer, K.N.; Johnson, C.K.; Todd, T.A.

    1995-02-01

    The dissolution of simulated Idaho Chemical Processing Plant pilot plant calcines, containing none of the radioactive actinides, lanthanides or fission products, was examined to evaluate the solubility of calcine matrix materials in acidic media. This study was a necessary precursor to dissolution and optimization experiments with actual radionuclide-containing calcines. The importance of temperature, nitric acid concentration, ratio of acid volume to calcine mass, and time on the amount, as a weight percentage of calcine dissolved, was evaluated. These parameters were studied for several representative pilot plant calcine types: (1) Run No. 74 Zirconia calcine; (2) Run No. 17 Zirconia/Sodium calcine; (3) Run No. 64 Zirconia/Sodium calcine; (3) Run No. 1027 Alumina calcine; and (4) Run No. 20 Alumina/Zirconia/Sodium calcine. Statistically designed experiments with the different pilot plant calcines indicated the effect of the studied process variables on the amount of calcine dissolved decreases in the order: Acid/Calcine Ratio > Temperature > HNO 3 Concentration > Dissolution Time. The following conditions are suitable to achieve greater than 90 wt. % dissolution of most Zr, Al, or Na blend calcines: (1) Maximum nitric acid concentration of 5M; (2) Minimum acid/calcine ratio of 10 mL acid/1 gram calcine; (3) Minimum dissolution temperature of 90 degrees C; and (4) Minimum dissolution time of 30 minutes. The formation of calcium sulphate (CaSO 4 ) precipitates was observed in certain dissolved calcine solutions during the dissolution experiments. Consequently, a study was initiated to evaluate if and under what conditions the resulting dissolved calcine solutions would be unstable with regards to precipitate formation. The results indicate that precipitate formation in the calcine solutions prepared under the above proposed dissolution conditions are not anticipated

  3. The effect of calcination conditions on the graphitizability of novel synthetic and coal-derived cokes

    Science.gov (United States)

    Bennett, Barbara Ellen

    The effects of calcination heating rate and ultimate calcination temperature upon calcined coke and subsequent graphitic material microstructures were studied for materials prepared from three different precursors. The pitch precursors used were Mitsubishi AR pitch (a synthetic, 100% mesophase pitch), the NMP-extracted portion of a raw coal, and the NMP-extracted fraction of a coal liquefaction residue obtained from an HTI pilot plant. These materials were all green-coked under identical conditions. Optical microscopy confirmed that the Mitsubishi coke was very anisotropic and the HTI coke was nearly as anisotropic. The coke produced from the direct coal extract was very isotropic. Crystalline development during calcination heating was verified by high-temperature x-ray diffraction. Experiments were performed to ascertain the effects of varying calcination heating rate and ultimate temperature. It was determined that calcined coke crystallite size increased with increasing temperature for all three materials but was found to be independent of heating rate. The graphene interplanar spacing decreased with increasing temperature for the isotropic NMP-extract material but increased with increasing temperature for the anisotropic materials---Mitsubishi and HTI cokes. Graphene interplanar spacing was also found to be independent of heating rate. Calcined coke real densities were, likewise, found to be independent of heating rate. The anisotropic cokes (Mitsubishi and HTI) exhibited increasing real density with increasing calcination temperature. The NMP-extract coke increased in density up to 1050°C and then suffered a dramatic reduction in real density when heated to 1250°C. This is indicative of puffing. Since there was no corresponding disruption in the crystalline structure, the puffing phenomena was determined to be intercrystalline rather than intracrystalline. After the calcined cokes were graphitized (under identical conditions), the microstructures were re

  4. Recovery of gold and uranium from calcines

    Energy Technology Data Exchange (ETDEWEB)

    Livesey-Goldblatt, E.

    1981-10-06

    The invention concerns the recovery of non-ferrous metals, such as gold, uranium or the like from iron oxide containing calcines which have the non-ferrous metal present in solid solution and/or encapsulated within the iron oxide. The calcine is reacted, while stirring vigorously, with sulphuric acid or another strong inorganic acid to cause the iron to form the ferric salt. The material obtained is mixed with water and the liquid and solid phases are separated from each other. The non-ferrous metal is then obtained from at least one of these phases by leaching, or the like.

  5. 1st International Conference on Calcined Clays for Sustainable Concrete

    CERN Document Server

    Favier, Aurélie

    2015-01-01

    This volume focuses on research and practical issues linked to Calcined Clays for Sustainable Concrete. The main subjects are geology of clays, hydration and performance of blended systems with calcined clays, alkali activated binders, economic and environmental impacts of the use of calcined clays in cement based materials. Topics addressed in this book include the influence of processing on reactivity of calcined clays, influence of clay mineralogy on reactivity, geology of clay deposits, Portland-calcined clay systems, hydration, durability, performance, Portland-calcined clay-limestone systems, hydration, durability, performance, calcined clay-alkali systems, life cycle analysis, economics and environmental impact of use of calcined clays in cement and concrete, and field applications. This book compiles the different contributions of the 1st International Conference on Calcined Clays for Sustainable Concrete, which took place in Lausanne, Switzerland, June, 23-25, 2015.The papers present the latest  res...

  6. Remotely replaceable fuel and feed nozzles for the new waste calcining facility calciner vessel

    International Nuclear Information System (INIS)

    Fletcher, R.D.; Carter, J.A.; May, K.W.

    1978-01-01

    The development and testing of remotely replaceable fuel and feed nozzles for calcination of liquid radioactive wastes in the calciner vessel of the New Waste Calcining Facility being built at the Idaho National Engineering Laboratory is described. A complete fuel nozzle assembly was fabricated and tested at the Remote Maintenance Development Facility to evolve design refinements, identify required support equipment, and develop handling techniques. The design also provided for remote replacement of the nozzle support carriage and adjacent feed and fuel pipe loops using two pairs of master-slave manipulators

  7. Evaluation of Calcine Disposition Path Forward

    International Nuclear Information System (INIS)

    Birrer, S.A.; Heiser, M.B.

    2003-01-01

    This document describes an evaluation of the baseline and two alternative disposition paths for the final disposition of the calcine wastes stored at the Idaho Nuclear Technology and Engineering Center at the Idaho National Engineering and Environmental Laboratory. The pathways are evaluated against a prescribed set of criteria and a recommendation is made for the path forward

  8. KINETICS OF SORPTION OF FLUORIDE ON CALCINED MAGNESITE IN BATCH

    DEFF Research Database (Denmark)

    Singano, J. J.; Mashauri, D. A.; Mtalo, F. W.

    1997-01-01

    on first-order reaction with respect to the concentration of fluoride. The rate constant is directly proportional to the dosage. The model takes into accounts the lag time observed. The kinetical model can be described for any given dosage and initial fluoride concentration in the water. The reaction rate...... parameter, K, varies however slightly for different initial concentrations of fluoride in the water and different dosage of calcined magnesia. These relationships are described separately by two linear equations. It is discussed that the observed lag time is due to the fact that magnesia cannot remove...... fluoride without hydrolysis, and it is probably this hydrolysis which constraint the start of the removal....

  9. Process for calcining a material

    International Nuclear Information System (INIS)

    Ross, D.R.

    1981-01-01

    This invention is directed to a method and an apparatus to heat certain particles. These certain particles are heated to make them more desirable. In the heating of these particles, it is often desirable to expand the particles to make a light-weight aggregate. The light-weight aggregate may be used in making a building material or the like. In carrying out the process of heating these particles, there is used air for combustion of the combustible fuel and only a minimum of air for carrying of the particles or expansion of the particles

  10. Corrosion evaluation of uranyl nitrate solution evaporator and denitrator in Tokai reprocessing plant

    International Nuclear Information System (INIS)

    Yamanaka, Atsushi; Hashimoto, Kowa; Uchida, Toyomi; Shirato, Yoji; Isozaki, Toshihiko; Nakamura, Yoshinobu

    2011-01-01

    The Tokai reprocessing plant (TRP) adopted the PUREX method in 1977 and has reprocessed spent nuclear fuel of 1140 tHM (tons of heavy metals) since then. The reprocessing equipment suffers from various corrosion phenomena because of high nitric acidity, solution ion concentrations, such as uranium, plutonium, and fission products, and temperature. Therefore, considering corrosion performance in such a severe environment, stainless steels, titanium steel, and so forth were employed as corrosion resistant materials. The severity of the corrosive environment depends on the nitric acid concentration and the temperature of the solution, and uranium in the solution reportedly does not significantly affect the corrosion of stainless steels and controls the corrosion rates of titanium steel. The TRP equipment that handles uranyl nitrate solution operates at a low nitric acid concentration and has not experienced corrosion problems until now. However, there is a report that corrosion rates of some stainless steels increase in proportion to rising uranium concentrations. The equipment that handles the uranyl nitrate solution in the TRP includes the evaporators, which concentrate uranyl nitrate to a maximum concentration of about 1000 gU/L (grams of uranium per liter), and the denitrator, where uranyl nitrate is converted to UO 3 powder at about 320degC. These equipments are therefore required to grasp the degree of the progress of corrosion to handle high-temperature and high-concentration uranyl nitrate. The evaluation of this equipment on the basis of thickness measurement confirmed only minor corrosion and indicated that the equipment would be fully adequate for future operation. (author)

  11. Dissolution studies with pilot plant and actual INTEC calcines

    International Nuclear Information System (INIS)

    Herbst, R.S.; Garn, T.G.

    1999-01-01

    The dissolution of Idaho Nuclear Technology and Engineering Center (INTEC) pilot plant calcines was examined to determine solubility of calcine matrix components in acidic media. Two representatives pilot plant calcine types were studied: Zirconia calcine and Zirconia/Sodium calcine. Dissolution of these calcines was evaluated using lower initial concentrations of nitric acid than used in previous tests to decrease the [H+] concentration in the final solutions. Lower [H+] concentrations contribute to more favorable TRUEX/SREX solvent extraction flowsheet performance. Dissolution and analytical results were also obtained for radioactive calcines produced using high sodium feeds blended with non-radioactive Al(NO 3 ) 3 solutions to dilute the sodium concentration and prevent bed agglomeration during the calcination process. Dissolution tests indicated >95 wt.% of the initial calcine mass can be dissolved using the baseline dissolution procedure, with the exception that higher initial nitric acid concentrations are required. The higher initial acid concentration is required for stoichiometric dissolution of the oxides, primarily aluminum oxide. Statistically designed experiments using pilot plant calcine were performed to determine the effect of mixing rate on dissolution efficiency. Mixing rate was determined to provide minimal effects on wt.% dissolution. The acid/calcine ratio and temperature were the predominate variables affecting the wt.% dissolution, a result consistent with previous studies using other similar types of pilot plant calcines

  12. Effects of pH and calcination temperature on structural and optical properties of alumina nanoparticles

    Science.gov (United States)

    Amirsalari, A.; Farjami Shayesteh, S.

    2015-06-01

    In this study, we describe the synthesis of alumina nanoparticles using a chemical wet method in at varying pH. The optimized prepared particles with pH equals to 9 were calcined at various temperatures. For characterization of structural and optical properties of nanoparticles had been used X-ray diffraction, Infrared Fourier transform spectroscopy, field effect-scanning electron microscopy, photoluminescence and ultraviolet-visible spectroscopy. The results revealed that the nanoparticles calcined at 500 °C consist of an Al2O3 tetragonal structure and tetragonal distortion decreases with increasing calcination temperature up to 750 °C then increased with increasing temperature. Another phase similar to γ-Al2O3 was formed instead of δ-Al2O3 in the transition sequence from the γ to θ phase. FT-IR analysis; suggests that there are a few different types of functional groups on the surface of the alumina nanoparticles such as hydroxy groups and oxy groups. The transmittance spectra showed that the absorption bands in the UV region strongly depend on the calcination temperature. Moreover, the results showed that alumina has an optical direct band gap and that the energy gap decreases with increasing the calcination temperature and pH of the reaction. Luminescence spectra showed that some luminescent centers such as OH-related radiative centers and oxygen vacancies (F, F22+ and F2 centers) centers exist in the nanoparticles.

  13. Wet calcining of trona (sodium sesquicarbonate) and bicarbonate in a mixed solvent

    Science.gov (United States)

    Gärtner, R. S.; Witkamp, G. J.

    2002-04-01

    Trona ore is used in large amounts for the production of soda ash. A key step in this process is the conversion of trona (sodium sesquicarbonate: Na 2CO 3·NaHCO 3·2H 2O) into soda (sodium carbonate anhydrate: Na 2CO 3). Currently, this conversion is done industrially by calcining of the raw ore in rotary calciners at ca. 120°C or higher (Natural Soda Ash—Occurrences, Processing, and Use, Van Nostrand Reinhold, New York, 1991, p. 267). Trona can however be converted at lower temperatures by using a "wet calcining" technique. In this technique, trona is contacted with an organic or mixed organic-aqueous solvent at a conversion temperature that depends on the water activity of the used solvent. In pure ethylene glycol this temperature can be as low as 55°C. The conversion by "wet calcining" occurs very similar to that in the regular dry calcining process via a solid phase conversion. The anhydrate crystals form directly from the solid trona. This produces pseudomorphs (J. Chem. Eng. Data 8(3) (1963) 301), i.e. agglomerates of fine anhydrate crystals (1-10 μm). At high temperatures, dense, finely pored agglomerates are formed, while the outer shape of the agglomerate retains the prism shape of the trona crystal. At low conversion temperatures, loosely packed or even unstable agglomerates are found.

  14. Redox calcination study of Synroc D powder containing simulated SRL waste

    International Nuclear Information System (INIS)

    Chen, C.

    1982-01-01

    According to Ringwood [A.E. Ringwood, W. Sinclair, and G.M. McLaughlin, Nuclear Waste Immobilization, Lawrence Livermore Laboratory, Livermore, Rept. UCRL-15147 (1979)], the iron oxidation state is important in controlling, the spinel mineralogy and composition if the amount of titania (TiO 2 ) consumed in spinel formation is to be minimized in favor of the formation of the Synroc phases, zirconolite, perovskite, and nepheline. In our redox calcination studies we observed that the iron oxidation state of FeO/Fe 2 O 3 can be controlled by the redoxcalcining atmosphere. In a CO atmosphere, the oxidation state was reduced to less than 7 wt % Fe 2 O 3 . With appropriate CO 2 /CO gas mixtures the resultant iron oxidation states were in the range of 45 to 59 wt % Fe 2 O 3 . Direct rotary redox calcination of spray dried powder at 600 0 C, without prior air calcination, showed increased redox efficiency when compared to powder that had been previously air calcined at 650 0 C. We believe this is caused by a reduction in particle size. Rotary calcination at 800 0 C in argon has no measurable reduction affect on the iron oxidation state of Synroc D powder

  15. The increase performance BMF-14 calcination unit

    International Nuclear Information System (INIS)

    Triyono

    2013-01-01

    The heating element of performance increase BMF-14 calcination unit has been installed. The activity includes: installation and function test heating element step by step. The main component includes: kanthal heating element type with size long 58,2 cm diameter 0,9 cm slot total 28, flexible cable resists heat 30 Amperes, band cable heat resists and flexible clamp. The heating elements installation includes from 3 groups and every groups have 4 heating elements to connectly series. Every group connecting to every phase RST and neutral for getting electric voltage 380 Volts follow contact relay 3 phases to controlling by digital temperature control. The resulting installation of heating element in the BMF-14 calcination unit showed that: BMF-14 calcination unit can be again of the setting temperature step by step. In the step I get optimal temperature 560 °C test time 1068 minutes with rate velocity heat 0 to 18,0 °C/minutes with current between 5,8 to 6,4 Amperes voltage 103 to 123 Volts (phase R and T). In the step II gets optimal temperature 600 °C test time 265 minutes getting rate velocity heat 0 to 40,3 °C/minutes with current 3,8 to 8,5 Amperes voltage 76 to 142 Volts (phase RST). In the step III gets optimal temperature 1000 °C test time 107 minutes getting rate velocity heat 0 to 53,5 °C/minutes with current 9,7 to 12,5 Amperes voltage 215 to 225 Volts (phase RST). (author)

  16. Waste Calcining Facility remote inspection report

    International Nuclear Information System (INIS)

    Patterson, M.W.; Ison, W.M.

    1994-08-01

    The purpose of the Waste Calcining Facility (WCF) remote inspections was to evaluate areas in the facility which are difficult to access due to high radiation fields. The areas inspected were the ventilation exhaust duct, waste hold cell, adsorber manifold cell, off-gas cell, calciner cell and calciner vessel. The WCF solidified acidic, high-level mixed waste generated during nuclear fuel reprocessing. Solidification was accomplished through high temperature oxidation and evaporation. Since its shutdown in 1981, the WCFs vessels, piping systems, pumps, off-gas blowers and process cells have remained contaminated. Access to the below-grade areas is limited due to contamination and high radiation fields. Each inspection technique was tested with a mock-up in a radiologically clean area before the equipment was taken to the WCF for the actual inspection. During the inspections, essential information was obtained regarding the cleanliness, structural integrity, in-leakage of ground water, indications of process leaks, indications of corrosion, radiation levels and the general condition of the cells and equipment. In general, the cells contain a great deal of dust and debris, as well as hand tools, piping and miscellaneous equipment. Although the building appears to be structurally sound, the paint is peeling to some degree in all of the cells. Cracking and spalling of the concrete walls is evident in every cell, although the east wall of the off-gas cell is the worst. The results of the completed inspections and lessons learned will be used to plan future activities for stabilization and deactivation of the facility. Remote clean-up of loose piping, hand tools, and miscellaneous debris can start immediately while information from the inspections is factored into the conceptual design for deactivating the facility

  17. Product removal and solids transport from fluidized-bed calciners

    International Nuclear Information System (INIS)

    Grimmett, E.S.; Munger, D.H.

    1978-09-01

    Methods of removing the solid product from pilot-plant and production fluidized-bed calciners, and transporting product to underground storage vaults are reported here. Testing of dense-phase solids transport systems in test loops during development of a 15-cm-diam. and 30-cm-diam. calciner are described. A lean-phase solid transport system is used with the Waste Calcining Facility. The results of some recent tests done in a lean-phase transport system connected to the 30-cm-diam. calciner are included in this report

  18. Flash calcination of kaolinite rich clay and impact of process conditions on the quality of the calcines

    DEFF Research Database (Denmark)

    Gebremariam, Abraham Teklay; Yin, Chungen; Rosendahl, Lasse

    2016-01-01

    Use of properly calcined kaolinite rich clay (i.e., metakaolin) to offset part of CO2-intensive clinkers not only reduces CO2 footprint from cement industry but also improves the performance of concrete. However, calcination under inappropriately high temperatures or long retention times may...... deplete metakaolin into unwanted products (e.g., mullite), which limits the use of the calcines as a supplementary cementitious material. With this regard, a dynamic model of flash calcination of kaolinite rich clay particles is developed using gPROMS (general PROcess Modeling System) to predict...... the impacts of calcination temperature and residence time on the transformation of the clay particles and to derive a favorable production path that is able to achieve optimum amount of the desired product. Flash calcination tests of the kaolinite rich clay particles are also performed in a pilot-scale gas...

  19. SYNROC production using a fluid bed calciner

    International Nuclear Information System (INIS)

    Ackerman, F.J.; Grens, J.Z.; Ryerson, F.J.; Hoenig, C.L.; Bazan, F.; Campbell, J.H.

    1982-01-01

    SYNROC is a titanate-based ceramic developed for immobilization of high-level nuclear reactor wastes in solid form. Fluid-bed SYNROC production permits slurry drying, calcining and redox to be carried out in a single unit. We present results of studies from two fluid beds; the Idaho Exxon internally-heated unit and the externally-heated unit constructed at Lawrence Livermore National laboratory. Bed operation over a range of temperature, feed rate, fluidizing rate and redox conditions indicate that high density, uniform particle-size SYNROC powders are produced which facilitate the densification step and give HUP parts with dense, well-developed phases and good leaching characteristics. 3 figures, 3 tables

  20. Role of Calcination Temperature on the Hydrotalcite Derived MgO–Al2O3 in Converting Ethanol to Butanol

    Energy Technology Data Exchange (ETDEWEB)

    Ramasamy, Karthikeyan K.; Gray, Michel J.; Job, Heather M.; Santosa, Daniel M.; Li, Xiaohong S.; Devaraj, Arun; Karkamkar, Abhijeet J.; Wang, Yong

    2015-10-09

    In the base catalyzed ethanol condensation reactions, the calcined MgO-Al2O3 derived hydrotalcites used broadly as catalytic material and the calcination temperature plays a big role in determining the catalytic activity. The characteristic of the hydrotalcite material treated between catalytically relevant temperatures 450ºC and 800ºC have been studied with respect to the physical, chemical, and structural properties and compared with catalytic activity testing. With the increasing calcination temperature, the total measured catalytic basicity dropped linearly with the calcination temperature and the total measured acidity stayed the same for all the calcination temperatures except 800ºC. However, the catalyst activity testing does not show any direct correlation between the measured catalytic basicity and the catalyst activity to the ethanol condensation reaction to form 1-butanol. The highest ethanol conversion of 44 percent with 1-butanol selectivity of 50 percent was achieved for the 600ºC calcined hydrotalcite material.

  1. Mission Need Statement: Calcine Disposition Project Major Systems Acquisition Project

    International Nuclear Information System (INIS)

    J. T. Beck

    2007-01-01

    This document identifies the need to establish the Calcine Disposition Project to determine and implement the final disposition of calcine including characterization, retrieval, treatment (if necessary), packaging, loading, onsite interim storage pending shipment to a repository or interim storage facility, and disposition of related facilities

  2. An assessment of the calcination characteristics of the mfamosing ...

    African Journals Online (AJOL)

    The suitability of the limestone for commercial lime production depends on its chemical purity (66.69% CaCO3) and calcination process. Consequently the limestone was calcined through a range of temperature (9500C, 10000C, 10500C and 11000C) for varied retention times (60, 90, 120 minutes) and the burning ...

  3. Effect of Calcination and Reduction Temperatures on the Reduction ...

    African Journals Online (AJOL)

    The effect of calcination and reduction temperatures on the reducibility, dispersion and Fischer-Tropsch activity of 10 wt% cobalt supported on titania catalyst modified by 0.1 wt% boron has been studied. The percentage reduction and percentage dispersion were found to decrease with increasing calcination temperature.

  4. Kinetic Study of Calcination of Jakura Limestone Using Power Rate ...

    African Journals Online (AJOL)

    investigation into kinetics of calcinations of some large commercial deposits of limestone in Nigeria. The study is aimed at finding kinetic parameters for the purpose of energy saving, lime kiln design, modeling and simulation of lime kiln. In this study, kinetic of Jakura limestone calcination process using power rate law has ...

  5. Characterization and Dissolution Kinetics Testing of Radioactive H-3 Calcine

    Energy Technology Data Exchange (ETDEWEB)

    Garn, Troy Gerry; Batcheller, Thomas Aquinas

    2002-09-01

    Characterization and dissolution kinetics testing were performed with Idaho radioactive H-3 calcine. Calcine dissolution is the key front-end unit operation for the Separations Alternative identified in the Idaho High Level Waste Draft EIS. The impact of the extent of dissolution on the feasibility of Separations must be clearly quantified.

  6. Properties of Formula 127 glass prepared with radioactive zirconia calcine

    International Nuclear Information System (INIS)

    Staples, B.A.; Pavlica, D.A.; Cole, H.S.

    1982-09-01

    Formula 127 glass has been developed to immobilize ICPP zirconia calcine. This glass has been prepared remotely on a laboratory scale basis with actual radioactive zirconia calcine retrieved after ten years of storage from Bin Set 2. The aqueous leachability of the glass produced was investigated and compared through application of the MCC-1, MCC-2 and Soxhlet leach tests with that of Formula 127 glass prepared with simulated calcine. The solid state properties of the glasses prepared with actual and simulated calcines were also measured by electron spectroscopy for chemical analysis (ESCA) and scanning electron microscopy energy dispersive x-ray (SEM-EDX). Based on the application of these leaching tests and analysis techniques the properties measured in this study are similar for 127 glass prepared with either simulated or radioactive calcine. 13 figures, 16 tables

  7. Effect of Na poisoning catalyst (V2O5-WO3/TiO2) on denitration process and SO3 formation

    Science.gov (United States)

    Xiao, Haiping; Chen, Yu; Qi, Cong; Ru, Yu

    2018-03-01

    This paper aims to study the effect of alkali metal sodium (Na) poisoning on the performance of the Selective Catalytic Reduction (SCR) catalyst. The result showed that Na2SO4 poisoning leads to a reduced denitration rate of the SCR catalyst and an increase in the SO3 generation rate. Na2O poisoning leads to a significant reduction in the denitration rate of the SCR catalyst and marginally improves the formation of SO3. The maximum of the SO3 generation rate for a Na2SO4-poisoned catalyst reached 1.35%, whereas it was only 0.85% for the SCR catalyst. When the SO2 was contained in flue gas, the denitration rate for the Na2O-poisoned catalyst clearly increased by more than 28%. However, the effect of SO2 on the Na2SO4-poisoned catalyst was very slight. The denitration rate of the SCR catalyst decreased with an increase in the Na content. The BET and XRD results showed that Na poisoning of the catalyst decreased the number of acid sites, the reducibility of the catalyst, the surface area, and pore volume. The H2-TPR and NH3-TPD results show that Na decreases the number of acid sites and the reducibility of the catalyst. The FT-IR and XPS results showed that Na2O poisoning led to the decrease of V5+dbnd O bonds and the consumptions of oxygen atoms. Na2SO4 poisoning can improve surface adsorbed oxygen, which was beneficial for the SO2-SO3 conversion reaction.

  8. Calcination of the cerium concentrate to be cerium oxide

    International Nuclear Information System (INIS)

    Suyanti; MV Purwani

    2016-01-01

    Calcination of the cerium concentrate to be cerium oxide has done. The cerium concentrate were obtained from the Ce making process wear KBrO 3 and without using KBrO 3 . The calcination were done with a variation of time 1, 2, 3 and 4 hours with the temperature variations of 700, 800 and 900°C. The easiest calcination of Ce concentrates to be CeO 2 containing majority of Ce(OH) 4 and contains least impurities as Th(OH) 4 , (NH 4 ) 2 Y(NO 3 ), H 4 N 5 O 12 La, H 12 N 3 NdO 15 and N 3 O 9 Sm. On the calcination of Ce concentrates process results without using KBrO 3 1, the calcination temperature 900°C was obtained CeO 2 content of 73.53% for calcination time of 4 hours, has little difference when compared with the predictions and calculation result of complete calcination was equal 73.84%. (author)

  9. Calcination/dissolution testing for Hanford Site tank wastes

    International Nuclear Information System (INIS)

    Colby, S.A.; Delegard, C.H.; McLaughlin, D.F.; Danielson, M.J.

    1994-07-01

    Thermal treatment by calcination offers several benefits for the treatment of Hanford Site tank wastes, including the destruction of organics and ferrocyanides and an hydroxide fusion that permits the bulk of the mostly soluble nonradioactive constituents to be easily separated from the insoluble transuranic residue. Critical design parameters were tested, including: (1) calciner equipment design, (2) hydroxide fusion chemistry, and (3) equipment corrosion. A 2 gal/minute pilot plant processed a simulated Tank 101-SY waste and produced a free flowing 700 C molten calcine with an average calciner retention time of 20 minutes and >95% organic, nitrate, and nitrite destruction. Laboratory experiments using actual radioactive tank waste and the simulated waste pilot experiments indicate that 98 wt% of the calcine produced is soluble in water, leaving an insoluble transuranic fraction. All of the Hanford Site tank wastes can benefit from calcination/dissolution processing, contingent upon blending various tank waste types to ensure a target of 70 wt% sodium hydroxide/nitrate/nitrite fluxing agent. Finally, corrosion testing indicates that a jacketed nickel liner cooled to below 400 C would corrode <2 mil/year (0.05 mm/year) from molten calcine attack

  10. Summary of Calcine Disposal Development Using Hot Isostatic Pressing

    Energy Technology Data Exchange (ETDEWEB)

    Bateman, Ken [Idaho National Lab. (INL), Idaho Falls, ID (United States); Wahlquist, Dennis [Idaho National Lab. (INL), Idaho Falls, ID (United States); Hart, Edward [Idaho National Lab. (INL), Idaho Falls, ID (United States); McCartin, William [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2015-03-01

    Battelle Energy Alliance, LLC, has demonstrated the effectiveness of the hot isostatic press (HIP) process for treatment of hazardous high-level waste known as calcine that is stored at the Idaho Nuclear Technology and Engineering Center (INTEC) at Idaho National Laboratory. HIP trials performed with simulated calcines at Idaho National Laboratory’s Materials and Fuels Complex and an Australian Nuclear Science and Technology Organization facility from 2007 to 2010 produced a dense, monolithic waste form with increased chemical durability and effective (storage) volume reductions of ~10 to ~70% compared to granular calcine forms. In December 2009, the U.S. Department of Energy signed an amended Record of Decision selecting HIP technology as the treatment method for the 4,400 m3 of granular zirconia and alumina calcine stored at INTEC. Testing showed that HIP treatment reduces the risks associated with radioactive and hazardous constituent release, post-production handling, and long-term (repository) storage of calcines and would result in estimated storage cost savings in the billions of dollars. Battelle Energy Alliance has the ability to complete pilot-scale HIP processing of INTEC calcine, which is the next necessary step in implementing HIP processing as a calcine treatment method.

  11. Development and Testing of the Advanced CHP System Utilizing the Off-Gas from the Innovative Green Coke Calcining Process in Fluidized Bed

    Energy Technology Data Exchange (ETDEWEB)

    Chudnovsky, Yaroslav [Gas Technology Inst., Des Plaines, IL (United States); Kozlov, Aleksandr [Gas Technology Inst., Des Plaines, IL (United States)

    2013-08-15

    Green petroleum coke (GPC) is an oil refining byproduct that can be used directly as a solid fuel or as a feedstock for the production of calcined petroleum coke. GPC contains a high amount of volatiles and sulfur. During the calcination process, the GPC is heated to remove the volatiles and sulfur to produce purified calcined coke, which is used in the production of graphite, electrodes, metal carburizers, and other carbon products. Currently, more than 80% of calcined coke is produced in rotary kilns or rotary hearth furnaces. These technologies provide partial heat utilization of the calcined coke to increase efficiency of the calcination process, but they also share some operating disadvantages. However, coke calcination in an electrothermal fluidized bed (EFB) opens up a number of potential benefits for the production enhancement, while reducing the capital and operating costs. The increased usage of heavy crude oil in recent years has resulted in higher sulfur content in green coke produced by oil refinery process, which requires a significant increase in the calcinations temperature and in residence time. The calorific value of the process off-gas is quite substantial and can be effectively utilized as an “opportunity fuel” for combined heat and power (CHP) production to complement the energy demand. Heat recovered from the product cooling can also contribute to the overall economics of the calcination process. Preliminary estimates indicated the decrease in energy consumption by 35-50% as well as a proportional decrease in greenhouse gas emissions. As such, the efficiency improvement of the coke calcinations systems is attracting close attention of the researchers and engineers throughout the world. The developed technology is intended to accomplish the following objectives: - Reduce the energy and carbon intensity of the calcined coke production process. - Increase utilization of opportunity fuels such as industrial waste off-gas from the novel

  12. Assessment of soda ash calcination treatment of Turkish trona ore

    Directory of Open Access Journals (Sweden)

    Gezer Sibel

    2016-01-01

    Full Text Available Trona is relatively rare, non-metallic mineral, Na2CO3 · NaHCO3 · 2H2O. The pure material contains 70.3% sodium carbonate and by calcination the excess CO2 and water can be driven off, yielding natural soda ash. The terms soda ash and sodium carbonate are used interchangeably. Trona calcining is a key process step in production of soda ash (sodium carbonate anhydrate from the relatively cheap trona ore. The calcination reaction may proceeds in a sequence of steps. Depending on the conditions, it may result in formation of either sodium carbonate monohydrate (Na2CO3 · H2O, sodium sesquicarbonate or weigschederite (Na2CO3 · 3NaHCO3. The Beypazarı Turkish trona deposit is the second largest deposit in the world with the content of 84% trona. The decomposition of trona appeared to be a single stage process across the temperature range studied (150-200 °C with the representative samples of different size fractions in the draught up metallurgical furnace. The optimum particle size and calcination time were −6.35 mm and 30 minutes, respectively, at calcination temperature of 175 °C in a metallurgical furnace. Microwave-induced dry calcination of trona was possible and 5 minutes of calcination time at a power level of 900 was sufficient for complete calcination of −6.35 mm feed. This includes short time calcinations with the goal of improving economics and simplifying the thermal process.

  13. Structural Integrity Program for INTEC Calcined Solids Storage Facilities

    Energy Technology Data Exchange (ETDEWEB)

    Jeffrey Bryant

    2008-08-30

    This report documents the activities of the structural integrity program at the Idaho Nuclear Technology and Engineering Center relevant to the high-level waste Calcined Solids Storage Facilities and associated equipment, as required by DOE M 435.1-1, 'Radioactive Waste Management Manual'. Based on the evaluation documented in this report, the Calcined Solids Storage Facilities are not leaking and are structurally sound for continued service. Recommendations are provided for continued monitoring of the Calcined Solids Storage Facilities.

  14. Calcine Waste Storage at the Idaho Nuclear Technology and Engineering Center

    Energy Technology Data Exchange (ETDEWEB)

    Staiger, Merle Daniel; M. C. Swenson

    2005-01-01

    This report documents an inventory of calcined waste produced at the Idaho Nuclear Technology and Engineering Center during the period from December 1963 to May 2000. The report was prepared based on calciner runs, operation of the calcined solids storage facilities, and miscellaneous operational information that establishes the range of chemical compositions of calcined waste stored at Idaho Nuclear Technology and Engineering Center. The report will be used to support obtaining permits for the calcined solids storage facilities, possible treatment of the calcined waste at the Idaho National Engineering and Environmental Laboratory, and to ship the waste to an off-site facility including a geologic repository. The information in this report was compiled from calciner operating data, waste solution analyses and volumes calcined, calciner operating schedules, calcine temperature monitoring records, and facility design of the calcined solids storage facilities. A compact disk copy of this report is provided to facilitate future data manipulations and analysis.

  15. Crystallographic transformation of limestone during calcination under CO2.

    Science.gov (United States)

    Valverde, Jose Manuel; Medina, Santiago

    2015-09-14

    The calcination reaction of limestone (CaCO3) to yield lime (CaO) is at the heart of many industrial applications as well as natural processes. In the recently emerged calcium-looping technology, CO2 capture is accomplished by the carbonation of CaO in a gas-solid reactor (carbonator). CaO is derived by the calcination of limestone in a calciner reactor under necessarily high CO2 partial pressure and high temperature. In situ X-ray diffraction (XRD) has been employed in this work to gain further insight into the crystallographic transformation that takes place during the calcination of limestone under CO2, at partial pressures (P) close to the equilibrium pressure (Peq) and at high temperature. Calcination under these conditions becomes extremely slow. The in situ XRD analysis presented here suggests the presence of an intermediate metastable CaO* phase stemming from the parent CaCO3 structure. According to the reaction mechanism proposed elsewhere, the exothermicity of the CaO* → CaO transformation and high values of P/Peq inhibit the nucleation of CaO at high temperatures. The wt% of CaO* remains at a relatively high level during slow calcination. Two diverse stages have been identified in the evolution of CaO crystallite size, L. Initially, L increases with CaCO3 conversion, following a logarithmic law. Slow calcination allows the crystallite size to grow up from a few nanometers at nucleation up to around 100 nm near the end of conversion. Otherwise, quick calcination at relatively lower CO2 concentrations limits CaO crystallite growth. Once calcination reaches an advanced state, the presence of CaO* drops to zero and the rate of increase of the CaO crystallite size is significantly hindered. Arguably, the first stage in CaO crystallite growth is driven by aggregation of the metastable CaO* nanocrystals, due to surface attractive forces, whereas the second one is consistent with sintering of the aggregated CaO crystals, and persists with time after full

  16. CSER 99-001: PFP LAB Dentirating calciner

    Energy Technology Data Exchange (ETDEWEB)

    MILLER, E.M.; DOBBIN, K.D.

    1999-02-22

    A criticality safety evaluation report was prepared for the Plutonium Finishing Plant (PFP) laboratory denigrating calciner, located in Glovebox 188-1, that converts Pu(NO{sub 3}){sub 4} solutions to the high fired stable oxide PuO{sub 2}. Fissile mass limits and volume limits are set for the glovebox for testing operations and training operators using only nitric acid feed to a plutonium oxide bed in the calciner.

  17. Modeling of calcination of single kaolinitic clay particle

    DEFF Research Database (Denmark)

    Gebremariam, Abraham Teklay; Yin, Chungen; Rosendahl, Lasse

    The present work aims at modeling of the calcination (dehydroxylation) process of clay particles, specifically kaolinite, and its thermal transformation. For such purpose, 1D single particle calcination model was developed based on the concept of shrinking core model to assess the dehydroxylation...... distribution within the clay particle and simultaneous density changes due to the reaction kinetics. Accordingly, a particular residence time was noticed as a point where kaolinitic clay particles attain optimum conversion to metakaolinite which is pozzolanic....

  18. Adsorption behavior of Zn(II) on calcinated Chinese loess

    Energy Technology Data Exchange (ETDEWEB)

    Tang Xiaowu [MOE Key Laboratory of Soft Soils and Geoenvironmental Engineering, Department of Civil Engineering, Zhejiang University, Zheda Road 38, Hangzhou 310027 (China)], E-mail: tangxiaowu@zju.edu.cn; Li Zhenze; Chen Yunmin [MOE Key Laboratory of Soft Soils and Geoenvironmental Engineering, Department of Civil Engineering, Zhejiang University, Zheda Road 38, Hangzhou 310027 (China)

    2009-01-30

    Chinese loess has proven to be effective in removing Zn(II) from aqueous solutions, but the resultant adsorbent-water slurry is difficult to separate. In this paper, the crude loess was calcinated to improve the separation efficiency of slurries in terms of sedimentary rate by increasing the particle sizes of the adsorbent. The sorption capacities of different sorbents, including crude loess, calcinated loess, de-organic crude loess and acid-treated calcinated loess, were obtained and sequenced. The adsorption capacity of the calcinated loess towards Zn(II) was found to be as high as 113.6 mg g{sup -1}. The adsorption isotherms and kinetics of calcinated loess were best-fit with the Freundlich isotherm and the pseudo-second order kinetics, respectively. The thermodynamic analysis revealed that the adsorption was exothermic and spontaneous with a high preference for Zn(II) removal. The adsorption of Zn(II) on calcinated loess implies an ion exchange of the solute with calcite and goethite due to the observed FT-IR and XRD patterns as well as the predicted mean free energies (-11.58 to -9.28 kJ mol{sup -1} by D-R model). The byproduct of adsorption can be purified and refreshed by using a 0.01 M HCl solution.

  19. High Temperature Calcination - MACT Upgrade Equipment Pilot Plant Test

    Energy Technology Data Exchange (ETDEWEB)

    Richard D. Boardman; B. H. O& #39; Brien; N. R. Soelberg; S. O. Bates; R. A. Wood; C. St. Michel

    2004-02-01

    About one million gallons of acidic, hazardous, and radioactive sodium-bearing waste are stored in stainless steel tanks at the Idaho Nuclear Technology and Engineering Center (INTEC), which is a major operating facility of the Idaho National Engineering and Environmental Laboratory. Calcination at high-temperature conditions (600 C, with alumina nitrate and calcium nitrate chemical addition to the feed) is one of four options currently being considered by the Department of Energy for treatment of the remaining tank wastes. If calcination is selected for future processing of the sodium-bearing waste, it will be necessary to install new off-gas control equipment in the New Waste Calcining Facility (NWCF) to comply with the Maximum Achievable Control Technology (MACT) standards for hazardous waste combustors and incinerators. This will require, as a minimum, installing a carbon bed to reduce mercury emissions from their current level of up to 7,500 to <45 {micro}g/dscm, and a staged combustor to reduce unburned kerosene fuel in the off-gas discharge to <100 ppm CO and <10 ppm hydrocarbons. The staged combustor will also reduce NOx concentrations of about 35,000 ppm by 90-95%. A pilot-plant calcination test was completed in a newly constructed 15-cm diameter calciner vessel. The pilot-plant facility was equipped with a prototype MACT off-gas control system, including a highly efficient cyclone separator and off-gas quench/venturi scrubber for particulate removal, a staged combustor for unburned hydrocarbon and NOx destruction, and a packed activated carbon bed for mercury removal and residual chloride capture. Pilot-plant testing was performed during a 50-hour system operability test January 14-16, followed by a 100-hour high-temperature calcination pilot-plant calcination run January 19-23. Two flowsheet blends were tested: a 50-hour test with an aluminum-to-alkali metal molar ratio (AAR) of 2.25, and a 50-hour test with an AAR of 1.75. Results of the testing

  20. Improved Low-Temperature Activity of V2O5-WO3/TiO2 for Denitration Using Different Vanadium Precursors

    OpenAIRE

    Lina Gan; Feng Guo; Jian Yu; Guangwen Xu

    2016-01-01

    This work tested two V2O5-WO3/TiO2 catalysts with different vanadium precursors for selective catalytic reduction (SCR) of flue gas NO using NH3 at 150–450 °C. While catalyst A was prepared using ammonium metavanadate (NH4VO3) through incipient impregnation, catalyst B was made according to the solvothermal method using vanadyl acetylacetonate (VO(acac)2) as the vanadium precursor. The catalytic evaluation for denitration was in a laboratory fixed bed reactor using simulated flue gas under co...

  1. Optimization of Calcine Blending During Retrieval From Binsets; TOPICAL

    International Nuclear Information System (INIS)

    Taylor, D.D.; Mohr, C.M.; Nelson, L.O.

    2000-01-01

    This report documents a study performed during advanced feasibility studies for the INTEC Technology Development Facility (ITDF). The study was commissioned to provide information about functional requirements for the ITDF related to development of equipment and procedures for retrieving radioactive calcine from binset storage at the Idaho Nuclear Technology and Engineering Center (INTEC) at the Idaho National Engineering and Environmental Laboratory (INEEL). Calcine will be retrieved prior to treating it for permanent disposal in a national repository for high level waste. The objective this study was to estimate the degree of homogenization of the calcine that might be achieved through optimized retrieval and subsequent blending. Such homogenization has the potential of reducing the costs for treatment of the calcine and for qualifying of the final waste forms for acceptance at the repository. Results from the study indicate that optimized retrieval and blending can reduce the peak c oncentration variations of key components (Al, Zr, F) in blended batches of retrieved calcine. During un-optimized retrieval these variations are likely to be 81-138% while optimized retrieval can reduce them to the 5-10% range

  2. Plutonium Immobilization Project (PIP) Precursor Material Calcine Temperature

    International Nuclear Information System (INIS)

    Cozzi, A.D.

    1999-01-01

    As a result of the end of the Cold War, approximately 50 metric tons of plutonium are no longer needed and have been identified for disposition. A ceramic waste form is the chosen option for immobilization of the excess plutonium. The plutonium ceramic form then will be encased in high-level waste glass using can-in-canister technology for final disposition. The precursor materials are the non-radioactive components that are added to the plutonium feed stream to form the desired phases in the immobilization product. The precursor materials are blended and calcined prior to being mixed with the plutonium feed stream. The purpose of the calcine step is to remove any physical or chemical water retained in the precursors and convert any hydroxides or carbonates to the oxides. Initially, a temperature of 750 degrees C for a period of one hour was chosen for the calcining of the precursors. In this effort, several different calcine temperatures were investigated to evaluate the effect on initial phase formation (in the calcined precursors), thermal expansion of the pressed pellets during heating, and mineralogy and porosity of the final product

  3. Calcined Waste Storage at the Idaho Nuclear Technology and Engineering Center

    Energy Technology Data Exchange (ETDEWEB)

    Staiger, M. Daniel, Swenson, Michael C.

    2011-09-01

    This comprehensive report provides definitive volume, mass, and composition (chemical and radioactivity) of calcined waste stored at the Idaho Nuclear Technology and Engineering Center. Calcine composition data are required for regulatory compliance (such as permitting and waste disposal), future treatment of the caline, and shipping the calcine to an off-Site-facility (such as a geologic repository). This report also contains a description of the calcine storage bins. The Calcined Solids Storage Facilities (CSSFs) were designed by different architectural engineering firms and built at different times. Each CSSF has a unique design, reflecting varying design criteria and lessons learned from historical CSSF operation. The varying CSSF design will affect future calcine retrieval processes and equipment. Revision 4 of this report presents refinements and enhancements of calculations concerning the composition, volume, mass, chemical content, and radioactivity of calcined waste produced and stored within the CSSFs. The historical calcine samples are insufficient in number and scope of analysis to fully characterize the entire inventory of calcine in the CSSFs. Sample data exist for all the liquid wastes that were calcined. This report provides calcine composition data based on liquid waste sample analyses, volume of liquid waste calcined, calciner operating data, and CSSF operating data using several large Microsoft Excel (Microsoft 2003) databases and spreadsheets that are collectively called the Historical Processing Model. The calcine composition determined by this method compares favorably with historical calcine sample data.

  4. Letter report: Evaluation of dryer/calciner technologies for testing

    International Nuclear Information System (INIS)

    Sevigny, G.

    1996-02-01

    This letter report describes some past experiences on the drying and calcination of radioactive materials or corresponding simulants; and the information needed from testing. The report also includes an assessment of informational needs including possible impacts to a full-scale plant. This includes reliability, maintenance, and overall size versus throughput. Much of the material was previously compiled and reported by Mike Elliott of PNL open-quotes Melter Performance Assessmentclose quotes and Larry Eisenstatt of SEG on contract to WHC in a letter to Rod Powell. Also, an annotated bibliography was prepared by Reagan Seymour of WHC. Descriptions of the drying and calciner technologies, development status, advantages and disadvantages of using a WFE or calciner, and recommendations for future testing are discussed in this report

  5. Apatite formation on calcined kaolin-white Portland cement geopolymer.

    Science.gov (United States)

    Pangdaeng, S; Sata, V; Aguiar, J B; Pacheco-Torgal, F; Chindaprasirt, P

    2015-06-01

    In this study, calcined kaolin-white Portland cement geopolymer was investigated for use as biomaterial. Sodium hydroxide and sodium silicate were used as activators. In vitro test was performed with simulated body fluid (SBF) for bioactivity characterization. The formation of hydroxyapatite bio-layer on the 28-day soaked samples surface was tested using SEM, EDS and XRD analyses. The results showed that the morphology of hydroxyapatite was affected by the source material composition, alkali concentration and curing temperature. The calcined kaolin-white Portland cement geopolymer with relatively high compressive strength could be fabricated for use as biomaterial. The mix with 50% white Portland cement and 50% calcined kaolin had 28-day compressive strength of 59.0MPa and the hydroxyapatite bio-layer on the 28-day soaked sample surface was clearly evident. Copyright © 2015 Elsevier B.V. All rights reserved.

  6. Industrial calcination of kaolinitic clays to make reactive pozzolans

    Directory of Open Access Journals (Sweden)

    Roger S. Almenares

    2017-06-01

    Full Text Available This paper presents the results of an industrial trial for the production of calcined clay to be used as pozzolan in cement manufacture. For the trial, a wet-process clinker rotary kiln was modified to process on dry basis the low grade kaolinitic clay used as raw material. The kaolinitic clay deposit was chosen through a screening based on geologic, chemical and mineralogical criteria, and a confirmation of reactivity with an experimental protocol at lab scale. During the calcination trial technological parameters such as rotation speed, fuel pressure and outer temperature of calcined clay were measured and coupled with the reactivity of the samples tested, thus, preliminary estimations of operational parameters can be made. The trial proved that it is possible to produce a reactive pozzolan at industrial scale by implementing small conversions on existing equipment of a typical clinker plant.

  7. Microstructural changes in porous hematite nanoparticles upon calcination

    DEFF Research Database (Denmark)

    Johnsen, Rune; Knudsen, Kenneth D.; Molenbroek, Alfons M.

    2011-01-01

    This combined study using small-angle neutron scattering (SANS), X-ray powder diffraction (XRPD), transmission electron microscopy (TEM) and adsorption isotherm techniques demonstrates radical changes in the microstructure of porous hematite (-Fe2O3) nanoparticles upon calcination in air. TEM...... images of the as-synthesized hematite sample show that it consists of subrounded nanoparticles [50 (8)–61 (11) nm in average minimum and maximum diameters] with an apparent porous structure of nanosized pores/ channels or cracks. SANS data confirm the presence of two characteristic sizes, one originating....... The change in microstructure also causes a reduction in the surface area as calculated by gaseous adsorption. The XRPD and SANS data show that the crystallite and SANS particle sizes are virtually unchanged by calcination at 623 K. Calcination at 973 K induces a significant alteration of the sample. The XRPD...

  8. Synthesis of NaY Zeolite Using Mixed Calcined Kaolins

    Directory of Open Access Journals (Sweden)

    Subagjo

    2015-12-01

    Full Text Available Kaolin is one of several types of clay minerals. The most common crystalline phase constituting kaolin minerals is kaolinite, with the chemical composition Al2Si2O5(OH4. Kaolin is mostly used for manufacturing traditional ceramics and also to synthesize zeolites or molecular sieves. The Si-O and Al-O structures in kaolin are inactive and inert, so activation by calcination is required. This work studies the conversion of kaolin originating from Bangka island in Indonesia into calcined kaolin phase as precursor in NaY zeolite synthesis. In the calcination process, the kaolinite undergoes phase transformations from metakaolin to mullite. The Bangka kaolin is 74.3% crystalline, predominantly composed of kaolinite, and 25.7% amorphous, with an SiO2/Al2O3 mass ratio of 1.64. Thermal characterization using simultaneous DSC/TGA identified an endothermic peak at 527°C and an exothermic peak at 1013°C. Thus, three calcination temperatures (700, 1013, and 1050 °C were selected to produce calcined kaolins with different phase distributions. The best product, with 87.8% NaY zeolite in the 54.7% crystalline product and an SiO2/Al2O3 molar ratio of 5.35, was obtained through hydrothermal synthesis using mixed calcined kaolins with a composition of K700C : K1013C : K1050C = 10 : 85 : 5 in %-mass, with seed addition, at a temperature of 93 °Cand a reaction time of 15 hours.

  9. Corrosion experience in calcination of liquid nuclear waste

    Energy Technology Data Exchange (ETDEWEB)

    Zimmerman, C A

    1980-01-01

    The Waste Calcining Facility (WCF) at the Idaho National Engineering Laboratory became operational in 1963. Since that time, approximately 13,337,137 litres (3,523,375 gallons) of liquid nuclear wastes, generated during the reprocessing of spent nuclear fuel materials, have been reduced to dry granular solids. The volume reduction is about seven or eight gallons of liquid waste to one gallon of dry granular solids. This paper covers some of the corrosion experiences encountered in over fifteen years of operating that calcination facility. 7 figures, 7 tables.

  10. Techniques for detection of transition phases in calcined alumina

    International Nuclear Information System (INIS)

    Pandolfelli, V.C.; Folgueras-Dominguez, S.

    1987-01-01

    Detection of transition phases in alumina, is very important in the receiving control and calcination of aluminium hydroxide. The non alfa or transition phases difficults the processability and causes localized shrinkage on sintering compromising the dimensional and mechanical aspects of the product. In this research using refraction index, absorption of dyes, specific density, X-ray diffraction and scanning electron microscopy, analyses, are done in calcined hydroxides submited to different thermal treatments. The limits and facilities of each technique are discussed and compared. (Author) [pt

  11. Calcine Waste Storage at the Idaho Nuclear Technology and Engineering Center

    Energy Technology Data Exchange (ETDEWEB)

    M. D. Staiger

    1999-06-01

    A potential option in the program for long-term management of high-level wastes at the Idaho Nuclear Technology and Engineering Center (INTEC), at the Idaho National Engineering and Environmental Laboratory, calls for retrieving calcine waste and converting it to a more stable and less dispersible form. An inventory of calcine produced during the period December 1963 to May 1999 has been prepared based on calciner run, solids storage facilities operating, and miscellaneous operational information, which gives the range of chemical compositions of calcine waste stored at INTEC. Information researched includes calciner startup data, waste solution analyses and volumes calcined, calciner operating schedules, solids storage bin capacities, calcine storage bin distributor systems, and solids storage bin design and temperature monitoring records. Unique information on calcine solids storage facilities design of potential interest to remote retrieval operators is given.

  12. Study of as-synthesized and calcined hydrocalumites as possible ...

    Indian Academy of Sciences (India)

    Administrator

    calcine at different temperatures Ca/Al hydrocalumite- type solids for evaluating their basic properties in vitro as antacid. Results are compared to those obtained with a commercial antacid based on hydrotalcite as active agent. 2. Experimental. 2.1 Synthesis of hydrocalumite (HC). Hydrocalumite was synthesized by the co- ...

  13. Effect of fly ash calcination in geopolymer synthesis

    Science.gov (United States)

    Samadhi, Tjokorde Walmiki; Jatiningrum, Mirna; Arisiani, Gresia

    2015-12-01

    Geopolymer, a largely amorphous class of inorganic polymer consisting of aluminosilicate repeat units, is an environmentally attractive engineering material due to its ability to consume aluminosilicate waste as raw materials. This work studies the effect of the calcination temperature of a coal fly ash generated by a low-efficiency boiler on the mechanical strength of geopolymer mortar synthesized using a mixture of the fly ash, potassium hydroxide as the alkali activator, and locally available sand as the filler aggregate. The calcination temperature is varied between 500-700 °C, with a calcination period of 2 hours in an electric furnace. Two sand samples with different particle size distributions are used. The key response variable is the compressive strength at room temperature, measured after curing at 80 °C for 7 and 14 days. Uncalcined ash, with a carbon content of approximately 31.0%, is not amenable for geopolymer synthesis. Analysis of experimental data using the ANOVA method for general factorial design identifies significant main effects for all three experimental variables. Two-way interactions are significant, except that between sand type and curing period. Higher calcination temperature significantly improves the strength of the mortar. However, the strength of the obtained geopolymer mortars are still significantly lower than that of ordinary Portland cement mortar.

  14. Screening Level Risk Assessment for the New Waste Calcining Facility

    Energy Technology Data Exchange (ETDEWEB)

    M. L. Abbott; K. N. Keck; R. E. Schindler; R. L. VanHorn; N. L. Hampton; M. B. Heiser

    1999-05-01

    This screening level risk assessment evaluates potential adverse human health and ecological impacts resulting from continued operations of the calciner at the New Waste Calcining Facility (NWCF) at the Idaho Nuclear Technology and Engineering Center (INTEC), Idaho National Engineering and Environmental Laboratory (INEEL). The assessment was conducted in accordance with the Environmental Protection Agency (EPA) report, Guidance for Performing Screening Level Risk Analyses at Combustion Facilities Burning Hazardous Waste. This screening guidance is intended to give a conservative estimate of the potential risks to determine whether a more refined assessment is warranted. The NWCF uses a fluidized-bed combustor to solidify (calcine) liquid radioactive mixed waste from the INTEC Tank Farm facility. Calciner off volatilized metal species, trace organic compounds, and low-levels of radionuclides. Conservative stack emission rates were calculated based on maximum waste solution feed samples, conservative assumptions for off gas partitioning of metals and organics, stack gas sampling for mercury, and conservative measurements of contaminant removal (decontamination factors) in the off gas treatment system. Stack emissions were modeled using the ISC3 air dispersion model to predict maximum particulate and vapor air concentrations and ground deposition rates. Results demonstrate that NWCF emissions calculated from best-available process knowledge would result in maximum onsite and offsite health and ecological impacts that are less then EPA-established criteria for operation of a combustion facility.

  15. Utilization of Microwave Energy in the Calcination and ...

    African Journals Online (AJOL)

    The application of microwave energy in the calcination and agglomeration of manganese carbonate ore from Nsuta, Ghana, has been investigated. The real and imaginary permittivities, which may be used to determine a substance's response to microwave heating, were measured and the permittivities of both the ore and ...

  16. Physical and chemical characterization of synthetic calcined sludge

    International Nuclear Information System (INIS)

    Slates, R.V.; Mosley, W.C. Jr.; Tiffany, B.; Stone, J.A.

    1982-03-01

    Calcined synthetic sludge was chemically characterized in support of engineering studies to design a processing plant to solidify highly radioactive waste at the Savannah River Plant. An analytical technique is described which provides quantitative data by mass spectrometric analysis of gases evolved during thermogravimetric analysis without measurements of gas flow rates or mass spectrometer sensitivities. Scanning electron microprobe analysis, Mossbauer spectroscopy, and several other common analytical methods were also used. Calcined sludge consists primarily of amorphous particles of hydrous oxides with iron, manganese, nickel, and calcium distributed fairly uniformly throughout the powder. Iron, manganese, nickel, and calcium exist in forms that are highly insoluble in water, but aluminum, sulfate, nitrate, and sodium exhibit relative water solubilities that increase in the given order from 60% to 94%. Evolved gas analysis in a helium atmosphere showed that calcined sludge is completely dehydrated by heating to 400 0 C, carbon dioxide is evolved between 100 to 700 0 C with maximum evolution at 500 0 C, and oxygen is evolved between 400 and 1000 0 C. Evolved gas analyses are also reported for uncalcined sludge. A spinel-type oxide similar to NiFe 2 O 4 was detected by x-ray diffraction analysis at very low-level in calcined sludge

  17. Ninth Processing Campaign in the Waste Calcining Facility

    International Nuclear Information System (INIS)

    Childs, K.F.; Donovan, R.I.; Swenson, M.C.

    1982-04-01

    This report discusses the Ninth (and final) Processing Campaign at the Waste Calcining Facility. Several processing interruptions were experienced during this campaign and the emphasis of this report is on process and equipment performance with operating problems and corrective actions discussed in detail

  18. Improvement of Gold Leaching from a Refractory Gold Concentrate Calcine by Separate Pretreatment of Coarse and Fine Size Fractions

    Directory of Open Access Journals (Sweden)

    Qian Li

    2017-05-01

    Full Text Available A total gold extraction of 70.2% could only be reached via direct cyanidation from a refractory As-, S- and C-bearing gold concentrate calcine, and the gold extraction varied noticeably with different size fractions. The reasons for unsatisfactory gold extraction from the calcine were studied through analyses of chemical composition, chemical phase and SEM-EDS of different sizes of particles. It was found that a significant segregation of compositions occurred during the grinding of gold ore before flotation. As a result, for the calcine obtained after oxidative roasting, the encapsulation of gold by iron oxides was easily engendered in finer particles, whilst in coarser particles the gold encapsulation by silicates was inclined to occur likely due to melted silicates blocking the porosity of particles. The improvement of gold leaching from different size fractions was further investigated through pretreatments with alkali washing, acid pickling or sulfuric acid curing-water leaching. Finally, a novel process was recommended and the total gold extraction from the calcine could be increased substantially to 93.6% by the purposeful pretreatment with alkali washing for the relatively coarse size fraction (+37 μm and sulfuric acid curing–water leaching for the fine size fraction (−37 μm.

  19. In Vitro Studies Evaluating Leaching of Mercury from Mine Waste Calcine Using Simulated Human Body Fluids

    OpenAIRE

    Gray, John E.; Plumlee, Geoffrey S.; Morman, Suzette A.; Higueras, Pablo L.; Crock, James G.; Lowers, Heather A.; Witten, Mark L.

    2010-01-01

    In vitro bioaccessibility (IVBA) studies were carried out on samples of mercury (Hg) mine-waste calcine (roasted Hg ore) by leaching with simulated human body fluids. The objective was to estimate potential human exposure to Hg due to inhalation of airborne calcine particulates and hand-to-mouth ingestion of Hg-bearing calcines. Mine waste calcines collected from Hg mines at Almad?n, Spain, and Terlingua, Texas, contain Hg sulfide, elemental Hg, and soluble Hg compounds, which constitute prim...

  20. Calcined iron rich clay as an adsorbent and a photocatalyst for the ...

    African Journals Online (AJOL)

    Photocatalytic degradation of phenol using the calcined clay obeys pseudo-first order kinetic model. The apparent rate constants (kapp) of the photocatalytic degradation of phenol using the calcined iron rich clay are higher than the reported kapp for the photocatalytic degradation of phenol using TiO2. The calcined iron rich ...

  1. Calcined Waste Storage at the Idaho Nuclear Technology and Engineering Center

    Energy Technology Data Exchange (ETDEWEB)

    M. D. Staiger

    2007-06-01

    This report provides a quantitative inventory and composition (chemical and radioactivity) of calcined waste stored at the Idaho Nuclear Technology and Engineering Center. From December 1963 through May 2000, liquid radioactive wastes generated by spent nuclear fuel reprocessing were converted into a solid, granular form called calcine. This report also contains a description of the calcine storage bins.

  2. Comparative evaluation of glasses reprocessing and reversible conditioning of calcinates; Evaluation comparative de la reprise des verres et du conditionnement reversible des calcinats

    Energy Technology Data Exchange (ETDEWEB)

    Boen, R

    2000-01-15

    Fission products and minor actinides separated during the spent fuel reprocessing treatment are industrially vitrified on-line and thus confined inside a glass matrix with admittedly durability properties. In the framework of the feasibility of a reversible conditioning, this document examines first the possible alternative ways of conditioning and storage of calcinates before vitrification, which may simplify the reversibility aspect. Such a conditioning must be compatible with the storage process, with a possible extraction of actinides and long-lived fission products, and with the vitrification process if no extraction is performed. Calcinates are pulverulent and comprise an important soluble fraction, a proportion of nitrates of about 30%, and release a high thermal power (17 kW/m{sup 3}) combined to a low thermal conductivity (0.1 to 0.15 W.m{sup -1} k{sup -1}). Among the different foreseeable solutions (denitration, mixing with another material, with or without compacting, dissolution inside another material..), the dissolution inside a borate seems to be the most acceptable with respect to the safety, feasibility and vitrification aspects. The thermal aspect of the storage remains complex as a specific container is necessary. In a second part, this report analyzes the possibility to re-extract back the long-lived radionuclides from vitrified wastes. The different possible ways to destroy the glass structure and to transfer the fission products and minor actinides in an aqueous solution compatible with an hydrometallurgical separation process are explored. Two processes are foreseeable: a low temperature dissolution process which requires a preliminary crushing and the handling of huge amounts of acids, and a both high and low temperature process which comprises the following steps: melting, fractionation by water tempering, addition of Na{sub 2}O or sodium tetraborate to make it sensible to hot leaching, separation of fission products and minor actinides

  3. Evaluation of ceramic materials to immobilize ICPP calcines

    International Nuclear Information System (INIS)

    Staples, B.A.; Cole, H.S.; Mittl, J.C.

    1982-01-01

    Various ceramic materials as well as Formula 127 glass have been developed to immobilize Idaho Chemical Processing Plant (ICPP) zirconia calcine. Tailored, titanate and matrix encapsulated ceramics were prepared by cold pressing and sintering reactants, while glass-ceramics were prepared by melting in a manner similar to that of preparing the glass. X-ray diffraction techniques were used to determine the presence of radionuclide and calcine matrix element host phases in each ceramic material. The aqueous leachability, practical loading capacity and the incorporation of waste elements into host phases was investigated and compared to those of Formula 127 glass through application of the Soxhlet and MCC-1 static leach tests. Potential process requirements for each material were evaluated based on the number of steps needed for laboratory-scale preparation. 5 figures, 4 tables

  4. Sulfuric acid leaching of high iron-bearing zinc calcine

    Science.gov (United States)

    Yang, Jin-lin; Liu, Ji-guang; Xiao, Han-xin; Ma, Shao-jian

    2017-11-01

    Sulfuric acid leaching of high iron-bearing zinc calcine was investigated to assess the effects of sulfuric acid concentration, liquid- to-solid ratio, leaching time, leaching temperature, and the stirring speed on the leaching rates of zinc and iron. The results showed that the sulfuric acid concentration, liquid-to-solid ratio, leaching time, and leaching temperature strongly influenced the leaching of zinc and iron, whereas stirring speed had little influence. Zinc was mainly leached and the leaching rate of iron was low when the sulfuric acid concentration was less than 100 g/L. At sulfuric acid concentrations higher than 100 g/L, the leaching rate of iron increased quickly with increasing sulfuric acid concentration. This behavior is attributed to iron-bearing minerals such as zinc ferrite in zinc calcine dissolving at high temperatures and high sulfuric acid concentrations but not at low temperatures and low sulfuric acid concentrations.

  5. Metal-support interaction: The key factor governing activity of Pd/SnO2 catalyst for denitration of ground water

    Directory of Open Access Journals (Sweden)

    Bošković Goran C.

    2008-01-01

    Full Text Available Two mesoporous nanocristalline Pd/SnO2 catalysts were prepared by modified solgel technique differing in the pH conditions (pH = 2 and 9.5 of the synthesis of their supports. Samples achieved different activity and selectivity in water denitration reaction using hydrogen. XPS results of reduced samples indicate a strong interaction between the Pd and the Sn possibly as a result of electron shift from Sn to Pd. The solid solution of Pd2+ and SnO2 is formed by taking O from the surface of the support. In such a way some SnO2-X species may stay onto the surface and be responsible for its pronounced activity.

  6. 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)

  7. Experimental Results of NWCF Run H4 Calcine Dissolution Studies Performed in FY-98 and -99

    Energy Technology Data Exchange (ETDEWEB)

    Garn, Troy Gerry; Herbst, Ronald Scott; Batcheller, Thomas Aquinas; Sierra, Tracy Laureena

    2001-08-01

    Dissolution experiments were performed on actual samples of NWCF Run H-4 radioactive calcine in fiscal years 1998 and 1999. Run H-4 is an aluminum/sodium blend calcine. Typical dissolution data indicates that between 90-95 wt% of H-4 calcine can be dissolved using 1gram of calcine per 10 mLs of 5-8M nitric acid at boiling temperature. Two liquid raffinate solutions composed of a WM-188/aluminum nitrate blend and a WM-185/aluminum nitrate blend were converted into calcine at the NWCF. Calcine made from each blend was collected and transferred to RAL for dissolution studies. The WM-188/aluminum nitrate blend calcine was dissolved with resultant solutions used as feed material for separation treatment experimentation. The WM-185/aluminum nitrate blend calcine dissolution testing was performed to determine compositional analyses of the dissolved solution and generate UDS for solid/liquid separation experiments. Analytical fusion techniques were then used to determine compositions of the solid calcine and UDS from dissolution. The results from each of these analyses were used to calculate elemental material balances around the dissolution process, validating the experimental data. This report contains all experimental data from dissolution experiments performed using both calcine blends.

  8. ICPP radioactive liquid and calcine waste technologies evaluation. Interim report

    Energy Technology Data Exchange (ETDEWEB)

    Murphy, J.A.; Pincock, L.F.; Christiansen, I.N.

    1994-06-01

    The Department of Energy (DOE) has received spent nuclear fuel (SNF) at the Idaho Chemical Processing Plant (ICPP) for interim storage since 1951 and reprocessing since 1953. Until recently, the major activity of the ICPP has been the reprocessing of SNF to recover fissile uranium; however, changing world events have raised questions concerning the need to recover and recycle this material. In April 1992, DOE chose to discontinue reprocessing SNF for uranium recovery and shifted its focus toward the management and disposition of radioactive wastes accumulated through reprocessing activities. Currently, 1.8 million gallons of radioactive liquid wastes (1.5 million gallons of radioactive sodium-bearing liquid wastes and 0.3 million gallons of high-level liquid waste) and 3,800 cubic meters (m{sup 3}) of calcine waste are in inventory at the ICPP. Legal drivers and agreements exist obligating the INEL to develop, demonstrate, and implement technologies for safe and environmentally sound treatment and interim storage of radioactive liquid and calcine waste. Candidate treatment processes and waste forms are being evaluated using the Technology Evaluation and Analysis Methodology (TEAM) Model. This process allows decision makers to (1) identify optimum radioactive waste treatment and disposal form alternatives; (2) assess tradeoffs between various optimization criteria; (3) identify uncertainties in performance parameters; and (4) focus development efforts on options that best satisfy stakeholder concerns. The Systems Analysis technology evaluation presented in this document supports the DOE in selecting the most effective radioactive liquid and calcine waste management plan to implement in compliance with established regulations, court orders, and agreements.

  9. Advanced fluid bed calciner information on IR-100 award

    International Nuclear Information System (INIS)

    Druby, M.C.; Owen, T.J.; Klem, M.J.

    1986-01-01

    The advanced fluidized bed calciner provides time, temperature and turbulence to change a liquid slurry such as ammonium diuranate into a uranium dioxide powder. The liquid is sprayed into a hot chamber (up to 700 0 C) which includes thousands of tiny metal beads, about the size of BB's. The constantly moving beads provide an efficient heat transfer media for the immediate transformation of the slurry droplets into dry particles of powder, which are carried out by hot nitrogen gas and recovered in a collector

  10. Remote process connectors for the new waste calcining facility

    International Nuclear Information System (INIS)

    Jacobs, R.T.; Carter, J.A.; Hohback, A.C.

    1978-01-01

    The remote process connectors developed, used, and tested at the Remote Maintenance Development Facility are described. These connectors, including the three-bolt kinematic-graphite flange and watertight electrical connectors, are assembled on master jigs (holding-welding fixture) to form interchangeable pump and valve loop assemblies. These assemblies, with their guide-in platforms, make possible a method of performing remote maintenance at the New Waste Calcining Facility which is a departure from methods that until now have been the standard of the industry

  11. Precipitation of plutonium (III) oxalate and calcination to plutonium oxide

    International Nuclear Information System (INIS)

    Esteban, A.; Orosco, E.H.; Cassaniti, P.; Greco, L.; Adelfang, P.

    1989-01-01

    The plutonium based fuel fabrication requires the conversion of the plutonium nitrate solution from nuclear fuel reprocessing into pure PuO2. The conversion method based on the precipitation of plutonium (III) oxalate and subsequent calcination has been studied in detail. In this procedure, plutonium (III) oxalate is precipitated, at room temperature, by the slow addition of 1M oxalic acid to the feed solution, containing from 5-100 g/l of plutonium in 1M nitric acid. Before precipitation, the plutonium is adjusted to trivalent state by addition of 1M ascorbic acid in the presence of an oxidation inhibitor such as hydrazine. Finally, the precipitate is calcinated at 700 deg C to obtain PuO2. A flowsheet is proposed in this paper including: a) A study about the conditions to adjust the plutonium valence. b) Solubility data of plutonium (III) oxalate and measurements of plutonium losses to the filtrate and wash solution. c) Characterization of the obtained products. Plutonium (III) oxalate has several potential advantages over similar conversion processes. These include: 1) Formation of small particle sizes powder with good pellets fabrication characteristics. 2) The process is rather insensitive to most process variables, except nitric acid concentration. 3) Ambient temperature operations. 4) The losses of plutonium to the filtrate are less than in other conversion processes. (Author) [es

  12. Dissolution kinetics of calcined ulexite in ammonium sulfate solutions

    Directory of Open Access Journals (Sweden)

    Nizamettin Demirkıran

    2018-03-01

    Full Text Available Ulexite is one of the boron minerals, which include a respectable amount of hydration water. It can be used as a raw material in the production of boron compounds. Some part of water in the composition of ulexite can be removed from the solid matrix applying dehydration treatment, and a porous structure can be obtained to increase the reaction rate. In the present study, the effect of dehydration temperature on dissolution kinetics of ulexite in ammonium sulfate solutions was researched in a batch reactor utilizing the parameters of solution concentration, solid-to-liquid ratio, stirring speed and reaction temperature. It was determined that the dissolution rate of calcined material increased with increasing solution concentration and reaction temperature and with decreasing solid-to-liquid ratio. The highest dissolution rate was attained with the sample calcined at 150 °C. It was found that the dissolution rate fit to the first order pseudo-homogeneous model. The activation energy of the dissolution process was estimated to be 42 kJ·mol-1.

  13. 46 CFR 148.04-17 - Petroleum coke, calcined, at 130 °F or above.

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Petroleum coke, calcined, at 130 °F or above. 148.04-17...-17 Petroleum coke, calcined, at 130 °F or above. (a) The requirements of this part do not apply to bulk shipments of petroleum coke, calcined, on any vessel when the material is less than 130 °F. (b...

  14. Nano-sized ceramic particles of hydroxyapatite calcined with an anti-sintering agent.

    Science.gov (United States)

    Okada, Masahiro; Furuzono, Tsutomu

    2007-03-01

    Nano-sized crystals of calcined hydroxyapatite (HAp) having spherical morphologies were fabricated by calcination at 800 degrees C for 1 h with an anti-sintering agent surrounding the original HAp particles and the agent was subsequently removed by washing after calcination. The original HAp particles were prepared by a modified emulsion system, and surrounded with poly(acrylic acid, calcium salt) (PAA-Ca) by utilizing a precipitation reaction between calcium hydroxide and poly(acrylic acid) adsorbed on the HAp particle surfaces in an aqueous medium. In the case of calcination without PAA-Ca, micron-sized particles consisting of sintered polycrystals were mainly observed by scanning electron microscopy, indicating the calcination-induced sintering among the crystals. On the other hand, most of the crystals calcined with the anti-sintering agent were observed as isolated particles, and the mean size of the HAp crystals was around 80 nm. This result indicates that PAA-Ca and its thermally decomposed product, CaO, surrounding the HAp crystals could protect them against calcination-induced sintering during calcination at 800 degrees C. The HAp crystals calcined with PAA-Ca showed high crystallinity, and no other calcium phosphate phases could be detected.

  15. In vitro studies evaluating leaching of mercury from mine waste calcine using simulated human body fluids

    Science.gov (United States)

    Gray, John E.; Plumlee, Geoffrey S.; Morman, Suzette A.; Higueras, Pablo L.; Crock, James G.; Lowers, Heather A.; Witten, Mark L.

    2010-01-01

    In vitro bioaccessibility (IVBA) studies were carried out on samples of mercury (Hg) mine-waste calcine (roasted Hg ore) by leaching with simulated human body fluids. The objective was to estimate potential human exposure to Hg due to inhalation of airborne calcine particulates and hand-to-mouth ingestion of Hg-bearing calcines. Mine waste calcines collected from Hg mines at Almadén, Spain, and Terlingua, Texas, contain Hg sulfide, elemental Hg, and soluble Hg compounds, which constitute primary ore or compounds formed during Hg retorting. Elevated leachate Hg concentrations were found during calcine leaching using a simulated gastric fluid (as much as 6200 μg of Hg leached/g sample). Elevated Hg concentrations were also found in calcine leachates using a simulated lung fluid (as much as 9200 μg of Hg leached/g), serum-based fluid (as much as 1600 μg of Hg leached/g), and water of pH 5 (as much as 880 μg of Hg leached/g). The leaching capacity of Hg is controlled by calcine mineralogy; thus, calcines containing soluble Hg compounds contain higher leachate Hg concentrations. Results indicate that ingestion or inhalation of Hg mine-waste calcine may lead to increased Hg concentrations in the human body, especially through the ingestion pathway.

  16. Feasibility of Carbonaceous Nanomaterial-Assisted Photocatalysts Calcined at Different Temperatures for Indoor Air Applications

    Directory of Open Access Journals (Sweden)

    Wan-Kuen Jo

    2012-01-01

    Full Text Available This study examined the characteristics and photocatalytic activity of multiwall carbon nanotube-assisted TiO2 (MWNT-TiO2 nanocomposites calcined at different temperatures to assess their potential indoor air applications. It was confirmed that the composites calcined at low temperatures (300 and 400°C contained TiO2 nanoparticles bound intimately to the MWNT networks. Meanwhile, almost no MWNTs were observed when the calcination temperature was increased to 500 and 600°C. The MWNT-TiO2 composites calcined at low temperatures showed higher photocatalytic decomposition efficiencies for aromatic hydrocarbons at indoor concentrations than those calcined at high temperatures. The mean efficiencies for benzene, toluene, ethyl benzene, and o-xylene (BTEX by the composite calcined at 300°C were 32, 70, 79, and 79%, respectively, whereas they were 33, 71, 78, and 78% for the composite calcined at 400°C, respectively. In contrast, the efficiencies decreased to close to zero when the calcination temperature was increased to 600°C. Moreover, the MWNT-TiO2 exhibited superior photocatalytic performance for the decomposition efficiencies compared to TiO2 under conventional UV-lamp irradiations. Consequently, these carbonaceous nanomaterial-assisted photocatalysts can be applied effectively to indoor air applications depending upon the calcination temperature.

  17. Modeling of in-line low-NOx calciners - a parametric study

    DEFF Research Database (Denmark)

    Iliuta, Ion; Dam-Johansen, Kim; Jensen, Anker

    2002-01-01

    parameter is the mixing rate of preheated combustion air into the sub-stoichiometric suspension leaving the reducing zone and the most important combustion parameter is the char reactivity. Also, the calcination rate modifies very much the temperature in the calciner, char and limestone conversion......Simulations with a heterogeneous model of an in-line low-NOx calciner, based on non-isothermal diffusion-reaction models for char combustion and limestone calcination combined with a kinetic model for NO formation and reduction, are reported. The analysis shows that the most important hydrodynamic...... and NO emission. Carbon monoxide is a key component for the reduction of NO and reliable data for the kinetics of NO reduction by CO over CaO are very important for the prediction of the NO emission. The internal surface area of char and limestone particles influences the combustion and calcination rates...

  18. LITERATURE REVIEW OF PUO2 CALCINATION TIME AND TEMPERATURE DATA FOR SPECIFIC SURFACE AREA

    Energy Technology Data Exchange (ETDEWEB)

    Daniel, G.

    2012-03-06

    The literature has been reviewed in December 2011 for calcination data of plutonium oxide (PuO{sub 2}) from plutonium oxalate Pu(C{sub 2}O{sub 4}){sub 2} precipitation with respect to the PuO{sub 2} specific surface area (SSA). A summary of the literature is presented for what are believed to be the dominant factors influencing SSA, the calcination temperature and time. The PuO{sub 2} from Pu(C{sub 2}O{sub 4}){sub 2} calcination data from this review has been regressed to better understand the influence of calcination temperature and time on SSA. Based on this literature review data set, calcination temperature has a bigger impact on SSA versus time. However, there is still some variance in this data set that may be reflecting differences in the plutonium oxalate preparation or different calcination techniques. It is evident from this review that additional calcination temperature and time data for PuO{sub 2} from Pu(C{sub 2}O{sub 4}){sub 2} needs to be collected and evaluated to better define the relationship. The existing data set has a lot of calcination times that are about 2 hours and therefore may be underestimating the impact of heating time on SSA. SRNL recommends that more calcination temperature and time data for PuO{sub 2} from Pu(C{sub 2}O{sub 4}){sub 2} be collected and this literature review data set be augmented to better refine the relationship between PuO{sub 2} SSA and its calcination parameters.

  19. Performance of Dolomite Calcination in a Bench-Scale Rotary Kiln

    Directory of Open Access Journals (Sweden)

    Wulandari Winny

    2018-01-01

    Full Text Available Dolomite calcination is one of process steps to prepare calcined dolomite for raw materials in magnesium production. Calcination of dolomite involves heating the raw material at sufficient temperature in order to release the carbon dioxide from its carbonate minerals. This process is commonly conducted in a rotary kiln. There have been a number of calcination studies in a laboratory scale, but the study of dolomite calcination in a larger scale is very scarce. This research is aimed to study the performance of dolomite calcination in a bench-scale rotary kiln with 500 gram of feed. The effect of various parameters, including temperatures, feed rate, rotating frequency, and particle size were examined. The temperature of rotary kiln was varied between 700 and 1000 °C, while the particle size of dolomite was varied between 0.149 – 0.297 mm and up to 10 – 15 mm. The temperature distribution inside the rotary kiln was also measured. It is obtained that a conversion of 92% was attained at operation temperature of 1000 °C, which is at a higher temperature compared to the laboratory scale, where a conversion of 100% was obtained at 900 °C. This imply that the effect of heat transfer also plays important role in the calcination of dolomite especially at a larger scale.

  20. Calcination effect of borate-bearing hydroxyapatite on the mobility of borate.

    Science.gov (United States)

    Sasaki, Keiko; Toshiyuki, Kenta; Guo, Binglin; Ideta, Keiko; Hayashi, Yoshikazu; Hirajima, Tsuyoshi; Miyawaki, Jin

    2018-02-15

    Discharge from accidental nuclear power plants includes boric acid, which is used as a neutron absorbent in nuclear reactors. Co-precipitation of borate with hydroxyapatite (HAp), using Ca(OH) 2 , is known to be an effectively fast method for stabilization of borate as well as coexisting radioactive nuclides. To reduce bulky volume of solid residues after co-precipitation, calcination is necessary to investigate the chemical stability of targets. Calcination at 850°C resulted in the high crystalization of HAp with formation of xCaO·B 2 O 3 as a by-phase in which x increased with a decrease in the borate contents. After calcination, the lattice parameter a of HAp showed a reentrant curve and c showed a convex curve with an increase in borate contents. A dissolution assay revealed that calcination sometimes increases the borate moiety and that the acceptable B contents in HAp are lower than 1.59mmol/g-calcined HAp. These results imply that during calcination of HAp, some borate is excluded to form the by-phase xCaO·B 2 O 3 , which is relatively insoluble in water, but some other fractions might be additionally emitted from the amorphous phase to weakly bind the calcined products. Copyright © 2017 Elsevier B.V. All rights reserved.

  1. Improved Low-Temperature Activity of V2O5-WO3/TiO2 for Denitration Using Different Vanadium Precursors

    Directory of Open Access Journals (Sweden)

    Lina Gan

    2016-02-01

    Full Text Available This work tested two V2O5-WO3/TiO2 catalysts with different vanadium precursors for selective catalytic reduction (SCR of flue gas NO using NH3 at 150–450 °C. While catalyst A was prepared using ammonium metavanadate (NH4VO3 through incipient impregnation, catalyst B was made according to the solvothermal method using vanadyl acetylacetonate (VO(acac2 as the vanadium precursor. The catalytic evaluation for denitration was in a laboratory fixed bed reactor using simulated flue gas under conditions of a gas hourly space velocity (GHSV of 40,000 h−1 and an NH3/NO molar ratio of 0.8. Without SO2 and water vapor in the flue gas at 200 °C, the realized NO conversion was 56% for catalyst A but 80% for B. The presence of 350 ppm SO2 and 10 vol. % water vapor in the flue gas slightly reduced the NO conversion over catalyst B, and its activity was stable in a 108-h continuous test at temperatures varying from 450 °C to 220 °C. Via fourier transformation infrared spectroscopy (FT-IR and thermogravimetric (TG analysis, it was shown that over catalyst B a dynamic balance between the formation and decomposition of ammonium sulfite or sulfate is built possibly at temperatures as low as 220 °C. For this catalyst there was a higher surface atomic concentration of vanadium and a higher ratio of V4+/(V4+ + V5+, while the NH3 adsorption test revealed more acidic sites on catalyst B. The study discloses a potentially new approach to prepare a V2O5-WO3/TiO2 catalyst with good performance for SCR of flue gas NO at 220–300 °C.

  2. Influence of different supports on the physicochemical properties and denitration performance of the supported Mn-based catalysts for NH3-SCR at low temperature

    Science.gov (United States)

    Yao, Xiaojiang; Kong, Tingting; Yu, Shuohan; Li, Lulu; Yang, Fumo; Dong, Lin

    2017-04-01

    The commonly used supports of SiO2, γ-Al2O3, TiO2, and CeO2 were synthesized, and used for preparing MnOx/SiO2, MnOx/γ-Al2O3, MnOx/TiO2, and MnOx/CeO2 catalysts with the purpose of investigating the influence of crystal structure and coordination status on the physicochemical properties and denitration performance of these supported Mn-based catalysts for low-temperature NH3-SCR. The obtained samples were characterized by XRD, Raman, BET, H2-TPR, NH3-TPD, in situ DRIFTS, NO + O2-TPD, XPS, and NH3-SCR model reaction. XRD results indicate that MnOx species can be highly dispersed on the surface of γ-Al2O3, TiO2, and CeO2, which is because that there are some octahedral and tetrahedral vacancy sites, octahedral vacancy site, and cubic vacancy site exist on the surface of defective spinel structure γ-Al2O3, anatase TiO2, and cubic fluorite-type structure CeO2, respectively. However, there is no any vacancy site on the surface of SiO2 due to its unique SiO4 tetrahedral structure, which results in the appearance of crystalline β-MnO2 on the surface of MnOx/SiO2 catalyst. Furthermore, H2-TPR results exhibit obvious different reduction behavior among these supported Mn-based catalysts, which is explained by the coordination status of Mn species. Finally, NH3-SCR model reaction results show that MnOx/γ-Al2O3 catalyst presents the best catalytic performance among these supported Mn-based catalysts due to its high dispersion, suitable reduction behavior, largest amount of acid sites, optimal NOx adsorption capacity, and abundant Mn4+ content.

  3. Microwave calcination for plutonium immobilization and residue stabilization

    International Nuclear Information System (INIS)

    Harris, M.J.; Rising, T.L.; Roushey, W.J.; Sprenger, G.S.

    1995-01-01

    In the late 1980's development was begun on a process using microwave energy to vitrify low level mixed waste sludge and transuranic mixed waste sludge generated in Building 374 at Rocky Flats. This process was shown to produce a dense, highly durable waste form. With the cessation of weapons production at Rocky Flats, the emphasis has changed from treatment of low level and TRU wastes to stabilizaiton of plutonium oxide and residues. This equipment is versatile and can be used as a heat source to calcine, react or vitrify many types of residues and oxides. It has natural economies in that it heats only the material to be treated, significantly reducing cycle times over conventional furnaces. It is inexpensive to operate in that most of the working components remain outside of any necessary contamination enclosure and therefore can easily be maintained. Limited testing has been successfully performed on cerium oxide (as a surrogate for plutonium oxide), surrogate electrorefining salts, surrogate residue sludge and residue ash. Future plans also include tests on ion exchange resins. In an attempt to further the usefullness of this technology, a mobile, self-contained microwave melting system is currently under development and expected to be operational at Rocky Flats Enviromental Technology Site by the 4th quarter of FY96

  4. Structural, optical and morphological properties of post-growth calcined TiO{sub 2} nanopowder for opto-electronic device application: Ex-situ studies

    Energy Technology Data Exchange (ETDEWEB)

    Sathyaseelan, B., E-mail: bsseelan03@gmail.com [Dept of Physics, University College of Engineering Arni (A Constituent College of Anna University Chennai) Arni 632326, Tamil Nadu (India); Manikandan, E., E-mail: maniphysics@gmail.com [Central Research Laboratory, Sree Balaji Medical College & Hospital, Bharath University, BIHER, Chrompet, Chennai 600044, Tamil Nadu (India); UNESCO UNISA Africa Chair in Nanosciences & Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, PO Box 392, Pretoria (South Africa); Lakshmanan, V. [Dept of Physics, A.C.T College of Engineering & Technology, Nelvoy 603107 Kancheepuram (Dt), Tamil Nadu (India); Baskaran, I. [Dept of Physics, Arignar Anna Government Arts College, Cheyyar 604407, Tamil Nadu (India); Sivakumar, K. [Dept of Physics, Anna University, Chennai 600025, Tamil Nadu (India); Ladchumananandasivam, Rasiah [Dept of Textile Engineering & Post Graduate Programme in Mechanical Engineering Centre of Technology, Federal University of Rio Grande do Norte, Natal (Brazil); Kennedy, J. [UNESCO UNISA Africa Chair in Nanosciences & Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, PO Box 392, Pretoria (South Africa); The MacDiarmid Institute for Advanced Materials and Nanotechnology, PO Box 600, Wellington (New Zealand); Maaza, M., E-mail: maaza@tlabs.ac.za [UNESCO UNISA Africa Chair in Nanosciences & Nanotechnology, College of Graduate Studies, University of South Africa, Muckleneuk Ridge, PO Box 392, Pretoria (South Africa)

    2016-06-25

    Nanocrystalline TiO{sub 2} powders have been selectively prepared by the simple combustion reaction method using urea as a fuel. The crystalline powder was obtained using a silica basin heated directly on a hot plate at 500 °C until self-ignition occurred. After combustion process, the calcined products were obtained by heating the as-prepared powders for 1 h in air atmosphere at various sintering temperatures [500–900 °C]. The obtained nanopowder materials were systematically characterized by X-day diffraction (XRD), micro-Raman, UV–visible absorption (UV–vis), and Fourier transform infrared (FT-IR) spectroscopics. Powder XRD pattern shows the good agreement rutile phase structured TiO{sub 2} and the sharp diffraction peaks indicates good for crystallinity. The size of a symmetry of the nanoparticles have been measured with aid of a scanning electron microscopy (SEM), high resolution transmission electron microscopy (HR-TEM), and Brunauer, Emmett and Teller (BET) surface studies. The crystallinity of the powders was found to increase with respect to calcination temperatures. The average specific surface area of the particle was probed using gas adsorption–desorption measurements. Raman spectroscopy experiment was performed to ascertain the nature of TiO{sub 2} powder quality. UV–vis absorption spectra results showed the changes in the absorption edges of TiO{sub 2} report to increasing the calcinations temperatures. - Highlights: • TiO{sub 2} Nanocrystalline powders were prepared by simple combustion reaction method. • Calcined TiO{sub 2} nanopowder obtained by heating for 1 hr in air atmosphere at 500–900 °C. • Systematic characterization employed by XRD, micro-Raman, Optical, SEM, HRTEM. • The size symmetry of nanoparticles measured by electron microscopes BET methods. • Calcinations raises the crystallinity size enhanced for future opto-electronic devices.

  5. Remotely replaceable fuel and feed nozzles for the NWCF calciner vessel

    International Nuclear Information System (INIS)

    Fletcher, R.D.; Carter, J.A.; May, K.W.

    1978-01-01

    The development and testing of remotely replaceable fuel and feed nozzles for calcination of liquid radioactive wastes in the calciner vessel of the New Waste Calcining Facility (NWCF) being built at the Idaho National Engineering Laboratory are described. A complete fuel nozzle assembly was fabricated and tested at the Remote Maintenance Development Facility to evolve design refinements, identify required support equipment, and develop handling techniques. The design also provided for remote replacement of the nozzle support carriage and adjacent feed and fuel pipe loops using two pairs of master-slave manipulators

  6. Interlock recovery during the drying, calcination and vitrification phase of Am/Cm processing

    International Nuclear Information System (INIS)

    Snyder, T.K.

    2000-01-01

    This document summarizes the results of five CIM5 [5-inch Cylindrical Induction Melter] runs designed to demonstrate power interlock recovery methods during the drying, calcination and vitrification phases of the Am/Cm melter cycle

  7. Preparation of orthorhombic Ba2YCu3O7 powder by single-step calcining

    International Nuclear Information System (INIS)

    Spann, J.R.; Kahn, M.; Lloyd, I.K.

    1990-01-01

    A single calcination step, solid-state process that provides orthohombic Ba 2 YCu 3 O 7 powder is described. BaCO 3 , Y 2 O 3 , and CuO are used as precursor materials. The only phase identifiable by x-ray diffraction is the orthorhombic Ba 2 YCu 3 O 7 . The use of a vacuum during the initial stages of the calcining process promotes complete decomposition of the carbonate, and no residual carbonate is observed. An oxygen atmosphere during the later stages of calcining ensures proper oxidation to Ba 2 YCu 3 O 7 . The use of a similar combination vacuum-oxygen calcining schedule should also be beneficial in the preparation of chemically derived powders

  8. Volatilization of cobalt, technetium, and uranium isotopes from soils through salt amendment and calcination

    International Nuclear Information System (INIS)

    Shor, Joel T.; Dial, Chris

    2000-01-01

    The effects of alkali and alkaline earth metal chloride salts on the decontamination (through volatilization) of radionuclides from clay soils in a calcination process were examined. Calcium chloride was found to decontaminate 60 Co-containing soils to a maximum extent of about 65% of 60 Co present before treatment by calcination for 8 h at 1000 deg. C with the addition of about 4 milliequivalents (meq) of chloride per gram of soil. Repeated calcination treatments raised the level of decontamination to 80%, but not beyond. Technetium could be removed from clay soils slightly more effectively using a similar salting and calcination process. No decontamination of strontium or uranium soils was found using this process under reducing or oxidizing conditions. The data presented indicate areas in which the presence of chlorides may result in problems in the thermal treatment of soils or similar matrices; however, no viable decontamination process was achieved

  9. Incorporation of Polymers into Calcined Clays as Improved Thermal Insulating Materials for Construction

    OpenAIRE

    Ng, Serina; Jelle, Bjørn Petter

    2017-01-01

    Calcined clay is a Type Q supplementary cementing material according to EN197-1:2000. It possesses lower thermal conductivity than cement. To further improve its thermal insulation property, polymer-calcined clay complexes (PCCs) were produced in a one-pot synthesis. Two contrasting polymers, polystyrene (PS) and polyethylene glycol (PEG), were employed. The hydrophilicity of the polymers influenced the thermal conductivity of PCC. Hydrophilic PEG entrapped more water molecules on clay layers...

  10. Origin of Activity and Stability Enhancement for Ag3PO4 Photocatalyst after Calcination

    Directory of Open Access Journals (Sweden)

    Pengyu Dong

    2016-11-01

    Full Text Available Pristine Ag3PO4 microspheres were synthesized by a co-precipitation method, followed by being calcined at different temperatures to obtain a series of calcined Ag3PO4 photocatalysts. This work aims to investigate the origin of activity and stability enhancement for Ag3PO4 photocatalyst after calcination based on the systematical analyses of the structures, morphologies, chemical states of elements, oxygen defects, optical absorption properties, separation and transfer of photogenerated electron-hole pairs, and active species. The results indicate that oxygen vacancies (VO˙˙ are created and metallic silver nanoparticles (Ag NPs are formed by the reaction of partial Ag+ in Ag3PO4 semiconductor with the thermally excited electrons from Ag3PO4 and then deposited on the surface of Ag3PO4 microspheres during the calcination process. Among the calcined Ag3PO4 samples, the Ag3PO4-200 sample exhibits the best photocatalytic activity and greatly enhanced photocatalytic stability for photodegradation of methylene blue (MB solution under visible light irradiation. Oxygen vacancies play a significantly positive role in the enhancement of photocatalytic activity, while metallic Ag has a very important effect on improving the photocatalytic stability. Overall, the present work provides some powerful evidences and a deep understanding on the origin of activity and stability enhancement for the Ag3PO4 photocatalyst after calcination.

  11. Characterization of magnetic biochar amended with silicon dioxide prepared at high temperature calcination

    Directory of Open Access Journals (Sweden)

    Baig Shams Ali

    2016-09-01

    Full Text Available Calcination is considered to increase the hardness of composite material and prevent its breakage for the effective applications in environmental remediation. In this study, magnetic biochar amended with silicon dioxide was calcined at high temperature under nitrogen environment and characterized using various techniques. X-ray diffraction (XRD analysis revealed elimination of Fe3O4 peaks under nitrogen calcination and formation of Fe3Si and iron as major constituents of magnetic biochar-SiO2 composite, which demonstrated its superparamagnetic behavior (>80 A2·kg−1 comparable to magnetic biochar. Thermogravimetric analysis (TGA revealed that both calcined samples generated higher residual mass (>96 % and demonstrated better thermal stability. The presence of various bands in Fourier transform infrared spectroscopy (FT-IR was more obvious and the elimination of H–O–H bonding was observed at high temperature calcination. In addition, scanning electron microscopy (SEM images revealed certain morphological variation among the samples and the presence of more prominent internal and external pores, which then judged the surface area and pore volume of samples. Findings from this study suggests that the selective calcination process could cause useful changes in the material composites and can be effectively employed in environmental remediation measures.

  12. Effects of rapid calcination on properties of calcium-based sorbents

    International Nuclear Information System (INIS)

    Yan, Chang-Feng; Grace, John R.; Lim, C. Jim

    2010-01-01

    The calcination process may influence subsequent fragmentation, sintering and swelling when CaO derived from limestone acts as a CO 2 or SO 2 -sorbent in combustion, gasification and reforming. Sorbent properties are affected by CO 2 partial pressure, total pressure, temperature, heating rate, impurities and sample size. In this study, the effect of calcination heating rate was investigated based on an electrically heated platinum foil. The effects of heating rate (up to 800 C/s), calcination temperature (700-950 C), particle size (90-180 μm) and sweep gas velocity were investigated. Higher initial heating rates led to lower extents of limestone calcination, but the extents of carbonation of the resulting CaO were similar to each other. Calcium utilization declined markedly during carbonation or sulphation of CaO after calcination by rapid heating. Experimental results show that carbonation and calcium utilization were most effective for carbonation temperatures between 503 and 607 C. Increasing the extent of calcination is not the best way to improve overall calcium utilization due to the vast increase in energy consumption. (author)

  13. ICPP calcined solids storage facility closure study. Volume III: Engineering design files

    International Nuclear Information System (INIS)

    1998-02-01

    The following information was calculated to support cost estimates and radiation exposure calculations for closure activities at the Calcined Solids Storage Facility (CSSF). Within the estimate, volumes were calculated to determine the required amount of grout to be used during closure activities. The remaining calcine on the bin walls, supports, piping, and floor was also calculated to approximate the remaining residual calcine volumes at different stages of the removal process. The estimates for remaining calcine and vault void volume are higher than what would actually be experienced in the field, but are necessary for bounding purposes. The residual calcine in the bins may be higher than was is experienced in the field as it was assumed that the entire bin volume is full of calcine before removal activities commence. The vault void volumes are higher as the vault roof beam volumes were neglected. The estimations that follow should be considered rough order of magnitude, due to the time constraints as dictated by the project's scope of work. Should more accurate numbers be required, a new analysis would be necessary

  14. The leaching of base minerals from the calcines produced by the roasting of pyrite concentrates

    International Nuclear Information System (INIS)

    Nicol, M.J.; Filmer, A.O.

    1985-01-01

    A number of gold and uranium plants in South Africa concentrate the pyrite in the ore residue by flotation and roast the concentrate for the production of sulphuric acid. The calcine produced, which is predominantly hematite, is generally subjected to cyanidation for the recovery of gold and silver. The calcines often contain economically significant quantities of copper, nickel , cobalt and uranium. Prior treatment of the calcine for the recovery of these metals would be desirable in terms of the value of the products. Several processes for the leaching of the base metals from plant calcines have been investigated, and an important general conclusion is that an adequate recovery of the base metals requires that a large proportion of the iron should also be extracted. This observation led to a more extensive investigation of the kinetics of leaching of various iron oxides. The application of electrochemical theory and techniques resulted in a fuller understanding of the various factors that govern the rate of leaching of iron oxides. As a result of this fundamental work, alternative treatment schemes that should yield more efficient extraction from calcines were suggested. Several of these possibilities were investigated, and the most promising were found to require reducing conditions during the leach, or prior partial reduction of the calcine to magnetite or wustite

  15. Effect of Calcination Temperature on Morphological and Topography of Nickel-Alumina Thin Film

    Directory of Open Access Journals (Sweden)

    Sarwani Khairul Ilman

    2016-01-01

    Full Text Available Dip coating process promises good potential of nickel-alumina catalyst deposition on metal substrate for various applications especially in gas conversion reaction. This study was conducted to investigate the effect of different calcination temperature on nickel-alumina catalysts thin film formation. Four different calcination temperature were used, which are 300°C, 400°C, 500°C and 600°C. The calculation process was conducted for a duration of 90 minutes. The deposited thin films were characterized using Atomic Force Microscopy (AFM and X-ray diffraction (XRD equipment. The AFM result showed that the surface roughness of the nickel-alumina increase proportionally from 56 to 275 nm when the calcination temperature increased from 300 to 600°C. From an observation at high calcination temperature, the atom of grains assisted diffusion at the crystallite point causing grain with lower surface energy become larger. As the calcination temperature increase, the surface profile becomes rough and uneven representing high surface roughness. Thus, the effect of calcination temperature greatly influences the surface roughness of the nickel-alumina thin film.

  16. Effect of Calcination Conditions on the Performance of Co-precipitation Catalyst

    Directory of Open Access Journals (Sweden)

    Lin Kai

    2016-01-01

    Full Text Available The Fe-Co-Ce composite catalysts were prepared by co-precipitation method, and the effect of calcination temperature and calcination time on the performances of the Fe-Co-Ce composite catalysts were investigated. The results indicated that the optimum calcination temperature and calcination time of the Fe-Co-Ce composite catalysts were 450 °C and 7 h, respectively. Using the catalysts which prepared under the optimum calcination conditions catalytic wet oxidation of methyl orange simulated wastewater, after 90 min, the COD, COD removal rate, absorbance, decolorization rate and pH of the methyl orange simulated wastewater were 737.7, 70.5%, 0.348, 95.3%, and 5.31, respectively. According to the analyses of the SEM, FTIR, and TG-DTA curves, the components of the catalysts which prepared under the optimum calcination conditions distributed evenly, and the chemical compositions of the catalysts including C-O, -OH, and H-O-H, showing a good thermal stability.

  17. Numerical modelling of flow and transport processes in a calciner for cement production

    Energy Technology Data Exchange (ETDEWEB)

    Fidaros, D.K.; Baxevanou, C.A.; Dritselis, C.D.; Vlachos, N.S. [University of Thessaly, Volos (Greece). Dept. for Mechanical & Industrial Engineering

    2007-02-15

    Controlling the calcination process in industrial cement kilns is of particular importance because it affects fuel consumption, pollutant emission and the final cement quality. Therefore, understanding the mechanisms of flow and transport phenomena in the calciner is important for efficient cement production. The main physico-chemical processes taking place in the calciner are coal combustion and the strongly endothermic calcination reaction of the raw materials. In this paper a numerical model and a parametric study are presented of the flow and transport processes taking place in an industrial calciner. The numerical model is based on the solution of the Navier-Stokes equations for the gas flow, and on Lagrangean dynamics for the discrete particles. All necessary mathematical models were developed and incorporated into a computational fluid dynamics model with the influence of turbulence simulated by a two-equation (k-epsilon) model. Distributions of fluid velocities, temperatures and concentrations of the reactants and products as well as the trajectories of particles and their interaction with the gas phase are calculated. The results of the present parametric study allow estimations to be made and conclusions to be drawn that help in the optimization of a given calciner.

  18. ICPP calcined solids storage facility closure study. Volume III: Engineering design files

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-02-01

    The following information was calculated to support cost estimates and radiation exposure calculations for closure activities at the Calcined Solids Storage Facility (CSSF). Within the estimate, volumes were calculated to determine the required amount of grout to be used during closure activities. The remaining calcine on the bin walls, supports, piping, and floor was also calculated to approximate the remaining residual calcine volumes at different stages of the removal process. The estimates for remaining calcine and vault void volume are higher than what would actually be experienced in the field, but are necessary for bounding purposes. The residual calcine in the bins may be higher than was is experienced in the field as it was assumed that the entire bin volume is full of calcine before removal activities commence. The vault void volumes are higher as the vault roof beam volumes were neglected. The estimations that follow should be considered rough order of magnitude, due to the time constraints as dictated by the project`s scope of work. Should more accurate numbers be required, a new analysis would be necessary.

  19. Effects of Calcination Holding Time on Properties of Wide Band Gap Willemite Semiconductor Nanoparticles by the Polymer Thermal Treatment Method

    Directory of Open Access Journals (Sweden)

    Ibrahim Mustapha Alibe

    2018-04-01

    Full Text Available Willemite is a wide band gap semiconductor used in modern day technology for optoelectronics application. In this study, a new simple technique with less energy consumption is proposed. Willemite nanoparticles (NPs were produced via a water–based solution consisting of a metallic precursor, polyvinylpyrrolidone (PVP, and underwent a calcination process at 900 °C for several holding times between 1–4 h. The FT–IR and Raman spectra indicated the presence of metal oxide bands as well as the effective removal of PVP. The degree of the crystallization and formation of the NPs were determined by XRD. The mean crystallite size of the NPs was between 18.23–27.40 nm. The morphology, particle shape and size distribution were viewed with HR-TEM and FESEM analysis. The willemite NPs aggregate from the smaller to larger particles with an increase in calcination holding time from 1–4 h with the sizes ranging between 19.74–29.71 nm. The energy values obtained from the experimental band gap decreased with increasing the holding time over the range of 5.39 eV at 1 h to at 5.27 at 4 h. These values match well with band gap obtained from the Mott and Davis model for direct transition. The findings in this study are very promising and can justify the use of these novel materials as a potential candidate for green luminescent optoelectronic applications.

  20. Calcination, Reduction and Sintering of ADU Spheres for HTGR Fuel

    International Nuclear Information System (INIS)

    Jeong, Kyung Chai; Eom, Sung Ho; Kim, Yeon Ku; Kim, Woong Ki; Kim, Young Min; Lee, Young Woo; Kim, Ju Hee; Cho, Hyo Jin; Cho, Moon Seoung

    2011-01-01

    formation of spheres is then formed by the dispersed in air and ammonia gases atmosphere. The gelation of polymer was induced at the surface of the droplets in this step. The surfaces of these liquid droplets are slightly solidified by reaction of ammonia gas and uranyl ion into the droplets. Spherical droplets are converted to aged-ADU gels in NH 4 OH solution. Then, many steps, such as the ageing and drying of ADU gel, the calcining to UO 3 , the sintering to UO 2 , were progressed continuously

  1. Direct activation of microcrystalline zeolites

    NARCIS (Netherlands)

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

    2013-01-01

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

  2. The calcination process in a system for washing, calcinating, and converting treated municipal solid waste incinerator fly ash into raw material for the cement industry.

    Science.gov (United States)

    Zhu, Fenfen; Takaoka, Masaki; Oshita, Kazuyuki; Morisawa, Shinsuke

    2011-07-01

    Calcination is the second step in a washing-calcination-conversion system in which treated municipal solid waste incinerator fly ash and bottom ash can be reused as raw material in the cement industry and can decompose or stabilize hazardous compounds, reduce residue amounts, and alter residue characteristics. In this research, only fly ash is discussed. Chloride reduction is important if treated fly ash is to be reused in cement; however, the relationship between washed fly ash properties and chloride reduction by calcination is not well understood. This study used washed residues of three types of fly ash-raw fly ash (RFA) from the boiler or economizer of an incineration system, fly ash collected in a bag filter injected with calcium hydroxide (Ca(OH)2) for acid removal (CaFA), and fly ash collected in a bag filter injected with sodium bicarbonate (NaHCO3) for acid removal (NaFA)-in calcination experiments with varying temperature (400-1100 degrees C) and atmosphere (100% nitrogen [N2] at 25 mL/min or 10% oxygen [O2] [90% N2] at fluxes of 25, 50, and 75 mL/min). From the perspective of chloride reduction, heating to 1000 degrees C with 1-hr heating time, 1-hr holding time, and an atmosphere of 10% O2/90% N2 was most suitable for calcination. Under these conditions, chloride levels were reduced by 91, 52, and 96% in washed residues of RFA, CaFA, and NaFA, respectively. Among the washed residues, the weight of the washed residue of NaFA decreased the most.

  3. Design and performance of a full-scale spray calciner for nonradioactive high-level-waste-vitrification studies

    International Nuclear Information System (INIS)

    Miller, F.A.

    1981-06-01

    In the spray calcination process, liquid waste is spray-dried in a heated-wall spray dryer (termed a spray calciner), and then it may be combined in solid form with a glass-forming frit. This mixture is then melted in a continuous ceramic melter or in an in-can melter. Several sizes of spray calciners have been tested at PNL- laboratory scale, pilot scale and full scale. Summarized here is the experience gained during the operation of PNL's full-scale spray calciner, which has solidified approx. 38,000 L of simulated acid wastes and approx. 352,000 L of simulated neutralized wastes in 1830 h of processing time. Operating principles, operating experience, design aspects, and system descriptions of a full-scale spray calciner are discussed. Individual test run summaries are given in Appendix A. Appendices B and C are studies made by Bechtel Inc., under contract by PNL. These studies concern, respectively, feed systems for the spray calciner process and a spray calciner vibration analysis. Appendix D is a detailed structural analysis made at PNL of the spray calciner. These appendices are included in the report to provide a complete description of the spray calciner and to include all major studies made concerning PNL's full-scale spray calciner

  4. LAB-SCALE DEMONSTRATION OF PLUTONIUM PURIFICATION BY ANION EXCHANGE, PLUTONIUM (IV) OXALATE PRECIPITATION, AND CALCINATION TO PLUTONIUM OXIDE TO SUPPORT THE MOX FEED MISSION

    Energy Technology Data Exchange (ETDEWEB)

    Crowder, M.; Pierce, R.

    2012-08-22

    H-Canyon and HB-Line are tasked with the production of PuO{sub 2} from a feed of plutonium metal. The PuO{sub 2} will provide feed material for the MOX Fuel Fabrication Facility. After dissolution of the Pu metal in H-Canyon, the solution will be transferred to HB-Line for purification by anion exchange. Subsequent unit operations include Pu(IV) oxalate precipitation, filtration and calcination to form PuO{sub 2}. This report details the results from SRNL anion exchange, precipitation, filtration, calcination, and characterization tests, as requested by HB-Line1 and described in the task plan. This study involved an 80-g batch of Pu and employed test conditions prototypical of HB-Line conditions, wherever feasible. In addition, this study integrated lessons learned from earlier anion exchange and precipitation and calcination studies. H-Area Engineering selected direct strike Pu(IV) oxalate precipitation to produce a more dense PuO{sub 2} product than expected from Pu(III) oxalate precipitation. One benefit of the Pu(IV) approach is that it eliminates the need for reduction by ascorbic acid. The proposed HB-Line precipitation process involves a digestion time of 5 minutes after the time (44 min) required for oxalic acid addition. These were the conditions during HB-line production of neptunium oxide (NpO{sub 2}). In addition, a series of small Pu(IV) oxalate precipitation tests with different digestion times were conducted to better understand the effect of digestion time on particle size, filtration efficiency and other factors. To test the recommended process conditions, researchers performed two nearly-identical larger-scale precipitation and calcination tests. The calcined batches of PuO{sub 2} were characterized for density, specific surface area (SSA), particle size, moisture content, and impurities. Because the 3013 Standard requires that the calcination (or stabilization) process eliminate organics, characterization of PuO{sub 2} batches monitored the

  5. Determination of the Rate of Formation of Hydroceramic Waste Forms made with INEEL Calcined Wastes

    Energy Technology Data Exchange (ETDEWEB)

    Barry Scheetz; Johnson Olanrewaju

    2001-10-15

    The formulation, synthesis, characterization and hydration kinetics of hydroceramic waste forms designed as potential hosts for existing INEEL calcine high-level wastes have been established as functions of temperature and processing time. Initial experimentations were conducted with several aluminosilicate pozzolanic materials, ranging from fly ash obtained from various power generating coal and other combustion industries to reactive alumina, natural clays and ground bottled glass powders. The final selection criteria were based on the ease of processing, excellent physical properties and chemical durability (low-leaching) determined from the PCT test produced in hydroceramic. The formulation contains vermiculite, Sr(NO32), CsC1, NaOH, thermally altered (calcined natural clay) and INEEL simulated calcine high-level nuclear wastes and 30 weight percent of fluorinel blend calcine and zirconia calcine. Syntheses were carried out at 75-200 degree C at autogeneous water pressure (100% relative humidity) at various time intervals. The resulting monolithic compact products were hard and resisted breaking when dropped from a 5 ft height. Hydroceramic host mixed with fluorinel blend calcine and processed at 75 degree C crumbled into rice hull-side grains or developed scaly flakes. However, the samples equally possessed the same chemical durability as their unbroken counterparts. Phase identification by XRD revealed that hydroceramic host crystallized type zeolite at 75-150 degree C and NaP1 at 175-200 degree C in addition to the presence of quartz phase originating from the clay reactant. Hydroceramic host mixed with either fluorinel blend calcine or zirconia calcine crystallized type A zeolite at 75-95 degree C, formed a mixture of type A zeolite and hydroxysodalite at 125-150 degree C and hydroxysodalite at 175-200 degree C. Quartz, calcium fluoride and zirconia phases from the clay reactant and the two calcine wastes were also detected. The PCT test solution

  6. Removal of Dissolved Silica using Calcinated Hydrotalcite in Real-life Applications.

    Energy Technology Data Exchange (ETDEWEB)

    Sasan, Koroush [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Brady, Patrick Vane. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Krumhansl, James L. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Nenoff, Tina M. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Sasan, Koroush [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Sasan, Koroush [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

    2017-09-01

    Water shortages are a growing global problem. Reclamation of industrial and municipal wastewater will be necessary in order to mitigate water scarcity. However, many operational challenges, such as silica scaling, prevent large scale water reuse. Previously, our team at Sandia has demonstrated the use of selective ion exchange materials, such as calcinated hydrotalcite (HTC, (Mg 6 Al 2 (OH) 16 (CO 3 )*4H 2 O)), for the low cost removal of silica from synthetic cooling tower water. However, it is not currently know if calcinated HTC has similar capabilities in realistic applications. The purpose of this study was to investigate the ability of calcinated HTC to remove silica from real cooling tower water. This was investigated under both batch and continuous conditions, and in the presence of competing ions. It was determined that calcinated HTC behaved similarly in real and synthetic cooling tower water; the HTC is highly selective for the silica even in the presence of competing cations. Therefore, the data concludes that calcinated HTC is a viable anti-scaling pretreatment for the reuse of industrial wastewaters.

  7. Chemistry of proposed calcination/dissolution processing of Hanford Site tank wastes

    International Nuclear Information System (INIS)

    Delegard, C.H.

    1995-01-01

    Plans exist to separate radioactive waste stored in underground tanks at the US Department of Energy's Hanford Site in south central Washington State into low-level and high-level fractions, and to immobilize the separate fractions in high-integrity vitrified forms for long-term disposal. Calcination with water dissolution has been proposed as a possible treatment for achieving low/high-level separation. Chemistry development activities conducted since 1992 with simulated and genuine tank waste show that calcination/dissolution destroys organic carbon and converts nitrate and nitrite to hydroxide and benign offgases. The process also dissolves significant quantities of bulk chemicals (aluminum, chromium, and phosphate), allowing their redistribution from the high-level to the low-level fraction. Present studies of the chemistry of calcination/dissolution processing of genuine wastes, conducted in the period October 1993 to September 1994, show the importance of sodium fluoride phosphate double salt in controlling phosphate dissolution. Peptization of waste solids is of concern if extensive washing occurs. Strongly oxidizing conditions imposed by calcination reactions were found to convert transition metals to soluble anions in the order chromate > manganate > > ferrate. In analogy with manganese behavior, plutonium dissolution, presumably by oxidation to more soluble anionic species, also occurs by calcination/dissolution. Methods to remove plutonium from the product low-level solution stream must be developed

  8. Spray Calciner/In-Can Melter high-level waste solidification technical manual

    International Nuclear Information System (INIS)

    Larson, D.E.

    1980-09-01

    This technical manual summarizes process and equipment technology developed at Pacific Northwest Laboratory over the last 20 years for vitrification of high-level liquid waste by the Spray Calciner/In-Can Melter process. Pacific Northwest Laboratory experience includes process development and demonstration in laboratory-, pilot-, and full-scale equipment using nonradioactive synthetic wastes. Also, laboratory- and pilot-scale process demonstrations have been conducted using actual high-level radioactive wastes. In the course of process development, more than 26 tonnes of borosilicate glass have been produced in 75 canisters. Four of these canisters contained radioactive waste glass. The associated process and glass chemistry is discussed. Technology areas described include calciner feed treatment and techniques, calcination, vitrification, off-gas treatment, glass containment (the canister), and waste glass chemistry. Areas of optimization and site-specific development that would be needed to adapt this base technology for specific plant application are indicated. A conceptual Spray Calciner/In-Can Melter system design and analyses are provided in the manual to assist prospective users in evaluating the process for plant application, to provide equipment design information, and to supply information for safety analyses and environmental reports. The base (generic) technology for the Spray Calciner/In-Can Melter process has been developed to a point at which it is ready for plant application

  9. RECONSTRUCTION OF CALCINED Zn -Al LAYERED DOUBLE HYDROXIDES DURING TETRACYCLINE ADSORPSION

    Directory of Open Access Journals (Sweden)

    G. M. Starukh

    2015-12-01

    Full Text Available Zn-Al mixed oxides containing ZnO different degree crystallinity were obtained by calcinations of Zn-Al layered double hydroxides (LDHs. The reconstruction of calcined Zn-Al LDHs has been performed under stirring in aqueous suspensions. The assynthesized LDHs, its decomposition products, as well as the reconstructed solids upon hydration were characterized by XRD, N2adsorption, differential and thermal gravimetric analysis. It was found that the ability of Zn-Al LDHs to recover a layered structure under the hydration of mixed oxides depends on the degree of ZnO crystallinity. The partial reconstruction of Zn-Al layered structure occurs in tetracycline solutions irrespective to the degree of ZnO crystallinity in calcined LDHs. Calcined Zn-Al LDHs demonstrate the higher adsorption capacity to tetracycline in comparison with as-prepared Zn-Al LDHs. The adsorption of TC on calcined and uncalcined ZnAl LDHs occurs on the centers of one particular type. It is suggested that surface complexation of the A-ring ligand of TC with Al-OH centers takes place.

  10. Preparation of plutonium waste forms with ICPP calcined high-level waste

    Energy Technology Data Exchange (ETDEWEB)

    Staples, B.A.; Knecht, D.A. [Lockheed Idaho Technologies Co., Idaho Falls, ID (United States); O`Holleran, T.P. [Argonne National Lab.-West, Idaho Falls, ID (United States)] [and others

    1997-05-01

    Glass and glass-ceramic forms developed for the immobilization of calcined high-level wastes generated by Idaho Chemical Processing Plant (ICPP) fuel reprocessing activities have been investigated for ability to immobilize plutonium and to simultaneously incorporate calcined waste as an anti-proliferation barrier. Within the forms investigated, crystallization of host phases result in an increased loading of plutonium as well as its incorporation into potentially more durable phases than the glass. The host phases were initially formed and characterized with cerium (Ce{sup +4}) as a surrogate for plutonium (Pu{sup +4}) and samarium as a neutron absorber for criticality control. Verification of the surrogate testing results were then performed replacing cerium with plutonium. All testing was performed with surrogate calcined high-level waste. The results of these tests indicated that a potentially useful host phase, based on zirconia, can be formed either by devitrification or solid state reaction in the glass studied. This phase incorporates plutonium as well as samarium and the calcined waste becomes part of the matrix. Its ease of formation makes it potentially useful in excess plutonium dispositioning. Other durable host phases for plutonium and samarium, including zirconolite and zircon have been formed from zirconia or alumina calcine through cold press-sintering techniques and hot isostatic pressing. Host phase formation experiments conducted through vitrification or by cold press-sintering techniques are described and the results discussed. Recommendations are given for future work that extends the results of this study.

  11. Spray Calciner/In-Can Melter high-level waste solidification technical manual

    Energy Technology Data Exchange (ETDEWEB)

    Larson, D.E. (ed.)

    1980-09-01

    This technical manual summarizes process and equipment technology developed at Pacific Northwest Laboratory over the last 20 years for vitrification of high-level liquid waste by the Spray Calciner/In-Can Melter process. Pacific Northwest Laboratory experience includes process development and demonstration in laboratory-, pilot-, and full-scale equipment using nonradioactive synthetic wastes. Also, laboratory- and pilot-scale process demonstrations have been conducted using actual high-level radioactive wastes. In the course of process development, more than 26 tonnes of borosilicate glass have been produced in 75 canisters. Four of these canisters contained radioactive waste glass. The associated process and glass chemistry is discussed. Technology areas described include calciner feed treatment and techniques, calcination, vitrification, off-gas treatment, glass containment (the canister), and waste glass chemistry. Areas of optimization and site-specific development that would be needed to adapt this base technology for specific plant application are indicated. A conceptual Spray Calciner/In-Can Melter system design and analyses are provided in the manual to assist prospective users in evaluating the process for plant application, to provide equipment design information, and to supply information for safety analyses and environmental reports. The base (generic) technology for the Spray Calciner/In-Can Melter process has been developed to a point at which it is ready for plant application.

  12. Preparation of plutonium waste forms with ICPP calcined high-level waste

    International Nuclear Information System (INIS)

    Staples, B.A.; Knecht, D.A.; O'Holleran, T.P.

    1997-05-01

    Glass and glass-ceramic forms developed for the immobilization of calcined high-level wastes generated by Idaho Chemical Processing Plant (ICPP) fuel reprocessing activities have been investigated for ability to immobilize plutonium and to simultaneously incorporate calcined waste as an anti-proliferation barrier. Within the forms investigated, crystallization of host phases result in an increased loading of plutonium as well as its incorporation into potentially more durable phases than the glass. The host phases were initially formed and characterized with cerium (Ce +4 ) as a surrogate for plutonium (Pu +4 ) and samarium as a neutron absorber for criticality control. Verification of the surrogate testing results were then performed replacing cerium with plutonium. All testing was performed with surrogate calcined high-level waste. The results of these tests indicated that a potentially useful host phase, based on zirconia, can be formed either by devitrification or solid state reaction in the glass studied. This phase incorporates plutonium as well as samarium and the calcined waste becomes part of the matrix. Its ease of formation makes it potentially useful in excess plutonium dispositioning. Other durable host phases for plutonium and samarium, including zirconolite and zircon have been formed from zirconia or alumina calcine through cold press-sintering techniques and hot isostatic pressing. Host phase formation experiments conducted through vitrification or by cold press-sintering techniques are described and the results discussed. Recommendations are given for future work that extends the results of this study

  13. Numerical evaluation of different pulverized coal and solid recovered fuel co-firing modes inside a large-scale cement calciner

    International Nuclear Information System (INIS)

    Mikulčić, Hrvoje; Berg, Eberhard von; Vujanović, Milan; Wang, Xuebin; Tan, Houzhang; Duić, Neven

    2016-01-01

    Highlights: • Substitution of coal by alternative fuels is a method for greenhouse gas mitigation. • Alternative fuels have an impact on the performance of existing pulverized fuel furnaces. • Numerical simulations are a useful tool for studying and control of co-firing process. • Six different co-firing modes inside a cement calciner were evaluated. • The thermal share of solid recovered fuel varied from 0% to 100%. - Abstract: Partial substitution of coal by alternative solid fuels, such as waste-derived fuels and biomass, is recognized as an advantageous method for greenhouse gas mitigation. However, due to different fuel properties than that of coal, alternative fuels have a direct impact on the performance of existing pulverized coal fired furnaces. Numerical simulations currently represent a useful approach for studying and controlling the co-firing process. Early comprehensive information, parametric studies and initial conclusions that can be gained from numerical simulations are very important in handling modern combustion units. In this study modelling approach for the combustion of pulverized coal, biomass, plastic, and solid recovered fuel is presented. The purpose of the present study is to evaluate six different pulverized coal and solid recovered fuel co-firing modes inside a cement calciner. The thermal share of the solid recovered fuel in these six simulations varied from 0% to 100%. The results obtained, which include the temperature and species concentrations, provide useful conclusions regarding the maximal allowed coal substitution rate for stable cement calciner operation.

  14. Effect of fly ash preliminary calcination on the properties of geopolymer.

    Science.gov (United States)

    Temuujin, J; van Riessen, A

    2009-05-30

    The influence of preliminary calcination of fly ashes on the geopolymerisation process has been studied. Preliminary calcination at 500 and 800 degrees C causes decarbonation of the fly ash while it also leads to a decrease of the amorphous content of the fly ashes from 60 to 57%. Geopolymer prepared using raw fly ash exhibited a compressive strength 55.7(9.2)MPa, while for 500 and 800 degrees C calcined samples it reduced to 54(5.8) and 44.4(5.4)MPa, respectively. The decrease in compressive strength of the geopolymers is discussed in terms of partial surface crystallisation of the fly ash particles. Reactivity of the fly ash also has been correlated with the shrinkage rate and presence of efflorescence on the surface of geopolymers.

  15. High-Temperature Release of SO2 from Calcined Cement Raw Materials

    DEFF Research Database (Denmark)

    Nielsen, Anders Rooma; Larsen, Morten B.; Glarborg, Peter

    2011-01-01

    During combustion of alternative fuels in the material inlet end of cement rotary kilns, local reducing conditions may occur and cause reductive decomposition of sulfates from calcined cement raw materials. Decomposition of sulfates is problematic because it increases the gas-phase SO2 concentrat......During combustion of alternative fuels in the material inlet end of cement rotary kilns, local reducing conditions may occur and cause reductive decomposition of sulfates from calcined cement raw materials. Decomposition of sulfates is problematic because it increases the gas-phase SO2...... concentration, which may cause deposit formation in the kiln system. In this study, the release of sulfur from calcined cement raw materials under both oxidizing and reducing conditions is investigated. The investigations include thermodynamic equilibrium calculations in the temperature interval of 800–1500 °C...

  16. Calcination of Fluorinel-sodium waste blends using sugar as a feed additive (formerly WINCO-11879)

    International Nuclear Information System (INIS)

    Newby, B.J.; Thomson, T.D.; O'Brien, B.H.

    1992-06-01

    Methods were studied for using sugar as a feed additive for converting the sodium-bearing wastes stored at the Idaho Chemical Processing Plant into granular, free flowing solids by fluidized-bed calcination at 500 degrees C. All methods studied blended sodium-bearing wastes with Fluorinel wastes but differed in the types of sugar (sucrose or dextrose) that were added to the blend. The most promising sugar additive was determined to be sucrose, since it is converted more completely to inorganic carbon than is dextrose. The effect of the feed aluminum-to-alkali metal mole ratio on calcination of these blends with sugar was also investigated. Increasing the aluminum-to-alkali metal ratio from 0.6 to 1.0 decreased the calcine product-to-fines ratio from 3.0 to 1.0 and the attrition index from 80 to 15%. Further increasing the ratio to 1.25 had no effect

  17. Ce - promoted catalyst from hydrotalcites for CO2 reforming of methane: calcination temperature effect

    Directory of Open Access Journals (Sweden)

    Carlos Enrique Daza

    2012-01-01

    Full Text Available Ce-promoted Ni-catalysts from hydrotalcites were obtained. The effect of calcination temperature on the chemical and physical properties of the catalysts was studied. Several techniques were used to determine the chemical and physical characteristics of oxides. The apparent activation energies of reduction were determined. Catalytic experiments at 48 L g-1h-1 without pre-reduction in CO2 reforming of methane were performed. The spinel-like phase in these oxides was only formed at 1000 ºC. The reduction of Ni2+ in the oxides was clearly affected by the calcination temperature which was correlated with catalytic performance. The catalyst calcined at 700 ºC showed the greatest activity.

  18. Effect of Calcination Temperature on the Alumina-Zirconia Nanostructures Prepared by Combustion Synthesis

    Directory of Open Access Journals (Sweden)

    M. Jafar Tafreshi

    2012-12-01

    Full Text Available In this research, a sol gel autocaombustion route has been proposed to synthesize alumina-zirconia composite powders, using ammonium bicarbonate as a new fuel. Then the effect of calcination temperature on phase transformation and crystallite sizes was investigated. To characterize the products XRD, TEM and BET analyses were used. XRD patterns of as-synthesized powder and calcined powders at 1100 ◦C and 1200 ◦C showed t-ZrO2 phase with small crystallite sizes (sintered at 1300 ◦C and the particle sizes after calcination were 14.90 nm and 50 nm for ZrO2 and Al2O3 phases, respectively as calculated from XRD and the transformation of t-ZrO2 to m-ZrO2 started at 1300 ◦C. TEM micrograph of as-synthesized powder revealed nanosize spherical particles of about 8 nm.

  19. Incorporation of Polymers into Calcined Clays as Improved Thermal Insulating Materials for Construction

    Directory of Open Access Journals (Sweden)

    Serina Ng

    2017-01-01

    Full Text Available Calcined clay is a Type Q supplementary cementing material according to EN197-1:2000. It possesses lower thermal conductivity than cement. To further improve its thermal insulation property, polymer-calcined clay complexes (PCCs were produced in a one-pot synthesis. Two contrasting polymers, polystyrene (PS and polyethylene glycol (PEG, were employed. The hydrophilicity of the polymers influenced the thermal conductivity of PCC. Hydrophilic PEG entrapped more water molecules on clay layers than the hydrophobic PS, making PEG-PCC more thermally conducting than PS-PCC. Contaminants in calcined clays played a role in affecting the overall thermal conductivity. PCC can improve thermal insulation properties for future construction applications.

  20. Calcined paper sludge -- pozzolanic admixture to improve sulfate resistance of concrete

    Energy Technology Data Exchange (ETDEWEB)

    Rols, S.; Ambroise, J.; Pera, J.; Chabannet, M. [National Institute of Applied Sciences, Lyon (France)

    2000-07-01

    A new admixture, calcined paper sludge, is described. It is a mixture of metakaolin and calcium carbonate which is used to improve the resistance of both portland cement and ground-granulated blast-furnace cement to ammonium sulfate solution, a substance which is harmful to concrete as it reacts with calcium hydroxide to form expansive gypsum in the presence of aluminates. Five concrete samples were subjected to repeated sulfate attack in alternate wetting-drying cycles. After four cycles only the concrete made with blast-furnace slag cement presented measurable residual strength, however, the presence of calcined paper sludge did not appear to have any significant effect. However, after five cycles the presence of at least 20 per cent calcined paper sludge increased the durability of concrete and limited mass loss. Expansion levels were measurable only in concrete specimen containing at least 20 per cent calcined paper sludge, the expansion level moving inversely with the calcined sludge content. Microstructural studies showed the presence of gypsum after a sulfate attack with the size of the gypsum crystals depending upon the type of binder used. These results led to the conclusion that the addition of calcined paper sludge limited the amount of calcium hydroxide in the matrix, which in turn influenced the formation of gypsum as a result of reaction with ammonium sulfate. It was also shown that the sludge (in amounts higher than 20 per cent) can be used to control the expansion level and enhance durability of the concrete.10 refs., 7 tabs., 11 figs.

  1. Study of variation grain size in desulfurization process of calcined petroleum coke

    Science.gov (United States)

    Pintowantoro, Sungging; Setiawan, Muhammad Arif; Abdul, Fakhreza

    2018-04-01

    Indonesia is a country with abundant natural resources, such as mineral mining and petroleum. In petroleum processing, crude oil can be processed into a source of fuel energy such as gasoline, diesel, oil, petroleum coke, and others. One of crude oil potentials in Indonesia is petroleum coke. Petroleum coke is a product from oil refining process. Sulfur reducing process in calcined petroleum cokes can be done by desulfurization process. The industries which have potential to become petroleum coke processing consumers are industries of aluminum smelting (anode, graphite block, carbon mortar), iron riser, calcined coke, foundry coke, etc. Sulfur reducing process in calcined petroleum coke can be done by thermal desulfurization process with alkaline substance NaOH. Desulfurization of petroleum coke process can be done in two ways, which are thermal desulfurization and hydrodesulphurization. This study aims to determine the effect of various grain size on sulfur, carbon, and chemical bond which contained by calcined petroleum coke. The raw material use calcined petroleum coke with 0.653% sulfur content. The grain size that used in this research is 50 mesh, then varied to 20 mesh and 100 mesh for each desulfurization process. Desulfurization are tested by ICP, UV-VIS, and FTIR to determine levels of sulfur, carbon, chemical bonding and sulfur dissolved water which contained in the residual washing of calcined petroleum coke. From various grain size that mentioned before, the optimal value is on 100 mesh grain size, where the sulfur content in petroleum coke is 0.24% and carbon content reaches the highest level of 97.8%. Meanwhile for grain size 100 mesh in the desulfurization process is enough to break the chemical bonds of organic sulfur in petroleum coke.

  2. ICPP radioactive liquid and calcine waste technologies evaluation final report and recommendation

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-04-01

    Using a formalized Systems Engineering approach, the Latched Idaho Technologies Company developed and evaluated numerous alternatives for treating, immobilizing, and disposing of radioactive liquid and calcine wastes at the Idaho Chemical Processing Plant. Based on technical analysis data as of March, 1995, it is recommended that the Department of Energy consider a phased processing approach -- utilizing Radionuclide Partitioning for radioactive liquid and calcine waste treatment, FUETAP Grout for low-activity waste immobilization, and Glass (Vitrification) for high-activity waste immobilization -- as the preferred treatment and immobilization alternative.

  3. Microwave energy for post-calcination treatment of high-level nuclear wastes

    International Nuclear Information System (INIS)

    Gombert, D.; Priebe, S.J.; Berreth, J.R.

    1980-01-01

    High-level radioactive wastes generated from nuclear fuel reprocessing require treatment for effective long-term storage. Heating by microwave energy is explored in processing of two possible waste forms: (1) drying of a pelleted form of calcined waste; and (2) vitrification of calcined waste. It is shown that residence times for these processes can be greatly reduced when using microwave energy rather than conventional heating sources, without affecting product properties. Compounds in the waste and in the glass frit additives couple very well with the 2.45 GHz microwave field so that no special microwave absorbers are necessary

  4. Volatilisation of ruthenium in vitrification. Isothermal calcination studies of 'Magnox' and thermal oxide simulates

    International Nuclear Information System (INIS)

    Cains, P.W.; Hay, D.A.

    1982-12-01

    Ru volatilities have been measured for the static, isothermal calcination of ''Magnox'' and Thermal Oxide HAL's (Highly Active Liquors) at temperatures up to 600 0 C. Model solutions containing Ru, HNO 3 , and nitrates of important individual cations have also been investigated. Experimental design was primarily based on the requirements of rotary calcination process development. The results have been interpreted in terms of a reaction model involving competition between the simple degradation of Ru(NO) complexes to RuO 2 and oxidative decomposition to volatile species (e.g. RuO 4 ). (author)

  5. Synthesis of alumina powder with seeds by Pechini Method using O2 as calcination atmosphere

    International Nuclear Information System (INIS)

    Salem, R.E.P.; Guilherme, K.A.; Chinelatto, A.S.A.; Chinelatto, A. L.

    2012-01-01

    Alumina is a very investigated material due to its excellent refractory characteristics and mechanical properties. Its alpha phase, the most stable one, has a formation temperature of about 1200 ° C. Due to its high temperature of formation, many researches have been trying to reduce it through addition of seeds of alpha phase in chemical processes of synthesis. This work aims to synthesize ultrafine powders of alpha-alumina by the Pechini method with seeding, and using an O 2 atmosphere in the pre-calcination (500 ° C) and calcination (1000 ° C and 1100° C) steps. The resulting powders were characterized through X-ray diffractometry, infrared spectroscopy and scanning electron microscopy. The results were compared with samples calcined on ai. It was verified that the presence of oxygen in the calcination atmosphere favored the elimination of residual carbon from the precursor powders, forthcoming from the great amount of organic material used on the synthesis, modifying its morphology and favoring reduction of particle size. (author)

  6. Effect of calcination conditions of pork bone sludge on behaviour of ...

    Indian Academy of Sciences (India)

    Permanent link: http://www.ias.ac.in/article/fulltext/boms/036/04/0755-0764. Keywords. Natural hydroxyapatite; simulated body fluid; incubation; biomaterial; pH changes; rotary calcining kiln; chamber oven. Abstract. The paper presents in vitro (in SBF) behaviour of hydroxyapatite (HAp) obtained from pork bone sludge from ...

  7. Effect of calcination methods on electrochemical performance of NiO ...

    Indian Academy of Sciences (India)

    Administrator

    reason was proposed. The charge storage mechanism of NiO positive electrode in aqueous electrolyte was dis- ... Keywords. NiO; calcination methods; electrochemical performance; electrode materials; supercapacitor. 1. Introduction ... double-layer capacitors, mainly focusing on carbon mate- rials with a high specific ...

  8. COMPARATIVE MAGNETIC AND PHOTOCATALYTIC PROPERTIES OF COPRECIPITATED ZINC FERRITE NANOPARTICLES BEFORE AND AFTER CALCINATION

    Directory of Open Access Journals (Sweden)

    M. Ebrahimi

    2017-03-01

    Full Text Available In this work, the effects of co-precipitation temperature and post calcination on the magnetic properties and photocatalytic activities of ZnFe2O4 nanoparticles were investigated. The structure, magnetic and optical properties of zinc ferrite nanoparticles were characterized by X-ray diffraction (XRD, vibrating sample magnetometry and UV–Vis spectrophotometry techniques.  The XRD results showed that the coprecipitated as well as calcined nanoparticles are single phase with partially inverse spinel structures. The magnetization and band gap decreased with the increasing of co-precipitation temperature through the increasing of the crystallite size. However, the post calcination at 500 °C was more effective on the decreasing of magnetization and band gap. Furthermore, photocatalytic activity of zinc ferrite nanoparticles was studied by the degradation of methyl orange under UV-light irradiation. Compare with the coprecipitated ZnFe2O4 nanoparticles with 5% degradation of methyl orange after 5 h UV-light light radiation, the calcined ZnFe2O4 nanoparticles exhibited a better photocatalytic activity with 20% degradation.

  9. Influence of calcined mud on the mechanical properties and shrinkage of self-compacting concrete

    Directory of Open Access Journals (Sweden)

    Fatima Taieb

    2018-01-01

    Full Text Available The use of SCC has a particular interest in terms of sustainable development. Indeed, their specific formulation leads to a greater volume of dough than for common concretes, thus, a larger quantity of cement. However, for economical, ecological and technical reasons, it is sought to limit their cement content [1]. It is therefore necessary to almost always use mineral additions as a partial replacement for cement because the technology of self-compacting concretes can consume large quantities of fines, in this case calcinated mud issued from dams dredging sediments that can give and/or ameliorate characteristics and performances of this type of concretes. Four SCCs had been formulated from the same composition where the only percentage of calcinated mud of Chorfa (west of Algeria dam changed (0%, 10%, 20% and 30%. The effect of calcinated mud on characteristics at fresh state of SCC according to AFGC was quantified. Mechanical strengths and shrinkage deformation (total, autogenous, drying were evaluated. The results show the possibility to make SCCs with different dosages of calcinated mud having strengths that can defy those of the control SCC. The analysis of free deformations indicates the beneficial impact of the mud by contributing to decrease the amplitudes of the shrinkage compared to those of the control SCC.

  10. CO{sub 2} capture behavior of shell during calcination/carbonation cycles

    Energy Technology Data Exchange (ETDEWEB)

    Li, Y.J.; Zhao, C.S.; Chen, H.C.; Duan, L.B.; Chen, X.P. [School of Energy and Environment, Southeast University, Nanjing (China)

    2009-08-15

    The cyclic carbonation performances of shells as CO{sub 2} sorbents were investigated during multiple calcination/carbonation cycles. The carbonation kinetics of the shell and limestone are similar since they both exhibit a fast kinetically controlled reaction regime and a diffusion controlled reaction regime, but their carbonation rates differ between these two regions. Shell achieves the maximum carbonation conversion for carbonation at 680-700 C. The mactra veneriformis shell and mussel shell exhibit higher carbonation conversions than limestone after several cycles at the same reaction conditions. The carbonation conversion of scallop shell is slightly higher than that of limestone after a series of cycles. The calcined shell appears more porous than calcined limestone, and possesses more pores >230 nm, which allow large CO{sub 2} diffusion-carbonation reaction rates and higher conversion due to the increased surface area of the shell. The pores of the shell that are greater than 230 nm do not sinter significantly. The shell has more sodium ions than limestone, which probably leads to an improvement in the cyclic carbonation performance during the multiple calcination/carbonation cycles. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  11. Silica-associated limited systemic sclerosis after occupational exposure to calcined diatomaceous earth.

    Science.gov (United States)

    Moisan, Stéphanie; Rucay, Pierre; Ghali, Alaa; Penneau-Fontbonne, Dominique; Lavigne, Christian

    2010-10-01

    Silica-associated systemic sclerosis can occur in persons using calcined diatomaceous earth for filtration purpose. A limited systemic sclerosis was diagnosed in a 52-year-old male winegrower who had a combination of Raynaud's phenomenon, oesophageal dysfunction, sclerodactyly and telangectasia. The anti-centromere antibodies titre was 1/5000. The patient was frequently exposed to high atmospheric concentrations of calcined diatomaceous earth when performing the filtration of wines. Calcined diatomaceous earth is almost pure crystalline silica under the cristobalite form. The diagnosis of silica-associated limited systemic sclerosis after exposure to calcined diatomaceous earth was made. The patient's disease met the medical, administrative and occupational criteria given in the occupational diseases list 22 bis of the agriculture Social Security scheme and thence was presumed to be occupational in origin, without need to be proved. The diagnosis of occupational disease had been recognized by the compensation system of the agricultural health insurance. Copyright © 2010 Société française de rhumatologie. Published by Elsevier SAS. All rights reserved.

  12. 46 CFR 148.04-15 - Petroleum coke, uncalcined; petroleum coke, uncalcined and calcined (mixture).

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Petroleum coke, uncalcined; petroleum coke, uncalcined and calcined (mixture). 148.04-15 Section 148.04-15 Shipping COAST GUARD, DEPARTMENT OF HOMELAND... Requirements for Certain Material § 148.04-15 Petroleum coke, uncalcined; petroleum coke, uncalcined and...

  13. Effect of the rate of calcination of kaolin on the properties of metakaolin-based geopolymers

    Directory of Open Access Journals (Sweden)

    B.B. Kenne Diffo

    2015-03-01

    Full Text Available Kaolin samples of the same mass were treated at 700 °C for the same duration of 30 min by varying the rate of calcination (1, 2.5, 5, 10, 15 and 20 °C/min in order to obtain metakaolins which were used to produce geopolymers. Depending on the nature of each type of material, kaolin, metakaolins and geopolymers were characterized using thermal analysis, chemical analysis, XRD, FTIR, particle size distribution, specific surface area, bulk density, setting time and compressive strength. FTIR and XRD analyses showed that metakaolins except at 1 °C/min contained residual kaolinite whose quantity increased with the rate of calcination of kaolin and which influenced the characteristics of geopolymers. Thus as the rate of calcination of kaolin increased, the setting time increased (226 min (rate of 1 °C/min–773 min (rate of 20 °C/min while the compressive strength reduced (49.4 MPa (rate of 1 °C/min–20.8 MPa (rate of 20 °C/min. From the obtained results the production of geopolymers having high compressive strength along with low setting time requires that the calcination of kaolin be carried out at a low rate.

  14. Effect of calcination conditions of pork bone sludge on behaviour of ...

    Indian Academy of Sciences (India)

    The paper presents in vitro (in SBF) behaviour of hydroxyapatite (HAp) obtained from pork bone sludge from meat plant via ... The results obtained proved that calcination conditions of pork bone sludge (temperature 750–950 ◦C, time and type of the ...... LeGeros R Z 1991 Calcium phosphates in oral biology and medicine.

  15. Cost Comparison for the Transfer of Select Calcined Waste Canisters to the Monitored Geologic Repository at Yucca Mountain, NV

    International Nuclear Information System (INIS)

    Michael B. Heiser; Clark B. Millet

    2005-01-01

    This report performs a life-cycle cost comparison of three proposed canister designs for the shipment and disposition of Idaho National Laboratory high-level calcined waste currently in storage at the Idaho Nuclear Technology and Engineering Center to the proposed national monitored geologic repository at Yucca Mountain, Nevada. Concept A (2 x 10-ft) and Concept B (2 x 15-ft) canisters are comparable in design, but they differ in size and waste loading options and vary proportionally in weight. The Concept C (5.5 x 17.5-ft) canister (also called the ''super canister''), while similar in design to the other canisters, is considerably larger and heavier than Concept A and B canisters and has a greater wall thickness. This report includes estimating the unique life-cycle costs for the three canister designs. Unique life-cycle costs include elements such as canister purchase and filling at the Idaho Nuclear Technology and Engineering Center, cask preparation and roundtrip consignment costs, final disposition in the monitored geologic repository (including canister off-loading and placement in the final waste disposal package for disposition), and cask purchase. Packaging of the calcine ''as-is'' would save $2.9 to $3.9 billion over direct vitrification disposal in the proposed national monitored geologic repository at Yucca Mountain, Nevada. Using the larger Concept C canisters would use 0.75 mi less of tunnel space, cost $1.3 billion less than 10-ft canisters of Concept A, and would be complete in 6.2 years

  16. CFD Modelling and Experimental Testing of Thermal Calcination of Kaolinite Rich Clay Particles - An Effort towards Green Concrete

    DEFF Research Database (Denmark)

    Gebremariam, Abraham Teklay

    processes in a calciner and develop a useful tool that can aid in design of a smart clay calcination technology, which makes the major objective of this study. In this thesis, a numerical approach is mainly used to investigate the flash calcination of clay particles. A transient one-dimensional particle...... are crucial not only to maximize the yield of the desired product but also minimize the energy consumption during operation. Thus, the experimentally validated calcination model and simulation results can aid in an improved understanding of clay calcination process and also new conceptual design......Cement industry is one of the major industrial emitters of greenhouse gases, generating 5-7% of the total anthropogenic CO2 emissions. Consequently, use of supplementary cementitious materials (SCM) to replace part of the CO2-intensive cement clinker is an attractive way to mitigate CO2 emissions...

  17. Design and performance of atomizing nozzles for spray calcination of high-level wastes

    International Nuclear Information System (INIS)

    Miller, F.A.; Stout, L.A.

    1981-05-01

    A key aspect of high-level liquid-waste spray calcination is waste-feed atomization by using air atomizing nozzles. Atomization substantially increases the heat transfer area of the waste solution, which enhances rapid drying. Experience from the spray-calciner operations has demonstrated that nozzle flow conditions that produce 70-μ median-volume-diameter or smaller spray droplets are required for small-scale spray calciners (drying capacity less than 80 L/h). For large-scale calciners (drying capacity greater than 300 L/h), nozzle flow conditions that produce 100-μ median-volume-diameter or smaller spray droplets are required. Mass flow ratios of 0.2 to 0.4, depending on nozzle size, are required for proper operation of internal-mix atomizing nozzles. Both internal-mix and external-mix nozzles have been tested at PNL. Due to the lower airflow requirements and fewer large droplets produced, the internal-mix nozzle has been chosen for primary development in the spray calciner program at PNL. Several nozzle air-cap materials for internal-mix nozzles have been tested for wear resistance. Results show that nozzle air caps of stainless steel and Cer-vit (a machineable glass ceramic) are suceptible to rapid wear by abrasive slurries, whereas air caps of alumina and reaction-bonded silicon nitride show only slow wear. Longer-term testing is necessary to determine more accurately the actual frequency of nozzle replacement. Atomizing nozzle air caps of alumina are subject to fracture from thermal shock, whereas air caps of silicon nitride and Cer-vit are not. Fractured nozzles are held in place by the air-cap retaining ring and continue to atomize satisfactorily. Therefore, fractures caused by thermal shocking do not necessarily result in nozzle failure

  18. Preparation of NiO nanoflakes under different calcination temperatures and their supercapacitive and optical properties

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Jiangshan; Liu, Hua; Zhang, Qiang, E-mail: zhangqiang6299@bit.edu.cn

    2017-01-15

    Highlights: • The NiO nanocrystals were prepared by calcinating Ni(OH){sub 2} nanoflakes synthesized via an ion diffusion controlled by ion exchange membrane. • The NiO sample calcinated at 400 °C exhibits the highest specific capacitance of 381 F g{sup −1} and specific surface area of 188.4 m{sup 2} g{sup −1}. • The NiO samples with the lower binding energy are harder to capture OH- than Ni(OH)2, which is disadvantageous to charge storage. • The UV–Vis absorption peak of NiO samples have a red shift with increasing the calcination temperature due to the increase in crystallinity. - Abstract: The NiO nanocrystals were successfully prepared by calcinating Ni(OH){sub 2} precursor synthesized via a facile ion diffusion controlled by ion exchange membrane without adding any solvent or template. X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) isotherm, X-ray photoelectron spectroscopy (XPS) and Ultraviolet–visible (UV–vis) analysis were used to investigate the crystallinity, morphology, surface and porosity characteristics, chemical composition and optical properties in more detail. The pseudocapacitive behavior of the NiO samples was investigated by cyclic voltammograms (CV) and galvanostatic charge-discharge tests in 2 M KOH. The results analysis reveals that both specific capacitance and surface area decrease with the increase of calcination temperatures. Among the NiO samples, the NiO-400 nanoflakes calcinated at 400 °C possess the highest specific capacitance of 381 F g{sup −1} at a current density of 2 A g{sup −1}, but much lower than the Ni(OH){sub 2} sample. In addition, the UV–vis analysis shows that there is a red shift of absorption peak for the three NiO samples with the increasing temperature and the NiO-400 has a broad band gap of 3.3 eV, which renders the material highly interesting for application in photocatalyst.

  19. Cyclic calcination/carbonation looping of dolomite modified with acetic acid for CO{sub 2} capture

    Energy Technology Data Exchange (ETDEWEB)

    Li, Ying-jie; Zhao, Chang-sui; Duan, Lun-bo; Liang, Cai; Li, Qing-zhao; Zhou, Wu; Chen, Hui-chao [Key Laboratory of Coal Power Generation and Combustion Technology of Ministry of Education, Southeast University, Nanjing 210096 (China)

    2008-12-15

    The dolomite modified with acetic acid solution was proposed as a CO{sub 2} sorbent for calcination/carbonation cycles. The carbonation conversions for modified and original dolomites in a twin fixed-bed reactor system with increasing the numbers of cycles were investigated. The carbonation temperature in the range of 630 C-700 C is beneficial to the carbonation reaction of modified dolomite. The carbonation conversion for modified dolomite is significantly higher than that for original sorbent at the same reaction conditions with increasing numbers of reaction cycles. The modified dolomite exhibits a carbonation conversion of 0.6 after 20 cycles, while the unmodified sorbent shows a conversion of 0.26 at the same reaction conditions, which is calcined at 920 C and carbonated at 650 C. At the high calcination temperature over 920 C modified dolomite can maintain much higher conversion than unmodified sorbent. The mean grain size of CaO derived from modified dolomite is smaller than that from original sorbent with increasing numbers of reaction cycles. The calcined modified dolomite possesses greater surface area and pore volume than calcined original sorbent during the multiple cycles. The pore volume and pore area distributions for calcined modified dolomite are also superior to those for calcined unmodified sorbent during the looping cycle. The modified dolomite is proved as a new and promising type of regenerable CO{sub 2} sorbent for industrial applications. (author)

  20. Influence of Calcination Temperature on Structural and Photoluminescence Properties of ZnO Nanoparticles via Precipitation Method

    International Nuclear Information System (INIS)

    Mahayatun Dayana Johan Ooi; Azlan Abdul Aziz; Mat Johar Abdullah

    2011-01-01

    ZnO nanoparticles were synthesized via precipitation of Zn and I 2 with assistance of DEA at different calcination temperatures ranging from 250 to 1150 degree Celsius. All the synthesized ZnO nanoparticles are pure and exhibit hexagonal wurtzite structure with preferred orientation growth in (101) plane. Spherical particles of size∼60 nm and strong violet emission peak of 417 nm (3.0 eV) has been observed for ZnO powder calcined at 850 degree Celsius. Our results reveal a strong influence of calcination temperature on ZnO microstructure and optical behaviour of synthesized particles. (author)

  1. EFFECT OF CALCINATION TEMPERATURE OF TUNISIAN CLAYS ON THE PROPERTIES OF GEOPOLYMERS

    Directory of Open Access Journals (Sweden)

    Essaidi N.

    2013-09-01

    Full Text Available Geopolymers are amorphous three dimensional aluminosilicate materials that may be synthesized at room or slightly higher temperature by alkaline activation of aluminosilicates obtained from industrial wastes, calcined clays and natural minerals. Among the different family of geopolymers, two Tunisian clays (a kaolinite clay from Tabarka and illito/kaolinitic clay from Medenine are tested for their feasibility of geopolymers at low temperature. The unfired and calcined clays were dissolved in strongly alkaline solution in order to produce consolidated materials whose pastes were characterized by their compressive strength. Hardened geopolymer samples were also submitted to X-Ray diffraction, FTIR spectroscopy and scanning electron microscopy analyses. The geopolymer strength is related to the structure and reactivity of the clay generated by thermal treatment and to the role of associated minerals in clays. The amorphous character of obtained geopolymers and the displacement of the IR wavenumber are signature of geopolymerisation reaction.

  2. Bone mineral change during experimental calcination: an X-ray diffraction study.

    Science.gov (United States)

    Galeano, Sergio; García-Lorenzo, Mari Luz

    2014-11-01

    The effects of calcination (400-1200°C) on pig bones have been studied using powder X-ray diffraction (XRD) and secondary modifications, such as color change and weight loss. The characterisation by powder XRD confirmed the presence of the crystalline phase of hydroxyapatite, and comparison of the results obtained at different temperatures suggested that at 650°C, all the organic components and carbonate substitutions were completely removed. Accordingly, these samples were white. In addition, the crystallinity degree and the crystallite size progressively increased with the calcination temperature until 650°C, remaining stable until 1200°C. Below 650°C, bone samples presented organic compounds, resulting in background noise in the diffractogram and gray or black color. In addition, impurities in the lattice correspond to low crystallite sizes. © 2014 American Academy of Forensic Sciences.

  3. A parametric study of a solar calcinator using computational fluid dynamics

    International Nuclear Information System (INIS)

    Fidaros, D.K.; Baxevanou, C.A.; Vlachos, N.S.

    2007-01-01

    In this work a horizontal rotating solar calcinator is studied numerically using computational fluid dynamics. The specific solar reactor is a 10 kW model designed and used for efficiency studies. The numerical model is based on the solution of the Navier-Stokes equations for the gas flow, and on Lagrangean dynamics for the discrete particles. All necessary mathematical models were developed and incorporated into a computational fluid dynamics model with the influence of turbulence simulated by a two-equation (RNG k-ε) model. The efficiency of the reactor was calculated for different thermal inputs, feed rates, rotational speeds and particle diameters. The numerically computed degrees of calcination compared well with equivalent experimental results

  4. Influence of calcination temperature in pozolanicity of gray sugar cane bagasse

    International Nuclear Information System (INIS)

    Santos, T.A.; Argolo, R.A.; Andrade, H.M.C.; Ribeiro, D.V.

    2016-01-01

    BCA (Sugar Cane Bagasse) is burned in boilers in the process of electricity cogeneration causing the generation of CBCA (Gray Sugar Cane Bagasse), which is the final residue of sucroalcooeira industry. Currently, several studies seek alternative materials that can replace Portland cement, promoting discussions on the use of pozzolanic materials in cementitious matrices. Thus, this research seeks to analyze the pozzolanicity the CBCA, obtained by calcining the residue at different temperatures, to be determined by TG / DTG and DTA tests. For analysis of pozzolanicity these ashes were used electrical conductivity techniques, chemical titration NP EN 196-5, chapelle modified NBR 15895/2010 and the IAP method (Activity Index pozzolanic NBR:5752). The results obtained during the study demostraramm no difference between the ash calcined at temperatures of 500 ° C, 600 ° C and 700 ° C. (author)

  5. Conceptual design for remote handling methods using the HIP process in the Calcine Immobilization Program

    Energy Technology Data Exchange (ETDEWEB)

    Berry, S.M.; Cox, C.G.; Hoover, M.A.

    1994-03-01

    This report recommends the remote conceptual design philosophy for calcine immobilization using the hot isostatic press (HIP) process. Areas of remote handling operations discussed in this report include: (1) introducing the process can into the front end of the HIP process, (2) filling and compacting the calcine/frit mixture into the process can, (3) evacuating and sealing the process can, (4) non-destructive testing of the seal on the process can, (5) decontamination of the process can, (6) HIP furnace loading and unloading the process can for the HIPing operation, (7) loading an overpack canister with processed HIP cans, (8) sealing the canister, with associated non-destructive examination (NDE) and decontamination, and (9) handling canisters for interim storage at the Idaho Chemical Processing Plant (ICPP) located on the Idaho National Engineering Laboratory (INEL) site.

  6. Conceptual design for remote handling methods using the HIP process in the Calcine Immobilization Program

    International Nuclear Information System (INIS)

    Berry, S.M.; Cox, C.G.; Hoover, M.A.

    1994-03-01

    This report recommends the remote conceptual design philosophy for calcine immobilization using the hot isostatic press (HIP) process. Areas of remote handling operations discussed in this report include: (1) introducing the process can into the front end of the HIP process, (2) filling and compacting the calcine/frit mixture into the process can, (3) evacuating and sealing the process can, (4) non-destructive testing of the seal on the process can, (5) decontamination of the process can, (6) HIP furnace loading and unloading the process can for the HIPing operation, (7) loading an overpack canister with processed HIP cans, (8) sealing the canister, with associated non-destructive examination (NDE) and decontamination, and (9) handling canisters for interim storage at the Idaho Chemical Processing Plant (ICPP) located on the Idaho National Engineering Laboratory (INEL) site

  7. A parametric study of a solar calcinator using computational fluid dynamics

    Energy Technology Data Exchange (ETDEWEB)

    Fidaros, D.K.; Baxevanou, C.A.; Vlachos, N.S. [University of Thessaly, Volos (Greece). Laboratory of Fluid Mechanics and Turbomachines, Department of Mechanical and Industrial Engineering

    2007-11-15

    In this work a horizontal rotating solar calcinator is studied numerically using computational fluid dynamics. The specific solar reactor is a 10 kW model designed and used for efficiency studies. The numerical model is based on the solution of the Navier-Stokes equations for the gas flow, and on Lagrangean dynamics for the discrete particles. All necessary mathematical models were developed and incorporated into a computational fluid dynamics model with the influence of turbulence simulated by a two-equation (RNG k-{epsilon}) model. The efficiency of the reactor was calculated for different thermal inputs, feed rates, rotational speeds and particle diameters. The numerically computed degrees of calcination compared well with equivalent experimental results. (author)

  8. In-situ investigation of the calcination process of mixed oxide xerogels with Raman spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Panitz, J.C. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1997-06-01

    The controlled calcination of materials derived by sol-gel reactions is important for the evolution of the final structure. Raman spectroscopy is an ideal tool for the identification of surface species under in-situ conditions, as demonstrated in the following for the example of a molybdenum oxide-silica xerogel. Raman spectra of this particular sample were recorded at temperatures as high as 1173 K, and compared with those of a reference material.(author) 3 figs., 4 refs.

  9. Étude de la calcination du phosphate clair de youssoufia (Maroc ...

    African Journals Online (AJOL)

    AKA Boko

    telles que le séchage, ou quelque autres techniques de séparation physique. Les différents aspects du traitement thermique ont été étudiés par de nombreux auteurs. [4-7]. Par contre, pour les phosphates BT et TBT, quelques autres techniques spéciales peuvent être aussi appliquées telles que la calcination, dont l'un des ...

  10. Spectroscopy research on the Guizhou Xingyi gangue of different calcined temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, B.; Sun, Y.; Xie, C. [Guizhou University, Guiyang (China). School of Science

    2008-09-15

    The major components, the decomposition mechanisms and the optimum calcination temperature of gangue at different temperatures were studied by XRF, XRD and FTIR. XRF shows that the primary chemical constituents of gangue are SiO{sub 2}, Al{sub 2}O{sub 3}, Fe{sub 2}O{sub 3} and so on. Moreover, the ignition loss is relatively high. XRD shows that the main mineral components of gangue are kaolinite, mica, spathic iron, iron pyrites, rutile, bischofite, quartz and calcite. XRD and FTIR at different calcination temperatures show that kaolinite and mica take part in a dehydration reaction as the temperatures increases. The amounts of SiO{sub 2} and Al{sub 2}O{sub 3}are increased, so the activity of gangue increases. At temperatures above 800{sup o}C, SiO{sub 2} reacts with Al{sub 2}O{sub 3} to produce andalusite, so the activity of the gangue decreases. Based on the experimental results, the optimum calcination temperature of the gangue from Guizhou Xingyi is 700 {sup o}C. 9 refs., 2 figs., 1 tab.

  11. Stabilization of As-, Pb-, and Cu-contaminated soil using calcined oyster shells and steel slag.

    Science.gov (United States)

    Moon, Deok Hyun; Wazne, Mahmoud; Cheong, Kyung Hoon; Chang, Yoon-Young; Baek, Kitae; Ok, Yong Sik; Park, Jeong-Hun

    2015-07-01

    In this study, As-, Pb-, and Cu-contaminated soil was stabilized using calcined oyster shells (COS) and steel slag (SS). The As-contaminated soil was obtained from a timber mill site where chromate copper arsenate (CCA) was used as a preservative. On the other hand, Pb- and Cu-contaminated soil was obtained from a firing range. These two soils were thoroughly mixed to represent As-, Pb-, and Cu-contaminated soil. Calcined oyster shells were obtained by treating waste oyster shells at a high temperature using the calcination process. The effectiveness of stabilization was evaluated by 1-N HCl extraction for As and 0.1-N HCl extraction for Pb and Cu. The treatment results showed that As, Pb, and Cu leachability were significantly reduced upon the combination treatment of COS and SS. The sole treatment of SS (10 wt%) did not show effective stabilization. However, the combination treatment of COS and SS showed a significant reduction in As, Pb, and Cu leachability. The best stabilization results were obtained from the combination treatment of 15 wt% COS and 10 wt% SS. The SEM-EDX results suggested that the effective stabilization of As was most probably achieved by the formation of Ca-As and Fe-As precipitates. In the case of Pb and Cu, stabilization was most probably associated with the formation of pozzolanic reaction products such as CSHs and CAHs.

  12. Fuel nitrogen conversion and release of nitrogen oxides during coal gangue calcination.

    Science.gov (United States)

    Zhang, Yingyi; Ge, Xinlei; Liu, Lili; Wang, Xidong; Zhang, Zuotai

    2015-05-01

    The pollution emission during the widespread utilization of coal gangue in construction industry has long been neglected. In present study, the NO x release behaviors in a simulation experiment of coal gangue calcination in construction industry were systematically investigated. The corresponding evolution of nitrogen functionalities in coal gangue was also discussed. Results showed that pyrrolic (N-5) and pyridine N-oxide (N-6-O) forms nitrogen were relatively abundant in the raw gangue. During calcination, the N-5 and N-6-O form nitrogen greatly decreased and converted to quaternary nitrogen (N-Q). It was found that NO2 was formed under slowly heating-up condition and at 600 °C under isothermal condition, while only NO was detected with further increase of temperature. From 600 to 1000 °C, the conversion ratio of fuel nitrogen to NO x increased from 8 to 12 %. The char nitrogen was found greatly contribute to NO formation, which may bring difficulty to the abatement of NO x emission during coal gangue calcination.

  13. Calcined clay lightweight ceramics made with wood sawdust and sodium silicate

    Energy Technology Data Exchange (ETDEWEB)

    Santis, Bruno Carlos de; Rossignolo, Joao Adriano, E-mail: desantis.bruno@gmail.com [Universidade de Sao Paulo (USP), Pirassununga, SP (Brazil); Morelli, Marcio Raymundo [Universidade Federal de Sao Carlos (UFSCar), SP (Brazil). Departamento de Engenharia de Materiais

    2016-11-15

    This paper aims to study the influence of including wood sawdust and sodium silicate in the production process of calcined clay lightweight ceramics. In the production process first, a sample used by a company that produces ceramic products in Brazil was collected. The sample was analysed by techniques of liquidity (LL) and plasticity (LP) limits, particle size analysis, specific mass, X-ray diffraction (XRD) and X ray fluorescence spectrometry (XRF). From the clay, specimens of pure clay and mixtures with wood sawdust (10%, 20% and 30% by mass) and sodium silicate were produced and fired at a temperature of 900 deg C. These specimens were submitted to tests of water absorption, porosity, specific mass and compressive strength. Results of this research indicate that the incorporation of wood sawdust and sodium silicate in the ceramic paste specimens can be useful to make calcined clay lightweight ceramics with special characteristics (low values of water absorption and specific mass and high values of compressive strength), which could be used to produce calcined clay lightweight aggregates to be used in structural concrete. (author)

  14. Selection of a glass-ceramic formulation to immobilize fluorinel- sodium calcine

    Energy Technology Data Exchange (ETDEWEB)

    Staples, B.A.; Wood, H.C.

    1994-12-01

    One option for immobilizing calcined high level wastes produced by nuclear fuel reprocessing activities at the Idaho Chemical Processing Plant (ICPP) is conversion to a glass-ceramic form through hot isostatic pressing. Calcines exist in several different chemical compositions, and thus candidate formulations have been developed for converting each to glass-ceramic forms which are potentially resistant to aqueous corrosion and stable enough to qualify for repository storage. Fluorinel/Na, a chemically complex calcine type, is one of the types being stored at ICPP, and development efforts have identified three formulations with potential for immobilizing it. These are a glass forming additive that uses aluminum metal to enhance reactivity, a second glass forming additive that uses titanium metal to enhance reactivity and a third that uses not only a combination of silicon and titanium metals but enough phosphorous pentoxide to form a calcium phosphate host phase in the glass-ceramic product. Glass-ceramics of each formulation performed well in restricted characterization tests. However, none of the three was subjected to rigorous testing that would provide information on whether each was processable, that is able to retain favorable characteristics over a practical range of processing conditions.

  15. Adsorption of basic chromium sulfate used in the tannery industries by calcined hydrotalcite

    International Nuclear Information System (INIS)

    Lopez M, B. E.; Rivera R, R.; Iturbe G, J. L.; Olguin G, M. T.

    2011-01-01

    The sorption behavior of the chemical species of Cr(III) from aqueous solutions by hydrotalcite calcined products was investigated considering the equilibrium ph (5.0 to 8.9) and the chromium concentration in aqueous solution (from 10.6 to 430.0 mmol/L) to obtain the corresponding isotherms. Each solution was prepared from basic Cr(III) sulphate which is a primary tanning agent used in the tannery industries. In this work no previous oxidation treatment was done to form Cr(vi) in order to remove the chromium from aqueous solutions by hydrotalcite. The amount of chromium in the remaining solutions after the sorption processes in a batch system by visible spectroscopy (Vis) was determined. The calcined hydrotalcite before and after the contact with the chromium(III) solutions by X-ray power diffraction, thermogravimetric analysis and Fourier transformed infrared spectroscopy, were characterized. The specific are by Brunauer, Emmett and Teller (Bet) method of each sample was also evaluated. It was found that under the experimental conditions of this work hydrolyzed species of Cr(III) are precipitated on the surface of the calcined hydrotalcite instead other adsorption mechanism, and the sulfate ions were the responsible to regenerated the crystalline structure of hydrotalcite, therefore the results are discussed in terms of both Cr(III) and sulfate chemical species. (Author)

  16. Adsorption of basic chromium sulfate used in the tannery industries by calcined hydrotalcite

    Energy Technology Data Exchange (ETDEWEB)

    Lopez M, B. E.; Rivera R, R.; Iturbe G, J. L.; Olguin G, M. T., E-mail: beatriz.lopez@inin.gob.mx [ININ, Departamento de Quimica, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

    2011-07-01

    The sorption behavior of the chemical species of Cr(III) from aqueous solutions by hydrotalcite calcined products was investigated considering the equilibrium ph (5.0 to 8.9) and the chromium concentration in aqueous solution (from 10.6 to 430.0 mmol/L) to obtain the corresponding isotherms. Each solution was prepared from basic Cr(III) sulphate which is a primary tanning agent used in the tannery industries. In this work no previous oxidation treatment was done to form Cr(vi) in order to remove the chromium from aqueous solutions by hydrotalcite. The amount of chromium in the remaining solutions after the sorption processes in a batch system by visible spectroscopy (Vis) was determined. The calcined hydrotalcite before and after the contact with the chromium(III) solutions by X-ray power diffraction, thermogravimetric analysis and Fourier transformed infrared spectroscopy, were characterized. The specific are by Brunauer, Emmett and Teller (Bet) method of each sample was also evaluated. It was found that under the experimental conditions of this work hydrolyzed species of Cr(III) are precipitated on the surface of the calcined hydrotalcite instead other adsorption mechanism, and the sulfate ions were the responsible to regenerated the crystalline structure of hydrotalcite, therefore the results are discussed in terms of both Cr(III) and sulfate chemical species. (Author)

  17. Study on Al2O3 extraction from activated coal gangue under different calcination atmospheres

    Science.gov (United States)

    Dong, Ling; Liang, Xinxing; Song, Qiang; Gao, Gewu; Song, Lihua; Shu, Yuanfeng; Shu, Xinqian

    2017-12-01

    Coal gangue was calcinated under air, nitrogen, carbon dioxide, air-hydrogen, and hydrogen atmospheres. The effects of different calcination temperatures and atmospheres on the mineral composition of activated coal gangue were investigated by X-ray diffraction. Moreover, the acid leaching kinetics of aluminum oxide from coal gangue was investigated with sulfuric acid. It showed that the air atmosphere promoted kaolinite decomposition during coal gangue calcination. The hydrogen atmosphere promoted the activation and decomposition of kaolinite at reaction temperatures exceeding 650°C. The carbon dioxide atmosphere eliminated the influence of residual carbon on coal gangue. When the ratio of acid/coal gangue was 1.5 and reaction temperature was 650°C, the sulfuric acid leaching rate under air, air-hydrogen, carbon dioxide, hydrogen and nitrogen atmospheres were 93.66%, 90.90%, 84.06%, 81.91% and 77.54% respectively. The acid leaching reaction process conformed to unreacted shrinking core model of particle unchanged, and was controlled by the interfacial chemical reaction. The reaction kinetic equation for the leaching process was 1-(1-x)1/3=kt with an apparent activation energy of 48.97 kJ/mol.

  18. Defluoridation of groundwater by calcined Mg/Al layered double hydroxide

    Directory of Open Access Journals (Sweden)

    A. Elhalil

    2016-03-01

    Full Text Available The present study evaluated calcined Mg/Al layered double hydroxide (CLDH availability for the removal of fluoride from local groundwaters. The Mg/Al layered double hydroxide (LDH was synthesized by co-precipitation method and characterized by XRD, FT-IR and TGA-TDA analyses. Batch defluoridation experiments were performed under various conditions such as calcination, solution pH, contact time, temperature, material dosage and reuse. Experimental results indicate that fluoride removal strongly increased after calcination of the LDH up to 600 °C. The maximum fluoride removal was obtained at solution pH of 6.85. Kinetics of fluoride removal followed the pseudo-second order kinetic model. The rise in solution temperature strongly enhances the removal efficiency. The adsorption mechanism involved surface adsorption, ion exchange interaction and original LDH structure reconstruction by rehydration of mixed metal oxides and concomitant intercalation of fluoride ions into the interlayer region. The optimum dosages required to meet the national standard for drinking water quality were found to be 0.29 and 0.8 g/L, respectively, for Bejaad and Settat goundwaters. A decrease in the fluoride uptake with increasing the number of regeneration cycles was observed.

  19. Adsorption of Anionic Dyes from Aqueous Solutions by Calcined and Uncalcined Mg/ Al Layered Double Hydroxide

    International Nuclear Information System (INIS)

    Siti Mariam Sumari; Zaini Hamzah; Kantasamy, N.

    2016-01-01

    The uptake of Acid Blue 29 (AB29), Reactive Orange 16 (RO16) and Reactive Red 120 (RR120) from aqueous solutions by calcined (CLDH) and uncalcined Mg/Al layered double hydroxide (LDH) has been investigated. The adsorption process was conducted in a batch mode at 25 degree Celcius. Anionic dye removal was more efficient using the CLDH rather than LDH. The adsorption process by CLDH involved reconstruction and hydration of the calcined LDH and intercalation of AB29, RO16 and RR120. Physical characterization using X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and Fourier Transform Infrared (FTIR) were used to ascertain the memory effect phenomenon that is structural reconstruction to regain its original LDH after rehydration. To gain insight into the mechanism of adsorption by CLDH, the pseudo-first order (PFO) and pseudo-second order (PSO) and intraparticle diffusion (IPD) kinetic models were used to analyse experimental data. Based on the correlation coefficient (R 2 ), the PSO has better fitting (R 2 =0.987-1.00) compared to PFO (R 2 =0.867-0.990). Furthermore the values of maximum adsorption capacity, (q e ) calculated from PSO model are consistent with the experimental q e indicating that the experimental kinetic data for AB29, RO16 and RR120 adsorption by CLDH are suitable for this model. Recycling of the adsorbent, in cycles of calcination-reconstruction process promised a possibility of regeneration of CLDH. (author)

  20. Preparation of controlled particle size U3O8 by uranyl formate precipitation and calcination

    International Nuclear Information System (INIS)

    Johnson, D.R.

    1978-11-01

    A conceptual process flowsheet for preparation of U 3 O 8 by precipitating uranyl formate monohydrate with excess formic acid and calcining it was developed and demonstrated on a laboratory scale. The product U 3 O 8 has a particle size distribution apropriate for fabrication of U 3 O 8 -Al fuel by powder metallurgy. The U 3 O 8 particles are crystalline, do not exceed 150 μm in diameter, and have a narrow particle size distribution with most particles within the range of 44 to 150 μm. A ten-fold decontamination of uranium from low-level fission products during uranyl formate precipitation was demonstrated. Minimal variations in U 3 O 8 particle size distribution as a function of various uranyl formate precipitation conditions were observed. Preliminary tests demonstrated that calcination of uranyl formate monohydrate recovered from solution by evaporation to dryness did not produce U 3 O 8 with the desired particle size distribution. Calcination of uranyl oxalate, uranous oxalate, or uranous formate also did not produce U 3 O 8 with the appropriate particle size distribution

  1. Connecting section and associated systems concept for the spray calciner/in-can melter process

    International Nuclear Information System (INIS)

    Petkus, L.L.; Gorton, P.S.; Blair, H.T.

    1981-06-01

    For a number of years, researchers at the Pacific Northwest Laboratory have been developing processes and equipment for converting high-level liquid wastes to solid forms. One of these processes is the Spray Calciner/In-Can Melter system. To immobilize high-level liquid wastes, this system must be operated remotely, and the calcine must be reliably conveyed from the calciner to the melting furnace. A concept for such a remote conveyance system was developed at the Pacific Northwest Laboratory, and equipment was tested under full-scale, nonradioactive conditions. This concept and the design of demonstration equipment are described, and the results of equipment operation during experimental runs of 7 d are presented. The design includes a connecting section and its associated systems - a canister sypport and alignment concept and a weight-monitoring system for the melting furnace. Overall, the runs demonstrated that the concept design is an acceptable method of connecting the two pieces of process equipment together. Although the connecting section has not been optimized in all areas of concern, it provides a first-generation design of a production-oriented system

  2. Processing of concentrated radioactive wastes into cement and bitumens following calcination

    International Nuclear Information System (INIS)

    Napravnik, J.; Sazavsky, P.; Ditl, P.; Prikryl, P.

    1985-01-01

    A brief characteristic is presented of the most frequently used processes of solidification of liquid radioactive wastes, viz., bituminization, cementation and their combination with calcination. The effect of individual parameters is assessed on the choice of the type of solidification process as is their importance in the actual process, in temporary storage, during transportation and under conditions of long-term storage. It has been found that a combination of the procedures could lead to a modular system of methods and equipment. This would allow to approach optimal solidification of wastes in the present period and to establish a research reserve for the development of more modern, economically advantageous and safer procedures. A rough estimate is made of the costs of the solidification of 1 m 3 of radioactive concentrate from the V-1 power plant at a production of 380 m 3 /year, this for the cementation-calcination and bituminization-calcination procedures. The said rough economic analysis only serves to identify the major operating components which have the greatest effect on the economic evaluation of the solidification procedures. (Z.M.)

  3. The effect of calcination temperature on the formation and magnetic properties of ZnMn2O4 spinel

    Science.gov (United States)

    Hermanto, B.; Ciswandi; Afriani, F.; Aryanto, D.; Sudiro, T.

    2018-03-01

    The spinel based on transition-metal oxides has a typical composition of AB2O4. In this study, the ZnMn2O4 spinel was synthesized using a powder metallurgy technique. The Zn and Mn metallic powders with an atomic ratio of 1:2 were mechanically alloyed for 3 hours in aqueous solution. The mixed powder was then calcined in a muffle furnace at elevated temperature of 400, 500 and 600 °C. The X-ray Diffractometer (XRD) was used to evaluate the formation of a ZnMn2O4 spinel structure. The magnetic properties of the sample at varying calcination temperatures were characterized by a Vibrating Sample Magnetometer (VSM). The results show that the fraction of ZnMn2O4 spinel formation increases with the increase of calcination temperature. The calcination temperature also affects the magnetic properties of the samples.

  4. Improvement of the crystallinity and photocatalytic property of zinc oxide as calcination product of Zn–Al layered double hydroxide

    International Nuclear Information System (INIS)

    Ahmed, Abdullah Ahmed Ali; Talib, Zainal Abidin; Hussein, Mohd Zobir bin; Zakaria, Azmi

    2012-01-01

    Highlights: ► ZnO phase and ZnAl 2 O 4 spinel can be formed as Zn–Al–NO 3 –LDH calcination products. ► The crystallinity of ZnO phase increased with an increase of calcination temperature. ► The optical band gaps of ZnO were improved with an increase in temperature. ► The oxygen vacancies in ZnO and ZnAl 2 O 4 generated the ESR signals. - Abstract: Zinc oxide with different degrees of crystallinity can be formed as Zn–Al-layered double hydroxide (Zn–Al–NO 3 –LDH) calcination products. ZnAl 2 O 4 spinel is also formed in a range of calcination temperatures from 600 to 1000 °C from the LDH. X-ray diffraction patterns showed that the crystallinity of the ZnO phase increased as calcination temperatures increased. The LDH structure was fully collapsed at and above 400 °C. The photocatalytic activity was determined by UV–VIS–NIR diffuse reflectance spectroscopy. The band gap of the calcined samples increased as the calcination temperature increased. Electron spin resonance (ESR) spectra of the fresh and calcined LDH at room temperature demonstrated that oxygen vacancies in the ZnO and ZnAl 2 O 4 were responsible for the generation of ESR signals. One BET specific surface area increased from 1 m 2 /g for the LDH to a maximum at 400 °C (43 m 2 /g) and decreased thereafter down to 6 m 2 /g at 1000 °C.

  5. 4.2. The kinetics of nitric acid decomposition of calcined borosilicate raw material of Ak-Arkhar Deposit

    International Nuclear Information System (INIS)

    Mirsaidov, U.M.; Kurbonov, A.S.; Mamatov, E.D.

    2015-01-01

    Present article is devoted to kinetics of nitric acid decomposition of calcined borosilicate raw material of Ak-Arkhar Deposit. The dependence of nitric acid decomposition of calcined boric raw material for extraction of boron oxide on temperature (20-100 deg C) and process duration (15-60 minutes) was defined. It was defined that at temperature increasing the extraction rate of boron oxide increases from 20.8 to 78.6%.

  6. Effect of calcination temperature on structural properties and photocatalytic activity of Mn-C-codoped TiO{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Cai, Jianbo; Xin, Wei; Liu, Guanglong; Lin, Die; Zhu, Duanwei, E-mail: liugl@mail.hzau.edu.cn [Laboratory of Eco-Environmental Engineering Research, College of Resources and Environment, Huazhong Agricultural University (HZAU), Wuhan (China)

    2016-03-15

    Mn-C-codoped TiO{sub 2} catalysts were synthesized by modified sol-gel method based on the self-assembly technique using polyoxyethylene sorbitan monooleate (Tween 80) as template and carbon precursor and the effect of calcination temperature on their structural properties and photocatalytic activity were investigated. The XRD results showed undoped and Mn-C-codoped TiO{sub 2} calcined at 400 deg C only include anatase phase and the rutile phase appears when the calcination temperature reached to 600 deg C. UV-vis absorption spectroscopy demonstrates that the absorption spectra are strongly modified by the calcination temperature. Moreover, the Mn-C-TiO{sub 2} calcined at 400 deg C showed the lowest PL intensity due to a decrease in the recombination rate of photogenerated electrons and holes under light irradiation. The photocatalytic activity of Mn-C-codoped TiO{sub 2} were evaluated by the degradation of methyl orange (MO) under the simulate daylight irradiation and all the prepared Mn-C-codoped TiO{sub 2} samples exhibited high photocatalytic activities for photocatalytic decolorisation of methyl orange aqueous solution. At 400 deg C, the Mn-C-codoped TiO{sub 2} samples showed the highest photocatalytic activity due to synergetic effects of good crystallize ation, appropriate phase composition and slower recombination rate of photogenerated charge carriers, which further confirms the calcination temperature could affect the properties of Mn-C-codoped TiO2 significantly. (author)

  7. Luminescence properties and color identification of Eu doped Ca3(PO4)2 phosphors calcined in air

    Science.gov (United States)

    Tong, Chao; Zhu, Yangguang; Xu, Chuanyan; Yang, Lei; Li, Yadong

    2017-09-01

    The Ca3(PO4)2:Eu (TCP) phosphor was synthesized by a high-temperature solid-state reaction in air atmosphere. X-ray powder diffraction(XRD) analysis indicates that the α-TCP↔β-TCP phase transition takes place under different calcination and cooling conditions. The luminescence properties of the two different phases of TCP were discussed according to the luminescence spectra during the heating and cooling transition. The CIE chromaticity coordinates of β-TCP phase located at the red region, α-TCP phase at bluish-green region because of the coexistence of Eu2+ and Eu3+ ions. The color-tunable emission of the products could also be directly observed under UV lamp. Pure red and bluish-green-emitting particles were observed respectively for the pure β-TCP phase and α-TCP phase samples whereas bluish-green and red mixture emitting particles were traced for the α-TCP /β-TCP phase co-existence samples. Therefore, results of this study suggested that Eu ion could be used as a spectroscopic probe to qualitatively identify the crystalline phase of TCP by a simple and convenient way to observe the color-tunable emission of the samples when irradiating it under 365 nm UV lamp.

  8. Synthesis and antibacterial evaluation of calcinated Ag-doped nano-hydroxyapatite with dispersibility.

    Science.gov (United States)

    Furuzono, Tsutomu; Motaharul, Mazumder; Kogai, Yasumichi; Azuma, Yoshinao; Sawa, Yoshiki

    2015-05-01

    Dispersible hydroxyapatite (HAp) nanoparticles are very useful for applying a monolayer to implantable medical devices using the nano-coating technique. To improve tolerance to infection on implanted medical devices, silver-doped HAp (Ag-HAp) nanoparticles with dispersiblity and crystallinity were synthesized, avoiding calcination-induced sintering, and evaluated for antibacterial activity. The Ca10-xAgx(PO4)6(OH)2 with x = 0 and 0.2 were prepared by wet chemical processing at 100°C. Before calcination at 700°C for 2 h, two kinds of anti-sintering agents, namely a Ca(NO3)2 (Ca salt) and a polyacrylic acid/Ca salt mixture (PAA-Ca), were used. Escherichia coli was used to evaluate the antibacterial activity of the nanopowder. When PAA-Ca was used as an anti-sintering agent in calcination to prepare the dispersible nanoparticles, strong metallic Ag peaks were observed at 38.1° and 44.3° (2θ) in the X-ray diffraction (XRD) profile. However, the Ag peak was barely observed when Ca salt was used alone as the anti-sintering agent. Thus, using Ca salt alone was more effective for preparation of dispersible Ag-HAp than PAA-Ca. The particle average size of Ag-HAp with 0.5 mol% of Ag content was found to be 325 ± 70 nm when the formation of large particleaggregations was prevented, as determined by dynamic light scattering instrument. The antibacterial activity of the Ag-HAp nanoparticles possessing 0.5 mol% against E. coli was greater than 90.0%. Dispersible and crystalline nano Ag-HAp can be obtained by using Ca salt alone as an anti-sintering agent. The nanoparticles showed antibacterial activity.

  9. Development of a SREX flowsheet for the separation of strontium from dissolved INEEL zirconium calcine

    International Nuclear Information System (INIS)

    Law, J.D.; Wood, D.J.; Todd, T.A.

    1999-01-01

    Laboratory experimentation has indicated that the SREX process is effective for partitioning 90 Sr from acidic radioactive waste solutions located at the Idaho Nuclear Technology and Engineering Center. These laboratory results were used to develop a flowsheet for countercurrent testing of the SREX process with dissolved pilot plant calcine. Testing was performed using 24 stages of 2-cm diameter centrifugal contactors which are installed in the Remote Analytical Laboratory hot cell. Dissolved Run No.64 pilot plant calcine spiked with 85 Sr was used as feed solution for the testing. The flowsheet tested consisted of an extraction section (0.15 M 4prime,4prime(5prime)-di-(tert-butylcyclohexo)-18-crown-6 and 1.5 M TBP in Isopar-L.), a 1.0 M NaNO 3 scrub section to remove extracted K from the SREX solvent, a 0.01 M HNO 3 strip section for the removal of Sr from the SREX solvent, a 0.25 M Na2CO 3 wash section to remove degradation products from the solvent, and a 0.1 M HNO 3 rinse section. The behavior of 85 Sr, Na, K, Al, B, Ca, Cr, Fe, Ni, and Zr was evaluated. The described flowsheet successfully extracted 85 Sr from the dissolved pilot plant calcine with a removal efficiency of 99.6%. Distribution coefficients for 85 Sr ranged from 3.6 to 4.5 in the extraction section. With these distribution coefficients a removal efficiency of approximately >99.99% was expected. It was determined that the lower than expected removal efficiency can be attributed to a stage efficiency of only 60% in the extraction section. Extracted K was effectively scrubbed from the SREX solvent with the 1.0 M NaNO 3 resulting in only 6.4% of the K in the HLW strip product. Sodium was not extracted from the dissolved calcine by the SREX solvent; however, the use of a 1.0 M NaNO 3 scrub solution resulted in a Na concentration of 70 mg/L (12.3% of the feed concentration) in the HLW strip product. Al, B, Ca, Cr, Fe, Ni, and Zr were determined to be essentially inextractable

  10. Removal of strontium-90 from calcined wastes with the SREX process

    International Nuclear Information System (INIS)

    Wood, D.J.; Mann, N.R.; Tillotson, R.; Tullock, P.A.; Todd, T.A.

    1997-01-01

    Experiments have been performed to formulate chemical procedures for the processing of radioactive dissolved calcine wastes for the removal of 90 Sr with the SREX (Strontium Extraction) solvent. Batch contact solvent extraction experiments have been performed to yield a processing scheme which is highly efficient for the extraction of Sr, while remaining free from insoluble precipitate formation and third phase formation. The effect of various scrubbing and stripping techniques and elevated temperature have been evaluated. The results of the batch contact experimentation has formed the basis for a proposed processing flowsheet which is scheduled soon for demonstration in centrifugal contactors

  11. Utilisation des os calcinés dans la défluoruration des eaux ...

    African Journals Online (AJOL)

    Le présent travail a consisté à une défluoruration des eaux souterraines de la localité de Essèkpa dans la commune de Dassa au Bénin dont la concentration en ions fluorures est de 6,2 mg/L. Les essais au laboratoire ont porté sur 250 ml d'eau traitée avec 20 g d'os de boeuf calcinés à différentes températures (de 100 °C ...

  12. Volume reduction of low- and medium-level waste by incineration/calcination

    International Nuclear Information System (INIS)

    Buzonniere, A. de; Gauthey, J.C.

    1993-01-01

    Nuclear installations generate large quantities of low- and medium-level radwaste. This waste comes from various installations in the fuel cycle, reactor operation, research institute, hospitals, nuclear plate dismantling, etc.. TECHNICATOME did the project development work for the incineration plant of PIERRELATE (France) on behalf of COGEMA (Compagnie Generale des d'Etudes Technique). This plant has been in active service since November 1987. In addition, TECHNICATOME was in charge of the incinerator by a turnkey contract. This incinerator was commissioned in 1992. For a number of years, TECHNICATOME has been examining, developing and producing incineration and drying/calcination installations. They are used for precessing low- and medium-level radwaste

  13. Idaho National Engineering and Environmental Laboratory, Old Waste Calcining Facility, Scoville vicinity, Butte County, Idaho -- Photographs, written historical and descriptive data. Historical American engineering record

    International Nuclear Information System (INIS)

    1997-01-01

    This report describes the history of the Old Waste Calcining Facility. It begins with introductory material on the Idaho National Engineering and Environmental Laboratory, the Materials Testing Reactor fuel cycle, and the Idaho Chemical Processing Plant. The report then describes management of the wastes from the processing plant in the following chapters: Converting liquid to solid wastes; Fluidized bed waste calcining process and the Waste Calcining Facility; Waste calcining campaigns; WCF gets a new source of heat; New Waste Calcining Facility; Last campaign; Deactivation and the RCRA cap; Significance/context of the old WCF. Appendices contain a photo key map for HAER photos, a vicinity map and neighborhood of the WCF, detailed description of the calcining process, and chronology of WCF campaigns

  14. Evaluation of calcination temperature and phase composition ratio for new hyroxyapatite

    Science.gov (United States)

    Salimi, M. N. Ahmad; Chin, H. S.

    2017-10-01

    The demand of production of hydroxyapatite (HA) has been increasing for the purpose of medical and dental application. HA possesses the excellent properties leads to the priority choice for ceramic bone replacement. Synthesis route by wet chemical precipitation is commonly practised in industrial scale. Calcium hydroxide and Orthophosphoric acid are the precursors for production scale. The synthesis of HA is conducted by varying the synthetic condition: stirring rate, calcium-phosphate and calcination temperature. This paper is focused on the properties of HA produced by regulating the synthetic condition so that the qualities of HA can be well performed. Characterization studies were also carried out by Fourier Transform Infrared Spectroscopy (FT-IR) for functional group identification, Scanning Electron Microscope (SEM) for surface morphology analysis and X-Ray Diffraction (XRD) for phase composition and crystallinity respectively. Narrow particle size distribution contributed to better quality of hydroxyapatite for bone replacement. Both calcium-phosphate ratio and calcination temperature would affect the phase composition of calcium phosphate.

  15. Effects of Composition and Calcination Temperature on Photocatalytic Evolution over from Glycerol and Water Mixture

    Directory of Open Access Journals (Sweden)

    Cancan Fan

    2012-01-01

    Full Text Available A series of sulfide coupled semiconductors supported on SiO2, (, was prepared by incipient wet impregnation method. The photocatalysts were characterized by XRD, XPS, TPR, and UV/Vis DRS. Characterization results show that the chemical actions between ZnS and CdS resulted in the formation of solid solutions on the surface of the support and the formation of them is affected by the molar ratio of ZnS/CdS and calcination temperature. Performance of photocatalysts was tested in the home made reactor under both UV light and solar-simulated light irradiation by detecting the rate of the photocatalytic H2 evolution from glycerol solution. The hydrogen production rates are related to the catalyst composition, surface structure, photoabsorption property, as well as the amount of solid solution. The maximum rate of hydrogen production, 550 μmol·h−1 under UV light irradiation and 210 μmol·h−1 under solar-simulated light irradiation, was obtained over Cd0.8Zn0.2S/SiO2 solid solution calcined at 723 K.

  16. Hydrothermal preparation of high saturation magnetization and coercivity cobalt ferrite nanocrystals without subsequent calcination

    International Nuclear Information System (INIS)

    Goh, S.C.; Chia, C.H.; Zakaria, S.; Yusoff, M.; Haw, C.Y.; Ahmadi, Sh.; Huang, N.M.; Lim, H.N.

    2010-01-01

    In this work, CoFe 2 O 4 nanocrystals with high saturation magnetization (M s ) and high coercivity (H c ) have been fabricated via a simple hydrothermal method and without subsequent calcination. The resulting CoFe 2 O 4 nanocrystals are characterized by X-ray diffraction, transmission electron microscopy, scanning electron microscopy, energy-dispersive X-ray spectrometry, differential scanning calorimetry and vibrating sample magnetometry. The results indicate that CoFe 2 O 4 nanocrystals are single crystal and the average crystallite size is increasing with the hydrothermal temperature. The electron micrographs show that the nanocrystals are well-dispersed and possess uniform size. The shape of CoFe 2 O 4 nanocrystals is transformed from spherical into rod by increasing the hydrothermal temperature. The nanocrystals show relatively high M s of 74.8 emu g -1 and H c of 2216 Oe, as compared to previous reported results. The obtained results reveal the applicability of this method for efficiently producing well crystallized and relatively high magnetic properties CoFe 2 O 4 nanocrystals as compared to other methods. More importantly, it does not require further calcination processes.

  17. Photocatalytic hydrogen evolution of palladium nanoparticles decorated black TiO2 calcined in argon atmosphere

    Science.gov (United States)

    Wu, Ming-Chung; Hsiao, Kai-Chi; Chang, Yin-Hsuan; Chan, Shun-Hsiang

    2018-02-01

    Black TiO2 nanoparticles (BTN) was prepared by sol-gel derived precursor calcined in an argon atmosphere. The synthesized BTN with trivalent titanium ion, structural defect, and oxygen vacancy shows a remarkably high absorbance in the visible light spectrum. BTN thus behaves a higher visible-active nanoreactor than white TiO2 nanoparticles (WTN) in the aqueous solution for organic pollutant degradation. Moreover, palladium decoration on the BTN surface (Pd-BTN) demonstrates a fascinating clean energy application. The obtained Pd-BTN fulfills a satisfied green material demand in the photocatalytic hydrogen production application. Pd-BTN calcined at 400 °C (Pd-BTN-400) shows the high photocatalytic hydrogen generation rate of 5200 μmol/g h under UV-A irradiation and 9300 μmol/g h under UV-B irradiation, respectively. The well-developed material, Pd-BTN-400, could be one of the best solutions in the concern of clean energy and water-purification with regard to the continuous environmental issue.

  18. Influence of calcination process on the formation of selected air pollutants

    Directory of Open Access Journals (Sweden)

    Wydrych Jacek

    2017-01-01

    Full Text Available The subject of the study is to analyze the phenomena of thermal flow in the precalcinator chamber of the exchanger's furnace tower including the combustion of coal dust and decarbonisation of raw lime powder. During the research were provided development of a mathematical model of particulate solid fuels combustion, calcining the raw material, NOx and COx formation. Moreover conducting the number for the current and the upgraded design of the precalcinator and analysis of the results. In this study, a mathematical model based on Euler's method to describe the motion of the gas phase and the Lagrange method to describe the motion of particles [1-4]. In the calculations there were assumed fractional particles raw material and fuel, and the following processes: flow of exhaust gases from the rotary kiln through the precalcinator chamber, heat exchange between the particles of raw material and exhaust gases, the additional fuel combustion in the precalcinator, the process of raw material calcination, transformation of gaseous substances, effect of the additional (tertiary air delivery on the processes in the chamber.

  19. Influence of calcination process on the formation of selected air pollutants

    Science.gov (United States)

    Wydrych, Jacek; Dobrowolski, Bolesław; Borsuk, Grzegorz; Pochwała, Sławomir

    2017-10-01

    The subject of the study is to analyze the phenomena of thermal flow in the precalcinator chamber of the exchanger's furnace tower including the combustion of coal dust and decarbonisation of raw lime powder. During the research were provided development of a mathematical model of particulate solid fuels combustion, calcining the raw material, NOx and COx formation. Moreover conducting the number for the current and the upgraded design of the precalcinator and analysis of the results. In this study, a mathematical model based on Euler's method to describe the motion of the gas phase and the Lagrange method to describe the motion of particles [1-4]. In the calculations there were assumed fractional particles raw material and fuel, and the following processes: flow of exhaust gases from the rotary kiln through the precalcinator chamber, heat exchange between the particles of raw material and exhaust gases, the additional fuel combustion in the precalcinator, the process of raw material calcination, transformation of gaseous substances, effect of the additional (tertiary) air delivery on the processes in the chamber.

  20. Study on calcination of bi-layered films produced by anodizing iron in dimethyl sulfoxide electrolyte

    International Nuclear Information System (INIS)

    Jagminas, Arūnas; Klimas, Vaclovas; Mažeika, Kęstutis; Mickevičius, Sigitas; Balakauskas, Saulius

    2012-01-01

    Research on well adherent, thick and nanoporous oxide film formation onto the metal substrates underwent a major burst throughout the last decade. In the current study, thick bi-layered films produced onto a pure iron surface by anodizing way in dimethyl sulfoxide (DMSO) electrolyte containing silica hexafluoride acid have been investigated upon the annealing in air. Compositional, phase and structural transformations of the film material to hematite, α-Fe 2 O 3 , were studied using Mössbauer spectroscopy at room to cryogenic temperatures, thermogravimetry (TG), differential thermal analysis (DTA), photoemission spectroscopy, scanning electron microscopy (SEM), and wave dispersive X-ray spectroscopy (WDX). Experimental findings indicated that much longer heating in air is required for these films to be fully transformed to hematite. This effect is linked here with the complex nature of DMSO films. Based on the combined WDX, photoemission and Mössbauer spectroscopy results, the transformations taken place during calcination of such amorphous films by heat-treatment in air to crystalline hematite have been determined. Investigations on the calcination effects of thick iron anodic films reported here offer opportunities for both fundamental research and practical applications.

  1. Uptake of chloride ion from aqueous solution by calcined layered double hydroxides: equilibrium and kinetic studies.

    Science.gov (United States)

    Lv, Liang; He, Jing; Wei, Min; Evans, D G; Duan, Xue

    2006-02-01

    Layered double hydroxides (LDH) calcined within a certain temperature range (denoted as CLDH) have been shown to recover their original layered structure in the presence of appropriate anions. In the light of this so-called "memory effect", uptake of chloride ion from aqueous solution by calcined MgAl-CO3 LDH was investigated in batch mode. The equilibrium isotherm showed that the uptake of chloride ion by CLDH was consistent with the Langmuir and Freundlich equations and that the Langmuir model gave a better fit to the experimental data than the Freundlich model. The maximum uptake capacity of CLDH for chloride ion was 149.5 mg/g, close to the stoichiometric uptake (168 mg/g). The influence of varying pH of solution, initial chloride concentration, adsorbent quantity, and temperature on the kinetics of chloride removal has also been explored. Four kinetic models were used to fit the experimental data, and it was found that the pseudo-second-order kinetics model could be used to describe the uptake process satisfactorily. The calculated value of Ea was found to be 56.8 kJ/mol, which suggests that the process of uptake of chloride ion is controlled by the rate of reaction of chloride ion with the CLDH rather than diffusion. A mechanism for removal of chloride ion has been confirmed by X-ray diffraction, FT-IR spectroscopy and TG-MS measurements.

  2. Calcination temperature influenced multiferroic properties of Ca-doped BiFeO3 nanoparticles

    Science.gov (United States)

    Dhir, Gitanjali; Uniyal, Poonam; Verma, N. K.

    2015-06-01

    The influence of Ca-doping and particle size on structural, morphological and magnetic properties of BiFeO3 nanoparticles has been studied. A sol-gel method was employed for the synthesis of nanoparticles and their particle size was tailored by varying the calcination temperature. Structural analysis revealed a rhombohedral distortion induced by Ca-substitution. The broadening of diffraction peaks with decreasing calcination temperature was indicative of reduction in crystallite size. The morphological analysis revealed the formation of agglomerated nanoparticles having average particle size ranging from 10-15 and 50-55 nm for C4 and C6, respectively. The agglomeration is attributed to high surface energy of nanoparticles. Ferromagnetism has been displayed by all the synthesized nanoparticles. Enhancement of saturation magnetization with Ca-substitution is attributed to suppression of spin cycloid structure by the reduction in size, lattice distortion and creation of oxygen vacancies by the substitution of divalent ion at trivalent site. Further, this value increases as a function of decreasing particle size. Strong particle size effects on magnetic properties of the synthesized nanoparticles are owed to increasing surface to volume ratio. All these observations are indicative of strong dependence of multiferroism on particle size.

  3. Mercury removal at Idaho National Engineering and Environmental Laboratory's New Waste Calciner Facility

    International Nuclear Information System (INIS)

    Ashworth, S.C.

    2000-01-01

    Technologies were investigated to determine viable processes for removing mercury from the calciner (NWCF) offgas system at the Idaho National Engineering and Environmental Laboratory. Technologies for gas phase and aqueous phase treatment were evaluated. The technologies determined are intended to meet EPA Maximum Achievable Control Technology (MACT) requirements under the Clean Air Act and Resource Conservation and Recovery Act (RCRA). Currently, mercury accumulation in the calciner off-gas scrubbing system is transferred to the tank farm. These transfers lead to accumulation in the liquid heels of the tanks. The principal objective for aqueous phase mercury removal is heel mercury reduction. The system presents a challenge to traditional methods because of the presence of nitrogen oxides in the gas phase and high nitric acid in the aqueous scrubbing solution. Many old and new technologies were evaluated including sorbents and absorption in the gas phase and ion exchange, membranes/sorption, galvanic methods, and UV reduction in the aqueous phase. Process modifications and feed pre-treatment were also evaluated. Various properties of mercury and its compounds were summarized and speciation was predicted based on thermodynamics. Three systems (process modification, NOxidizer combustor, and electrochemical aqueous phase treatment) and additional technology testing were recommended

  4. Mercury Removal at Idaho National Engineering and Environmental Laboratory's New Waste Calcining Facility

    Energy Technology Data Exchange (ETDEWEB)

    Ashworth, Samuel Clay; Wood, R. A.; Taylor, D. D.; Sieme, D. D.

    2000-03-01

    Technologies were investigated to determine viable processes for removing mercury from the calciner (NWCF) offgas system at the Idaho National Engineering and Environmental Laboratory. Technologies for gas phase and aqueous phase treatment were evaluated. The technologies determined are intended to meet EPA Maximum Achievable Control Technology (MACT) requirements under the Clean Air Act and Resource Conservation and Recovery Act (RCRA). Currently, mercury accumulation in the calciner off-gas scrubbing system is transferred to the tank farm. These transfers lead to accumulation in the liquid heels of the tanks. The principal objective for aqueous phase mercury removal is heel mercury reduction. The system presents a challenge to traditional methods because of the presence of nitrogen oxides in the gas phase and high nitric acid in the aqueous scrubbing solution. Many old and new technologies were evaluated including sorbents and absorption in the gas phase and ion exchange, membranes/sorption, galvanic methods, and UV reduction in the aqueous phase. Process modifications and feed pre-treatment were also evaluated. Various properties of mercury and its compounds were summarized and speciation was predicted based on thermodynamics. Three systems (process modification, NOxidizer combustor, and electrochemical aqueous phase treatment) and additional technology testing were recommended.

  5. Mercury removal at Idaho National Engineering and Environmental Laboratory's New Waste Calcining Facility

    Energy Technology Data Exchange (ETDEWEB)

    S. C. Ashworth

    2000-02-27

    Technologies were investigated to determine viable processes for removing mercury from the calciner (NWCF) offgas system at the Idaho National Engineering and Environmental Laboratory. Technologies for gas phase and aqueous phase treatment were evaluated. The technologies determined are intended to meet EPA Maximum Achievable Control Technology (MACT) requirements under the Clean Air Act and Resource Conservation and Recovery Act (RCRA). Currently, mercury accumulation in the calciner off-gas scrubbing system is transferred to the tank farm. These transfers lead to accumulation in the liquid heels of the tanks. The principal objective for aqueous phase mercury removal is heel mercury reduction. The system presents a challenge to traditional methods because of the presence of nitrogen oxides in the gas phase and high nitric acid in the aqueous scrubbing solution. Many old and new technologies were evaluated including sorbents and absorption in the gas phase and ion exchange, membranes/sorption, galvanic methods, and UV reduction in the aqueous phase. Process modifications and feed pre-treatment were also evaluated. Various properties of mercury and its compounds were summarized and speciation was predicted based on thermodynamics. Three systems (process modification, NOxidizer combustor, and electrochemical aqueous phase treatment) and additional technology testing were recommended.

  6. A low-temperature process for the denitration of Hanford single-shell tank, nitrate-based waste utilizing the nitrate to ammonia and ceramic (NAC) or nitrate to ammonia and glass (NAG) process: Phase 2 report

    International Nuclear Information System (INIS)

    Mattus, A.J.; Walker, J.F. Jr.; Youngblood, E.L.; Farr, L.L.; Lee, D.D.; Dillow, T.A.; Tiegs, T.N.

    1994-12-01

    Continuing benchtop studies using Hanford single-shell tank (SST) simulants and actual Oak Ridge National Laboratory (ORNL) low-level waste (LLW), employing a new denitration process for converting nitrate to ammonia and ceramic (NAC), have conclusively shown that between 85 and 99% of the nitrate can be readily converted to gaseous ammonia. In this process, aluminum powders can be used to convert alkaline, nitrate-based supernate to ammonia and an aluminum oxide-sodium aluminate-based solid. The process may be able to use contaminated aluminum scrap metal from DOE sites to effect the conversion. The final, nitrate-free ceramic product can be pressed and sintered like other ceramics or silica and/or fluxing agents can be added to form a glassy ceramic or a flowable glass product. Based upon the starting volumes of 6.2 and 3.1 M sodium nitrate solution, volume reductions of 50 to 70% were obtained for the waste form produced. Sintered pellets produced from supernate from Melton Valley Storage Tanks (MVSTs) have been leached in accordance with the 16.1 leach test for the radioelements 85 Sr and 137 Cs. Despite lengthy counting times, 85 Sr could not be detected in the leachates. 137 Cs was only slightly above background and corresponded to a leach index of 12.2 to 13.7 after 8 months of leaching. Leach testing of unsintered and sintered reactor product spiked with hazardous metals proved that both sintered and unsintered product passed the Toxicity Characteristic Leaching Procedure (TCLP) test. Design of the equipment and flowsheet for a pilot demonstration-scale system to prove the nitrate destruction portion of the NAC process and product formation is under way

  7. Effect of calcination temperature on microstructural and magnetic properties of CuFe2O4 spinel

    Energy Technology Data Exchange (ETDEWEB)

    Costa, A.F.; Melo, D.M.A.; Gomes, D.K.S.; Araujo, J.H.; Lima, A.C. [Universidade Federal do Rio Grande do Norte (UFRN), RN (Brazil); Pimentel, P.M. [Universidade Federal Rural do Semi-Arido (UFERSA), Mossoro, RN (Brazil); Santana, R.S.; Oliveira, R.M.P.B. [Universidade Federal de Sergipe (UFS), SE (Brazil)

    2014-07-01

    In this research, we report a study of nanostructured CuFe{sub 2}O{sub 4} Spinel obtained by a method which makes uses of gelatin as an organic precursor. The structural and magnetic properties were investigated in function of calcination temperature. The precursor powders were calcined at 700 and 900 deg C to obtain spinel phase. Then were characterized using X-ray diffraction combined with the Rietveld refinement method, infrared spectroscopy (FTIR), and magnetic measurements. The X-ray diffraction patterns revealed the presence of an inverse spinel phase, corresponding to copper ferrite in all samples. Moreover, Fe{sub 2}O{sub 3} and CuO phases were also identified. The results reveal that the calcination temperature strongly influences the magnetic properties of the prepared oxides. (author)

  8. Preparation and thermal energy storage properties of paraffin/calcined diatomite composites as form-stable phase change materials

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Zhiming [School of Chemical and Environmental Engineering, China University of Mining and Technology, Beijing 100083 (China); Chemistry Discipline, Faculty of Science and Technology, Queensland University of Technology, 2 George Street, GPO Box 2434, Brisbane, Queensland 4001 (Australia); Zhang, Yuzhong [School of Chemical and Environmental Engineering, China University of Mining and Technology, Beijing 100083 (China); Zheng, Shuilin, E-mail: shuilinzh@yahoo.com.cn [School of Chemical and Environmental Engineering, China University of Mining and Technology, Beijing 100083 (China); Park, Yuri [Chemistry Discipline, Faculty of Science and Technology, Queensland University of Technology, 2 George Street, GPO Box 2434, Brisbane, Queensland 4001 (Australia); Frost, Ray L., E-mail: r.frost@qut.edu.au [Chemistry Discipline, Faculty of Science and Technology, Queensland University of Technology, 2 George Street, GPO Box 2434, Brisbane, Queensland 4001 (Australia)

    2013-04-20

    Highlights: ► Composite phase change material (PCM) was prepared by blending composite paraffin and calcined diatomite. ► The optimum mixed proportion was obtained through differential scanning calorimetry. ► Thermal energy storage properties of the composite PCMs were determined by DSC. ► Thermal cycling test showed that the prepared PCMs are thermally reliable and chemically stable. - Abstract: A composite paraffin-based phase change material (PCM) was prepared by blending composite paraffin and calcined diatomite through the fusion adsorption method. In this study, raw diatomite was purified by thermal treatment in order to improve the adsorption capacity of diatomite, which acted as a carrier material to prepare shape-stabilized PCMs. Two forms of paraffin (paraffin waxes and liquid paraffin) with different melting points were blended together by the fusion method, and the optimum mixed proportion with a suitable phase-transition temperature was obtained through differential scanning calorimetry (DSC) analysis. Then the prepared composite paraffin was adsorbed in calcined diatomite. The prepared paraffin/calcined diatomite composites were characterized by the scanning electron microscope (SEM) and Fourier transformation infrared (FT-IR) analysis techniques. Thermal energy storage properties of the composite PCMs were determined by DSC method. DSC results showed that there was an optimum adsorption ratio between composite paraffin and calcined diatomite and the phase-transition temperature and the latent heat of the composite PCMs were 33.04 °C and 89.54 J/g, respectively. Thermal cycling test of composite PCMs showed that the prepared material is thermally reliable and chemically stable. The obtained paraffin/calcined diatomite composites have proper latent heat and melting temperatures, and show practical significance and good potential application value.

  9. Preparation and thermal energy storage properties of paraffin/calcined diatomite composites as form-stable phase change materials

    International Nuclear Information System (INIS)

    Sun, Zhiming; Zhang, Yuzhong; Zheng, Shuilin; Park, Yuri; Frost, Ray L.

    2013-01-01

    Highlights: ► Composite phase change material (PCM) was prepared by blending composite paraffin and calcined diatomite. ► The optimum mixed proportion was obtained through differential scanning calorimetry. ► Thermal energy storage properties of the composite PCMs were determined by DSC. ► Thermal cycling test showed that the prepared PCMs are thermally reliable and chemically stable. - Abstract: A composite paraffin-based phase change material (PCM) was prepared by blending composite paraffin and calcined diatomite through the fusion adsorption method. In this study, raw diatomite was purified by thermal treatment in order to improve the adsorption capacity of diatomite, which acted as a carrier material to prepare shape-stabilized PCMs. Two forms of paraffin (paraffin waxes and liquid paraffin) with different melting points were blended together by the fusion method, and the optimum mixed proportion with a suitable phase-transition temperature was obtained through differential scanning calorimetry (DSC) analysis. Then the prepared composite paraffin was adsorbed in calcined diatomite. The prepared paraffin/calcined diatomite composites were characterized by the scanning electron microscope (SEM) and Fourier transformation infrared (FT-IR) analysis techniques. Thermal energy storage properties of the composite PCMs were determined by DSC method. DSC results showed that there was an optimum adsorption ratio between composite paraffin and calcined diatomite and the phase-transition temperature and the latent heat of the composite PCMs were 33.04 °C and 89.54 J/g, respectively. Thermal cycling test of composite PCMs showed that the prepared material is thermally reliable and chemically stable. The obtained paraffin/calcined diatomite composites have proper latent heat and melting temperatures, and show practical significance and good potential application value

  10. Retrofit design of remotely removable decontamination spray nozzles for the new waste calcining facility at the Idaho National Engineering Laboratory

    International Nuclear Information System (INIS)

    Gay, J.A.

    1988-01-01

    High level radioactive liquid waste is converted to a solid form at the Idaho Chemical Processing Plant (ICPP). The conversion is done by a fluidized bed combustion process in the calciner vessel. The interior decontamination system for the calciner vessel uses a common header bolted to four decontamination nozzles around the upper head. The retrofit was required to eliminate hands-on maintenance and difficulty in nozzle removal because of nozzle plugging. The retrofit design for this project demonstrates the solution of problems associated with thermal phenomena, structural supports, seismic requirements, remote handling and installations into extremely restricted spaces

  11. Physical and chemical characteristics of fluorinel/sodium calcine generated during 30 cm Pilot-Plant Run 17

    International Nuclear Information System (INIS)

    Brewer, K.N.; Kessinger, G.F.; Littleton, L.L.; Olson, A.L.

    1993-07-01

    The 30 centimeter (cm) pilot plant calciner Run 17, of March 9, 1987, was performed to study the calcination of fluroinel-sodium blended waste blended at the ratio 3.5:1 fluorinel to sodium, respectively. The product of the run was analyzed by a variety of analytical techniques that included X-ray powder diffraction (XRD), inductively coupled plasma spectroscopy (ICP), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS) to deduce physical and chemical characteristics. The analytical data, as well as data analyses and conclusions drawn from the data, are presented

  12. Influence of Solids-to-liquid and Activator Ratios on Calcined Kaolin Cement Powder

    Science.gov (United States)

    Liew, Y. M.; Kamarudin, H.; Bakri, A. M. Mustafa Al; Binhussain, M.; Luqman, M.; Nizar, I. Khairul; Ruzaidi, C. M.; Heah, C. Y.

    This paper summarizes the effect of activator ratio on the processing of cement powder. Geopolymer slurry was produced via alkaline activation of calcined kaolin. Once the geopolymer slurry solidified, it was crushed and ground to obtain cement powder. Ultilizing the concept of "just adding water", hardened cement paste could be produced from cement powder. This paper concluded that solids-to-liquid and sodium silicate-to-sodium hydroxide ratios have a significant effect on compressive strength of hardened cement paste. The optimum solids-to-liquid and sodium silicate-to-sodium hydroxide ratios were 0.80 and 0.20, respectively. SEM micrographs showed that a processing route to produce cement powder by "just adding water" was possible, and the structure became denser and fewer unreacted particles were observed.

  13. Influence of temperature on the synthesis of calcining cement α--tricalcium phosphate

    International Nuclear Information System (INIS)

    Vieira, R.S.; Thurmer, M.B.; Coelho, W.T.; Fernandes, J.M.; Santos, L.A.

    2011-01-01

    The calcium phosphate cement (CFCs) bone substitutes are of great potential use in medical and dental. However, one of the great difficulties of using this type of cement is its low mechanical strength due to the presence of undesirable phases, such as beta-tricalcium phosphate. The step of obtaining this compound is done at high temperature by solid state reaction. With the aim of obtaining calcium phosphate cements more resistant, we studied the conditions for obtaining an alpha-TCP at temperatures of 1300, 1400 and 1500 ° C with time 2h calcination. The samples were analyzed for crystalline phases, density, porosity and mechanical strength. The results show that the synthesis parameters studied strongly influence the obtained phases and the mechanical properties of cement. (author)

  14. ANTI-ULCER ACTIVITY OF SHANKHA BHASMA (CALCINED CONCH-SHELL

    Directory of Open Access Journals (Sweden)

    T. K. Sur

    2013-06-01

    Full Text Available The anti-ulcer activities along with chemical identification of purified Shankha Bhasma (SBM or calcined conch-shell was undertaken. Shankha Bhasma (SBM was prepared by traditional process used in India. The chemical composition of SBM was studied by atomic absorption spectrometry and infra-red spectral analysis. Acute oral toxicity of SBM was done in Swiss mice. SBM (25 mg/kg and 50 mg/kg was studied for anti-ulcer effect on ethanol induced and pylorus ligature induced model in Wistar rats. SBM showed significant (P<0.001 positive results in both the models in comparison with respective control and standard control (omeprazole 20 mg/kg and ranitidine 50 mg/kg.

  15. Surface complexation modeling calculation of Pb(II) adsorption onto the calcined diatomite

    Science.gov (United States)

    Ma, Shu-Cui; Zhang, Ji-Lin; Sun, De-Hui; Liu, Gui-Xia

    2015-12-01

    Removal of noxious heavy metal ions (e.g. Pb(II)) by surface adsorption of minerals (e.g. diatomite) is an important means in the environmental aqueous pollution control. Thus, it is very essential to understand the surface adsorptive behavior and mechanism. In this work, the Pb(II) apparent surface complexation reaction equilibrium constants on the calcined diatomite and distributions of Pb(II) surface species were investigated through modeling calculations of Pb(II) based on diffuse double layer model (DLM) with three amphoteric sites. Batch experiments were used to study the adsorption of Pb(II) onto the calcined diatomite as a function of pH (3.0-7.0) and different ionic strengths (0.05 and 0.1 mol L-1 NaCl) under ambient atmosphere. Adsorption of Pb(II) can be well described by Freundlich isotherm models. The apparent surface complexation equilibrium constants (log K) were obtained by fitting the batch experimental data using the PEST 13.0 together with PHREEQC 3.1.2 codes and there is good agreement between measured and predicted data. Distribution of Pb(II) surface species on the diatomite calculated by PHREEQC 3.1.2 program indicates that the impurity cations (e.g. Al3+, Fe3+, etc.) in the diatomite play a leading role in the Pb(II) adsorption and dominant formation of complexes and additional electrostatic interaction are the main adsorption mechanism of Pb(II) on the diatomite under weak acidic conditions.

  16. Characterization of red mud derived from a combined Bayer Process and bauxite calcination method.

    Science.gov (United States)

    Liu, Yong; Lin, Chuxia; Wu, Yonggui

    2007-07-19

    Red mud can be derived from the processing of bauxite using different methods. The chemical and mineralogical composition of the combined Bayer Process and bauxite calcination red mud (BPBCRM) differs markedly from those of the pure Bayer Process red mud (PBPRM). In this study, red mud derived from a combined Bayer Process and bauxite calcination method was characterized. The results show that pH of the red mud decreased with increasing duration of storage time. Na dominated among the soluble cations, but the concentration of soluble Na decreased with increasing duration of storage time as a result of leaching. Cation exchange capacity also decreased with increasing duration of storage time, probably due to a decrease in pH causing a reduction in negatively charged sites on the red mud particles. Ca was the predominant exchangeable cation in the fresh red mud but the concentration of exchangeable Ca markedly decreased in the old red mud, which was dominated by exchangeable Na. The degree of crystallization and thermal stability of the red mud increased with increasing duration of storage. The acid neutralizing capacity of red mud obtained from this study was about 10 mol kg(-1), which is much greater than the reported values for the pure Bayer Process red mud. Column filtering experiment indicates that the red mud also had a very strong capacity to remove Cu, Zn and Cd from the filtering solution. It is conservatively estimated that the simultaneous removal rates of Cd, Zn and Cu by red mud are over 22,250 mg kg(-1), 22,500 mg kg(-1) and 25,000 mg kg(-1), respectively. The affinity of these metals to the red mud was in the following decreasing order: Cu>Zn>Cd. In general, the fresh red mud retained more heavy metals than the old red mud did.

  17. Development of mesoporosity in scandia-stabilized zirconia: particle size, solvent, and calcination effects.

    Science.gov (United States)

    Cahill, James T; Ruppert, Jesse N; Wallis, Bryce; Liu, Yanming; Graeve, Olivia A

    2014-05-20

    We present the mechanisms of formation of mesoporous scandia-stabilized zirconia using a surfactant-assisted process and the effects of solvent and thermal treatments on the resulting particle size of the powders. We determined that cleaning the powders with water resulted in better formation of a mesoporous structure because higher amounts of surfactant were preserved on the powders after washing. Nonetheless, this resulted in agglomerate sizes that were larger. The water-washed powders had particle sizes of >5 μm in the as-synthesized state. Calcination at 450 and 600 °C reduced the particle size to ∼1-2 and 0.5 μm, respectively. Cleaning with ethanol resulted in a mesoporous morphology that was less well-defined compared to the water-washed powders, but the agglomerate size was smaller and had an average size of ∼250 nm that did not vary with calcination temperature. Our analysis showed that surfactant-assisted formation of mesoporous structures can be a compromise between achieving a stable mesoporous architecture and material purity. We contend that removal of the surfactant in many mesoporous materials presented in the literature is not completely achieved, and the presence of these organics has to be considered during subsequent processing of the powders and/or for their use in industrial applications. The issue of material purity in mesoporous materials is one that has not been fully explored. In addition, knowledge of the particle (agglomerate) size is essential for powder handling during a variety of manufacturing techniques. Thus, the use of dynamic light scattering or any other technique that can elucidate particle size is essential if a full characterization of the powders is needed for achieving postprocessing effectiveness.

  18. Chemistry of application of calcination/dissolution to the Hanford tank waste inventory

    International Nuclear Information System (INIS)

    Delegard, C.H.; Elcan, T.D.; Hey, B.E.

    1994-05-01

    Approximately 330,000 metric tons of sodium-rich radioactive waste originating from separation of plutonium from irradiated uranium fuel are stored in underground tanks at the Hanford Site in Washington State. Fractionation of the waste into low-level waste (LLW) and high-level waste (HLW) streams is envisioned via partial water dissolution and limited radionuclide extraction operations. Under optimum conditions, LLW would contain most of the chemical bulk while HLW would contain virtually all of the transuranic and fission product activity. Calcination at around 850 C, followed by water dissolution, has been proposed as an alternative initial treatment of Hanford Site waste to improve waste dissolution and the envisioned LLW/HLW split. Results of literature and laboratory studies are reported on the application of calcination/dissolution (C/D) to the fractionation of the Hanford Site tank waste inventory. Both simulated and genuine Hanford Site waste materials were used in the lab tests. To evaluation confirmed that C/D processing reduced the amount of several components from the waste. The C/D dissolutions of aluminum and chromium allow redistribution of these waste components from the HLW to the LLW fraction. Comparisons of simple water-washing with C/D processing of genuine Hanford Site waste are also reported based on material (radionuclide and chemical) distributions to solution and solid residue phases. The lab results show that C/D processing yielded superior dissolution of aluminum and chromium sludges compared to simple water dissolution. 57 refs., 26 figs., 18 tabs

  19. Chemistry of application of calcination/dissolution to the Hanford tank waste inventory

    Energy Technology Data Exchange (ETDEWEB)

    Delegard, C.H.; Elcan, T.D.; Hey, B.E.

    1994-05-01

    Approximately 330,000 metric tons of sodium-rich radioactive waste originating from separation of plutonium from irradiated uranium fuel are stored in underground tanks at the Hanford Site in Washington State. Fractionation of the waste into low-level waste (LLW) and high-level waste (HLW) streams is envisioned via partial water dissolution and limited radionuclide extraction operations. Under optimum conditions, LLW would contain most of the chemical bulk while HLW would contain virtually all of the transuranic and fission product activity. Calcination at around 850 C, followed by water dissolution, has been proposed as an alternative initial treatment of Hanford Site waste to improve waste dissolution and the envisioned LLW/HLW split. Results of literature and laboratory studies are reported on the application of calcination/dissolution (C/D) to the fractionation of the Hanford Site tank waste inventory. Both simulated and genuine Hanford Site waste materials were used in the lab tests. To evaluation confirmed that C/D processing reduced the amount of several components from the waste. The C/D dissolutions of aluminum and chromium allow redistribution of these waste components from the HLW to the LLW fraction. Comparisons of simple water-washing with C/D processing of genuine Hanford Site waste are also reported based on material (radionuclide and chemical) distributions to solution and solid residue phases. The lab results show that C/D processing yielded superior dissolution of aluminum and chromium sludges compared to simple water dissolution. 57 refs., 26 figs., 18 tabs.

  20. Stabilized γ-BIMNVOX solid electrolyte: Ethylene glycol–citrate sol–gel synthesis, microwave-assisted calcination, and structural and electrical characterization

    Energy Technology Data Exchange (ETDEWEB)

    Al-Areqi, Niyazi A.S., E-mail: niyazi.alareqi@gmail.com [Department of Chemistry, Faculty of Applied Science, Taiz University, Taiz, Republic of Yemen (Yemen); Beg, Saba [Department of Chemistry, Aligarh Muslim University, Aligarh 202002 (India); Al-Alas, Ahlam [Department of Chemistry, Faculty of Applied Science, Taiz University, Taiz, Republic of Yemen (Yemen); Hafeez, Shehla [Department of Chemistry, Aligarh Muslim University, Aligarh 202002 (India)

    2013-12-25

    Highlights: •γ-BIMNVOX was synthesized by ethylene glycol–citrate sol–gel route. •γ-BIMNVOX crystallizes by 25-min microwave-assisted calcination. •Smaller particle sizes for microwave calcined BIMNVOX samples. •Best oxide-ion performance for microwave calcined BIMNVOX samples. -- Abstract: Samples of γ-BIMNVOX (Bi{sub 2}V{sub 1−x}Mn{sub x}O{sub 5.5−x/2}; 0.13 ⩽ x ⩽ 0.20) system were synthesized by an ethylene glycol–citrate sol–gel route. The resulting xerogels were then calcined by the microwave heating using a modified domestic microwave oven operated at 2.45 GHz. Microwave-assisted calcination samples in comparison with other conventionally calcined samples were characterized in terms of phase crystallization, stabilization and particle size using simultaneous thermogravimetric–differential thermal analysis (TG–DTA), X-ray powder diffraction (XRPD) and scanning electron microscopy (SEM). The AC impedance spectroscopy was employed for electrical characterization. It was found that the microwave-assisted calcination route successfully produces better crystalline stabilized γ-BIMNVOX samples with appreciably small average particle sizes after only 25 min of microwave heating. The electrical properties of microwave calcined γ-BIMNVOX system make it an advanced low-temperature solid electrolyte suitable for use in oxide-ion based electrochemical applications.

  1. Use of calcination in exposing the entrapped Fe particles from multi-walled carbon nanotubes grown by chemical vapour deposition

    CSIR Research Space (South Africa)

    Kesavan Pillai, Sreejarani

    2009-03-01

    Full Text Available Multi-walled carbon nanotubes (MWCNTs) were synthesized by a chemical vapour deposition method. The effect of calcination at temperatures ranging from 300 to 550°C in exposing the metal nanoparticles within the nanotube bundles was studied...

  2. Effect of calcination temperature and time on the structural and electrical properties of SrFe12O19 nanoparticles

    Directory of Open Access Journals (Sweden)

    M Zargar Shoushtari

    2015-01-01

    Full Text Available In this paper, nanoparticles of strontium hexaferrite (SrFe12O19 were synthesized via sol–gel technique. For preparation of the SrFe12O19 nanoparticles, the nitrates of the metal with a specified ratio of molar and citric acid were used. By using the thermogravimetric analysis (DTA/TGA the final product was studied. On the basis of this analysis, the samples at different temperatures from 600°C to 1100 °C and calcination time from 0.5 h to 3 h were synthesized. The effect of calcination temperature with different times on the structural and electrical properties was studied. The structural and morphology of the samples were investigated by the X- ray diffraction (XRD, Fourier transform infrared spectroscopy (FT- IR and scanning electron microscopy (SEM. Also, the DC resistivity of the samples was measured by four-probe method. The results of XRD revealed that the optimum temperature and calcination time of the single-phase SrFe12O19 nanoparticles were 1000°C and 2h, respectively. The results of the electrical properties at room temperature showed that the DC resistivity of the samples decreased by increasing the calcination temperature

  3. Influence of calcination temperature on the zirconia microstructure synthesized by complex polymerization method (CPM): a comparative study

    Energy Technology Data Exchange (ETDEWEB)

    Santos, R.L.P.; Mota, F.V.; Nascimento, R.M.; Henriques, B.P.; Silva, F.S.; Assis, R. [Universidade Federal do Rio Grande do Norte (UFRN), Natal, RN (Brazil)

    2016-07-01

    Full text: The aim of this study was to accomplish a previous characterization of the zirconia synthesized by Complex Polymerization Method (CPM) using yttria as stabilizing agent and different calcination temperatures. The powders were crystallized at 800, 900 and 1000 °C for 2h. The structural evolution Y-TZP powders were characterized by X-Ray Diffraction (XRD) and Micro-Raman Spectroscopy. The thermal properties of the calcined pre-pyrolyzed (350 °C for 4 h), samples were investigated by simultaneous thermo analysis (TGA/DTA). After heat treatment the phase Y-TZP was obtained of a single-phase, with absence of the deleterious phases. The results show that average crystallite size of the powder synthesized with 3% of Yttria dopant, increased from 11.5 to 27.9 nm when the calcination temperature increased from 800 to 1000 °C. This behavior was observed for all specimens independent of the Yttria content. The micro-Raman indicate the presence of the tetragonal phase for all samples independent of the calcination temperature employed. (author)

  4. Removal of an Acid Dye from Water Using Calcined and Uncalcined ZnAl-r Anionic Clay.

    Science.gov (United States)

    Bessaha, Hassiba; Bouraada, Mohamed; de Ménorval, Louis Charles

    2017-09-01

      The present report describes the removal of indigo carmine dye from water via adsorption on ZnAl-r hydrotalcite. Two grades of clay based on Zn/Al molar ratios of 3 and 4, uncalcined and calcined, were used. The adsorbents characterization using X-ray diffraction (XRD), Fourier transform infrared (FTIR), differential thermal and thermogravimetric analysis (DTA and TGA, respectively) revealed a layered structure for the hydrotalcite clays, whereas their calcination favored the formation of ZnO and ZnAl2O4 mixed metal oxides. The calcined materials immobilized much larger amounts of indigo carmine dye than the uncalcined layered double hydroxides (LDHs) specimens. The maximum adsorption capacities obey the order: CZnAl-4 (520.8 mg/g) > CZnAl-3 (358.4 mg/g) > ZnAl-3 (67.25 mg/g) > ZnAl-4 (21.65 mg/g). The adsorption isotherms are best described by Langmuir model. The sorption process is spontaneous in nature and its kinetics data are best described by a pseudo-second-order model. Adsorption tests on re-used calcined clays demonstrate its reusability after three thermal cycles.

  5. Effect of feed atomization and vessel configuration of fines formation and entrainment from fluidized-bed calciners

    International Nuclear Information System (INIS)

    Bonder, S.S.

    1978-11-01

    Fines and granules are produced during fluidized-bed calcination of liquid radioactive wastes. Fines are generated by attrition of larger bed particles and spray drying of atomized feed droplets. Some of the fines have sufficient residence time in the bed to provide seed particles for the particle growth; the remainder are elutriated from the bed or withdrawn with the product. Methods which were tested to reduce the generation and entrainment of fines during the calcination process are discussed. A pneumatic, flat-faced, feed atomizing nozzle has proven adequate for feed introduction, bed particle size control, and seed particle generation. Other pneumatic nozzle types (the extended divergent, long extended convergent, and short extended convergent) did not control bed particle size. Testing of a single-fluid pressure nozzle and the combination nozzle and cyclone fines return jet was discontinued before completion. However, no further testing to improve nozzle operating characteristics is presently justifiable, as the flat-faced nozzle has proven adequate. Limited tests confirmed that a cylindrical fluid bed with an expanded vapor space results in lower entrainment rates than a conventional cylindrical fluid bed. A reduction of the superficial gas velocity in the expanded vapor space by a factor of 3.2 reduced entrainment by a factor of 8. Double ''venetian blind'' baffles in the calciner vapor space were 20% more effective in suppressing fines entrainment than single ''venetian blind'' and fan baffles. Submerged baffles increased bed particle attrition and subsequent fines entrainment. The New Waste Calcining Facility will have a cylindrical calciner vessel with an expanded vapor space containing a double ''venetian blind'' baffle

  6. Direct cementitious waste option study report

    Energy Technology Data Exchange (ETDEWEB)

    Dafoe, R.E.; Losinski, S.J.

    1998-02-01

    A settlement agreement between the Department of Energy (DOE) and the State of Idaho mandates that all high-level radioactive waste (HLW) now stored at the Idaho Chemical Processing Plant (ICPP) will be treated so that it is ready to be moved out of Idaho for disposal by a target data of 2035. This study investigates the direct grouting of all ICPP calcine (including the HLW dry calcine and those resulting from calcining sodium-bearing liquid waste currently residing in the ICPP storage tanks) as the treatment method to comply with the settlement agreement. This method involves grouting the calcined waste and casting the resulting hydroceramic grout into stainless steel canisters. These canisters will be stored at the Idaho National Engineering and Environmental Laboratory (INEEL) until they are sent to a national geologic repository. The operating period for grouting treatment will be from 2013 through 2032, and all the HLW will be treated and in interim storage by the end of 2032.

  7. Direct cementitious waste option study report

    International Nuclear Information System (INIS)

    Dafoe, R.E.; Losinski, S.J.

    1998-02-01

    A settlement agreement between the Department of Energy (DOE) and the State of Idaho mandates that all high-level radioactive waste (HLW) now stored at the Idaho Chemical Processing Plant (ICPP) will be treated so that it is ready to be moved out of Idaho for disposal by a target data of 2035. This study investigates the direct grouting of all ICPP calcine (including the HLW dry calcine and those resulting from calcining sodium-bearing liquid waste currently residing in the ICPP storage tanks) as the treatment method to comply with the settlement agreement. This method involves grouting the calcined waste and casting the resulting hydroceramic grout into stainless steel canisters. These canisters will be stored at the Idaho National Engineering and Environmental Laboratory (INEEL) until they are sent to a national geologic repository. The operating period for grouting treatment will be from 2013 through 2032, and all the HLW will be treated and in interim storage by the end of 2032

  8. Infrared detection of the mineralogical aspects that influence the processing of calcined kaolin

    Science.gov (United States)

    Groenheide, Stefan; Guatame-Garcia, Adriana; Buxton, Mike; van der Werff, Harald

    2017-04-01

    Calcined kaolin is an industrial minerals product used in the production of paper, paint, rubber and other specialty applications. It is produced from kaolinite through a series of refinement steps and final calcination at temperatures of above 900°C, with the aim of generating a whiter and more abrasive material. The raw kaolin ore is a mixture of clay minerals, quartz and feldspars, where kaolinite is the main constituent. The optimal kaolin ores to feed the processing plant should ideally have high kaolinite abundance, be free in Fe-bearing mineralogy (to avoid influence in the colour of the product), and the kaolinite itself should be of high crystallinity (to ensure the correct abrasiveness after calcination). This work presents a case study from the kaolin deposits in the St. Austell Granite (South-West England), which are known for their high quality and world-class size. In this area, the kaolin is of primary-hydrothermal origin, with mineral associations that are related to the genetic history. The eventual depletion of the high-quality reserves is bringing now the attention to the lower grade zones, where the amount of impurities increases. As a consequence, it is critical to developing strategies that ensure the supply of high-quality ore to the processing plant. For this, it is necessary to acquire a thorough knowledge of the ore, including relative abundance of the minerals and their textural relationships. Hyperspectral images in the visible-near infrared (VNIR) and short-wave infrared (SWIR) ranges were collected from drill cores and run-off-mine (ROM) samples, obtained from one of the kaolin pits in the St. Austell area, where the kaolin quality is known to be lower than in the rest of the deposit. A series of mineral maps were generated to assess the distribution, texture and abundance of the Fe-bearing mineralogy and the other kaolin-associated minerals, as well as the variations in the crystallinity of kaolinite. The mineral maps enabled the

  9. Generalized Test Plan for the Vitrification of Simulated High-Level -Waste Calcine in the Idaho National Laboratory‘s Bench -Scale Cold Crucible Induction Melter

    Energy Technology Data Exchange (ETDEWEB)

    Vince Maio

    2011-08-01

    This Preliminary Idaho National Laboratory (INL) Test Plan outlines the chronological steps required to initially evaluate the validity of vitrifying INL surrogate (cold) High-Level-Waste (HLW) solid particulate calcine in INL's Cold Crucible Induction Melter (CCIM). Its documentation and publication satisfies interim milestone WP-413-INL-01 of the DOE-EM (via the Office of River Protection) sponsored work package, WP 4.1.3, entitled 'Improved Vitrification' The primary goal of the proposed CCIM testing is to initiate efforts to identify an efficient and effective back-up and risk adverse technology for treating the actual HLW calcine stored at the INL. The calcine's treatment must be completed by 2035 as dictated by a State of Idaho Consent Order. A final report on this surrogate/calcine test in the CCIM will be issued in May 2012-pending next fiscal year funding In particular the plan provides; (1) distinct test objectives, (2) a description of the purpose and scope of planned university contracted pre-screening tests required to optimize the CCIM glass/surrogate calcine formulation, (3) a listing of necessary CCIM equipment modifications and corresponding work control document changes necessary to feed a solid particulate to the CCIM, (4) a description of the class of calcine that will be represented by the surrogate, and (5) a tentative tabulation of the anticipated CCIM testing conditions, testing parameters, sampling requirements and analytical tests. Key FY -11 milestones associated with this CCIM testing effort are also provided. The CCIM test run is scheduled to be conducted in February of 2012 and will involve testing with a surrogate HLW calcine representative of only 13% of the 4,000 m3 of 'hot' calcine residing in 6 INL Bin Sets. The remaining classes of calcine will have to be eventually tested in the CCIM if an operational scale CCIM is to be a feasible option for the actual INL HLW calcine. This remaining calcine

  10. Phase and morphology evolution of (Na1-xKxNbO3 powders related to calcinations and K2CO3 content

    Directory of Open Access Journals (Sweden)

    Steven J. Milne

    2007-03-01

    Full Text Available Sodium-potassium niobate ((Na1-xKxNbO3 powders with x = 0.2, 0.4, 0.6 and 0.8 were prepared following the conventional mixed oxide method and characterized by TG-DTA, XRD and SEM techniques.The effects of calcination temperature, dwell time and K2CO3 content on phase formation behavior and morphology of the powders were investigated. The calcination temperature and dwell time were found tohave a pronounced effect on the phase formation of the calcined sodium-potassium niobate powders. It was found that the crystallized phase depended on calcination conditions. The high calcination temperature andlong dwell time clearly favored particle growth and the formation of large and hard agglomerates. All the (Na1-xKxNbO3 powders showed a similar orthorhombic phase structure. The K2CO3 content significantlyaffected the calcination temperature and particle size and shape. Large particle size, cubic shape and a lower calcined condition were observed in (Na1-xKxNbO3 powder with low K2CO3 content (x = 0.2.

  11. Stabilization of lead and copper contaminated firing range soil using calcined oyster shells and fly ash.

    Science.gov (United States)

    Moon, Deok Hyun; Park, Jae-Woo; Cheong, Kyung Hoon; Hyun, Seunghun; Koutsospyros, Agamemnon; Park, Jeong-Hun; Ok, Yong Sik

    2013-12-01

    A stabilization/solidification treatment scheme was devised to stabilize Pb and Cu contaminated soil from a firing range using renewable waste resources as additives, namely waste oyster shells (WOS) and fly ash (FA). The WOS, serving as the primary stabilizing agent, was pre-treated at a high temperature to activate quicklime from calcite. Class C FA was used as a secondary additive along with the calcined oyster shells (COS). The effectiveness of the treatment was evaluated by means of the toxicity characteristic leaching procedure (TCLP) and the 0.1 M HCl extraction tests following a curing period of 28 days. The combined treatment with 10 wt% COS and 5 wt% FA cause a significant reduction in Pb (>98 %) and Cu (>96 %) leachability which was indicated by the results from both extraction tests (TCLP and 0.1 M HCl). Scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDX) analyses are used to investigate the mechanism responsible for Pb and Cu stabilization. SEM-EDX results indicate that effective Pb and Cu immobilization using the combined COS-FA treatment is most probably associated with ettringite and pozzolanic reaction products. The treatment results suggest that the combined COS-FA treatment is a cost effective method for the stabilization of firing range soil.

  12. Heavy metal stabilization in contaminated soil by treatment with calcined cockle shell.

    Science.gov (United States)

    Islam, Mohammad Nazrul; Taki, Golam; Nguyen, Xuan Phuc; Jo, Young-Tae; Kim, Jun; Park, Jeong-Hun

    2017-03-01

    In several previous studies, the efficacy of various liming waste materials on the immobilization of heavy metals has been tested and it was found that soils contaminated with heavy metals can be stabilized using this technique. Since lime (CaO) has been identified as the main phase of calcined cockle shell (CCS), it was hypothesized that CCS could be used as a soil amendment to immobilize heavy metals in soil. However, to date, no studies have been conducted using CCS. In this study, the effectiveness of CCS powder on the immobilization of Cd, Pb, and Zn in mine tailing soil was evaluated. After 28 days of incubation, the treated soil samples were exposed to weathering (four cycles of freezing-thawing and four cycles of wetting-drying) for 8 days before being subjected to a leaching test. The results of this study revealed that the soil pH increased from 7.5 to 12.2 with the addition of 5% CCS. A similar soil pH was obtained when the soil was amended with 5% pure CaO. By leaching with 0.1 M HCl, extracted Cd, Pb, and Zn were reduced by up to 85, 85, and 91%, respectively. Therefore, CCS is suggested as a low-cost lime-based soil amendment for stabilizing heavy metals in abandoned mining sites.

  13. Environmental assessment: Closure of the Waste Calcining Facility (CPP-633), Idaho National Engineering Laboratory

    International Nuclear Information System (INIS)

    1996-07-01

    The U.S. Department of Energy (DOE) proposes to close the Waste Calcining Facility (WCF). The WCF is a surplus DOE facility located at the Idaho Chemical Processing Plant (ICPP) on the Idaho National Engineering Laboratory (INEL). Six facility components in the WCF have been identified as Resource Conservation and Recovery Ace (RCRA)-units in the INEL RCRA Part A application. The WCF is an interim status facility. Consequently, the proposed WCF closure must comply with Idaho Rules and Standards for Hazardous Waste contained in the Idaho Administrative Procedures Act (IDAPA) Section 16.01.05. These state regulations, in addition to prescribing other requirements, incorporate by reference the federal regulations, found at 40 CFR Part 265, that prescribe the requirements for facilities granted interim status pursuant to the RCRA. The purpose of the proposed action is to reduce the risk of radioactive exposure and release of hazardous constituents and eliminate the need for extensive long-term surveillance and maintenance. DOE has determined that the closure is needed to reduce potential risks to human health and the environment, and to comply with the Idaho Hazardous Waste Management Act (HWMA) requirements

  14. Thermokinetic study of the rehydration process of a calcined MgAl-layered double hydroxide.

    Science.gov (United States)

    Pfeiffer, Heriberto; Lima, Enrique; Lara, Víctor; Valente, Jaime S

    2010-03-16

    The rehydration process of a calcined MgAl-layered double hydroxide (LDH) with a Mg/Al molar ratio of 3 was systematically analyzed at different temperatures and relative humidity. Qualitative and quantitative experiments were done. In the first set of samples, the temperature or the relative humidity was varied, fixing the second variable. Both adsorption and absorption phenomena were present; absorption process was associated to the LDH regeneration. Of course, in all cases the LDH regeneration was confirmed by other techniques such as TGA, solid state NMR, and SAXS. In the second set of experiments, a kinetic analysis was performed, the results allowed to obtain different activation enthalpies for the LDH regeneration as a function of the relative humidity. The activation enthalpies varied from 137.6 to 83.3 kJ/mol as a function of the relative humidity (50 and 80%, respectively). All these experiments showed that LDH regeneration is highly dependent on the temperature and relative humidity.

  15. Characterization of Calcined Jade and its immunomodulatory effect on macrophage isolated from Swiss albino mice

    Directory of Open Access Journals (Sweden)

    Asif Elahi

    2017-10-01

    Full Text Available Calcined Jade (CJ is a metasilicate frequently used in traditional system of medicine as tonic to vital organs with several other pharmacological activities. X-ray powder diffraction (XRPD, inductively coupled plasma mass spectrometry (ICP-MS, atomic absorption spectroscopy (AAS and CHNS analyzer techniques were used to characterize CJ sample. CJ was administered orally to Swiss albino mice at a dose of 50, 75, 100 and 200 μg/kg body weight for 10 days and modulation of the macrophage mediated innate immune responses was studied. Flow cytometric analysis of TLR-2/4 on peritoneal macrophage revealed elevated expression of TLR-2 as compared to control. Significant increase in phagocytic activity was observed in peritoneal macrophage. The lymphoid organs weight and other toxicity parameters did not exhibit any harmful effect. To evaluate the presence of nanoparticles, CJ was dissolved in milli Q water, filtered and lyophilized. Transmission electron microscopic (TEM analysis revealed the presence of spherical nanoparticles in CJ [14.7–142.0 nm dimension with average particle size of 64.6 nm]. In conclusion, we report stimulation of innate immune responses by CJ may partly be due to the formation of nanoparticles. Further experiments using isolated nanoparticles may further validate the role of nanoparticles.

  16. 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.

  17. Chloride adsorption by calcined layered double hydroxides in hardened Portland cement paste

    KAUST Repository

    Yoon, Seyoon

    2014-06-01

    This study investigated the feasibility of using calcined layered double hydroxides (CLDHs) to prevent chloride-induced deterioration in reinforced concrete. CLDHs not only adsorbed chloride ions in aqueous solution with a memory effect but also had a much higher binding capacity than the original layered double hydroxides (LDHs) in the cement matrix. We investigated this adsorption in hardened cement paste in batch cultures to determine adsorption isotherms. The measured and theoretical binding capacities (153 mg g -1 and 257 mg g-1, respectively) of the CLDHs were comparable to the theoretical capacity of Friedel\\'s salt (2 mol mol-1 or 121 mg g-1), which belongs to the LDH family among cementitious phases. We simulated chloride adsorption by CLDHs through the cement matrix using the Fickian model and compared the simulation result to the X-ray fluorescence (XRF) chlorine map. Based on our results, it is proposed that the adsorption process is governed by the chloride transport through the cement matrix; this process differs from that in an aqueous solution. X-ray diffraction (XRD) analysis showed that the CLDH rebuilds the layered structure in a cementitious environment, thereby demonstrating the feasibility of applying CLDHs to the cement and concrete industries. © 2014 Published by Elsevier B.V. All rights reserved.

  18. Mineral Phase and Physical Properties of Red Mud Calcined at Different Temperatures

    Directory of Open Access Journals (Sweden)

    Chuan-sheng Wu

    2012-01-01

    Full Text Available Different characterizations were carried out on red mud uncalcined and samples calcined in the range of 100°C–1400°C. In the present paper, the phase composition and structural transition of red mud heated from room temperature are indicated by XRD, TG-DTA, and SEM techniques. The mean particle diameter, density, and bond strength of these samples also have been investigated. The results indicate the decomposition of gibbsite into Al2O3 and H2O between 300°C and 550°C and calcite into CaO and CO2 in the interval of 600–800°C. Tricalcium aluminate and gehlenite are formed in the range of 800–900°C. Combined with the SEM images, the results of physical property testing show that the particle size and the strength each has a continuous rise during the heat treatment from 150°C to 1350°C. But the value of density will undergo a little drop before 450°C and then increases to a higher value at the temperature of 1200°C. These obtained results provide an important base for the further studies of comprehensive utilization of red mud.

  19. Adsorption of methyl orange from aqueous solution onto calcined Lapindo volcanic mud

    International Nuclear Information System (INIS)

    Jalil, Aishah A.; Triwahyono, Sugeng; Adam, S. Hazirah; Rahim, N. Diana; Aziz, M. Arif A.; Hairom, N. Hanis H.; Razali, N. Aini M.; Abidin, Mahani A.Z.; Mohamadiah, M. Khairul A.

    2010-01-01

    In this study, calcined Lapindo volcanic mud (LVM) was used as an adsorbent to remove an anionic dye, methyl orange (MO), from an aqueous solution by the batch adsorption technique. Various conditions were evaluated, including initial dye concentration, adsorbent dosage, contact time, solution pH, and temperature. The adsorption kinetics and equilibrium isotherms of the LVM were studied using pseudo-first-order and -second-order kinetic equations, as well as the Freundlich and Langmuir models. The experimental data obtained with LVM fits best to the Langmuir isotherm model and exhibited a maximum adsorption capacity (q max ) of 333.3 mg g -1 ; the data followed the second-order equation. The intraparticle diffusion studies revealed that the adsorption rates were not controlled only by the diffusion step. The thermodynamic parameters, such as the changes in enthalpy, entropy, and Gibbs free energy, showed that the adsorption is endothermic, random and spontaneous at high temperature. The results indicate that LVM adsorbs MO efficiently and could be utilized as a low-cost alternative adsorbent for the removal of anionic dyes in wastewater treatment.

  20. The influence of calcination temperature on catalytic activities in a Co based catalyst for CO2 dry reforming

    International Nuclear Information System (INIS)

    Song, Sang-Hoon; Son, Ju-Hee; Budiman, Anatta Wahyu; Choi, Myoung-Jae; Chang, Tae-Sun; Shin, Chae-Ho

    2014-01-01

    The carbon dioxide dry reforming of methane (CDR) reaction could be thermodynamically favored in the range of 800 to 1,000 .deg. C. However, the catalyst in this reaction should be avoided at the calcination temperature over 800 .deg. C since strong metal support interaction (SMSI) in this temperature range can decrease activity due to loss of active sites. Therefore, we focused on optimizing the temperature of pretreatment and a comparison of surface characterization results for CDR. Results related to metal sintering over support, re-dispersion by changing of particle size of metal-support, and strong metal support interaction were observed and confirmed in this work. In our conclusion, optimum calcination temperature for a preparation of catalyst was proposed that 400 .deg. C showed a higher and more stable catalytic activity without changing of support characteristics

  1. Comparative studies on physico-mechanical properties of composite materials of low density polyethylene and raw/calcined kaolin

    Directory of Open Access Journals (Sweden)

    Amit Mallik

    2015-06-01

    Full Text Available The paper describes the preparation of the composite materials of low density polyethylene (LDPE as the base mixed separately with raw kaolin and the same calcined at 800 °C under the same variation in weight percentage using single-screw extruder and a mixing machine operated at a temperature between 190 and 200 °C. Some of the mechanical and physical properties such as Young's modulus, elongation at break, shore hardness and water absorption were determined at different weight fractions of filler (0, 2, 7, 10 and 15%. It was found that the addition of filler increases the mechanical properties. Absorption test was done in water at different immersion times for different composites. The degree of water absorption of composite materials was found to decrease with increasing wt% of kaolin filler (0–15% according to Fick's law. Calcined kaolin produces better mechanical properties than raw kaolin.

  2. Effect of the calcining temperature on the porosity of the titanium dioxide powders obtained by Polymeric Precursor Method

    International Nuclear Information System (INIS)

    Silva, D.W.; Granado, S.R.; Ciola, R.A.; Cavalheiro, A.A.

    2011-01-01

    Ceramics materials obtained by Polymeric Precursor Method exhibit mechanisms of the pore formation and elimination dependents on the decomposition kinetics of the residual organic matter of the polyester. The mechanism of pore elimination seems to occur by disrupting of the wall among the pores because it leads to the consequent pore coalescence and increasing in pore volume, which posses higher pore diameters. In this case, it was observed that the porosity decreasing occurs by pore wall moving after that the residual organic matter is eliminated from the pore inside. The pore diameter associated to the highest volume desorption occurred for the material obtained after calcining at 450°C is approximately 1,7 nm, what seems to be related to the amorphous carbon accumulated inside the pores, once that the pore volume decreases more effectively for the material obtained by calcining at 550°C, making the maximum volume situates at 2,0 nm. (author)

  3. Modeling for the Calcination Process of Industry Rotary Kiln Using ANFIS Coupled with a Novel Hybrid Clustering Algorithm

    Directory of Open Access Journals (Sweden)

    Yongchang Cai

    2017-01-01

    Full Text Available Rotary kiln is important equipment in heavy industries and its calcination process is the key impact to the product quality. Due to the difficulty in obtaining the accurate algebraic model of the calcination process, an intelligent modeling method based on ANFIS and clustering algorithms is studied. In the model, ANFIS is employed as the core structure, and aiming to improve both its performance in reduced computation and accuracy, a novel hybrid clustering algorithm is proposed by combining FCM and Subtractive methods. A quasi-random data set is then hired to test the new hybrid clustering algorithm and results indicate its superiority to FCM and Subtractive methods. Further, a set of data from the successful control activity of sophisticated workers in manufacturing field is used to train the model, and the model demonstrates its advantages in both fast convergence and more accuracy approaching.

  4. Characterization and use of in natura and calcined rice husks for biosorption of heavy metals ions from aqueous effluents

    Directory of Open Access Journals (Sweden)

    M. G. A. Vieira

    2012-09-01

    Full Text Available Heavy metal removal by adsorption using rice husks as a bioadsorbent was evaluated as an alternative for wastewater treatment. Batch equilibrium experiments and kinetic sorption studies were performed using monocomponent solutions of Ni(II, Cd(II, Zn(II, Pb(II and Cu(II in surface samples of in natura(RH and calcined rice husks (RHA. RHA showed higher potential for removing lead and copper. Experimental data for adsorption isotherms of lead and copper were adjusted by Langmuir, Freundlich and Dubinin-Radushkevick (D-R models, being better represented by the Langmuir model. The calcination of RH increased its surface area, improving its adsorption properties. From a morphological analysis obtained by SEM and diffraction patterns (XRD, a longitudinal fibrous and amorphous structure was observed for RH. TGA resultsindicated a total mass loss of around 60% for RH and 24.5% for RHA.

  5. Influence of the carbonate-free clay calcination temperature and curing conditions on the properties of alkali-activated mortar

    OpenAIRE

    Bumanis, Girts; Bajare, Diana; Korjakins, Aleksandrs

    2014-01-01

    Alkali-activated materials (AAMs) are one of the most perspective alternatives to the traditional Portland cement based materials. AAMs could reduce the environmental pollution and greenhouse gas emission due to the lower heat consumption in production (up to 80% compared to the ordinary Portland cement). In the current research alkali-activated mortar was developed from the locally available low-carbonate Illite clay. Experimental work consisted of Illite clay calcination at different temper...

  6. Decomposition of methane over alumina supported Fe and Ni–Fe bimetallic catalyst: Effect of preparation procedure and calcination temperature

    Directory of Open Access Journals (Sweden)

    A.S. Al-Fatesh

    2018-02-01

    Full Text Available Catalytic decomposition of methane has been studied extensively as the production of hydrogen and formation of carbon nanotube is proven crucial from the scientific and technological point of view. In that context, variation of catalyst preparation procedure, calcination temperature and use of promoters could significantly alter the methane conversion, hydrogen yield and morphology of carbon nanotubes formed after the reaction. In this work, Ni promoted and unpromoted Fe/Al2O3 catalysts have been prepared by impregnation, sol–gel and co-precipitation method with calcination at two different temperatures. The catalysts were characterized by X-ray diffraction (XRD, N2 physisorption, temperature programmed reduction (TPR and thermogravimetric analysis (TGA techniques. The catalytic activity was tested for methane decomposition reaction. The catalytic activity was high when calcined at 500 °C temperature irrespective of the preparation method. However while calcined at high temperature the catalyst prepared by impregnation method showed a high activity. It is found from XRD and TPR characterization that disordered iron oxides supported on alumina play an important role for dissociative chemisorptions of methane generating molecular hydrogen. The transmission electron microscope technique results of the spent catalysts showed the formation of carbon nanotube which is having length of 32–34 nm. The Fe nanoparticles are present on the tip of the carbon nanotube and nanotube grows by contraction–elongation mechanism. Among three different methodologies impregnation method was more effective to generate adequate active sites in the catalyst surface. The Ni promotion enhances the reducibility of Fe/Al2O3 oxides showing a higher catalytic activity. The catalyst is stable up to six hours on stream as observed in the activity results.

  7. Operation of a 25 kWth Calcium Looping Pilot-plant with High Oxygen Concentrations in the Calciner.

    Czech Academy of Sciences Publication Activity Database

    Erans, M.; Jeremiáš, Michal; Manovic, V.; Anthony, E.J.

    2017-01-01

    Roč. 128, 25 OCT (2017), č. článku e56112. ISSN 1940-087X Grant - others:RFCS(XE) RFCR-CT-2014-00007 Institutional support: RVO:67985858 Keywords : calcium looping * CO2 capture * oxy-fuel calcination Subject RIV: JE - Non-nuclear Energetics, Energy Consumption ; Use OBOR OECD: Energy and fuels Impact factor: 1.232, year: 2016

  8. Effects of Calcination on the Crystallography and Nonbiogenic Aragonite Formation of Ark Clam Shell under Ambient Condition

    Directory of Open Access Journals (Sweden)

    Chee Wah Loy

    2016-01-01

    Full Text Available This paper presents a study of crystallographic evolution of disposed ark clam shell (ACS after calcination at 400–1400°C which was kept at room temperature under ambient condition in Malaysia during nine months. A better understanding of hydration and recarbonation of ACS powder (≤63 μm after calcination was discovered by PXRD and FTIR. The research focuses on the crystallographic transformation, biogenic calcite decomposition, and unusual atmospheric aragonite formation in ACS after calcination and atmospheric air exposure. Ex situ PXRD showed calcite present in ACS at ≤900°C. ACS transformed to pyrogenic fcc CaO at ≥800°C after three months. Long term atmospheric air exposure of decarbonized ACS caused nucleation of nonbiogenic aragonite, vaterite, calcite, and portlandite. However, in situ PXRD analysis of ACS at instantaneous temperature without cooling process does not indicate the presence of aragonite, vaterite, and portlandite crystals. FTIR spectra revealed CaO–CO2 bond in ACS dissociated with temperature (600–900°C to form CaO and CO2. Ca–OH bond was also traced in FTIR spectra of ≥700°C. It resulted by hydroadsorption of CaO with H2O in atmospheric air.

  9. Maximizing Sustainability of Concrete through the Control of Moisture Rise and Drying Shrinkage Using Calcined Clay Pozzolan

    Directory of Open Access Journals (Sweden)

    John Solomon Ankrah

    2016-01-01

    Full Text Available The Ghanaian concrete industry is really a booming industry due to many infrastructural developments and the surge in residential development. However, many developmental projects that utilize concrete do suffer from the negative impact of moisture rise including paint peeling-off, bacterial and fungi growth, and microcracks as well as unpleasant looks on buildings. Such negative outlook resulting from the effects of moisture rise affects the longevity of concrete and hence makes concrete less sustainable. This study seeks to develop materials that could minimize the rise of moisture or ions through concrete medium. The experimental works performed in this study included pozzolanic strength activity index, water sorptivity, and shrinkage test. Calcined clay produced from clay was used as pozzolan to replace Portland cement at 20%. The strength activity test showed that the cement containing the calcined material attained higher strength activity indices than the control. The thermal gravimetric analysis showed that the pozzolan behaved partly as a filler material and partly as a pozzolanic material. The sorptivity results also showed that the blended mix resulted in lower sorptivity values than the control mortar. The study recommends that calcined clay and Portland cement mixtures could be used to produce durable concrete to maximize sustainability.

  10. Reduced graphene oxide modified NiFe-calcinated layered double hydroxides for enhanced photocatalytic removal of methylene blue

    Science.gov (United States)

    Zhao, Guoqing; Li, Caifeng; Wu, Xia; Yu, Jingang; Jiang, Xinyu; Hu, Wenjihao; Jiao, Feipeng

    2018-03-01

    Calcined layered double hydroxides (CLDH) are one of the remarkable photocatalysts passionately studied for photodecolorization of organic dyes. NiFe-CLDH was successfully modified by reduced graphene oxide (RGO) through a facile in situ crystallization technique. The obtained RGO/NiFe-CLDH composites were fully characterized by powder X-ray diffraction (XRD), Scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), Fourier transform infrared (FT-IR), and UV-vis diffuse reflectance spectroscopy (DRS). The results analysis indicated that RGO sheets could work as base course to prompt the growth of LDH crystallites and NiFe-LDH lamellar crystal promiscuously distributed on the sheets with a strong interplay between each other. The photocatalytic performance of RGO/NiFe-CLDH composites toward decolorization of methylene blue tightly depended on the mass fraction of RGO and calcinated temperature. At the RGO weight loading of 1%, calcination temperature of 500 °C, the photocatalytic degradation efficiency of RGO/NiFe-CLDH composites reached 93.0% within 5.0 h. The enhanced activity of RGO/NiFe-CLDH composites may be due to the concerted catalysis effect between two constituents of as-prepared composites.

  11. Atmospheric pressure plasma assisted calcination by the preparation of TiO2 fibers in submicron scale

    Science.gov (United States)

    Medvecká, Veronika; Kováčik, Dušan; Zahoranová, Anna; Černák, Mirko

    2018-01-01

    Atmospheric pressure plasma assisted calcination by the preparation of TiO2 submicron fibers as a low-temperature alternative to the conventional thermal annealing was studied. A special type of dielectric barrier discharge was used for plasma treatment of hybrid titanium butoxide/polyvinylpyrrolidone (Ti(Bu)/PVP) fibers prepared by forcespinning to decompose and oxidize the base polymer and precursor. The obtained fibers were characterized by changes in chemical bonds on the surface using Fourier Transform Infrared Spectroscopy (FTIR), chemical composition by using Energy-Dispersive X-Ray Spectroscopy (EDX), X-ray Photoelectron Spectroscopy (XPS). The morphology of fibers was investigated by Scanning Electron Microscopy (SEM). A significant decrease of organic components was reached by short plasma exposure times less than 1 h. The obtained fibers exhibit a high surface porosity without degradation of the fibrous structure. The results obtained indicate that atmospheric pressure plasma assisted calcination can be a viable low-temperature, energy- and time-saving alternative or pre-treatment method for the conventional high-temperature thermal calcination.

  12. Synthesis of type A zeolite from calcinated kaolin; Sintese de zeolita tipo A a partir de caulim calcinado

    Energy Technology Data Exchange (ETDEWEB)

    Rodrigues, E.C.; Neves, R.F.; Souza, J.A.S. [Universidade Federal do Para (PPEQ/UFPA), Abaetetuba, PA (Brazil). Instituto de Engenharia Quimica. Programa de Pos-Graduacao; Moraes, C.G.; Macedo, E.N., E-mail: mersone7@yahoo.com.br [Universidade Federal do Para (PRODERNA/UFPA), Abaetetuba, PA (Brazil). Programa de Pos-Graduacao em Engenharia de Recursos Naturais da Amazonia

    2011-07-01

    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)

  13. Calcined Eggshell Waste for Mitigating Soil Antibiotic-Resistant Bacteria/Antibiotic Resistance Gene Dissemination and Accumulation in Bell Pepper.

    Science.gov (United States)

    Ye, Mao; Sun, Mingming; Feng, Yanfang; Li, Xu; Schwab, Arthur P; Wan, Jinzhong; Liu, Manqiang; Tian, Da; Liu, Kuan; Wu, Jun; Jiang, Xin

    2016-07-13

    The combined accumulation of antibiotics, heavy metals, antibiotic-resistant bacteria (ARB)/antibiotic resistance genes (ARGs) in vegetables has become a new threat to human health. This is the first study to investigate the feasibility of calcined eggshells modified by aluminum sulfate as novel agricultural wastes to impede mixed contaminants from transferring to bell pepper (Capsicum annuum L.). In this work, calcined eggshell amendment mitigated mixed pollutant accumulation in bell pepper significantly, enhanced the dissipation of soil tetracycline, sulfadiazine, roxithromycin, and chloramphenicol, decreased the water-soluble fractions of antibiotics, and declined the diversity of ARB/ARGs inside the vegetable. Moreover, quantitative polymerase chain reaction analysis detected that ARG levels in the bell pepper fruits significantly decreased to 10(-10) copies/16S copies, indicating limited risk of ARGs transferring along the food chain. Furthermore, the restoration of soil microbial biological function suggests that calcined eggshell is an environmentally friendly amendment to control the dissemination of soil ARB/ARGs in the soil-vegetable system.

  14. The decrease of carbonation efficiency of CaO along calcination-carbonation cycles: Experiments and modelling

    Energy Technology Data Exchange (ETDEWEB)

    Bouquet, E.; Leyssens, G.; Schonnenbeck, C.; Gilot, P. [Laboratoire de Gestion des Risques et Environnement, Mulhouse (France)

    2009-05-15

    Successive calcination-carbonation cycles, using CaO as sorbent, have been performed either in a classical fixed bed reactor or using a thermogravimetric analyser. Significant differences in carbonation efficiencies were obtained, possibly due to different conditions prevailing for CaO sintering during the calcination stage. The effect of the presence of CO{sub 2} on sintering was confirmed. A simple model of the decay of the carbonation capacity along cycles based on the specific surface area of non-sintered micrograins of CaO is able to predict the decrease of the extent of conversion obtained after 40 carbonations along calcination-carbonation cycles. The asymptotic extent of conversion is obtained when all the micrograins present within a grain are sintered. A detailed model of the carbonation shows that the voids present between the micrograins are filled up by carbonate when a critical thickness of the carbonate layer around each micrograin reaches 43 nm. Then, carbonation becomes controlled by diffusion at the scale of the whole grain, with the CO{sub 2} diffusion coefficient decreasing (at 650 {sup o}C) from 2 x 10{sup -12} to 6.5 x 10{sup -14} m{sup 2}/s as carbonation proceeds from 50% conversion to 76% (first cycle). This scale change for diffusion is responsible for the drastic decrease of the carbonation rate after the voids between micrograins are filled up.

  15. Effect of calcinations temperature on the luminescence intensity and fluorescent lifetime of Tb3+-doped hydroxyapatite (Tb-HA nanocrystallines

    Directory of Open Access Journals (Sweden)

    Hairong Yin

    2017-06-01

    Full Text Available Hydroxyapatite luminescent nanocrystallines doped with 6 mol.% Tb3+ (Tb-HA were prepared via chemical deposition method and calcined at different temperature, and the effects of calcinations temperature on the luminescence intensity and fluorescent lifetime were studied. TEM image of Tb-HA revealed that the shape of nanocrystallines changed from needle-like to short rod-like and sphere-like with the increase of calcinations temperature; while the particles sizes decreased from 190 nm to 110 nm. The crystallinity degree increased. The typical emission peaks attributed to Tb3+ ions were observed in emission spectra of 6 mol.% Tb-HA under 378 nm excitation. The luminescent intensity of Tb-HA, which showed the fluorescence quenching, firstly enhanced and then decreased at 700 °C; while the fluorescent lifetime increased firstly and then decreased after 600 °C. Furthermore, the ratio of intensity between 545 nm and 490 nm corresponding to electric-dipole and magnetic-dipole transition (IR: IO increases firstly and then decreases, which revealed that the proportion of substitute type and site of Ca2+ ions by Tb3+ ions were helpful to realize the substitute process and functional structure design.

  16. Application of calcined waste fish (Labeo rohita) scale as low-cost heterogeneous catalyst for biodiesel synthesis.

    Science.gov (United States)

    Chakraborty, R; Bepari, S; Banerjee, A

    2011-02-01

    This paper explores the feasibility of converting waste Rohu fish (Labeo rohita) scale into a high-performance, reusable, low-cost heterogeneous catalyst for synthesis of biodiesel from soybean oil. The thermo-gravimetric analysis (TGA) and X-ray diffraction (XRD) analysis revealed that a significant portion of the main component of fish scale i.e. HAP (hydroxyapatite) could be transformed into β-tri-calcium phosphate when calcined above 900°C for 2 h. Scanning Electron Microscopy (SEM) morphology studies of the calcined scale depicted a fibrous layer of porous structure; while a BET surface area of 39 m(2)/g was measured. Response surface methodology (RSM) was employed to determine the optimal parametric conditions viz. methanol/oil molar ratio, 6.27:1, calcination temperature, 997.42°C and catalyst concentration, 1.01 wt.% of oil corresponding to a maximum FAME yield of 97.73%. Reusability results confirmed that the prepared catalyst could be reemployed up to six times, procreating a potentially applicable avenue in biodiesel synthesis. Copyright © 2010 Elsevier Ltd. All rights reserved.

  17. Effect of calcination temperature on formaldehyde oxidation performance of Pt/TiO2 nanofiber composite at room temperature

    Science.gov (United States)

    Xu, Feiyan; Le, Yao; Cheng, Bei; Jiang, Chuanjia

    2017-12-01

    Catalytic oxidation at room temperature over well-designed catalysts is an environmentally friendly method for the abatement of indoor formaldehyde (HCHO) pollution. Herein, nanocomposites of platinum (Pt) and titanium dioxide (TiO2) nanofibers with various phase compositions were prepared by calcining the electrospun TiO2 precursors at different temperatures and subsequently depositing Pt nanoparticles (NPs) on the TiO2 through a NaBH4-reduction process. The phase compositions and structures of Pt/TiO2 can be easily controlled by varying the calcination temperature. The Pt/TiO2 nanocomposites showed a phase-dependent activity towards the catalytic HCHO oxidation. Pt/TiO2 containing pure rutile phase showed enhanced activity with a turnover frequency (TOF) of 16.6 min-1 (for a calcination temperature of 800 °C) as compared to those containing the anatase phase or mixed phases. Density functional theory calculation shows that TiO2 nanofibers with pure rutile phase have stronger adsorption ability to Pt atoms than anatase phase, which favors the reduction of Pt over rutile phase TiO2, leading to higher contents of metallic Pt in the nanocomposite. In addition, the Pt/TiO2 with rutile phase possesses more abundant oxygen vacancies, which is conducive to the activation of adsorbed oxygen. Consequently, the Pt/rutile-TiO2 nanocomposite exhibited better catalytic activity towards HCHO oxidation at room temperature.

  18. Denitration of High Nitrate Salts Using Reductants

    Energy Technology Data Exchange (ETDEWEB)

    HD Smith; EO Jones; AJ Schmidt; AH Zacher; MD Brown; MR Elmore; SR Gano

    1999-05-03

    This report describes work conducted by Pacific Northwest National Laboratory (PNNL), in conjunction with Idaho National Engineering and Environmental Laboratory (INEEL), to remove nitrates in simulated low-activity waste (LAW). The major objective of this work was to provide data for identifying and demonstrating a technically viable and cost-effective approach to condition LAW for immobilization (grout).

  19. Performance of Cobalt-Based Fischer-Tropsch Synthesis Catalysts Using Dielectric-Barrier Discharge Plasma as an Alternative to Thermal Calcination

    International Nuclear Information System (INIS)

    Bai Suli; Huang Chengdu; Lv Jing; Li Zhenhua

    2012-01-01

    Co-based catalysts were prepared by using dielectric-barrier discharge (DBD) plasma as an alternative method to conventional thermal calcination. The characterization results of N 2 -physisorption, temperature programmed reduction (TPR), transmission electron microscope (TEM), and X-ray diffraction (XRD) indicated that the catalysts prepared by DBD plasma had a higher specific surface area, lower reduction temperature, smaller particle size and higher cobalt dispersion as compared to calcined catalysts. The DBD plasma method can prevent the sintering and aggregation of active particles on the support due to the decreased treatment time (0.5 h) at lower temperature compared to the longer thermal calcination at higher temperature (at 500° C for 5 h). As a result, the catalytic performance of the Fischer-Tropsch synthesis on DBD plasma treated Co/SiO 2 catalyst showed an enhanced activity, C 5+ selectivity and catalytic stability as compared to the conventional thermal calcined Co/SiO 2 catalyst.

  20. Extended Development Work to Validate a HLW Calcine Waste Form via INL's Cold Crucible Induction Melter

    Energy Technology Data Exchange (ETDEWEB)

    James A. King; Vince Maio

    2011-09-01

    To accomplish calcine treatment objectives, the Idaho Clean-up Project contractor, CWI, has chosen to immobilize the calcine in a glass-ceramic via the use of a Hot-Isostatic-Press (HIP); a treatment selection formally documented in a 2010 Record of Decision (ROD). Even though the HIP process may prove suitable for the calcine as specified in the ROD and validated in a number of past value engineering sessions, DOE is evaluating back-up treatment methods for the calcine as a result of the technical, schedule, and cost risk associated with the HIPing process. Consequently DOE HQ has requested DOE ID to make INL's bench-scale cold-crucible induction melter (CCIM) available for investigating its viability as a process alternate to calcine treatment. The waste form is the key component of immobilization of radioactive waste. Providing a solid, stable, and durable material that can be easily be stored is the rationale for immobilization of radioactive waste material in glass, ceramic, or glass-ceramics. Ceramic waste forms offer an alternative to traditional borosilicate glass waste forms. Ceramics can usually accommodate higher waste loadings than borosilicate glass, leading to smaller intermediate and long-term storage facilities. Many ceramic phases are known to possess superior chemical durability as compared to borosilicate glass. However, ceramics are generally multiphase systems containing many minor phase that make characterization and prediction of performance within a repository challenging. Additionally, the technologies employed in ceramic manufacture are typically more complex and expensive. Thus, many have proposed using glass-ceramics as compromise between in the more inexpensive, easier to characterize glass waste forms and the more durable ceramic waste forms. Glass-ceramics have several advantages over traditional borosilicate glasses as a waste form. Borosilicate glasses can inadvertently devitrify, leading to a less durable product that could

  1. Catalyst used in 1,2-epoxyalkane preparation is obtained by heating tetraalkyl ammonium salts, tetraalkyl siloxanes and amines, calcining and treating with a tetraalkoxy compound

    DEFF Research Database (Denmark)

    2001-01-01

    NOVELTY - The catalyst, used in 1,2-epoxyalkane preparation, is obtained by heat treating an aqueous composition comprising tetraalkyl ammonium salts, tetraalkyl siloxanes and amines, removing the template by calcining and treating with a tetraalkoxy compound......NOVELTY - The catalyst, used in 1,2-epoxyalkane preparation, is obtained by heat treating an aqueous composition comprising tetraalkyl ammonium salts, tetraalkyl siloxanes and amines, removing the template by calcining and treating with a tetraalkoxy compound...

  2. Radiant-heat spray-calcination process for the solid fixation of radioactive waste. Part 1, Non-radioactive pilot unit

    Energy Technology Data Exchange (ETDEWEB)

    Allemann, R.T.; Johnson, B.M. Jr.

    1960-11-14

    The fixation of radioactive waste in a stable solid media by means of calcination of these aqueous solutions has been the subject of considerable-effort throughout the U. S. Atomic Energy Commission and by atomic energy organizations in other countries. Several methods of doing this on a continuous or semi-continuous basis have been devised, and a fev have been demonstrated to be feasible for the handling of non-radioactive, or low-activity, simulated wastes. Notable among methods currently under development are: (a) batch-operated pot calcination of waste generated from reprocessing stainless steel clad fuel elements (Darex process) and Purex waste, (b) combination rotary kiln and ball mill calcination of aluminum nitrate (TBP-25 and Redox process), and (c) fluidized bed calcination of TBP-25 and Purex wastes. Although a considerable amount of engineering experience has been obtained on the calcination of dissolved salts in a fluidized bed, and the other methods have been the subjects of a great deal of study, none of them have been developed to-the extent which would rule out the desirability of further investigation of other possible methods of calcination.

  3. Preparation and Characterization of Au/Pd Modified-TiO2 Photocatalysts for Phenol and Toluene Degradation under Visible Light—The Effect of Calcination Temperature

    Directory of Open Access Journals (Sweden)

    Anna Cybula

    2014-01-01

    Full Text Available Rutile loaded with Au/Pd nanoparticles was prepared using a water-in-oil microemulsion system of water/AOT/cyclohexane followed by calcination. The effect of calcination temperature (from 350 to 700°C on the structure of Au/Pd nanoparticles deposited at rutile matrix and the photocatalytic properties of Au/Pd-TiO2 was investigated in two model reactions (toluene degradation in gas phase and phenol degradation in aqueous phase. Toluene was irradiated over Au/Pd-TiO2 using light emitting diodes (LEDs, λmax⁡ = 415 nm. The sample 0.5 mol% Pd/TiO2 exhibited the highest activity under visible light irradiation in gas and aqueous phase reaction among all photocatalysts calcined at 350°C, while the sample modified only with gold nanoparticles showed the lowest activity. The Au/Pd-TiO2 sample calcinated at 350°C possesses the highest photocatalytic activity when degrading phenol under visible light, which is 14 times higher than that of the one calcinated at 450°C. It was observed that increasing temperature from 350 to 700°C during calcination step caused segregation of metals and finally resulted in photoactivity drop.

  4. Effect of the calcination temperature on the photocatalytic efficiency of acidic sol-gel synthesized TiO2nanoparticles in the degradation of alprazolam.

    Science.gov (United States)

    Romeiro, Andreia; Freitas, Diana; Emília Azenha, M; Canle, Moisés; Burrows, Hugh D

    2017-06-14

    We report a comparative study on the photodegradation of the widely used benzodiazepine psychoactive drug alprazolam (8-chloro-1-methyl-6-phenyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine, ALP) using direct photolysis, and titanium dioxide photocatalyzed reaction. Titanium dioxide photocatalysts were prepared as nanoparticles by acidic sol-gel methods, calcined at two different temperatures, and their behavior compared with P25 (Degussa type) TiO 2 . Efficient photodegradation was observed in the photocatalytic process, with over 90% degradation after 90 minutes under optimized conditions. Triazolaminoquinoline, 5-chloro-(5-methyl-4H-1,2,4-triazol-4-yl)benzophenone, triazolbenzophenone, and α-hydroxyalprazolam were identified as the degradation products by fluorescence spectroscopy and HPLC-MS. A comparison with the literature suggests that 8H-alprazolam may also be formed. Good mineralization was observed with TiO 2 photocatalysts. ALP photodegradation with TiO 2 follows pseudo-first order kinetics, with rates depending on the photocatalyst used. The effects of the quantity of the photocatalyst and concentration of alprazolam were studied.

  5. Obtaining a pozzolanic addition from the controlled calcination of paper mill sludge. Performance in cement matrices

    Directory of Open Access Journals (Sweden)

    San José, J. T.

    2006-09-01

    Full Text Available Mineralogically, the paper mill sludge consists essentially of calcite, kaolinite, talc and other philosilicates (illite, chlorite. When such sludge is subjected to controlled thermal treatment, its kaolinite component may be transformed into metakaolin, yielding a product with high pozzolanic reactivity. This study was designed to analyze a number of scientific questions around the production of pozzolanic additions via controlled thermal activation of paper mill sludge and to evaluate the performance of such additions when included in a cement matrix. The findings show that paper mill waste activation is optimal when the sludge is calcined for 2 hours at 700 ºC in the 700-800 ºC interval. A comparative study between the cement made with the new addition and a commercial cement (CEM I-42.5R used as a reference led to highlight the scientific and technical viability of this waste as a cementing secondary material.Los lodos de destintado del papel están constituidos,mineralógicamente, por calcita, caolinita, talco y otros filosilicatos (ilita, clorita. Cuando al lodo se le somete aun tratamiento térmico controlado, la caolinita puede transformarse en metacaolín, dando origen a un producto de alta reactividad puzolánica.El objeto de este trabajo es analizar diferentes aspectos científicos relativos al proceso de obtención de una adiciónpuzolánica a partir de la activación térmica controlada de lodos de destintado del papel, así como evaluar el comportamiento de la nueva adición cuando se incorpora en una matriz de cemento. Los resultados obtenidos ponen de manifiesto la recomendación de utilizar 700 ºC durante 2 horas de permanencia en el horno, como condiciones más óptimas para activar los residuos de lodos de papel en el intervalo 700-800 ºC. Del estudio comparativo del cemento elaborado con la nueva adición con respecto a un cemento comercial (CEM I-42,5R, se puede destacar la viabilidad científica y técnica de

  6. Influences of air calcination and steam activation on microstructure and photocatalytic activity of continuous TiO2 fibers

    International Nuclear Information System (INIS)

    You, Yang; Zhang, Shiying; Xu, Difa

    2013-01-01

    Graphical abstract: Display Omitted Highlights: ► Effects of air calcination and steam activation on TiO 2 fibers were studied. ► The photocatalytic activity was evaluated by degradation of formaldehyde. ► Steam activation promoted the anatase–rutile phase transformation. ► Steam activation decreased grain size and increased special surface area. ► Steam activation improved photocatalytic activity of TiO 2 fibers. -- Abstract: Effects of air calcination and steam activation, on phase transformation, microstructure and photocatalytic activity of continuous TiO 2 fibers prepared by sol–gel method were studied. The fibers were characterized by XRD, SEM, and N 2 adsorption–desorption. The photocatalytic activity was evaluated by photocatalytic degradation of formaldehyde. Results showed that 100% rutile fibers heat-treated in air and steam were obtained at 800 °C and 600 °C, respectively. The anatase grain sizes and special surface areas of the fibers heat-treated at 500 °C in air and steam were 31.6 nm, 22.7 nm, 26.7 m 2 /g and 32.3 m 2 /g, respectively. The degradation rates of formaldehyde over the fibers heat-treated at 500 °C in air and steam were 92.3% and 98.6% after 14 h under UV irradiation, respectively. Compared with the air calcination, the steam activation promoted the anatase–rutile phase transformation, reduced the grain size, increased the special surface area, and improved photocatalytic activity of continuous TiO 2 fibers.

  7. Performance assessment of CO2 capture with calcination carbonation reaction process driven by coal and concentrated solar power

    International Nuclear Information System (INIS)

    Zhang, Xuelei; Liu, Yingguang

    2014-01-01

    Calcination carbonation reaction (CCR) process is regarded as a promising option for pulverized coal power plant to mitigate CO 2 emission. In this paper, concentrated solar power (CSP) substitutes for coal to supply part of the calcination energy in order to reduce the fossil fuel consumption associated with the calciner. A CCR process driven by coal and CSP is examined from the perspective of energy efficiency. This paper focuses on the parameters of heat recovery efficiency, CSP capacity, compression energy, air separation energy and recycled energy to determine the contribution of each to the overall energy penalty. In addition, the effects of heat recovery efficiency, CSP capacity, purge percentage and CO 2 capture efficiency on the co-driven case are analyzed through a sensitivity analysis. The results indicate that the thermal efficiency of integrating CCR co-driven process into an ultra-supercritical 1019 MW power plant is 35.37%, which means that the overall efficiency penalty is 9.63 percentage points. Moreover, the co-driven case reduces the fossil fuel consumption and the mass flow rate of fresh sorbent and circulation solids compared with coal-driven case. Increasing heat recovery efficiency and CSP efficiency can improve the co-driven case performance. - Highlights: • We examine a CCR process driven by coal and concentrated solar power simultaneously. • The contributors to the overall energy penalty are quantitatively identified. • Obvious coal-saving effect has been found in the co-driven system. • A sensitivity analysis is conducted to find the impact of key parameters

  8. Adsorption of a cationic dye (Yellow Basic 28 ontothe calcined mussel shells: Kinetics, Isotherm and Thermodynamic Parameters

    Directory of Open Access Journals (Sweden)

    Imane EL Ouahabi

    2015-11-01

    Full Text Available The aim of this study is to valorise the mussel shells and evaluate the adsorption capacity of calcined mussel shells for the cationic dyes.  The adsorbent was characterized by DRX, FTIR, BET and SEM, respectively. The adsorption of Yellow Basic28 on calcined mussel shells was investigated using the parameters such as concentrations (10-50mg/L, pH (3-10, ionic strength (0-2 mol / L and temperature (288 - 318 °C.  The adsorption rate data were analysed according to the first and second-order kinetic models.  The adsorption kinetics was found to be best represented by the pseudo-second-order kinetic model.  The experimental isotherm data were analyzed using Langmuir, Freundlich, Temkin, Elovich and Dubinin–Radushkevich isotherm equations on the dye-adsorbent system. The experimental data yielded excellent fits with Freundlich isotherm equation (R² = 0.966. It was indicative of the heterogeneity of the adsorption sites on the CMS particles.  Various thermodynamic parameters such as enthalpy of adsorption ΔH°, free energy change ΔG°and entropy ΔS° were estimated.  The positive value of ΔH°(30.321 kJ/mol and negative values of ΔG° (from -5.392 to -2.873 kJ/mol show the process is endothermic and spontaneous.  The negative value of entropy ΔS° (-87.172 J/mol K suggest the decreased randomness at the solid-liquid interface during the adsorption of dyes onto calcined mussel shells.

  9. Synthesis of cubic yttrium aluminum garnet (YAG) powders by co-precipitation and two-step calcinations

    Science.gov (United States)

    Girish, H. N.; Zhu, C.; Ma, F. F.; Shao, G. Q.

    2017-04-01

    YAG powders were synthesized by co-precipitation and two-step moderate calcinations at 600/800 °C or 600/900 °C in air, respectively. Two kinds of the synthesized powders both possess pure cubic YAG phases without any secondary phases such as YAH, YAP and YAM, etc.. The former has low agglomeration with nano-sized primary particles and large active energy, and the latter has homogeneously dispersed and well-crystallized particles, with a narrow particle size distribution of 8 - 13 µm.

  10. Determination of the Index of Consumption of Petroleum of the Calcining Kiln of the Ernesto Che Guevara Commander Undertaking

    Directory of Open Access Journals (Sweden)

    Yarilys Gaínza-Delgado

    2016-07-01

    Full Text Available This work presents the results obtained in carrying out the mass and energy balances in the calcining kiln of the company commander Ernesto Che Guevara, for determining the consumption index of petroleum used for obtaining nickel oxide through thermal decomposition of the basic nickel carbonate. It was shown that for a production of basic nickel carbonate of              12 t / h with 69% moisture, it is necessary to feed about 1100 kg / h of fuel, for an consumption index of 91.67 kg of fuel per ton of load.

  11. Effect of aluminum and silicon reactants and process parameters on glass-ceramic waste form characteristics for immobilization of high-level fluorinel-sodium calcined waste

    International Nuclear Information System (INIS)

    Vinjamuri, K.

    1993-06-01

    In this report, the effects of aluminum and silicon reactants, process soak time and the initial calcine particle size on glass-ceramic waste form characteristics for immobilization of the high-level fluorinel-sodium calcined waste stored at the Idaho Chemical Processing Plant (ICPP) are investigated. The waste form characteristics include density, total and normalized elemental leach rates, and microstructure. Glass-ceramic waste forms were prepared by hot isostatically pressing (HIPing) a pre-compacted mixture of pilot plant fluorinel-sodium calcine, Al, and Si metal powders at 1050 degrees C, 20,000 psi for 4 hours. One of the formulations with 2 wt % Al was HIPed for 4, 8, 16 and 24 hours at the same temperature and pressure. The calcine particle size range include as calcined particle size smaller than 600 μm (finer than -30 mesh, or 215 μm Mass Median Diameter, MMD) and 180 μm (finer than 80 mesh, or 49 μm MMD)

  12. New DC conductivity spectra of Zn–Al layered double hydroxide (Zn–Al–NO3–LDH and its calcined product of ZnO phase

    Directory of Open Access Journals (Sweden)

    Abdullah Ahmed Ali Ahmed

    2017-05-01

    Full Text Available Zn–Al–NO3–LDH nanostructure was synthesized via the coprecipitation method at molar ratio Zn2+/Al3+ = 4 and pH = 7. The resultant sample was thermally treated at calcined temperatures of 50, 100, 150, 200, 250 and 300 °C. The layered structure of the Zn–Al–NO3–LDH samples was stable below the calcination temperature 200 °C as shown in powder X-ray diffraction (PXRD patterns of calcined samples. The calcination products showed a collapse of LDH structure and ZnO phase was formed at 200 °C and above. The dielectric spectroscopy of LDH was explained using anomalous low frequency dispersion (ALFD due to the low mobility of LDH carriers. The conductivity spectra of LDH can be theoretically described according to the effective phase within the calcination products of LDH. In the comparison with previously researches, this study presented higher values of DC conductivity for all studied samples.

  13. Evaluation of blends bauxite-calcination-method red mud with other industrial wastes as a cementitious material: Properties and hydration characteristics

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Na, E-mail: zhangna06@mails.tsinghua.edu.cn [State Key Lab of New Ceramics and Fine Processing, Department of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China); Liu Xiaoming [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Sun Henghu [School of Engineering and Computer Science, University of the Pacific, Stockton, CA 95211 (United States); Li Longtu [State Key Lab of New Ceramics and Fine Processing, Department of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China)

    2011-01-15

    Red mud is generated from alumina production, and its disposal is currently a worldwide problem. In China, large quantities of red mud derived from bauxite calcination method are being discharged annually, and its utilization has been an urgent topic. This experimental research was to evaluate the feasibility of blends red mud derived from bauxite calcination method with other industrial wastes for use as a cementitious material. The developed cementitious material containing 30% of the bauxite-calcination-method red mud possessed compressive strength properties at a level similar to normal Portland cement, in the range of 45.3-49.5 MPa. Best compressive strength values were demonstrated by the specimen RSFC2 containing 30% bauxite-calcination-method red mud, 21% blast-furnace slag, 10% fly ash, 30% clinker, 8% gypsum and 1% compound agent. The mechanical and physical properties confirm the usefulness of RSFC2. The hydration characteristics of RSFC2 were characterized by XRD, FTIR, {sup 27}Al MAS-NMR and SEM. As predominant hydration products, ettringite and amorphous C-S-H gel are principally responsible for the strength development of RSFC2. Comparing with the traditional production for ordinary Portland cement, this green technology is easier to be implemented and energy saving. This paper provides a key solution to effectively utilize bauxite-calcination-method red mud.

  14. Efficiency of sodium hypochlorite and calcinated calcium in killing Escherichia coli O157:H7, Salmonella spp., and Staphylococcus aureus attached to freshly shredded cabbage.

    Science.gov (United States)

    Fukuyama, Satomi; Watanabe, Yuko; Kondo, Nozomi; Nishinomiya, Takashi; Kawamoto, Shinichi; Isshiki, Kenji; Murata, Masatsune

    2009-01-01

    The effects of the disinfectants NaClO and calcinated calcium on the food-borne pathogens Staphylococcus aureus, Escherichia coli O157:H7, and Salmonella spp. attached to shredded cabbage leaves were examined. After these bacteria were attached to shredded leaves for 1 h, the leaves were treated with NaClO and/or calcinated calcium. About 2.6-log and 3.5-log reductions of E. coli O157 were achieved by treatment with NaClO (100 ppm, pH 6.0, 10 min) and calcinated calcium (0.1%, 20 min), respectively. The combination of 100 ppm NaClO and 0.1% calcinated calcium resulted in a 3- to 4-log reduction in the pathogen populations without apparent deteriorative effects. The bacterial numbers in the treated cabbage did not increase during storage at 4 degrees C. However, sensory evaluation including appearance and flavor indicated that the quality of the treated cabbage declined during storage. In conclusion, the combination of NaClO and calcinated calcium was useful in treatment before eating.

  15. Beneficiation of Low-Grade Phosphate Deposits by a Combination of Calcination and Shaking Tables: Southwest Iran

    Directory of Open Access Journals (Sweden)

    Shahram Shariati

    2015-06-01

    Full Text Available Three quarters of the world’s phosphate deposits are of sedimentary origin and 75%–80% of those include carbonate gangue. In this study, carbonate sedimentary phosphate deposits of the Lar Mountains of southwest Iran are studied. These deposits consist mainly of calcite, fluorapatite, quartz, kaolinite and illite, with an average P2O5 grade of 9%–10% (low-grade. Various pre-processing and processing methods have been developed for concentrating low-grade phosphate up to marketable grade and this study aims to select the optimal method to produce an economically viable grade of phosphate concentrate from low-grade ore. Different concentration methods, including calcination and gravity separation, were applied on samples at both a laboratory and semi-industrial scale (pilot scale. Using an integrated method of calcination (performed in a rotary kiln and shaking table for concentrating the low-grade phosphate ore, the results show promise at producing grades of 30.77% P2O5 with 60.7%–63.2% recovery.

  16. Production of U3O8 by uranyl formate precipitation and calcination in a full-scale pilot facility

    International Nuclear Information System (INIS)

    Kendrick, L.S.; Wilson, W.A.; Mosley, W.C.

    1984-08-01

    The uranyl formate process for the production of U 3 O 8 with a controlled particle size has been extensively studied on a laboratory scale. Based on this study, a pilot-scale facility (the Uranyl Formate Facility) was built to investigate the key steps of the process on a larger scale. These steps were the precipitation of a uranyl formate monohydrate salt and the calcination of this salt to U 3 O 8 . Tests of the facility and process were conducted at conditions recommended by the laboratory-scale studies for a full-scale production facility. These tests demonstrated that U 3 O 8 of the required particle size for the PM process can be produced on a plant scale by the calcination of uranyl formate crystals. The performance of the U 3 O 8 produced by the uranyl formate process in fuel tube fabrication was also investigated. Small-scale extrusion tests of U 3 O 8 -Al cores which used the U 3 O 8 produced in the Uranyl Formate Facility were conducted. These tests demonstrated that the U 3 O 8 quality was satisfactory for the PM process

  17. A comparative study of thermal calcination and an alkaline hydrolysis method in the isolation of hydroxyapatite from Thunnus obesus bone

    Energy Technology Data Exchange (ETDEWEB)

    Venkatesan, Jayachandran; Ryu, BoMi; Thomas, Noel Vinay; Kim, Se Kwon [Department of Chemistry, Pukyong National University, Busan 608-737 (Korea, Republic of); Qian Zhongji, E-mail: sknkim@pknu.ac.kr [Marine Bioprocess Research Center, Pukyong National University, Busan 608-737 (Korea, Republic of)

    2011-06-15

    In the present study, hydroxyapatite (HAp) was isolated from Thunnus obesus bone using alkaline hydrolysis and thermal calcination methods. The obtained ceramic has been characterized by thermal gravimetric analysis (TGA), Fourier transform infrared spectroscopy (FT-IR), powder x-ray diffraction analysis (XRD), field-emission scanning electron microscopy, energy-dispersive x-ray analysis, transmission electron microscopy (TEM), selected area diffraction analysis, cytotoxic analysis and cell proliferation analysis. The results indicate that there are significant differences between the ceramics and T. obesus bone. FT-IR and TGA results affirmed that the collagen and organic moieties have been eliminated by both the proposed methods. XRD results were in agreement with JCPDS data. TEM and selective area diffraction images have signified that the thermal calcination method produces good crystallinity with dimensions 0.3-1.0 {mu}m, whereas the alkaline hydrolysis method produces nanostructured HAp crystals with 17-71 nm length and 5-10 nm width. Biocompatibility of HAp crystals was evaluated by cytotoxicity and cell proliferation with human osteoblast-like cell MG-63.

  18. Adsorptive removal of 2,4,6-trichlorophenol in aqueous solution using calcined kaolinite-biomass composites.

    Science.gov (United States)

    Olu-Owolabi, Bamidele I; Alabi, Alimoh H; Diagboya, Paul N; Unuabonah, Emmanuel I; Düring, Rolf-Alexander

    2017-05-01

    Synergistically combined low-cost composites may be effective for the potential treatment of effluents containing organic pollutants. Hence, preparation of Carica-papaya-modified-kaolinite (CPK) and pine-cone-modified-kaolinite (PCK) composites via calcination of pure kaolinite (KAC), Carica-papaya and pine-cone seeds is demonstrated. The composites' specific surface areas were reduced by more than 57% but no structural modification in KAC lattice d-spacing, indicating impregnation of calcined biomass on clay surfaces and pores. However, composites' cation exchange capacities were enhanced over 4-fold, indicating higher potential for adsorption. Adsorption of 2,4,6-trichlorophenol on composites and KAC showed that CPK and PCK attained equilibrium relatively faster (30 min) compared to KAC (60 min). Modeling studies showed that 2,4,6-trichlorophenol removal mechanisms involved electrostatic interactions on sites of similar energy. Modification enhanced adsorption by 52 and 250% in PCK and CPK, respectively, and adsorption increased with temperature. Copyright © 2017 Elsevier Ltd. All rights reserved.

  19. Effects of Calcination Temperature and Acid-Base Properties on Mixed Potential Ammonia Sensors Modified by Metal Oxides

    Science.gov (United States)

    Satsuma, Atsushi; Katagiri, Makoto; Kakimoto, Shiro; Sugaya, Satoshi; Shimizu, Kenichi

    2011-01-01

    Mixed potential sensors were fabriated using yttria-stabilized zirconia (YSZ) as a solid electrolyte and a mixture of Au and various metal oxides as a sensing electrode. The effects of calcination temperature ranging from 600 to 1,000 °C and acid-base properties of the metal oxides on the sensing properties were examined. The selective sensing of ammonia was achieved by modification of the sensing electrode using MoO3, Bi2O3 and V2O5, while the use of WO3, Nb2O5 and MgO was not effective. The melting points of the former group were below 820 °C, while those of the latter group were higher than 1,000 °C. Among the former group, the selective sensing of ammonia was strongly dependent on the calcination temperature, which was optimum around melting point of the corresponding metal oxides. The good spreading of the metal oxides on the electrode is suggested to be one of the important factors. In the former group, the relative response of ammonia to propene was in the order of MoO3 > Bi2O3 > V2O5, which agreed well with the acidity of the metal oxides. The importance of the acidic properties of metal oxides for ammonia sensing was clarified. PMID:22319402

  20. Effect of Different Calcination Temperatures on the Structural and Photocatalytic Performance of Bi-TiO2/SBA-15

    Directory of Open Access Journals (Sweden)

    Jing Ma

    2013-01-01

    Full Text Available The new novel material Bi-TiO2/SBA-15 was synthesized by an easy wet impregnation method. A combination of XRD, XPS, Raman, N2 adsorption-desorption isotherm measurement, TEM, and solid state UV-Vis spectroscopy has been used to characterize the Bi-TiO2/SBA-15 material. It was found that SBA-15 retained the ordered hexagonal mesostructure after incorporation of TiO2 and Bi. The photodecomposition of rhodamine B (RhB in aqueous medium was selected to evaluate the photocatalytic performance of Bi-TiO2/SBA-15 under visible light irradiation (λ≥420 nm. The experiment results indicated that Bi-TiO2/SBA-15 exhibited higher photocatalytic activities than pure TiO2 and Bi2O3. The influences of calcination temperature were studied. It strongly influenced the activity of the samples. The sample calcined at 550°C shows the highest photocatalytic activity in the decomposition of RhB under visible light. The catalyst preserved almost its initial photocatalytic activity after six reuses.

  1. Effects of Calcination Temperature and Acid-Base Properties on Mixed Potential Ammonia Sensors Modified by Metal Oxides

    Directory of Open Access Journals (Sweden)

    Kenichi Shimizu

    2011-02-01

    Full Text Available Mixed potential sensors were fabriated using yttria-stabilized zirconia (YSZ as a solid electrolyte and a mixture of Au and various metal oxides as a sensing electrode. The effects of calcination temperature ranging from 600 to 1,000 °C and acid-base properties of the metal oxides on the sensing properties were examined. The selective sensing of ammonia was achieved by modification of the sensing electrode using MoO3, Bi2O3 and V2O5, while the use of WO3, Nb2O5 and MgO was not effective. The melting points of the former group were below 820 °C, while those of the latter group were higher than 1,000 °C. Among the former group, the selective sensing of ammonia was strongly dependent on the calcination temperature, which was optimum around melting point of the corresponding metal oxides. The good spreading of the metal oxides on the electrode is suggested to be one of the important factors. In the former group, the relative response of ammonia to propene was in the order of MoO3 > Bi2O3 > V2O5, which agreed well with the acidity of the metal oxides. The importance of the acidic properties of metal oxides for ammonia sensing was clarified.

  2. Calcined dolomite, magnesite, and calcite for cleaning hot gas from a fluidized bed biomass gasifier with steam: Life and usefulness

    Energy Technology Data Exchange (ETDEWEB)

    Delgado, J.; Aznar, M.P. [Univ. of Saragossa (Spain). Dept. of Chemical and Environmental Engineering; Corella, J. [Univ. Complutense of Madrid (Spain). Dept. of Chemical Engineering

    1996-10-01

    Calcined dolomites, limestones, and magnesites are active and inexpensive solids for cleaning raw hot gas from biomass gasifiers with steam. The variations of their activities with time-on-stream are studied here. Simultaneous coke formation and coke elimination by steam gasification increases the life of these naturally occurring catalysts under some circumstances. The lives of these solids are studied at different temperatures (800--880 C), space times (0.08--0.32 kg of dolomite{center_dot}h/nm{sup 3}), particle diameters (1--4 mm), and types of solid. Not much deactivation was observed for tar concentration in the raw gas below 48 g/nm{sup 3}, particle diameters of less than 1.9 mm, temperatures above 800 C, and space times above 0.13 kg{center_dot}h/nm{sup 3}. The effectiveness of these calcined minerals is compared with that of an inert material (silica sand) and with a commercial steam reforming catalyst (R-67 from Haldor Topsoee).

  3. Electro-oxidation nitrite based on copper calcined layered double hydroxide and gold nanoparticles modified glassy carbon electrode

    International Nuclear Information System (INIS)

    Cui Lin; Meng Xiaomeng; Xu Minrong; Shang Kun; Ai Shiyun; Liu Yinping

    2011-01-01

    Highlights: → A nitrite sensor fabricated based on copper calcined layered double hydroxides and gold nanoparticles modified electrode. → This sensor exhibited excellent electrocatalytic oxidation to nitrite. → This nitrite sensor exhibited very good analytical performance with low cost, convenient preparation and rapid detection. - Abstract: In this paper, a novel nitrite sensor was constructed based on electrodeposition of gold nanoparticles (AuNPs) on a copper calcined layered double hydroxide (Cu-CLDH) modified glassy carbon electrode. Electrochemical experiments showed that AuNPs/CLDH composite film exhibited excellent electrocatalytic oxidation activity with nitrite due to the synergistic effect of the Cu-CLDH with AuNPs. The fabricated sensor exhibited excellent performance for nitrite detection within a wide concentration interval of 1-191 μM and with a detection limit of 0.5 μM. The superior electrocatalytic response to nitrite was mainly attributed to the large surface area, minimized diffusion resistance, and enhanced electron transfer of the Cu-CLDH and AuNPs composition film. This platform offers a novel route for nitrite sensing with wide analytical applications and will supply the practical applications for a variety of simple, robust, and easy-to-manufacture analytical approaches in the future.

  4. Effects of calcination temperature and heating rate on the photocatalytic properties of ZnO prepared by pyrolysis.

    Science.gov (United States)

    He, Lingling; Tong, Zhifang; Wang, Zhonghua; Chen, Ming; Huang, Ni; Zhang, Wei

    2018-01-01

    A series of ZnO nanorods were prepared by pyrolysis of zinc acetate at different calcination temperatures and heating rates under ambient atmosphere. The as-prepared ZnO nanorods were characterized by X-ray diffractometer (XRD), scanning electron microscopy (SEM), UV-visible diffuse reflectance spectroscopy (DRS) and X-ray photoelectron spectroscopy (XPS). The photocatalytic performances of the ZnO nanorods were evaluated by the photodegradation of methyl orange (MO) and 4-nitrophenol (4-NP). The morphology, optical property, surface composition, and photocatalytic performance of the ZnO samples were affected by both calcination temperature and heating rate. The photocatalytic activity of the ZnO sample was obviously decreased with increased heating rate, which might be ascribed to the simultaneous decrease of oxygen vacancies and surface adsorption oxygen species. The ZnO nanorods prepared at 300°C with a heating rate of 1°C/min exhibited good photocatalytic activity and photochemical stability, allowing good potential practical application in environmental remediation. Copyright © 2017 Elsevier Inc. All rights reserved.

  5. Removal of indigo carmine dye from water to Mg-Al-CO(3)-calcined layered double hydroxides.

    Science.gov (United States)

    El Gaini, L; Lakraimi, M; Sebbar, E; Meghea, A; Bakasse, M

    2009-01-30

    Layered double hydroxides (LDHs) calcined, denoted as CLDHs, have been shown to recover their original layered structure in the presence of appropriate anions. In the light of this so-called "memory effect", the removal of indigo carmine (IC), an anionic dye, from aqueous solution by calcined Mg-Al-CO(3) LDHs was investigated in batch mode. We looked at the influence of pH values, dye-adsorbent contact time, initial dye concentration and various temperatures of heating of LDHs on the decolorization rate of IC. The adsorption isotherms, described by Freundlich model are L-type. The characterization of the solids CLDHs, both fresh and after removal of IC, by X-ray diffraction and infrared spectroscopy shows that the IC adsorption on CLDHs is enhanced by reconstruction of a matrix hydrotalcite intercaled by the dye, and the intercalation of the organic ion was clearly evidenced by the net increase in the basal spacing from 0.76 nm for [Mg-Al-CO(3)] to 2.13 nm for the organic derivative.

  6. Removal of indigo carmine dye from water to Mg-Al-CO3-calcined layered double hydroxides

    International Nuclear Information System (INIS)

    El Gaini, L.; Lakraimi, M.; Sebbar, E.; Meghea, A.; Bakasse, M.

    2009-01-01

    Layered double hydroxides (LDHs) calcined, denoted as CLDHs, have been shown to recover their original layered structure in the presence of appropriate anions. In the light of this so-called 'memory effect', the removal of indigo carmine (IC), an anionic dye, from aqueous solution by calcined Mg-Al-CO 3 LDHs was investigated in batch mode. We looked at the influence of pH values, dye-adsorbent contact time, initial dye concentration and various temperatures of heating of LDHs on the decolorization rate of IC. The adsorption isotherms, described by Freundlich model are L-type. The characterization of the solids CLDHs, both fresh and after removal of IC, by X-ray diffraction and infrared spectroscopy shows that the IC adsorption on CLDHs is enhanced by reconstruction of a matrix hydrotalcite intercaled by the dye, and the intercalation of the organic ion was clearly evidenced by the net increase in the basal spacing from 0.76 nm for [Mg-Al-CO 3 ] to 2.13 nm for the organic derivative

  7. Removal of indigo carmine dye from water to Mg-Al-CO{sub 3}-calcined layered double hydroxides

    Energy Technology Data Exchange (ETDEWEB)

    El Gaini, L. [Faculty of Science, University Chouaib Doukkali, 24000 El Jadida (Morocco); Lakraimi, M. [ENS Ecole Normale Superieure, 40000 Marrakech (Morocco); Sebbar, E. [Faculty of Science, University Chouaib Doukkali, 24000 El Jadida (Morocco); Meghea, A. [University POLITEHNICA of Bucharest (Romania); Bakasse, M. [Faculty of Science, University Chouaib Doukkali, 24000 El Jadida (Morocco)], E-mail: bakassem@yahoo.fr

    2009-01-30

    Layered double hydroxides (LDHs) calcined, denoted as CLDHs, have been shown to recover their original layered structure in the presence of appropriate anions. In the light of this so-called 'memory effect', the removal of indigo carmine (IC), an anionic dye, from aqueous solution by calcined Mg-Al-CO{sub 3} LDHs was investigated in batch mode. We looked at the influence of pH values, dye-adsorbent contact time, initial dye concentration and various temperatures of heating of LDHs on the decolorization rate of IC. The adsorption isotherms, described by Freundlich model are L-type. The characterization of the solids CLDHs, both fresh and after removal of IC, by X-ray diffraction and infrared spectroscopy shows that the IC adsorption on CLDHs is enhanced by reconstruction of a matrix hydrotalcite intercaled by the dye, and the intercalation of the organic ion was clearly evidenced by the net increase in the basal spacing from 0.76 nm for [Mg-Al-CO{sub 3}] to 2.13 nm for the organic derivative.

  8. Spring 2009 Semiannual (III.H. and I.U.) Report for the HWMA/RCRA Post-Closure Permit for the INTEC Waste Calcining Facility at the INL Site

    Energy Technology Data Exchange (ETDEWEB)

    Boehmer, Ann M.

    2009-05-31

    The Waste Calcining Facility is located at the Idaho Nuclear Technology and Engineering Center. In 1999, the Waste Calcining Facility was closed under and approved Hazardous Waste Management Act/Resource Conservation and Recovery Act Closure plan. Vessels and spaces were grouted and then covered with a concrete cap. This permit sets forth procedural requirements for groundwater characterization and monitoring, maintenance, and inspections of the Waste Calcining Facility to ensure continued protection of human health and the environment.

  9. Glass-ceramic waste forms for immobilization of the fluorinel-sodium, alumina, and zirconia calcines stored at the Idaho Chemical Processing Plant

    Energy Technology Data Exchange (ETDEWEB)

    Vinjamuri, K. [Idaho National Engineering Lab., Idaho Falls, ID (United States)

    1994-12-31

    Glass-ceramics appear to be very good candidate waste forms for immobilization of the calcined high level solid wastes, fluorinel-sodium (Fl/Na), alumina and zirconia that are stored at the Idaho Chemical Processing Plant (ICPP). Candidate experimental glass-ceramics were synthesized at ICPP by hot isostatically pressing (HIPing) a mixture of precompacted pilot plant calcine and additives. The glass-ceramic waste forms for immobilization of the Fl/Na, alumina, and zirconia calcines consist of 70 wt% Fl/Na calcine, 23.9 wt% SiO{sub 2}, 5 wt% Ti, 1.1 wt% B{sub 2}O{sub 3}; 70 wt% alumina calcine, 30 wt% SiO{sub 2}; and 70 wt% zirconia calcine, 20.25 wt% SiO{sub 2}, 5 wt% Ti, 2.25 wt% Na{sub 2}O, 1.75 wt% B{sub 2}O{sub 3}, 0.75 wt% Li{sub 2}O, respectively. The characteristics of the waste forms including density, chemical durability, glass and crystalline phases, and the microstructure are investigated. The 14-day MCC-1 total mass loss rates and the normalized elemental leach rates for aluminum, boron, calcium, cadmium, chromium, cesium, potassium, silicon, sodium, strontium, titanium, and zirconium are all less than 1 g/m{sup 2}-day. The crystalline phases for the Fl/Na and zirconia waste forms include zirconia, zircon, calcium fluoride, and titanates. In addition, cadmium sulphide in Fl/Na, and cadmium metal in zirconia waste form were also identified. The crystalline phases for the alumina waste form are alpha, gamma, and delta alumina, cristobalite, albite, and mullite. Glass phase separation was not observed in alumina and zirconia waste forms. The observed glass phase separation in Fl/Na waste form appears to be chemically durable.

  10. Hot isostatically-pressed aluminosilicate glass-ceramic with natural crystalline analogues for immobilizing the calcined high-level nuclear waste at the Idaho Chemical Processing Plant

    Energy Technology Data Exchange (ETDEWEB)

    Raman, S.

    1993-12-01

    The additives Si, Al, MgO, P{sub 2}O{sub 5} were mechanically blended with fluorinelsodium calcine in varying proportions. The batches were vacuum sealed in stainless steel canisters and hot isostatically pressed at 20,000 PSI and 1000 C for 4 hours. The resulting suite of glass-ceramic waste forms parallels the natural rocks in microstructural and compositional heterogeneity. Several crystalline phases ar analogous in composition and structure to naturally occurring minerals. Additional crystalline phases are zirconia and Ca-Mg borate. The glasses are enriched in silica and alumina. Approximately 7% calcine elements occur dissolved in this glass and the total glass content in the waste forms averages 20 wt%. The remainder of the calcine elements are partitioned into crystalline phases at 75 wt% calcine waste loading. The waste forms were tested for chemical durability in accordance with the MCC1-test procedure. The leach rates are a function of the relative proportions of additives and calcine, which in turn influence the composition and abundances of the glass and crystalline phases. The DOE leach rate criterion of less than 1 g/m{sup 2}-day is met by all the elements B, Cs and Na are increased by lowering the melt viscosity. This is related to increased crystallization or devitrification with increases in MgO addition. This exploratory work has shown that the increases in waste loading occur by preferred partitioning of the calcine components among crystalline and glass phases. The determination of optimum processing parameters in the form of additive concentration levels, homogeneous blending among the components, and pressure-temperature stabilities of phases must be continued to eliminate undesirable effects of chemical composition, microstructure and glass devitrification.

  11. Employing Calcination as a Facile Strategy to Reduce the Cytotoxicity in CoFe2O4and NiFe2O4Nanoparticles.

    Science.gov (United States)

    Lima, Débora R; Jiang, Ning; Liu, Xin; Wang, Jiale; Vulcani, Valcinir A S; Martins, Alessandro; Machado, Douglas S; Landers, Richard; Camargo, Pedro H C; Pancotti, Alexandre

    2017-11-15

    CoFe 2 O 4 and NiFe 2 O 4 nanoparticles (NPs) represent promising candidates for biomedical applications. However, in these systems, the knowledge over how various physical and chemical parameters influence their cytotoxicity remains limited. In this article, we investigated the effect of different calcination temperatures over cytotoxicity of CoFe 2 O 4 and NiFe 2 O 4 NPs, which were synthesized by a sol-gel proteic approach, toward L929 mouse fibroblastic cells. More specifically, we evaluated and compared CoFe 2 O 4 and NiFe 2 O 4 NPs presenting low crystallinity (that were calcined at 400 and 250 °C, respectively) with their highly crystalline counterparts (that were calcined at 800 °C). We found that the increase in the calcination temperature led to the reduction in the concentration of surface defect sites and/or more Co or Ni atoms located at preferential crystalline sites in both cases. A reduction in the cytotoxicity toward mouse fibroblast L929 cells was observed after calcination at 800 °C. Combining with inductively coupled plasma mass spectrometry data, our results indicate that the calcination temperature can be employed as a facile strategy to reduce the cytotoxicity of CoFe 2 O 4 and NiFe 2 O 4 , in which higher temperatures contributed to the decrease in the dissolution of Co 2+ or Ni 2+ from the NPs. We believe these results may shed new insights into the various parameters that influence cytotoxicity in ferrite NPs, which may pave the way for their widespread applications in biomedicine.

  12. Effect of hexagonal boron nitride and calcined petroleum coke on friction and wear behavior of phenolic resin-based friction composites

    International Nuclear Information System (INIS)

    Yi Gewen; Yan Fengyuan

    2006-01-01

    Calcined petroleum coke (CPC) and hexagonal boron nitride (h-BN) were used as the friction modifiers to improve the friction and wear properties of phenolic resin-based friction composites. Thus, the composites with different relative amounts of CPC and h-BN as the friction modifiers were prepared by compression molding. The hardness and bending strength of the friction composites were measured. The friction and wear behaviors of the composites sliding against cast iron at various temperatures were evaluated using a pin-on-disc test rig. The worn surfaces and wear debris of the friction composites were analyzed by means of scanning electron microscopy, energy dispersive spectroscopy, and X-ray photoelectron spectroscopy. It was found that the hybrid of the two friction modifiers was effective to significantly decrease the wear rate and stabilize the friction coefficient of the friction composites at various temperatures by forming a uniform lubricating and/or transferred film on the rubbing surfaces. The uniform and durable transfer films were also able to effectively diminish the direct contact between the friction composite and the cast iron counterpart and hence prevent severe wear of the latter as well. The effectiveness of the hybrid of CPC and h-BN in improving the friction and wear behavior of the phenolic resin-based friction modifiers could be attributed to the complementary action of the 'low temperature' lubricity of CPC and the 'high temperature' lubricity of h-BN. The optimum ratio of the two friction modifiers CPC and h-BN in the friction composites was suggested to be 1:1, and the corresponding friction composite showed the best friction-reducing and antiwear abilities

  13. Avaliação de erosão a quente de concretos refratários para calcinadores de leito fluidizado Hot erosion evaluation of fluid flash calciner refractory castables

    Directory of Open Access Journals (Sweden)

    L. R. G. Gonçalves

    2011-06-01

    Full Text Available Revestimentos refratários são severamente solicitados pela erosão causada por partículas que se movem pneumaticamente através de vasos e dutos em calcinadores de leito fluidizado. Esse tipo de desgaste constitui um fator chave para a degradação do revestimento desse equipamento. Consequentemente, o desempenho desses refratários tem um efeito imediato no lucro da empresa, uma vez que paradas para reparos tem um impacto direto no cronograma operacional e nos custos de manutenção da unidade produtiva. Apesar da temperatura de operação dos calcinadores variar entre 200 e 1250 ºC, a resistência a erosão, que é uma das principais propriedades selecionadas para avaliar materiais usados nessa aplicação, geralmente é medida somente à temperatura ambiente. Porém, esse tipo de avaliação não representa fielmente as condições de operação. Portanto, é necessário um estudo mais realista na tentativa de encontrar alguma relação entre a severidade de erosão e a temperatura. Visando alcançar esse objetivo, o presente trabalho apresenta o desenvolvimento e aplicação de um equipamento de erosão à quente para avaliação de concretos refratários para calcinadores de leito fluidizado.Refractory linings are heavily damaged by the erosion caused by particles moving pneumatically through vessels and pipes in fluid flash calciners. This sort of wearing constitutes one of the key factors for equipment lining degradation. Consequently, the performance of materials has an immediate effect on a company's profit, as each maintenance call has a direct impact on the operational schedule and costs. Although the operation temperature of the calciners ranges from 200 up to 1250 ºC, the erosion resistance, which is one of the main properties selected to evaluate the materials used in this application, is mostly measured only at room temperature. Nevertheless, this sort of evaluation does not represent the actual working environment. Therefore

  14. Study of the behavior of aggregate of calcined clay for use in permeable pavements for the city of Manaus

    International Nuclear Information System (INIS)

    Oliveira, M.S.; Vilela, P.A.T.; Araujo, V.S.

    2016-01-01

    Research on the production of ceramic aggregates and their use in paving in the country began in the 80’s in the search for an alternative material that could replace the pebble or crushed stone, studied the clay, considered an abundant mineral resource by virtue of being the predominant soil in this region and which were made synthetic calcinated clay aggregates (ASAC), for their application in permeable paving concrete motivated by the lack of permeable areas. The study consists of the characterization of materials for manufacture of concrete slabs permeable and the assessment of the effects of synthetic aggregate on its properties in fresh and hardened state. The ceramic bodies were subjected to tests of X-ray diffraction, determination of chemical composition and plasticity. The results indicate that the use of synthetic clusters is a viable alternative for the production of porous concrete. (author)

  15. Effectiveness factors for a commercial steam reforming (Ni) catalyst and for a calcined dolomite used downstream biomass gasifiers

    Energy Technology Data Exchange (ETDEWEB)

    Corella, J.; Narvaez, I.; Orio, A. [Madrid Univ. (Spain). Dept. of Chem. Eng.

    1996-12-31

    A commercial steam reforming catalyst from BASF, the G1-25 S one, and a calcined dolomite, Norte-1, from Cantabria-Spain, have been used, once crushed and sieved to different particle fractions between 1.0 and 4.0 mm. The materials have been tested downstream small pilot biomass gasifiers, bubbling fluidized bed type, gasifying with air and with steam. The Thiele modulus and the effectiveness factor have been calculated at temperatures of 750-850 deg C. It is experimentally shown that diffusion control plays an important part when particle size is larger than ca. 0.5 mm. This has to be taken into account when comparing the quality of the solids for tar elimination. (author) (5 refs.)

  16. Géopolymère à base d'argiles calcinées : formulation et caractérisation

    OpenAIRE

    SEIFI, Sahar

    2015-01-01

    L'utilisation de kaolin et de métakaolin (kaolin calciné) comme matériau pouzzolanique pour fabriquer des géopolymères a attiré l'intérêt à travers le monde notamment dans l'industrie des mortiers et des bétons. Les géopolymères sont des polymères minéraux issus de processus géochimique. La formation des géopolymères se fait avec des quantités spécifiques de silice et d'alumine, dissoutes en milieu alcalin. Dans cette étude, la rhéologie des mélanges de métakaolin ARGICAL M-1000 et de solutio...

  17. Thermal and catalytic cracking of ethylene in presence of CaO, MgO, zeolite and calcined dolomite

    Energy Technology Data Exchange (ETDEWEB)

    Taralas, G.; Sjoestroem, K.; Jaeraas, S.; Bjoernbom, E. [Royal Inst. of Tech., Stockholm (Sweden). Dept. of Chemical Technology

    1993-12-31

    The subject of the present work is to study the effect of catalysts such as calcined dolomite (CaO.MgO), CaO (quicklime), MgO and Zeolite (EKZ-4) on the cracking of ethylene in the presence and absence of steam. N-heptane, toluene, naphthalene, thiophene have been some suitable model compounds for studies of the thermal and catalytic decomposition of tar. Previous results showed that the reaction scheme of the thermal decomposition of n-heptane was consistent with the high yield of ethylene observed in thermal decomposition of n-heptane. The effect of the reactor wall and the ferric impurities in the dolomite are also subjects of the research in this study. The results may also throw some additional light on the nature of the gas-phase thermal and catalytic reactions occurring in the use of dolomite as tar cracking catalysts. 28 refs

  18. Molecular dynamics simulations of the effect of NaCl-doping on the calcination characteristics in desulfurization processes

    Energy Technology Data Exchange (ETDEWEB)

    Murakami, T.; Kurita, N.; Naruse, I. [Toyohashi University of Technology, Toyohashi (Japan)

    2003-03-01

    Desulfurization performance of wasted seashells was found to be over twice as high as that of limestone, which was currently used as a desulfurizer in fluidized bed coal combustors. NaCl-doping into limestone was also found to be effective in improving the desulfurization efficiency. From X-ray diffraction (XRD) analyses of calcined seashell, limestone and NaCl-doped limestone, on the other hand, not only the calcined seashell but also the NaCl-doped limestone had strong peaks of CaO crystal, and those two materials also had high desulfurization activity. This improvement was hypothesized to be due to NaCl causing a change in the crystal structure of CaO. In order to elucidate the effect of NaCl addition on the CaO crystal structure in the incineration of CaCO{sub 3} the change of structures was simulated by means of molecular dynamics simulations of CaO. In the simulation one molecule of NaCl was exchanged into one molecule of CaO. A pair correlation functions and the distances between Ca and O atoms, which were obtained by the simulations, were compared with those from the crystal CaO. NaCl-doping affected the crystalization temperature of CaO. The crystallization temperature increased due to adding a little bit of NaCl. From the result of the pair correlation functions obtained in NaCl-doped CaO, the difference of the potential energy of NaCl from that of CaO seemed to contribute to the crystallization of the bulk of CaO. The simulation and experimental results obtained suggested that NaCl-doping contributed to crystallizing the CaO molecules.

  19. Intercalation behavior of amino acids into Zn-Al-layered double hydroxide by calcination-rehydration reaction

    Science.gov (United States)

    Aisawa, Sumio; Kudo, Hiroko; Hoshi, Tomomi; Takahashi, Satoshi; Hirahara, Hidetoshi; Umetsu, Yoshio; Narita, Eiichi

    2004-11-01

    The intercalation of amino acids for the Zn-Al-layered double hydroxide (LDH) has been investigated by the calcination-rehydration reaction at 298 K using mainly phenylalanine (Phe) as a guest amino acid. The Zn-Al oxide precursor prepared by the calcination of Zn-Al-carbonated LDH at 773 K for 2 h was used as the host material. The amount of Phe intercalated by the rehydration was remarkably influenced by the initial solution pH and reached ca. 2.7 times for anion exchange capacity (AEC) of the LDH at neutral and weak alkaline solutions, suggesting that Phe was intercalated as amphoteric ion form into the LDH interlayer. As Phe is intercalated for the LDH as monovalent anion in alkaline solution, the amount of Phe intercalated at pH 10.5 corresponded with AEC of the LDH. The solid products were found to have the expanded LDH structure, which confirmed that Phe was intercalated into the LDH interlayer as amphoteric ion or anion form. The basal spacing, d003, of the Phe/LDH was 1.58 nm at pH 7.0 and 0.80 nm at pH 10.5; two kinds of expansion suggested for Phe in the interlayer space as vertical (pH 7.0) and horizontal (pH 10.5) orientations. The intercalation behavior of various amino acids for the LDH was also found to be greatly influenced by the feature of the amino acid side-chain, namely, its carbon-chain length, structure and physicochemical property. In particular, α-amino acids possessing a hydrophobic or negative-charged side-chain were preferentially intercalated for the LDH.

  20. Limestone calcined clay cement as a low-carbon solution to meet expanding cement demand in emerging economies

    Directory of Open Access Journals (Sweden)

    Yudiesky Cancio Díaz

    Full Text Available This paper aims at assessing the return on investment and carbon mitigation potentials of five investment alternatives for the Cuban cement industry in a long-term horizon appraisal (15 years. Anticipated growing demand for cement, constrained supply and an urgent need for optimisation of limited capital while preserving the environment, are background facts leading to the present study. This research explores the beneficial contribution of a new available technology, LC3 cement, resulting from the combination of clinker, calcined clay and limestone, with a capacity of replacing up to 50% of clinker in cement. Global Warming Potential (GWP is calculated with Life Cycle Assessment method and the economic investment's payback is assessed through Return on Capital Employed (ROCE approach. Main outcomes show that projected demand could be satisfied either by adding new cement plants—at a high environmental impact and unprofitable performance— or by introducing LC3 strategy. The latter choice allows boosting both the return on investment and the production capacity while reducing greenhouse gas (GHG emissions up to 20–23% compared to business-as-usual practice. Overall profitability for the industry is estimated to overcome BAU scenario by 8–10% points by 2025, if LC3 were adopted. Increasing the production of conventional blended cements instead brings only marginal economic benefits without supporting the needed increase in production capacity. The conducted study also shows that, in spite of the extra capital cost required for the calcination of kaolinite clay, LC3 drops production costs in the range of 15–25% compared to conventional solutions. Keywords: Cement, Alternative, ROCE, CO2, LCA, Investment

  1. Synthesis of zeolites Na-A and Na-X from tablet compressed and calcinated coal fly ash

    Science.gov (United States)

    Hu, Tao; Gao, Wenyan; Liu, Xin; Zhang, Yifu; Meng, Changgong

    2017-10-01

    Zeolites Na-A and Na-X are important synthetic zeolites widely used for separation and adsorption in industry. It is of great significance to develop energy-efficient routines that can synthesize zeolites Na-A and Na-X from low-cost raw materials. Coal fly ash (CFA) is the major residue from the combustion of coal and biomass containing more than 85% SiO2 and Al2O3, which can readily replace the conventionally used sodium silicate and aluminate for zeolite synthesis. We used Na2CO3 to replace the expensive NaOH used for the calcination of CFA and showed that tablet compression can enhance the contact with Na2CO3 for the activation of CFA through calcination for the synthesis of zeolites Na-A and Na-X under mild conditions. We optimized the control variables for zeolite synthesis and showed that phase-pure zeolite Na-A can be synthesized with CFA at reactant molar ratio, hydrothermal reaction temperature and reaction time of 1.3Na2O: 0.6Al2O3: 1SiO2: 38H2O at 80°C for 6 h, respectively, while phase-pure zeolite Na-X can be synthesized at 2.2Na2O: 0.2Al2O3: 1SiO2: 88H2O at 100°C for 8 h, respectively. The composition, morphology, specific surface area, vibration spectrum and thermogravimetry of synthesized Na-A and Na-X were further characterized.

  2. Effect of Calcination Temperatures and Mo Modification on Nanocrystalline (γ-χ-Al2O3 Catalysts for Catalytic Ethanol Dehydration

    Directory of Open Access Journals (Sweden)

    Tharmmanoon Inmanee

    2017-01-01

    Full Text Available The mixed gamma and chi crystalline phase alumina (M-Al catalysts prepared by the solvothermal method were investigated for catalytic ethanol dehydration. The effects of calcination temperatures and Mo modification were elucidated. The catalysts were characterized by X-ray diffraction (XRD, N2 physisorption, transmission electron microscopy (TEM, and NH3-temperature programmed desorption (NH3-TPD. The catalytic activity was tested for ethylene production by dehydration reaction of ethanol in gas phase at atmospheric pressure and temperature between 200°C and 400°C. It was found that the calcination temperatures and Mo modification have effects on acidity of the catalysts. The increase in calcination temperature resulted in decreased acidity, while the Mo modification on the mixed phase alumina catalyst yielded increased acidity, especially in medium to strong acids. In this study, the catalytic activity of ethanol dehydration to ethylene apparently depends on the medium to strong acid. The mixed phase alumina catalyst calcined at 600°C (M-Al-600 exhibits the complete ethanol conversion having ethylene yield of 98.8% (at 350°C and the Mo-modified catalysts promoted dehydrogenation reaction to acetaldehyde. This can be attributed to the enhancement of medium to strong acid with metal sites of catalyst.

  3. Manufacture of barium hexaferrite (BaO3.98Fe2O3) from iron oxide waste of grinding process by using calcination process

    Science.gov (United States)

    Idayanti, N.; Dedi; Kristiantoro, T.; Mulyadi, D.; Sudrajat, N.; Alam, G. F. N.

    2018-03-01

    The utilization of iron oxide waste of grinding process as raw materials for making barium hexaferrite has been completed by powder metallurgy method. The iron oxide waste was purified by roasting at 800 °C temperature for 3 hours. The method used varying calcination temperature at 1000, 1100, 1200, and 1250 °C for 3 hours. The starting iron oxide waste (Fe2O3) and barium carbonate (BaCO3) were prepared by mol ratio of Fe2O3:BaCO3 from the formula BaO3.98Fe2O3. Some additives such as calcium oxide (CaO), silicon dioxide (SiO2), and polyvinyl alcohol (PVA) were added after calcination process. The samples were formed at the pressure of 2 ton/cm2 and sintered at the temperature of 1250 °C for 1 hour. The formation of barium hexaferrite compounds after calcination is determined by X-Ray diffraction. The magnetic properties were observed by Permagraph-Magnet Physik with the optimum characteristic at calcination temperature of 1250 °C with the induction of remanence (Br) = 1.38 kG, coercivity (HcJ) = 4.533 kOe, product energy maximum (BHmax) = 1.086 MGOe, and density = 4.33 g/cm3.

  4. Comparison of the rotary calciner-metallic melter and the slurry-fed ceramic melter technologies for vitrifying West Valley high-level wastes

    International Nuclear Information System (INIS)

    Chapman, C.C.

    1983-01-01

    Two processes which are believed applicable and available for vitrification of West Valley's high-level (HLW) wastes were technically evaluated and compared. The rotary calciner-metallic melter (AVH) and the slurry-fed ceramic melter (SFCM) were evaluated under the following general categories: process flow sheet, remote operability, safety and environmental considerations, and estimated cost and schedules

  5. Aqueous chemical route synthesis and the effect of calcination temperature on the structural and optical properties of ZnO nanoparticles

    Directory of Open Access Journals (Sweden)

    Mohammad Ramzan Parra

    2014-10-01

    Full Text Available This article reports the controlled size of ZnO nanoparticles synthesized via simple aqueous chemical route without the involvement of any capping agent. The effect of different calcination temperatures on the size of the ZnO nanoparticles was investigated. X-ray diffraction (XRD results indicated that all the samples have crystalline wurtzite phase, and peak broadening analysis was used to evaluate the average crystallite size and lattice strain using Scherrer's equation and Williamson–Hall (W–H method. Morphology and elemental compositions were investigated using atomic force microscopy (AFM and scanning electron microscopy (SEM with energy-dispersive X-ray (EDX spectroscopy. The average crystallite size of ZnO nanoparticles estimated from Scherrer's formula and W–H analysis was found to increase with the increase in calcination temperature. These results were in good agreement with AFM results. Optical properties were investigated using UV–vis spectroscopy in diffused reflectance (DR mode, with a sharp increase in reflectivity at 375 nm and the material has a strong reflective characteristic after 420 nm at 500 °C calcination temperature. Furthermore, photoluminescence spectroscopic results revealed intensive ultraviolet (UV emission with reduced defect concentrations and a slight shifting in band gap energies with increased calcination temperature from 200 °C to 500 °C. This study suggests that the as-prepared ZnO nanoparticles with bandgap tunability might be utilized as window layer in optoelectronic devices.

  6. Negative Effect of Calcination to Catalytic Performance of Coal Char-loaded TiO2 Catalyst in Styrene Oxidation with Hydrogen Peroxide as Oxidant

    Directory of Open Access Journals (Sweden)

    Mukhamad Nurhadi

    2018-01-01

    How to Cite: Nurhadi, M., Kusumawardani, R., Nur, H. (2018. Negative Effect of Calcination to Catalytic Performance of Coal Char-loaded TiO2 Catalyst in Styrene Oxidation with Hydrogen Peroxide as Oxidant. Bulletin of Chemical Reaction Engineering & Catalysis, 13 (1: 113-118 (doi:10.9767/bcrec.13.1.1171.113-118

  7. Removal of indigo carmine and green bezanyl-F2B from water using calcined and uncalcined Zn/Al + Fe layered double hydroxide

    Directory of Open Access Journals (Sweden)

    Hassiba Bessaha

    2017-06-01

    Full Text Available Layered double hydroxide Zn/(Al + Fe with a molar ratio of 3:(0.85 + 0.15, designated as ZAF-HT, was synthetized by co-precipitation. Its calcined product CZAF was obtained by heat treatment of ZAF-HT at 500°C. The calcined and uncalcined materials were used to remove the acid dyes indigo carmine (IC and green bezanyl-F2B (F2B from water in batch mode. The synthetized materials were characterized by X-ray diffraction, scanning electron microscopy, Brunauer–Emmett–Teller analysis, Fourier transform infra-red spectroscopy and thermogravimetric/differential thermal analysis. The sorption kinetic data fitted a pseudo-second-order model. The adsorbed amounts of the calcined material were much larger than ZAF-HT. The maximum adsorption capacity of CZAF was found to be 617.3 mg g−1 for IC and 1,501.4 mg g−1 for F2B. The isotherms showed that the removal of IC and F2B by ZAF-HT and CZAF could be described by a Langmuir model. The thermodynamic parameters were also calculated. The negative values of standard free energy ΔG° indicate the spontaneity of sorption process. The reuse of CZAF was studied for both dyes and the calcined material showed a good stability for four thermal cycles.

  8. Preparation of Calcined Zirconia-Carbon Composite from Metal Organic Frameworks and Its Application to Adsorption of Crystal Violet and Salicylic Acid

    Directory of Open Access Journals (Sweden)

    Zubair Hasan

    2016-03-01

    Full Text Available Zirconia-carbon (ZC composites were prepared via calcination of Zr-based metal organic frameworks, UiO-66 and amino-functionalized UiO-66, under N2 atmosphere. The prepared composites were characterized using a series of instrumental analyses. The surface area of the ZC composites increased with the increase of calcination temperature, with the formation of a graphite oxide phase observed at 900 °C. The composites were used for adsorptive removal of a dye (crystal violet, CV and a pharmaceutical and personal care product (salicylic acid, SA. The increase of the calcination temperature resulted in enhanced adsorption capability of the composites toward CV. The composite calcined at 900 °C exhibited a maximum uptake of 243 mg·g−1, which was much greater than that by a commercial activated carbon. The composite was also effective in SA adsorption (102 mg·g−1, and N-functionalization of the composite further enhanced its adsorption capability (109 mg·g−1. CV adsorption was weakly influenced by solution pH, but was more dependent on the surface area and pore volume of the ZC composite. Meanwhile, SA adsorption showed strong pH dependence, which implies an active role of electrostatic interactions in the adsorption process. Base-base repulsion and hydrogen bonding are also suggested to influence the adsorption of CV and SA, especially for the N-functionalized composite.

  9. Continuous plutonium(IV) oxalate precipitation, filtration, and calcination process. [From product streams from Redox, Purex, or Recuplex solvent extraction plants

    Energy Technology Data Exchange (ETDEWEB)

    Beede, R L

    1956-09-27

    A continuous plutonium (IV) oxalate precipitation, filtration, and calcination process has been developed. Continuous and batch decomposition of the oxalate in the filtrates has been demonstrated. The processes have been demonstrated in prototype equipment. Plutonium (IV) oxalate was precipitated continuously at room temperature by the concurrent addition of plutonium (IV) nitrate feed and oxalic acid into the pan of a modified rotary drum filter. The plutonium (IV) oxalate was calcined to plutonium dioxide, which could be readily hydrofluorinated. Continuous decomposition of the oxalate in synthetic plutonium (IV) oxalate filtrates containing plutonium (IV) oxalate solids was demonstrated using co-current flow in a U-shaped reactor. Feeds containing from 10 to 100 g/1 Pu, as plutonium (IV) nitrate, and 1.0 to 6.5 M HNO/sub 3/, respectively, can be processed. One molar oxalic acid is used as the precipitant. Temperatures of 20 to 35/sup 0/C for the precipitation and filtration are satisfactory. Plutonium (IV) oxalate can be calcined at 300 to 400/sup 0/C in a screw-type drier-calciner to plutonium dioxide and hydrofluorinated at 450 to 550/sup 0/C. Plutonium dioxide exceeding purity requirements has been produced in the prototype equipment. Advantages of continuous precipitation and filtration are: uniform plutonium (IV) oxalate, improved filtration characteristics, elimination of heating and cooling facilities, and higher capacities through a single unit. Advantages of the screw-type drier-calciner are the continuous production of an oxide satisfactory for feed for the proposed plant vibrating tube hydrofluorinator, and ease of coupling continuous precipitation and filtration to this proposed hydrofluorinator. Continuous decomposition of oxalate in filtrates offers advantages in decreasing filtrate storage requirements when coupled to a filtrate concentrator. (JGB)

  10. Facile synthesis of both needle-like and spherical hydroxyapatite nanoparticles: Effect of synthetic temperature and calcination on morphology, crystallite size and crystallinity

    Energy Technology Data Exchange (ETDEWEB)

    Wijesinghe, W.P.S.L.; Mantilaka, M.M.M.G.P.G. [Department of Chemistry, Faculty of Science, University of Peradeniya, Peradeniya 20400 (Sri Lanka); Post-graduate Institute of Science, P.O. Box: 25, University of Peradeniya, Peradeniya 20400 (Sri Lanka); Premalal, E.V.A. [Department of Materials Science, Shizuoka University, Johoku, Naka-ku Hamamatsu, 432-8011 (Japan); Herath, H.M.T.U. [Department of Medical Laboratory Science, Faculty of Allied Health Sciences, University of Peradeniya, Peradeniya 20400 (Sri Lanka); Mahalingam, S.; Edirisinghe, M. [Department of Mechanical Engineering, University College London, London WC1E 7JE (United Kingdom); Rajapakse, R.P.V.J. [Department of Veterinary Pathobiology, Faculty of Veterinary, University of Peradeniya, Peradeniya 20400 (Sri Lanka); Rajapakse, R.M.G., E-mail: rmgr@pdn.ac.lk [Department of Chemistry, Faculty of Science, University of Peradeniya, Peradeniya 20400 (Sri Lanka); Post-graduate Institute of Science, P.O. Box: 25, University of Peradeniya, Peradeniya 20400 (Sri Lanka)

    2014-09-01

    Synthetic hydroxyapatite (HA) nanoparticles, that mimic natural HA, are widely used as biocompatible coatings on prostheses to repair and substitute human bones. In this study, HA nanoparticles are prepared by precipitating them from a precursor solution containing calcium sucrate and ammonium dihydrogen orthophosphate, at a Ca/P mole ratio of 1.67:1, at temperatures, ranging from 10 °C to 95 °C. A set of products, prepared at different temperatures, is analyzed for their crystallinity, crystallite size, morphology, thermal stability and composition, by X-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA) and Fourier transform infrared (FT-IR) spectroscopic techniques, while the other set is analyzed after calcining the respective products, soon after their synthesis, for 3 h, at 700 °C. The as-prepared products, after 2 h of drying, without any calcination, are not crystalline, but they grow very slowly into needle-like morphologies, as they are ripened with time. The percentage crystallinity of the final products increases from 15% to 52%, with increasing the preparative temperature. The calcined samples always produce spherical nanoparticles of essentially the same diameter, between 90 nm and 100 nm, which does not change due to aging and preparative temperatures. Therefore, the same method can be utilized to synthesize both spherical and needle-like nanoparticles of hydroxyapatite, with well-defined sizes and shapes. The ability to use readily available cheap raw materials, for the synthesis of such well-defined crystallites of hydroxyapatite, is an added advantage of this method, which may be explored further for the scaling up of the procedures to suit to industrial scale synthesis of such hydroxyapatite nanoparticles. - Highlights: • Hydroxyapatite nanoparticles are synthesized using a simple precipitation method. • Both needle-like and spherical hydroxyapatite nanoparticles are synthesized. • The prepared

  11. Heavy metal behavior in "Washing-Calcination-Changing with Bottom Ash" system for recycling of four types of fly ashes.

    Science.gov (United States)

    Zhu, Fenfen; Xiong, Yiqun; Wang, Yingying; Wei, Xiang; Zhu, Xuemei; Yan, Fawei

    2018-01-30

    The Washing-Calcination-Changing with Bottom Ash (WCCB) system, effective at reducing chloride, was proposed to treat fly ash (FA) from a municipal solid waste incinerator (MSWI) before recycling FA in cement kiln as raw material. This study analyzed the behavior of heavy metals in four types of FA during WCCB treatment via Tessier and X-ray absorption fine structure (XANES) method. One FA was from the bag filter of a typical MSWI in Beijing, China (CFA), and the other three were from Japan (RFA, CaFA, and NaFA). All the metals were reduced especially Pb, Cd, and Hg (38.4-82.4%, 21.8-34.7%, and 100%, respectively). Besides Cr almost all heavy metals were stabilized according to Tessier analysis. Cr should be given more attention in WCCB as the formation of exchangeable Cr in the final residue. XANES result indicated that PbCl 2 could be the main species of Pb in FA, while CaFA contains some PbO. The treated FAs contain PbCO 3 and PbO besides PbCl 2 . The Tessier results of Ni, Pb, Cd, Cr, and Cu showed that NaFA was better at heavy metal stabilization than the other FA, so NaHCO 3 is a more suitable neutralizer in WCCB. Copyright © 2018 Elsevier Ltd. All rights reserved.

  12. Influences of the calcination temperature and polymethyl methacrylate templates to characteristic pore membrane of bioceramic titanium dioxide

    Science.gov (United States)

    Ady, Jan; Viandari, Eka; Hasanah, Dewi W.

    2017-05-01

    The synthesis of the bioceramics titanium dioxide on its template by polymethyl methacrylate to be a sample with forming TiO2/PMMA was made with sol-gel process, and its pore membrane characteristics has also been studied. Different calcination temperatures 500°C, 550°C, and 600°C were given to sample for 17 hours. This purpose themselves was to fill TiO2 fissures with PMMA on different concentrations of 0.0, 2.0 wt%, 3.0 wt%, 4.0 wt%. Template leaching technique was used to remove PMMA from samples, and it was then sequentially found of the pore size of the membrane in approximate ranges (1900 nm - 2000 nm), (860.5 nm - 1669 nm), (312.8 nm-382.5 nm), and (136.1 nm - 269.7 nm). SEM test using and fourth it has average thickness in about 6.7 nm with Ellipsometer measurement. The percentage values of titanium and oxygen atoms are found by SEM-EDX from 3.03 at.% up to 66.81 at.% and there is amount 99.99% of the sample in anatase phase forming at 550 0C with angle of diffraction is 25.410 and it was prepared by XRD measurement.

  13. Development of Al2O3 electrospun fibers prepared by conventional sintering method or plasma assisted surface calcination

    Science.gov (United States)

    Mudra, E.; Streckova, M.; Pavlinak, D.; Medvecka, V.; Kovacik, D.; Kovalcikova, A.; Zubko, P.; Girman, V.; Dankova, Z.; Koval, V.; Duzsa, J.

    2017-09-01

    In this paper, the electrospinning method was used for preparation of α-Al2O3 microfibers from PAN/Al(NO3)3 precursor solution. The precursor fibers were thermally treated by conventional method in furnace or low-temperature plasma induced surface sintering method in ambient air. The four different temperatures of PAN/Al(NO3)3 precursors were chosen for formation of α-Al2O3 phase by conventional sintering way according to the transition features observed in the TG/DSC analysis. In comparison, the low-temperature plasma treatment at atmospheric pressure was used as an alternative sintering method at the exposure times of 5, 10 and 30 min. FTIR analysis was used for evaluation of residual polymer after plasma induced calcination and for studying the mechanism of polymer degradation. The polycrystalline alumina fibers arranged with the nanoparticles was created continuously throughout the whole volume of the sample. On the other side the low temperature approach, high density of reactive species and high power density of plasma generated at atmospheric pressure by used plasma source allowed rapid removal of polymer in preference from the surface of fibers leading to the formation of composite ceramic/polymer fibers. This plasma induced sintering of PAN/Al(NO3)3 can have obvious importance in industrial applications where the ceramic character of surface with higher toughness of the fibers are required.

  14. Palm oil biodiesel synthesized with potassium loaded calcined hydrotalcite and effect of biodiesel blend on elastomer properties

    Energy Technology Data Exchange (ETDEWEB)

    Trakarnpruk, Wimonrat; Porntangjitlikit, Suriya [Petrochemistry and Polymer Science, Department of Chemistry, Faculty of Science, Chulalongkorn University, Bangkok 10330 (Thailand)

    2008-07-15

    Biodiesel was prepared from palm oil by transesterification with methanol in the presence of 1.5%K loaded-calcined Mg-Al hydrotalcite. Fatty acid methyl esters content of 96.9% and methyl ester yield of 86.6% were achieved using a 30:1 methanol to oil molar ratio at 100{sup o}C for 6 h and 7 wt% catalyst. The biodiesel was characterized and its impact on elastomer properties was evaluated. The compatibility of B10 diesel blend (10% biodiesel) with six types of elastomers commonly found in fuel systems (NBR, HNBR, NBR/PVC, acrylic rubber, co-polymer FKM, and terpolymer FKM) were investigated. The physical properties of elastomers after immersion in tested fuels (for 22, 670, and 1008 h at 100{sup o}C) were measured according to American Society of Testing and Materials (ASTM). These include swelling (mass change and volume change), hardness, tensile and elongation, as well as the dynamic mechanical property. The results showed that properties of NBR, NBR/PVC and acrylic rubber were affected more than other elastomers. This is due to the absorption and dissolving of biodiesel by rubber in these samples. Co-polymer FKM and terpolymer FKM which are fluoroelastomers show little property change. (author)

  15. Sorption kinetics and equilibrium for the removal of nickel ions from aqueous phase on calcined Bofe bentonite clay.

    Science.gov (United States)

    Vieira, M G A; Neto, A F Almeida; Gimenes, M L; da Silva, M G C

    2010-05-15

    In this paper the kinetics and dynamics of nickel adsorption on calcined Bofe bentonite clay were studied. The clay was characterized through EDX, surface area (BET) and XRD analysis. The influence of parameters (pH, amount of adsorbent, adsorbate concentration and temperature) was investigated. Kinetic models were evaluated in order to identify potential adsorption process mechanisms. The Langmuir and Freundlich models were utilized for the analysis of adsorption equilibrium. Thermodynamic parameters were assessed as a function of the process temperature. The kinetics data were better represented by the second-order model. The process was found to be strongly influenced by the factors studied. The Bofe clay removed nickel with maximum adsorption capacity of 1.91 mg metal/g of clay (20 degrees C; pH 5.3) and that the thermodynamic data indicated that the adsorption reaction is spontaneous and of an exothermal nature. The Langmuir model provided the best fit for sorption isotherms. Copyright (c) 2009 Elsevier B.V. All rights reserved.

  16. Hydration mechanism and leaching behavior of bauxite-calcination-method red mud-coal gangue based cementitious materials

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Na; Li, Hongxu [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Beijing Key Laboratory of Rare and Precious Metals Green Recycling and Extraction, University of Science and Technology Beijing, Beijing 100083 (China); Liu, Xiaoming, E-mail: liuxm@ustb.edu.cn [School of Metallurgical and Ecological Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Beijing Key Laboratory of Rare and Precious Metals Green Recycling and Extraction, University of Science and Technology Beijing, Beijing 100083 (China)

    2016-08-15

    Highlights: • Nanocrystalline regions in size of ∼5 nm were found in the amorphous C-A-S-H gel. • A hydration model was proposed to clarify the hydration mechanism. • The developed cementitious materials are environmentally acceptable. - Abstract: A deep investigation on the hydration mechanism of bauxite-calcination-method red mud-coal gangue based cementitious materials was conducted from viewpoints of hydration products and hydration heat analysis. As a main hydration product, the microstructure of C-A-S-H gel was observed using high resolution transmission electron microscopy. It was found that the C-A-S-H gel is composed of amorphous regions and nanocrystalline regions. Most of regions in the C-A-S-H gel are amorphous with continuous distribution, and the nanocrystalline regions on scale of ∼5 nm are dispersed irregularly within the amorphous regions. The hydration heat of red mud-coal gangue based cementitious materials is much lower than that of the ordinary Portland cement. A hydration model was proposed for this kind of cementitious materials, and the hydration process mainly consists of four stages which are dissolution of materials, formation of C-A-S-H gels and ettringite, cementation of hydration products, and polycondensation of C-A-S-H gels. There are no strict boundaries among these four basic stages, and they proceed crossing each other. Moreover, the leaching toxicity tests were also performed to prove that the developed red mud-coal gangue based cementitious materials are environmentally acceptable.

  17. Kinetics and Mechanism of NaOH-Impregnated Calcined Oyster Shell-Catalyzed Transesterification of Soybean Oil

    Directory of Open Access Journals (Sweden)

    Han Jin

    2017-11-01

    Full Text Available The objective of this research is to develop a kinetic model to describe the transesterification of soybean oil with methanol using NaOH-impregnated calcined oyster shell (Na-COS. Batch experiments were performed via a two-factor randomized complete block design using a molar ratio of methanol to oil (MR of 6, 12, and 18 and catalyst loadings (CL (mass of catalyst/mass of oil in % of 2%, 4%, 6%, and 8% to obtain fatty acid methyl ester yields. In addition, the catalyst was studied by X-ray diffraction (XRD, X-ray photoelectron spectroscopy (XPS, and time-of-flight secondary ion spectrometry (TOF-SIMS to elucidate the role of the catalyst in the transesterification reaction. XRD and XPS analyses suggested that the formation of sodium peroxide (Na2O2 on the surface contributed to catalytic activity. The TOF-SIMS analysis suggested that the transesterification occurred between adsorbed triglyceride and free methanol, similar to the Eley-Rideal mechanism. The transesterification of adsorbed triglyceride to adsorbed diglyceride was found to be the rate-determining step with a rate constant of 0.0059 ± 0.0002 L mol−1 min−1.

  18. Effect of Calcined Hard Kaolin Dosage on the Strength Development of CPB of Fine Tailings with Sulphide

    Directory of Open Access Journals (Sweden)

    Juanrong Zheng

    2017-01-01

    Full Text Available This study presents the effect of calcined hard kaolin (CHK as replacement (15–50 wt.% to Portland cement (PC on the strength development of cemented paste backfill (CPB of fine tailings containing sulphide. PC is used as binder at 20 wt.% dosage. The results show that CPB sample containing 30 wt.% CHK replacements produces the desired strength and durability (i.e., 26.1% increase in strength over the curing period between 28 d and 360 d. CPB without CHK does not produce the desired strength and durability (i.e., 32.8% losses in strength over the curing period between 90 d and 360 d. The quantity of expansive gypsum of CPB containing 30 wt.% CHK is obviously less than that of CPB without CHK. The porosity of the fine pore for pore diameter < 0.3 μm is obviously higher in CPB containing 30 wt.% CHK than in CPB without CHK, regardless of curing time. It can be concluded that CHK can be suitably exploited for CPB of fine tailings with sulphide to improve the strength and stability in short and long terms.

  19. In Situ IR Characterization of CO Interacting with Rh Nanoparticles Obtained by Calcination and Reduction of Hydrotalcite-Type Precursors

    Directory of Open Access Journals (Sweden)

    F. Basile

    2011-01-01

    Full Text Available Supported Rh nanoparticles obtained by reduction in hydrogen of severely calcined Rh/Mg/Al hydrotalcite-type (HT phases have been characterized by FT-IR spectroscopy of adsorbed CO [both at room temperature (r.t. and nominal liquid nitrogen temperature] and Transmission Electron Microscopy (TEM. The effect of reducing temperature has been investigated, showing that Rh crystal size increases from 1.4 nm to 1.8 nm when the reduction temperature increases from 750°C to 950°C. The crystal growth favours the formation of bridged CO species and linear monocarbonyl species with respect to gem-dicarbonyl species; when CO adsorbs at r.t., CO disproportionation occurs on Rh and it accompanies the formation of RhI(CO2. The role of interlayer anions in the HT precursors to affect the properties of the final materials has been also investigated considering samples prepared from silicate-instead of carbonate-containing precursors. In this case, formation of RhI(CO2 and CO disproportionation do not occur, and this evidence is discussed in terms of support effect.

  20. Effects of Calcination Temperatures on Photocatalytic Activity of Ordered Titanate Nanoribbon/SnO2 Films Fabricated during an EPD Process

    Directory of Open Access Journals (Sweden)

    Li Zhao

    2012-01-01

    Full Text Available Ordered titanate nanoribbon (TNR/SnO2 films were fabricated by electrophoretic deposition (EPD process using hydrothermally prepared titanate nanoribbon as a precursor. The formation mechanism of ordered TNR film on the fluorine-doped SnO2 coated (FTO glass was investigated by scanning electron microscopy (SEM. The effects of calcination temperatures on the phase structure and photocatalytic activity of ordered TNR/SnO2 films were investigated and discussed. The X-ray diffraction (XRD results indicate that the phase transformation of titanate to anatase occurs at 400°C and with increasing calcination temperature, the crystallization of anatase increases. At 600°C, the nanoribbon morphology still hold and the TiO2/SnO2 film exhibits the highest photocatalytic activity due to the good crystallization, unique morphology, and efficient photogenerated charge carriers separation and transfer at the interface of TiO2 and SnO2.

  1. Influence of calcination temperature in pozolanicity of gray sugar cane bagasse; Influencia da temperatura de calcinacao na pozolanicidade da cinza de bagaco de cana-de-acucar (CBCA))

    Energy Technology Data Exchange (ETDEWEB)

    Santos, T.A.; Argolo, R.A.; Andrade, H.M.C.; Ribeiro, D.V., E-mail: tiagoassuncao@hotmail.com [Universidade Federal da Bahia (UFBA), Salvador, BA (Brazil)

    2016-07-01

    BCA (Sugar Cane Bagasse) is burned in boilers in the process of electricity cogeneration causing the generation of CBCA (Gray Sugar Cane Bagasse), which is the final residue of sucroalcooeira industry. Currently, several studies seek alternative materials that can replace Portland cement, promoting discussions on the use of pozzolanic materials in cementitious matrices. Thus, this research seeks to analyze the pozzolanicity the CBCA, obtained by calcining the residue at different temperatures, to be determined by TG / DTG and DTA tests. For analysis of pozzolanicity these ashes were used electrical conductivity techniques, chemical titration NP EN 196-5, chapelle modified NBR 15895/2010 and the IAP method (Activity Index pozzolanic NBR:5752). The results obtained during the study demostraramm no difference between the ash calcined at temperatures of 500 ° C, 600 ° C and 700 ° C. (author)

  2. Superb adsorption capacity of hierarchical calcined Ni/Mg/Al layered double hydroxides for Congo red and Cr(VI) ions

    Energy Technology Data Exchange (ETDEWEB)

    Lei, Chunsheng [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China); College of Environmental & Safety Engineering, Changzhou University, Changzhou 213164 (China); Zhu, Xiaofeng [College of Environmental & Safety Engineering, Changzhou University, Changzhou 213164 (China); Zhu, Bicheng; Jiang, Chuanjia; Le, Yao [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China); Yu, Jiaguo, E-mail: jiaguoyu@yahoo.com [State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070 (China); Department of Physics, Faculty of Science, King Abdulaziz University, Jeddah 21589 (Saudi Arabia)

    2017-01-05

    Highlights: • Ni/Mg/Al layered double hydroxides (NMA-LDHs) synthesized. • NMA-LDHs with hierarchically hollow microsphere structure. • Calcined NMA-LDHs have large adsorption capacities for CR and Cr(VI) ions. - Abstract: The preparation of hierarchical porous materials as catalysts and sorbents has attracted much attention in the field of environmental pollution control. Herein, Ni/Mg/Al layered double hydroxides (NMA-LDHs) hierarchical flower-like hollow microspheres were synthesized by a hydrothermal method. After the NMA-LDHs was calcined at 600 °C, NMA-LDHs transformed into Ni/Mg/Al layered double oxides (NMA-LDOs), which maintained the hierarchical flower-like hollow structure. The crystal phase, morphology, and microstructure of the as-prepared samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy elemental mapping, Fourier transform infrared spectroscopy, and nitrogen adsorption−desorption methods. Both the calcined and non-calcined NMA-LDHs were examined for their performance to remove Congo red (CR) and hexavalent chromium (Cr(VI)) ions in aqueous solution. The maximum monolayer adsorption capacities of CR and Cr(VI) ions over the NMA-LDOs sample were 1250 and 103.4 mg/g at 30 °C, respectively. Thermodynamic studies indicated that the adsorption process was endothermic in nature. In addition, the addition of coexisting anions negatively influenced the adsorption capacity of Cr(VI) ions, in the following order: CO{sub 3}{sup 2−} > SO{sub 4}{sup 2−} > H{sub 2}PO{sub 4}{sup −} > Cl{sup −}. This work will provide new insight into the design and fabrication of advanced adsorption materials for water pollutant removal.

  3. Choice of precipitant and calcination temperature of precursor for synthesis of NiCo2O4 for control of CO-CH4 emissions from CNG vehicles.

    Science.gov (United States)

    Trivedi, Suverna; Prasad, Ram

    2018-03-01

    Compressed natural gas (CNG) is most appropriate an alternative of conventional fuel for automobiles. However, emissions of carbon-monoxide and methane from such vehicles adversely affect human health and environment. Consequently, to abate emissions from CNG vehicles, development of highly efficient and inexpensive catalysts is necessary. Thus, the present work attempts to scan the effects of precipitants (Na 2 CO 3 , KOH and urea) for nickel cobaltite (NiCo 2 O 4 ) catalysts prepared by co-precipitation from nitrate solutions and calcined in a lean CO-air mixture at 400°C. The catalysts were used for oxidation of a mixture of CO and CH 4 (1:1). The catalysts were characterized by X-ray diffractometer, Brunauer-Emmett-Teller surface-area, X-ray photoelectron spectroscopy; temperature programmed reduction and Scanning electron microscopy coupled with Energy-Dispersive X-Ray Spectroscopy. The Na 2 CO 3 was adjudged as the best precipitant for production of catalyst, which completely oxidized CO-CH 4 mixture at the lowest temperature (T 100 =350°C). Whereas, for catalyst prepared using urea, T 100 =362°C. On the other hand the conversion of CO-CH 4 mixture over the catalyst synthesized by KOH limited to 97% even beyond 400°C. Further, the effect of higher calcination temperatures of 500 and 600°C was examined for the best catalyst. The total oxidation of the mixture was attained at higher temperatures of 375 and 410°C over catalysts calcined at 500 and 600°C respectively. Thus, the best precipitant established was Na 2 CO 3 and the optimum calcination temperature of 400°C was found to synthesize the NiCo 2 O 4 catalyst for the best performance in CO-CH 4 oxidation. Copyright © 2017. Published by Elsevier B.V.

  4. ICPP calcined solids storage facility closure study. Volume II: Cost estimates, planning schedules, yearly cost flowcharts, and life-cycle cost estimates

    International Nuclear Information System (INIS)

    1998-02-01

    This document contains Volume II of the Closure Study for the Idaho Chemical Processing Plant Calcined Solids Storage Facility. This volume contains draft information on cost estimates, planning schedules, yearly cost flowcharts, and life-cycle costs for the four options described in Volume I: (1) Risk-Based Clean Closure; NRC Class C fill, (2) Risk-Based Clean Closure; Clean fill, (3) Closure to landfill Standards; NRC Class C fill, and (4) Closure to Landfill Standards; Clean fill

  5. Effect of calcination temperature on the photocatalytic activity of TiO2 powders prepared by co-precipitation of TiCl3

    International Nuclear Information System (INIS)

    Yudoyono, Gatut; Ichzan, Nur; Zharvan, Vicran; Daniyati, Rizqa; Santoso, Hadi; Indarto, Bachtera; Pramono, Yono Hadi; Zainuri, Mochamad; Darminto

    2016-01-01

    The adsorption of basic dye methylene blue (MB) onto titanium dioxide (titania) powder that were prepared by coprecipitation method of TiCl 3 and NH 4 OH as iniatial material with different calcination temperature was studied to examine the photocatalytic activity. Synthesis process carried out by the solution pH was adjusted to be 8. Effect of calcination temperature on the titania powder were characterized with Differential Scanning Calorimetry/Thermogravimetry (DSC/TG), X-ray diffraction (XRD), and Scanning Electron Microscopy (SEM). The result of TG and XRD showed that the NH 4 Cl decomposed between 235-372°C. The XRD result showed that the anatase TiO 2 only contained a single phase when the calcination temperature of the precursor at 800°C, and over which it began to grow rutile phase. The influence of synthesis condition on the photocatalytic activity of TiO 2 powder was determined by the photodegradation of MB dye under UV light.

  6. Effect of calcination temperature on the crystallite growth of cerium oxide nano-powders prepared by the co-precipitation process

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Jian-Chih [Department of Orthopaedics, Kaohsiung Medical University Hospital, Kaohsiung 807, Taiwan (China); Chen, Wen-Cheng [School of Dentistry, College of Dental Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan (China); Tien, Yin-Chun [Department of Orthopaedics, Kaohsiung Medical University Hospital, Kaohsiung 807, Taiwan (China); Shih, Chi-Jen, E-mail: cjshih@kmu.edu.t [Department of Fragrance and Cosmetics Science, Kaohsiung Medical University, 100 Shi-Chuan1st Road, Kaohsiung 80708, Taiwan (China)

    2010-04-30

    Cerium oxide nanocrystallites were synthesized by a co-precipitation process at a relatively low temperature, using cerium (III) nitrate as the starting material in a water solution with pH in the range of 8-9. The effect of calcination temperature on the crystallite growth of cerium oxide nano-powders was investigated by X-ray diffraction, transmission electron microscopy and electron diffraction. The crystallization temperature of the cerium oxide powders was estimated to be about 273 K, by XRD analysis. When calcined at temperatures from 473 to 1273 K, face-centered cubic phase crystallization was observed by XRD. The crystallite size of the cerium oxide increased from 12.0 to 48 nm as the calcining temperature increased from 473 to 1273 K, in the pH range 8-9. The activation energy for the growth of cerium oxide nanoparticles was found to have very low values of 17.5 kJ/mol for pH = 8 and 16.0 kJ/mol for pH = 9.

  7. Formation of Rosette-Shaped Cd(II) Thiolate Coordination Polymer in Aqueous Solution and Conversion to CdS by Calcination

    International Nuclear Information System (INIS)

    Han, Sung June; Lee, Myung Han; Jeon, Young Jin

    2010-01-01

    We have synthesized rosette-shaped Cd-MSA CPs by a reaction between Cd(II) ions and MSA in aqueous solution and calcined the obtained CPs to obtain CdS microstructures. Upon calcination, the morphology of the CPs does not undergo any significant change, but the particle diameter decreases by 74%. This indicates that our strategy can be used for the synthesis of CPs from other metal thiolates as well. We expect this strategy to be suitable for the preparation of important metal chalcogenide nanostructures and microstructures that can be used in future applications. Coordination polymers (CPs) have attracted considerable attention because of their potential applications in gas storage, catalysis, ion exchange, separation, biomedicine, etc. For use in the above mentioned applications, the structure and morphology of these CPs have been controlled by judicious choice of metals, ligands, and reaction conditions. Recently, Oh and coworkers have reported that CPs can be successfully converted into metal oxides by calcination without causing any significant change in their morphology

  8. Repetitive carbonation-calcination reactions of Ca-based sorbents for efficient CO{sub 2} sorption at elevated temperatures and pressures

    Energy Technology Data Exchange (ETDEWEB)

    Kuramoto, K.; Fujimoto, S.; Morita, A.; Shibano, S.; Suzuki, Y.; Hatano, H.; Lin, S.Y.; Harada, M.; Takarada, T. [National Institute of Advanced Industrial Science and Technology, Tsukaba (Japan). Clean Fuel Research Group

    2003-03-05

    In an effort to develop a novel hydrogen production process in which coal is gasified with high-pressure steam in the presence of CO{sub 2} sorbents, the fundamental CO{sub 2} sorption characteristics of Ca-based sorbents during repetitive carbonation-calcination reactions at different pressures were investigated using a conventional TG/DTA analyzer and a laboratory-scale horizontal-tube reactor. The results revealed that, as a result of sintering and crystal growth, Ca-based sorbents were significantly deactivated by high-temperature calcination treatment. As a consequence, the CO{sub 2} uptake capacity of the sorbents decreased with cycle number under both atmospheric and pressurized conditions. An intermediate hydration treatment was found to enhance the reactivity and durability of the sorbents for multicycle CO{sub 2} sorption. Because of the presence of eutectics in the CaO-Ca(OH){sub 2}-CaCO{sub 3} ternary system, the formation of sorbent melts was observed in repetitive calcination-hydration-carbonation reactions at elevated pressures at 923 and 973 K. Even under eutectic conditions, the sorbents retained their high reactivity for CO{sub 2} sorption.

  9. Hot gas cleaning and upgrading with a calcined dolomite located downstream a biomass fluidized bed gasifier operating with steam-oxygen mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Perez, P.; Aznar, M.P.; Caballero, M.A.; Gil, J.; Martin, J.A.; Corella, J. [University of Zaragoza, Zaragoza (Spain). Dept. of Chemical and Environmental Engineering

    1997-11-01

    Cleaning and upgrading of the hot raw gas from a biomass gasifier, bubbling fluidized bed type, is studied at small pilot plant scale (10 kg biomass fed/h) using a calcined dolomite located downstream from the gasifier. Gasification is made with steam-oxygen mixtures at 800-850{degree}C and atmospheric pressure. Main variables studied are the gas residence time in the bed of dolomite and the gas atmosphere composition, which depends on the gasifying agent (H{sub 2}O + O{sub 2})-to-biomass and H{sub 2}O/O{sub 2} ratios. H{sub 2} and CO content in the flue gas increases by 16-23 vol% and decrease by 15-22 vol % (dry basis), respectively. Although CH{sub 4} conversion (elimination) higher than 30 vol % has never been reached, tar conversion (elimination) of 90-95 vol% are obtained with space times of 0.06 - 0.15 kg calcined dolomite h{sup -1} m{sup -3}. A detailed study is here presented on how the calcined dolomite significantly cleans and upgrades the flue gas, increasing also the gas yield by 0.15-0.40 m{sup 3} (STP)/kg daf biomass fed. 14 refs., 20 figs., 3 tabs.

  10. Impact of natural and calcined starfish (Asterina pectinifera) on the stabilization of Pb, Zn and As in contaminated agricultural soil.

    Science.gov (United States)

    Lim, Jung Eun; Sung, Jwa Kyung; Sarkar, Binoy; Wang, Hailong; Hashimoto, Yohey; Tsang, Daniel C W; Ok, Yong Sik

    2017-04-01

    Metal stabilization using soil amendments is an extensively applied, economically viable and environmentally friendly remediation technique. The stabilization of Pb, Zn and As in contaminated soils was evaluated using natural starfish (NSF) and calcined starfish (CSF) wastes at different application rates (0, 2.5, 5.0 and 10.0 wt%). An incubation study was conducted over 14 months, and the efficiency of stabilization for Pb, Zn and As in soil was evaluated by the toxicity characteristic leaching procedure (TCLP) test. The TCLP-extractable Pb was reduced by 76.3-100 and 91.2-100 % in soil treated with NSF and CSF, respectively. The TCLP-extractable Zn was also reduced by 89.8-100 and 93.2-100 % in soil treated with NSF and CSF, respectively. These reductions could be associated with the increased metal adsorption and the formation of insoluble metal precipitates due to increased soil pH following application of the amendments. However, the TCLP-extractable As was increased in the soil treated with NSF, possibly due to the competitive adsorption of phosphorous. In contrast, the TCLP-extractable As in the 10 % CSF treatment was not detectable because insoluble Ca-As compounds might be formed at high pH values. Thermodynamic modeling by visual MINTEQ predicted the formation of ettringite (Ca 6 Al 2 (SO 4 ) 3 (OH) 12 ·26H 2 O) and portlandite (Ca(OH) 2 ) in the 10 % CSF-treated soil, while SEM-EDS analysis confirmed the needle-like structure of ettringite in which Pb was incorporated and stabilized in the 10 % CSF treatment.

  11. The effect of calcinated calcium and chlorine treatments on Escherichia coli O157:H7 87-23 population reduction in radish sprouts.

    Science.gov (United States)

    Fransisca, Lilia; Zhou, Bin; Park, Heekyung; Feng, Hao

    2011-08-01

    The effect of calcinated calcium spray on Escherichia coli O157:H7 87-23 population reduction during radish sprout production was studied. Artificially inoculated radish seeds were soaked in sodium hypochlorite (NaOCl) solutions (200 and 20000 ppm), rinsed in distilled water, and sprayed with water or a calcinated calcium solution during sprouting. Microbial plate count was obtained at each step of the process and germination rate was determined after 72 h of sprouting. Scanning electron microscopy (SEM) was done on treated seeds and sprouts to locate which parts were populated by the E. coli cells. The results showed that the active compound in the calcinated calcium was calcium oxide. The treatment of 200 ppm NaOCl soaking followed by 0.04% calcinated calcium spray resulted in no microbial growth after a 72-h sprouting, while maintaining a high germination rate. The 0.4% calcinated calcium spray significantly reduced the germination rate and is therefore not recommended. Soaking the seeds in a 20000 ppm chlorine solution achieved the highest E. coli count reduction (1.65 log CFU/g). However, the E. coli cells that survived the 20000 ppm chlorine soak grew to 6 log CFU/g sprouts after a 72-h sprouting, significantly higher than the initial count on the seeds. The SEM microimages showed that the bacteria were mostly located in the roots of the radish sprouts and all across the seed surface. The E. coli O157:H7 87-23 cells appeared to be located in biofilms or embedded into the radish sprout tissues during sprouting. The seed sanitation treatment with 20000 ppm chlorine solution that is currently used by the sprout industry was once again found to be ineffective in eliminating inoculated pathogenic cells. More importantly, the remaining cells that have survived the chlorine wash would grow during sprouting to reach an alarmingly high cell concentration. The new observation of E. coli cells and sprout tissue interaction manifested as embedding

  12. Effect of calcination temperature on structure and photocatalytic activity under UV and visible light of nanosheets from low-cost magnetic leucoxene mineral

    Science.gov (United States)

    Charerntanom, Wissanu; Pecharapa, Wisanu; Pavasupree, Suttipan; Pavasupree, Sorapong

    2017-07-01

    This research has experimentally synthesized the nanosheets from the naturally-mineral magnetic leucoxene under the hydrothermal synthesis condition of 105 °C for 24 h. Magnetic leucoxene was utilized as the starting material due to its high TiO2 content (70-80%) and inexpensiveness. The characterization of the synthesized nanosheets was subsequently carried out: the crystalline structure, the chemical composition, the shape, the size and the specific surface area, by the X-ray diffraction (XRD), X-ray fluorescence (XRF), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Brunauer-Emmett-Teller (BET) specific surface area analysis. The analysis results indicated that the starting magnetic leucoxene is of rutile phase while the synthesized nanosheets are of titanate structure (H2TixO2x + 1). After calcination at the temperature range of 300 and 400 °C, the calcined samples demonstrated TiO2 (B). At 500 and 600 °C, the calcined nanosheets revealed a bi-crystalline mixture consisting of TiO2 (B) and anatase TiO2. At 700-1000 °C, the crystalline structure shows anatase and rutile phase. At 1100 °C, the prepared samples consisted of a mixture of anatase, rutile phase of TiO2, and Fe2O3 phase. The synthesized product also exhibited the flower-like morphology with 2-5 μm in diameter, and the nanosheets structure was slightly curved, with 100 nm to 2 μm in width and 1-3 nm in thickness. At 100-200 °C showed sheets-like structure. At 300-1100 °C, the calcined nanosheets became unstable and began to decompose and transform into nanoparticles. The increasing size of nanoparticle decreased the specific surface area of the nanosheets, caused by increasing calcination temperature. Furthermore, the BET specific surface area of the nanosheets was approximately 279.8 m2/g. More importantly, the synthesized nanosheets achieved the higher photocatalytic activity under UV and visible light than did the commercial TiO2 nanoparticles (JRC-01, JRC-03

  13. Role of Mg{sub x}Ca{sub 1−x}CO{sub 3} on the physical–chemical properties and cyclic CO{sub 2} capture performance of dolomite by two-step calcination

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Ke; Han, Dongtai, E-mail: handongtai@cumt.edu.cn; Zhao, Pengfei, E-mail: zhaopfcumt@163.com; Hu, Xiumeng; Yin, Zeguang; Wu, Di

    2015-08-20

    Highlights: • Two-step calcination treated dolomite sorbent was prepared and characterized. • An intermediate phase (Mg{sub x}Ca{sub 1−x}CO{sub 3}) was observed by TG and XRD results. • Mg-calcite hindered the de-mixing of Ca and Mg. • Smaller grains, larger specific surface area and pore volume were obtained. • This favorable structure resulted in a high and stable CO{sub 2} capture performance. - Abstract: Two-step calcination (CO{sub 2} and N{sub 2} atmospheres) was used to modify the microstructure of natural dolomite for high-temperature CO{sub 2} capture. Two other one-step calcinations (CO{sub 2} or N{sub 2} atmosphere) were provided for comparison. Different morphological characterizations (thermal decomposition, phase composition, morphology, and nitrogen adsorption) were performed, followed by an analysis of 30 carbonation/calcination cycles in a fixed bed reactor. During primary calcination in a CO{sub 2} atmosphere, an intermediate phase (Mg{sub x}Ca{sub 1−x}CO{sub 3}) was observed by TG and XRD results, which hindered the de-mixing of CaO and MgO in the secondary calcination in a N{sub 2} atmosphere. Therefore, two-step calcination produced smaller grains (CaO: 45.2 nm; MgO: 32.6 nm), larger specific surface area (21.08 m{sup 2}/g) and pore volume (0.082 cm{sup 3}/g) and uniform distribution of CaO and MgO, which resulted in a higher and more stable uptake of CO{sub 2} compared to the results from one-step calcinations.

  14. Rheology and zeta potential of cement pastes containing calcined silt and ground granulated blast-furnace slag

    Directory of Open Access Journals (Sweden)

    Safi, B.

    2011-09-01

    Full Text Available This study aimed to analyse the re-use of dam silt as a supplementary binder for self-compacting concrete (SCC. When burnt, silt becomes more reactive because the kaolin it contains is converted into metakaolin. Portland cement, calcined or burnt silt and ground granulated blast furnace slag were used in this research. Cement pastes were prepared with blends containing two or three of these materials. The replacement ratio for burnt silt in both cases was 10 % and 20 % by cement weight and the ratio for the slag was a constant 30 % by weight of the blend. Rheological and zeta potential tests were conducted to evaluate paste electrokinetics and rheological behaviour. The findings showed that burnt silt is apt for use as an addition to cement for SCC manufacture.

    En el presente trabajo se ha analizado la posibilidad de utilizar los lodos procedentes de embalses como adición en la fabricación del hormigón autocompactante (HAC. Con la calcinación, estos materiales se vuelven más reactivos debido a la transformación en metacaolín, del caolín que forma parte de su composición. Las materias primas empleadas en esta investigación son: cemento Pórtland, lodos de embalse calcinados y escorias granuladas de horno alto. Se prepararon pastas de cemento con mezclas que contenían dos o tres de estos materiales. El porcentaje de reemplazo de los lodos calcinados osciló entre el 10 y el 20 % en peso del cemento, mientras que el de la escoria fue del 30 % en peso de la mezcla. Se llevaron a cabo ensayos reológicos y de potencial zeta para evaluar el comportamiento electrocinético y reológico de las distintas pastas. De acuerdo con los resultados obtenidos, una vez calcinados, los lodos de embalse son aprovechables como adición al cemento con destino a la preparación de HAC.

  15. Effect of metal ratio and calcination temperature of chromium based mixed oxides catalyst on FAME density from palm fatty acid distillate

    Science.gov (United States)

    Wan, Z.; Fatimah, S.; Shahar, S.; Noor, A. C.

    2017-09-01

    Mixed oxides chromium based catalysts were synthesized via sol-gel method for the esterification of palm fatty acid distillate (PFAD) to produce fatty acid methyl ester (FAME). The reactions were conducted in a batch reactor at reaction temperature of 160 °C for 4 h and methanol to PFAD molar ratio of 3:1. The effects of catalyst preparation conditions which are the mixed metal ratio and calcination temperature were studied. The various metal ratio of Cr:Mn (1:0, 0:1, 1:1, 1:2 and 2:1) and Cr:Ti (0:1, 1:1, 1:2 and 2:1) resulted in FAME density ranges from 1.041 g/cm3 to 0.853 g/cm3 and 1.107 g/cm3 to 0.836 g/cm3, respectively. The best condition catalyst was found to be Cr:Ti metal ratio of 1:2 and Cr:Mn metal ratio of 1:1. The calcination temperature of the mixed oxides between 300 °C to 700°C shows effect on the FAME density obtained in the reaction. The calcination at 500°C gave the lowest FAME density of 0.836 g/cm3 and 0.853 g/cm3 for Cr:Ti and Cr:Mn mixed oxides, respectively. The density of FAME is within the value range of the biodiesel fuel property. Thus, mixed oxides of Cr-Ti and Cr-Mn have good potentials as heterogeneous catalyst for FAME synthesis from high acid value oils such as PFAD.

  16. Superb adsorption capacity of hierarchical calcined Ni/Mg/Al layered double hydroxides for Congo red and Cr(VI) ions.

    Science.gov (United States)

    Lei, Chunsheng; Zhu, Xiaofeng; Zhu, Bicheng; Jiang, Chuanjia; Le, Yao; Yu, Jiaguo

    2017-01-05

    The preparation of hierarchical porous materials as catalysts and sorbents has attracted much attention in the field of environmental pollution control. Herein, Ni/Mg/Al layered double hydroxides (NMA-LDHs) hierarchical flower-like hollow microspheres were synthesized by a hydrothermal method. After the NMA-LDHs was calcined at 600°C, NMA-LDHs transformed into Ni/Mg/Al layered double oxides (NMA-LDOs), which maintained the hierarchical flower-like hollow structure. The crystal phase, morphology, and microstructure of the as-prepared samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy elemental mapping, Fourier transform infrared spectroscopy, and nitrogen adsorption-desorption methods. Both the calcined and non-calcined NMA-LDHs were examined for their performance to remove Congo red (CR) and hexavalent chromium (Cr(VI)) ions in aqueous solution. The maximum monolayer adsorption capacities of CR and Cr(VI) ions over the NMA-LDOs sample were 1250 and 103.4mg/g at 30°C, respectively. Thermodynamic studies indicated that the adsorption process was endothermic in nature. In addition, the addition of coexisting anions negatively influenced the adsorption capacity of Cr(VI) ions, in the following order: CO 3 2- >SO 4 2- >H 2 PO 4 - >Cl - . This work will provide new insight into the design and fabrication of advanced adsorption materials for water pollutant removal. Copyright © 2016 Elsevier B.V. All rights reserved.

  17. The Influence of Calcined Clay Pozzolan, Low-Cao Steel Slag and Granite Dust On the Alkali-Silica Reaction in Concrete

    OpenAIRE

    James Sarfo-Ansah; Eugene Atiemo

    2015-01-01

    The influence of low CaO steel slag, calcined clay and granite dust on the alkali-silica reaction was investigated over a period of 35 days under accelerated curing conditions. The mineral admixtures were used to replace varying portions of high alkali Portland limestone cement up to an admixture content of 25% in order to study their effect on the alkali-silica reaction (ASR). Portland limestone cement used for the study had a total Na2Oeq of 4.32. XRD analysis of hydrated mortar...

  18. Fall Semiannual Report for the HWMA/RCRA Post Closure Permit for the INTEC Waste Calcining Facility at the INL Site

    Energy Technology Data Exchange (ETDEWEB)

    D. F. Gianotto

    2007-01-12

    The Waste Calcining Facility (WCF) is located at the Idaho Nuclear Technology and Engineering Center. In 1998, the WCF was closed under an approved Hazardous Waste Management Act/Resource Conservation and Recovery Act (HWMA/RCRA) Closure Plan. Vessels and spaces were grouted and then covered with a concrete cap. The Idaho Department of Environmental Quality issued a final HWMA/RCRA post-closure permit on September 15, 2003, with an effective date of October 16, 2003. This permit sets forth procedural requirements for groundwater characterization and monitoring, maintenance, and inspections of the WCF to ensure continued protection of human health and the environment.

  19. Structual evolution during calcination and sintering of a (La0.6Sr0.4)0.99CoO3-δ nanofiber prepared by electrospinning

    DEFF Research Database (Denmark)

    Simonsen, Søren Bredmose; Shao, Jing; Zhang, Wenjing (Angela)

    2017-01-01

    Design of 3-dimensional metal oxide nanofibers by electrospinning is being widely explored. However, the impacts of calcination and sintering on the resulting morphology remain unknown. For the first time, (La0.6Sr0.4)0.99CoO3-δ(LSC) nanofiber, which is among the most promising electrode materials...... for solid oxide fuel cells, was synthesized by sol-gel electrospinning. By elevating the temperature in oxygen using in situ transmission electron microscopy, we discovered the structural transitions from nanofibers to nanotubes and then to nano-pearl strings. This facile and up-scalable method can...

  20. Particle morphology and magnetic properties of Ba{sub 0.5}Sr{sub 0.5}Fe{sub 12}O{sub 19} powder calcined conventionally and by microwave heating

    Energy Technology Data Exchange (ETDEWEB)

    Kanagesan, S., E-mail: kanagu1980@gmail.com [Materials Synthesis and Characterization Laboratory (MSCL), Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, Serdang 43400, Selangor (Malaysia); Hashim, M. [Materials Synthesis and Characterization Laboratory (MSCL), Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, Serdang 43400, Selangor (Malaysia); Physics Department, Faculty of Science, Universiti Putra Malaysia, Serdang 43400, Selangor (Malaysia); Jesurani, S. [Department of Physics, Jeyaraj Annapackium College for Women, Periyakulam 625601, Tamil Nadu (India); Kalaivani, T. [Center for material science and Nano Devices, Department of Physics, SRM University, Kattankulathur 603203, Tamil Nadu (India); Ismail, I.; Shafie, M.S.E. [Materials Synthesis and Characterization Laboratory (MSCL), Institute of Advanced Technology (ITMA), Universiti Putra Malaysia, Serdang 43400, Selangor (Malaysia)

    2012-12-05

    Highlights: Black-Right-Pointing-Pointer Synthesis of Ba{sub 0.5}Sr{sub 0.5}Fe{sub 12}O{sub 19} by sol-gel technique. Black-Right-Pointing-Pointer Crystallization temperature is reduced to 900 Degree-Sign C due to the addition of D-Fructose. Black-Right-Pointing-Pointer Results of conventional and microwave calcined samples are reported. - Abstract: Barium strontium hexaferrite (Ba{sub 0.5}Sr{sub 0.5}Fe{sub 12}O{sub 19}-BSF) has been prepared by sol-gel process involving use of D-Fructose as a fuel. The prepared precursor was calcined in two different calcinations techniques conventional and microwave furnace. X-ray powder diffraction studies confirmed the formation of single phase Ba{sub 0.5}Sr{sub 0.5}Fe{sub 12}O{sub 19}. HR-SEM results show the morphology of the particles is hexagonal structures in platelet form. The average particle size of conventionally calcined BSF powder is 100-250 nm and that of microwave calcined powder is 30-100 nm. The broad hysteresis loop reveals that powder is well crystallized and exhibits hard magnetic properties.

  1. Fabrication of TiO2 nanorods/nanosheets photoelectrode on Ti mesh by hydrothermal method for degradation of methylene blue:influence of calcination temperature

    Science.gov (United States)

    Deng, Xiaoyong; Ma, Qiuling; Cui, Yuqi; Cheng, Xiuwen; Cheng, Qingfeng

    2017-10-01

    In the study, Using the strategy of hydrothermal reaction followed by annealing at different temperatures, TiO2 nanorods/nanosheets (NRs/NSs) photoelectrodes with diverse microcosmic morphologies and crystal structures were successfully fabricated. Moreover, all samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM) and Ultraviolet-visible diffuse reflectance spectroscopy (UV-vis DRS). Meanwhile the photoelectrochemical (PECH) properties were recorded through open circuit potential (OCP) and electrochemical impedance spectroscopy (EIS) curves. The photocatalytic (PC) activity of TiO2 NRs/NSs photoelectrodes were further measured by methylene blue (MB) degradation. Results suggest that the nanosheets possessed the width and thickness in the range of 100-400 and 10-20 nm, and the nanorods possessed the diameter in the range of around 10-20 nm, respectively. Also, the TiO2 NRs/NSs photoelectrode calcined at 500 °C exhibited the best proportion of both nanosheets and nanorods and higher photocatalytic activity (73.56%) than those of other TiO2 NRs/NSs photoelectrodes within 150 min under visible light illumination, which was ascribed to higher photoproduction electrons-holes (e/h+) pairs separation and visible light absorption. Therefore, the calcination temperature plays a significant role in altering the morphology and crystal structure of TiO2 NRs/NSs photoelectrode, and then enhanced PC performance.

  2. The Synergistic Effect of Nitrogen Dopant and Calcination Temperature on the Visible-Light-Induced Photoactivity of N-Doped TiO2

    Directory of Open Access Journals (Sweden)

    Yao-Tung Lin

    2013-01-01

    Full Text Available The synergistic effect of nitrogen content and calcinations temperature on the N-doped TiO2 catalysts prepared by sol-gel method was investigated. The phase and structure, chemical state, optical properties, and surface area/pore distribution of N-doped TiO2 were characterized using X-ray diffraction spectrometer, high-resolution transmission electron microscope, X-ray photoelectron spectroscopy, UV-vis diffusion reflectance spectroscopy, and Brunauer-Emmett-Teller specific surface area. Finding showed that the photocatalytic activity of N-doped TiO2 was greatly enhanced compared to pure TiO2 under visible irradiation. N dopants could retard the transformation from anatase to rutile phase. Namely, N-doping effect is attributed to the anatase phase stabilization. The results showed nitrogen atoms were incorporated into the interstitial positions of the TiO2 lattice. Ethylene was used to evaluate the photocatalytic activity of samples under visible-light illumination. The results suggested good anatase crystallization, smaller particle size, and larger surface are beneficial for photocatalytic activity of N-doped TiO2. The N-doped TiO2 catalyst prepared with ammonia to titanium isopropoxide molar ratio of 2.0 and calcinated at 400°C showed the best photocatalytic ability.

  3. Morphological Changes of Limestone Sorbent Particles during Carbonation/Calcination Looping Cycles in a Thermogravimetric Analyzer (TGA) and Reactivation with Steam

    KAUST Repository

    Wu, Y.

    2010-04-15

    Carbonation and calcination looping cycles were carried out on four limestones in a thermogravimetric analyzer (TGA). The CO2 carrying capacity of a limestone particle decays very quickly in the first 10 cycles, reducing to about 20% of its original uptake capacity after 10 cycles for the four limestones studied in this work, and it decreases further to 6-12% after 50 cycles. A new steam reactivation method was applied on the spent sorbent to recover the loss of reactivity. The steam reactivation of multi-cycled samples was conducted at atmospheric pressure. Steam reactivation for 5 min at 130 °C of particles that had undergone 10 cycles resulted in an immediate increase (by 45-60% points) in carrying capacity. The morphological changes of limestone particles during the cycling and steam reactivation were studied using both an optical microscope and scanning electron microscopy (SEM). The diameters of limestone particles shrank by about 2-7% after 10 carbonation/calcination cycles, and the particle diameters swelled significantly (12-22% increase) after steam reactivation. These size changes are important for studies of attrition and mathematical modeling of carbonation. © 2010 American Chemical Society.

  4. Investigation of the possibility of copper removal from industrial leachate by raw and calcined phosphogypsum: D-optimal and Taguchi designs

    Energy Technology Data Exchange (ETDEWEB)

    Mesci, Basak [Engineering Faculty, Department of Material Science and Engineering, Ondokuz Mayis University, Kurupelit, Samsun (Turkey); Turan, Nurdan Gamze [Engineering Faculty, Department of Environmental Engineering, Ondokuz Mayis University, Kurupelit, Samsun (Turkey); Ozgonenel, Okan [Engineering Faculty, Department of Electric and Electronic Engineering, Ondokuz Mayis University, Kurupelit, Samsun (Turkey)

    2012-08-15

    In the present study, the removal of Cu(II) was evaluated by raw and calcined phosphogypsum (PG) as an industrial product. The role of experimental factors on the removal of Cu(II) was examined by using D-optimal and Taguchi designs. The experimental factors and their related levels were selected as initial pH of 3-6-8, adsorbent content of 5, 10, and 25 g L{sup -1}, contact time of 5, 10, and 20 min, and temperature of 20, 40, and 60 C. The results are evaluated by ANOVA test to extract important experimental factors and their levels. The performances of the suggested factorial designs were then compared and regression models that took into account the significant main and interaction effects were suggested. Taguchi design was found as a reliable solution with less number of experiments for adsorption studies with the optimized values. The resultant removal efficiency is calculated as 78.34%. The results revealed that calcined PG is an appropriate adsorbent for Cu(II) removal from leachate of industrial waste. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  5. Adsorptive performance of un-calcined sodium exchanged and acid modified montmorillonite for Ni2+ removal: Equilibrium, kinetics, thermodynamics and regeneration studies

    International Nuclear Information System (INIS)

    Ijagbemi, Christianah Olakitan; Baek, Mi-Hwa; Kim, Dong-Su

    2010-01-01

    The efficacy of un-calcined sodium exchanged (Na-MMT) and acid modified montmorillonite (A-MMT) has been investigated for adsorptive removal of Ni 2+ from aqueous solution. Physico-chemical parameters such as pH, initial Ni 2+ concentration, and equilibrium contact time were studied in a series of batch adsorption experiments. The equilibrium time of contact for both adsorbents was about 230 min. The Redlich-Peterson model best described the equilibrium sorption of Ni 2+ onto Na-MMT and the Dubinin-Radushkevich model was the best model in predicting the equilibrium sorption of Ni 2+ onto A-MMT. The kinetics of Ni 2+ uptake by Na-MMT and A-MMT followed the pseudo second-order chemisorption mechanism. Sorptions of Ni 2+ onto Na-MMT and A-MMT were spontaneous and endothermic. Regeneration was tried for several cycles with a view to recover the adsorbed Ni 2+ and also to restore Na-MMT and A-MMT to their original states. The un-calcined Na-MMT and A-MMT have adsorptive potentials for removal of Ni 2+ from aqueous bodies.

  6. Transesterification of edible, non-edible and used cooking oils for biodiesel production using calcined layered double hydroxides as reusable base catalysts.

    Science.gov (United States)

    Sankaranarayanan, Sivashunmugam; Antonyraj, Churchil A; Kannan, S

    2012-04-01

    Fatty acid methyl esters (FAME) were produced from edible, non-edible and used cooking oils with different fatty acid contents by transesterification with methanol using calcined layered double hydroxides (LDHs) as solid base catalysts. Among the catalysts, calcined CaAl2-LDH (hydrocalumite) showed the highest activity with >90% yield of FAME using low methanol:oil molar ratio (<6:1) at 65 °C in 5 h. The activity of the catalyst was attributed to its high basicity as supported by Hammett studies and CO(2)-TPD measurements. The catalyst was successfully reused in up to four cycles. Some of the properties such as density, viscosity, neutralization number and glycerol content of the obtained biodiesel matched well with the standard DIN values. It is concluded that a scalable heterogeneously catalyzed process for production of biodiesel in high yields from a wide variety of triglyceride oils including used oils is possible using optimized conditions. Copyright © 2012 Elsevier Ltd. All rights reserved.

  7. The influence of calcination temperatures on the acid-based properties and catalytic activity for the 1,3-butadiene synthesis from ethanol/acetaldehyde mixture

    Science.gov (United States)

    Gao, Meixiang; Jiang, Haoxi; Zhang, Minhua

    2018-05-01

    The influences of the calcination temperature on the catalysts' acid-based properties and catalytic activity for the 1,3-butadiene synthesis from ethanol are investigated. The results show that the 2 wt% ZrO2/Nano-SiO2 calcined at 773 K shows the best performance with the selectivity of 93.18% and conversion of 58.52% when reacted at 593 K, a WHSV of 1.8 h-1 and 3.5:1 volume ratio ethanol-to-acetaldehyde in an atmospheric fixed-bed reactor. Prepared catalysts were characterized by N2 adsorption-desorption, XRD, temperature-programmed desorption of NH3 and CO2, FTIR spectroscopy of adsorbed pyridine and CO2. Based on the relationship between the catalyst activity and its properties, the fact can be presumed that the formation and strength of Zrsbnd Osbnd Si bond determines the acid-based properties of the catalyst. In addition, moderate-intensity weak acid-basic sites are more suitable for ethanol conversion to BD with the amount of acid and basic sites as close as possible.

  8. Direct fabrication of 238PuO2 fuel forms

    International Nuclear Information System (INIS)

    Burney, G.A.; Congdon, J.W.

    1982-07-01

    The current process for the fabrication of 238 PuO 2 heat sources includes precipitation of small particle plutonium oxalate crystals (4 to 6 μm diameter), a calcination to PuO 2 , ball milling, cold pressing, granulation (60 to 125 μm), and granule sintering prior to hot pressing the fuel pellet. A new two-step direct-strike Pu(III) oxalate precipitation method which yields mainly large well-developed rosettes (50 to 100 μm diameter) has been demonstrated in the laboratory and in the plant. These large rosettes are formed by agglomeration of small (2 to 4 μm) crystals, and after calcining and sintering, were directly hot pressed into fuel forms, thus eliminating several of the powder conditioning steps. Conditions for direct hot pressing of the large heat-treated rosettes were determined and a full-scale General Purpose Heat Source pellet was fabricated. The pellet had the desired granule-type microstructure to provide dimensional stability at high temperature. 27 figures

  9. Thermal denitration of high concentration nitrate salts waste water

    International Nuclear Information System (INIS)

    Hwang, D. S.; Oh, J. H.; Choi, Y. D.; Hwang, S. T.; Park, J. H.; Latge, C.

    2003-01-01

    This study investigated the thermodynamic and the thermal decomposition properties of high concentration nitrate salts waste water for the lagoon sludge treatment. The thermodynamic property was carried out by COACH and GEMINI II based on the composition of nitrate salts waste water. The thermal decomposition property was carried out by TG-DTA and XRD. Ammonium nitrate and sodium nitrate were decomposed at 250 .deg. C and 730 . deg. C, respectively. Sodium nitrate could be decomposed at 450 .deg. C in the case of adding alumina for converting unstable Na 2 O into stable Na 2 O.Al 2 O 3 . The flow sheet for nitrate salts waste water treatment was proposed based on the these properties data. These will be used by the basic data of the process simulation

  10. Effects of calcining temperature on photocatalysis of g-C{sub 3}N{sub 4}/TiO{sub 2} composites for hydrogen evolution from water

    Energy Technology Data Exchange (ETDEWEB)

    Qu, Ailan, E-mail: elainqal@163.com; Xu, Xinmei; Xie, Haolong; Zhang, Yangyu; Li, Yuyu; Wang, Junxian

    2016-08-15

    Highlights: • TiO{sub 2} promotes melon to form at 400 °C, whereas it forms at 500 °C for only melamine. • The highest photocatalytic activity was achieved when calcination was performed at 400 °C. • Coordinated N−Ti−N bonds were formed in MA/TiO{sub 2} (400) and disappeared at high temperature. • The surface area decreased and the pore size increased with increasing of temperature. • Only MA/TiO{sub 2} (400) has a narrower band gap than pure g-C{sub 3}N{sub 4}. - Abstract: A composite of graphitic carbon nitride and TiO{sub 2} (g-C{sub 3}N{sub 4}/TiO{sub 2}) with enhanced photocatalytic hydrogen evolution capacity was achieved by calcining melamine and TiO{sub 2} sol-gel precursor. Characterization results reveal that heating temperature had a great influence on the structure, surface area and properties of the composites. Compared with the polycondensation of pure melamine, the presence of TiO{sub 2} precursor can promote the formation of melon at a low temperature. The highest photocatalytic activity of g-C{sub 3}N{sub 4}/TiO{sub 2}(400) was achieved when the calcination was performed at 400 °C, exhibiting H{sub 2} production rate of 76.25 μmol/h under UV–vis light irradiation (λ > 320 nm) and 35.44 μmol/h under visible light irradiation (λ > 420 nm). The highest photocatalytic performance of g-C{sub 3}N{sub 4}/TiO{sub 2}(400) can be attributed to: (1) the strong UV–vis light absorption due to the narrow bandgap caused by synergic effect of TiO{sub 2} and g-C{sub 3}N{sub 4}, (2) high surface area and porosity, (3) the effective separation of photo-generated electron-holes owing to the favorable heterojunction between TiO{sub 2} and g-C{sub 3}N{sub 4}.

  11. Influence of temperature on the synthesis of calcining cement α--tricalcium phosphate; Influencia da temperatura de calcinacao na sintese de cimento de α-fosfato tricalcico

    Energy Technology Data Exchange (ETDEWEB)

    Vieira, R.S.; Thurmer, M.B.; Coelho, W.T.; Fernandes, J.M.; Santos, L.A., E-mail: rafaelasv.eng@gmail.com [Universidade Federal do Rio Grande do Sul (UFRS), Porto Alegre (Brazil). Escola de Engenharia. Laboratorio de Biomateriais

    2011-07-01

    The calcium phosphate cement (CFCs) bone substitutes are of great potential use in medical and dental. However, one of the great difficulties of using this type of cement is its low mechanical strength due to the presence of undesirable phases, such as beta-tricalcium phosphate. The step of obtaining this compound is done at high temperature by solid state reaction. With the aim of obtaining calcium phosphate cements more resistant, we studied the conditions for obtaining an alpha-TCP at temperatures of 1300, 1400 and 1500 ° C with time 2h calcination. The samples were analyzed for crystalline phases, density, porosity and mechanical strength. The results show that the synthesis parameters studied strongly influence the obtained phases and the mechanical properties of cement. (author)

  12. Enhanced Removal of Arsenic and Antimony in the Mining Site by Calcined γ-Fe2O3/Layered Double Hydroxide Nanocomposite

    Science.gov (United States)

    Lee, Sang-Ho; Choi, Heechul; Kim, Kyoung-Woong

    2016-04-01

    Arsenic (As) and Antimony (Sb) have been recognized as harmful contaminants in aquatic environment due to its high toxicity and carcinogenicity. Especially, the contamination of arsenic in the mining areas is considered as a serious emerging environmental issue in Korea. Due to the hazardous effect of arsenic, the United States Environmental Protection Agency (US EPA) regulated maximum contamination level of arsenic to 10 μg/L in drinking water. The harmful effect on human health by excessive intake of antimony was also reported by previous studies, and severe contamination level (100 - 7,000 μg/L) of antimony reported in surface and groundwater of abandoned mining area in China and Slovakia. Therefore, US EPA regulated maximum contaminants level of antimony in drinking water to 6 μg/L. In order to remove anionic contaminants in drinking water, various type of nanomaterials have been developed. Layered double hydroxide (LDH) is the artificial anionic clay that is based on the layered structure of positively charged brucite-like layers with interlayers of anions. The LDH is one of the promising nanomaterials for the removal of anionic contaminants because it has high selectivity for arsenic, phosphate, chromium and antimony. However, the biggest problem of LDH for wastewater treatment is that the particles cannot be easily separated after the removal of contaminants. In this study, magnetic nanoparticles (γ-Fe2O3) supported LDH nanocomposite (γ-Fe2O3/LDH) was investigated to enhance magnetic particle recovery and removal efficiency for arsenic and antimony. The calcined γ-Fe2O3/LDH nanocomposites synthesized by co-precipitation method, and the crystallographic properties of maghemite (γ-Fe2O3) and layered structure of LDH were confirmed by X-ray diffraction. The nano-sized γ-Fe2O3 (30 to 50 nm) was stably attached on the surface of LDH (100 to 150 nm) and O1s spectrum by X-ray photoelectron spectroscopy (XPS) explained that there are both physical and

  13. Calcination and solid state reaction of ceramic-forming components to provide single-phase superconducting materials having fine particle size

    Science.gov (United States)

    Balachandran, Uthamalingam; Poeppel, Roger B.; Emerson, James E.; Johnson, Stanley A.

    1992-01-01

    An improved method for the preparation of single phase, fine grained ceramic materials from precursor powder mixtures where at least one of the components of the mixture is an alkali earth carbonate. The process consists of heating the precursor powders in a partial vacuum under flowing oxygen and under conditions where the partial pressure of CO.sub.2 evolved during the calcination is kept to a very low level relative to the oxygen. The process has been found particularly suitable for the preparation of high temperature copper oxide superconducting materials such as YBa.sub.2 Cu.sub.3 O.sub.x "123" and YBa.sub.2 Cu.sub.4 O.sub.8 "124".

  14. Preparation of a sup(99m) Tc generator for use in nuclear medicine, using calcinated (10000C) alumina as an adsorber for 99Mo

    International Nuclear Information System (INIS)

    Gasiglia, H.T.; Enoshita, M.

    1980-12-01

    The preparation of 99 sup(m) Tc generator using calcinated (1000 0 C) alumina as adsorber for 99 Mo is described. The adsorption of 99 Mo and the elution of 99 sup(m) Tc were studied. When the generator is autoclaved (30 minutes, 121 0 C), after the loading of 99 Mo, elution yields of 99 sup(m) Tc fall to the half if compared whith generators not autoclaved. However, by autoclaving 99 Mo loading solution and alumina column separately and than preparing the generator, 80% elution yields of 99 sup(m) Tc were obtained. The contamination of the generator by microorganism is avoided when the loading of the 99 Mo is carried out in a hot-cell under UV ligth. The radioactive, radiochemical, chemical and microbiological purity criteria were examined for 99 sup(m) Tc solutions. The generator is considered safe for medical purposes. (Author) [pt

  15. Fabrication and characterization of ZnO nanowires array electrodes with high photocurrent densities: Effects of the seed layer calcination time

    International Nuclear Information System (INIS)

    Lu, Yi-Jing; Liu, Ching-Fang; Hu, Chi-Chang; Kuo, Jen-Hou; Boddula, Rajender

    2017-01-01

    In this work, we demonstrate that vertically grown ZnO nanowire (NW) arrays of the wurzite phase were successfully fabricated on fluorine doped tin oxide (FTO) substrates via a hydrothermal method. The coating of a seed layer onto the FTO substrates was found to favor the growth of a uniform ZnO NWs array which shows saturation in the photocurrent density with a relatively low potential bias. Furthermore, prolonging the calcination time of the seed layer makes the ZnO NWs behave the better charge separation and improve the photo-electrochemical performance. Under the irradiation at a 75 mW cm −2 from a simulated sunlight source, the ZnO NWs array electrode prepared from the seed layer with calcination at 350 °C for 5 h shows a saturated photocurrent density of 514 μA cm −2 and a maximum half-cell solar-to-hydrogen (HC-STH) efficiency of 0.26% was obtained at 0.6 V versus reversible hydrogen electrode (RHE) in neutral electrolyte. - Highlights: • The seed layer annealing time strongly influences the textural and photo-activity of ZnO NWs. • The average diameter and density of ZnO NWs were controlled to 47–70 nm and 46–70 NWs μm −2 , respectively. • ZnO NWs show promising application potential in solar-electrocatalytic water splitting under potential bias. • The ZnO NWs with SL annealing time = 5 h achieve the highest HC-STH efficiency of 0.26% at 0.6 V.

  16. Fabrication and characterization of ZnO nanowires array electrodes with high photocurrent densities: Effects of the seed layer calcination time

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Yi-Jing; Liu, Ching-Fang; Hu, Chi-Chang, E-mail: cchu@che.nthu.edu.tw; Kuo, Jen-Hou; Boddula, Rajender

    2017-03-01

    In this work, we demonstrate that vertically grown ZnO nanowire (NW) arrays of the wurzite phase were successfully fabricated on fluorine doped tin oxide (FTO) substrates via a hydrothermal method. The coating of a seed layer onto the FTO substrates was found to favor the growth of a uniform ZnO NWs array which shows saturation in the photocurrent density with a relatively low potential bias. Furthermore, prolonging the calcination time of the seed layer makes the ZnO NWs behave the better charge separation and improve the photo-electrochemical performance. Under the irradiation at a 75 mW cm{sup −2} from a simulated sunlight source, the ZnO NWs array electrode prepared from the seed layer with calcination at 350 °C for 5 h shows a saturated photocurrent density of 514 μA cm{sup −2} and a maximum half-cell solar-to-hydrogen (HC-STH) efficiency of 0.26% was obtained at 0.6 V versus reversible hydrogen electrode (RHE) in neutral electrolyte. - Highlights: • The seed layer annealing time strongly influences the textural and photo-activity of ZnO NWs. • The average diameter and density of ZnO NWs were controlled to 47–70 nm and 46–70 NWs μm{sup −2}, respectively. • ZnO NWs show promising application potential in solar-electrocatalytic water splitting under potential bias. • The ZnO NWs with SL annealing time = 5 h achieve the highest HC-STH efficiency of 0.26% at 0.6 V.

  17. Water-n-BuOH solvothermal synthesis of ZnAl-LDHs with different morphologies and its calcined product in efficient dyes removal.

    Science.gov (United States)

    Huang, Gailing; Sun, Yingying; Zhao, Chencong; Zhao, Yifei; Song, Zhaoyuan; Chen, Junli; Ma, Shulan; Du, Junping; Yin, Zhigang

    2017-05-15

    In this study, water-n-BuOH mixed solvents were used to synthesize the ZnAl-layered double hydroxides (ZnAl-LDHs) via hydrothermal method. The XRD, FT-IR, SEM, ICP and CHN analyses revealed that the type of intercalated anions, the layer Zn/Al ratios, and morphologies of the LDHs depended on the ratio of V(water)/V(n-BuOH) in the mixed solvents. When the ratio of V(water)/V(n-BuOH) is 3 or 0.3, the as-prepared LDHs had 3D "silk flowers" (ZnAl-LDH-3) or "Sedimentary rock" morphology (ZnAl-LDH-0.3). Adsorption properties of dyes on calcined LDHs were studied. Compared with ZnAl-LDO-0.3 and ZnAl-LDO-w (calcined from the LDHs obtained in pure water), ZnAl-LDO-3 showed much better adsorption efficiency for anionic dyes thanks to its much larger BET-specific surface area. The sorption kinetics for dyes was appropriately described by the pseudo-second-order model and sorption isotherms can be fitted more satisfactorily by the Langmuir model. With the increasing concentrations of dyes from 10mg/L to 400mg/L, the maximum absorption capacities of ZnAl-LDO-3 were 1540mg/g (2.21mmol/g) for congo red, 1153mg/g (3.52mmol/g) for methyl orange and 390mg/g (0.63mmol/g) for active red (X-3B), respectively. The adsorption dyes onto the external surface is still the main mechanism for LDO adsorbents. The ZnAl-LDO-3 was a potential adsorbent for dyeing wastewater treatment. Copyright © 2017 Elsevier Inc. All rights reserved.

  18. MoO3/SiO2-ZrO2 Catalyst: Eeffect of Calcination Temperature on Physico-chemical Properties and Activities in Nitration of Toluene

    Directory of Open Access Journals (Sweden)

    Sunil Madhavrao Kemdeo

    2012-12-01

    Full Text Available 12 wt % molybdena was deposited over 1:1 silica zirconia mixed oxide support and the resultant catalyst was calcined between the 500 to 700 oC range of temperature. The samples were characterized by XRD, FT-IR, BET, SEM, NH3-TPD and pyridine adsorbed FT-IR techniques.  Nitration of toluene was studied as a model reaction over the prepared catalysts and parameters like effect of reaction temperature, effect of various solvents, catalyst reusability are studied. It was found that conversion of toluene varies with the presence of Brönsted acid sites over the catalyst surface and para-nitrotoulene selectivity is associated with pore size of the catalyst. Over the same catalysts, nitration was extended for some other aromatics. Avoid of sulfuric acid in the present process is an interesting concern in view of green chemistry. Copyright © 2012 by BCREC UNDIP. All rights reservedKeywords: MoO3/SiO2-ZrO2; SO2-ZrO2; NH3-TPD; Nitration; ortho-nitro tolueneReceived: 19th May 2012, Revised: 24th May 2012, Accepted: 26th May 2012[How to Cite: S.M. Kemdeo. (2012. MoO3/SiO2-ZrO2 Catalyst: Effect of Calcination Temperature on Physico-chemical Properties and Activities in Nitration of Toluene. Bulletin of Chemical Reaction Engineering & Catalysis, 7 (2: 92-104. doi:10.9767/bcrec.7.2.3521.92-104] [How to Link / DOI: http://dx.doi.org/10.9767/bcrec.7.2.3521.92-104 || or local: http://ejournal.undip.ac.id/index.php/bcrec/article/view/3521] | View in 

  19. Estudio de la adición de arcillas calcinadas en la durabilidad de hormigones Study of the addition of calcined clays in the durability of concrete

    Directory of Open Access Journals (Sweden)

    Rancés Castillo Lara

    2011-01-01

    conveniente para el hormigón ante la posible acción de diferentes mecanismos de degradación.Currently economical and environmental advantages of cement clinker replacement by other supplementary cementious materials are well known. For example calcined clays, such as metakaolin, have drawn special attention during recent years. It is well known that these admixtures added to mortars and concretes improve mechanical strength as well as durability. The purpose of this study is to evaluate the behavior of physical-mechanical properties and durability in micro-concretes, by employing calcinated and grinded clays as replacement material, by 30% of ordinary Portland cement (OPC. Therefore, clay soil was employed, which is mainly composed by low-purity-kaolin mineral, so as to obtain calcined clays to be used as supplementary cementious minerals. Best results for compressive strength at 28 days were obtained by sedimentary calcined clays, which have higher content of kaolin mineral thanks to a purification process by means of raw material sedimentation conducted on this admixture only. Nevertheless, capillary water absorption tests delivered best results for calcined clay soil, which finesse is quite high. Lower values showed by this admixture, as much for capillary porosity and sorptivity, revealed there was a predominance of compaction and impermeability phenomena achieved by cementious matrix using such fine material, over the effect of puzzolanic reaction. Micro-structure studies on C-S-H gel, employing energy dispersive x-ray (EDX technique, demonstrated that the use of calcined clays as replacement of RPC favors the creation of quite stable hydration products, mainly monosulfos of hemicabo and monocarbo types, which is convenient for concrete against possible deterioration actions from different mechanisms.

  20. Directed homology

    DEFF Research Database (Denmark)

    Fahrenberg, Uli

    2004-01-01

    We introduce a new notion of directed homology for semicubical sets. We show that it respects directed homotopy and is functorial, and that it appears to enjoy some good algebraic properties. Our work has applications to higher-dimensional automata.......We introduce a new notion of directed homology for semicubical sets. We show that it respects directed homotopy and is functorial, and that it appears to enjoy some good algebraic properties. Our work has applications to higher-dimensional automata....

  1. Multivariate optimization of process parameters in the synthesis of calcined Ca‒Al (NO3) LDH for defluoridation using 3(3) factorial, central composite and Box-Behnken design.

    Science.gov (United States)

    Ghosal, Partha S; Gupta, Ashok K; Sulaiman, Ayoob

    2016-01-01

    Response surface methodology was applied for the first time in the optimization of the preparation of layered double hydroxide (LDH) for defluoridation. The influence of three vital process parameters (viz. pH, molar ratio and calcination temperature) in the synthesis of the adsorbent 'Calcined Ca‒Al (NO3) LDH' was thoroughly examined to maximize its fluoride scavenging potential. The process parameters were optimized using the 3(3) factorial, face centered central composite and Box-Behnken designs and a comparative assessment of the methods was conducted. The maximum fluoride removal efficiency was achieved at a calcination temperature of approximately 500ºC; however, the efficiency decreased with increasing pH and molar ratio. The outcome of the comparative assessment clearly delineates the case specific nature of the models. A better predictability over the entire experimental domain was obtained with the 3(3) factorial method, whereas the Box-Behnken design was found to be the most efficient model with lesser number of experimental runs. The desirability function technique was performed for optimizing the response, wherein face centered central composite design exhibited a maximum desirability. The calcined Ca‒Al (NO3) LDH, synthesized under the optimum conditions, demonstrated the removal efficiencies of 95% and 99% for the doses of 3 g L(-1) and 5 g L(-1), respectively.

  2. Direct Democracy

    DEFF Research Database (Denmark)

    Beramendi, Virginia; Ellis, Andrew; Kaufman, Bruno

    of direct democracy mechanisms in specific contexts. These country case studies allow for in depth discussion of particular issues, including signature collection and voter participation, campaign financing, media coverage, national variations in the usage of direct democracy procedures and national lessons...

  3. Influence of calcination parameters on the synthesis of N-doped TiO{sub 2} by the polymeric precursors method

    Energy Technology Data Exchange (ETDEWEB)

    Dawson, Margaret, E-mail: missmargaretdawson@gmail.com [Department of Materials Engineering, Universidade Federal de São Carlos, Rodovia Washington Luis KM 235 SP-310, São Carlos CEP 13565-905, São Paulo (Brazil); Soares, Gabriela Byzynski, E-mail: gabi.byzynski@gmail.com [Department of Chemistry, Universidade Federal de São Carlos, Rodovia Washington Luis KM 235 SP-310, São Carlos CEP 13565-905, São Paulo (Brazil); Embrapa Instrumentação, Rua XV de Novembro 1452, São Carlos CEP 13560-970, São Paulo (Brazil); Ribeiro, Caue, E-mail: caue.ribeiro@embrapa.br [Embrapa Instrumentação, Rua XV de Novembro 1452, São Carlos CEP 13560-970, São Paulo (Brazil)

    2014-07-01

    In this paper, the influence of calcination parameters on the synthesis of N:TiO{sub 2} catalysts obtained through the polymeric precursors method was evaluated. The powders were prepared by annealing Ti{sup 4+} precursor resins at different temperature-time conditions in air, resulting in powders with different degrees of crystallinity for N doping, which was done by adding urea to the as-prepared powders and calcining in N{sub 2} atmosphere. The N doping process resulted in band gap narrowing of TiO{sub 2} and, varying annealing temperature and time, can be an alternative method for preferential formation of substitutional N or interstitial N. It was found that the percentage of interstitial N increased with an increase in annealing temperature, resulting in the complete absence of substitutional N at 400 °C. The photocatalytic performance of the powders was evaluated using Rhodamine-B and Atrazine solutions under ultraviolet and visible irradiations. The coefficients revealed that interstitial N had a positive correlation to both ultraviolet and visible photoactivity. In contrast, substitutional N showed a negative correlation. Further, the ratio of substitutional N to interstitial N indicated a strong negative correlation to ultraviolet light photoactivity and no correlation to visible light photoactivity. However, substitutional N should be controlled for better photocatalytic properties. - Graphical abstract: The temperature influences to promote higher quantities of Interstitial N doped TiO{sub 2} than Substitutional and due to difference between energies levels for substitutional N doped TiO{sub 2} and Interstitial N doped TiO{sub 2}, it is presented difference on photocatalytic activity. - Highlights: • Temperature and time of synthesis of N doping TiO{sub 2} could affect the type of N (interstitial and substitutional N). • The percentage of interstitial N increased with an increase in annealing temperature. • Interstitial N improves ultraviolet and

  4. Computer software configuration management plan for the Honeywell modular automation system

    International Nuclear Information System (INIS)

    Cunningham, L.T.

    1997-01-01

    This document provides a Computer Software management plan for a new Honeywell Modular Automation System (MAS) being installed in the Plutonium Finishing Plant (PFP). This type of system will be used to control new thermal stabilization furnaces, a vertical denitrator calciner, and a pyrolysis furnace

  5. Honeywell Modular Automation System Computer Software Documentation

    International Nuclear Information System (INIS)

    CUNNINGHAM, L.T.

    1999-01-01

    This document provides a Computer Software Documentation for a new Honeywell Modular Automation System (MAS) being installed in the Plutonium Finishing Plant (PFP). This system will be used to control new thermal stabilization furnaces in HA-211 and vertical denitration calciner in HC-230C-2

  6. Advance Directives

    Science.gov (United States)

    ... Types Bladder Cancer Breast Cancer Colorectal Cancer Kidney (Renal Cell) Cancer Leukemia Liver Cancer Lung Cancer Lymphoma ... about advance directives. Two well-known ones are: Aging With Dignity Aging with Dignity is a national ...

  7. Directing Creativity

    DEFF Research Database (Denmark)

    Darsø, Lotte; Ibbotson, Piers

    2008-01-01

    . Like leaders, who are caught in paradoxical situations where they have to manage production and logistics simultaneously with making space for creativity and innovation, theatre directors need to find the delicate balance between on one hand renewal of perceptions, acting and interaction......In this article we argue that leaders facing complex challenges can learn from the arts, specifically that leaders can learn by examining how theatre directors direct creativity through creative constraints. We suggest that perceiving creativity as a boundary phenomenon is helpful for directing it...... and on the other hand getting ready for the opening night. We conclude that the art of directing creativity is linked to developing competencies of conscious presence, attention and vigilance, whereas the craft of directing creativity concerns communication, framing and choice....

  8. Direct Heat

    Energy Technology Data Exchange (ETDEWEB)

    Lienau, P.J.

    1990-01-01

    Potential resources and applications of earth heat in the form of geothermal energy are large. United States direct uses amount to 2,100 MWt thermal and worldwide 8,850 MWt above a reference temperature of 35 degrees Celsius. Space and district heating are the major direct uses of geothermal energy. Equipment employed in direct use projects is of standard manufacture and includes downhole and circulation pumps, transmission and distribution pipelines, heat exchangers and convectors, heat pumps and chillers. Direct uses of earth heat discussed are space and district heating, greenhouse heating and fish farming, process and industrial applications. The economic feasibility of direct use projects is governed by site specific factors such as location of user and resource, resource quality, system load factor and load density, as well as financing. Examples are presented of district heating in Klamath Falls, and Elko. Further developments of direct uses of geothermal energy will depend on matching user needs to the resource, and improving load factors and load density.

  9. Calcination Method Synthesis of SnO2/g-C3N4 Composites for a High-Performance Ethanol Gas Sensing Application

    Science.gov (United States)

    Cao, Jianliang; Qin, Cong; Wang, Yan; Zhang, Bo; Gong, Yuxiao; Zhang, Huoli; Sun, Guang; Bala, Hari; Zhang, Zhanying

    2017-01-01

    The SnO2/g-C3N4 composites were synthesized via a facile calcination method by using SnCl4·5H2O and urea as the precursor. The structure and morphology of the as-synthesized composites were characterized by the techniques of X-ray diffraction (XRD), the field-emission scanning electron microscopy and transmission electron microscopy (SEM and TEM), energy dispersive spectrometry (EDS), thermal gravity and differential thermal analysis (TG-DTA), and N2-sorption. The analysis results indicated that the as-synthesized samples possess the two dimensional structure. Additionally, the SnO2 nanoparticles were highly dispersed on the surface of the g-C3N4nanosheets. The gas-sensing performance of the as-synthesized composites for different gases was tested. Moreover, the composite with 7 wt % g-C3N4 content (SnO2/g-C3N4-7) SnO2/g-C3N4-7 exhibits an admirable gas-sensing property to ethanol, which possesses a higher response and better selectivity than that of the pure SnO2-based sensor. The high surface area of the SnO2/g-C3N4 composite and the good electronic characteristics of the two dimensional graphitic carbon nitride are in favor of the elevated gas-sensing property. PMID:28468245

  10. Transition metal modified and partially calcined inorganic-organic pillared clays for the adsorption of salicylic acid, clofibric acid, carbamazepine, and caffeine from water.

    Science.gov (United States)

    Cabrera-Lafaurie, Wilman A; Román, Félix R; Hernández-Maldonado, Arturo J

    2012-11-15

    Pharmaceutical and Personal Care Products (PPCPs) are considered emerging contaminants, and their efficient removal from water is going to be a challenging endeavor. Microporous adsorbent materials, including pillared clays, could offer a potential solution if tailored properly. Although pillared clays have been employed previously for the removal of organics, the effective removal of PPCPs will only be possible if their surface and textural properties are manipulated from the bottom-up. This work presents the use of modified inorganic-organic pillared clays (IOCs) for the adsorption of salicylic acid, clofibric acid, carbamazepine, and caffeine. The IOCs have been modified with Co(2+), Cu(2+), or Ni(2+) to induce complexation-like adsorbate-adsorbent interactions at ambient conditions, in an attempt to provide an efficient and yet reversible driving force in the sub-ppm concentration range. Furthermore, the IOCs were partially calcined to increase effective surface area by an order of magnitude while preserving some hydrophobicity. In general, the Ni(2+) IOCs exhibited the greatest interaction with salicylic and clofibric acids, respectively, while the Co(2+) adsorbents excelled at adsorbing caffeine at low concentrations. All of the metal-modified IOCs showed comparable adsorption capacities for the case of carbamazepine, probably due to the lack of availability of particular functional groups in this adsorbate. Copyright © 2012 Elsevier Inc. All rights reserved.

  11. Hydrogen-Rich Gas Production by Sorption Enhanced Steam Reforming of Woodgas Containing TAR over a Commercial Ni Catalyst and Calcined Dolomite as CO2 Sorbent

    Directory of Open Access Journals (Sweden)

    Vincenzo Naso

    2013-07-01

    Full Text Available The aim of this work was the evaluation of the catalytic steam reforming of a gaseous fuel obtained by steam biomass gasification to convert topping atmosphere residue (TAR and CH4 and to produce pure H2 by means of a CO2 sorbent. This experimental work deals with the demonstration of the practical feasibility of such concepts, using a real woodgas obtained from fluidized bed steam gasification of hazelnut shells. This study evaluates the use of a commercial Ni catalyst and calcined dolomite (CaO/MgO. The bed material simultaneously acts as reforming catalyst and CO2 sorbent. The experimental investigations have been carried out in a fixed bed micro-reactor rig using a slipstream from the gasifier to evaluate gas cleaning and upgrading options. The reforming/sorption tests were carried out at 650 °C while regeneration of the sorbent was carried out at 850 °C in a nitrogen environment. Both combinations of catalyst and sorbent are very effective in TAR and CH4 removal, with conversions near 100%, while the simultaneous CO2 sorption effectively enhances the water gas shift reaction producing a gas with a hydrogen volume fraction of over 90%. Multicycle tests of reforming/CO2 capture and regeneration were performed to verify the stability of the catalysts and sorbents to remove TAR and capture CO2 during the duty cycle.

  12. Effect of the calcining temperature on the porosity of the titanium dioxide powders obtained by Polymeric Precursor Method; Efeito da temperatura de calcinacao na porosidade de pos de dioxido de titanio obtidos pelo Metodo dos Precursores Polimericos

    Energy Technology Data Exchange (ETDEWEB)

    Silva, D.W.; Granado, S.R.; Ciola, R.A.; Cavalheiro, A.A., E-mail: douglas_levis@hotmail.com [Universidade Estadual de Mato Grosso do Sul (CPTREN/UEMS), Navirai, MS (Brazil). Centro de Pesquisas Tecnologicas em Recursos Naturais

    2011-07-01

    Ceramics materials obtained by Polymeric Precursor Method exhibit mechanisms of the pore formation and elimination dependents on the decomposition kinetics of the residual organic matter of the polyester. The mechanism of pore elimination seems to occur by disrupting of the wall among the pores because it leads to the consequent pore coalescence and increasing in pore volume, which posses higher pore diameters. In this case, it was observed that the porosity decreasing occurs by pore wall moving after that the residual organic matter is eliminated from the pore inside. The pore diameter associated to the highest volume desorption occurred for the material obtained after calcining at 450°C is approximately 1,7 nm, what seems to be related to the amorphous carbon accumulated inside the pores, once that the pore volume decreases more effectively for the material obtained by calcining at 550°C, making the maximum volume situates at 2,0 nm. (author)

  13. Effects of calcination treatment on the morphology, crystallinity, and photoelectric properties of all-solid-state dye-sensitized solar cells assembled by TiO2 nanorod arrays.

    Science.gov (United States)

    Sun, Xianmiao; Sun, Qiong; Li, Yang; Sui, Lina; Dong, Lifeng

    2013-11-14

    TiO2 has been extensively investigated due to its unique photoelectric properties. In this study, oriented single-crystal rutile TiO2 nanorod arrays were synthesized and then calcined at different temperatures in the atmosphere. The morphology and crystalline characterization indicated that the length of TiO2 nanorods increased rapidly and the nanorods became aggregated and fragile after calcination, yet the sintering treatment seemed to have almost no effect on the crystallinity. To obtain the all-solid-state, dye-sensitized solar cells (DSSCs), a newly reported solid inorganic semiconductor, CsSnI2.95F0.05, was employed as the electrolyte, and the Pt deposited on the conductive side of the fluorine-doped tin oxide (FTO) glass substrate was used as the counter-electrode. The effects of the calcination treatment on the photoelectric properties of the solar cells, including external quantum efficiency (EQE), open circuit voltage (V(OC)), short-circuit current (J(SC)), and photoelectric conversion efficiency (η), were investigated under the illumination of a solar simulator. As a result, all of the EQE, V(OC), J(SC), and η values of the cells first increased and then declined with the increase of calcination temperatures, and the highest η of 2.81% was obtained by the cell assembled with its TiO2 electrode sintered at 450 °C for 3 h, a value almost 2.5 times that of the non-sintered sample (1.1%).

  14. Direct marketing

    Directory of Open Access Journals (Sweden)

    Čičić Muris

    2002-01-01

    Full Text Available Direct Marketing (DM is usually treated as unworthy activity, with actions at the edge of legality and activities minded cheating. Despite obvious problems regarding ethics and privacy threat, DM with its size, importance and role in a concept of integrated marketing communication deserves respect and sufficient analysis and review

  15. Effect of calcination temperature of a copper ferrite synthesized by a sol-gel method on its structural characteristics and performance as Fenton catalyst to remove gallic acid from water.

    Science.gov (United States)

    López-Ramón, María V; Álvarez, Miguel A; Moreno-Castilla, Carlos; Fontecha-Cámara, María A; Yebra-Rodríguez, África; Bailón-García, Esther

    2018-02-01

    A copper ferrite synthesized by a sol-gel combustion method was calcined at different temperatures up to 800°C, determining changes in its structural characteristics and magnetic measurements and studying its catalytic performance in gallic acid removal by Fenton reaction. The main objective was to study the effect of the calcination temperature of copper ferrite on its crystalline phase formation and transformation, activity and metal ion leaching. The cubic-to-tetragonal transformation of the spinel occurred via its reaction with the CuO phase, displacing Fe 3+ ions in B (octahedral) sites out of the spinel structure by the following reaction: 2Fe 3+ B +3CuO→Fe 2 O 3 +3Cu 2+ B . The catalysts showed superparamagnetic or substantial superparamagnetic behaviour. At higher calcination temperatures, catalyst activity was lower, and Cu ion leaching was markedly decreased. There was no Fe ion leaching with any catalyst. The as-prepared catalyst showed better catalytic performance than a commercial copper ferrite. Leached Cu ions acted as homogeneous catalysts, and their contribution to the overall removal mechanism was examined. Cu 2 O present in the as-prepared catalysts made only a small contribution to their activity. Finally, the reutilization of various catalysts was studied by performing different catalytic cycles. Copyright © 2017 Elsevier Inc. All rights reserved.

  16. Micro-structural characterization of the hydration products of bauxite-calcination-method red mud-coal gangue based cementitious materials

    International Nuclear Information System (INIS)

    Liu, Xiaoming; Zhang, Na; Yao, Yuan; Sun, Henghu; Feng, Huan

    2013-01-01

    Highlights: • Al IV and Al VI both exist in the hydration products. • Increase of Ca/Si ratio promotes the conversion from [AlO 4 ] to [AlO 6 ]. • Polymerization degree of [SiO 4 ] in the hydration products declines. -- Abstract: In this research, the micro-structural characterization of the hydration products of red mud-coal gangue based cementitious materials has been investigated through SEM-EDS, 27 Al MAS NMR and 29 Si MAS NMR techniques, in which the used red mud was derived from the bauxite calcination method. The results show that the red mud-coal gangue based cementitious materials mainly form fibrous C-A-S-H gel, needle-shaped/rod-like AFt in the early hydration period. With increasing of the hydration period, densification of the pastes were promoted resulting in the development of strength. EDS analysis shows that with the Ca/Si of red mud-coal gangue based cementitious materials increases, the average Ca/Si and Ca/(Si + Al) atomic ratio of C-A-S-H gel increases, while the average Al/Si atomic ratio of C-A-S-H gel decreases. MAS NMR analysis reveals that Al in the hydration products of red mud-coal gangue based cementitious materials exists in the forms of Al IV and Al VI , but mainly in the form of Al VI . Increasing the Ca/Si ratio of raw material promotes the conversion of [AlO 4 ] to [AlO 6 ] and inhibits the combination between [AlO 4 ] and [SiO 4 ] to form C-A-S-H gel. Meanwhile, the polymerization degree of [SiO 4 ] in the hydration products declines

  17. Reduction of Acute Inflammatory Effects of Fumed Silica Nanoparticles in the Lung by Adjusting Silanol Display through Calcination and Metal Doping.

    Science.gov (United States)

    Sun, Bingbing; Pokhrel, Suman; Dunphy, Darren R; Zhang, Haiyuan; Ji, Zhaoxia; Wang, Xiang; Wang, Meiying; Liao, Yu-Pei; Chang, Chong Hyun; Dong, Juyao; Li, Ruibin; Mädler, Lutz; Brinker, C Jeffrey; Nel, André E; Xia, Tian

    2015-09-22

    The production of pyrogenic (fumed) silica is increasing worldwide at a 7% annual growth rate, including expanded use in food, pharmaceuticals, and other industrial products. Synthetic amorphous silica, including fumed silica, has been generally recognized as safe for use in food products by the Food and Drug Administration. However, emerging evidence from experimental studies now suggests that fumed silica could be hazardous due to its siloxane ring structure, high silanol density, and "string-of-pearl-like" aggregate structure, which could combine to cause membrane disruption, generation of reactive oxygen species, pro-inflammatory effects, and liver fibrosis. Based on this structure-activity analysis (SAA), we investigated whether calcination and rehydration of fumed silica changes its hazard potential in the lung due to an effect on silanol density display. This analysis demonstrated that the accompanying change in surface reactivity could indeed impact cytokine production in macrophages and acute inflammation in the lung, in a manner that is dependent on siloxane ring reconstruction. Confirmation of this SAA in vivo, prompted us to consider safer design of fumed silica properties by titanium and aluminum doping (0-7%), using flame spray pyrolysis. Detailed characterization revealed that increased Ti and Al doping could reduce surface silanol density and expression of three-membered siloxane rings, leading to dose-dependent reduction in hydroxyl radical generation, membrane perturbation, potassium efflux, NLRP3 inflammasome activation, and cytotoxicity in THP-1 cells. The reduction of NLRP3 inflammasome activation was also confirmed in bone-marrow-derived macrophages. Ti doping, and to a lesser extent Al doping, also ameliorated acute pulmonary inflammation, demonstrating the possibility of a safer design approach for fumed silica, should that be required for specific use circumstances.

  18. Direct ELISA.

    Science.gov (United States)

    Lin, Alice V

    2015-01-01

    First described by Engvall and Perlmann, the enzyme-linked immunosorbent assay (ELISA) is a rapid and sensitive method for detection and quantitation of an antigen using an enzyme-labeled antibody. Besides routine laboratory usage, ELISA has been utilized in medical field and food industry as diagnostic and quality control tools. Traditionally performed in 96-well or 384-well polystyrene plates, the technology has expanded to other platforms with increase in automation. Depending on the antigen epitope and availability of specific antibody, there are variations in ELISA setup. The four basic formats are direct, indirect, sandwich, and competitive ELISAs. Direct ELISA is the simplest format requiring an antigen and an enzyme-conjugated antibody specific to the antigen. This chapter describes the individual steps for detection of a plate-bound antigen using a horseradish peroxidase (HRP)-conjugated antibody and luminol-based enhanced chemiluminescence (ECL) substrate. The methodological approach to optimize the assay by chessboard titration is also provided.

  19. Synthesis of aluminum oxide by the polymer precursor method (Pechini) in 4: 1 ratio of citric acid: metal cation: calcination temperature effect; Sintese do oxido de aluminio pelo metodo dos precursores polimericos (Pechini) na relacao 4:1 de acido citrico: cation metalico: efeito da temperatura de calcinacao

    Energy Technology Data Exchange (ETDEWEB)

    Silva, M.C.; Lira, H.L.; Ribeiro, P.C.; Freitas, N.L., E-mail: mirelecsilva@hotmail.com [Universidade Federal de Campina Grande (UFCG), PB (Brazil). Unidade Academica de Engenharia de Materiais

    2014-07-01

    The technology field is nanopowders prominent in science since these materials fall in various sectors regarding their applications. This work aims at the synthesis of aluminum oxide by polymeric precursors in 4:1 ratio of citric acid:metal cation and evaluate the influence of calcination temperature on their structural and morphological characteristics. The samples after reaction were characterized by XRD and thermal analysis. After calcination 500-1200°C the samples were characterized by XRD, SEM and particle size distribution. The results showed that the variation of the calcination temperature is sufficient to achieve a same material with different structural and morphological characteristics. The most stable phase aluminum oxide arose only after calcination at 1100°C, below 900°C, the amorphous material appeared. As regards the morphology, the change was not as significant as compared to the structure. (author)

  20. Fall 2010 Semiannual (III.H. and I.U.) Report for the HWMA/RCRA Post Closure Permit for the INTEC Waste Calcining Facility and the CPP 601/627/640 Facility at the INL Site

    Energy Technology Data Exchange (ETDEWEB)

    Boehmer, Ann

    2010-11-01

    The Waste Calcining Facility is located at the Idaho Nuclear Technology and Engineering Center. In 1999, the Waste Calcining Facility was closed under an approved Hazardous Waste Management Act/Resource Conservation and Recovery Act (HWMA/RCRA) Closure Plan. Vessels and spaces were grouted and then covered with a concrete cap. The Idaho Department of Environmental Quality issued a final HWMA/RCRA post-closure permit on September 15, 2003, with an effective date of October 16, 2003. This permit sets forth procedural requirements for groundwater characterization and monitoring, maintenance, and inspections of the Waste Calcining Facility to ensure continued protection of human health and the environment. The post closure permit also includes semiannual reporting requirements under Permit Conditions III.H. and I.U. These reporting requirements have been combined into this single semiannual report, as agreed between the Idaho Cleanup Project and Idaho Department of Environmental Quality. The Permit Condition III.H. portion of this report includes a description and the results of field methods associated with groundwater monitoring of the Waste Calcining Facility. Analytical results from groundwater sampling, results of inspections and maintenance of monitoring wells in the Waste Calcining Facility groundwater monitoring network, and results of inspections of the concrete cap are summarized. The Permit Condition I.U. portion of this report includes noncompliances not otherwise required to be reported under Permit Condition I.R. (advance notice of planned changes to facility activity which may result in a noncompliance) or Permit Condition I.T. (reporting of noncompliances which may endanger human health or the environment). This report also provides groundwater sampling results for wells that were installed and monitored as part of the Phase 1 post-closure period of the landfill closure components in accordance with HWMA/RCRA Landfill Closure Plan for the CPP-601 Deep

  1. Production of BaAl2O4 doped with Eu3+ in low temperature: research of the influence of the synthesis route, temperature and calcination time in the optical properties

    International Nuclear Information System (INIS)

    Gomes, Manasses Almeida

    2017-01-01

    In this work, the synthesis condition (complexing agent and temperature and time of calcination) were studied aiming to produce BaAl 2 O 4 samples in the ferroelectric hexagonal phase. Pure and Eu 3+ - doped samples were produced and its luminescent properties were investigated. BaAl 2 O 4 was prepared using several thermal treatment conditions, via an alternative sol-gel route, using coconut water or PVA as the complexing agents. The sample production at 600 °C/5h is quite interesting, since to date the lowest calcination temperatures found in the literature was 650 ° C using reagents with high degree of toxicity DTA / TG measurements indicated a possible start of the crystallization of the material at approximately 600 ° C, and the X-ray powder diffraction (XRD) confirm the formation of the desired phase of the calcined barium aluminate at that temperature. The results of the Rietveld refinements showed the occurrence of secondary phase in the samples produced at 600 ° C / 5h, presenting 5% of phase Ba(NO 3 ) 2 , while single phase was found for samples calcined at 1200 ° C for 2 and 5h. Analysis of the diffractogram by the Scherrer equation showed smaller crystallite size for samples calcified at 600 °C/5h, but apparently with a lower degree of crystallinity than the sample prepared at 1200 ° C/ 2 and 5h. The photoluminescence measurements showed that the emission spectra of the samples have great dependence on the times, temperatures and complexing agents used. In particular, samples calcined at 600 ° C have very different characteristics with regard to the probabilities of emissions associated with Eu 3+ when compared with samples produced at higher temperatures. Differences observed in the spectra of samples produced via different complexing agents are possibly due to defects created in the materials by impurities present in the coconut water. Samples produced using PVA present sites with higher symmetry, which was evidenced by a lower relative

  2. Effects of calcining temperatures of Eu{sup 2+} and Dy{sup 3+} ion-codoped calcia-alumina binary compounds on their phase transition and luminescence properties

    Energy Technology Data Exchange (ETDEWEB)

    Liang, Chen-Jui, E-mail: cjliang@fcu.edu.tw; Siao, Hao-Yi

    2017-06-01

    In this study, phase evolution as a function of calcining temperature in calcia-alumina binary compound phosphors was examined to interpret their luminescence properties. The binary compounds were prepared through a coprecipitation method employing potassium carbonate as the precipitant to obtain precursors with a high-precision stoichiometric composition for the calcination. The results indicate that the morphology, surface properties, and infrared transmittance of the prepared phosphors were affected by the calcining temperature. X-ray diffraction analysis results enabled identification of Ca{sub 12}Al{sub 14}O{sub 33}, CaAl{sub 2}O{sub 4}, and CaAl{sub 4}O{sub 7} phase transitions at various calcining temperatures. The amount of the CaAl{sub 2}O{sub 4} phase increased with the calcining temperature within the range of 700–1060 °C. The Ca{sub 12}Al{sub 14}O{sub 33} and CaAl{sub 4}O{sub 7} phases exhibited trends opposite to that of the CaAl{sub 2}O{sub 4} phase. When the calcining temperature reached 980 °C, the CaAl{sub 2}O{sub 4} phase (60.5%) was determined to be the main phase in the structure, and excellent emission intensity at an emission band of 449 nm was observed as a result of the complete substitution of Eu{sup 2+} for Ca{sup 2+}. The emission intensity corresponding to Eu{sup 2+} 4f{sup 6}5d{sup 1} → 4f{sup 7} decreased slightly when the temperature reached 1060 °C because of more monoclinic reciprocal CaAl{sub 4}O{sub 7} phase (81.5%) formation, causing the transfer of some Eu{sup 2+} to Eu{sup 3+}, during which strong photoluminescence spectra of Eu{sup 3+5}D{sub 0} → {sup 7}F{sub j} (j = 0, 1, 2, 3, 4) within the wavelength range of 570–720 nm were observed. Because the strong photoluminescence spectra of the Eu{sup 2+} and Eu{sup 3+} emissions were together within the wavelength range of 449–720 nm in this phosphor, the photoluminescence was white light. One moderately intense emission band in the infrared region was observed and

  3. A combined self-assembly and calcination method for preparation of nanoparticles-assembled cobalt oxide nanosheets using graphene oxide as template and their application for non-enzymatic glucose biosensing.

    Science.gov (United States)

    Zhang, Haiyan; Liu, Sen

    2017-01-01

    Cobalt oxide (Co 3 O 4 )-based materials have been extensively investigated as efficient electrocatalysts for non-enzymatic glucose biosensing. The proper tuning the structure of Co 3 O 4 -based materials could improve sensing performances for glucose detection. Herein, we have developed a combined self-assembly and calcination method to prepare nanoparticles-assembled Co 3 O 4 nanosheets, which exhibit good sensing performances for glucose biosensing. The Co 3 O 4 nanosheets were prepared by the following three steps: (i) the Co 2+ modified graphene oxide (GO) was prepared by the self-assembly of Co 2+ and GO in aqueous solution firstly, and then Co 2+ modified GO film was obtained by vacuum filtration method; (ii) after calcination of Co 2+ modified GO film in N 2 atmosphere, Co 3 O 4 nanoparticles modified reduced GO (RGO) was obtained; (iii) finally, nanoparticles-assembled Co 3 O 4 nanosheets were obtained by calcination of Co 3 O 4 modified RGO in air to remove RGO template. Most importantly, Co 3 O 4 nanosheets exhibit good electrocatalytic activity for oxidation of glucose, leading to high-performance glucose sensor. The detection limit and linear range of Co 3 O 4 nanosheets-based glucose sensor in the present work are 0.15μM, and 1-50μM, respectively. Furthermore, such sensor also shows excellent selectivity for glucose detection, compared to the commonly interfering species including dopamine, and uric acid. Copyright © 2016 Elsevier Inc. All rights reserved.

  4. Effects of FeO{sub x}, CoO{sub x}, and NiO catalysts and calcination temperatures on the synthesis of single-walled carbon nanotubes through chemical vapor deposition of methane

    Energy Technology Data Exchange (ETDEWEB)

    Tan, S.-M. [School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, Seri Ampangan, 14300 Nibong Tebal, S.P.S. Pulau Pinang (Malaysia); Chai, S.-P. [School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, Seri Ampangan, 14300 Nibong Tebal, S.P.S. Pulau Pinang (Malaysia); School of Engineering, Monash University, Jalan Lagoon Selatan, 46150 Bandar Sunway, Selangor (Malaysia); Liu, W.-W. [School of Materials Science and Mineral Resources Engineering, Engineering Campus, Universiti Sains Malaysia, Seri Ampangan, 14300 Nibong Tebal, S.P.S. Pulau Pinang (Malaysia); Mohamed, Abdul Rahman [School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, Seri Ampangan, 14300 Nibong Tebal, S.P.S. Pulau Pinang (Malaysia)], E-mail: chrahman@eng.usm.my

    2009-05-27

    The oxides of cobalt, iron, and nickel catalysts were tested in chemical vapor deposition (CVD) of methane in synthesizing single-walled carbon nanotubes (SWNTs). All catalysts used in this study were prepared using impregnation method and calcined at temperatures ranging from 300 to 850 deg. C. The catalyst samples after CVD of methane were characterized using transmission electron microscopy (TEM). The TEM study elucidates that iron oxide serves as an effective catalyst for growing SWNTs. The presence of SWNTs on the catalyst was confirmed in the Raman study.

  5. Effects of FeOx, CoOx, and NiO catalysts and calcination temperatures on the synthesis of single-walled carbon nanotubes through chemical vapor deposition of methane

    International Nuclear Information System (INIS)

    Tan, S.-M.; Chai, S.-P.; Liu, W.-W.; Mohamed, Abdul Rahman

    2009-01-01

    The oxides of cobalt, iron, and nickel catalysts were tested in chemical vapor deposition (CVD) of methane in synthesizing single-walled carbon nanotubes (SWNTs). All catalysts used in this study were prepared using impregnation method and calcined at temperatures ranging from 300 to 850 deg. C. The catalyst samples after CVD of methane were characterized using transmission electron microscopy (TEM). The TEM study elucidates that iron oxide serves as an effective catalyst for growing SWNTs. The presence of SWNTs on the catalyst was confirmed in the Raman study.

  6. Hydrothermal synthesis of zeolite T from kaolin using two different structure-directing agents

    Science.gov (United States)

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

    2018-01-01

    Zeolite T was synthesized from the molar chemical composition of 1SiO2:0.04Al2O3:0.26Na2O:0.09K2O:14H2O in the form of a homogenous milky solution in the presence of the two different structure-directing agents TMAOH and TEAOH respectively. Modification of the composition of silica was undertaken using metakaolin from calcined kaolin at 750 °C for 4 h, while the molar composition of each different SDA was variated from 0.05, 0.10, 0.15, 0.20 and 0.25. The homogenous mixture was left at room temperature for 24 h before undergoing hydrothermal synthesis at 100 °C for 168 h. The synthesized samples were filtered and aged at 120 °C for 2 h and each sample was calcined at high temperatures (545 °C for TMAOH and 520 °C for TEAOH) for template removal before characterization using XRD and SEM. Crystallization of the zeolite T in its major form only took place at a molar ratio of 0.10 of TMAOH, while TEAOH showed the species evolution of zeolite T into zeolite L and W for other molar ratios.

  7. Study of the behavior of aggregate of calcined clay for use in permeable pavements for the city of Manaus; Estudo do comportamento de agregado sintetico de argila calcinada para uso em pavimentos permeaveis para a cidade de Manaus

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, M.S.; Vilela, P.A.T.; Araujo, V.S., E-mail: oliveirasmichelle@gmail.com [Universidade do Estado do Amazonas (UEAM), AM (Brazil)

    2016-07-01

    Research on the production of ceramic aggregates and their use in paving in the country began in the 80’s in the search for an alternative material that could replace the pebble or crushed stone, studied the clay, considered an abundant mineral resource by virtue of being the predominant soil in this region and which were made synthetic calcinated clay aggregates (ASAC), for their application in permeable paving concrete motivated by the lack of permeable areas. The study consists of the characterization of materials for manufacture of concrete slabs permeable and the assessment of the effects of synthetic aggregate on its properties in fresh and hardened state. The ceramic bodies were subjected to tests of X-ray diffraction, determination of chemical composition and plasticity. The results indicate that the use of synthetic clusters is a viable alternative for the production of porous concrete. (author)

  8. Elaboration d'un catalyseur supporté micronique par un procédé en voie sèche combinant imprégnation - calcination en lit fluidisé et broyage

    OpenAIRE

    Torré, Jean-Philippe; Alavi, Shila; Le Bolay, Nadine; Hemati, Mehrdji

    2007-01-01

    L'étude porte sur la production d'un catalyseur supporté à base d'oxyde de manganèse de taille micronique par une étape d'imprégnation – calcination en lit fluidisé sur support millimétrique, suivie de broyage. Les conditions opératoires ont permis de réaliser un dépôt métallique uniforme au sein d'un support constitué d'alumine poreuse. La distribution homogène sur l'ensemble du volume du support a été contrôlée par microscopie électronique à balayage sur coupe, mais aussi par comparaison de...

  9. Synthesis and photoluminescence properties of Eu3+-doped silica@coordination polymer core-shell structures and their calcinated silica@Gd2O3:Eu and hollow Gd2O3:Eu microsphere products.

    Science.gov (United States)

    Lee, Hee Jung; Park, Ju-Un; Choi, Sora; Son, Juhee; Oh, Moonhyun

    2013-02-25

    The conjugation of Eu(3+)-doped coordination polymers constructed from Gd(3+) and isophthalic acid (H(2)IPA) with silica particles is investigated for the production of luminescent microspheres. A series of doping ratio-controlled silica@coordination polymer core-shell spheres is easily synthesized by altering the amounts of metal nodes used in the reactions, where the ratios of Gd(3+) and Eu(3+) are 10:0 (1a), 9:1 (1b), 8:2 (1c), 7:3 (1d), 5:5 (1e), and 0:10 (1f). The formation of monodisperse uniform core-shell structures is achieved throughout the entirety of a series. Investigations of the photoluminescence property of the resulting series of silica@coordination polymer core-shell spheres reveal that 20% Eu(3+)-doped product (1c) has the strongest emission intensity. The subsequent calcination process on the silica@coordination polymer core-shell structures (1a-f) results in the formation of a series of doping ratio-controlled silica@Gd(2)O(3):Eu core-shell microspheres (2a-f) with uniform shell thickness. During the calcination step, the coordination polymers within silica@coordination polymer core-shells are transformed into metal oxides, resulting in silica@Gd(2)O(3):Eu core-shell structures. The final etching process on the silica@Gd(2)O(3):Eu core-shell microspheres (2a-f) produces a series of hollow Gd(2)O(3):Eu microspheres (3a-f) as a result of the elimination of silica cores. The luminescence intensities of silica@Gd(2)O(3):Eu core-shell (2a-f) and hollow Gd(2) O(3):Eu microspheres (3a-f) also vary depending upon the doping ratio of Eu(3+) ions. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. High activity wastes immobilization in sintered glasses: simulated wastes of the HWR (heavy water reactors) type in a new formulation glass

    International Nuclear Information System (INIS)

    Bevilacqua, A.M.; Messi de Bernasconi, N.B.; Audero, M.A.

    1987-01-01

    The new formulation of boron silicate glass, of German origin, SG7, was specifically developed for high activity wastes immobilization by a sintering process. Using the pressing technique at room temperature and subsequent sintering, the sintering conditions of the pure glass and the incorporation of the 10% in weight of simulated wastes of the HWR type recently developed, have been studied. Besides, three ways of incorporation of wastes are presented: a) incorporation of a coincidental compound obtained from chemical and thermal denitration; b) incorporation of a calcination only obtained from thermal denitration; c) incorporation of the nitric solution, mixing this one with the glass, and subsequent calcination. The results from the sintering studies and from the leaching assays of the MCC-1 are presented, and the microstructures observed are described. These results are compared with those previously obtained from boron silicate glasses of the VG type. Finally, results from long duration leaching assays, performed in samples obtained years before, are presented. (Author)

  11. Direct preparation of La2Zr2O7 microspheres by cathode plasma electrolysis.

    Science.gov (United States)

    Liu, Chenxu; Zhang, Jin; Deng, Shunjie; Wang, Peng; He, Yedong

    2016-07-15

    La2Zr2O7 microspheres were directly prepared by cathode plasma electrolysis (CPE) in the electrolyte of Zr(NO3)4·5H2O and La(NO3)3·6H2O. Compared with high temperature sintering methods, the energy of plasma was completely used by CPE and made it possible to prepare the microspheres without calcining. The diameters of microspheres were mostly in the range of 0.5-5μm and the microspheres consisted of fluorite and pyrochlore structures of La2Zr2O7. Moreover, the microspheres possessed potential photocatalytic activity and fluorescence property, owing to the high crystallinity and large surface area of the microspheres. Copyright © 2016 Elsevier Inc. All rights reserved.

  12. An ingenious strategy of preparing TiO2/g-C3N4 heterojunction photocatalyst: In situ growth of TiO2 nanocrystals on g-C3N4 nanosheets via impregnation-calcination method

    Science.gov (United States)

    Zhang, Guanghui; Zhang, Tianyong; Li, Bin; Jiang, Shuang; Zhang, Xia; Hai, Li; Chen, Xingwei; Wu, Wubin

    2018-03-01

    An ingenious method was employed to design and fabricate the TiO2/g-C3N4 heterojunction photocatalysts in this study. The thermal oxidation etching of g-C3N4 nanosheets and the in situ growth of TiO2 nanocrystal on the surface of g-C3N4 nanosheets were completed simultaneously by the calcination process. The g-C3N4 nanosheets played a crucial role in regulating and assembling the structures and morphologies of TiO2. Furthermore, the thickness and content of g-C3N4, and the crystallinity of TiO2 in TiO2/g-C3N4 composites could be regulated and controlled by the calcination temperature. Among the resultant TiO2/g-C3N4 samples, the TiO2/g-C3N4 sample with 41.6 wt% g-C3N4 exhibited the highest photocatalytic activity. It could degrade almost all MO molecules under visible light irradiation within 3 h. Moreover, it displayed higher visible light photocatalytic performance for degrading MO solution than pure g-C3N4 and D-TiO2. The synergistic effect between TiO2 and g-C3N4 makes significant contributions to the enhancement of the visible light photocatalytic activity. In addition, the favorable photocatalytic performance of TiO2/g-C3N4 nanocomposites is also attributed to the porous structures and uniform morphologies, and large surface area. Furthermore, the resultant TiO2/g-C3N4 exhibits excellent photocatalytic stability. Radical trapping experiments indicated that rad O2- and h+ were the main reactive species during the photodegradation process under visible light irradiation. Hopefully, the results can offer new design and strategy for preparing other g-C3N4-based nanocomposites for environmental and energy applications.

  13. Direct Dating and Physico-Chemical Analyses Cast Doubts on the Coexistence of Humans and Dwarf Hippos in Cyprus.

    Directory of Open Access Journals (Sweden)

    Antoine Zazzo

    Full Text Available In the Mediterranean, the island dwarf megafaunas became extinct around the end of the Pleistocene, during a period of rapid and global climate change. In Cyprus, this coincided with the first human presence on the island, as attested by the rock shelter of Akrotiri-Aetokremnos where an Epipaleolithic anthropogenic layer (stratum 2 was found overlying a massive accumulation of pygmy hippopotamus (Phanourios minor (Desmarest, 1822 [Boekschoten and Sondaar, 1972] bones (stratum 4. The relationship between the two layers is highly controversial and the role played by humans in hippo extinction remains fiercely debated. Here, we provide new, direct radiocarbon and physico-chemical analyses on calcined bones which elucidates the complex depositional history of the assemblage. Bone turquoise was identified using micro-PIXE analysis and depth-profiling together with Vis spectroscopy, demonstrating that these bones were not freshly burned. Bayesian modeling of the radiocarbon dates indicates that stratum 4 accumulated during the first half of the 13th mill cal BP and that calcination occurred several hundred years later. We conclude that accumulation occurred naturally during the beginning of the Younger Dryas and that Epipalaeolithic visitors subsequently used the bones as fuel, starting from the mid-13th mill cal BP. At that time, dwarf hippos were probably already extinct or at least highly endangered. Our results shed new light on the possible causes of hippo extinction, on the subsequent introduction of the wild boar and on the earliest occupation of the island by humans.

  14. WEEE directive application: vitrification of e-waste

    International Nuclear Information System (INIS)

    Silva, A.C.; Pidone, L.; Mello-Castanho, S.R.H.

    2011-01-01

    The aim of the WEEE directive is the electrical and electronic equipment waste (e-waste) mitigation and reduce life-cycle-end environmental impact of the this kind of equipment. Currently applied to electrical and electronic equipment manufacturers and distributors in European Union, it's Pigovian principle based, where the person that place potentially polluting products at the environment, is also legal and financial responsible for the resultant life-cycle-end pollution. This policy is a worldwide trend, and implies a growing demand in the search for new proper waste disposal technological solutions. In this context of broad spectrum, are also entered the medical equipment that make use of electronic devices. This study aims to obtain glasses which can be used as a product of commercial value containing up to 40% by mass of hospital apparatus e-waste. The residues were previously crushed and calcined. Copper and iron aventurine glass were prepared through the modification of the basic composition of soda-lime-borosilicate glass. After the melting temperature of 1300°C, the glasses were characterized by FT-IR and XRD. The chemical stability was evaluated by hydrolytic attack test. The glasses showed a high chemistry and environmental stability, like commercial soda-lime glass, in addition the obtained material present attractive appearance, allowing its use in decoration or architecture products. (author)

  15. Single and multi-component adsorption of salicylic acid, clofibric acid, carbamazepine and caffeine from water onto transition metal modified and partially calcined inorganic-organic pillared clay fixed beds.

    Science.gov (United States)

    Cabrera-Lafaurie, Wilman A; Román, Félix R; Hernández-Maldonado, Arturo J

    2015-01-23

    Fixed-beds of transition metal (Co(2+), Ni(2+) or Cu(2+)) inorganic-organic pillared clays (IOCs) were prepared to study single- and multi-component non-equilibrium adsorption of a set of pharmaceutical and personal care products (PPCPs: salicylic acid, clofibric acid, carbamazepine and caffeine) from water. Adsorption capacities for single components revealed that the copper(II) IOCs have better affinity toward salicylic and clofibric acid. However, multi-component adsorption tests showed a considerable decrease in adsorption capacity for the acids and an unusual selectivity toward carbamazepine depending on the transition metal. This was attributed to a combination of competition between PPCPs for adsorption sites, adsorbate-adsorbate interactions, and plausible pore blocking caused by carbamazepine. The cobalt(II) IOC bed that was partially calcined to fractionate the surfactant moiety showcased the best selectivity toward caffeine, even during multi-component adsorption. This was due to a combination of a mildly hydrophobic surface and interaction between the PPCP and cobalt(II). In general, the tests suggest that these IOCs may be a potential solution for the removal of PPCPs if employed in a layered-bed configuration, to take care of families of adsorbates in a sequence that would produce sharpened concentration wavefronts. Copyright © 2014 Elsevier B.V. All rights reserved.

  16. Preparation and catalytic performance of copper-containing magnetic catalysts for degradation of azo dye (direct violet).

    Science.gov (United States)

    Duan, Qiannan; Lee, Jianchao; Chen, Han; Zheng, Yunyun

    2017-12-01

    A novel magnetically separable magnetic activated carbon supporting-copper (MCAC) catalyst for catalytic wet peroxide oxidation (CWPO) was prepared by chemical impregnation. The prepared samples were characterized by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) method, and scanning electron microscopy (SEM) equipped with energy dispersive spectrometry (EDS). The catalytic performance of the catalysts was evaluated by direct violet (D-BL) degradation in CWPO experiments. The influence of preparative and operational parameters (dipping conditions, calcination temperature, catalyst loading H 2 O 2 dosage, pH, reaction temperature, additive salt ions and initial D-BL concentration) on degradation performance of CWPO process was investigated. The resulting MCAC catalyst showed higher reusability in direct violet oxidation than the magnetic activated carbon (MAC). Besides, dynamic tests also showed the maximal degradation rate reached 90.16% and its general decoloring ability of MCAC was 34 mg g -1 for aqueous D-BL.

  17. Invariants of directed spaces

    DEFF Research Database (Denmark)

    Raussen, Martin

    2007-01-01

    Directed spaces are the objects of study within directed algebraic topology. They are characterised by spaces of directed paths associated to a source and a target, both elements of an underlying topological space. The algebraic topology of these path spaces and their connections are studied from...... a categorical perspective. In particular, we study the preorder category associated to a directed space and various "quotient" categories arising from algebraic topological functors. Furthermore, we propose and study a new notion of directed homotopy equivalence between directed spaces....

  18. Direct selling particularities

    OpenAIRE

    Greifová, Daniela

    2009-01-01

    Bachelor thesis is focused on the parcularities of direct selling, self regulation of this industry, multi-level marketing which is the most used sales method in the field of direct selling. The part of the thesis is dedicated to the issue of customer psychology that is very important for achieving success in direct selling. Main goals are to provide readers with the general view of direct selling and analysis of growing possibilities of the industry in the future.

  19. Direct immunofluorescence microscopy

    NARCIS (Netherlands)

    Diercks, G.F.H.; Pas, Hendrikus; Jonkman, Marcel

    2016-01-01

    Direct immunofluorescence plays an important role in the diagnosis of autoimmune bullous diseases. The purpose of direct immunofluorescence microscopy is to detect in vivo antibodies in patient's skin or mucosa. Direct immunofluorescence of pemphigus shows depositions of immunoglobulins and/or

  20. Effect of calcination temperature on microstructure and magnetic properties of Ni{sub 0.5}Zn{sub 0.25}Cu{sub 0.25} Fe{sub 2}O{sub 4} nanoparticles synthesized by sol-gel method

    Energy Technology Data Exchange (ETDEWEB)

    Pransisco, Prengki, E-mail: prengkipransisco@gmail.com, E-mail: afza@petronas.com.my; Shafie, Afza, E-mail: prengkipransisco@gmail.com, E-mail: afza@petronas.com.my [Department of Fundamental and Applied Sciences, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 31750 Tronoh, Perak (Malaysia); Guan, Beh Hoe, E-mail: beh.hoeguan@petronas.com.my

    2014-10-24

    This paper examines the effect of calcination process on the structural and magnetic properties material nanostructure composite of Ni{sub 0Ð}œ‡{sub 5}Zn{sub 0Ð}œ‡{sub 25}Cu{sub 0.25} Fe{sub 2}O{sub 4} ferrites. The samples were successfully prepared by sol-gel method at different calcination temperature, which are 600°C, 700°C, 800°C and 900°C. Morphological investigation, average crystallite size and microstructure of the material were examined by using X-ray diffraction (XRD) and confirmed by high resolution transmission electron microscope (HRTEM) and field emission scanning electron microscope (FESEM). The effects of calcination temperature on the magnetic properties were calculated by using vibrating sample magnetometer (VSM). The XRD result shows single-phase cubic spinel structure with interval average size 5.9-38 nm, and grain size microstructure of the material was increasing with temperature increases. The highest magnetization saturation was reached at a temperature 800°C with value 53.89 emu/g, and the value coercive force (Hc) was inversely with the grain size.

  1. [Acupuncture direction and analgesia].

    Science.gov (United States)

    Sun, Lu; Kou, Renzhong; Liu, Lanqing; Fan, Gangqi

    2017-03-12

    The acupuncture direction is closely related with the efficacy of acupuncture analgesia. In this article, the relationship between efficacy of acupuncture analgesia and factors, such as whether the needle towards disease location, whether the needle towards meridian direction, whether the needle following spinal cord direction and whether the needle following muscle direction, were analyzed. The previous clinical and literature research indicated that the needle towards disease location was superior to reverse direction, however, the efficacy of analgesia between needle following and reversing meridian, needle towards and at disease location, needles following and reversing spinal cord direction, needles following and reversing muscle direction was controversial. Therefore, the solutions to these problems will benefit the optimized acupuncture treatment plan for pain disorders.

  2. Process for denitrating waste solutions containing nitrates and actinides with simultaneous separation of the actinides

    International Nuclear Information System (INIS)

    Gompper, K.

    1986-01-01

    The invention is intended to reduce the acid and nitrate content of nitrate waste solutions, to reduce the total salt content of the waste solution, to remove the actinides contained in it by precipitation, without any danger of violent reactions or an increase in the volume of the waste solution. The invention achieves this by mixing the waste solution with diethyl oxalate at room temperature and heating the mixture to at least 80 0 C. (orig./PW) [de

  3. Process for denitrating waste solutions containing nitric acid actinides simultaneously separating the actinides

    International Nuclear Information System (INIS)

    Gompper, K.

    1984-01-01

    The invention should reduce the acid and nitrate content of waste solutions containing nitric acid as much as possible, should reduce the total salt content of the waste solution, remove the actinides contained in it by precipitation and reduce the α radio-activity in the remaining solution, without having to worry about strong reactions or an increase in the volume of the waste solution. The invention achieves this by mixing the waste solution with diethyl oxalate at room temperature and heating the mixture to at least 80 0 C. (orig.) [de

  4. Applications of Fuzzy adaptive PID control in the thermal power plant denitration liquid ammonia evaporation

    Directory of Open Access Journals (Sweden)

    Li Jing

    2016-01-01

    Full Text Available For the control of the liquid level of liquid ammonia in thermal power plant’s ammonia vaporization room, traditional PID controller parameter tuning is difficult to adapt to complex control systems, the setting of the traditional PID controller parameters is difficult to adapt to the complex control system. For the disadvantage of bad parameter setting, poor performance and so on the fuzzy adaptive PID control is proposed. Fuzzy adaptive PID control combines the advantages of traditional PID technology and fuzzy control. By using the fuzzy controller to intelligent control the object, the performance of the PID controller is further improved, and the control precision of the system is improved[1]. The simulation results show that the fuzzy adaptive PID controller not only has the advantages of high accuracy of PID controller, but also has the characteristics of fast and strong adaptability of fuzzy controller. It realizes the optimization of PID parameters which are in the optimal state, and the maximum increase production efficiency, so that are more suitable for nonlinear dynamic system.

  5. Methanol-to-hydrocarbons conversion over MoO3/H-ZSM-5 catalysts prepared via lower temperature calcination: a route to tailor the distribution and evolution of promoter Mo species, and their corresponding catalytic properties.

    Science.gov (United States)

    Liu, Bonan; France, Liam; Wu, Chen; Jiang, Zheng; Kuznetsov, Vladimir L; Al-Megren, Hamid A; Al-Kinany, Mohammed; Aldrees, Saud A; Xiao, Tiancun; Edwards, Peter P

    2015-09-01

    A series of MoO 3 /H-ZSM-5 (Si/Al = 25) catalysts were prepared via calcination at a lower-than-usual temperature (400 °C) and subsequently evaluated in the methanol-to-hydrocarbon reaction at that same temperature. The catalytic properties of those catalysts were compared with the sample prepared at the more conventional, higher temperature of 500 °C. For the lower temperature preparations, molybdenum oxide was preferentially dispersed over the zeolite external surface, while only the higher loading level of MoO 3 (7.5 wt% or higher) led to observable inner migration of the Mo species into the zeolite channels, with concomitant partial loss of the zeolite Brønsted acidity. On the MoO 3 modified samples, the early-period gas yield, especially for valuable propylene and C 4 products, was noticeably accelerated, and is gradually converted into an enhanced liquid aromatic formation. The 7.5 wt% MoO 3 /H-ZSM-5 sample prepared at 400 °C thereby achieved a balance between the zeolite surface dispersion of Mo species, their inner channel migration and the corresponding effect on the intrinsic Brønsted acidity of the acidic zeolite. That loading level also possessed the highest product selectivity (after 5 h reaction) to benzene, toluene and xylenes, as well as higher early-time valuable gas product yields in time-on-stream experiments. However, MoO 3 loading levels of 7.5 wt% and above also resulted in earlier catalyst deactivation by enhanced coke accumulation at, or near, the zeolite channel openings. Our research illustrates that the careful adoption of moderate/lower temperature dispersion processes for zeolite catalyst modification gives considerable potential for tailoring and optimizing the system's catalytic performance.

  6. Descendants and advance directives.

    Science.gov (United States)

    Buford, Christopher

    2014-01-01

    Some of the concerns that have been raised in connection to the use of advance directives are of the epistemic variety. Such concerns highlight the possibility that adhering to an advance directive may conflict with what the author of the directive actually wants (or would want) at the time of treatment. However, at least one objection to the employment of advance directives is metaphysical in nature. The objection to be discussed here, first formulated by Rebecca Dresser and labeled by Allen Buchanan as the slavery argument and David DeGrazia the someone else problem, aims to undermine the legitimacy of certain uses of advance directives by concluding that such uses rest upon an incorrect assumption about the identity over time of those ostensibly governed by the directives. There have been numerous attempts to respond to this objection. This paper aims to assess two strategies that have been pursued to cope with the problem.

  7. Directional radiation detectors

    Science.gov (United States)

    Dowell, Jonathan L.

    2017-09-12

    Directional radiation detectors and systems, methods, and computer-readable media for using directional radiation detectors to locate a radiation source are provided herein. A directional radiation detector includes a radiation sensor. A radiation attenuator partially surrounds the radiation sensor and defines an aperture through which incident radiation is received by the radiation sensor. The aperture is positioned such that when incident radiation is received directly through the aperture and by the radiation sensor, a source of the incident radiation is located within a solid angle defined by the aperture. The radiation sensor senses at least one of alpha particles, beta particles, gamma particles, or neutrons.

  8. Directed Energy Anechoic Chamber

    Data.gov (United States)

    Federal Laboratory Consortium — The Directed Energy Anechoic Chamber comprises a power anechoic chamber and one transverse electromagnetic cell for characterizing radiofrequency (RF) responses of...

  9. Mathematical modelling of the calcination process | Olayiwola ...

    African Journals Online (AJOL)

    High quality lime is an essential raw material for Electric Arc Furnaces and Basic Oxygen Furnaces, steelmaking, alumina production etc. Decrease in fuel consumption in metallurgical furnaces is a tremendous opportunity for reduction of greenhouse gas emissions into the atmosphere. In this paper, a mathematical model ...

  10. The Consumer Rights Directive

    NARCIS (Netherlands)

    Luzak, J.A.; Mak, V.; Hartkamp, A.S.; Sieburgh, C.H.; Keus, L.A.D.; Kortmann, J.S.; Wissink, M.H.

    2014-01-01

    This contribution discusses the impact of the CRD on Dutch private law. How will the new directive influence consumer rights and how does this fit with existing law? Considering the background of the directive and its importance for European consumer law, however, we discuss these questions in the

  11. Direct RF modulation transmitter

    NARCIS (Netherlands)

    Fukuda, Shuichi; Nauta, Bram

    2013-01-01

    PROBLEM TO BE SOLVED: To provide a direct RF modulation transmitter capable of saving more power consumption. SOLUTION: The direct RF modulation transmitter comprises: a passive mixer circuit 100 which inputs digital baseband data D of 1 bit, inverted data DN, a first RF signal, and a second RF

  12. Directionality effects in percolation

    Science.gov (United States)

    Redner, Sidney

    The percolation properties of random networks containing resistors (two-way streets) and/or diodes (one-way streets) are considered. The directionality constraints of the diodes are found to lead to novel geometrical behavior. As a simple example, various random cluster models with a preferred direction, such as directed random walks or directed lattice animals, are shown to be anisotropic in character. The critical behavior of directed percolation is then treated and its connection with branching Markov processes is explained. A closely related "reverse" percolation problem, a transition from one-way percolation to isotropic percolation, is introduced. Finally, the geometrical properties of a network containing arbitrarily oriented diodes are treated. Symmetry and duality arguments are applied to yield exact results for certain aspects of its critical behavior.

  13. Mesoporous nanoplate multi-directional assembled Bi2WO6for high efficient photocatalytic oxidation of NO.

    Science.gov (United States)

    Wan, Jun; Du, Xiao; Wang, Ruimiao; Liu, Enzhou; Jia, Jia; Bai, Xue; Hu, Xiaoyun; Fan, Jun

    2018-02-01

    Herein, a mesoporous nanoplate multi-directional assembled Bi 2 WO 6 architecture was successfully prepared and applied for the photocatalytic removal of NOx pollutants at low concentrations under visible light and simulated solar light irradiation. Bi 2 WO 6 -180-C synthesized at a hydrothermal temperature of 180 °C with calcination exhibited an excellent conversion efficiency in the photocatalytic oxidation of gaseous NO. The crystallinity, morphology, specific surface area, pore environment, light absorption, and separation of photogenerated electrons and holes were investigated by various techniques; the excellent photocatalytic performance of Bi 2 WO 6 -180-C was attributed to its special hierarchical mesoporous structure with an appropriate pore size and interconnected porous network, which imparted good gas permeability and fast mass transfer of reaction intermediates and final products of NO oxidation. Furthermore, hierarchical mesoporous Bi 2 WO 6 showed excellent photocatalytic durability and reusability. Copyright © 2017 Elsevier Ltd. All rights reserved.

  14. Direction of time

    International Nuclear Information System (INIS)

    Mirman, R.

    1975-01-01

    The meaning of the phrase ''the direction of time'' and the physical problems involved are considered. These problems are discussed, and plausibility arguments are given to show that all clocks run in the same direction (almost always), that the most probable development of the universe during the early stages of the expansion would result in the introduction of some internal organization, and that the expansion of the universe and the increase in entropy define time directions that have the same sense. The question of what properties of the laws governing the universe lead to these results is studied

  15. Effects of La{sup 3+}–Nd{sup 3+} ions and pre-calcination on the growth of hexaferrite nanoparticles prepared by gel to crystallization technique: Non-isothermal crystallization kinetics analysis

    Energy Technology Data Exchange (ETDEWEB)

    Thakur, Ankush [Department of Physics, Jaipur Engineering College and Research Centre, Jaipur (India); Barman, P.B. [Department of Physics and Materials Science, Jaypee University of Information Technology, Waknaghat (India); Singh, R.R., E-mail: raginirajsingh@gmail.com [Department of Physics and Materials Science, Jaypee University of Information Technology, Waknaghat (India)

    2015-04-15

    This is the first report ever on La{sup 3+}–Nd{sup 3+} doped M-type hexaferrite nanoparticles: SrNd{sub x}La{sub y}Fe{sub 12−x−y}O{sub 19} (0 ≤ x ≤ 1) prepared by citrate precursor using the sol–gel technique followed by gel to crystallization. The substitution effects of ions and molar ratio of Fe{sup 3+}/Sr{sup 2+} on the formation of ferrite phase were examined using powder differential thermal analysis (DTA) technique, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (Mid-IR) and vibrating sample magnetometer (VSM). The present work aim to study the crystallization of binary La{sup 3+}- Nd{sup 3+} doped hexaferrite nanoparticles. DTA technique was employed to investigate the formation of nanocrystalline SrNd{sub 0.4}La{sub 0.4}Fe{sub 11.2}O{sub 19} and revealed that the formation of ferrite phase was occurred in steps and crystallization take place by the means of endothermic reactions. The value of activation energy and crystallization temperature has been obtained from DTA data using different non-isothermal methods. XRD and Mid-IR studies have confirmed the formation of ferrite phase. Through this work an optimum calcination condition was established for the synthesis of single phase hexaferrite nanoparticles even after the substitution of binary rare earth elements. Magnetic properties were determined by using a vibrating sample magnetometer. The magnetic results revealed that the synthesized nanoparticles are suitable for perpendicular recording media due to their high coercivity value. - Highlights: • First report of studies on Nd{sup 3+}–La{sup 3+} doped M-type strontium hexaferrite nanoparticles. • Studied the crystallization of binary (Nd{sup 3+}–La{sup 3+}) doped hexaferrite nanoparticles. • Studied the effects of La{sup 3+}–Nd{sup 3+} & molar ratio of Fe{sup 3+}/Sr{sup 2+} on the formation of ferrite phase. • Established an optimum condition to obtain single phase hexaferrite nanoparticles. • Magnetic

  16. Modelación del proceso de calcinación flash durante la activación de arcillas // Modeling of the flash calcination process during clay activation

    Directory of Open Access Journals (Sweden)

    Rubén Borrajo‐Pérez

    2012-01-01

    temperatureof particles are obtained as a function of the gas parameters. The calculation includes the heat losses andthe model predicts the residence time of a particle in an activation unit.Key words: puzzolan, flash, calcinations, modeling.

  17. Efeito da argila calcinada sobre a durabilidade de argamassas reforçadas com fibras curtas de sisal Effect of calcined clay on aging of sisal short fiber reinforced mortar

    Directory of Open Access Journals (Sweden)

    João de Farias Filho

    2010-10-01

    Full Text Available O interesse pelo uso de fibras vegetais como reforço de matrizes, à base de cimento, tem crescido em todo o mundo nos últimos anos, sendo limitado pela baixa durabilidade das fibras no meio alcalino. Com o tempo, as fibras podem mineralizar devido à migração de hidróxido de cálcio (CH da matriz para o lúmen e paredes das fibro-células. Procurou-se consumir, no presente estudo, o CH livre utilizando-se resíduo de tijolo moído e metacaulinita em substituição parcial, de 20 e 40% em peso, do cimento portland. Compósitos com fibras de sisal e matrizes cimento-pozolana foram submetidos a ensaios de resistência a flexão, após 28 dias de cura em água, 135 e 180 dias de envelhecimento natural e após 94 ciclos de molhagem e secagem. Os resultados indicaram que é possível consumir todo o CH da matriz, o que resultou na manutenção da tenacidade inicial do compósito e no aumento da sua resistência a flexão após exposição natural ou ciclos de molhagem e secagem.In the last few years a growing interest in the use of sisal fibers as reinforcement in cement based composites has been observed. However, the main concern for its use is related with the durability of the fibers in the alkaline water of concrete as they can mineralize due to the migration of calcium hydroxide to the fiber lumen and cell walls. In this study, the alkalinity of the matrix was reduced using metakaolin and crushed waste calcined clay bricks as cement replacement. The percentage of cement replacement ranged from 20 to 40% on weight basis. Flexural tests were carried out in the composites after 28 days of cure in water, 135 and 180 days of ageing in the open air and after 94 cycles of wetting and drying. These results indicated that the mixture with cement replacement consumed all calcium hydroxide and kept the toughness over time.

  18. Potencialidades da metacaolinita e do tijolo queimado moído como substitutos parciais do cimento Portland Potentialities of metakaolin and crushed waste calcined clay brick as partial replacement of Portland cement

    Directory of Open Access Journals (Sweden)

    João de Farias Filho

    2000-12-01

    Full Text Available Avalia-se, neste trabalho, a potencialidade do uso da metacaolinita e dos resíduos de produção de tijolos cerâmicos queimados finamente moídos, como substitutos parciais do cimento Portland. Os materiais foram caracterizados física, química e mineralogicamente, além de determinado o índice de atividade pozolânica com cimento Portland. A evolução da resistência a compressão e a flexão das argamassas foi avaliada até as idades de, respectivamente, 365 e 208 dias. As porcentagens de substituição do cimento Portland, em peso, pelos materiais pozolânicos, variaram de 20 a 50%, enquanto o fator água/cimento variou de 0,37 a 0,45. Os resultados obtidos indicaram que a metacaolinita e o tijolo moído queimado possuem elevada atividade pozolânica e que a resistência a compressão, aos 28 dias, das argamassas mistas, foi superior à das argamassas de cimento Portland para os níveis de substituição e fatores água/cimento estudados. Um modelo matemático para predição da resistência à compressão das argamassas mistas é proposto com base em um desenho fatorial de experimentos.This paper evaluates the potentiality of metakaolin and crushed waste fired clay brick as cement replacement materials. They were characterised physically, chemically and mineralogically and their activity with Portland cement determined. The influence of the partial replacement of Portland cement on the development of compressive and flexural strength was evaluated until the age of, respectively, 365 and 208 days. The percentage of cement replacement, in weight, ranged from 20 to 50%, whereas the water/cement ratio ranged from 0.37 to 0.45. The results obtained show that the metakaolin and crushed calcined clay brick presented a good pozolanic activity and that the compressive strength of the blended mortars after 28 days of cure was higher than that observed for the reference Portland cement for all levels of cement replacement and water/cement ratio. A

  19. Advance Directives - Multiple Languages

    Science.gov (United States)

    ... Expand Section Advance Directives - 简体中文 (Chinese, Simplified (Mandarin dialect)) Bilingual PDF Health Information Translations Chinese, Traditional (Cantonese dialect) (繁體中文) Expand Section Advance ...

  20. Direct Conversion of Energy

    Energy Technology Data Exchange (ETDEWEB)

    Corliss, William R

    1964-01-01

    Topics include: direct versus dynamic energy conversion; laws governing energy conversion; thermoelectricity; thermionic conversion; magnetohydrodynamic conversion; chemical batteries; the fuel cell; solar cells; nuclear batteries; and advanced concepts including ferroelectric conversion and thermomagnetic conversion.

  1. Directed GF-spaces

    Directory of Open Access Journals (Sweden)

    F.G. Arenas

    2001-10-01

    Full Text Available In this paper we introduce the concept of directed fractal structure, which is a generalization of the concept of fractal structure (introduced by the authors. We study the relation with transitive quasiuniformities and inverse limits of posets. We define the concept of GF-compactification and apply it to prove that the Stone-Cech compactification can be obtained as the GF-compactification of the directed fractal structure associated to the Pervin quasi-uniformity.

  2. Directional gear ratio transmissions

    Science.gov (United States)

    Lafever, A. E. (Inventor)

    1984-01-01

    Epicyclic gear transmissions which transmit output at a gear ratio dependent only upon the input's direction are considered. A transmission housing envelops two epicyclic gear assemblies, and has shafts extending from it. One shaft is attached to a sun gear within the first epicyclic gear assembly. Planet gears are held symmetrically about the sun gear by a planet gear carrier and are in mesh with both the sun gear and a ring gear. Two unidirectional clutches restrict rotation of the first planet gear carrier and ring gear to one direction. A connecting shaft drives a second sun gear at the same speed and direction as the first planet gear carrier while a connecting portion drives a second planet gear carrier at the same speed and direction as the first ring gear. The transmission's output is then transmitted by the second ring gear to the second shaft. Input is transmitted at a higher gear ratio and lower speed for all inputs in the first direction than in the opposite direction.

  3. Desempenho mecânico de misturas asfálticas confeccionadas com agregados sintéticos de argila calcinada Mechanical performance of asphalt mixtures composed of synthetic calcinated clay aggregates

    Directory of Open Access Journals (Sweden)

    C. A. Frota

    2007-09-01

    .A substantial number of municipal districts in the State of Amazonas are located in areas which are poor in stony materials. And this has led pavement builders into adopting alternatives which have historically produced pavements with low mechanical strength. Whist more effective and appropriate from a technical standpoint, the asphalt concrete has been usually left aside due to the referred lack of stony materials. Because of the specific situation in the State of Amazonas the adoption of synthetic calcinated clay aggregates (SCCA, with an abundant raw material (clay in the State of Amazonas is recommended in lieu of the traditional practice. Previous works carried out by the Federal University of Amazonas Geotechny Group have demonstrated that the clay soil commonly used in the production of ceramic materials can yield synthetic aggregates with adequate mechanical properties. In this research work, samples featuring similar characteristics as those of the soils in question have been found along the BR-319 highway connecting the Manaus (AM city to Porto Velho (RO city. The transportation structure in general is in deplorable conditions. Justifiably so, the recovery of this highway has been earmarked as one of the targets for the Ministry of Transportation. In this study, asphalt mixtures were blended with synthetic aggregates and pebbles taken from the river bed in order to compare the mechanical performance of such mixtures by means of the determination of the resilient modulus (RM. The results, as a rule, have shown that the asphalt mixtures comprising synthetic calcinated clay aggregates when compared with those comprising the naturally-found material (river bed pebbles have shown: (a greater tensile and resilient modulus strengths; (b low deformation tendency, as well as a considerable elastic recovery and (c less susceptibility to permanent deformation.

  4. Directed network modules

    International Nuclear Information System (INIS)

    Palla, Gergely; Farkas, Illes J; Pollner, Peter; Derenyi, Imre; Vicsek, Tamas

    2007-01-01

    A search technique locating network modules, i.e. internally densely connected groups of nodes in directed networks is introduced by extending the clique percolation method originally proposed for undirected networks. After giving a suitable definition for directed modules we investigate their percolation transition in the Erdos-Renyi graph both analytically and numerically. We also analyse four real-world directed networks, including Google's own web-pages, an email network, a word association graph and the transcriptional regulatory network of the yeast Saccharomyces cerevisiae. The obtained directed modules are validated by additional information available for the nodes. We find that directed modules of real-world graphs inherently overlap and the investigated networks can be classified into two major groups in terms of the overlaps between the modules. Accordingly, in the word-association network and Google's web-pages, overlaps are likely to contain in-hubs, whereas the modules in the email and transcriptional regulatory network tend to overlap via out-hubs

  5. Microstructure and magnetic properties of M-type Sr{sub 0.61−x}La{sub 0.39}Ca{sub x}Fe{sub 11.7}Co{sub 0.3}O{sub 19} hexaferrite prepared by microwave calcination

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Zhongyan, E-mail: chenzhongyan88@163.com; Wang, Fan; Yan, Shuoqing; Feng, Zekun

    2014-03-15

    Highlights: • We successfully prepared M-type Sr{sub 0.61−z}La{sub 0.39}Ca{sub z}Fe{sub 11.7}Co{sub 0.3}O{sub 19} ferrites samples using microwave calcining technique, which is an effective method for preparing the hexaferrites and controling the grain size. • The magnetic properties of the samples with the composition of Sr{sub 0.61−z}La{sub 0.39}Ca{sub z}Fe{sub 11.7}Co{sub 0.3}O{sub 19} were markedly improved when x ≤ 0.2. With the composition of Sr0.41La0.39Ca0.2Fe11.7Co0.3O19 calcined at 1140 °C for 30 min using microwave calcining, the largest saturation magnetization of 68.3 emu/g and coercivity of 5320 Oe were observed for the sample. -- Abstract: M-type Sr{sub 0.61−x}La{sub 0.39}Ca{sub x}Fe{sub 11.7}Co{sub 0.3}O{sub 19} ferrites with various calcium concentrations (x = 0, 0.1, 0.2, 0.3) were prepared through microwave calcining. The microstructure, morphology and magnetic properties of the samples were evaluated by X-ray diffraction, scanning electron microstructure and vibrating sample magnetometry, respectively. Results showed that more Fe{sup 3+} ions were substituted by Co{sup 2+} with the increase of calcium substitution, which suppressed the formation of the impurity phases to improve the magnetic properties. The coercivity and saturation magnetization of the samples with the composition of Sr{sub 0.61−x}La{sub 0.39}Ca{sub x}Fe{sub 11.7}Co{sub 0.3}O{sub 19} can be remarkably improved when x = 0.2.

  6. Direct reading dosimeter

    International Nuclear Information System (INIS)

    Thomson, I.

    1985-01-01

    This invention is a direct reading dosimeter which is light, small enough to be worn on a person, and measures both dose rates and total dose. It is based on a semiconductor sensor. The gate threshold voltage change rather than absolute value is measured and displayed as a direct reading of the dose rate. This is effected by continuously switching the gate of an MOS transistor from positive to negative bias. The output can directly drive a digital readout or trigger an audible alarm. The sensor device can be a MOSFET, bipolar transistor, or MOSFET capacitor which has its electrical characteristics change due to the trapped charge in the insulating layer of the device

  7. DIRECT KICKS IN BOXING

    Directory of Open Access Journals (Sweden)

    Izet Kahrović

    2009-11-01

    Full Text Available Hit directly, giving any impact maximum muscle strength is skill, and it is neces- sary to the exercise and learning to make it perfect. Training begins with oral statement, so that students get to know with the techni- que that works. After oral exposure, it is necessary to create a good notion on technology that is adopted. The best way for the creation of good notion is a good demonstration. In direct training kicks in the box, you need patience and gradualness and there- fore uses a large number of additional exercises. In their work with beginners, in the first class, individual elements of technology, and also direct blow, it is necessary to separate the parts and run them on multiple commands, to later come to the confluence in one command. Direct wounds, with left and right hand, can be run from the towns, on the head and body, from the movement, to step forward, step back and step aside, the remedy to the left and right side. Left direct is taking out from a running protrusion hands, but kick, which is a pro- duct of the system, ankle-knee-pelvis and shoulder forward horizontaly. Set at the time of stripes, body weight over the left leg. Right direct from the place, starting ekscentrical reflecsive impuls of a extensor muscle in ankle, knee and joint of a hip.This kind of a sud- den movement is running simultaneously with the rotation of the body around vertical (longitudinal axis, with the transfer body weight on the left leg. Further movement to the hand which serves as a lever, which is transmitted through the power stroke

  8. Directed flux motor

    Science.gov (United States)

    Wilson, Andrew (Inventor); Punnoose, Andrew (Inventor); Strausser, Katherine (Inventor); Parikh, Neil (Inventor)

    2011-01-01

    A directed flux motor described utilizes the directed magnetic flux of at least one magnet through ferrous material to drive different planetary gear sets to achieve capabilities in six actuated shafts that are grouped three to a side of the motor. The flux motor also utilizes an interwoven magnet configuration which reduces the overall size of the motor. The motor allows for simple changes to modify the torque to speed ratio of the gearing contained within the motor as well as simple configurations for any number of output shafts up to six. The changes allow for improved manufacturability and reliability within the design.

  9. Direct subdural scintigraphy

    Energy Technology Data Exchange (ETDEWEB)

    Keren, G.; Barzilay, Z.; Czerniak, P.; Cohen, B.E.

    1980-06-01

    We report a case of pneumococcal meningitis in an 8 weeks old female infant followed by persistent subdural effusion successsfully treated by repeated subdural taps. The initial delineation of the subdural effusion, the decrease in size and the disappearance of the fluid were demonstrated by direct subdural scintigraphy (D.S.S.). The literature of pneumoccocal meningitis, its diagnosis, treatment and complications are reviewed, and it is suggested that direct subdural scintigraphy should be employed as a diagnostic aid in the evaluation and follow up of subdural effusions.

  10. Handedness of direct photons

    International Nuclear Information System (INIS)

    Kopeliovich, B.Z.; Rezaeian, A.H.; Schmidt, Ivan

    2008-01-01

    The azimuthal asymmetry of direct photons originating from primary hard scatterings between partons is calculated. This can be accounted for by the inclusion of the color dipole orientation, which is sensitive to the rapid variation of the nuclear profile. To this end we introduce the dipole orientation within the saturation model of Golec-Biernat and Wuesthoff, while preserving all its features at the cross-section level. We show that the direct photon elliptic anisotropy v2 coming from this mechanism changes sign and becomes negative for peripheral collisions, albeit it is quite small for nuclear collisions at the RHIC energy. (author)

  11. The direction of time

    CERN Document Server

    Reichenbach, Hans

    1999-01-01

    Ever a source of philosophical conjecture and debate, the concept of time represents the beating heart of physics. This final work by the distinguished physicist Hans Reichenbach represents the culmination and integration of a lifetime's philosophical contributions and inquiries into the analysis of time. The result is an outstanding overview of such qualitative, or topological, attributes of time as order and direction.Beginning with a discussion of the emotive significance of time, Reichenbach turns to an examination of the time order of mechanics, the time direction of thermodynamics and m

  12. Polymer Directed Protein Assemblies

    Directory of Open Access Journals (Sweden)

    Patrick van Rijn

    2013-05-01

    Full Text Available Protein aggregation and protein self-assembly is an important occurrence in natural systems, and is in some form or other dictated by biopolymers. Very obvious influences of biopolymers on protein assemblies are, e.g., virus particles. Viruses are a multi-protein assembly of which the morphology is dictated by poly-nucleotides namely RNA or DNA. This “biopolymer” directs the proteins and imposes limitations on the structure like the length or diameter of the particle. Not only do these bionanoparticles use polymer-directed self-assembly, also processes like amyloid formation are in a way a result of directed protein assembly by partial unfolded/misfolded biopolymers namely, polypeptides. The combination of proteins and synthetic polymers, inspired by the natural processes, are therefore regarded as a highly promising area of research. Directed protein assembly is versatile with respect to the possible interactions which brings together the protein and polymer, e.g., electrostatic, v.d. Waals forces or covalent conjugation, and possible combinations are numerous due to the large amounts of different polymers and proteins available. The protein-polymer interacting behavior and overall morphology is envisioned to aid in clarifying protein-protein interactions and are thought to entail some interesting new functions and properties which will ultimately lead to novel bio-hybrid materials.

  13. Direct vision internal urethrotomy

    DEFF Research Database (Denmark)

    Jakobsen, H; Willumsen, H; Søndergaard Jensen, L

    1984-01-01

    During a five-year period, direct vision internal urethrotomy was used for the treatment of urethral strictures in 34 men. After the primary operation the patients were followed for an average period of 29 months (range 3-73 months). During this period 53% of the patients were found to have one...

  14. CGH Future Directions

    Science.gov (United States)

    Looking ahead, we have three major future directions that we believe will help us push forward in achieving NCI’s goal of advancing global cancer research, building expertise, and leveraging resources across nations to address the challenges of cancer and reduce cancer deaths worldwide.

  15. Summary and future directions

    Science.gov (United States)

    Janaki R.R. Alavalapati; D. Evan Mercer

    2004-01-01

    This chapter summarizes the main results from the preceding chapters, identifies gaps, and provides direction for fbture economics research on agroforestry systems. Although a common theme throughout the 1990s was that economic research on agroforestry continued to lag the advances made in the bio-physical sciences, the wide range of systems, regions, and techniques...

  16. Directional loudness perception

    DEFF Research Database (Denmark)

    Sivonen, Ville Pekka

    developed. The research and modeling of loudness have mainly been concerned with the temporal and spectral aspects of sounds, while the spatial aspects have mostly been overlooked. This PhD thesis investigates the spatial aspects of loudness perception, namely, how does the direction from which a sound...

  17. Direct Sulfation of Limestone

    DEFF Research Database (Denmark)

    Hu, Guilin; Dam-Johansen, Kim; Wedel, Stig

    2007-01-01

    The direct sulfation of limestone was studied in a laboratory fixed-bed reactor. It is found that the direct sulfation of limestone involves nucleation and crystal grain growth of the solid product (anhydrite). At 823 K and at low-conversions (less than about 0.5 %), the influences of SO2, O-2...... and CO2 on the direct sulfation of limestone corresponds to apparent reaction orders of about 0.2, 0.2 and -0.5, respectively. Water is observed to promote the sulfation reaction and increase the apparent reaction orders of SO2 and O-2. The influence of O-2 at high O-2 concentrations (> about 15...... %) becomes negligible. In the temperature interval from 723 K to 973 K, an apparent activation energy of about 104 kJ/mol is observed for the direct sulfation of limestone. At low temperatures and low conversions, the sulfation process is most likely under mixed control by chemical reaction and solid...

  18. Direct contamination - seasonality

    International Nuclear Information System (INIS)

    Aarkrog, A.

    1994-01-01

    Direct contamination is the primary pathway to terrestrial vegetation in the first period after an activity release to the atmosphere. All radionuclides are able to be transferred via this pathway. Deposition, interception and retention are the three processes involved in direct contamination of crops. Wet deposition is more important than dry deposition in temperature regions. Resuspension and rainsplash both belong to secondary direct deposition and became evident for e.g. radiocaesium after the Chernobyl accident. Seasonality is the varying response to radioactive contamination of crops according to the time of the year when the contamination occurs. Shortlived radionuclides (as 131 I) and those that mainly enter the foodchain by direct contamination (e.g. 137 Cs) are especially important in this connection. In particular, the contamination of cereal crops is influenced by seasonality. As a result of seasonality the impact of the Chernobyl accident on the radioactive contamination of human diet was for the same deposition density higher in southern than in northern Europe. (orig.)

  19. Direct fired heat exchanger

    Science.gov (United States)

    Reimann, Robert C.; Root, Richard A.

    1986-01-01

    A gas-to-liquid heat exchanger system which transfers heat from a gas, generally the combustion gas of a direct-fired generator of an absorption machine, to a liquid, generally an absorbent solution. The heat exchanger system is in a counterflow fluid arrangement which creates a more efficient heat transfer.

  20. Direction des Publications

    African Journals Online (AJOL)

    Synthese

    Experimental research of fluid flow and convection heat transfer in plate channels filled with glass or metallic particles, Experimental Thermal and Fluid. Science, Vol.20, Issue.1, 45-54. [7] Rahimian M.H., Pourshaghaghy A.,. 2002. Direct simulation of forced convection flow in a parallel plate channel filled with porous media, ...

  1. Advanced directives: open issues

    Directory of Open Access Journals (Sweden)

    Gabriella Negrini

    2013-05-01

    Full Text Available BACKGROUND In Italy Advanced directives have not been regulated by law yet. Moreover, there is a confusion of concepts: advanced directives, refusal of treatment, medical futility and euthanasia are not synonymous.DISCUSSION The following aspects are then discussed: object of directives; elapse of time between their expression and their application; knowledge of the directives and their obligatory nature. The refusal of a treatment that can save a person’s life is a critical subject. There are different ethical points of view: according to lay ethics, the patient’s self-determination prevails; the religious viewpoint, instead, says that life is a gift which we cannot dispose of. In any case, the patient will be confronted with the professional autonomy of the doctor. Should the doctor save a patient’s life in any case or should he achieve best clinical practice, in respect of his will? The doctor should interpret the patient’s will but with caution and judgment. An exemption from responsibility should be provided by law for doctors who respect patient’s living will.

  2. The Directed Case Method.

    Science.gov (United States)

    Cliff, William H.; Curtin, Leslie Nesbitt

    2000-01-01

    Provides an example of a directed case on human anatomy and physiology. Uses brief real life newspaper articles and clinical descriptions of medical reference texts to describe an actual, fictitious, or composite event. Includes interrelated human anatomy and physiology topics in the scenario. (YDS)

  3. Potencialidades de um caulim calcinado como material de substituição parcial do cimento portland em argamassas Potentialities of a calcined kaolin as material of partial replacement of portland cement in mortars

    Directory of Open Access Journals (Sweden)

    Marilia P. de Oliveira

    2006-06-01

    Full Text Available A utilização de argilas calcinadas na forma de metacaulinita, como material pozolânico para argamassas e concretos, tem recebido atenção considerável nos últimos anos. Este trabalho objetivou avaliar o desempenho mecânico de argamassas, nas quais foi utilizado um caulim calcinado proveniente do Estado da Paraíba, como material de substituição parcial do cimento Portland. Utilizaram-se duas finuras do caulim: passando nas peneiras ABNT 200 (0,074 mm e 325 (0,044 mm e calcinados nas temperaturas de 700, 800 e 900 ºC pelo tempo de 2 h. As amostras foram caracterizadas através de análise química, análise térmica diferencial, difração de raios-X e área específica. Obteve-se o índice de atividade pozolânica com a cal e o cimento Portland. O percentual de substituição adotado foi de 0, 10, 20, 30 e 40%. A relação aglomerante: areia foi de 1:1,5 e a relação água/aglomerante fixada igual 0,4. O efeito da substituição parcial do cimento na argamassa foi avaliado através da resistência à compressão simples, nas idades de 7, 28 e 90 dias. As argamassas estudadas apresentaram resistência superior em relação à da referência, até o nível de 30% de substituição.The use of burnt clays, in the metakaolin form, as pozzolanic material for mortars and concretes has received a remarkable attention in the last years. This paper aimed to evaluate the mechanical property of mortars, in which a calcined kaolin originating from the State of Paraiba, was used as partial cement replacement material. Two finess of the kaolin were used: ABNT 200 (0.074 mm and 325 (0.044 mm and burnt at temperatures of 700, 800 and 900 ºC for a period of 2 h. Both materials were characterized by chemical analysis, differential thermal analysis, X-ray diffraction, specific area tests. The pozolanic activity index was obtanied using lime and cement Portland. The amounts of replacement were 10, 20, 30 and 40%, besides the reference mortar. The binder

  4. Technological advances in (U,Pu)O2 CRO recycling using microwave heating

    International Nuclear Information System (INIS)

    Das, D.K.; Singh, G.; Khot, P.M; Kumar, S.; Mishra, A.K.; Behere, P.G.; Afzal, Mohd; Kumar, Arun

    2014-01-01

    A batch type wet recycling process viz. microwave direct de-nitration and calcination technique (MWDDC) has been developed at Advanced Fuel Fabrication Facility (AFFF), BARC, Tarapur, India. The process was developed for complete and multiple recycling of PFBR clean rejected (U,Pu)O 2 MOX fuel pellets (CRO) up to 30(wt%) of PuO 2 . The complete recycling of CRO containing higher Pu content with conventional dry recycling was difficult to achieve and certain amount of virgin powder is always needed to obtain the required product characteristics. The conditioned co-de-nitrated powder via MWDDC process have more or less similar characteristics to that of virgin powder with respect to particle size, apparent and tap density, surface area. This paper presents an insight into MWDDC process details and recent advancements made for improvement of powder and product characteristics. Low temperature microwave calcination (LTMC) was incorporated to improve the quality of co-de-nitrated powder with regard to volatile impurities and nitrate content. MWDDC powder and pellets were subjected to extensive chemical and physical characterization as per PFBR specification document. MOX pellets were fabricated from virgin and MWDDC powder via powder oxide pelletizing route and characterized. The homogeneity in the MOX pellets fabricated from MWDDC powder was found as good as that of virgin. Industrial microwave heating systems are indigenously developed and have advanced applicator and wave transmission designs to achieve high throughput, precise control of microwave power hence the temperature during the course of the process. It was demonstrated that MWDDC is a novel technique for (U,Pu)O 2 MOX rejects recycling in view of complete and multiple recycling. Key words: (U,Pu)O 2 MOX, CRO, Recycling, MWDDC. (authors)

  5. Preparation and Performance of Modified Red Mud-Based Catalysts for Selective Catalytic Reduction of NOx with NH3

    Directory of Open Access Journals (Sweden)

    Jingkun Wu

    2018-01-01

    Full Text Available Bayer red mud was selected, and the NH3-SCR activity was tested in a fixed bed in which the typical flue gas atmosphere was simulated. Combined with XRF, XRD, BET, SEM, TG and NH3-Temperature Programmed Desorption (TPD characterization, the denitration characteristics of Ce-doped red mud catalysts were studied on the basis of alkali-removed red mud. The results showed that typical red mud was a feasible material for denitration catalyst. Acid washing and calcining comprised the best treatment process for raw red mud, which reduced the content of alkaline substances, cleared the catalyst pore and optimized the particle morphology with dispersion. In the temperature range of 300–400 °C, the denitrification efficiency of calcined acid washing of red mud catalyst (ARM was more than 70%. The doping of Ce significantly enhanced NH3 adsorption from weak, medium and strong acid sites, reduced the crystallinity of α-Fe2O3 in ARM, optimized the specific surface area and broadened the active temperature window, which increased the NOx conversion rate by an average of nearly 20% points from 250–350 °C. The denitration efficiency of Ce0.3/ARM at 300 °C was as high as 88%. The optimum conditions for the denitration reaction of the Ce0.3/ARM catalyst were controlled as follows: Gas Hourly Space Velocity (GHSV of 30,000 h−1, O2 volume fraction of 3.5–4% and the NH3/NO molar ratio ([NH3/NO] of 1.0. The presence of SO2 in the feed had an irreversible negative effect on the activity of the Ce0.3/ARM catalyst.

  6. Incretin secretion: direct mechanisms

    DEFF Research Database (Denmark)

    Balk-Møller, Emilie; Holst, Jens Juul; Kuhre, Rune Ehrenreich

    2014-01-01

    enzyme responsible for incretin degradation (dipeptidyl peptidase-4) is inhibited (drugs are already on the market) while the secretion of endogenous GLP-1 secretion is stimulated at the same time may prove particularly rewarding. In this section we review current knowledge on the mechanisms for direct......The incretin hormones glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide 1 (GLP-1) are secreted from gastro-intestinal K- and L-cells, respectively, and play an important role in post-prandial blood glucose regulation. They do this by direct stimulation of the pancreatic β....... This suggests that the therapeutic potential of GIP for the treatment for T2D is limited, whereas GLP-1 based treatments have been on the market since 2005. Research is now pursuing novel approaches to utilize the effects of GLP-1 for T2D treatment. A combinatorial approach by which the activity of the major...

  7. Direct thermal neutron capture

    International Nuclear Information System (INIS)

    Raman, S.; Kahane, S.; Lynn, J.E.

    1987-01-01

    We discuss the direct-capture theory pertaining to primary electric dipole (E1) transitions following slow-neutron capture. For light nuclides that we have studied (including 9 Be, 12 C, 13 C, 24 Mg, 25 Mg, 26 Mg, 32 S, 33 S, 34 S, 40 Ca, and 44 Ca), estimates of direct-capture cross sections using optical-model potentials with physically realistic parameters, are in reasonable agreement with the data. Minor disagreements that exist are consistent with extrapolations to light nuclides of generally accepted formulations of compound-nucleus capture. We also discuss the channel-capture approximation which is, in general, a good representation of these cross sections in heavier nuclei particularly if the scattering lengths are not different from the corresponding potential radii. We also draw attention to cases where the use of this formula leads to inaccurate predictions. 9 refs., 1 fig., 2 tab

  8. Incretin secretion: direct mechanisms

    DEFF Research Database (Denmark)

    Balk-Møller, Emilie; Holst, Jens Juul; Kuhre, Rune Ehrenreich

    2014-01-01

    The incretin hormones glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide 1 (GLP-1) are secreted from gastro-intestinal K- and L-cells, respectively, and play an important role in post-prandial blood glucose regulation. They do this by direct stimulation of the pancreatic β......-cell, accounting for some 25-70% of postprandial insulin secretion in healthy subjects. In patients with type 2 diabetes (T2D, however, this effect is greatly reduced or lost due to a combination of severely impaired or eliminated insulinotrophic effect of GIP and reduced meal stimulated GLP-1 secretion...... enzyme responsible for incretin degradation (dipeptidyl peptidase-4) is inhibited (drugs are already on the market) while the secretion of endogenous GLP-1 secretion is stimulated at the same time may prove particularly rewarding. In this section we review current knowledge on the mechanisms for direct...

  9. Direction sensitive neutron detector

    Science.gov (United States)

    Ahlen, Steven; Fisher, Peter; Dujmic, Denis; Wellenstein, Hermann F.; Inglis, Andrew

    2017-01-31

    A neutron detector includes a pressure vessel, an electrically conductive field cage assembly within the pressure vessel and an imaging subsystem. A pressurized gas mixture of CF.sub.4, .sup.3He and .sup.4He at respective partial pressures is used. The field cage establishes a relatively large drift region of low field strength, in which ionization electrons generated by neutron-He interactions are directed toward a substantially smaller amplification region of substantially higher field strength in which the ionization electrons undergo avalanche multiplication resulting in scintillation of the CF.sub.4 along scintillation tracks. The imaging system generates two-dimensional images of the scintillation patterns and employs track-finding to identify tracks and deduce the rate and direction of incident neutrons. One or more photo-multiplier tubes record the time-profile of the scintillation tracks permitting the determination of the third coordinate.

  10. Direct use in Hawaii

    International Nuclear Information System (INIS)

    Beck, A.G.

    1990-01-01

    This paper reports on a public laboratory, Noi'i O Puna, that was established in Hawaii to support direct use research in 1985, tapping the previously unutilized heat in brines from the HGP-A well. Two rounds of small grants were offered to entrepreneurs. With the closure of the HGP-A power plant in late 1989, Noi'i O Puna is expanding its facilities. When the HGP-A well is back in service, Noi'i O Puna will be able to support additional research and development projects, as well as pre-commercial ventures. Direct use industries, which support existing agricultural activities in the region have good potential

  11. Future directions for QCD

    International Nuclear Information System (INIS)

    Bjorken, J.D.

    1996-10-01

    New directions for exploring QCD at future high-energy colliders are sketched. These include jets within jets. BFKL dynamics, soft and hard diffraction, searches for disoriented chiral condensate, and doing a better job on minimum bias physics. The new experimental opportunities include electron-ion collisions at HERA, a new collider detector at the C0 region of the TeVatron, and the FELIX initiative at the LHC

  12. Direct hydrocarbon fuel cells

    Science.gov (United States)

    Barnett, Scott A.; Lai, Tammy; Liu, Jiang

    2010-05-04

    The direct electrochemical oxidation of hydrocarbons in solid oxide fuel cells, to generate greater power densities at lower temperatures without carbon deposition. The performance obtained is comparable to that of fuel cells used for hydrogen, and is achieved by using novel anode composites at low operating temperatures. Such solid oxide fuel cells, regardless of fuel source or operation, can be configured advantageously using the structural geometries of this invention.

  13. AngularJS directives

    CERN Document Server

    Vanston, Alex

    2013-01-01

    This book uses a practical, step-by-step approach, starting with how to build directives from the ground up before moving on to creating web applications comprised of multiple modules all working together to provide the best user experience possible.This book is intended for intermediate JavaScript developers who are looking to enhance their understanding of single-page web application development with a focus on AngularJS and the JavaScript MVC frameworks.It is expected that readers will understand basic JavaScript patterns and idioms and can recognize JSON formatted data.

  14. Direction des Publications

    African Journals Online (AJOL)

    Synthese

    pulvérulente. La poudre de fer réduite est la matière de base la plus utilisée dans l‟industrie de la métallurgie de poudres. Le processus de réduction direct est communément utilisé par plusieurs compagnies (tels que Höganäs en Suède,. Kawasaki au Japon et Pyron aux USA) pour obtenir le fer métallique en poudre.

  15. Directions for further research

    DEFF Research Database (Denmark)

    Minsaas, Atle; Psaraftis, Harilaos N.

    2015-01-01

    Green transportation logistics is an area that combines the following: (a) it is relatively new in terms of research carried out thus far, (b) it has become increasingly important for both industry and society, and (c) it is rich in topics for further research, both basic and applied. In this final...... chapter of this book we discuss directions for further research in this area. We do so by taking stock of (1) related recommendations of project SuperGreen, and (2) related activities mainly in European research. Links between research and policy-making as two activities that should go hand in hand...

  16. The direct manipulation shell

    International Nuclear Information System (INIS)

    Allen, M.E.; Christiansen, M.

    1992-01-01

    Accelerator controls systems provide parameter display pages which allow the operator to monitor and manipulate selected control points in the system. Display pages are generally implemented as either hand-crafted, purpose-built programs; or by using a specialized display page layout tool. These two methods of display page development exhibit the classic trade-off between functionality vs. ease of implementation. In the Direct Manipulation Shell we approach the process of developing a display page in a manifestly object-oriented manner. This is done by providing a general framework for interactively instantiating and manipulating display objects. (author)

  17. Direct olive oil analysis

    Directory of Open Access Journals (Sweden)

    Peña, F.

    2002-03-01

    Full Text Available The practical impact of “direct analysis” is undeniable as it strong contributes to enhance the so-called productive analytical features such as expeditiousness, reduction of costs and minimisation of risks for the analysts and environment. The main objective is to establish a reliable bypass to the conventional preliminary operations of the analytical process. This paper offers a systematic approach in this context and emphasises the great field of action of direct methodologies in the routine analysis of olive oil. Two main types of methodologies are considered. On the one hand, the direct determination of volatile components is systematically considered. On the other hand, simple procedures to automatically implement the preliminary operations of the oil analysis using simple devices in which the sample is directly introduced with/without a simple dilution are present and discussed.El impacto práctico del análisis directo es tan innegable como que el contribuye decisivamente a mejorar las denominadas características analíticas relacionadas con la productividad como la rapidez, la reducción de costes y la minimización de riesgos para los analistas y el ambiente. El principal objetivo es establecer un adecuado "bypass" a las operaciones convencionales preliminares del proceso analítico. Este artículo ofrece una propuesta sistemática en este contexto y resalta el gran campo de acción de las metodologías directas en los análisis de rutina del aceite de oliva. Se analizan los dos tipos principales de metodologías. Por una lado, se analiza la determinación directa de los compuestos volátiles. Por el otro, se presentan y discuten los procedimientos simples para implementar automáticamente las operaciones preliminares del análisis del aceite usando sistemas simples en los que la muestra se introduce directamente con/sin un dilución simple.

  18. Direct thermal dyes

    Science.gov (United States)

    Ehlinger, Edward

    1990-07-01

    Direct thermal dyes are members of a class of compounds referred to in the imaging industry as color formers or leuco dyes. The oldest members of that class have simple triarylmethane structures, and have been employed for years in various dyeing applications. More complex triarylmethane compounds, such as phthalides and fluorans, are now used in various imaging systems to produce color. Color is derived from all of these compounds via the same mechanism, on a molecular level. That is, an event of activation produces a highly resonating cationic system whose interaction with incident light produces reflected light of a specific color. The activation event in the case of a direct thermal system is the creation of a melt on the paper involving dye and an acidic developer. The three major performance parameters in a thermal system are background color, image density, and image stability. The three major dye physical parameters affecting thermal performance are chemical constituency, purity, and particle size. Those dyes having the best combination of characteristics which can also be manufactured economically dominate the marketplace. Manufacturing high performance dyes for the thermal market involves multi-step, convergent reaction sequences performed on large scale. Intermediates must be manufactured at the right time, and at the right quality to be useful.

  19. Direct access to INIS

    International Nuclear Information System (INIS)

    Zheludev, I.S.; Romanenko, A.G.

    1981-01-01

    Librarians, researchers, and information specialists throughout the world now have the opportunity for direct access to coverage of almost 95% of the world's literature dealing with the peaceful uses of atomic energy and nuclear science. This opportunity has been provided by the International Nuclear Information System (INIS) of the IAEA. INIS, with the voluntary collaboration of more than 60 of the Agency's Member States, maintains a comprehensive, computer-resident data-base, containing the bibliographic details plus informative abstracts of the bulk of the world's literature on nuclear science and technology. Since this data-base is growing at a rate of 75,000 items per year, and already contains more than 500,000 items, it is obviously important to be able to search this collection conveniently and efficiently. The usefulness of this ability is enhanced when other data-bases on related subjects are made available on an information network. During the early 1970s, on-line interrogation of large bibliographic data-bases became the accepted method for searching this type of information resource. Direct interaction between the searcher and the data-base provides quick feed-back resulting in improved literature listings for launching research and development projects. On-line access enables organizations which cannot store a large data-base on their own computer to expand the information resources at their command. Because of these advantages, INIS undertook to extend to interested Member States on-line access to its data-base in Vienna

  20. Remote direct memory access

    Science.gov (United States)

    Archer, Charles J.; Blocksome, Michael A.

    2012-12-11

    Methods, parallel computers, and computer program products are disclosed for remote direct memory access. Embodiments include transmitting, from an origin DMA engine on an origin compute node to a plurality target DMA engines on target compute nodes, a request to send message, the request to send message specifying a data to be transferred from the origin DMA engine to data storage on each target compute node; receiving, by each target DMA engine on each target compute node, the request to send message; preparing, by each target DMA engine, to store data according to the data storage reference and the data length, including assigning a base storage address for the data storage reference; sending, by one or more of the target DMA engines, an acknowledgment message acknowledging that all the target DMA engines are prepared to receive a data transmission from the origin DMA engine; receiving, by the origin DMA engine, the acknowledgement message from the one or more of the target DMA engines; and transferring, by the origin DMA engine, data to data storage on each of the target compute nodes according to the data storage reference using a single direct put operation.