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Sample records for calcined wastes

  1. 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.

  2. 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.

  3. 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

  4. 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.

  5. 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.

  6. 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.

  7. 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.

  8. 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

  9. 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.

  10. 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.

  11. HWMA closure plan for the Waste Calcining Facility at the Idaho National Engineering Laboratory

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-05-01

    The Waste Calcining Facility (WCF) calcined and evaporated aqueous wastes generated from the reprocessing of spent nuclear fuel. The calciner operated from 1963 to 1981, primarily processing high level waste from the first cycle of spent fuel extraction. Following the calciner shutdown the evaporator system concentrated high activity aqueous waste from 1983 until 1987. In 1988, US Department of Energy Idaho Operations Office (DOE-ID) requested interim status for the evaporator system, in anticipation of future use of the evaporator system. The evaporator system has not been operated since it received interim status. At the present time, DOE-ID is completing construction on a new evaporator at the New Waste Calcining Facility (NWCF) and the evaporator at the WCF is not needed. The decision to not use the WCF evaporator requires Lockheed Idaho Technologies Company (LITCO) and DOE-ID to close these units. After a detailed evaluation of closure options, LITCO and DOE-ID have determined the safest option is to fill the voids (grout the vessels, cells and waste pile) and close the WCF to meet the requirements applicable to landfills. The WCF will be covered with a concrete cap that will meet the closure standards. In addition, it was decided to apply these closure standards to the calcining system since it is contained within the WCF building. The paper describes the site, waste inventory, closure activities, and post-closure care plans.

  12. 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.

  13. 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.

  14. Heat Transfer Characteristics of Calcined Petroleum Coke in Waste Heat Recovery Process

    Directory of Open Access Journals (Sweden)

    Bin Zheng

    2016-01-01

    Full Text Available This paper reports the results of heat transfer characteristics of calcined petroleum coke in waste heat recovery process. The model of heat exchanger was set up. The model has been used to investigate the effects of porosity (0.58 to 0.79, equivalent heat conductivity coefficient (0.9 to 1.1, and equivalent specific heat (0.9 to 1.1. The calculated values of calcined petroleum coke temperature showed good agreement with the corresponding available experimental data. The temperature distribution of calcined petroleum coke, the calcined petroleum coke temperature at heat exchanger outlet, the average heat transfer coefficient, and the heat recovery efficiency were studied. It can also be used in deriving much needed data for heat exchanger designs when employed in industry.

  15. 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

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-12-31

    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.

  16. Chemical and mineralogical modifications of simplified radioactive waste calcine during heat treatment

    Energy Technology Data Exchange (ETDEWEB)

    Monteiro, A. [CEA, DEN, DTCD/SECM/LDMC Marcoule, BP 17171, F-30207 Bagnols-sur-Cèze cedex (France); Schuller, S., E-mail: sophie.schuller@cea.fr [CEA, DEN, DTCD/SECM/LDMC Marcoule, BP 17171, F-30207 Bagnols-sur-Cèze cedex (France); Toplis, M.J. [CNRS, Observatoire Midi Pyrénées, IRAP (UMR 5277), F-31400 Toulouse (France); Podor, R.; Ravaux, J.; Clavier, N.; Brau, H.P. [ICSM UMR 5257 CEA/CNRS/UMR/ENSCM Site de Marcoule, BP 17171, F-30207 Bagnols-sur-Cèze cedex (France); Charpentier, T. [UMR CEA/CNRS 3299, IRAMIS, SIS2M, LSDRM Saclay, F-91191 Gif-sur-Yvette cedex (France); Angeli, F. [CEA, DEN, DTCD/SECM/LCLT Marcoule, BP 17171, F-30207 Bagnols-sur-Cèze cedex (France); Leterrier, N. [CEA, DEN, DM2S/SFME/LSFT Saclay, F-91191 Gif-sur-Yvette cedex (France)

    2014-05-01

    The microstructural and mineralogical changes associated with heating calcined mixtures of Al(NO{sub 3}){sub 3}⋅9H{sub 2}O–NaNO{sub 3} have been studied. This system is a simplified analogue of high-level radioactive waste calcine, one of the raw materials used in the vitrification process employed for waste management. The decomposition (dehydration and denitration) and formation of secondary crystalline phases have been studied by differential thermal and gravimetric analysis (DTA and TGA), and heat-treated products characterized by X-ray diffraction, Raman spectroscopy, Nuclear Magnetic Resonance (NMR) and Transmission Electron Microscopy (TEM). It is found that pure Al(NO{sub 3}){sub 3}⋅9H{sub 2}O transforms to amorphous Al{sub 2}O{sub 3} at a temperature of ∼180 °C, well below that of the calcination process (500 °C). This amorphous Al{sub 2}O{sub 3} is highly porous with a high specific surface area, but may in turn convert to denser γ-Al{sub 2}O{sub 3} and α-Al{sub 2}O{sub 3} with increasing temperature. On the other hand, pure NaNO{sub 3} remains stable up to ∼880 °C, despite a solid–liquid transition at ∼320 °C. For Al(NO{sub 3}){sub 3}⋅9H{sub 2}O–NaNO{sub 3} mixtures, the products of calcination at 500 °C are found to consist of very fine porous material containing Na, Al and O, in addition to a variable proportion of well-defined crystals consisting of Na, and O. Heating these mixtures to temperatures of up to 1000 °C shows that for the case 80% Al(NO{sub 3}){sub 3}⋅9H{sub 2}O −20% NaNO{sub 3} (weight%) a variety of crystalline sodium aluminates is formed (NaAlO{sub 2}, NaAl{sub 11}O{sub 17}, NaAl{sub 6}O{sub 9.5}), while for the 50–50 mixture, only NaAlO{sub 2} is found. In large amounts, addition of alumina thus leads to the formation of crystalline phases rich in Al{sub 2}O{sub 3} that are responsible for hardening the calcine as the temperature rises. The kinetics of nitrogen loss from NaNO{sub 3} are also found to be

  17. Biodiesel production from palm oil using calcined waste animal bone as catalyst.

    Science.gov (United States)

    Obadiah, Asir; Swaroopa, Gnanadurai Ajji; Kumar, Samuel Vasanth; Jeganathan, Kenthorai Raman; Ramasubbu, Alagunambi

    2012-07-01

    Waste animal bones was employed as a cost effective catalyst for the transesterification of palm oil. The catalyst was calcined at different temperatures to transform the calcium phosphate in the bones to hydroxyapatite and 800 °C was found to give the best yield of biodiesel. The catalyst was characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), energy dispersive spectrometry (EDS) and Fourier transform infrared spectrometry (FT-IR). Under the optimal reaction conditions of 20 wt.% of catalyst, 1:18 oil to methanol molar ratio, 200 rpm of stirring of reactants and at a temperature of 65 °C, the methyl ester conversion was 96.78% and it was achieved in 4h. The catalyst performed equally well as the laboratory-grade CaO. Animal bone is therefore a useful raw material for the production of a cheap catalyst for transesterification. Copyright © 2012 Elsevier Ltd. All rights reserved.

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

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    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.

  19. Research about the pozzolanic activity of waste materials from calcined clay

    Directory of Open Access Journals (Sweden)

    Sánchez de Rojas, M. I.

    2001-03-01

    Full Text Available To recycle and reutilise waste materials and find definite applications for their use, it is necessary to have a deep knowledge of them. The aim of this study is to study the possibility of using waste materials from calcined clay, actually ceramic tile, once crushed and grounded, as pozzolanic material. For this purpose, different tests are carried out in order to establish the pozzolanic activity of this material. At the same time, these results are compared to those of other industrial by-products, fly ash and silica fume, which are pozzolanic materials usually employed to elaborate mortars and concretes.

    Para llevar a cabo labores encaminadas al reciclado y revalorización de residuos es necesario un conocimiento profundo de los mismos, de forma que se busquen aplicaciones concretas de uso. El objetivo de este estudio es investigar la posibilidad de utilizar materiales de desecho procedentes de arcilla cocida, concretamente teja cerámica, una vez triturada y molida, como puzolana. Para ello, se efectúan diferentes ensayos dirigidos a establecer la actividad puzolanica del material. A su vez, estos resultados son comparados con otros residuos industriales, ceniza volante y humo de sílice, habituales en la elaboración de morteros y hormigones.

  20. Draft environmental assessment -- Closure of the Waste Calcining Facility (CPP-633), Idaho National Engineering Laboratory

    Energy Technology Data Exchange (ETDEWEB)

    Braun, J.B.; Irving, J.S.; Staley, C.S.; Stanley, N.

    1996-04-01

    The DOE-Idaho Operations Office has prepared an environmental assessment (EA) to analyze the environmental impacts of closing the Waste Calcining Facility (WCF) at the Idaho National Engineering Laboratory (INEL). The purpose of the action is to reduce the risk of radioactive exposure and release of radioactive and hazardous constituents and eliminate the need for extensive long-term surveillance and maintenance. DOE has determined that the closure is needed to reduce these risks to human health and the environment and to comply with Resource Conservation and Recovery Act requirements. The WCF closure project is described in the DOE Programmatic Spent Nuclear Fuel Management and Idaho National Engineering Laboratory Environmental Restoration and Waste Management Programs Final Environmental Impact Statement (Programmatic EIS). DOE determined in the Programmatic EIS Record of Decision (ROD) that certain actions would be implemented and other actions deferred. The EA examined the potential environmental impacts of the proposed action and evaluated reasonable alternatives, including the no action alternative in accordance with the Council on Environmental Quality Regulations. Based on the analysis in the EA, the action will not have a significant effect on the human environment.

  1. Regeneration of Waste Edible Oil by the Use of Virgin and Calcined Magnesium Hydroxide as Adsorbents.

    Science.gov (United States)

    Ogata, Fumihiko; Kawasaki, Naohito

    2016-01-01

    In this study, we prepared virgin (S, L) and calcined (S-380, S-1000, L-380, L-1000) magnesium hydroxide for regeneration of waste edible oil. Deterioration of soybean oil, rapeseed oil, and olive oil was achieved by heat and aeration treatment. The properties of the different adsorbents were investigated using specific surface area measurements, scanning electron microscopy, X-ray diffraction analysis, thermogravimetric-differential thermal analysis, and surface pH measurement. Moreover, the relationship between the changes in acid value (AV) and carbonyl value (CV) and the adsorbent properties were evaluated. The specific surface areas of S-380 and L-380 were greater than that of other adsorbents. In addition, the XRD results show that S-380 and L-380 contain both magnesium hydroxide and magnesium oxide structures. The decreases in AV and CV using S-380 and L-380 were greater than achieved using other adsorbents. The correlation coefficients between the decrease in AV and CV and specific surface area were 0.947 for soybean oil, 0.649 for rapeseed oil, and 0.773 for olive oil, respectively. The results obtained in this study suggest that a physical property of the adsorbent, namely specific surface area, was primarily responsible for the observed decreases in AV and CV. Overall, the results suggest that S-380 and L-380 are useful for the regeneration of waste edible oil.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. 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.

  8. 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

  9. Implementation of industrial waste ferrochrome slag in conventional and low cement castables: Effect of calcined alumina

    Directory of Open Access Journals (Sweden)

    Pattem Hemanth Kumar

    2014-12-01

    Full Text Available A new class of conventional and low-cement ferrochrome slag-based castables were prepared from 40 wt.% ferrochrome slag and 45 wt.% calcined bauxite. Rest fraction varied between high alumina cement (HAC acting as hydraulic binder and calcined alumina as pore filling additive. Standard ASTM size briquettes were prepared for crushing and bending strengths evaluation, and the samples were then subjected to firing at 800, 1100 and 1300 °C for a soaking period of 3 h. The microstructure and refractory properties of the prepared castables have been investigated using X-ray diffraction (XRD, scanning electron microscopy (SEM, cold crushing strength, modulus of rupture and permanent linear changes (PLCs test. Castables show good volume stability (linear change <0.7% at 1300 °C. The outcomes of these investigations were efficacious and in accordance with previously reported data of similar compositions. High thermo-mechanical and physico-chemical properties were attained pointing out an outstanding potential to increase the refractory lining working life of non-recovery coke oven and reheating furnaces.

  10. 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.

  11. 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.

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

    Science.gov (United States)

    Zhang, Na; Liu, Xiaoming; Sun, Henghu; Li, Longtu

    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, (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. Copyright © 2010 Elsevier B.V. All rights reserved.

  13. The extraction of rare earth elements from ICPP sodium-bearing waste and dissolved zirconium calcine by CMP and TRUEX solvents

    Energy Technology Data Exchange (ETDEWEB)

    Todd, T.A.; Glagolenko, I.Y.; Herbst, R.S.; Brewer, K.N.

    1995-11-01

    The extraction of stable isotopes of Eu and Ce was investigated from simulated sodium-bearing waste (SBW) and dissolved zirconium calcine by TRUEX and CMP solvents at the Idaho Chemical Processing Plant (ICPP). Single batch contacts were carried out in order to evaluate the rare earth behavior in the extraction, scrub, strip and wash sections for the proposed flowsheets. It has been shown that these lanthanides are efficiently extracted from the sodium-bearing wastes into either solvent, are not scrubbed and are stripped from both of the extractants with dilute HEDPA. The extraction distribution coefficients for Ce and Eu are higher in the TRUEX solvent (D{sub Ce} = 11.7, D{sub Eu} = 14.9) compared with CMP (D{sub Ce} = 9.3, D{sub Eu} = 7.23) for SBW. The extraction distribution coefficients for Ce and Eu are considerably less in the TRUEX solvent (D{sub Ce}=1.13, D{sub Eu}=1.8) than in the CMP solvent (D{sub Ce}=7.4, D{sub Eu=}6.1) for dissolved zirconium calcine feeds. The lower distribution coefficients for the extraction of lanthanides in the TRUEX/dissolved zirconium calcine system can be explained by zirconium loading of the solvent. The data obtained also confirmed that Ce and Eu can be used as non-radioactive surrogates for Am in separation experiments with acidic solutions.

  14. Alternative calcination development status report

    Energy Technology Data Exchange (ETDEWEB)

    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.

  15. 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.

  16. 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

  17. 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.

  18. 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

  19. Enrichment Of Calcined Magnesite

    OpenAIRE

    GENCE, Nermin

    2017-01-01

    In this study, the possibility ofconcentration of magnesite are which contains high dolomite, low iron andsiliceous gangue was investigated by heavy medium separation, shaking table and vashing-screeningafter calcination.

  20. 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.

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

    Energy Technology Data Exchange (ETDEWEB)

    Grutzeck, Michael W.

    2005-06-27

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

  2. 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.

  3. One-pot synthesis of carbon supported calcined-Mg/Al layered double hydroxides for antibiotic removal by slow pyrolysis of biomass waste

    Science.gov (United States)

    Tan, Xiaofei; Liu, Shaobo; Liu, Yunguo; Gu, Yanling; Zeng, Guangming; Cai, Xiaoxi; Yan, Zhili; Yang, Chunping; Hu, Xinjiang; Chen, Bo

    2016-12-01

    A biochar supported calcined-Mg/Al layered double hydroxides composite (CLDHs/BC) was synthesized by a one-pot slow pyrolysis of LDHs preloaded bagasse biomass. Multiple characterizations of the product illustrated that the calcined-Mg/Al layered double hydroxides (CLDHs) were successfully coated onto the biochar in slow pyrolysis of pre-treated biomass. The as-synthesized CLDHs/BC could efficiently remove antibiotic tetracycline from aqueous solutions. The coating of CLDHs significantly increased the adsorption ability of biochar, and CLDHs/BC exhibited more than 2 times higher adsorption capacity than that of the pristine biochar (BC) in the tested pH range. The maximum adsorption capacity of CLDHs/BC for tetracycline was 1118.12 mg/g at 318 K. The experimental results suggested that the interaction with LDHs on biochar played a dominant role in tetracycline adsorption, accompanied with π-π interaction and hydrogen bond. This study provides a feasible and simple approach for the preparation of high-performance material for antibiotics contaminated wastewater treatment in a cost-effective way.

  4. 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.

  5. 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.

  6. 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

  7. The Properties of Calcined Anthracite

    OpenAIRE

    Holm, Katrine

    2017-01-01

    The aim of this thesis has been to look at the thermal behaviour of anthracite, coke and charcoal regarding their expansion during heating and their release of off-gases. Furthermore, to look at how the porosity and expansion of the anthracite is affected by the different temperatures during the calcining process. Two anthracites (A11 and A19), two cokes (C3 and C7) and one charcoal (BIO) were investigated. The porosity and surface area of A11 calcined at different temperatures were inves...

  8. 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

    at inappropriately high temperatures or long retention time will not only waste energy but also decrease the reactivity of the calcines due to possible recrystallization of the reactive phase into a stable crystalline phase. Therefore, it is very crucial to achieve an in-depth understanding of the calcination...... 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...... model which fully addresses not only the particle-ambient flow interaction but also the intra-particle processes has been successfully developed in a C++ program to examine calcination of clay particles suspended in a hot gas. The calcination process is also numerically studied using gPROMS (a general...

  9. 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

  10. Nuclear waste solidification

    Science.gov (United States)

    Bjorklund, William J.

    1977-01-01

    High level liquid waste solidification is achieved on a continuous basis by atomizing the liquid waste and introducing the atomized liquid waste into a reaction chamber including a fluidized, heated inert bed to effect calcination of the atomized waste and removal of the calcined waste by overflow removal and by attrition and elutriation from the reaction chamber, and feeding additional inert bed particles to the fluidized bed to maintain the inert bed composition.

  11. The Kinetic Model of Calcination and Carbonation of Anadara Granosa

    OpenAIRE

    Rashidi, Nor Adilla; Mohamed, Mustakimah; Yusup, Suzana

    2016-01-01

    Utilization of calcium-based adsorbent in carbon dioxide (CO2) separation from the gas stream through the calcination and carbonation process is extensively applied in the gas purification process, especially at the elevated reaction temperature. Typically, natural calcium carbonates (CaCO3) such as the limestone, magnesite and dolomite are widely consumed in the process due to their low cost and large abundance of these materials. However, in this research study, the potential of waste cockl...

  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. Modeling and control of a calcination furnace

    OpenAIRE

    Wilson, Øyvind

    2017-01-01

    Calcined anthracite is the primary material used in Søderberg electrode paste, prebaked carbon electrodes, aluminium cathodes, and a variety of other carbon products used in the metallurgical industries. In electrical calcination of anthracite current is passed through the raw material. This heat treats the anthracite, which gets rid of volatile matter and water, and graphitizes the anthracite. The graphitization lower the anthracite's electrical resistivity. The object of the process is...

  14. 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...

  15. Actinide partitioning from actual ICPP dissolved zirconium calcine using the TRUEX solvent

    Energy Technology Data Exchange (ETDEWEB)

    Brewer, K.N.; Herbst, R.S.; Tranter, T.J. [and others

    1995-05-01

    The TRansUranic EXtraction process (TRUEX), as developed by E.P. Horwitz and coworkers at Argonne National Laboratory (ANL), is being evaluated as a TRU extraction process for Idaho Chemical Processing Plant (ICPP) wastes. A criteria that must be met during this evaluation, is that the aqueous raffinate must be below the 10 nCi/g limit specified in 10 CFR 61.55. A test was performed where the TRUEX solvent (0.2 M octyl(phenyl)-N-N-diisobutyl-carbamoylmethyl-phosphine oxide (CMPO), and 1.4 M tributylphosphate (TBP) in an Isopar-L diluent) was contacted with actual ICPP dissolved zirconium calcine. Two experimental flowsheets were used to determine TRU decontamination factors, and TRU, Zr, Fe, Cr, and Tc extraction, scrub, and strip distribution coefficients. Results from these two flowsheets show that >99.99% of the TRU alpha activity was removed from the acidic feed after three contacts with the TRUEX solvent (fresh solvent being used for each contact). The resulting aqueous raffinate solution contained an approximate TRU alpha activity of 0.02 nCi/g, which is well below the non-TRU waste limit of 10 nCi/g specified in 10 CFR 61.55. Favorable scrub and strip distribution coefficients were also observed for Am-241, Pu-238, and Pu-239, indicating the feasibility of recovering these isotopes from the TRUTEX solvent. A solution of 0.04 M 1-hydroxyethane-1,1-diphosphonic acid (HEDPA) in 0.04 M HNO{sub 3} was used to successfully strip the TRUs from the TRUEX solvent. The results of the test using actual ICPP dissolved zirconium calcine, and subsequent GTM evaluation, show the feasibility of removing TRUs from the dissolved zirconium calcine with the TRUEX solvent and the deleterious effects zirconium poses with the ICPP zirconium calcine waste. Test results using actual ICPP zirconium calcine reveal the necessity of preventing zirconium from following the TRUs.

  16. Actinide partitioning studies using dihexyl-N,N-diethycarbamolymehtyl phosphonate and dissolved zirconium calcine

    Energy Technology Data Exchange (ETDEWEB)

    Brewer, K.N.; Herbst, R.S.; Law, J.D.; Garn, T.G.; Tillotson, R.D.; Todd, T.A.

    1996-01-01

    A baseline flowsheet capable of partitioning the transuranic (TRU) elements from dissolved zirconium calcines has been developed. The goal of the TRU partitioning process is to remove the TRUs from solutions of dissolved zirconium calcines to below the 10 CFR 61.55 Class A waste limit of 10 nCi/g. Extraction, scrub, strip, and wash distribution coefficients for several elements, including the actinides, were measured in the laboratory by performing equal volume batch contacts. A solvent containing diheyl-N, N- diethylcarbamoylmethyl phosphonate (CMP), tributylphosphate (TBP), and a branched chain hydrocarbon as the diluent were used to develop this process. A non-radioactive zirconium pilot-plant calcine was spiked with the TRUs, U, Tc, or a radioactive isotope of zirconium to simulate the behavior of these elements in actual dissolved zirconium calcine feed. Distribution coefficient data obtained from laboratory testing were used to recommend: (1) solvent composition, (2) scrub solutions capable of selectively removing extracted zirconium while minimizing actinide recycle, (3) optimized strip solutions which quantitatively recover extracted actinides, and (4) feed adjustments necessary for flowsheet efficiency. Laboratory distribution coefficients were used in conjunction with the Generic TRUEX Model (GTM) to develop and recommend a flowsheet for testing in the 5.5-cm Centrifugal Contractor Mockup. GTM results indicate that the recommended flowsheet should remove the actinides from dissolved zirconium calcine feed to below the Class A waste limit of 10 nCi/g. Less than 0.01 wt% of the extracted zirconium will report to the high- activity waste (HAW) fraction using the 0.05 M H{sub 2}C{sub 2}O{sub 4} in 3.0 M HNO{sub 3} scrub, and greater than 99% of the extracted actinides are recovered with 0.001 M HEDPA.

  17. Dissolution Studies With Pilot Plant and Actual INTEC Calcines

    Energy Technology Data Exchange (ETDEWEB)

    Herbst, Ronald Scott; Garn, Troy Gerry

    1999-04-01

    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 A1(NO3)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.

  18. Calcination of calcium carbonate and blend therefor

    Science.gov (United States)

    Mallow, William A.; Dziuk, Jr., Jerome J.

    1989-01-01

    A method for calcination of a calcium carbonate material comprising heating the calcium carbonate material to a temperature and for a time sufficient to calcine the material to the degree desired while in the presence of a catalyst; said catalyst comprising at least one fused salt having the formula MCO.sub.3.CaCO.sub.3.CaO.H.sub.2 O.sub.x, wherein M is an alkali metal and x is 0 to 1 and formed by fusing MCO.sub.3 and CaCO.sub.3 in a molar ratio of about 1:2 to 2:1, and a blend adapted to be heated to CaO comprising a calcium carbonate material and at least one such fused salt.

  19. Waste disposal options report. Volume 2

    Energy Technology Data Exchange (ETDEWEB)

    Russell, N.E.; McDonald, T.G.; Banaee, J.; Barnes, C.M.; Fish, L.W.; Losinski, S.J.; Peterson, H.K.; Sterbentz, J.W.; Wenzel, D.R.

    1998-02-01

    Volume 2 contains the following topical sections: estimates of feed and waste volumes, compositions, and properties; evaluation of radionuclide inventory for Zr calcine; evaluation of radionuclide inventory for Al calcine; determination of k{sub eff} for high level waste canisters in various configurations; review of ceramic silicone foam for radioactive waste disposal; epoxides for low-level radioactive waste disposal; evaluation of several neutralization cases in processing calcine and sodium-bearing waste; background information for EFEs, dose rates, watts/canister, and PE-curies; waste disposal options assumptions; update of radiation field definition and thermal generation rates for calcine process packages of various geometries-HKP-26-97; and standard criteria of candidate repositories and environmental regulations for the treatment and disposal of ICPP radioactive mixed wastes.

  20. Comparison of Dolomite Crystal Structure, Calcinations Dolomite and Magnesium Hydroxide in Partial Calcinations and Slaking Process

    Science.gov (United States)

    Sulistiyono, E.; Firdiyono, F.; Natasha, NC; Amalia, Y.

    2017-02-01

    Dolomite is a mineral that consists of calcium carbonate and magnesium carbonate with various mole ratio depend on the formation of mineral source. Recently, Utilization of dolomite only used as raw material for fertilizer and building materials, so that the enhancement of its added value becomes low. If the components in dolomite can be separated, magnesium carbonate and calcium carbonate will be produced then provide high added value. To separate these two components in dolomite is through partial calcinations followed by slaking process. The purpose of this paper is to prove that the partial calcinations can be used as a fundamental process for calcium and magnesium separation process in dolomite. SEM-EDX and XRD analysis proved that partial calcinations at 675°C for 6 hours is able to produce magnesium oxide (MgO) and calcium oxide (CaO). Then sea water was added to calcinations product so magnesium hydroxide and calcium carbonate that easily separated by sea water. The weakness of partial calcinations process at 675°C and processing time 2 hours is the dolomite has not perfectly reacted yet. XRD analysis showed that MgCO3. CaCO3 compounds still exist, so there is a possibility that magnesium was not fetched after the separation process.

  1. 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; Kozlov, Aleksandr

    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

  2. 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.

  3. Calcination of kaolinite clay particles for cement production

    DEFF Research Database (Denmark)

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

    2014-01-01

    Kaolinite rich clay particles calcined under certain conditions can attain favorable pozzolanic properties and can be used to substitute part of the CO2 intensive clinker in cement production. To better guide calcination of a clay material, a transient one-dimensional single particle model...

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

    Indian Academy of Sciences (India)

    Administrator

    properties, when it is calcined at different temperatures. Thus, for ... controlling the pH in the stomach. They could act as neu- tralizing of stomach acidity and maintaining an adequate. pH in the stomach. Normally, such antacids can be for- mulated as ... calcine at different temperatures Ca/Al hydrocalumite- type solids for ...

  5. 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.

  6. 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...

  7. 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.

  8. Numerical study of co-firing pulverized coal and biomass inside a cement calciner.

    Science.gov (United States)

    Mikulčić, Hrvoje; von Berg, Eberhard; Vujanović, Milan; Duić, Neven

    2014-07-01

    The use of waste wood biomass as fuel is increasingly gaining significance in the cement industry. The combustion of biomass and particularly co-firing of biomass and coal in existing pulverized-fuel burners still faces significant challenges. One possibility for the ex ante control and investigation of the co-firing process are computational fluid dynamics (CFD) simulations. The purpose of this paper is to present a numerical analysis of co-firing pulverized coal and biomass in a cement calciner. Numerical models of pulverized coal and biomass combustion were developed and implemented into a commercial CFD code FIRE, which was then used for the analysis. Three-dimensional geometry of a real industrial cement calciner was used for the analysis. Three different co-firing cases were analysed. The results obtained from this study can be used for assessing different co-firing cases, and for improving the understanding of the co-firing process inside the calculated calciner. © The Author(s) 2014.

  9. 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.

  10. Calcinated egg shell as a candidate of biosecurity enhancement material

    National Research Council Canada - National Science Library

    OTA, Mari; TOYOFUKU, Chiharu; THAMMAKARN, Chanathip; SANGSRIRATANAKUL, Natthanan; YAMADA, Masashi; NAKAJIMA, Katsuhiro; KITAZAWA, Minori; HAKIM, Hakimullah; ALAM, Md. Shahin; SHOHAM, Dany; TAKEHARA, Kazuaki

    2016-01-01

    Calcinated egg shell (Egg-CaO), of which the main component is calcium oxide, was evaluated in the forms of powder and aqueous solutions for their efficacies as disinfectants against avian influenza virus (AIV...

  11. CSER 97-004: PFP production denitration calciner system

    Energy Technology Data Exchange (ETDEWEB)

    Hillesland, K.E.

    1997-09-11

    The plutonium stabilization program at the Plutonium Finishing Plant (PFP) includes conversion of acidic plutonium nitrate solution into plutonium oxide. Conversion is facilitated through use of a vertical calciner installed in Glovebox HC-23OC-2, which is located in RM 230C of this facility. This evaluation supports the Criticality Prevention Specification for the calcining process inside this glovebox. As the product of the calciner is a high density plutonium oxide, a number of limits are required to insure criticality safety. The containers allowed are product receiver vessels and 0.5 C slip lid cans and polyjars. The limits allow for two ``unit masses`` of 2 V total volume each, separated by a distance of at least 25.4 cm (10 in.). This evaluation allows for operation of the calciner for product densities not in excess of 5.5 g Pu/cm{sup 3}.

  12. 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

  13. Magnesium Production by Vacuum Aluminothermic Reduction of a Mixture of Calcined Dolomite and Calcined Magnesite

    Science.gov (United States)

    Hu, Wen-xin; Feng, Nai-xiang; Wang, Yao-wu; Wang, Zhi-hui

    A new method of magnesium production was proposed that using a mixture of calcined dolomite and calcined magnesite as raw materials with the molar ratio of MgO to CaO was 6:1 by vacuum aluminothermic reduction. The reduction process was studied by thermodynamic analysis and X-ray diffraction analysis of reduction residue. The reaction of reduction process was CaO+6MgO+4Al=CaO•2Al2O3+6Mg. The effect of briquetting pressure, reduction temperature, time and CaF2 (MgF2) on reduction ratio of MgO was investigated. And the reduction residue that the main phase of CaO•2Al2O3 was leached in alkaline solution for producing sodium aluminateme raw material for special alumina. The results show that the reduction ratio is increased with increasing of the temperature, time, briquetting pressure in range from 40 to 100 MPa and addition of CaF2 or MgF2 in range from 0 to 3%. The alumina leaching ratio of reduction residue reached 88% at the conditions of leaching temperature 95 °C and the concentration ratio of Na2CO3 to NaOH was 100:75 in leaching solution.

  14. 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....

  15. 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.

  16. Mechanism of boron uptake by hydrocalumite calcined at different temperatures.

    Science.gov (United States)

    Qiu, Xinhong; Sasaki, Keiko; Takaki, Yu; Hirajima, Tsuyoshi; Ideta, Keiko; Miyawaki, Jin

    2015-04-28

    Hydrocalumite (Ca-Al-layered double hydroxide (LDH)) was prepared and applied for the removal of borate. The properties of Ca-Al-LDH calcined at different temperatures were diverse, which affected the sorption density and mechanism of boron species. The sorption density increased with increase in calcined temperature and the sample calcined at 900°C (Ca-Al-LDH-900) showed the maximum sorption density in this work. The solid residues after sorption were characterized by (11)B NMR, (27)Al NMR, SEM, and XRD to investigate the sorption mechanism. Dissolution-reprecipitation was the main mechanism for sorption of borate in Ca-Al-LDH. For Ca-Al-LDH calcined at 300 and 500°C, regeneration occurred in a short time and the newly forming LDHs were decomposed to release Ca(2+) ions and formed ettringite with borate. Two stages occurred in the sorption of boron by Ca-Al-LDH calcined at 900°C. In the first stage, boron species adsorbed on the alumina gel resulting from the hydration of calcined products. In this stage, borate was included as an interlayer anion into the newly forming LDHs in the following stage, and then immobilized as HBO3(2-) into the interlayer, most the LDHs. Copyright © 2015 Elsevier B.V. All rights reserved.

  17. Total oxidation of toluene over calcined trimetallic hydrotalcites type catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Palacio, Luz A. [Instituto Superior Tecnico, IBB - Centro de Engenharia Biologica e Quimica, Universidade Tecnica de Lisboa, Av. Rovisco Pais, 1049-001 Lisboa (Portugal); Grupo Catalizadores y Adsorbentes, Universidad de Antioquia 1-317, A.A. 1226 Medellin (Colombia); Velasquez, Juliana; Echavarria, Adriana [Grupo Catalizadores y Adsorbentes, Universidad de Antioquia 1-317, A.A. 1226 Medellin (Colombia); Faro, Arnaldo [Departamento de Fisicoquimica, Instituto de Quimica, Universidade Federal do Rio de Janeiro, Ilha do Fundao, CT bloco A, Rio de Janeiro (Brazil); Ramoa Ribeiro, F. [Instituto Superior Tecnico, IBB - Centro de Engenharia Biologica e Quimica, Universidade Tecnica de Lisboa, Av. Rovisco Pais, 1049-001 Lisboa (Portugal); Ribeiro, M. Filipa, E-mail: filipa.ribeiro@ist.utl.pt [Instituto Superior Tecnico, IBB - Centro de Engenharia Biologica e Quimica, Universidade Tecnica de Lisboa, Av. Rovisco Pais, 1049-001 Lisboa (Portugal)

    2010-05-15

    Two trimetallic ZnCuAl and MnCuAl hydrotalcites have been successfully synthesized by a co-precipitation method. The manganese based material was identified as a new hydrotalcite phase. Both lamellar precursors were calcined at 450 and 600 deg. C and the resulting catalysts were tested on reaction of total oxidation of toluene. The solids were characterized by X-ray diffraction, thermal analysis, atomic absorption spectroscopy, Fourier transformed infrared spectroscopy, N{sub 2} adsorption and H{sub 2} temperature-programmed reduction. It was found that ZnCuAl materials are composed of copper and zinc oxides supported on alumina; while MnCuAl ones comprise basically spinel phases, which were not completely identified. The catalytic behavior of the calcined samples showed that Mn hydrotalcite calcined at 450 deg. C exhibited the best catalytic performance that corresponds to 100% toluene conversion into CO{sub 2} at about 300 deg. C.

  18. CSER 95-005: PFP vertical denitration calciner

    Energy Technology Data Exchange (ETDEWEB)

    Geiger, J.L.

    1995-05-31

    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.

  19. 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.

  20. Talc-based cementitious products: Effect of talc calcination

    Directory of Open Access Journals (Sweden)

    C.J. Ngally Sabouang

    2015-09-01

    Full Text Available This study reports the use of calcined talc for cementitious products making. The calcination is used to enhance the availability of magnesium from talc to react with phosphate for cement phase formation. It is shown that previous calcination of talc leads to products having enhanced mechanical performance due to the formation of more cement phase than in products based on raw talc. Talc fired at 900 °C was found to be the one in which magnesium release was maximal. Firing at temperature higher than 900 °C leads to the stabilization of enstatite, which decreased the magnesium availability. The cement phase is struvite, which was better detected on the X-ray patterns of the products involving fired talc. All the products have very rapid setting time and low shrinkage.

  1. 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.

  2. 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.

  3. Modeling the Gas-Solid Flow in Calcining Furnace

    Directory of Open Access Journals (Sweden)

    Haiyan Luo

    2011-03-01

    Full Text Available Gas-solid two-phase flow in calcining furnace is investigated in this paper. The turbulent fluid phase is calculated using the RNG k-e two-equation model in the Eulerain framework while the solid phase being handled via the particle stochastic trajectory model is calculated in the Lagrangian framework. Flow pattern characteristics of the fluid phase and the particle trajectories of the solid phase were predicted subject to a range of flow conditions and different particle sizes. The computed results provided useful information in the preview of kinetics regulation of the gas-solid two-phase in calcining furnace.

  4. Development of a SREX Flowsheet for the Separation of Strontium from Dissolved INEEL Zirconium Calcine

    Energy Technology Data Exchange (ETDEWEB)

    Law, Jack Douglas; Wood, David James; Todd, Terry Allen

    1999-02-01

    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 #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 4',4'(5')-di-(tert-butylcyclohexo)-18-crown-6 and 1.5 M TBP in Isopar-L.), a 1.0 M NaNO3 scrub section to remove extracted K from the SREX solvent, a 0.01 M HNO3 strip section for the removal of Sr from the SREX solvent, a 0.25 M Na2CO3 wash section to remove degradation products from the solvent, and a 0.1 M HNO3 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 NaNO3 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 NaNO3 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.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1999-01-01

    Laboratory experimentation has indicated that the SREX process is effective for partitioning {sup 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 {sup 85}Sr was used as feed solution for the testing. The flowsheet tested consisted of an extraction section (0.15 M 4{prime},4{prime}(5{prime})-di-(tert-butylcyclohexo)-18-crown-6 and 1.5 M TBP in Isopar-L.), a 1.0 M NaNO{sub 3} scrub section to remove extracted K from the SREX solvent, a 0.01 M HNO{sub 3} strip section for the removal of Sr from the SREX solvent, a 0.25 M Na2CO{sub 3} wash section to remove degradation products from the solvent, and a 0.1 M HNO{sub 3} rinse section. The behavior of {sup 85}Sr, Na, K, Al, B, Ca, Cr, Fe, Ni, and Zr was evaluated. The described flowsheet successfully extracted {sup 85}Sr from the dissolved pilot plant calcine with a removal efficiency of 99.6%. Distribution coefficients for {sup 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{sub 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{sub 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

  6. Calcined eggshell (CES): An efficient natural catalyst for ...

    Indian Academy of Sciences (India)

    A convenient, eco-friendly and economic method for Knoevenagel condensation of aromatic aldehydes with active methylene compounds using calcined eggshell (CES) as an efficient natural catalyst in aqueous medium has been reported. CES is a new, ecologically safe and inexpensive green catalyst obtained from ...

  7. 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 ...

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

    African Journals Online (AJOL)

    The current demand of hydrated lime [Ca(OH)2] worldwide has necessitated 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.

  9. 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 ... The reduction temperature did not affect the product selectivity. South African Journal of ...

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

    African Journals Online (AJOL)

    2003-12-05

    Dec 5, 2003 ... 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 ...

  11. Mechanical and electrical properties of calcinated tea-based cellulose composite films

    Science.gov (United States)

    Tippabattini, Jayaramudu; Kim, Jung Woong; Ko, Hyun-U.; Kafy, Abdullahil; Li, Yaguang; Kim, Jaehwan

    2017-04-01

    In the present investigation, calcinated tea-based cellulose composite films were fabricated via solution casting technique. The fabricated films were characterized by using Fourier transform infrared spectroscopy and differential scanning calorimetry. The effect of calcinated tea loading on the properties of the calcinated tea-based cellulose composite films was studied. The results were showed that the calcinated tea composite films display better mechanical properties and dielectric constant than the pure cellulose films.

  12. Vitrified waste option study report

    Energy Technology Data Exchange (ETDEWEB)

    Lopez, D.A.; Kimmitt, R.R.

    1998-02-01

    A {open_quotes}Settlement Agreement{close_quotes} between the Department of Energy and the State of Idaho mandates that all radioactive high-level 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 date of 2035. This report investigates vitrification treatment of all ICPP calcine, including the existing and future HLW calcine resulting from calcining liquid Sodium-Bearing Waste (SBW). Currently, the SBW is stored in the tank farm at the ICPP. Vitrification of these wastes is an acceptable treatment method for complying with the Settlement Agreement. This method involves vitrifying the calcined waste and casting the vitrified mass into stainless steel canisters that will be ready to be moved out of the Idaho for disposal by 2035. These canisters will be stored at the Idaho National Engineering and Environmental Laboratory (INEEL) until they are sent to a HLW national repository. The operating period for vitrification treatment will be from 2013 through 2032; all HLW will be treated and in storage by the end of 2032.

  13. Reutilization of low-grade magnesium oxides for flue gas desulfurization during calcination of natural magnesite: A closed-loop process

    OpenAIRE

    del Valle Zermeño, Ricardo; Formosa Mitjans, Joan; Aparicio, J.A,; Chimenos Ribera, Josep Maria

    2014-01-01

    The European Commission is encouraging the Cement, Lime and Magnesium Oxide Manufacturing Industries to reutilize collected particulate matter or wastes in the emission control of SO2 with a 100% removal efficiency. Following this directive, three different by-products from the calcination of natural magnesite were selected in order to evaluate their desulfurization capacity. The saturation time, defined as the time for the total neutralization of SO2 was used to determine consumption values ...

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

    DEFF Research Database (Denmark)

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

    2002-01-01

    The reduction of the NOx content in in-line-calciner-type kiln systems can be made by optimization of the primary filing in the rotary kiln and of the secondary firing in the calciner. Because the optimization of calciner offers greater opportunities the mathematical modeling of this reactor...... 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...

  15. PROCESSING OF RADIOACTIVE WASTE

    Science.gov (United States)

    Johnson, B.M. Jr.; Barton, G.B.

    1961-11-14

    A process for treating radioactive waste solutions prior to disposal is described. A water-soluble phosphate, borate, and/or silicate is added. The solution is sprayed with steam into a space heated from 325 to 400 deg C whereby a powder is formed. The powder is melted and calcined at from 800 to 1000 deg C. Water vapor and gaseous products are separated from the glass formed. (AEC)

  16. The influence of calcination on the physical and chemical properties of petroleum and mixed cokes

    Energy Technology Data Exchange (ETDEWEB)

    Sikora, K.; Syrek, H.

    1980-01-01

    Freshly prepared petroleum and coal-petroleum cokes, before utilization for the production of various materials, are subjected to calcining--thermal treatment in a neutral or reducing atmosphere without the admission of air at less than or equal to 1400/sup 0/. During calcining, stabilization of the physical and chemical properties of the cokes takes place. The properties of the obtained coke depend chiefly on the calcining time and temperature. During calcining, volatile substances are removed almost completely from the coke; the coke density is increased, and its structure is put in order; the electrical conductivity is improved; the mechanical strength is increased; and the reactivity of the coke is decreased. Laboratory studies were conducted on calcining mixed coal-petroleum cokes of two grades at 1200, 1250, and 1300/sup 0/ for 2-6 h. In the calcining products the content of volatile substances, the ash content, S content, and density were determined. It was ascertained that calcining of mixed coal-petroleum cokes goes analogously to calcining of pure petroleum cokes. Raising the temperature and increasing the time of calcining has a substantial effect on improvement of coke physical and chemical properties. For high-quality coke, calcining is to be carried out at greater than or equal to 1300/sup 0/ for 4-6 h, for ordinary coke at > 1200/sup 0/ and greater than or equal to 4 h. The results are regarded as starting data for an industrial study of the calcining process.

  17. Genesis of Cr(VI) in Sri Lankan soils and its adsorptive removal by calcined gibbsite

    Science.gov (United States)

    Rajapaksha, A. U.; Wijesundara, D. M.; Vithanage, M. S.; Ok, Y. S.

    2012-12-01

    Hexavalent chromium is highly toxic to biota and considered as a priority pollutant. Industrial sources of Cr(VI) include leather tanning, plating, electroplating, anodizing baths, rinse waters, etc. In addition, weathering of ultramafic rocks rich in chromium, such as serpentine, is known to Cr(VI) sources into natural water. The Cr(III) is the most stable in the environment, however, conversion of Cr(III) into Cr(VI) occurs in soil due to presence of naturally occurring minerals such as manganese dioxides. We investigated the amount of Cr(VI) recorded from the soils from anthropogenically and naturally contaminated soils (serpentine soils) in Sri Lanka and the removal efficacy of Cr(VI) by calcined gibbsite (Al oxides). The effect of pH on Cr(VI) adsorption was determined by adjusting the pH in the range of 4-10. In the experiments, the adsorbent concentration was kept at 1 g/l of solution containing 10 mg/l Cr(VI) at 25 0C. Total chromium recorded were around 11,000 mg kg-1 and 6,000 mg kg-1 for serpentine soil and tannery waste-contaminated soil, respectively. Although total Cr was high in the contaminated soils, Cr(VI) concentration was only about 28 mg kg-1 and 210 mg kg-1 in the serpentine and tannery soils, respectively. The calcined gibbsite has maximum adsorption of 85 % around pH 4 and adsorption generally decreased with increase of pH.

  18. 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.

  19. 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.

  20. 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...

  1. 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...

  2. Influence of roasting-quenching pretreatment on the rice husk silica prepared by calcination method

    Science.gov (United States)

    Maksum, Ahmad; Rustandi, Andi; Permana, Sulaksana; Soedarsono, Johny Wahyuadi

    2017-03-01

    Calcination is a simple method to produce silica from rice husk (RH). One of the key to obtain higher purity silica from rice husk by calcination method is the effectiveness of impurities removal, especially potassium, from RH surface before calcination process. So, in the present study, an attempt has been made to produce high purity silica powder by using calcination method with the combination of roasting-quenching and acid leaching as a pretreatment to eliminate metal impurities, especially potassium, detected by using inductively coupled plasma mass spectrometry (ICP-MS). Finally, the high purity silica, 99.928% was obtained by roasting and calcination temperature of 300°C and 650°C, respectively. However, by considering less energy usage and silica purity achievement, the combination of 300°C roasting-quenching, 1M hydrochloric acid leaching, and calcination at the temperature of 600°C was the best route.

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

    Indian Academy of Sciences (India)

    Ni(OH)2 precursors were prepared via the precipitation transformation method, which was originated from Na2C2O4, NiSO4.6H2O and urea. NiO samples were successfully obtained by calcining Ni(OH)2 precursor with different calcination methods. Some were calcination in a tube furnace under the nitrogen flow and ...

  4. Cyclic Carbonation Calcination Studies of Limestone and Dolomite for CO2 Separation From Combustion Flue Gases

    OpenAIRE

    Sivalingam, S.;Gleis, S.;Hartmut, S.;Yrjas, P.;Hupa, M.

    2017-01-01

    Naturally occurring limestone and dolomite samples, originating from different geographical locations, were tested as potential sorbents for carbonation/calcination based CO2 capture from combustion flue gases. Samples have been studied in a thermogravimetric analyzer under simulated flue gas conditions at three calcination temperatures,viz., 750textdegreeC, 875textdegreeC, and 930textdegreeC for four carbonation calcination reaction (CCR) cycles. The dolomite sample exhibited the highest rat...

  5. Potential dispositioning flowsheets for ICPP SNF and wastes

    Energy Technology Data Exchange (ETDEWEB)

    Olson, A.L. [ed.; Anderson, P.A.; Bendixsen, C.L. [and others

    1995-11-01

    The Idaho Chemical Processing Plant (ICPP), located at the Idaho National Laboratory (INEL), has reprocessed irradiated nuclear fuels for the US Department of Energy (DOE) since 1953. This activity resulted mainly in the recovery of uranium and the management of the resulting wastes. The acidic radioactive high-level liquid waste was routinely stored in stainless steel tanks and then calcined to form a dry granular solid. The calcine is stored in stainless steel bins that are housed in underground concrete vaults. In April 1992, the DOE discontinued the practice of reprocessing irradiated nuclear fuels. This decision has left a legacy of 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), 3800 cubic meters of calcine waste, and 289 metric tons of heavy metal within unprocessed spent nuclear fuel (SNF) left in inventory at the ICPP. The nation`s radioactive waste policy has been established by the Nuclear Waste Policy Act (NWPA), which requires the final disposal of SNF and radioactive waste in accordance with US Environmental Protection Agency (EPA) and Nuclear Regulatory Commission (NRC) standards. In accordance with these regulations and other legal agreements between the State of Idaho and the DOE, the DOE must, among other requirements, (1) complete a final Environmental Impact Statement by April 30, 1995, (2) evaluate and test sodium-bearing waste pre-treatment technologies, (3) select the sodium-bearing and calcine waste pre-treatment technology, if necessary, by June 1, 1995, and (4) select a technology for converting calcined waste into an appropriate disposal form by June 1, 1995.

  6. Method of preparing nuclear wastes for tansportation and interim storage

    Science.gov (United States)

    Bandyopadhyay, Gautam; Galvin, Thomas M.

    1984-01-01

    Nuclear waste is formed into a substantially water-insoluble solid for temporary storage and transportation by mixing the calcined waste with at least 10 weight percent powdered anhydrous sodium silicate to form a mixture and subjecting the mixture to a high humidity environment for a period of time sufficient to form cementitious bonds by chemical reaction. The method is suitable for preparing an interim waste form from dried high level radioactive wastes.

  7. 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.

  8. Process for solidifying high-level nuclear waste

    Science.gov (United States)

    Ross, Wayne A.

    1978-01-01

    The addition of a small amount of reducing agent to a mixture of a high-level radioactive waste calcine and glass frit before the mixture is melted will produce a more homogeneous glass which is leach-resistant and suitable for long-term storage of high-level radioactive waste products.

  9. Carbothermic reduction of electric arc furnace dust and calcination of waelz oxide by semi-pilot scale rotary furnace

    Directory of Open Access Journals (Sweden)

    Morcali M.H.

    2012-01-01

    Full Text Available The paper gives a common outline about the known recycling techniques from electric arc furnace dusts and describes an investigation of a pyrometallurgical process for the recovery of zinc and iron from electric arc furnace dusts (EAFD. In the waelz process, the reduction of zinc and iron from the waste oxides using solid carbon (lignite coal was studied. In the reduction experiments; temperature, time and charge type (powder and pellet were investigated in detail. It was demonstrated that zinc and iron recovery (% increases with increasing temperature as well as time. Pelletizing was found to be a better method than using the powder as received for the zinc recovery and iron conversion (. In the calcination (roasting process, crude zinc oxide, which evaporated from non-ferric metals were collected as condensed product (crude waelz oxide, was heated in air atmosphere. Lead, cadmium as well as chlorine and other impurities were successfully removed from crude waelz oxide by this method. In the calcination experiments; temperature and time are investigated in detail. It was demonstrated that zinc purification (% increases with increasing temperature. The highest zinc refining (% was obtained at 1200°C for 120 minutes. A kinetic study was also undertaken to determine the activation energy of the process. Activation energies were 242.77 kJ/mol for the zinc recovery with powder forms, 261.99 kJ/mol for the zinc recovery with pellet forms respectively. It was found that, initially, the reaction was chemically controlled.

  10. 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.

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

    African Journals Online (AJOL)

    Calcined iron rich clay as an adsorbent and a photocatalyst for the degradation of phenol. ... Nigerian Journal of Technological Research ... This study investigates the potential of a calcined iron rich clay for the removal of phenol from aqueous solutions (adsorption) and subsequent degradation of the adsorbed phenol ...

  12. Test Plan for Radioactive Testing of a Vertical Direct Denitration Calciner

    Energy Technology Data Exchange (ETDEWEB)

    COMPTON, J.A.

    1999-10-05

    A vertical calciner will be used to demonstrate the direct denitration process for converting plutonium-bearing liquors to stable plutonium rich solids. The calciner and some of its associated equipment were previously tested with non-radioactive chemicals to demonstrate operability.

  13. Calcination effects on CeZrOx geometry and styrene production from ethylbenzene

    NARCIS (Netherlands)

    Kovacevic, M.; Brunet Espinosa, Roger; Lefferts, Leonardus; Mojet, Barbara

    2014-01-01

    A series of CeZrOx catalysts was prepared by calcination of hydrothermally obtained metal oxide precipitate at increasing temperatures. The samples were characterized by HRSEM, XRD and Raman spectroscopy, showing a change in morphology and particle size as a function of calcination temperature.

  14. Model for the sulfidation of calcined limestone and its use in reactor models.

    NARCIS (Netherlands)

    Heesink, Albertus B.M.; Brilman, Derk Willem Frederik; van Swaaij, Willibrordus Petrus Maria

    1998-01-01

    A mathematical model describing the sulfidation of a single calcined limestone particle was developed and experimentally verified. This model, which includes no fitting parameters, assumes a calcined limestone particle to consist of spherical grains of various sizes that react with H2S according to

  15. Waste Treatment of Acidic Solutions from the Dissolution of Irradiated LEU Targets for 99-Mo Production

    Energy Technology Data Exchange (ETDEWEB)

    Bakel, Allen J. [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division; Conner, Cliff [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division; Quigley, Kevin [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division; Vandegrift, George F. [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division

    2016-10-01

    One of the missions of the Reduced Enrichment for Research and Test Reactors (RERTR) program (and now the National Nuclear Security Administrations Material Management and Minimization program) is to facilitate the use of low enriched uranium (LEU) targets for 99Mo production. The conversion from highly enriched uranium (HEU) to LEU targets will require five to six times more uranium to produce an equivalent amount of 99Mo. The work discussed here addresses the technical challenges encountered in the treatment of uranyl nitrate hexahydrate (UNH)/nitric acid solutions remaining after the dissolution of LEU targets. Specifically, the focus of this work is the calcination of the uranium waste from 99Mo production using LEU foil targets and the Modified Cintichem Process. Work with our calciner system showed that high furnace temperature, a large vent tube, and a mechanical shield are beneficial for calciner operation. One- and two-step direct calcination processes were evaluated. The high-temperature one-step process led to contamination of the calciner system. The two-step direct calcination process operated stably and resulted in a relatively large amount of material in the calciner cup. Chemically assisted calcination using peroxide was rejected for further work due to the difficulty in handling the products. Chemically assisted calcination using formic acid was rejected due to unstable operation. Chemically assisted calcination using oxalic acid was recommended, although a better understanding of its chemistry is needed. Overall, this work showed that the two-step direct calcination and the in-cup oxalic acid processes are the best approaches for the treatment of the UNH/nitric acid waste solutions remaining from dissolution of LEU targets for 99Mo production.

  16. 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.

  17. ICPP Waste Management Technology Development Program

    Energy Technology Data Exchange (ETDEWEB)

    Hogg, G.W.; Olson, A.L.; Knecht, D.A. [Westinghouse Idaho Nuclear Co., Inc., Idaho Falls, ID (United States); Bonkoski, M.J. [USDOE, Washington, DC (United States)

    1993-01-01

    As a result of the decision to curtail reprocessing at the Idaho Chemical Processing Plant (ICPP), a Spent fuel and Waste Management Technology Development plan has been implemented to identify acceptable options for disposing of the (1) sodium-bearing liquid radioactive waste, (2) radioactive calcine, and (3) irradiated spent fuel stored at the Idaho National Engineering Laboratory (INEL). The plan was developed jointly by DOE and WINCO.

  18. 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

  19. 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.

  20. Enhanced photocatalytic activity of calcined natural sphalerite under visible light irradiation

    Directory of Open Access Journals (Sweden)

    Abdulhamid Hamza

    2017-01-01

    Full Text Available The photocatalytic activity of natural sphalerite (the main mineral ore of ZnS is relatively low in the absence of sacrificial donors. Present work focuses on the improvement of the photocatalytic activity of a natural sphalerite obtained from Abuni deposit, Nigeria, via calcination at 600 °C, 700 °C and 800 °C. The raw and calcined natural sphalerite samples were characterized using X-ray diffraction (XRD, scanning electron microscopy (SEM, and specific surface area analysis. The activity of the raw and calcined samples was evaluated using photocatalytic decolorization of methyl orange (MO as the model reaction. The kinetics of photocatalytic decolorization of MO on the raw and calcined natural sphalerite samples was fitted to the pseudo-first order approximation of the Langmuir–Hinshelwood model. The photocatalytic activity of the natural sphalerite was doubled upon calcination at 700 °C. The natural sphalerite calcined at 700 °C is also more active than the ones calcined at 600 °C and 800 °C due to the combined effects of chemical composition, crystallite size, specific surface area and oxygen vacancies.

  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. 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.

  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. SYNTHESIS OF SnO2 NANOCRYSTALS BY SOLID STATE REACTION FOLLOWED BY CALCINATION

    Institute of Scientific and Technical Information of China (English)

    Shanmin Gao; Li Pang; Hongwei Che; Xiaoping Zhou

    2004-01-01

    Nanocrystalline SnO2 was synthesized by direct mixing and grinding of SnCl4·5H2O and NaOH at roomtemperature, followed by calcination at different temperatures for different times in air. Product samples were characterized by X-ray diffraction and transmission electron microscope, revealing that the amorphous precursor SnO2 was transformed to crystals at 200 ℃ for 3 h, and that the average particle size increased upon raising the calcining temperature or prolonging the calcining time. The mechanism of the phase transformation of the products is discussed.

  5. Defense waste vitrification studies during FY 1980

    Energy Technology Data Exchange (ETDEWEB)

    Bjorklund, W.J.

    1981-08-01

    During FY-1980, Pacific Northwest Laboratory (PNL) tested three vitrification processes on simulated high-level radioactive waste typical of that stored or being produced at US defense facilities. Processes tested included a spray calciner/in-can melter, spray calciner/ceramic melter and direct liquid feeding of a ceramic melter. Tests were made on pilot-scale as well as fullscale equipment. Over 16,000 kg of glass product were produced from 68,000 L of simulated waste. Several compositions were tested, and the glass products were evaluated. Emphasis was placed on determining the processing rates and the ability of the waste to be processed. Off-gas data were collected on several runs. Major conclusions drawn from this test program are divided into processing results, glass-product results, and general information.

  6. Calcined eggshell as a cost effective material for removal of dyes from aqueous solution

    Science.gov (United States)

    Borhade, A. V.; Kale, A. S.

    2017-04-01

    The removal of Rhodamine B, Eriochrome black T and Murexide dyes from aqueous solutions using calcined eggshell powder were investigated. In this study, calcined eggshell powder was applied for its potential use as an adsorbent for the removal of Rhodamine B, Eriochrome black T and Murexide dyes from their aqueous solutions. The calcined eggshell powder obtained was characterized by Fourier Transform Infrared Spectroscopy (FT-IR), Thermogravimetric Analysis (TGA), Scanning Electron Microscopy (SEM) and X-ray Diffraction (XRD). The various parameters such as initial concentration, pH, adsorbent dose and contact time were studied. Various isotherms including Langmuir, Freundlich, Temkin and Dubinin-Radushkevich isotherm models were applied for the equilibrium adsorption data. The kinetic study of Rhodamine B, Eriochrome black T and Murexide dyes on calcined eggshell powder follows pseudo-second order kinetics.

  7. Test Plan for Radioactive Testing of a Vertical Direct Denitration Calciner

    Energy Technology Data Exchange (ETDEWEB)

    COMPTON, J.A.

    2000-02-03

    Stored solutions containing plutonium and nitric acid and possibly uranium thorium and minor amounts of other substances will be used for development and demonstration of a vertical calciner direct denitration process for conversion of those to stable storable PuO{sub 2} rich solids. Some of those solutions are quite dilute and very impure these require either pretreatment to make them suitable for calciner feed or an alternate stabilization method. Untreated scrap solutions containing some amounts of sulfate phosphate sodium and/or potassium may also be tested for suitability of direct denitration for conversion directly to PuO{sub 2}-rich solids. A vertical calciner will be used to demonstrate the direct denitration process for converting plutonium-bearing liquors to stable plutonium rich solids. The calciner and some of its associated equipment were previously tested with non-radioactive chemicals to demonstrate operability.

  8. Spectral-Luminescence Characteristics of Laser Dyes in a Calcined Xerogel

    Science.gov (United States)

    Bezkrovnaya, O. N.; Maslov, V. V.; Pritula, I. M.; Yurkevych, A. G.; Chayka, M. A.; Gurkalenko, Yu. A.; Pereverzev, N. V.

    2017-03-01

    Spectral and luminescence characteristics of three laser dyes incorporated into xerogel matrices preliminarily calcined under 700oC were studied in the spectral range of 600-700 nm. A stabilizing effect of these matrices on the dye molecules in the S1 exited state was revealed. This effect manifested in decreasing nonradiative losses in this state and increasing the quantum yield of the dye luminescence in a calcined xerogel as compared with methanol.

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

    African Journals Online (AJOL)

    AKA Boko

    refroidissement. Mots-clés : Phosphate, matière organique, calcination, Youssoufia, Maroc. Abstract ... Moreover, we note that the granulometric distribution of calcined phosphates varies according to the rate of its .... 50,079 ; 20,885), et les carbonates qui sont sous forme de la dolomite CaMg(CO3)2 (2θ : 30,917 ; 50,674 ...

  10. Sorption characteristics of fluoride on to magnesium oxide-rich phases calcined at different temperatures.

    Science.gov (United States)

    Sasaki, Keiko; Fukumoto, Naoyuki; Moriyama, Sayo; Hirajima, Tsuyoshi

    2011-07-15

    The effect of calcination temperature during production of magnesium oxide-rich phases from MgCO(3) on the sorption of F(-) ions in the aqueous phase has been investigated. Magnesium oxide-rich phases were formed by calcination at over 873 K for 1h. Higher calcination temperatures produced more crystalline MgO with smaller specific surface area and provided larger values of the total basicity per unit surface area. The higher calcination temperatures lead to slower F(-) removal rate, and lower equilibrium F(-) concentrations, when the equilibrium F(-) concentrations are less than 1 mmol dm(-3). Larger total basicity per unit surface area made the reactivity with F(-) ions in aqueous phase more feasible, resulting in a greater degree of F(-) sorption. For equilibrium F(-) concentrations more than 1 mmol dm(-3), lower calcination temperatures favored the co-precipitation of F(-) with Mg(OH)(2), probably leading to the formation of Mg(OH)(2-x)F(x), and the achievement of larger sorption density. This is the first paper which describes the relationship between the solid base characteristics obtained by CO(2)-TPD for MgO with different calcination temperatures as a function of the reactivity of F(-) sorption in the aqueous phase. Copyright © 2011 Elsevier B.V. All rights reserved.

  11. Carbon dioxide absorption and release properties of pyrolysis products of dolomite calcined in vacuum atmosphere.

    Science.gov (United States)

    Wang, Fei; Kuzuya, Toshihiro; Hirai, Shinji; Li, Jihua; Li, Te

    2014-01-01

    The decomposition of dolomite into CaO and MgO was performed at 1073 K in vacuum and at 1273 K in an Ar atmosphere. The dolomite calcined in vacuum was found to have a higher specific surface area and a higher micropore volume when compared to the dolomite calcined in the Ar atmosphere. These pyrolysis products of dolomite were reacted with CO2 at 673 K for 21.6 ks. On the absorption of CO2, the formation of CaCO3 was observed. The degree of absorption of the dolomite calcined in vacuum was determined to be above 50%, which was higher than the degree of absorption of the dolomite calcined in the Ar atmosphere. The CO2 absorption and release procedures were repeated three times for the dolomite calcined in vacuum. The specific surface area and micropore volume of calcined dolomite decreased with successive repetitions of the CO2 absorption and release cycles leading to a decrease in the degree of absorption of CO2.

  12. 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.

  13. 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.

  14. Transportation and transformation of mercury in a calcine profile in the Wanshan Mercury Mine, SW China.

    Science.gov (United States)

    Yin, Runsheng; Gu, Chunhao; Feng, Xinbin; Zheng, Lirong; Hu, Ningning

    2016-12-01

    Calcination of Hg ores has resulted in serious contamination of mercury (Hg) in the environment. To understand the mobilization of Hg in the calcine pile, the speciation of Hg in a profile of a large calcine pile in the Wanshan Mercury Mine, SW China was investigated using the X-ray absorption spectroscopy (XANES), to understand the mobilization of Hg in the calcine pile. Higher concentrations of Hg were observed at the 30-50 cm depth of the profile, corresponding to a cemented layer. This layer is observed in the entire pile, and was formed due to cementation of calcines. Hg species in calcines include cinnabar (α-HgS), metacinnabar (β-HgS), elemental Hg(0), and minor mercuric chloride (HgCl2), but these Hg species show dramatic changes in the profile. Variations in Hg speciation suggest that extensive mobilization of Hg can occur during weathering processes. We show that the cemented layer can prevent the leaching of Hg and the emission of Hg(0) from the pile. High MeHg concentrations were found near the cemented layer, indicating Hg methylation occurs. This study provides important insights into the environmental risk of Hg in mining areas. Copyright © 2016 Elsevier Ltd. All rights reserved.

  15. 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.

  16. Process analysis of CO{sub 2} capture from flue gas using carbonation/calcination cycles

    Energy Technology Data Exchange (ETDEWEB)

    Li, Z.S.; Cai, N.S.; Croiset, E. [Tsinghua University, Beijing (China). Dept. for Thermal Engineering

    2008-07-15

    Process analysis of CO{sub 2} capture from flue gas using Ca-based carbonation/calcination cycles is presented here. A carbonation/calcination system is composed essentially of two reactors (an absorber and a regenerator) with Ca-based sorbent circulating between the two reactors (assumed here as fluidized beds). CO{sub 2} is, therefore, transferred from the absorber to the regenerator. Because of the endothermicity of the calcination reaction, a certain amount of coal is burned with pure oxygen in the regenerator. Detailed mass balance, heat balance and cost of electricity and CO{sub 2} mitigation for the carbonation/calcination cycles with three Ca-based sorbents in dual fluidized beds were calculated and analyzed to study the effect of the Ca-based sorbent activity decay on CO{sub 2} capture from flue gas. The three sorbents considered were: limestone, dolomite and CaO/Ca{sub 12}Al{sub 14}O{sub 33} (75/25 wt %) sorbent. All results, including the amount of coal and oxygen required, are presented with respect to the difference in calcium oxide conversion between the absorber and the regenerator, which is an important design parameter. Finally, costs of electricity and CO{sub 2} mitigation costs using carbonation/calcination cycles for the three sorbents were estimated. The results indicate that the economics of the carbonation/calcination process compare favorably with competing technologies for capturing CO{sub 2}.

  17. Carbon Dioxide Absorption and Release Properties of Pyrolysis Products of Dolomite Calcined in Vacuum Atmosphere

    Science.gov (United States)

    Wang, Fei; Kuzuya, Toshihiro; Hirai, Shinji; Li, Jihua; Li, Te

    2014-01-01

    The decomposition of dolomite into CaO and MgO was performed at 1073 K in vacuum and at 1273 K in an Ar atmosphere. The dolomite calcined in vacuum was found to have a higher specific surface area and a higher micropore volume when compared to the dolomite calcined in the Ar atmosphere. These pyrolysis products of dolomite were reacted with CO2 at 673 K for 21.6 ks. On the absorption of CO2, the formation of CaCO3 was observed. The degree of absorption of the dolomite calcined in vacuum was determined to be above 50%, which was higher than the degree of absorption of the dolomite calcined in the Ar atmosphere. The CO2 absorption and release procedures were repeated three times for the dolomite calcined in vacuum. The specific surface area and micropore volume of calcined dolomite decreased with successive repetitions of the CO2 absorption and release cycles leading to a decrease in the degree of absorption of CO2. PMID:25136696

  18. Adsorptive removal of phosphate from aqueous solutions using raw and calcinated dolomite.

    Science.gov (United States)

    Karaca, S; Gürses, A; Ejder, M; Açikyildiz, M

    2006-02-06

    This study explored the feasibility of utilizing raw and calcinated dolomite under CO2 atmosphere for phosphate removal in laboratory experiments. The experimental work emphasized the evaluation of phosphate adsorption characteristics of this adsorbent material. Studies were conducted to delineate the effect of contact time, initial phosphate concentration, temperature, pH, stirring speed, adsorbent dose and calcination temperature. Phosphate removal decreased with increasing temperature and slightly increased with increasing of pH. The observed decrease in the adsorption capacity with increase of the temperature from 20 to 40 and to 60 degrees C indicates that the low temperatures favor the phosphate removal by adsorption onto dolomite. Phosphate removal was seen to decrease with increasing calcination temperature due to the structural changes occurring in the structure and pore size distribution of dolomite samples during calcination. The experimental data obtained were applied to the Freundlich, Langmuir, BET, Halsey, Harkins-Jura, Smith and Henderson isotherm equations to test the fit of these equations to raw and calcinated dolomite samples. By considering the experimental results and adsorption models applied in this study, it can be concluded that adsorption of phosphate occurs predominantly through physical interactions, and the dolomite sample has a heteroporous structure. The large values of the constants for Henderson equation and the high value of y(m) obtained from BET equation indicate the microporous structure is more stable in raw and calcinated dolomite samples.

  19. 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.

  20. 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.

  1. Mechanical and Thermal Properties of Polypropylene Reinforced by Calcined and Uncalcined Zeolite

    Directory of Open Access Journals (Sweden)

    Nurdin Bukit

    2013-04-01

    Full Text Available This study was carried out to compare mechanical and thermal properties of polypropylene (PP reinforced with uncalcined and calcined zeolites. The PP samples were reinforced with zeolites at various quantities of 2, 4, and 6 (wt %. The comparison of the two types of zeolite was based  on mechanical properties, including tensile strength, elongation at break, and Young’s modulus, and thermal characteristics analyzed using DSC, and DTA/TGA technique. The results obtained clearly revealed that both zeolites were able to significantly increase tensile strength and Young’s modulus of the samples, with calcined zeolite was found to work better. Addition of calcined zeolite was found to result in increased fracture elongation of the samples reinforced with up to 4 wt% zeolite but decreased sharply for the sample reinforced with 6 wt% zeolite, while for the samples reinforced with uncalcined zeolite, no consistent trend was observed. Thermal analyses demonstrated that the samples reinforced with calcined zeolite are more resistant to thermal treatment than those reinforced with uncalcined zeolite, as indicated by their higher decomposition temperature. DSC analysis revealed that there  was no significant difference  of the melting points of the samples was observed, but the effect of the quantity of zeolite on enthalphy was quite evident, in which the enthalpies of the samples reinforced with calcined zeolites were relatively lower than those of the samples reinforced with uncalcined zeolites. 

  2. Hot isostatic press waste option study report

    Energy Technology Data Exchange (ETDEWEB)

    Russell, N.E.; Taylor, D.D.

    1998-02-01

    A Settlement Agreement between the Department of Energy and the State of Idaho mandates that all high-level radioactive waste now stored at the Idaho Chemical Processing Plant be treated so that it is ready to move out of Idaho for disposal by the target date of 2035. This study investigates the immobilization of all Idaho Chemical Processing Plant calcine, including calcined sodium bearing waste, via the process known as hot isostatic press, which produces compact solid waste forms by means of high temperature and pressure (1,050 C and 20,000 psi), as the treatment method for complying with the settlement agreement. The final waste product would be contained in stainless-steel canisters, the same type used at the Savannah River Site for vitrified waste, and stored at the Idaho National Engineering and Environmental Laboratory until a national geological repository becomes available for its disposal. The waste processing period is from 2013 through 2032, and disposal at the High Level Waste repository will probably begin sometime after 2065.

  3. 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.

  4. CALCINATION TEMPERATURE EFFECTS ON OPTICAL PROPERTIES OF NANO-POROUS SILICA THIN FILMS

    Directory of Open Access Journals (Sweden)

    Mohammadreza Mojab

    2015-06-01

    Full Text Available Silica nano-porous thin films at various calcination temperatures were deposited on glass substrates with a layer by layer method. The structure, morphology, surface composition, transmittance and reflectance of the films were investigated by X-ray diffraction, field emission scanning electron microscopy, attenuated total reflectance fourier transform infrared spectroscopy and UV-VIS-NIR spectrophotometer, respectively. The results indicated that the transmittance of the films is increased by increasing the calcinations temperatures to 300oC and at higher temperature, it is decreased. The deposition of silica nano-porous film on the glass at the optimum calcination temperature (300oC decreased refractive index of the glass at a wavelength of 550 nm from 1.5 to 1.37.

  5. 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.

  6. 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.

  7. Influence of calcinated and non calcinated nanobioglass particles on hardness and bioactivity of sol-gel-derived TiO2-SiO2 nano composite coatings on stainless steel substrates.

    Science.gov (United States)

    Dadash, Mohammad Saleh; Karbasi, Saeed; Esfahani, Mojtaba Nasr; Ebrahimi, Mohammad Reza; Vali, Hojatollah

    2011-04-01

    Thick films of calcinated and non calcinated nanobioglass (NBG)-titania composite coatings were prepared on stainless steel substrates by alkoxide sol-gel process. Dip-coating method was used for the films preparation. The morphology, structure and composition of the nano composite films were evaluated using environmental scanning electron microscope, X-ray diffraction and Fourier transform infrared spectroscope. The SEM investigation results showed that prepared thick NBG-titania films are smooth and free of macrocracking, fracture or flaking. The grain size of these films was uniform and nano scale (50-60 nm) which confirmed with TEM. Also FTIR confirmed the presence of Si-O-Si bands on the calcinated NBG-titania films. The hardness of the prepared films (TiO(2)-calcinated NBG and TiO(2)-Non calcinated NBG) was compared by using micro hardness test method. The results verified that the presence of calcinated NBG particles in NBG-titania composite enhanced gradually the mechanical data of the prepared films. The in vitro bioactivity of these films was discussed based on the analysis of the variations of Ca and P concentrations in the simulated body fluid (SBF) and their surface morphologies against immersion time. Surface morphology and Si-O-Si bands were found to be of great importance with respect to the bioactivity of the studied films. The results showed that calcinated NBG-titania films have better bioactivity than non calcinated NBG-titania films.

  8. 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.

  9. Zeolite Beta: The Relationship Between Calcination Procedure, Aluminum Configuration and Lewis Acidity

    NARCIS (Netherlands)

    Koningsberger, D.C.; Kunkeler, P.J.; Zuurdeeg, B.J.; Waal, J.C. van der; Bokhoven, J.A. van; Bekkum, H. van

    1998-01-01

    Zeolite Beta was calcined under a variety of carefully controlled conditions to study the influence of (hydro)thermal treatments on the catalytic activity of zeolite Beta in the Lewis acid-catalyzed Meerwein-Ponndorf-Verley reduction of ketones. The activity of (H)Beta can be increased by several

  10. Oxidative dehydrogenation of ethylbenzene to styrene over alumina : effect of calcination

    NARCIS (Netherlands)

    Nederlof, Christian; Zarubina, Valeriya; Melian-Cabrera, Ignacio; Heeres, Hero Jan (Eric); Kapteijn, Freek; Makkee, Michiel

    2013-01-01

    Commercially available gamma-Al2O3 was calcined at temperatures between 500 and 1200 degrees C and tested for its performance in the oxidative ethylbenzene dehydrogenation (ODH) over a wide range of industrially-relevant conditions. The original gamma-Al2O3, as well as Z- and alpha-Al2O3, were

  11. Enhanced pyroelectric properties of PZT/PVDF-TrFE composites using calcined PZT ceramic powders

    Science.gov (United States)

    Wu, Chuan-Gui; Cai, Guang-Qiang; Luo, Wen-Bo; Peng, Qiang-Xiang; Sun, Xiang-Yu; Zhang, Wan-Li

    2013-04-01

    The effects of calcined lead-zirconate-titanate (PZT) powders on the electric properties of PZT/polyvinylidene-trifluorethylene copolymer (PVDF-TrFE) composites thick films were studied in this paper. Firstly, the PZT powders synthesized by hydrothermal method were calcined at different temperatures ranging from 300°C to 900°C, and then the PZT/PVDF-TrFE composites films were produced by casting PZT/PVDF-TrFE suspension onto the indium-tin-oxide (ITO)-coated glass substrates. Electric properties, including dielectric and pyroelectric performances of thick films consisting of PZT powders calcined at different temperatures were tested. The highest pyroelectric coefficient obtained in the sample using 700°C calcined PZT powders was 96 μCm-2K-1, which was 20% higher than the composites made of uncalcined powders. Additionally, the highest detectivity figure-of-merit (FOM) (FD) of the composite was 1.36 × 10-5Pa-1/2, which increased about 13.5% compared to the one using uncalcined powders.

  12. 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 two essentially different calcination methods using a stationary, electrically heated chamber oven and enlarged laboratory scale rotary kiln designed by the authors, heated by gas combustion methods ...

  13. Hydroxyapatite nanoparticles: electrospinning and calcination of hydroxyapatite/polyvinyl butyral nanofibers and growth kinetics

    NARCIS (Netherlands)

    Zakaria, S.M.; Zein, S.H. Sharif; Othman, M.R.; Jansen, J.A.

    2013-01-01

    Electrospinning of hydroxyapatite (HA)/polyvinyl butyral solution resulted in the formation of fibers with average diameter of 937-1440 nm. These fibers were converted into HA nanoparticles with size <100 nm after undergoing calcination treatment at 600 degrees C. The diameter of the fiber was

  14. 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.

  15. 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.

  16. 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.)

  17. Alliance between chemical industry Astral Calcining, India, and energy company E.On Benelux; Verbond chemie en energie [tussen Astral Calcining, India en E.On Benelux

    Energy Technology Data Exchange (ETDEWEB)

    Roggen, M. (ed.)

    2003-03-01

    The Indian chemical concern Astral Calcining (produces carbon for the aluminium industry) will supply high-pressure steam to the energy company E.ON Benelux, to be used by Lyondell Bayer (producer of propylene oxide). In exchange, Astral will receive electricity from E.On Benelux. This is a unique co-operation between companies with different production processes and cultures. [Dutch] Het Indiase chemieconcern Astral gaat aan E.ON Benelux hogedruk stoom leveren die bestemd is voor Lyondell Bayer. In ruil daarvoor ontvangt Astral elektriciteit. Een unieke samenwerking tussen concerns met totaal andere productieprocessen en uiteenlopende culturen.

  18. 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)

  19. Cobalt-lanthanum catalyst precursors for ammonia synthesis: determination of calcination temperature and storage conditions

    Directory of Open Access Journals (Sweden)

    Zybert Magdalena

    2017-06-01

    Full Text Available A thermal decomposition of a cobalt-lanthanum catalyst precursor containing a mixture of cobalt and lanthanum compounds obtained by co-precipitation were studied using thermal analysis coupled with mass spectrometry (TG-MS. Studies revealed that the calcination in air at 500°C is sufficient to transform the obtained cobalt precipitate into Co3O4, but it leads to only partial decomposition of lanthanum precipitate. In order to obtain Co/La catalyst precursor containing La2O3 the calcination in air at the temperature about 800°C is required. However, it is unfavorable from the point of view of textural properties of the catalyst precursor. A strong effect of storage conditions on the phase composition of the studied cobalt-lanthanum catalyst precursor, caused by the formation of lanthanum hydroxide and lanthanum carbonates from La2O3 when contacting with air, was observed.

  20. 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...... 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...... and experiments in a tube furnace reactor in the temperature interval of 900–1100 °C. The investigated conditions resemble actual conditions in the material inlet end of cement rotary kilns. It was found that the sulfates CaSO4, K2SO4, and Na2SO4 were all stable under oxidizing conditions but began to decompose...

  1. 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.

  2. Ce-doped titania nanoparticles: The effects of doped amount and calcination temperature on photocatalytic activity

    Science.gov (United States)

    Shi, Jianwen; Zou, Yajun; Ma, Dandan

    2017-01-01

    A series of Ce-doped TiO2 nanoparticles with different doped amount and calcination temperature were prepared by sol-gel method. These obtained samples were characterized with X-ray diffraction (XRD), transmission electron microscope (TEM) and ultraviolet-visible diffuse reflectance spectra (DRS), and their photocatalytic activities were evaluated by the photocatalytic degradation of methyl orange. Results showed that Ce doping inhibits the growth of crystal size and the phase transformation from anatase to rutile, leads to lattice distortion and expansion of TiO2. Furthermore, Ce doping brings the red-shift of absorption profile and the increase of photons absorption in the range of 400-600 nm. Photocatalytic degradation of methyl orange shows that Ce doping improves the photocatalytic activity of TiO2. The optimal doped amount is 0.05 mol% and the optimal calcined temperature is 600 °C for the maximum photocatalytic degradation efficiency in our experiment.

  3. Evaluation and selection of aqueous-based technology for partitioning radionuclides from ICPP calcine

    Energy Technology Data Exchange (ETDEWEB)

    Olson, A.L.; Schulz, W.W.; Burchfield, L.A.; Carlson, C.D.; Swanson, J.L.; Thompson, M.C.

    1993-02-01

    Early in 1993 Westinghouse Idaho Nuclear Company (WINCO) chartered a Panel of Nuclear Separations Experts. The purpose of this Panel was to assist WINCO scientists and engineers in selecting, evaluating, and ranking candidate aqueous-based processes and technologies for potential use in partitioning selected radionuclides from nitric acid solutions of retrieved Idaho Chemical Processing Plant (ICPP) calcine. Radionuclides of interest are all transuranium elements, {sup 90}Sr, {sup 99}Tc, {sup 129}I, and {sup 137}Cs. The six man Panel met for 4 days (February 16--19, 1993) on the campus of the Idaho State University in Pocatello, Idaho. Principal topics addressed included: Available radionuclide removal technology; applicability of separations technology and processes to ICPP calcine; and potential integrated radionuclide partitioning schemes. This report, prepared from contributions from all Panel members, presents a comprehensive account of the proceedings and significant findings of the February, 1993 meeting in Pocatello.

  4. Hydroxyapatite nanoparticles: electrospinning and calcination of hydroxyapatite/polyvinyl butyral nanofibers and growth kinetics.

    Science.gov (United States)

    Zakaria, Siti Maisurah; Sharif Zein, Sharif Hussein; Othman, Mohd Roslee; Jansen, John A

    2013-07-01

    Electrospinning of hydroxyapatite (HA)/polyvinyl butyral solution resulted in the formation of fibers with average diameter of 937-1440 nm. These fibers were converted into HA nanoparticles with size <100 nm after undergoing calcination treatment at 600°C. The diameter of the fiber was found to be influenced by applied voltage and spinning distance. The injection flowrate did not affect the diameter significantly. The electrospinning method successfully reduced the commercial HA particle size in the range of 400-1100 nm into <100 nm. The dispersion of the finally calcined HA nanoparticles was improved significantly after anionic sodium dodecyl sulfate surfactant was introduced. The experimental data of HA growth kinetics were subjected to the integral method of analysis, and the rate law of the reaction was found to follow the first order reaction. Copyright © 2012 Wiley Periodicals, Inc.

  5. Environmental evaluation of alternatives for long-term management of Defense high-level radioactive wastes at the Idaho Chemical Processing Plant

    Energy Technology Data Exchange (ETDEWEB)

    1982-09-01

    The U.S. Department of Energy (DOE) is considering the selection of a strategy for the long-term management of the defense high-level wastes at the Idaho Chemical Processing Plant (ICPP). This report describes the environmental impacts of alternative strategies. These alternative strategies include leaving the calcine in its present form at the Idaho National Engineering Laboratory (INEL), or retrieving and modifying the calcine to a more durable waste form and disposing of it either at the INEL or in an offsite repository. This report addresses only the alternatives for a program to manage the high-level waste generated at the ICPP. 24 figures, 60 tables.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-08-15

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

  7. Biodiesel production via the transesterification of soybean oil using waste starfish (Asterina pectinifera).

    Science.gov (United States)

    Jo, Yong Beom; Park, Sung Hoon; Jeon, Jong-Ki; Ko, Chang Hyun; Ryu, Changkook; Park, Young-Kwon

    2013-07-01

    Calcined waste starfish was used as a base catalyst for the production of biodiesel from soybean oil for the first time. A batch reactor was used for the transesterification reaction. The thermal characteristics and crystal structures of the waste starfish were investigated by thermo-gravimetric analysis and X-ray diffraction. The biodiesel yield was determined by measuring the content of fatty acid methyl esters (FAME). The calcination temperature appeared to be a very important parameter affecting the catalytic activity. The starfish-derived catalyst calcined at 750 °C or higher exhibited high activity for the transesterification reaction. The FAME content increased with increasing catalyst dose and methanol-over-oil ratio.

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

    DEFF Research Database (Denmark)

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

    2002-01-01

    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...... and thereby the char and limestone conversion and the NO emission. (C) 2002 Elsevier Science Ltd. All rights reserved....

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1977-10-14

    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.

  11. 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)

  12. Effect of Calcination at Synthesis of Mg-Al Hydrotalcite Using co-Precipitation Method

    Directory of Open Access Journals (Sweden)

    Niar Kurnia Julianti

    2017-01-01

    Full Text Available The use of hydrotalcite in catalysis has wide attention in academic research and industrial parties. Based on its utilization, hydrotalcite can be active catalyst or support. This research is focused on the investigation of characteristic like spesific surface area of Mg-Al hydrotalcite which is prepared with different temperature of calcination. Synthesis of Mg-Al hydrotalcites with Mg/Al molar ratio 3:1 were prepared by co-precipitation method. Mg(NO33.6H2O and Al(NO33.9H2O as precursors of Mg-Al hydrotalcite. Na2CO3 was used as precipitant agent and NaOH was used as buffer solution. The solution was mixed and aging for 5 hours at 650oC. The dried precipitate was calcined at 2500oC, 3500oC, 4500oC, 5500oC and 6500oC. The characterization of functional group was determined by Fourier Transform Infra Red (FT-IR. The Identical peaks diffractogram were analyzed by X-Ray Diffraction (XRD. The spesific surface area was determined by adsorption-desorption of nitrogen. The largest surface area that obtained from the calcination temperature of 650oC is 156.252 m2/g.

  13. Calcination temperature effect on the microstructure and dielectric properties of M-type strontium hexagonal ferrites

    Science.gov (United States)

    Mohammed, J.; Sharma, Jyoti; Kumar, Sachin; Trudel, T. T. Carol; Srivastava, A. K.

    2017-07-01

    M-type hexagonal ferrites have found wide application in electronics industry due to the possibility of tuning properties such as dielectric properties. An improved dielectric property is useful in high frequency application. In this paper, we studied the effect of calcination temperature on structural and dielectric properties of Al-Mn substituted M-type strontium hexagonal ferrites with chemical composition Sr1-xAlxFe12-yMnyO19 (x=0.3 and y=0.6) synthesized by sol-gel auto-combustion method. The prepared sample was sintered at four different temperatures (T=750°C, 850°C, 950°C and 1050°C) for 5 hours. Characterisations of the synthesized samples were carried out using X-ray diffraction (XRD), impedance analyser, field emission electron microscope (FE-SEM) and energy dispersive X-ray (EDX) spectroscopy. The dielectric properties were explained on the basis of Koop's phenomenological theory and Maxwell Wagner theory. The sample calcinated at 750°C shows the highest value of dielectric constant and AC conductivity whereas that calcinated at 1050°C exhibit the lowest dielectric losses.

  14. 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.

  15. 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)

  16. 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.

  17. ANSTO's waste forms for the 31. century

    Energy Technology Data Exchange (ETDEWEB)

    Vance, E.R.; Begg, B. D.; Day, R. A.; Moricca, S.; Perera, D. S.; Stewart, M. W. A.; Carter, M. L.; McGlinn, P. J.; Smith, K. L.; Walls, P. A.; Robina, M. La

    2004-07-01

    ANSTO waste form development for high-level radioactive waste is directed towards practical applications, particularly problematic niche wastes that do not readily lend themselves to direct vitrification. Integration of waste form chemistry and processing method is emphasised. Some longstanding misconceptions about titanate ceramics are dealt with. We have a range of titanate-bearing waste form products aimed at immobilisation of tank wastes and sludges, actinide-rich wastes, INEEL calcines and Na-bearing liquid wastes, Al-rich wastes arising from reprocessing of Al-clad fuels, Mo-rich wastes arising from reprocessing of U-Mo fuels, partitioned Cs-rich wastes, and {sup 99}Tc. Waste form production techniques cover hot isostatic and uniaxial pressing, sintering, and cold-crucible melting, and these are strongly integrated into waste form design. Speciation and leach resistance of Cs and alkalis in cementitious products and geo-polymers are being studied. Recently we have embarked on studies of candidate inert matrix fuels for Pu burning. We also have a considerable program directed at basic understanding of the waste forms in regard to crystal chemistry, dissolution behaviour in aqueous media, radiation damage effects and optimum processing techniques. (authors)

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

    National Research Council Canada - National Science Library

    Qian Li; Yan Zhang; Xiaoliang Liu; Bin Xu; Yongbin Yang; Tao Jiang

    2017-01-01

    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...

  19. Reuse of spent FCC catalyst, waste serpentine and kiln rollers waste for synthesis of cordierite and cordierite-mullite ceramics.

    Science.gov (United States)

    Ramezani, A; Emami, S M; Nemat, S

    2017-09-15

    Spent fluid catalytic cracking (FCC) was gathered from several petrochemical plants and calcined in a rotary furnace between 1000 and 1100°C in order to remove sulphur and hydrocarbon based impurities. Calcining process on FCC led to formation of AlVO4 ceramic phase, so converted the hazardous waste to non-hazardous applicable raw material. In this study, two ceramic bodies as cordierite and cordierite-mullite were synthesized with calcined spent FCC, waste serpentine, kiln rollers waste and high grade kaolin as raw materials. The XRD results showed that the cordierite and cordierite-mullite were synthesized successfully so that 96.4% of F1 (cordierite) sample fired at 1400°C was cordierite phase and F2 (cordierite-mullite) sample fired at 1450°C was completely cordierite and mullite phases. The synthesized cordierite and cordierite-mullite samples had lower porosity values and coefficient of thermal expansion (CTE) than similar industrial products. The negative CTE value that obtained from the cordierite sample up to 800°C is favorable for some applications. The considerable results of the synthesized cordierite and cordierite-mullite from this work present cost reduction of the two ceramic bodies production and may help to solve the environmental problems with the use of three waste sources in large scales. Copyright © 2017 Elsevier B.V. All rights reserved.

  20. 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)

  1. 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.

  2. Waste Sites - Municipal Waste Operations

    Data.gov (United States)

    NSGIC Education | GIS Inventory — A Municipal Waste Operation is a DEP primary facility type related to the Waste Management Municipal Waste Program. The sub-facility types related to Municipal Waste...

  3. Effect of aluminum and silicon reactants and hip soak time on characteristics of glass-ceramic waste forms

    Energy Technology Data Exchange (ETDEWEB)

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

    1994-12-31

    The effects of aluminum and silicon reactants and process soak time on total and normalized elemental leach rates and microstructure of glass-ceramic waste forms are investigated. 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, 138 MPa for 4 hours. The formulation with 2 wt% Al was HIPed for 4, 8, 16 and 24 hours at 1050{degrees}C and 138 MPa. The leach rates remained essentially constant for the 2 wt% Al waste form that was HIPed for 4, 8, 16 and 24 hours at the same temperature and pressure. However, the leach rates increased in the waste forms where the Si content was increased. The 2 wt% Al waste form appears to be the potential candidate for immobilization of the fluorinel-sodium calcine stored onsite at the Idaho Chemical Processing Plant.

  4. PREPARATION AND PROPERTIES OF Co-Fe MIXED OXIDES OBTAINED BY CALCINATION OF LAYERED DOUBLE HYDROXIDES

    Directory of Open Access Journals (Sweden)

    M. E. Pérez Bernal

    2004-12-01

    Full Text Available Solids containing Co(II and Fe(III with molar ratios of 2/1, 3/2, 1/1, 2/3 and 1/2 have been synthetised by coprecipitation at constant pH. All they displayed a hydrotalcite-like structure with interlayer carbonate, which crystallinity decreases as the iron content was increased. No other crystalline phase was identified, even in the Fe-rich samples. They have been characterised by powder X-ray diffraction, FT-IR spectroscopy, thermal analysis (differential thermal analysis, thermogravimetric analysis and temperature-programmed reduction, in addition to specific surface area assessment by nitrogen adsorption at -196°C. A minor oxidation of Co(II to Co(III is observed in the Co-rich samples, although it reverses again to Co(II upon calcination in oxygen at ca. 850°C. Thermal decomposition takes place in a single step up to ca. 350°C, and the specific surface area increases with the iron content, probably because of the presence of hydrated amorphous iron oxides. The solids calcined at 1200°C in air contain crystalline CoO, Co3O4 and CoFe2O4 (spinel, this one being the dominant phase, and only phase detected for large Fe contents. Metallic species are more easily reduced in the original solids than in the calcined ones, and in all cases iron seems to be reduced at a higher temperature than cobalt.

  5. Phosphate interaction with calcined form of Mg-Al-CO3 hydrotalcite in aqueous solutions

    OpenAIRE

    Kostura, Bruno; Matýsek, Dalibor; Kukutschová, Jana; Leško, Juraj

    2012-01-01

    In this study the sorption removal of phosphates from aqueous solutions was investigated. The sorbent used was Mg-Al-CO3 hydrotalcite with a molar ratio of 2:1 calcined at 450 oC. The retention capacity of cLDH was 2.88 mmol P/g. The sorption can be characterized by a kinetic model of the pseudo-second order. Laboratory tests proved the existence of two steps – fast and slow. The fast step is associated with regeneration of the layered structure accompanied by surface adsorption of phosphates...

  6. Large scale production of SrFe12O19 nanoparticles with low calcination temperature

    Science.gov (United States)

    Kumar, M. Rajesh; Yu, Z. J.; Pan, Q.

    2017-09-01

    High quality SrFe12O19 nanoparticles were successfully synthesized by a co-precipitation method with low calcination temperature. Structural, morphological and magnetic properties of SrFe12O19 nanoparticles were investigated by means of x-ray diffraction (XRD), Fourier transform infrared spectra (FT-IR), scanning electron microscopy (SEM), and vibrating sample magnetometer (VSM) analysis. The formation of SrFe12O19 nanoparticles were confirmed by XRD analysis. The actual size and morphology of the nanoparticles were characterized by SEM.

  7. Residential Waste

    DEFF Research Database (Denmark)

    Christensen, Thomas Højlund; Fruergaard, Thilde; Matsufuji, Y.

    2011-01-01

    Residential waste comes from residential areas with multi-family and single-family housing and includes four types of waste: household waste, garden waste, bulky waste and household hazardous waste. Typical unit generation rates, material composition, chemical composition and determining factors...... are discussed in this chapter. Characterizing residential waste is faced with the problem that many residences already divert some waste away from the official collection systems, for example performing home composting of vegetable waste and garden waste, having their bundled newspaper picked up by the scouts...... twice a year or bringing their used furniture to the flea markets organized by charity clubs. Thus, much of the data available on residential waste represents collected waste and not necessarily all generated waste. The latter can only be characterized by careful studies directly at the source...

  8. Preparation of Nanosized LaCoO3 through Calcination of a Hydrothermally Synthesized Precursor

    Directory of Open Access Journals (Sweden)

    L. Tepech-Carrillo

    2016-01-01

    Full Text Available A method for obtaining nanosized LaCoO3 crystals from calcination of a precursor powder synthesized by a hydrothermal route is reported. Details concerning the evolution of the microstructure and formation mechanism of the perovskite phase were studied by powder X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, Raman spectroscopy, and thermal analysis. It was found that the morphology of the sample progressively turns from a mix of fibers and rods to interconnected nanocrystals. It is determined that LaCoO3 phase is produced by a reaction of cobalt and lanthanum oxides, the latter produced by a two-step dehydration process of La(OH3. Finally, it was found that nearly stoichiometric LaCoO3 nanocrystals can be obtained at temperatures as low as 850°C. Nevertheless, whether higher calcination temperatures are used, appropriate reaction times and a controlled atmosphere are required in order to avoid formation of lanthanum carbonates and high density of lattice defects.

  9. 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.

  10. 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.

  11. 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.

  12. Preparation of mesoporous MgO: phenomena occurred during the calcination

    Science.gov (United States)

    Thanh Huyen, Pham; Callone, Emanuela; Campostrini, Renzo; Carturan, Giovanni; Thi Hong, Tran; Nhat, Hoang Nam; Dang Chinh, Huynh

    2013-10-01

    Mesoporous MgO has been synthesized in the presence of the neutral block co-polymer surfactant Pluronic F127. The characterization of synthesized material was carried out by mean of X-ray diffraction (XRD), scanning electron microscope (SEM) and Brunauer-Emmett-Teller technique (BET). The obtained MgO exhibited a value of the surface area of 157 m2/g and showed a narrow pore size distribution centered at 4.3 nm. The phenomena and gas evolved during calcinations have been investigated by thermogravimeter-mass spectrometer (TG-MS). During the calcinations, the precursor Mg(OH)2 was converted to MgO with a mass loss of 29% and with the formation of H2O (>60% of the gas evolved). The desorption of CO2 and a small amount of CO and/or N2 which were adsorbed from air on the surface of Mg(OH)2 were also observed. No organic compounds were found which indicated that F127 was completely removed by Soxhlet extraction.

  13. Calcined Solution-Based PVP Influence on ZnO Semiconductor Nanoparticle Properties

    Directory of Open Access Journals (Sweden)

    Halimah Mohamed Kamari

    2017-02-01

    Full Text Available A water-based solution of polyvinylpyrrolidone (PVP at various concentrations and zinc nitrates were used in conjunction with calcination to produce zinc oxide semiconductor nanoparticles. The extent to which the zinc oxide semiconductor nanoparticles had become crystallized was measured using X-ray diffraction (XRD, whilst morphological characteristics were determined using scanning electron microscopy (SEM. Transmission electron microscopy (TEM supported by XRD results were used to evaluate the average particle size. Fourier transform infrared spectroscopy (FT-IR was then carried out in order to identify the composition phase, since this suggested that the samples contained metal oxide bands and that all organic compounds had been effectively removed after calcination. A UV-VIS spectrophotometer was used to determine the energy band gap and illustrate optical features. Additionally, photoluminescence (PL spectra revealed that the intensity of photoluminescence decreased with a decrease in particle size. The obtained results have mainly been inclusive for uses by several semiconductor applications in different fields, such as environmental applications and studies, since an absorption process for energy wavelengths could efficiently occur.

  14. Calcination temperature influenced multiferroic properties of Ca-doped BiFeO{sub 3} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Dhir, Gitanjali, E-mail: gitanjali.thaprian@gmail.com; Uniyal, Poonam; Verma, N. K. [Nano Research Lab, School of Physics and Materials Science, Thapar University, Patiala-147004 (India)

    2015-06-24

    The influence of Ca-doping and particle size on structural, morphological and magnetic properties of BiFeO{sub 3} 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.

  15. Easily recycled Bi2O3 photocatalyst coatings prepared via ball milling followed by calcination

    Science.gov (United States)

    Cheng, Lijun; Hu, Xumin; Hao, Liang

    2017-06-01

    Bi2O3 photocatalyst coatings derived from Bi coatings were first prepared by a two-step method, namely ball milling followed by the calcination process. The as-prepared samples were characterized by XRD, SEM, XPS and UV-Vis spectra, respectively. The results showed that monoclinic Bi2O3 coatings were obtained after sintering Bi coatings at 673 or 773 K, while monoclinic and triclinic mixed phase Bi2O3 coatings were obtained at 873 or 973 K. The topographies of the samples were observably different, which varied from flower-like, irregular, polygonal to nanosized particles with the increase in calcination temperature. Photodegradation of malachite green under simulated solar irradiation for 180 min showed that the largest degradation efficiency of 86.2% was achieved over Bi2O3 photocatalyst coatings sintered at 873 K. The Bi2O3 photocatalyst coatings, encapsulated with Al2O3 ball with an average diameter around 1 mm, are quite easily recycled, which provides an alternative visible light-driven photocatalyst suitable for practical water treatment application.

  16. 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.

  17. High Pressure Synthesis versus Calcination – Different Approaches to Crystallization of Zirconium Dioxide

    Directory of Open Access Journals (Sweden)

    Kaszewski Jarosław

    2014-06-01

    Full Text Available Calcination and microwave-assisted hydrothermal processing of precipitated zirconium dioxide are compared. Characterization of synthesized products of these two technologies is presented. The infiuence of thermal treatment up to 1200oC on the structural and spectroscopic properties of the so-obtained zirconium dioxide is examined. It was found that initial crystallization of material inhibits the crystal growth up to the 800oC (by means of XRD and TEM techniques, while the material crystallized from amorphous hydroxide precursor at 400oC, exhibits 26 nm sized crystallites already. It was found using the TG technique that the temperature range 100–200oC during the calcination process is equivalent to a microwave hydrothermal process by means of water content. Mass loss is estimated to be about 18%. Based on X-ray investigations it was found that the initial hydroxide precursor is amorphous, however, its luminescence activity suggests the close range ordering in a material.

  18. Manganese oxide phases and morphologies: A study on calcination temperature and atmospheric dependence.

    Science.gov (United States)

    Augustin, Matthias; Fenske, Daniela; Bardenhagen, Ingo; Westphal, Anne; Knipper, Martin; Plaggenborg, Thorsten; Kolny-Olesiak, Joanna; Parisi, Jürgen

    2015-01-01

    Manganese oxides are one of the most important groups of materials in energy storage science. In order to fully leverage their application potential, precise control of their properties such as particle size, surface area and Mn (x) (+) oxidation state is required. Here, Mn3O4 and Mn5O8 nanoparticles as well as mesoporous α-Mn2O3 particles were synthesized by calcination of Mn(II) glycolate nanoparticles obtained through an economical route based on a polyol synthesis. The preparation of the different manganese oxides via one route facilitates assigning actual structure-property relationships. The oxidation process related to the different MnO x species was observed by in situ X-ray diffraction (XRD) measurements showing time- and temperature-dependent phase transformations occurring during oxidation of the Mn(II) glycolate precursor to α-Mn2O3 via Mn3O4 and Mn5O8 in O2 atmosphere. Detailed structural and morphological investigations using transmission electron microscopy (TEM) and powder XRD revealed the dependence of the lattice constants and particle sizes of the MnO x species on the calcination temperature and the presence of an oxidizing or neutral atmosphere. Furthermore, to demonstrate the application potential of the synthesized MnO x species, we studied their catalytic activity for the oxygen reduction reaction in aprotic media. Linear sweep voltammetry revealed the best performance for the mesoporous α-Mn2O3 species.

  19. Manganese oxide phases and morphologies: A study on calcination temperature and atmospheric dependence

    Directory of Open Access Journals (Sweden)

    Matthias Augustin

    2015-01-01

    Full Text Available Manganese oxides are one of the most important groups of materials in energy storage science. In order to fully leverage their application potential, precise control of their properties such as particle size, surface area and Mnx+ oxidation state is required. Here, Mn3O4 and Mn5O8 nanoparticles as well as mesoporous α-Mn2O3 particles were synthesized by calcination of Mn(II glycolate nanoparticles obtained through an economical route based on a polyol synthesis. The preparation of the different manganese oxides via one route facilitates assigning actual structure–property relationships. The oxidation process related to the different MnOx species was observed by in situ X-ray diffraction (XRD measurements showing time- and temperature-dependent phase transformations occurring during oxidation of the Mn(II glycolate precursor to α-Mn2O3 via Mn3O4 and Mn5O8 in O2 atmosphere. Detailed structural and morphological investigations using transmission electron microscopy (TEM and powder XRD revealed the dependence of the lattice constants and particle sizes of the MnOx species on the calcination temperature and the presence of an oxidizing or neutral atmosphere. Furthermore, to demonstrate the application potential of the synthesized MnOx species, we studied their catalytic activity for the oxygen reduction reaction in aprotic media. Linear sweep voltammetry revealed the best performance for the mesoporous α-Mn2O3 species.

  20. 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.

  1. Cyclic carbonation calcination studies of limestone and dolomite for CO{sub 2} separation from combustion flue gases - article no. 011801

    Energy Technology Data Exchange (ETDEWEB)

    Senthoorselvan, S.; Gleis, S.; Hartmut, S.; Yrjas, P.; Hupa, M. [TUM, Garching (Germany)

    2009-01-15

    Naturally occurring limestone and dolomite samples, originating from different geographical locations, were tested as potential sorbents for carbonation/calcination based CO{sub 2} capture from combustion flue gases. Samples have been studied in a thermogravimetric analyzer under simulated flue gas conditions at three calcination temperatures, viz., 750{sup o}C, 875{sup o}C, and 930{sup o}C for four carbonation calcination reaction (CCR) cycles. The dolomite sample exhibited the highest rate of carbonation than the tested limestones. At the third cycle, its CO{sub 2} capture capacity per kilogram of the sample was nearly equal to that of Gotland, the highest reacting limestone tested. At the fourth cycle it surpassed Gotland, despite the fact that the CaCO{sub 3} content of the Sibbo dolomite was only 2/3 of that of the Gotland. Decay coefficients were calculated by a curve fitting exercise and its value is lowest for the Sibbo dolomite. That means, most probably its capture capacity per kilogram of the sample would remain higher well beyond the fourth cycle. There was a strong correlation between the calcination temperature, the specific surface area of the calcined samples, and the degree of carbonation. It was observed that the higher the calcination temperature, the lower the sorbent reactivity. For a given limestone/dolomite sample, sorbents CO{sub 2} capture capacity depended on the number of CCR cycles and the calcination temperature. According to the equilibrium thermodynamics, the CO{sub 2} partial pressure in the calciner should be lowered to lower the calcination temperature. This can be achieved by additional steam supply into the calciner. Steam could then be condensed in an external condenser to single out the CO{sub 2} stream from the exit gas mixture of the calciner. A calciner design based on this concept is illustrated.

  2. Hazardous Waste

    Science.gov (United States)

    ... you throw these substances away, they become hazardous waste. Some hazardous wastes come from products in our homes. Our garbage can include such hazardous wastes as old batteries, bug spray cans and paint ...

  3. 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

  4. RECENT PROGRESS IN DOE WASTE TANK CLOSURE

    Energy Technology Data Exchange (ETDEWEB)

    Langton, C

    2008-02-01

    The USDOE complex currently has over 330 underground storage tanks that have been used to process and store radioactive waste generated from the production of weapons materials. These tanks contain over 380 million liters of high-level and low-level radioactive waste. The waste consists of radioactively contaminated sludge, supernate, salt cake or calcine. Most of the waste exists at four USDOE locations, the Hanford Site, the Savannah River Site, the Idaho Nuclear Technology and Engineering Center and the West Valley Demonstration Project. A summary of the DOE tank closure activities was first issued in 2001. Since then, regulatory changes have taken place that affect some of the sites and considerable progress has been made in closing tanks. This paper presents an overview of the current regulatory changes and drivers and a summary of the progress in tank closures at the various sites over the intervening six years. A number of areas are addressed including closure strategies, characterization of bulk waste and residual heel material, waste removal technologies for bulk waste, heel residuals and annuli, tank fill materials, closure system modeling and performance assessment programs, lessons learned, and external reviews.

  5. 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)

  6. Preliminary assessment of candidate immobilization technologies for retrieved single-shell tank wastes

    Energy Technology Data Exchange (ETDEWEB)

    Wiemers, K.D.; Mendel, J.E.; Kruger, A.A.; Bunnell, L.R.; Mellinger, G.B.

    1992-01-01

    This report describes the initial work that has been performed to select technologies for immobilization of wastes that may be retrieved from Hanford single-shell tanks (SSTs). Two classes of waste will require immobilization. One is the combined high-level waste/transuranic (HLW/TRU) fraction, the other the low-level waste (LLW) fraction. A number of potential immobilization technologies are identified for each class of waste. Immobilization technologies were initially selected based on a number of considerations, including (1) the waste loading that could likely be achieved within the constraint of producing acceptable waste forms, (2) process flexibility (primarily compatibility with anticipated waste variability), (3) process complexity, and (4) state of development. Immobilization technologies selected for further development include the following: for HLW/TRU waste -- borosilicate glass, lead-iron phosphate glass, glass-calcine composites, glass-ceramics, and cement based forms; for non-denitrated LLW -- grout, laxtex-modified concrete, and polyethylene; and for denitrated LLW -- silicate glass, phosphate glass, and clay calcination or tailored ceramic in various matrices.

  7. Evaluation of defense-waste glass produced by full-scale vitrification equipment

    Energy Technology Data Exchange (ETDEWEB)

    Lukacs, J.M.; Petkus, L.L.; Mellinger, G.B.

    1981-09-01

    Three full-scale vitrification processes at the Pacific Northwest Laboratory produced over 67,000 kg of simulated nuclear-waste glass from March 1979 to August 1980. Samples were analyzed to monitor process operation and evaluate the resulting glass product. These processes are: Spray Calciner/In-Can Melter (SC/ICM); Spray Calciner/Calcine-Fed Ceramic Melter (SC/CFCM); and Liquid-Fed Ceramic Melter (LFCM). Waste components in the process feed varied less than +- 10%. The SC/ICM and SC/CFCM which use separate waste and frit feed systems showed larger glass compositional variation than the LFCM, which processed only premixed feed during this period. The SC/ICM and SC/CFCM product contained significant amounts of acmite crystals, while the LFCM product was largely amorphous. In addition, the lower portion of all SC/ICM-filled canisters contained a zone rich in waste components. A product chemical durability as determined by pH4 and soxhlet leach tests varied considerably. Aside from increased durability under pH4 conditions with decreasing waste content, glass composition, microstructure and melting process did not correlate with glass durability. For all samples analyzed, the weight loss under pH4 conditions ranged from 17.7 to 85.2 wt %. Soxhlet conditions produced weight losses from 1.78 to 3.56 wt %.

  8. 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.

  9. Twofold role of calcined hydrotalcites in the degradation of methyl parathion pesticide

    Directory of Open Access Journals (Sweden)

    Alvaro Sampieri

    2011-02-01

    Full Text Available Methyl parathion (MP is a very toxic organophosphate pesticide used as a non-systematic insecticide and acaricide on many corps. As MP and its by-products are highly toxic, they have to be retained to avoid pollution of rivers and lakes. Highly efficient sorbents are hydrotalcites (HTs (or anionic clays. We have correlated the degradation of an aqueous solution of MP at room temperature, with the basicity of the adsorbing materials. It was found that the metal composition of hydrotalcites determines both the surface electronic properties (basic or acidic and the sorption capacity. Depending on the basic strength, some calcined hydrotalcites can catalyze the transformation of MP to p-nitrophenol (p-NP and retain its by-products. Such a process has the advantage of being able to be carried out at room temperature and at the pH of the pesticide solution.

  10. Twofold role of calcined hydrotalcites in the degradation of methyl parathion pesticide

    Science.gov (United States)

    Fetter, Geolar; Villafuerte-Castrejon, María Elena; Tejeda-Cruz, Adriana; Bosch, Pedro

    2011-01-01

    Summary Methyl parathion (MP) is a very toxic organophosphate pesticide used as a non-systematic insecticide and acaricide on many corps. As MP and its by-products are highly toxic, they have to be retained to avoid pollution of rivers and lakes. Highly efficient sorbents are hydrotalcites (HTs) (or anionic clays). We have correlated the degradation of an aqueous solution of MP at room temperature, with the basicity of the adsorbing materials. It was found that the metal composition of hydrotalcites determines both the surface electronic properties (basic or acidic) and the sorption capacity. Depending on the basic strength, some calcined hydrotalcites can catalyze the transformation of MP to p-nitrophenol (p-NP) and retain its by-products. Such a process has the advantage of being able to be carried out at room temperature and at the pH of the pesticide solution. PMID:21977419

  11. Positron annihilation lifetime spectroscopy (PALS) study of the as prepared and calcined MFI zeolites

    Science.gov (United States)

    Bosnar, Sanja; Vrankić, Martina; Bosnar, Damir; Ren, Nan; Šarić, Ankica

    2017-11-01

    The synthesis of high silica zeolites in many cases implies the usage of organic structural direction agents (SDA). However, to manifest their functionalities, the SDA occluded inside the channels of the as-synthesized structure should be removed, usually by a high temperature treatment (calcination). In this paper, the positron annihilation lifetime spectroscopy (PALS) was used to monitor the development of accessible spaces, their sizes and distributions in MFI zeolites, ZSM-5 and silicalite-1 in order to give an additional insight in the process of the SDA removal. For that purpose, a conventional PALS setup with 22Na positron source was applied. It was established that there is a pronounced difference between positron annihilation data for these two zeolites of the same structural type. The samples were additionally analysed by X-ray powder diffraction at room temperature with a crystal structure refinement and thermogravimetry.

  12. Assessment of natural and calcined starfish for the amelioration of acidic soil.

    Science.gov (United States)

    Moon, Deok Hyun; Yang, Jae E; Cheong, Kyung Hoon; Koutsospyros, Agamemnon; Park, Jeong-Hun; Lim, Kyoung Jae; Kim, Sung Chul; Kim, Rog-Young; Ok, Yong Sik

    2014-01-01

    Quality improvement of acidic soil (with an initial pH of approximately 4.5) with respect to soil pH, exchangeable cations, organic matter content, and maize growth was attempted using natural (NSF) and calcined starfish (CSF). Acidic soil was amended with NSF and CSF in the range of 1 to 10 wt.% to improve soil pH, organic matter content, and exchangeable cations. Following the treatment, the soil pH was monitored for periods up to 3 months. The exchangeable cations were measured after 1 month of curing. After a curing period of 1 month, the maize growth experiment was performed with selected treated samples to evaluate the effectiveness of the treatment. The results show that 1 wt.% of NSF and CSF (700 and 900 °C) were required to increase the soil pH to a value higher than 7. In the case of CSF (900 °C), 1 wt.% was sufficient to increase the soil pH value to 9 due to the strong alkalinity in the treatment. No significant changes in soil pHs were observed after 7 days of curing and up to 3 months of curing. Upon treatment, the cation exchange capacity values significantly increased as compared to the untreated samples. The organic content of the samples increased upon NSF treatment, but it remains virtually unchanged upon CSF treatment. Maize growth was greater in the treated samples rather than the untreated samples, except for the samples treated with 1 and 3 wt.% CSF (900 °C), where maize growth was limited due to strong alkalinity. This indicates that the amelioration of acidic soil using natural and calcined starfish is beneficial for plant growth as long as the application rate does not produce alkaline conditions outside the optimal pH range for maize growth.

  13. Spent Fuel and Waste Management Technology Development Program. Annual progress report

    Energy Technology Data Exchange (ETDEWEB)

    Bryant, J.W.

    1994-01-01

    This report provides information on the progress of activities during fiscal year 1993 in the Spent Fuel and Waste Management Technology Development Program (SF&WMTDP) at the Idaho Chemical Processing Plant (ICPP). As a new program, efforts are just getting underway toward addressing major issues related to the fuel and waste stored at the ICPP. The SF&WMTDP has the following principal objectives: Investigate direct dispositioning of spent fuel, striving for one acceptable waste form; determine the best treatment process(es) for liquid and calcine wastes to minimize the volume of high level radioactive waste (HLW) and low level waste (LLW); demonstrate the integrated operability and maintainability of selected treatment and immobilization processes; and assure that implementation of the selected waste treatment process is environmentally acceptable, ensures public and worker safety, and is economically feasible.

  14. Cementitious waste option scoping study report

    Energy Technology Data Exchange (ETDEWEB)

    Lee, A.E.; Taylor, D.D.

    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) on the Idaho National Engineering and Environmental Laboratory (INEEL) will be treated so that it is ready to be moved out of Idaho for disposal by a target date of 2035. This study investigates the nonseparations Cementitious Waste Option (CWO) as a means to achieve this goal. Under this option all liquid sodium-bearing waste (SBW) and existing HLW calcine would be recalcined with sucrose, grouted, canisterized, and interim stored as a mixed-HLW for eventual preparation and shipment off-Site for disposal. The CWO waste would be transported to a Greater Confinement Disposal Facility (GCDF) located in the southwestern desert of the US on the Nevada Test Site (NTS). All transport preparation, shipment, and disposal facility activities are beyond the scope of this study. CWO waste processing, packaging, and interim storage would occur over a 5-year period between 2013 and 2017. Waste transport and disposal would occur during the same time period.

  15. 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.

  16. 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: CI - Industrial Chemistry, Chemical Engineering Impact factor: 1.232, year: 2016

  17. 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)

  18. 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.

  19. 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...

  20. Effect of calcination environments and plasma treatment on structural, optical and electrical properties of FTO transparent thin films

    Science.gov (United States)

    Kafle, Madhav; Kapadi, Ramesh K.; Joshi, Leela Pradhan; Rajbhandari, Armila; Subedi, Deepak P.; Gyawali, Gobinda; Lee, Soo W.; Adhikari, Rajendra; Kafle, Bhim P.

    2017-07-01

    The dependence of the structural, optical and electrical properties of the FTO thin films on the film thickness (276 nm - 546 nm), calcination environment, and low temperature plasma treatment were examined. The FTO thin films, prepared by spray pyrolysis, were calcinated under air followed by either further heat treatment under N2 gas or treatment in low temperature atmospheric plasma. The samples before and after calcination under N2, and plasma treatment will be represented by Sair, SN2 and SPl, respectively, hereafter. The thin films were characterized by measuring the XRD spectra, SEM images, optical transmittance and reflectance, and sheet resistance of the films before and after calcination in N2 environment or plasma treatment. The presence of sharp and narrow multiple peaks in XRD spectra hint us that the films were highly crystalline (polycrystalline). The samples Sair with the thickness of 471 nm showed as high as 92 % transmittance in the visible range. Moreover, from the tauc plot, the optical bandgap Eg values of the Sair found to be noticeably lower than that of the samples SN2. Very surprisingly, the electrical sheet resistance (Rsh) found to decrease following the trend as Rshair > RshN2 > RshPl. The samples exposed to plasma found to possess the lowest RshPl (for film with thickness 546 nm, the RshPl was 17 Ω /sq.).

  1. Separation technologies for the treatment of Idaho National Engineering Laboratory wastes

    Energy Technology Data Exchange (ETDEWEB)

    Todd, T.A. [Idaho National Engineering Lab., Idaho Falls, ID (United States)

    1997-10-01

    Currently about 6.8 million L of acidic, radioactive liquid waste that is not amenable to calcination, and about 3800 m{sup 3} of calcine exist at the ICPP. Legal drivers (court orders) and agreements between the state of Idaho, the U.S. Navy, and DOE exist that obligate INEL to develop, demonstrate, and implement technologies for treatment and interim storage of the radioactive liquid and calcine wastes. Per these agreements, all tank waste must be removed from the underground liquid storage tanks by the year 2012, and high-level radioactive waste must be treated and removed from INEL by 2035. Separation of the radionuclides from the wastes, followed by immobilization of the high-activity and low-activity fractions in glass and grout, respectively, is the approach preferred by INEL. Technologies to remove actinides (U, Np, Pu, and Am), Cs, Sr, and possibly Tc from highly acidic solutions are required to process INEL wastes. Decontamination of the wastes to NRC Class A low-level waste (LLW) is planned. Separation and isolation of Resource Conservation and Recovery Act (RCRA) metals (Hg, Pb, Cd, and Cr) from the highly radioactive waste streams may also be required. Remediation efforts will begin in FY 1997 to remove volatile organic compounds (VOCs) and radionuclides (Cs and Sr) from groundwater located at the Test Area North facility at INEL. A plume of VOCs and radionuclides has spread from the former TSF-05 injection well, and a Comprehensive Environmental Response, Conservation, and Liability Act (CERCLA) remediation action is under way. A Record of Decision was signed in August 1995 that commits INEL to remediate the plume from TSF-05. Removal of Sr and Cs from the groundwater using commercially available ion-exchange resins has been unsuccessful at meeting maximum contaminant levels, which are 119 pCi/L and 8 pCi/L for Cs and Sr, respectively. Cesium and Sr are the major contaminants that must be removed from the groundwater.

  2. Effect of RhOx/CeO2 Calcination on Metal-Support Interaction and Catalytic Activity for N2O Decomposition

    Directory of Open Access Journals (Sweden)

    Verónica Rico-Pérez

    2014-09-01

    Full Text Available The effect of the calcination conditions on the catalytic activity for N2O decomposition of 2.5% RhOx/CeO2 catalysts has been investigated. Ramp and flash calcinations have been studied (starting calcinations at 25 or 250/350 °C, respectively both for cerium nitrate and ceria-impregnated rhodium nitrate decomposition. The cerium nitrate calcination ramp has neither an effect on the physico-chemical properties of ceria, observed by XRD, Raman spectroscopy and N2 adsorption, nor an effect on the catalysts performance for N2O decomposition. On the contrary, flash calcination of rhodium nitrate improved the catalytic activity for N2O decomposition. This is attributed to the smaller size of RhOx nanoparticles obtained (smaller than 1 nm which allow a higher rhodium oxide-ceria interface, favoring the reducibility of the ceria surface and stabilizing the RhOx species under reaction conditions.

  3. Waste management

    DEFF Research Database (Denmark)

    Bruun Hansen, Karsten; Jamison, Andrew

    2000-01-01

    The case study deals with public accountability issues connected to household waste management in the municipality of Copenhagen, Denmark.......The case study deals with public accountability issues connected to household waste management in the municipality of Copenhagen, Denmark....

  4. Food waste

    OpenAIRE

    Arazim, Lukáš

    2015-01-01

    This thesis looks into issues related to food waste and consists of a theoretical and a practical part. Theoretical part aims to provide clear and complex definition of wood waste related problems, summarize current findings in Czech and foreign sources. Introduction chapter explains important terms and legal measures related to this topic. It is followed by description of causes, implications and possibilities in food waste reduction. Main goal of practical part is analyzing food waste in Cz...

  5. Automotive Wastes.

    Science.gov (United States)

    Guigard, Selma E; Shariaty, Pooya; Niknaddaf, Saeid; Lashaki, Masoud Jahandar; Atkinson, John D; Hashisho, Zaher

    2015-10-01

    A review of the literature from 2014 related to automotive wastes is presented. Topics include solid wastes from autobodies and tires as well as vehicle emissions to soil and air as a result of the use of conventional and alternative fuels. Potential toxicological and health risks related to automotive wastes are also discussed.

  6. Radioactive Waste.

    Science.gov (United States)

    Blaylock, B. G.

    1978-01-01

    Presents a literature review of radioactive waste disposal, covering publications of 1976-77. Some of the studies included are: (1) high-level and long-lived wastes, and (2) release and burial of low-level wastes. A list of 42 references is also presented. (HM)

  7. 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.

  8. [Based on Curing Age of Calcined Coal Gangue Fine Aggregate Mortar of X-Ray Diffraction and Scanning Electron Microscopy Analysis].

    Science.gov (United States)

    Dong, Zuo-chao; Xia, Jun-wu; Duan, Xiao-mu; Cao, Ji-chang

    2016-03-01

    By using X-ray diffraction (XRD) and environmental scanning electron microscope (SEM) analysis method, we stud- ied the activity of coal gangue fine aggregate under different calcination temperature. In view of the activity of the highest-700 degrees C high temperature calcined coal gangue fine aggregate mortar of hydration products, microstructure and strength were discussed in this paper, and the change laws of mortar strength with curing age (3, 7, 14, 28, 60 and 90 d) growth were analyzed. Test results showed that coal gangue fine aggregate with the increase of calcination temperature, the active gradually increases. When the calcination temperature reaches 700 degrees C, the activity of coal gangue fine aggregate is the highest. When calcining temperature continues to rise, activity falls. After 700 degrees C high temperature calcined coal gangue fine aggregate has obvious ash activity, the active components of SiO2 and Al2 O3 can be with cement hydration products in a certain degree of secondary hydration reaction. Through on the top of the activity of different curing age 700 degrees C high temperature calcined coal gangue fine aggregate mortar, XRD and SEM analysis showed that with the increase of curing age, secondary hydration reaction will be more fully, and the amount of hydration products also gradually increases. Compared with the early ages of the cement mortar, the products are more stable hydration products filling in mortar microscopic pore, which can further improve the microstructure of mortar, strengthen the interface performance of the mortar. The mortar internal structure is more uniform, calcined coal gangue fine aggregate and cement mortar are more of a strong continuous whole, which increase the later strength of hardened cement mortar, 700 degrees C high temperature calcined coal gangue fine aggregate pozzolanic effect is obvious.

  9. The effect of calcination on reactive milling of anthracite as potential precursor for graphite production

    Energy Technology Data Exchange (ETDEWEB)

    Burgess-Clifford, Caroline E.; Van Essendelft, Dirk T. [The EMS Energy Institute, C211 Coal Utilization Laboratory, Penn State University, University Park, PA 16802 (United States); Narayanan, Deepa L. [Puget Sound Energy, 10885 NE 4th PSE-09S, Bellevue, WA 98004 (United States); Jain, Puja; Lueking, Angela D. [Department of Energy and Mineral Engineering, Pennsylvania State University, 120 Hosler, University Park, PA 16802 (United States); Sakti, Apurba [School of Earth Atmospheric and Environmental Sciences, University of Manchester, Manchester (United Kingdom)

    2009-12-15

    The effect of a pretreatment using reactive ball milling and calcination on the graphitizability of an anthracite coal is explored. A thermal anneal of Buck Mountain anthracite at 1400 C in argon increased the L{sub c} crystallite dimension (from 12 to 20 A) and led to an increase in the oxidation temperature of the product. Ball milling of the coal reduced particle size with a nominal effect on carbon order and the degree of graphitization after the 1400 C thermal anneal (L{sub c} from 18 to 29 A). Ball milling in cyclohexene led to a substantial increase in the graphitizability at 1400 C (L{sub c} from 12 to 50 A). The enhanced reactivity was due to both carbon structure and introduced metal. The products of the mechano-chemical pretreatment and thermal anneal consisted of nanographene ribbons and multi-walled nanopolyhedral particles. It oxidized at moderate temperatures and had a high (74.3%) degree of graphitization based on X-ray diffraction analysis; the derived material has potential as filler for production of graphite. (author)

  10. 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.

  11. Enhancement of biohydrogen production from brewers' spent grain by calcined-red mud pretreatment.

    Science.gov (United States)

    Zhang, Jishi; Zang, Lihua

    2016-06-01

    This paper investigated the utilization of calcined-red mud (CRM) pretreatment to enhance fermentative hydrogen yields from brewers' spent grain (BSG). The BSG samples were treated with different concentrations (0.0-20g/L) of CRM at 55°C for 48h, before the biohydrogen process with heat-treated anaerobic sludge inoculum. The highest specific hydrogen production of 198.62ml/g-VS was obtained from the BSG treated with 10g/L CRM, with the corresponding lag time of 10.60h. Hydrogen yield increments increased by 67.74%, compared to the control tests without CRM. The results demonstrated that the CRM could hydrolyze more cellulose and further provided adequate broth and suitable pH value for efficient fermentative hydrogen. The model-based analysis showed that the modified Gompertz model presented a better fit for the experimental data than the first-order model. Copyright © 2016 Elsevier Ltd. All rights reserved.

  12. Advanced mineral calciner for regeneration of lime. Final report, March 1995--May 1997

    Energy Technology Data Exchange (ETDEWEB)

    Namazian, M.; Nickeson, R.; Lovas, B.; Miller, G.; Kelly, J.

    1997-12-31

    There are approximately 800 pulp, paper and paperboard mills in the United States. Pulp and paper is the ninth largest industry in US, uses 2.8 quads of energy per year and ranks third among all domestic US industries in the cost of energy consumed. A significant fraction of the energy consumed in pulp and paper plants is needed to recover chemicals that are used in breaking down the wood chips into pulp. In particular, 0.1 quads of energy per year are used to regenerate lime. Furthermore, pulp and paper plant operations generate 9,870 tons of NOx per year. Additionally over two million tons of spent lime are sent to landfills each year. In addition, growth in paper demand and changes in plant processes (e.g., bleaching), as a result of environmental pressures, will continue to drive the need for more lime regeneration capacity. Unless the increased capacity can be delivered productively and inexpensively, the growth in pulp and paper may occur in overseas markets. Furthermore, if new environmental constraints cannot be met at low cost, existing US pulp and paper production capacity may also move off-shore. The advanced mineral calciner (AMC) technology was developed to address this lime regeneration need. Prior to describing the technology, and the program of work that was used to test the concept, conventional lime regeneration systems and their limitations are described.

  13. CO{sub 2} capture with calcined dolomite: the effect of sorbent particle size

    Energy Technology Data Exchange (ETDEWEB)

    Stendardo, Stefano [Italian National Agency for New Technologies, Energy and Sustainable Economic Development, Rome (Italy); Di Felice, Luca; Gallucci, Katia; Foscolo, Pier Ugo [University of L' Aquila, L' Aquila (Italy)

    2011-09-15

    This investigation is set in the more comprehensive study of an innovative fluidized bed reformer configuration for producing hydrogen from either biomass/coal syngas or natural gas, in which capture of carbon dioxide by-product occurs in parallel with steam reforming and water-gas shift reactions. Reported here are experimental data of carbon dioxide absorption by particles of calcined dolomite included in a bed of otherwise inert material; the bed, initially fluidized by nitrogen, was subjected to a step concentration input of carbon dioxide and the sorption kinetics was obtained from the outlet response of the entire system. The influence of dolomite particle size was investigated - from 98 to 1,550 {mu}m - and a previously developed grain model was used to relate the observed effect of particle diameter to the complex mechanism of carbon dioxide capture in a solid sorbent. The results show that pore shrinking effects during the carbon dioxide capture process become increasingly more significant as the particle size is increased. (orig.)

  14. Linking the Physicochemical Properties of Calcined Titania Nanoparticles with Their Biocidal Activity

    Directory of Open Access Journals (Sweden)

    Changseok Han

    2016-12-01

    Full Text Available Titanium dioxide nanoparticles (nTiO2 show biocidal activity when exposed to UV illumination. Modification of their physical properties can expand their photoresponse region toward visible light. In this study, such modification was made through a sol-gel synthesis followed by calcination at a range of temperatures (250–900 °C, generating a series of nTiO2 particles with different crystal phases, sizes, porosities, zeta potentials, and BET surface areas. The unique properties of nTiO2 were linked to their toxicity to the marine bacterium, Vibrio fischeri. A modified “Flash” high-through put assay was used to test the viability of these marine organisms after short term (15–60 min exposure under visible light only to the individual groups of nTiO2 (500–2000 μg/mL. Linear regression analysis indicated that across all concentrations and time points, high biocidal activity correlated with the amorphous and anatase crystal phases, high BET surface area, high pore volume and small crystal size. The linkage between physicochemistry and nanotoxicity would be helpful for future design of more efficient and sustainable nTiO2.

  15. Electron transfer behavior and water photodecomposition ability of calcined material from a cerium-S-phenylene-O-holmium-O-phenylene-S hybrid copolymer.

    Science.gov (United States)

    Matsui, Hideo; Otsuki, Keigo; Yamada, Hiroyoshi; Kawahara, Tetsuro; Yoshihara, Masakuni

    2006-05-15

    Calcination of a cerium-S-phenylene-O-holmium-O-phenylene-S hybrid copolymer under a vacuum gave cerium oxide-carbon cluster-holmium oxide composite material. The material calcined at 600 degrees C loaded with Pt particles could decompose water to H2 and O2 with a H2/O2 ratio of 2 under visible light irradiation. ESR spectral examinations of the calcined materials revealed the possibility of a two-step electron transfer in the process of CeO2 --> carbon cluster --> Ho2O3 --> Pt with an oxidation site at CeO2 particles and a reduction site at Pt particles.

  16. Agricultural Waste.

    Science.gov (United States)

    Xue, Ling; Zhang, Panpan; Shu, Huajie; Chang, Chein-Chi; Wang, Renqing; Zhang, Shuping

    2016-10-01

    In recent years, the quantity of agricultural waste has been rising rapidly all over the world. As a result, the environmental problems and negative impacts of agricultural waste are drawn more and more attention. Therefore, there is a need to adopt proper approaches to reduce and reuse agricultural waste. This review presented about 200 literatures published in 2015 relating to the topic of agricultural waste. The review examined research on agricultural waste in 2015 from the following four aspects: the characterization, reuse, treatment, and management. Researchers highlighted the importance to reuse agricultural waste and investigated the potential to utilize it as biofertilizers, cultivation material, soil amendments, adsorbent, material, energy recycling, enzyme and catalyst etc. The treatment of agricultural waste included carbonization, biodegradation, composting hydrolysis and pyrolysis. Moreover, this review analyzed the differences of the research progress in 2015 from 2014. It may help to reveal the new findings and new trends in this field in 2015 comparing to 2014.

  17. Solution combustion synthesis: Effect of calcination and sintering temperature on structural, dielectric and ferroelectric properties of five layer Aurivillius oxides

    Science.gov (United States)

    Dubey, Shivangi; Subohi, Oroosa; Kurchania, Rajnish

    2017-09-01

    The effect of calcination temperature on phase formation and sintering temperature on structural, dielectric, electrical and ferroelectric properties of Ba2Bi4Ti5O18 (BBT), Pb2Bi4Ti5O18 (PBT) and Sr2Bi4Ti5O18 (SBT) ceramics prepared by solution combustion route using glycine as a fuel are investigated in this paper. Calcination temperature was optimized at 650 °C for BBT and 750 °C for SBT and PBT, at which these compounds showed pure phase formation. It was observed that density and grain size of the sintered pellets increases with increasing sintering temperature. The dielectric constant was found to be dependent on grain size and density. Transition temperature, activation energy and remnant polarization were found to increase with an increase in sintering temperature. Porosity and conductivity decreases with an increase in the sintering temperature. Thus improving the dielectric, electrical and ferroelectric properties of five layered Aurivillius oxides.

  18. 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.

  19. 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.

  20. Influence of calcinated starfish powder on growth, yield, spawn run and primordial germination of king oyster mushroom (Pleurotus eryngii).

    Science.gov (United States)

    Choi, Ung-Kyu; Bajpai, Vivek K; Lee, Nan-Hee

    2009-11-01

    This study was undertaken to assess the calcium absorption efficacy of Pleurotus eryngii (king oyster mushroom) in sawdust medium supplemented with starfish powder and to determine the effect of starfish powder as calcium supplement on growth, yield, spawn run and primordial germination of P. eryngii. Optimum calcination of starfish powder was achieved at the temperature ranging from 560.1 to 649.5 degrees C. A 1% supplementation of starfish powder in sawdust medium did not suppress the growth of P. eryngii. Also the supplementation of 1% calcinated starfish powder to sawdust medium potentially increased the calcium content up to a level of 256.0+/-16.3 in the fruiting body of P. eryngii without extension of spawn run period and the retardation of the days to primordial germination.

  1. Effects of calcination temperature on microstructures and photocatalytic activity of titanate nanotube films prepared by an EPD method.

    Science.gov (United States)

    Yu, Jiaguo; Zhou, Minghua

    2008-01-30

    Titanate nanotube films are fabricated on F-doped SnO(2)-coated glass substrates via an electrophoretic deposition method using hydrothermally prepared titanate nanotubes as precursors. The effects of calcination temperature on the microstructures and photoactivity of as-prepared titanate nanotube films are investigated and discussed. The results indicate that the intercalated sodium ions (Na(+)) in the as-prepared titanate nanotubes are easily removed during the electrophoretic deposition. The phase transformation of titanate to anatase and diffusion of Na(+) ions from glass substrates into films occur at 400 °C. With increasing calcination temperature, the crystallization of anatase enhances and sodium content in the films increases. At 500 °C, the tubular structure still holds and the films show the highest photocatalytic activity probably due to their good crystallization, large specific surface areas and tubular structures.

  2. 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.

  3. Consolidated waste forms: glass marbles and ceramic pellets

    Energy Technology Data Exchange (ETDEWEB)

    Treat, R.L.; Rusin, J.M.

    1982-05-01

    Glass marbles and ceramic pellets have been developed at Pacific Northwest Laboratory as part of the multibarrier concept for immobilizing high-level radioactive waste. These consolidated waste forms served as substrates for the application of various inert coatings and as ideal-sized particles for encapsulation in protective matrices. Marble and pellet formulations were based on existing defense wastes at Savannah River Plant and proposed commercial wastes. To produce marbles, glass is poured from a melter in a continuous stream into a marble-making device. Marbles were produced at PNL on a vibratory marble machine at rates as high as 60 kg/h. Other marble-making concepts were also investigated. The marble process, including a lead-encapsulation step, was judged as one of the more feasible processes for immobilizing high-level wastes. To produce ceramic pellets, a series of processing steps are required, which include: spray calcining - to dry liquid wastes to a powder; disc pelletizing - to convert waste powders to spherical pellets; sintering - to densify pellets and cause desired crystal formation. These processing steps are quite complex, and thereby render the ceramic pellet process as one of the least feasible processes for immobilizing high-level wastes.

  4. Method for solidification of radioactive and other hazardous waste

    Science.gov (United States)

    Anshits, Alexander G.; Vereshchagina, Tatiana A.; Voskresenskaya, Elena N.; Kostin, Eduard M.; Pavlov, Vyacheslav F.; Revenko, Yurii A.; Tretyakov, Alexander A.; Sharonova, Olga M.; Aloy, Albert S.; Sapozhnikova, Natalia V.; Knecht, Dieter A.; Tranter, Troy J.; Macheret, Yevgeny

    2002-01-01

    Solidification of liquid radioactive waste, and other hazardous wastes, is accomplished by the method of the invention by incorporating the waste into a porous glass crystalline molded block. The porous block is first loaded with the liquid waste and then dehydrated and exposed to thermal treatment at 50-1,000.degree. C. The porous glass crystalline molded block consists of glass crystalline hollow microspheres separated from fly ash (cenospheres), resulting from incineration of fossil plant coals. In a preferred embodiment, the porous glass crystalline blocks are formed from perforated cenospheres of grain size -400+50, wherein the selected cenospheres are consolidated into the porous molded block with a binder, such as liquid silicate glass. The porous blocks are then subjected to repeated cycles of saturating with liquid waste, and drying, and after the last cycle the blocks are subjected to calcination to transform the dried salts to more stable oxides. Radioactive liquid waste can be further stabilized in the porous blocks by coating the internal surface of the block with metal oxides prior to adding the liquid waste, and by coating the outside of the block with a low-melting glass or a ceramic after the waste is loaded into the block.

  5. 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.

  6. Enhanced remediation of Cr(VI)-contaminated soil by incorporating a calcined-hydrotalcite-based permeable reactive barrier with electrokinetics.

    Science.gov (United States)

    Zhang, Jia; Xu, Yunfeng; Li, Wentao; Zhou, Jizhi; Zhao, Jun; Qian, Guangren; Xu, Zhi Ping

    2012-11-15

    This paper describes the enhanced Cr(VI)-contaminated soil remediation via a combination of electrokinetics (EK) with a calcined-hydrotalcite-based permeable reactive barrier (PRB). First, this combination proved to be feasible, and remarkably facilitated Cr(VI) remediation in a column test. Then, lightly-to-severely (0.16-1.65 mg/g) Cr(VI)-contaminated soil was remediated in a simulated test with the calcined hydrotalcite as the PRB under an voltage of 10-30 V (i.e. an electric field intensity of 0.7-2.0 V/cm). The observations demonstrated that both PRB and EK are critical to efficient remediation and the high de-contamination efficiency is supposedly attributed to the synergistic effect, for which EK concentrates anionic chromate to the anode region and PRB media (calcined hydrotalcite) absorbs and immobilizes it. Thus we have shown that the combined PRB-EK system is highly adaptive and effective in remediation of a larger area contaminated with chromate and various anionic pollutants. Copyright © 2012 Elsevier B.V. All rights reserved.

  7. 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.

  8. 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.

  9. Kinetics and equilibrium studies for the adsorption of Acid Red 57 from aqueous solutions onto calcined-alunite.

    Science.gov (United States)

    Tunali, Sibel; Ozcan, A Safa; Ozcan, Adnan; Gedikbey, Tevfik

    2006-07-31

    The adsorption of Acid Red 57 (AR57) onto calcined-alunite was examined in aqueous solution in a batch system with respect to contact time, pH and temperature. The first-order, pseudo-second-order kinetic and the intraparticle diffusion models were used to describe the kinetic data and the rate constants were evaluated. The experimental data fitted very well the pseudo-second-order kinetic model and also followed the intraparticle diffusion model up to 90 min. The Langmuir and Freundlich adsorption models were applied to describe the equilibrium isotherms and the isotherm constants were also determined. The equilibrium data are successfully fitted to the Langmuir adsorption isotherm. The Langmuir isotherm constant, K(L), was used to evaluate the changes of free energy, enthalpy and entropy of adsorption for the adsorption of AR57 onto calcined-alunite. The results indicate that calcined-alunite could be employed as low-cost material for the removal of acid dyes from textile effluents.

  10. Effects of Calcination Temperature on Preparation of Boron-Doped TiO2 by Sol-Gel Method

    Directory of Open Access Journals (Sweden)

    Wenjie Zhang

    2012-01-01

    Full Text Available Boron-doped TiO2 photocatalyst was prepared by a modified sol-gel method. Being calcinated at temperatures from 300°C to 600°C, all the 3% B-TiO2 samples presented anatase TiO2 phase, and TiO2 crystallite sizes were calculated to be 7.6, 10.3, 13.6, and 27.3 nm, respectively. The samples were composed of irregular particles with rough surfaces in the size range within 3 μm. Ti atoms were in an octahedron skeleton and existed mainly in the form of Ti4+, while the Ti-O-B structure was the main boron existing form in the 3% B-TiO2 sample. When calcination temperature increased from 300°C to 600°C, specific surface area decreased sharply from 205.6 m2/g to 31.8 m2/g. The average pore diameter was 10.53 nm with accumulative pore volume of 0.244 mL/g for the 3% B-TiO2 sample calcinated at 400°C, which performed optimal photocatalytic degradation activity. After 90 min of UV-light irradiation, degradation rate of methyl orange was 96.7% on the optimized photocatalyst.

  11. 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.

  12. Effect of calcination temperature on the structure and catalytic performance of 80Ni20CO/SiO2 catalyst for CO2 methanation

    Science.gov (United States)

    Md Ali, S. A.; Hamid, K. H. K.; Ismail, K. N.

    2017-09-01

    The 80Ni20Co/SiO2 catalysts prepared using co-precipitate and incipient wetness impregnation method were used for production of methane through CO2 methanation reaction between CO and H2 gases. The effect of a range of calcination temperature on the structure and catalytic performance of 80Ni20Co/SiO2 catalyst was investigated using microactivity fixed bed reactor. It was found that the catalyst calcined at 400°C for 4.5 h under air atmosphere has shown the best catalytic performance for CO2 methanation. Characterization of 80Ni20Co/SiO2 catalyst calcined fresh samples was carried out using TPR-H2 analysis, Brunauere Emmette Teller (BET) measurements and X-ray diffraction (XRD. It was observed that calcination temperature influenced the structure, morphology and catalytic performance of the catalysts.

  13. Biocompatibility of calcined mesoporous silica particles with ventricular myocyte structure and function.

    Science.gov (United States)

    Aburawi, Elhadi H; Qureshi, Mohammed Anwar; Oz, Deniz; Jayaprakash, Petrilla; Tariq, Saeed; Hameed, Rashed S; Das, Sayantani; Goswami, Anandarup; Biradar, Ankush V; Asefa, Tewodros; Souid, Abdul-Kader; Adeghate, Ernest; Howarth, Frank Christopher

    2013-01-18

    In vivo and in vitro systems were employed to investigate the biocompatibility of two forms of calcined mesoporous silica microparticles, MCM41-cal and SBA15-cal, with ventricular myocytes. These particles have potential clinical use in delivering bioactive compounds to the heart. Ventricular myocytes were isolated from 6 to 8 week male Wistar rats. The distribution of the particles in ventricular myocytes was investigated by transmission electron microscopy and scanning electron microscopy. The distribution of particles was also examined in cardiac muscle 10 min after intravenous injection of 2.0 mg/mL MCM41-cal. Myocyte shortening and the Ca(2+) transient were determined following exposure to 200 μg/mL MCM41-cal or SBA15-cal for 10 min. Within 10 min of incubation at 25 °C, both MCM41-cal and SBA15-cal were found attached to the plasma membrane, and some particles were observed inside ventricular myocytes. MCM41-cal was more abundant inside the myocytes than SBA15-cal. The particles had a notable affinity to mitochondrial membranes, where they eventually settled. Within 10 min of intravenous injection (2.0 mg/mL), MCM41-cal traversed the perivascular space, and some particles entered ventricular myocytes and localized around the mitochondrial membranes. The amplitude of shortening was slightly reduced in myocytes superperfused with MCM41-cal or SBA15-cal. The amplitude of the Ca(2+) transient was significantly reduced in myocytes superperfused with MCM41-cal but was only slightly reduced with SBA15-cal. Overall, the results show reasonable bioavailability and biocompatibility of MCM41-cal and SBA15-cal with ventricular myocytes.

  14. Synthesis and crystal structure of As-synthesized and calcined pure silica zeolite ITQ-12.

    Science.gov (United States)

    Yang, Xiaobo; Camblor, Miguel A; Lee, Yongjae; Liu, Haiming; Olson, David H

    2004-08-25

    The small-pore pure silica zeolite ITQ-12 has been synthesized with fumed silica as the silica source in the presence of 1,3,4-trimethylimidazolium hydroxide and hydrofluoric acid under hydrothermal conditions at 448 K. Rietveld refinement using synchrotron X-ray diffraction data of the calcined ITQ-12 product taken at 298 K confirms the proposed topology, framework type code ITW, which can be described by a monoclinic unit cell [Si(24)O(48)] having Cm symmetry. Unit cell parameters are a = 10.3360(4), b = 15.0177(6), and c = 8.8639(4) A, beta = 105.356(3) degrees, and cell volume V = 1326.76(9) A(3). For as-synthesized ITQ-12, the occluded fluoride anion is located inside the double four-membered ring, while the flat 1,3,4-trimethylimidazolium cation lies on the equatorial plane of the slit-shaped [4(4)5(4)6(4)8(4)] cage, with its longest dimension in the [010] direction. The monoclinic unit cell |(C(6)N(2)H(11))(+)(2)F(-)(2)|[Si(24)O(48)], having Cm symmetry, has parameters a = 10.4478(3), b = 14.9854(4), and c = 8.8366(3) A, beta = 105.935(2) degrees, and cell volume V = 1330.34(7) A(3) at 298 K. Cooperative structure-directing effects during the crystallization of ITQ-12 are discussed in terms of the structure of the as-made material.

  15. Feasibility Study for Vitrification of Sodium-Bearing Waste

    Energy Technology Data Exchange (ETDEWEB)

    J. J. Quigley; B. D. Raivo; S. O. Bates; S. M. Berry; D. N. Nishioka; P. J. Bunnell

    2000-09-01

    Treatment of sodium-bearing waste (SBW) at the Idaho Nuclear Technology and Engineering Center (INTEC) within the Idaho National Engineering and Environmental Laboratory is mandated under a Settlement Agreement between the Department of Energy and the State of Idaho. One of the requirements of the Settlement Agreement is the complete calcination (i.e., treatment) of all SBW by December 31, 2012. One of the proposed options for treatment of SBW is vitrification. This study will examine the viability of SBW vitrification. This study describes the process and facilities to treat the SBW, from beginning waste input from INTEC Tank Farm to the final waste forms. Schedules and cost estimates for construction and operation of a Vitrification Facility are included. The study includes a facility layout with drawings, process description and flow diagrams, and preliminary equipment requirements and layouts.

  16. Industrial Waste

    DEFF Research Database (Denmark)

    Christensen, Thomas Højlund

    2011-01-01

    Industrial waste is waste from industrial production and manufacturing. Industry covers many industrial sectors and within each sector large variations are found in terms of which raw materials are used, which production technology is used and which products are produced. Available data on unit...... generation rates and material composition as well as determining factors are discussed in this chapter. Characterizing industrial waste is faced with the problem that often only a part of the waste is handled in the municipal waste system, where information is easily accessible. In addition part...... of the industrial waste may in periods, depending on market opportunities and prices, be traded as secondary rawmaterials. Production-specificwaste from primary production, for example steel slag, is not included in the current presentation. In some countries industries must be approved or licensed and as part...

  17. Waste indicators

    Energy Technology Data Exchange (ETDEWEB)

    Dall, O.; Lassen, C.; Hansen, E. [Cowi A/S, Lyngby (Denmark)

    2003-07-01

    The Waste Indicator Project focuses on methods to evaluate the efficiency of waste management. The project proposes the use of three indicators for resource consumption, primary energy and landfill requirements, based on the life-cycle principles applied in the EDIP Project. Trial runs are made With the indicators on paper, glass packaging and aluminium, and two models are identified for mapping the Danish waste management, of which the least extensive focuses on real and potential savings. (au)

  18. 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...

  19. Sintering and reactivity of CaCO{sub 3}-based sorbents for in situ CO{sub 2} capture in fluidized beds under realistic calcination conditions

    Energy Technology Data Exchange (ETDEWEB)

    Lu, D.Y.; Hughes, R.W.; Anthony, E.J.; Manovic, V. [Natural Resources Canada, Ottawa, ON (Canada)

    2009-06-15

    Sintering during calcination/carbonation may introduce substantial economic penalties for a CO{sub 2} looping cycle using limestone/dolomite-derived sorbents. Cyclic carbonation and calcination reactions were investigated for CO{sub 2} capture under fluidized bed combustion (FBC) conditions. The cyclic carbonation characteristics of CaCO{sub 3}-derived sorbents were compared at various calcination temperatures (700-925{sup o} C) and different gas stream compositions: pure -2 and a realistic calciner environment where high concentrations of CO{sub 2}>80-90% are expected. The conditions during carbonation were 700 {sup o}C and 15% CO{sub 2} in N{sub 2} and 0.18% or 0.50% SO{sub 2} in selected tests. Up to 20 calcination/carbonation cycles were conducted using a thermogravimetric analyzer (TGA) apparatus. Three Canadian limestones were tested: Kelly Rock, Havelock, and Cadomin, using a prescreened particle size range of 400-650 {mu} m. Calcined Kelly Rock and Cadomin samples were hydrated by steam and examined. Sorbent reactivity was reduced whenever SO{sub 2} was introduced to either the calcining or carbonation streams. The multicyclic capture capacity of CaO for CO{sub 2} was substantially reduced at high concentrations of CO{sub 2} during the sorbent regeneration process and carbonation conversion of the Kelly Rock sample obtained after 20 cycles was only 10.5%. Hydrated sorbents performed better for CO{sub 2} capture but showed deterioration following calcination in high CO{sub 2} gas streams indicating that high CO{sub 2} and SO{sub 2} levels in the gas stream lead to lower CaO conversion because of enhanced sintering and irreversible formation of CaSO{sub 4}.

  20. 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.

  1. Vitrification of high-level alumina nuclear waste

    Energy Technology Data Exchange (ETDEWEB)

    Brotzman, J.R.

    1979-01-01

    Borophosphate glass compositions have been developed for the vitrification of a high-alumina calcined defense waste. The effect of substituting SiO/sub 2/, P/sub 2/O/sub 5/ and CuO for B/sub 2/O/sub 3/ on the viscosity and leach resistance was measured. The effect of the alkali to borate ratio and the Li/sub 2/O:Na/sub 2/O ratio on the melt viscosity and leach resistance was also measured.

  2. Catalytic cracking of HDPE wastes to liquid fuel in the presence of siliceous mesoporous molecular sieves

    Science.gov (United States)

    Ramli, Anita; Majid, Noor Diana Abdul; Yusup, Suzana

    2014-10-01

    A siliceous gel was synthesized at 80°C and aged for 5 days at 120°C before it was dried at 120°C for 16 hours and calcined at 500 and 700°C. The calcined Na-Si-MMS samples were then undergone ion exchange with ammonia solution to form NH4- Si - MMS . All samples were characterized for their physicochemical properties using nitrogen (N2) adsorption-desorption isotherm for surface area and porosity; and temperature programme desorption of ammonia (TPD-NH3) for determination of acidity. The catalytic activity of all samples was tested in pyrolysis of high density polyethylene (HDPE) waste at catalyst to HDPE ratio of 0.2. The organic liquid product (OLP) collected was analysed using gas chromatography (GC). Results show that presence of Na-Si-MMS calcined at 500°C promotes the formation of gasoline-like product while presence of Na-Si-MMS calcined at 700°C promotes the formation of both diesel-like and kerosene-like products. On the other hand, presence of all NH4-Si-MMS catalysts promotes the formation of gasoline-like product. These show that the activation process of Si-MMS has a significant effect on the production of fuel-like product from pyrolysis of HDPE.

  3. Minimum Additive Waste Stabilization Using Vitreous Ceramics Interim Progress Report October 1994-September 1995

    Energy Technology Data Exchange (ETDEWEB)

    Feng, X; Hahn, W K; Gong, M [Pacific Northwest Lab., Richland, WA (United States); Gong, W; Wang, L; Ewing, R C [Univ. of New Mexico, Albuquerque, NM (United States). Dept. of Earth and Planetary Sciences

    1995-01-01

    Vitreous ceramic waste forms are being developed at Pacific Northwest Laboratory to complement glass waste forms in implementing the Minimum Additive Waste Stabilization (MAWS) Program to support the US Department of Energy`s environmental restoration efforts. These vitreous ceramics are composed of various metal-oxide crystalline phases embedded in a silicate-glass phase. This work extends the success of vitreous ceramic waste forms to treat wastes with both high metal and high alkali contents. Two successful approaches are discussed: developing high-durability alkali-binding crystals in a durable glassy matrix, and developing water-soluble crystals in a durable and continuous glassy matrix. Nepheline-vitreous ceramics were demonstrated for the immobilization of high-alkali wastes with alkali contents up to 21 wt%. The chemical durability of the nepheline-vitreous ceramics is better than the corresponding glasses, especially in over longer times. Vitreous ceramics with Cs{sub 2}O loading up to 35.4 wt% have been developed. Vitreous ceramic waste forms were developed from 90 and 100% Oak Ridge National Laboratory K-25 pond sludge. Heat treatment resulted in targeted crystal formation of spinels, potassium feldspar, and Ca-P phases. The K-25 pond sludge vitreous ceramics were up to 42 times more durable than high-level environmental assessments (EA) glass. The toxicity characteristics leach procedure (TCLP) concentration of LVC-6 is at least 2,000 times lower than US Environmental Protection Agency limits. Idaho Chemical Process Plant (ICPP) calcined wastes were immobilized into vitreous ceramics with calcine loading up to 88%. These ICPP-vitreous ceramics were more durable than the EA glass by factors of 5 to 30. Vitreous ceramic waste forms are being developed to complement, not to replace, glass waste forms.

  4. Effects of doping amounts of potassium ferricyanide with titanium dioxide and calcination durations on visible-light degradation of pharmaceuticals.

    Science.gov (United States)

    Lin, Justin Chun-Te; de Luna, Mark Daniel G; Gotostos, Mary Jane N; Lu, Ming-Chun

    2016-11-01

    Acetaminophen (ACT) is one of the most frequently detected pharmaceuticals in aqueous environments, and treatment of ACT were generally carried out by photocatalytic degradations under high energy UV irradiation. In this study, potassium ferricyanide was utilized as a quadruple-elemental dopant in a TiO2 photocatalyst in order to enhance its visible-light activity. Two critical parameters (amounts of dopants and durations of calcination) of the synthesis of the photocatalyst by a sol-gel method were systematically evaluated. Crystal structure of the doping TiO2 was examined by X-ray diffraction while the effects of the two parameters on the photocatalytic activity were elucidated by various characterizations. Increasing the amount of dopant or the duration of calcination red-shifted the UV-vis DRS of the doped TiO2. The estimated band gap energy of the doped TiO2 decreased slightly as the amount of dopant increased, but it increased as the duration of calcination increased. The FT-IR yielded characteristic peaks that revealed the effects of the two parameters, whereas the SEM images revealed the morphological evolutions of each effect. The photocatalyst, synthesized at optimum conditions was able to remove 99.1 % acetaminophen with rate constant of 7.9 × 10(-3) min(-1), which was 4.88 times greater than virgin TiO2. In general, this study not only optimized synthetic conditions of the new visible-light active photocatalyst for ACT degradation but also presented characterizations conducted by SEM, XRD, UV-vis DRS, and FTIR to elucidate the relationship between modified structure and the photocatalytic activity. Graphical abstract Effects of doping amounts of K3[Fe(CN)6] and calcunation duration on visible light absorbance of TiO2 photocatalysts.

  5. [Enhanced visible-light absorbance of nanosized AgI/TiO2 by using calcination combined with light irradiation].

    Science.gov (United States)

    Liang, Zhu; Ni, Jin-Ren

    2009-07-15

    With the aim to enhance visible-light absorbance, calcination combined with light irradiation was used to modify nanosized AgI/TiO2. UV-Vis spectrum curves indicated that the modified sample exhibited an intense absorption in the whole visible light range and a spectrum shifted from 465 nm to 800 nm, and that absorbance at 500 nm was improved three times as much as that of the reported pertinent material. XRD analytic results demonstrated that calcined AgI/TiO2 possessed more rutile phase with reduced band gap from 2.89 eV to 2.81 eV, and that the following xenon-light irradiation further enhanced the relative contents of anatase TiO2, rutile TiO2 and AgI accompanied with produced AgCl phase, leading to the decrease in band gap to 1.55 eV. Formation of AgCl and increases in the relative contents of rutile TiO2 and AgI should take the main responsibilities for the decrease in the band gap and enlargement of visible-light absorbance. Additionally, it was confirmed that only the spectrum absorption of the calcined AgI/TiO2 could be improved by light irradiation, and that ultraviolet light played more role than visible part during the light irradiation. Moreover, it was proposed here that two or more silver halides supported on TiO2 could show more capabilities to stimulate visible-light activation of TiO2.

  6. Sorption behaviour of manganese-coated calcined-starfish and manganese-coated sand for Mn(II).

    Science.gov (United States)

    Lee, Seung-Mok; Kim, Won-Gee; Yang, Jae-Kyu; Tiwari, Diwakar

    2010-04-01

    The objective of the present investigation was to explore the sorption behaviour of manganese-coated samples of calcined starfish (MCCSF) (i.e. the impregnation of calcined starfish with manganese) for the removal of low levels of an important heavy metal toxic ion, Mn(II), from aqueous solutions. The suitability of this solid was further compared with two different samples of manganese-coated sands (MCS): MCS4 and MCS9 impregnated at pH 4.0 and pH 9.0, respectively. These comparative studies were performed in both batch and column experiments. Batch data indicated that a fairly good stability of the coating was obtained for these three samples in the pH region 2.5 to 10.0. The removal efficiency of MCCSF was fairly good in comparison with the MCS4 and MCS9 samples. These last two samples possessed similar Mn(II) removal capacities. Moreover, a small dose of sodium hypochlorite further enhanced the uptake of Mn(II) by these solids. The sorbate concentration dependence data fitted reasonably well to the Freundlich adsorption isotherm. The column data indicated that MCCSF possessed a relatively higher adsorption capacity compared with the MCS4 and MCS9 samples. The breakthrough curves obtained were then used to evaluate the apparent removal capacity of these solids under the dynamic conditions using the Thomas equation. The SEM images obtained for these manganese-coated solids along with the virgin base materials, i.e. sand and calcined starfish, showed that manganese oxides occupied the surfaces or pores of the base materials and formed clusters on the base surface.

  7. 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.

  8. Effect of calcination temperature on the photodegradation efficiency of Ni/ZnO composite in removal of organic dye

    Science.gov (United States)

    Thein, Myo Thuya; Pung, Swee-Yong; Aziz, Azizan; Lockman, Zainovia; Itoh, Mitsuru

    2017-07-01

    ZnO based composite is an attractive UV light driven semiconductor photocatalyst to degrade organic compounds attributed to its wide bandgap (3.37 eV). In this study, Ni/ZnO composites were synthesized via solution precipitation method. The composites were calcinated at various temperature, i.e. from 250 °C to 700 °C and subsequently annealed at 500°C in reductive environment (hydrogen atmosphere). The diffraction peaks of all samples could be indexed to the hexagonal wurtzite ZnO. No diffraction peaks from Ni could be observed in all samples, suggesting that the amount of Ni in the composites were below the detection limit of X-ray diffraction (XRD). The field emission scanning electron microscope (FESEM) images confirm that all samples were rod-like structure with hexagonal tips. In addition, small Ni particles were homogeneously deposited on the surface of ZnO rods. This observation is supported by energy dispersive X-ray spectroscopy (EDX) analysis, showing present of Zn, O and Ni elements. It is noted that ZnO rods coupled with Ni experienced quenching of visible emission and enhancing of UV emission in room temperature photoluminescence (RTPL) analysis. The photodegradation efficiency of Ni/ZnO rods was improved when a higher calcination temperature was used. The removal of RhB dye under UV light (352 nm) by these photocatalysts followed pseudo first-order kinetic reaction. The Ni/ZnO composites synthesized at calcination temperature of 500 °C demonstrated the highest photodegradation efficiency of 37 % and the largest rate constant of 0.0053 min-1 after 75 min UV irradiation.

  9. Page 1 12 S R Sawant and R N Patil Fe2O3 were calcinated at 700 ...

    Indian Academy of Sciences (India)

    Fe2O3 were calcinated at 700°C for 24 hr. Powders of these oxides were fired to. 950°C for 24 hr and furnace cooled at the rate of 80°Chr. Pellets of 1 cm diameter and 2 mm thickness were prepared and sintered at a temperature 950°C for 8 hr and furnace cooled at the rate of 80°C/hr. Retaining a series of. Cu, Zn;– Fe3O4 ...

  10. Arsenic removal from aqueous solutions using Fe3O4-HBC composite: effect of calcination on adsorbents performance.

    Directory of Open Access Journals (Sweden)

    Shams Ali Baig

    Full Text Available The presence of elevated concentration of arsenic in water sources is considered to be health hazard globally. Calcination process is known to change the surface efficacy of the adsorbent. In current study, five adsorbent composites: uncalcined and calcined Fe3O4-HBC prepared at different temperatures (400°C and 1000°C and environment (air and nitrogen were investigated for the adsorptive removal of As(V and As(III from aqueous solutions determining the influence of solution's pH, contact time, temperature, arsenic concentration and phosphate anions. Characterizations from FTIR, XRD, HT-XRD, BET and SEM analyses revealed that the Fe3O4-HBC composite at higher calcination temperature under nitrogen formed a new product (fayalite, Fe2SiO4 via phase transformation. In aqueous medium, ligand exchange between arsenic and the effective sorbent site ( = FeOOH was established from the release of hydroxyl group. Langmuir model suggested data of the five adsorbent composites follow the order: Fe3O4-HBC-1000°C(N2>Fe3O4-HBC (uncalcined>Fe3O4-HBC-400°C(N2>Fe3O4-HBC-400°C(air>Fe3O4-HBC-1000°C(air and the maximum As(V and As(III adsorption capacities were found to be about 3.35 mg g(-1 and 3.07 mg g(-1, respectively. The adsorption of As(V and As(III remained stable in a wider pH range (4-10 using Fe3O4-HBC-1000°C(N2. Additionally, adsorption data fitted well in pseudo-second-order (R2>0.99 rather than pseudo-first-order kinetics model. The adsorption of As(V and As(III onto adsorbent composites increase with increase in temperatures indicating that it is an endothermic process. Phosphate concentration (0.0l mM or higher strongly inhibited As(V and As(III removal through the mechanism of competitive adsorption. This study suggests that the selective calcination process could be useful to improve the adsorbent efficiency for enhanced arsenic removal from contaminated water.

  11. Waste Cooking Oil Conversion To Biodeisel Catalized By Egg Shell Of Purebred Chiken With Ethanol As A Solvent

    Directory of Open Access Journals (Sweden)

    Hellna Tehubijuluw

    2014-08-01

    Full Text Available The synthesis of biodiesel from the waste cooking oil was carried out using the catalyst from egg shell of purebred chiken with ethanol as a solvent. Synthesis of biodiesel was prepared in two steps, esterification and transesterification. Esterification was conducted in mol ratio of ethanol and waste cooking oil of  9:1 with H2SO4 as a catalyst. Mol ratio of ethanol and used cooking oil in the transesterification of  12:1 with the CaO catalyst of shell eggs. CaO catalyst was yielded by calcinations egg shell of purebred chicken on 1000 for two hours. Calcination product was characterized with XRD to determine of CaO. Result of biodiesel was characterized based on FTIR, H-NMR, dan ASTM (American Standard Testing of Materials. Theoretically,yielded of biodiesel was 58% and experiment was 36.779%.

  12. Waste Facilities

    Data.gov (United States)

    Vermont Center for Geographic Information — This dataset was developed from the Vermont DEC's list of certified solid waste facilities. It includes facility name, contact information, and the materials...

  13. Development of New Ecological Ceramic Tiles by Recycling of Waste Glass and Ceramic Materials; Incorporacion de residuos derivados de la fabricacion ceramica y del vidrio reciclado en el proceso ceramico integral

    Energy Technology Data Exchange (ETDEWEB)

    Lazaro, C.; Ramon Trilles, V.; Gomez, F.; Allepuz, S.; Fraga, D.; Carda, J. B.

    2012-07-01

    The following research work shows the results of the introduction of waste generated by the ceramic industry, such as the calcined clay from fired porcelain of stoneware and raw biscuit, sludge and cleaning water, as well as waste from other sectors like the recycling glass. In this way, it can be obtained a stoneware porcelain slab, engobe-glaze and satin glaze that contains high percentage of recyclable raw materials. (Author)

  14. Hydrogen Production by Steam Reforming of Ethanol over Nickel Catalysts Supported on Sol Gel Made Alumina: Influence of Calcination Temperature on Supports.

    Science.gov (United States)

    Yaakob, Zahira; Bshish, Ahmed; Ebshish, Ali; Tasirin, Siti Masrinda; Alhasan, Fatah H

    2013-05-30

    Selecting a proper support in the catalyst system plays an important role in hydrogen production via ethanol steam reforming. In this study, sol gel made alumina supports prepared for nickel (Ni) catalysts were calcined at different temperatures. A series of (Ni/AlS.G.) catalysts were synthesized by an impregnation procedure. The influence of varying the calcination temperature of the sol gel made supports on catalyst activity was tested in ethanol reforming reaction. The characteristics of the sol gel alumina supports and Ni catalysts were affected by the calcination temperature of the supports. The structure of the sol gel made alumina supports was transformed in the order of γ → (γ + θ) → θ-alumina as the calcination temperature of the supports increased from 600 °C to 1000 °C. Both hydrogen yield and ethanol conversion presented a volcano-shaped behavior with maximum values of 4.3 mol/mol ethanol fed and 99.5%, respectively. The optimum values were exhibited over Ni/AlS.G800 (Ni catalyst supported on sol gel made alumina calcined at 800 °C). The high performance of the Ni/AlS.G800 catalyst may be attributed to the strong interaction of Ni species and sol gel made alumina which lead to high nickel dispersion and small particle size.

  15. 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.

  16. Multibarrier waste forms. Part II. Characterization and evaluation.

    Energy Technology Data Exchange (ETDEWEB)

    Rusin, J.M.; Gray, W.J.; Wald, J.W.

    1979-08-01

    The multibarrier concept for the storage of radioactive waste is to use up to three barriers to isolate radionuclides from the environment: a solidified waste inner core, an impervious coating, and a metal matrix. The four multibarrier waste forms were evaluated for thermal stability (volatility), mechanical strength (impact resistance), and leach resistance. This report discusses the characterization of the multibarrier waste forms and compares them to reference calcine and glass waste forms. The weight loss of supercalcine-ceramics after 4 h in dry air ranges between 0.01 and 1.6 wt % from 1000 to 1200/sup 0/C and is dependent upon composition. Glass marbles in a cast lead alloy offer approximately an order of magnitude decease in the wt % fines < 37 ..mu..m released after impact as compared to a glass monolith. CVD-coated supercalcine in a sintered 410 SS matrix offers up to two orders of magnitude decrease. Hot-pressed supercalcine ceramics may offer no increase in impact resistance or leach resistance over that of a glass monolith. Supercalcine may offer no advantage over waste glasses in leach resistance. Glass and PyC/Al/sub 2/O/sub 3/ coatings provide effective inert leaching barriers.

  17. Efficacy assessment of acid mine drainage treatment with coal mining waste using Allium cepa L. as a bioindicator.

    Science.gov (United States)

    Geremias, Reginaldo; Bortolotto, Tiago; Wilhelm-Filho, Danilo; Pedrosa, Rozangela Curi; de Fávere, Valfredo Tadeu

    2012-05-01

    The aim of this study was to evaluate the efficacy of the treatment of acid mine drainage (AMD) with calcinated coal mining waste using Allium cepa L. as a bioindicator. The pH values and the concentrations of aluminum, iron, manganese, zinc, copper, lead and sulfate were determined before and after the treatment of the AMD with calcinated coal mining waste. Allium cepa L. was exposed to untreated and treated AMD, as well as to mineral water as a negative control (NC). At the end of the exposure period, the inhibition of root growth was measured and the mean effective concentration (EC(50)) was determined. Oxidative stress biomarkers such as lipid peroxidation (TBARS), protein carbonyls (PC), catalase activity (CAT) and reduced glutathione levels (GSH) in the fleshy leaves of the bulb, as well as the DNA damage index (ID) in meristematic cells, were evaluated. The results indicated that the AMD treatment with calcinated coal mining waste resulted in an increase in the pH and an expressive removal of aluminum, iron, manganese and zinc. A high sub-chronic toxicity was observed when Allium cepa L. was exposed to the untreated AMD. However, after the treatment no toxicity was detected. Levels of TBARS and PC, CAT activity and the DNA damage index were significantly increased (P<0.05) in Allium cepa L. exposed to untreated AMD when compared to treated AMD and also to negative controls. No significant alteration in the GSH content was observed. In conclusion, the use of calcinated coal mining waste associated with toxicological tests on Allium cepa L. represents an alternative system for the treatment and biomonitoring of these types of environmental contaminants. Copyright © 2011 Elsevier Inc. All rights reserved.

  18. 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.

  19. 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.

  20. Fabrication, optical properties and laser outputs of Nd:YAG ceramics based on laser ablated and pre-calcined powders

    Science.gov (United States)

    Osipov, V. V.; Maksimov, R. N.; Shitov, V. A.; Lukyashin, K. E.; Toci, G.; Vannini, M.; Ciofini, M.; Lapucci, A.

    2017-09-01

    Transparent Nd:YAG ceramic was fabricated by the solid-state reaction method with an additional round of pre-calcining using nanopowders of 1 at.% Nd:Y2O3 and Al2O3 synthesized by laser ablation. The pre-calcining step and addition of tetraethyl orthosilicate was found crucial for fabricating high optical quality Nd:YAG ceramic from such nanoparticles. The transmittance of the obtained 2-mm-thick Nd:YAG ceramic was 83.6% at the wavelength of 1064 nm, which is very close to the theoretical value. The uniformity of the optical quality of ceramic was mapped by analyzing the point-by-point transmission of a focused laser beam. The average volume of the scattering centers in the obtained ceramic was evaluated by direct count method to be 17 ppm. The Nd distribution was determined by fluorescence imaging to be homogeneous throughout the sample. Output power of 4.9 W with a slope efficiency of 52.7% was obtained in 1.5-mm-thick Nd:YAG ceramic under a quasi-continuous wave (QCW) laser diode end pumping at 805 nm.

  1. 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.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. Heavy metal removal and speciation transformation through the calcination treatment of phosphorus-enriched sewage sludge ash.

    Science.gov (United States)

    Li, Rundong; Zhao, Weiwei; Li, Yanlong; Wang, Weiyun; Zhu, Xuan

    2015-01-01

    On the basis of the heavy metal (Cd, As, Pb, Zn, Cu, Cr, and Ni) control problem during the thermochemical recovery of phosphorus (P) from sewage sludge (SS), P-enriched sewage sludge ash (PSSA) was calcined at 1100°C. The effect of organic chlorinating agent (PVC) and inorganic chlorinating agent (MgCl2) on the fixed rate of P removal and the speciation transformation of heavy metal was studied. The removal of heavy metals Cd, Pb, As, Zn, and Cr exhibited an increasing tendency with the addition of chlorinating agent (PVC). However, an obvious peak under 100gCl/kg of PSSA appeared for Cu, owing to the presence of carbon and hydrogen in PVC. MgCl2 was found to be more effective than PVC in the removal of most heavy metals, such that up to 98.9% of Cu and 97.3% of Zn was effectively removed. Analyses of heavy metal forms showed that Pb and Zn occurred in the residue fraction after calcination. Meanwhile, the residue fraction of Cr, Ni, Cd, and Cu exhibited a decreasing tendency with the increase in the added chlorinating agent (MgCl2). Losses of P from PSSA were around 16.6% without the addition of chlorinating agent, which were greatly reduced to around 7.7% (PVC) and to only 1.7% (MgCl2). Copyright © 2014 Elsevier B.V. All rights reserved.

  7. Long-term calcination/carbonation cycling and thermal pretreatment for CO{sub 2} capture by limestone and dolomite

    Energy Technology Data Exchange (ETDEWEB)

    Zhongxiang Chen; Hoon Sub Song; Miguel Portillo; C. Jim Lim; John R. Grace; E.J. Anthony [University of British Columbia, Vancouver, BC (Canada). Department of Chemical and Biological Engineering

    2009-03-15

    Capturing carbon dioxide is vital for the future of climate-friendly combustion, gasification, and steam-re-forming processes. Dry processes utilizing simple sorbents have great potential in this regard. Long-term calcination/carbonation cycling was carried out in an atmospheric-pressure thermogravimetric reactor. Although dolomite gave better capture than limestone for a limited number of cycles, the advantage declined over many cycles. Under some circumstances, decreasing the carbonation temperature increased the rate of reaction because of the interaction between equilibrium and kinetic factors. Limestone and dolomite, after being pretreated thermally at high temperatures (1000 or 1100{sup o}C), showed a substantial increase in calcium utilization over many calcination/carbonation cycles. Lengthening the pretreatment interval resulted in greater improvement. However, attrition was significantly greater for the pretreated sorbents. Greatly extending the duration of carbonation during one cycle was found to be capable of restoring the CO{sub 2} capture ability of sorbents to their original behavior, offering a possible means of countering the long-term degradation of calcium sorbents for dry capture of carbon dioxide. 12 refs., 12 figs., 2 tabs.

  8. 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

  9. Relevance of the Physicochemical Properties of Calcined Quail Eggshell (CaO as a Catalyst for Biodiesel Production

    Directory of Open Access Journals (Sweden)

    Leandro Marques Correia

    2017-01-01

    Full Text Available The CaO solid derived from natural quail eggshell was calcined and employed as catalyst to produce biodiesel via transesterification of sunflower oil. The natural quail eggshell was calcined at 900°C for 3 h, in order to modify the calcium carbonate present in its structure in CaO, the activity phase of the catalyst. Both precursor and catalyst were characterized using Hammett indicators method, X-ray fluorescence (XRF, X-ray diffraction (XRD, thermogravimetric analysis (TG/DTG, CO2 temperature-programmed desorption (CO2-TPD, X-ray photoelectronic spectroscopy (XPS, Fourier infrared spectroscopy (FTIR, scanning electron microscopy (SEM, N2 adsorption-desorption at −196°C, and distribution particle size. The maximum biodiesel production was of 99.00 ± 0.02 wt.% obtained in the following transesterification reaction conditions: XMR (sunflower oil/methanol molar ratio of 1 : 10.5 mol : mol, XCAT (catalyst loading of 2 wt.%, XTIME (reaction time of 2 h, stirring rate of 1000 rpm, and temperature of 60°C.

  10. Sodium-bearing Waste Treatment Technology Evaluation Report

    Energy Technology Data Exchange (ETDEWEB)

    Charles M. Barnes; Arlin L. Olson; Dean D. Taylor

    2004-05-01

    Sodium-bearing waste (SBW) disposition is one of the U.S. Department of Energy (DOE) Idaho Operation Office’s (NE-ID) and State of Idaho’s top priorities at the Idaho National Engineering and Environmental Laboratory (INEEL). The INEEL has been working over the past several years to identify a treatment technology that meets NE-ID and regulatory treatment requirements, including consideration of stakeholder input. Many studies, including the High-Level Waste and Facilities Disposition Environmental Impact Statement (EIS), have resulted in the identification of five treatment alternatives that form a short list of perhaps the most appropriate technologies for the DOE to select from. The alternatives are (a) calcination with maximum achievable control technology (MACT) upgrade, (b) steam reforming, (c) cesium ion exchange (CsIX) with immobilization, (d) direct evaporation, and (e) vitrification. Each alternative has undergone some degree of applied technical development and preliminary process design over the past four years. This report presents a summary of the applied technology and process design activities performed through February 2004. The SBW issue and the five alternatives are described in Sections 2 and 3, respectively. Details of preliminary process design activities for three of the alternatives (steam reforming, CsIX, and direct evaporation) are presented in three appendices. A recent feasibility study provides the details for calcination. There have been no recent activities performed with regard to vitrification; that section summarizes and references previous work.

  11. Tribal Waste Management Program

    Science.gov (United States)

    The EPA’s Tribal Waste Management Program encourages environmentally sound waste management practices that promote resource conservation through recycling, recovery, reduction, clean up, and elimination of waste.

  12. Effect of different alcohols, gelatinizing times, calcination and microwave on characteristics of TiO2 nanoparticles synthesized by sol-gel method

    Science.gov (United States)

    Bahar, Mahmoud; Mozaffari, Masoud; Esmaeili, Sahar

    2017-03-01

    In this work, nanoparticles of titanium dioxide (TiO2) were synthesized by means of TiCl4 as precursor. Effects of alcohol type, calcination, gelatinizing time and microwave exposure on the particle size, morphology, crystallinity and particle phase are studied using XRD patterns and SEM images. Results showed that alcohols such as ethanol increased the particle size; calcination increased the particle size and improved the crystallinity of particles. Microwave exposure of particles resulted in smaller particles; adding water increased the impact of microwave. Effect of microwave exposure in rutile phase formation is also observed during this study.

  13. Effect of the preparation conditions on the catalytic activity of calcined Ca/Al-layered double hydroxides for the synthesis of glycerol carbonate

    OpenAIRE

    Salagre, P.; Granados-Reyes, J.; Cesteros, Y.

    2017-01-01

    Effect of the preparation conditions on the catalytic activity of calcined Ca/Al-layered double hydroxides for the synthesis of glycerol carbonate DOI: 10.1016/j.apcata.2017.02.013 URL: http://www.sciencedirect.com/science/article/pii/S0926860X17300686 Filiació URV: SI Memòria The effect of the preparation conditions of several calcined Ca/Al layered double hydroxide compounds (CaAl-LDH) on the catalytic transesterification of glycerol with dimethyl carbonate to obtain glycerol...

  14. Effects of surface features on sulfur dioxide adsorption on calcined NiAl hydrotalcite-like compounds.

    Science.gov (United States)

    Zhao, Ling; Li, Xinyong; Quan, Xie; Chen, Guohua

    2011-06-15

    The hydrotalcite-based NiAl mixed oxides were synthesized by coprecipitation and urea hydrolysis approaches and employed for SO₂ removal. The samples were well characterized by inductively coupled plasma (ICP) elemental analysis, X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and N₂ adsorption/desorption isotherm analyses. The acid-base properties were characterized by pyridine chemisorption and CO₂ temperature-programmed desorption (TPD). The calcined NiAlO from the urea method showed excellent SO₂ adsorption and its adsorption equilibrium showed a type I isotherm, which significantly improved the adsorption performance for low-concentration SO₂. Both the physical structure and the acidic-basic sites were found to play important roles in the SO₂ adsorption process. In situ Fourier transform infrared spectroscopy (FTIR) investigation revealed that adsorbed SO₂ molecules formed surface bisulfite, sulfite, and bidentate binuclear sulfate. The mechanisms for SO₂ adsorption and transformation are discussed in detail.

  15. 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

  16. 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.)

  17. 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

  18. 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.

  19. Waste disposal

    CERN Multimedia

    2006-01-01

    We should like to remind you that you can have all commonplace, conventional waste (combustible, inert, wood, etc.) disposed of by the TS-FM Group. Requests for the removal of such waste should be made by contacting FM Support on tel. 77777 or by e-mail (Fm.Support@cern.ch). For requests to be acted upon, the following information must be communicated to FM Support: budget code to be debited for the provision and removal of the skip / container; type of skip required (1m3, 4 m3, 7 m3, 15 m3, 20 m3, 30 m3); nature of the waste to be disposed of (bulky objects, cardboard boxes, etc.); building concerned; details of requestor (name, phone number, department, group, etc.). We should also like to inform you that the TS-FM Group can arrange for waste to be removed from work-sites for firms under contract to CERN, provided that the prior authorisation of the CERN Staff Member in charge of the contract is obtained and the relevant disposal/handling charges are paid. You are reminded that the selective sorting...

  20. Waste disposal

    CERN Multimedia

    2006-01-01

    We should like to remind you that you can have all commonplace, conventional waste (combustible, inert, wood, etc.) disposed of by the TS-FM Group. Requests for the removal of such waste should be made by contacting FM Support on tel. 77777 or by e-mail (Fm.Support@cern.ch). For requests to be acted upon, the following information must be communicated to FM Support: budget code to be debited for the provision and removal of the skip / container. type of skip required (1m3, 4 m3, 7 m3, 15 m3, 20 m3, 30 m3). nature of the waste to be disposed of (bulky objects, cardboard boxes, etc.). building concerned. details of requestor (name, phone number, department, group, etc.). We should also like to inform you that the TS-FM Group can arrange for waste to be removed from work-sites for firms under contract to CERN, provided that the prior authorisation of the CERN Staff Member in charge of the contract is obtained and the relevant disposal/handling charges are paid. You are reminded that the selective sorting o...

  1. Human waste

    NARCIS (Netherlands)

    Amin, Md Nurul; Kroeze, Carolien; Strokal, Maryna

    2017-01-01

    Many people practice open defecation in south Asia. As a result, lot of human waste containing nutrients such as nitrogen (N) and phosphorus (P) enter rivers. Rivers transport these nutrients to coastal waters, resulting in marine pollution. This source of nutrient pollution is, however, ignored in

  2. Dairy Wastes.

    Science.gov (United States)

    Pico, Richard F.

    1978-01-01

    Presents a literature review of wastes from the dairy industry covering publications of 1976-77. This review covers: (1) government regulations; (2) ion-plant control of dairy effluents; (3) dairy effluent treatment methods; and (4) research on dairy effluents. A list of 26 references is also presented. (HM)

  3. 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.

  4. 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.

  5. Structural and paramagnetic behavior of spinel NiCr2O4 nanoparticles synthesized by thermal treatment method: Effect of calcination temperature

    Science.gov (United States)

    Bakar, Syuhada Abu; Soltani, Nayereh; Yunus, W. Mahmood Mat; Saion, Elias; Bahrami, Afarin

    2014-08-01

    Spinel nickel chromite nanoparticles were synthesized using a simple thermal treatment method. The effect of calcination temperatures on the final properties of obtained materials was carefully examined using various characterization techniques.The infrared spectra of nickel chromite (NiCr2O4) revealed the characteristic bonds of metal-oxygen for Nisbnd O and Crsbnd O bands around 600 and 470 cm-1, respectively. The powder X-ray diffraction patterns exhibited the formation of normal spinel phase of NiCr2O4 in the calcination process at temperature between 550 and 850 °C. From transmission electron micrographs, nanosized particles with average size of ~7-64 nm were observed at calcination temperatures of 550-850 °C, respectively. The calcined samples at 750 and 850 °C exhibited paramagnetic behavior with g-factor values of 1.92 and 2.15, peak-to-peak line width of 25.59 and 117.02 Oe and resonance magnetic field of 342.04 and 306.49 Oe, respectively. Variation in the value of g-factor, peak-to-peak line width and resonance magnetic field can be attributed to the dipole-dipole and super exchange interactions.

  6. Effects of calcination temperature for rate capability of triple-shelled ZnFe2O4 hollow microspheres for lithium ion battery anodes

    Science.gov (United States)

    Hwang, Hojin; Shin, Haeun; Lee, Wan-Jin

    2017-04-01

    Triple-shelled ZnFe2O4 hollow microspheres (ZFO) as anode materials for lithium ion battery are prepared through a one-pot hydrothermal reaction using the composite solution consisting of sucrose in water and metal ions in ethylene glycol (EG), followed by different calcination processes. The architectures of ZFO micro spheres are differently synthesized through a mutual cooperation of inward and outward ripening with three different calcination temperatures. Thin triple-shelled ZnFe2O4 hollow microspheres calcined at 450 °C (ZFO-450) delivers a high reversible capacity of 932 mA h g-1 at a current density of 2 A g-1 even at the 200th cycle without obvious decay. Furthermore, ZFO-450 delivers 1235, 1005, 865, 834, and 845 mA h g-1 at high current densities of 0.5, 2, 5, 10, and 20 A g-1 after 100 cycles. Thin triple-shelled hollow microsphere prepared at an optimum calcination temperature provides exceptional rate capability and outstanding rate retention due to (i) the formation of nanoparticles leading to thin shell with morphological integrity, (ii) the facile mass transfer by thin shell with mesoporous structure, and (iii) the void space with macroporous structure alleviating volume change occurring during cycling.

  7. 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.

  8. Effect of doped SiO2 and calcinations temperature on phase transformation of TiO2 photocatalyst prepared by sol-gel method

    Directory of Open Access Journals (Sweden)

    Sutham Niyomwas

    2008-05-01

    Full Text Available The purpose of this research was to study the effect of calcinations temperature and SiO2 addition on phase transformation,crystallite size, and photocatalytic activity of SiO2/TiO2 thin films by using indigo carmine as an indicator. Thecomposite particles were prepared by sol-gel method via calcinations at a temperature range of 300-700oC for 2 h, and thecomposite thin films were prepared by means of spin coating. The microstructure and crystallite size of pure TiO2 and SiO2/TiO2 composite powders were characterized by using XRD, SEM and DTA. It was found that anatase structures wereformed at a calcinations temperature range of 300-600oC and mixed phases of anatase and rutile were observed at a temperatureof 700oC. Crystallite size of pure TiO2 tends to increase with an increase in calcinations temperature. Doped SiO2in the TiO2 has an effect on crystal phases and crystallite size of the composite powders and thin films, resulting in thechange of the photocatalytic activity of TiO2.

  9. 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.

  10. Production of calcium hydroxide from the waste of Cariri stone; Producao de hidroxido de calcio a partir de residuo da pedra Cariri

    Energy Technology Data Exchange (ETDEWEB)

    Alves, T.M.E.; Santos, A.M.M.; Brasileiro, M.I.; Pinheiro, S.F.L.; Prado, A.C.A., E-mail: tiagomaiaea@gmail.com [Universidade Federal do Cariri (UFCA), Juazeiro do Norte, CE (Brazil)

    2016-07-01

    The extraction of Cariri stone in the northeast is a frequent activity because of its ornamental application as well as for the construction sector. However, by this extraction, untapped waste formation grows and becomes a problem for the environment. The objective of this work is to produce calcium hydroxide, from this limestone residue, with controlled porosity, solubility and particle size. The waste was characterized with X-Ray Diffraction (XRD), X-Ray Fluorescence (XRF) and thermal analysis (TGA). The limestone was calcined at 850°C and 950°C for 45 minutes and three hours, being characterized by XRD, XRF and TGA. Once calcined, it was hydrated with 17,5g and 22g oxide to 100mL water and manually mixed for 15 and 25 minutes. The calcium hydroxides have been submitted for tests in vivo in rats and will be characterized by XRD, Scanning Electron Microscopy (SEM) and Infrared. (author)

  11. 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.

  12. Increased photocatalytic activity of NiO and ZnO in photodegradation of a model drug aqueous solution: Effect of coupling, supporting, particles size and calcination temperature

    Energy Technology Data Exchange (ETDEWEB)

    Derikvandi, Hadis [Department of Chemistry, Shahreza Branch, Islamic Azad University, P.O. Box 311-86145, Shahreza, Isfahan, Iran (Iran, Islamic Republic of); Young Researchers and Elite Club, Shahreza Branch, Islamic Azad University, Shahreza (Iran, Islamic Republic of); Nezamzadeh-Ejhieh, Alireza, E-mail: arnezamzadeh@iaush.ac.ir [Department of Chemistry, Shahreza Branch, Islamic Azad University, P.O. Box 311-86145, Shahreza, Isfahan, Iran (Iran, Islamic Republic of); Young Researchers and Elite Club, Shahreza Branch, Islamic Azad University, Shahreza (Iran, Islamic Republic of); Razi Chemistry Research Center (RCRC), Shahreza Branch, Islamic Azad University, Isfahan (Iran, Islamic Republic of)

    2017-01-05

    Highlights: • Increased photoactivity of hybridized/supported NiO-ZnO whit respect to monocomponent one. • Strong dependence of photocatalytic activity of NiO-ZnO to calcination temperature. • Calcination temperature varied the crystallite forms of the semiconductors. • Red shifts in band gaps of the supported coupled semiconductors whit respect to monocomponent one. - Abstract: Mechanically ball-mill prepared clinoptilolite nanoparticles (NC) were used for increasing photocatalytic activity of NiO and ZnO as alone and binary systems. The semiconductors were supported onto the zeolite during calcination of Ni(II)-Zn(II)-exchanged NC at different calcinations temperatures. XRD, FTIR, SEM-EDX, X-ray mapping, DRS, TEM and BET techniques were used for characterization of the samples. The calcined catalysts at 400 °C for 4 h showed the best photocatalytic activity for metronidazole (MNZ) in aqueous solution. The mole ratio of ZnO/NiO affected the photodegradation efficiency because activity of the coupled catalysts depends to the both e/h production and electron scavenging processes. In the used system, NiO acted as e/h production source and ZnO as an electron sink. Red shifts in band gaps of the supported coupled semiconductors was observed whit respect to monocomponent one, confirming formation of nanoparticles of the semiconductors onto the zeolitic bed. The best activities were obtained for the NiO{sub 1.3}–ZnO{sub 1.5}/NC (NZ-NC) and NiO{sub 0.7}–ZnO{sub 4.3}/NC (NZ{sub 3}-NC) catalysts at pH 3, 1.2 g L{sup −1} of the catalysts and 1 g L{sup −1} of MNZ.

  13. Secondary Waste Form Down Selection Data Package – Ceramicrete

    Energy Technology Data Exchange (ETDEWEB)

    Cantrell, Kirk J.; Westsik, Joseph H.

    2011-08-31

    binder is formed through an acid-base reaction between calcined magnesium oxide (MgO; a base) and potassium hydrogen phosphate (KH{sub 2}PO{sub 4}; an acid) in aqueous solution. The reaction product sets at room temperature to form a highly crystalline material. During the reaction, the hazardous and radioactive contaminants also react with KH{sub 2}PO{sub 4} to form highly insoluble phosphates. In this data package, physical property and waste acceptance data for Ceramicrete waste forms fabricated with wastes having compositions that were similar to those expected for secondary waste effluents, as well as secondary waste effluent simulants from the Hanford Tank Waste Treatment and Immobilization Plant were reviewed. With the exception of one secondary waste form formulation (25FA+25 W+1B.A. fabricated with the mixed simulant did not meet the compressive strength requirement), all the Ceramicrete waste forms that were reviewed met or exceeded Integrated Disposal Facility waste acceptance criteria.

  14. Optimization of the Transesterification of Waste Cooking Oil with Mg-Al Hydrotalcite Using Response Surface Methodology

    Directory of Open Access Journals (Sweden)

    Laureano Costarrosa

    2018-01-01

    Full Text Available Nowadays, biodiesel has become a very promising alternative to fossil diesel fuel, regarding environmental concerns and fuel resource depletion. Biodiesel is usually produced through homogeneous or heterogeneous transesterification of different fatty raw materials. Although main research has been carried out with homogenous catalysts, heterogeneous catalysts may be of interest due to ease of recovery and recycling, as well as readiness for continuous processing. In this work, calcined Mg-Al hydrotalcite (HT was used for the heterogeneous transesterification of waste cooking oil. Three reaction parameters, namely, reaction time, amount of catalyst, and methanol-to-oil molar ratio, were optimized by means of Response Surface Methodology (RSM at constant temperature (65 °C, using a Box-Behnken design. Optimal fatty acid methyl ester (FAME content (86.23% w/w FAME/sample was predicted by the model with an R-squared value of 98.45%, using 3.39 g of HT (8.5% w/w oil and an 8:1 methanol-oil molar ratio, for a duration of 3.12 h. It was observed that calcination of HT, while avoiding the previous washing step, allowed the presence of chemical species that enhanced the effect of the catalyst. It can be concluded from this field trial that calcined and nonwashed Mg-Al hydrotalcite may be considered an effective basic catalyst for the production of biodiesel from waste cooking oil. Also, RSM proved to be a useful tool for predicting biodiesel yield.

  15. Rethinking the waste hierarchy

    Energy Technology Data Exchange (ETDEWEB)

    Rasmussen, C.; Vigsoe, D. (eds.)

    2005-03-01

    There is an increasing need to couple environmental and economic considerations within waste management. Consumers and companies alike generate ever more waste. The waste-policy challenges of the future lie in decoupling growth in waste generation from growth in consumption, and in setting priorities for the waste management. This report discusses the criteria for deciding priorities for waste management methods, and questions the current principles of EU waste policies. The basis for the discussion is the so-called waste hierarchy which has dominated the waste policy in the EU since the mid-1970s. The waste hierarchy ranks possible methods of waste management. According to the waste hierarchy, the very best solution is to reduce the amount of waste. After that, reuse is preferred to recycling which, in turn, is preferred to incineration. Disposal at a landfill is the least favourable solution. (BA)

  16. Investigation of the possibility of using hydrogranulation in reprocessing radioactive wastes of radiochemical production facilities

    Energy Technology Data Exchange (ETDEWEB)

    Revyakin, V.; Borisov, L.M. [All Russian Scientific and Research Institute of Non-Organic Materials, Moscow (Russian Federation)

    1996-05-01

    Radio-chemical production facilities are constantly accumulating liquid radioactive wastes (still residues as the result of evaporation of extraction and adsorption solutions etc.) which are a complex multicomponent mixtures. The wastes are frequently stored for extended periods of time while awaiting disposition and in some cases, and this is much worse, they are released into the environment. In this report, I would like to draw your attention to some results we have obtained from investigations aimed at simplifying handing of such wastes by the precipitation of hard to dissolve metal hydroxides, the flocculation of the above into granules with the help of surface-active agents (in this case a polyacrylamide - PAA), quickly precipitated and easily filtered. The precipitate may be quickly dried and calcinated, if necessary, and transformed into a dense oxide sinter. In other words it may be transformed into a material convenient for storage or burial.

  17. Other Special Waste

    DEFF Research Database (Denmark)

    Brogaard, Line Kai-Sørensen; Christensen, Thomas Højlund

    2011-01-01

    separately from MSW. Some of these other special wastes are briefly described in this chapter with respect to their definition, quantity and composition, and management options. The special wastes mentioned here are batteries, tires, polyvinylchloride (PVC) and food waste.......In addition to the main types of special waste related to municipal solid waste (MSW) mentioned in the previous chapters (health care risk waste, WEEE, impregnated wood, hazardous waste) a range of other fractions of waste have in some countries been defined as special waste that must be handled...

  18. Performance assessment of the direct disposal in unsaturated tuff or spent nuclear fuel and high-level waste owned by USDOE: Volume 2, Methodology and results

    Energy Technology Data Exchange (ETDEWEB)

    Rechard, R.P. [ed.

    1995-03-01

    This assessment studied the performance of high-level radioactive waste and spent nuclear fuel in a hypothetical repository in unsaturated tuff. The results of this 10-month study are intended to help guide the Office of Environment Management of the US Department of Energy (DOE) on how to prepare its wastes for eventual permanent disposal. The waste forms comprised spent fuel and high-level waste currently stored at the Idaho National Engineering Laboratory (INEL) and the Hanford reservations. About 700 metric tons heavy metal (MTHM) of the waste under study is stored at INEL, including graphite spent nuclear fuel, highly enriched uranium spent fuel, low enriched uranium spent fuel, and calcined high-level waste. About 2100 MTHM of weapons production fuel, currently stored on the Hanford reservation, was also included. The behavior of the waste was analyzed by waste form and also as a group of waste forms in the hypothetical tuff repository. When the waste forms were studied together, the repository was assumed also to contain about 9200 MTHM high-level waste in borosilicate glass from three DOE sites. The addition of the borosilicate glass, which has already been proposed as a final waste form, brought the total to about 12,000 MTHM.

  19. Hanford Site annual dangerous waste report: Volume 1, Part 1, Generator dangerous waste report, dangerous waste

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1994-12-31

    This report contains information on hazardous wastes at the Hanford Site. Information consists of shipment date, physical state, chemical nature, waste description, waste number, weight, and waste designation.

  20. Fabrication of hydroxyapatite from fish bones waste using reflux method

    Science.gov (United States)

    Cahyanto, A.; Kosasih, E.; Aripin, D.; Hasratiningsih, Z.

    2017-02-01

    The aim of this present study was to investigate the fabrication of hydroxyapatites, which were synthesized from fish bone wastes using reflux method. The fish bone wastes collected from the restaurant were brushed and boiled at 100°C for 10 minutes to remove debris and fat. After drying, the fish bones were crushed, and ball milled into a fine powder. The fish bone wastes were then processed by refluxing using KOH and H3PO4 solutions. The samples were calcined at 900°C and characterized by X-Ray Diffraction (XRD) and Fourier Transform Infrared Spectrometry (FT-IR). The XRD pattern of samples after treatment revealed that the peak of hydroxyapatite was observed and the bands of OH- and PO4 3- were observed by FT-IR. The scanning electron microscope evaluation of sample showed the entangled crystal and porous structure of hydroxyapatite. In conclusion, the hydroxyapatite was successfully synthesized from fish bone wastes using reflux method.

  1. Technology Evaluations Related to Mercury, Technetium, and Chloride in Treatment of Wastes at the Idaho Nuclear Technology and Engineering Center of the Idaho National Engineering and Environmental Laboratory

    Energy Technology Data Exchange (ETDEWEB)

    C. M. Barnes; D. D. Taylor; S. C. Ashworth; J. B. Bosley; D. R. Haefner

    1999-10-01

    The Idaho High-Level Waste and Facility Disposition Environmental Impact Statement defines alternative for treating and disposing of wastes stored at the Idaho Nuclear Technology and Engineering Center. Development is required for several technologies under consideration for treatment of these wastes. This report contains evaluations of whether specific treatment is needed and if so, by what methods, to remove mercury, technetium, and chlorides in proposed Environmental Impact Statement treatment processes. The evaluations of mercury include a review of regulatory requirements that would apply to mercury wastes in separations processes, an evaluation of the sensitivity of mercury flowrates and concentrations to changes in separations processing schemes and conditions, test results from laboratory-scale experiments of precipitation of mercury by sulfide precipitation agents from the TRUEX carbonate wash effluent, and evaluations of methods to remove mercury from New Waste Calcining Facility liquid and gaseous streams. The evaluation of technetium relates to the need for technetium removal and alternative methods to remove technetium from streams in separations processes. The need for removal of chlorides from New Waste Calcining Facility scrub solution is also evaluated.

  2. 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

  3. Waste remediation

    Energy Technology Data Exchange (ETDEWEB)

    Halas, Nancy J.; Nordlander, Peter; Neumann, Oara

    2017-01-17

    A system including a steam generation system and a chamber. The steam generation system includes a complex and the steam generation system is configured to receive water, concentrate electromagnetic (EM) radiation received from an EM radiation source, apply the EM radiation to the complex, where the complex absorbs the EM radiation to generate heat, and transform, using the heat generated by the complex, the water to steam. The chamber is configured to receive the steam and an object, wherein the object is of medical waste, medical equipment, fabric, and fecal matter.

  4. Waste Reduction Model

    Science.gov (United States)

    To help solid waste planners and organizations track/report GHG emissions reductions from various waste management practices. To assist in calculating GHG emissions of baseline and alternative waste management practices and provide the history of WARM.

  5. Hazardous Waste Generators

    Data.gov (United States)

    Vermont Center for Geographic Information — The HazWaste database contains generator (companies and/or individuals) site and mailing address information, waste generation, the amount of waste generated etc. of...

  6. The temporality of waste

    DEFF Research Database (Denmark)

    Madsen, Katrine Dahl; Jordt Jørgensen, Nanna; Læssøe, Jeppe

    Waste is, indisputably, one of the key issues of environmental concerns of our times. In an environment and sustainability education perspective, waste offers concrete entry points to issues of consumption, sustainability and citizenship. Still, waste education has received relatively little...

  7. Household hazardous waste

    DEFF Research Database (Denmark)

    Fjelsted, Lotte; Christensen, Thomas Højlund

    2007-01-01

    .) comprised 15-25% and foreign items comprised 10-20%. Water-based paint was the dominant part of the paint waste. The chemical composition of the paint waste and the paint-like waste was characterized by an analysis of 27 substances in seven waste fractions. The content of critical substances was tow......'Paint waste', a part of the 'household hazardous waste', amounting to approximately 5 tonnes was collected from recycling stations in two Danish cities. Sorting and analyses of the waste showed paint waste comprised approximately 65% of the mass, paint-like waste (cleaners, fillers, etc...... and the paint waste was less contaminated with heavy metals than was the ordinary household waste. This may suggest that households no longer need to source-segregate their paint if the household waste is incinerated, since the presence of a small quantity of solvent-based paint will not be harmful when...

  8. Informative document waste plastics

    NARCIS (Netherlands)

    Nagelhout D; Sein AA; Duvoort GL

    1989-01-01

    This "Informative document waste plastics" forms part of a series of "informative documents waste materials". These documents are conducted by RIVM on the indstruction of the Directorate General for the Environment, Waste Materials Directorate, in behalf of the program of

  9. Informative document packaging waste

    NARCIS (Netherlands)

    Joosten JM; Nagelhout D; Duvoort GL; Weerd M de

    1989-01-01

    This "informative document packaging waste" forms part of a series of "informative documents waste materials". These documents are conducted by RIVM on the instructions of the Direcotrate General for the Environment, Waste Materials Directorate, in behalf of the program of

  10. 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.

  11. 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)

  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. Evolution of porous structure and texture in nanoporous SiO2/Al2O3 materials during calcination

    Science.gov (United States)

    Glazkova, Elena A.; Bakina, Olga V.

    2016-11-01

    The study focuses on the evolution of porous structure and texture of silica/alumina xerogels during calcination in the temperature range from 500 to 1200°C. The xerogel was prepared via sol-gel method using subcritical drying. The silica/alumina xerogels were examined using transmission electron microscopy-energy dispersive spectroscopy (TEM-EDS), Brunauer Emmett Teller-Barrett Joyner Halenda (BET-BJH), differential scanning calorimetry (DSC), and Fourier transform infrared (FTIR) spectroscopy. SiO2 primary particles of size about 10 nm are connected with each other to form a porous xerogel structure. Alumina is uniformly distributed over the xerogel volume. The changes of textural characteristics under heat treatment of samples are radical; the specific surface area and pore size attain their maximum at 500-700°C. The heat treatment of samples causes dehydroxylation of the xerogel surface, and at 1200°C the sample is sintered, loses mesoporosity, and its specific surface area reduces considerably down to 78 m2/g.

  14. Feasibility analysis of As(III) removal in a continuous flow fixed bed system by modified calcined bauxite (MCB).

    Science.gov (United States)

    Bhakat, P B; Gupta, A K; Ayoob, S

    2007-01-10

    This study examine the feasibility of As(III) removal from aqueous environment by an adsorbent, modified calcined bauxite (MCB) in a continuous flow fixed bed system. MCB exhibited excellent adsorption capacity of 520.2 mg/L (0.39 mg/g) with an adsorption rate constant 0.7658 L/mgh for an influent As(III) concentration of 1mg/L. In a 2 cm diameter continuous flow fixed MCB bed, a depth of only 1.765 cm was found necessary to produce effluent As(III) concentration of 0.01 mg/L, from an influent of 1 mg/L at a flow rate of 8 mL/min. Also, bed heights of 10, 20, and 30 cm could treat 427.85, 473.88 and 489.17 bed volumes of water, respectively, to breakthrough. A reduction in adsorption capacity of MCB was observed with increase in flow rates. The theoretical service times evaluated from bed depth service time (BDST) approach for different flow rates and influent As(III) concentrations had shown good correlation with the corresponding experimental values. The theoretical breakthrough curve developed from constantly mixed batch reactor (CMBR) isotherm data also correlated well with experimental breakthrough curve.

  15. 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.

  16. Competitive adsorption characteristics of fluoride and phosphate on calcined Mg-Al-CO3 layered double hydroxides.

    Science.gov (United States)

    Cai, Peng; Zheng, Hong; Wang, Chong; Ma, Hongwen; Hu, Jianchao; Pu, Yubing; Liang, Peng

    2012-04-30

    With synthetic wastewater, competitive adsorption characteristics of fluoride and phosphate on calcined Mg-Al-CO(3) layered double hydroxides (CLDH) were investigated. A series of batch experiments were performed to study the influence of various experimental parameters, such as pH, contact time, and order of addition of the anions on the competitive adsorption of fluoride and phosphate on CLDH. It was found that the optimal pH is around 6 and it took 24 h to attain equilibrium when fluoride and phosphate were simultaneous added. The order of addition of anions influenced the adsorption of fluoride and phosphate on CLDH. The kinetic data were analyzed using the pseudo first-order and pseudo second-order models and they were found to fit very well the pseudo second-order kinetic model. Data of equilibrium experiments were fitted well to Langmuir isotherm and the competitive monolayer adsorption capacities of fluoride and phosphate were found to be obviously lower than those of single anion at 25 °C. The results of X-ray diffraction, Scanning Electron Microscopy with energy-dispersive X-ray analyses, and ATR-FTIR demonstrate that the adsorption mechanism involves the rehydration of mixed metal oxides and concomitant intercalation of fluoride and phosphate ions into the interlayer to reconstruct the initial LDHs structure. Copyright © 2012 Elsevier B.V. All rights reserved.

  17. DEVELOPMENT OF CRYSTALLINE CERAMICS FOR IMMOBILIZATION OF ADVANCED FUEL CYCLE REPROCESSING WASTES

    Energy Technology Data Exchange (ETDEWEB)

    Fox, K.; Brinkman, K.

    2011-09-22

    its stability may be rate dependent, therefore limiting the activity of the waste for which it can be employed. Overall, these preliminary results indicate good radiation damage tolerance for the crystalline ceramic materials. The PCT results showed that, for all of the waste forms tested, the normalized release values for most of the elements measured, including all of the lanthanides and noble metals, were either very small or below the instrument detection limits. Elevated normalized release values were measured only for Cs, Mo, and Rb. It is difficult to draw further conclusions from these data until a benchmark material is developed for the PCT with this type of waste form. Calcined, simulated CS/LN/TM High Mo waste without additives had relatively low normalized release values for Cs, Mo, and Rb. A review of the chemical composition data for this sample showed that these elements were well retained after the calcination. Therefore, it will be useful to further characterize the calcined material to determine what form these elements are in after calcining. This, along with single phase studies on Cs containing crystal structures such as hollandite, should provide insight into the most ideal phases to incorporate these elements to produce a durable waste form.

  18. Municipal Solid Waste Management

    OpenAIRE

    Soni, Ajaykumar; Patil, Deepak; Argade, Kuldeep

    2016-01-01

    Waste management covers newly generated waste or waste from an onging process. When steps to reduce or even eliminate waste are to be considered, it is imperative that considerations should include total oversight, technical and management services of the total process.From raw material to the final product this includes technical project management expertise, technical project review and pollution prevention technical support and advocacy.Waste management also includes handling of waste, in...

  19. Supermarket food waste

    OpenAIRE

    Eriksson, Mattias

    2015-01-01

    Food waste occurs along the entire food supply chain and gives rise to great financial losses and waste of natural resources. The retail stage of the supply chain contributes significant masses of waste. Causes of this waste need to be identified before potential waste reduction measures can be designed, tested and evaluated. Therefore this thesis quantified retail food waste and evaluated selected prevention and valorisation measures, in order to determine how the carbon footprint of food ca...

  20. Test Summary Report INEEL Sodium-Bearing Waste Vitrification Demonstration RSM-01-1

    Energy Technology Data Exchange (ETDEWEB)

    Goles, Ronald W.; Perez, Joseph M.; Macisaac, Brett D.; Siemer, Darryl D.; Mccray, John A.

    2001-05-21

    The U.S. Department of Energy's Idaho National Engineering and Environmental Laboratory is storing large amounts of radioactive and mixed wastes. Most of the sodium-bearing wastes have been calcined, but about a million gallons remain uncalcined, and this waste does not meet current regulatory requirements for long-term storage and/or disposal. As a part of the Settlement Agreement between DOE and the State of Idaho, the tanks currently containing SBW are to be taken out of service by December 31, 2012, which requires removing and treatment the remaining SBW. Vitrification is the option for waste disposal that received the highest weighted score against the criteria used. Beginning in FY 2000, the INEEL high-level waste program embarked on a program for technology demonstration and development that would lead to conceptual design of a vitrification facility in the event that vitrification is the preferred alternative for SBW disposal. The Pacific Northwest National Laborator's Research-Scale Melter was used to conduct these initial melter-flowsheet evaluations. Efforts are underway to reduce the volume of waste vitrified, and during the current test, an overall SBW waste volume-reduction factor of 7.6 was achieved.

  1. Waste Transfer Stations

    DEFF Research Database (Denmark)

    Christensen, Thomas Højlund

    2011-01-01

    tion and transport is usually the most costly part of any waste management system; and when waste is transported over a considerable distance or for a long time, transferring the waste from the collection vehicles to more efficient transportation may be economically beneficial. This involves...... a transfer station where the transfer takes place. These stations may also be accessible by private people, offering flexibility to the waste system, including facilities for bulky waste, household hazardous waste and recyclables. Waste transfer may also take place on the collection route from small...... describes the main features of waste transfer stations, including some considerations about the economical aspects on when transfer is advisable....

  2. Chemical Waste and Allied Products.

    Science.gov (United States)

    Hung, Yung-Tse; Aziz, Hamidi Abdul; Ramli, Siti Fatihah; Yeh, Ruth Yu-Li; Liu, Lian-Huey; Huhnke, Christopher Robert

    2016-10-01

    This review of literature published in 2015 focuses on waste related to chemical and allied products. The topics cover the waste management, physicochemical treatment, aerobic granular, aerobic waste treatment, anaerobic granular, anaerobic waste treatment, chemical waste, chemical wastewater, fertilizer waste, fertilizer wastewater, pesticide wastewater, pharmaceutical wastewater, ozonation. cosmetics waste, groundwater remediation, nutrient removal, nitrification denitrification, membrane biological reactor, and pesticide waste.

  3. 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.

  4. Steam reforming of tar derived from lignin over pompom-like potassium-promoted iron-based catalysts formed on calcined scallop shell.

    Science.gov (United States)

    Guan, Guoqing; Kaewpanha, Malinee; Hao, Xiaogang; Zhu, Ai-Min; Kasai, Yutaka; Kakuta, Seiji; Kusakabe, Katsuki; Abudula, Abuliti

    2013-07-01

    In order to understand the improvement effect of potassium (K) on the catalytic activity of iron-loaded calcined scallop shell (CS) for the steam reforming tar derived from biomass, various K precursors were applied for the catalyst preparation. It is found that pompom-like iron-based particles with a mesoporous structure were easily formed on the surface of calcined scallop shell (CS) when K2CO3 was used as K precursor while no such kind of microsphere was formed when other kinds of K precursors such as KOH and KNO3 were applied. The optimum K-loading amount for the preparation of this catalyst was investigated. Based on the experimental results obtained, a mechanism for the formation of these microspheres was proposed. This pompom-like potassium-promoted iron-based catalyst showed a better catalytic activity and reusability for the steam reforming of tar derived from lignin. Copyright © 2013 Elsevier Ltd. All rights reserved.

  5. 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)

  6. Solid recovered fuels in the cement industry with special respect to hazardous waste.

    Science.gov (United States)

    Thomanetz, Erwin

    2012-04-01

    Cements with good technical properties have been produced in Europe since the nineteenth century and are now worldwide standardized high-quality mass products with enormous production numbers. The basic component for cement is the so-called clinker which is produced mainly from raw meal (limestone plus clay plus sands) in a rotary kiln with preheater and progressively with integrated calciner, at temperatures up to 1450 °C. This process requires large amounts of fossil fuels and is CO₂-intensive. But most CO₂ is released by lime decomposition during the burning process. In the 1980s the use of alternative fuels began--firstly in the form of used oil and waste tyres and then increasingly by pre-conditioned materials from commercial waste and from high calorific industrial waste (i.e. solid recovered fuel (SRF))--as well as organic hazardous waste materials such as solvents, pre-conditioned with sawdust. Therefore the cement industry is more and more a competitor in the waste-to-energy market--be it for municipal waste or for hazardous waste, especially concerning waste incineration, but also for other co-incineration plants. There are still no binding EU rules identifying which types of SRF or hazardous waste could be incinerated in cement kilns, but there are some well-made country-specific 'positive lists', for example in Switzerland and Austria. Thus, for proper planning in the cement industry as well as in the waste management field, waste disposal routes should be considered properly, in order to avoid surplus capacities on one side and shortage on the other.

  7. 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.

  8. ICPP calcined solids storage facility closure study. Volume II: Cost estimates, planning schedules, yearly cost flowcharts, and life-cycle cost estimates

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    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.

  9. Synthesis of microporous material faujasite-type from kaolin waste; Sintese de material microporoso do tipo faujasita a partir de rejeito de caulim

    Energy Technology Data Exchange (ETDEWEB)

    Hildebrando, E.A.; Valenzuela-Diaz, F.R., E-mail: edemarino@usp.b [Universidade de Sao Paulo (USP), SP (Brazil). Dept. de Engenharia Metalurgica e de Materiais. Lab. de Materias-Primas Particuladas e Solidos nao Metalicos; Angelica, R.S. [Universidade Federal do Para (UFPA), Belem, PA (Brazil). Inst. de Geociencias. Fac. de Geologia; Neves, R.F. [Universidade Federal do Para (UFPA), Belem, PA (Brazil). Inst. de Tecnologia. Fac. de Engenharia Quimica

    2010-07-01

    Zeolite with structure faujasite was synthesized using kaolin waste from kaolin processing industries for paper coating as predominant source of silicon and aluminum; the starting material was characterized by XRF, XRD, DTA/TG, SEM, and products obtained by XRD and SEM. Synthesis in hydrothermal conditions occurred on autoclave and time-temperature effects, as well as the relationship Si/Al were considered. The results show that the methodology developed with the waste of calcined kaolin reacting at 90 deg C for 20 hours in an alkaline medium, in the presence of an additional source of silica was obtained zeolite Y as single phase present in the product. (author)

  10. Introduction to Waste Management

    DEFF Research Database (Denmark)

    Christensen, Thomas Højlund

    2011-01-01

    Solid waste management is as old as human civilization, although only considered an engineering discipline for about one century. The change from the previous focus on public cleansing of the cities to modern waste management was primarily driven by industrialization, which introduced new materials...... and chemicals, dramatically changing the types and composition of waste, and by urbanization making waste management in urban areas a complicated and costly logistic operation. This book focuses on waste that commonly appears in the municipal waste management system. This chapter gives an introduction to modern...... waste management, including issues as waste definition, problems associated with waste, waste management criteria and approaches to waste management. Later chapters introduce aspects of engineering (Chapter 1.2), economics (Chapter 1.3) and regulation (Chapter 1.4)....

  11. The effect of calcination temperature on the capacitive properties of WO3-based electrochemical capacitors synthesized via a sol-gel method

    Science.gov (United States)

    Susanti, Diah; Wibawa, Rizky Narendra Dwi; Tananta, Lucky; Purwaningsih, Hariyati; Fajarin, Rindang; Kusuma, George Endri

    2013-12-01

    Electrochemical capacitor (EC) is a promising energy storage device which can be hybridized with other energy conversion or energy storage devices. One type of ECs is pseudocapacitor made of metal oxides. WO3 is an inexpensive semiconductor metal oxide which has many applications. However the application of WO3 as an EC material was rarely reported. Therefore in this research EC was prepared from WO3 nanomaterial synthesized by a sol-gel process. The WO3 gel was spin-coated on graphite substrates and calcined at various temperatures of 300°C, 400°C, 500°C and 600°C for 1 h. Cyclic voltammetry (CV) measurements were used to observe the capacitive property of the WO3 samples. SEM, XRD, FTIR and Brunauer-Emmett-Teller (BET) analyses were used to characterize the material structures. WO3 calcined at 400°C was proved to have the highest capacitance of 233.63 F·g-1 (1869 mF·cm-2) at a scan rate of 2 mV·s-1 in 1 mol/L H2SO4 between potentials -0.4 and 0.4 V vs. SCE. Moreover it also showed the most symmetric CV curves as the indication of a good EC. Hence WO3 calcined at 400°C is a potential candidate for EC material of pseudocapacitor type.

  12. Occupational exposure to carbon/coke fibers in plants that produce green or calcined petroleum coke and potential health effects: 2. Fiber concentrations.

    Science.gov (United States)

    Maxim, L Daniel; Galvin, Jennifer B; Niebo, Ron; Segrave, Alan M; Kampa, Otto A; Utell, Mark J

    2006-01-01

    We monitored exposure to various fibers among workers in eight plants operated by ConocoPhillips that produce green or calcined petroleum coke. Carbon/coke and other fibers, including calcium silicate, cellulose, gypsum, and iron silicate, were found in occupational samples. Carbon/coke fibers were found in bulk samples of calcined petroleum coke, the probable source of these fibers in occupational samples. Time-weighted average (TWA) total fiber concentrations were approximately lognormally distributed; 90% were fiber concentrations varied with plant, job (tasks), and type of coke. This was expected given the substantial differences in plant configuration, technology, and workplace practices among refineries and carbon plants. Carbon/coke fibers (identified and measured using transmission electron microscopy [TEM]) were found at all plants producing all types of calcined coke and not detected at any plant producing only green coke. Approximately 98% of all carbon/coke TWAs were carbon/coke TLA is certainly < or = 0.05 f/ml and probably < 0.03 f/ml.

  13. Waste shells of mollusk and egg as biodiesel production catalysts.

    Science.gov (United States)

    Viriya-Empikul, N; Krasae, P; Puttasawat, B; Yoosuk, B; Chollacoop, N; Faungnawakij, K

    2010-05-01

    The solid oxide catalysts derived from waste shells of egg, golden apple snail, and meretrix venus were employed to produce biodiesel from transesterification of palm olein oil. The shell materials were calcined in air at 800 degrees C with optimum time of 2-4h to transform calcium species in the shells into active CaO catalysts. All catalysts showed the high biodiesel production activity over 90% fatty acid methyl ester (FAME) in 2h, whilst the eggshell-derived catalyst showed comparable activity to the one derived from commercial CaCO(3). The catalytic activity was in accordance with the surface area of and the Ca content in the catalysts. Copyright 2009 Elsevier Ltd. All rights reserved.

  14. Hanford Site annual dangerous waste report: Volume 3, Part 1, Waste Management Facility report, dangerous waste

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1994-12-31

    This report contains information on hazardous wastes at the Hanford Site. Information consists of shipment date, physical state, chemical nature, waste description, handling method and containment vessel, waste number, waste designation, and amount of waste.

  15. Hanford Site annual dangerous waste report: Volume 3, Part 2, Waste Management Facility report, dangerous waste

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1944-12-31

    This report contains information on hazardous wastes at the Hanford Site. Information consists of shipment date, physical state, chemical nature, waste description, handling and containment vessel, waste number, waste designation and amount of waste.

  16. 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

  17. 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.

  18. Waste Package Lifting Calculation

    Energy Technology Data Exchange (ETDEWEB)

    H. Marr

    2000-05-11

    The objective of this calculation is to evaluate the structural response of the waste package during the horizontal and vertical lifting operations in order to support the waste package lifting feature design. The scope of this calculation includes the evaluation of the 21 PWR UCF (pressurized water reactor uncanistered fuel) waste package, naval waste package, 5 DHLW/DOE SNF (defense high-level waste/Department of Energy spent nuclear fuel)--short waste package, and 44 BWR (boiling water reactor) UCF waste package. Procedure AP-3.12Q, Revision 0, ICN 0, calculations, is used to develop and document this calculation.

  19. Commercial and Institutional Waste

    DEFF Research Database (Denmark)

    Christensen, Thomas Højlund; Fruergaard, Thilde

    2011-01-01

    Commercial and institutional waste is primarily from retail (stores), hotels, restaurants, health care (except health risk waste), banks, insurance companies, education, retirement homes, public services and transport. Within some of these sectors, e.g. retail and restaurants, large variations...... is handled in the municipal waste system, where information is easily accessible. An important part of commercial and institutional waste is packaging waste, and enterprises with large quantities of clean paper, cardboard and plastic waste may have their own facilities for baling and storing their waste...

  20. Understanding radioactive waste

    Energy Technology Data Exchange (ETDEWEB)

    Murray, R.L.

    1981-12-01

    This document contains information on all aspects of radioactive wastes. Facts are presented about radioactive wastes simply, clearly and in an unbiased manner which makes the information readily accessible to the interested public. The contents are as follows: questions and concerns about wastes; atoms and chemistry; radioactivity; kinds of radiation; biological effects of radiation; radiation standards and protection; fission and fission products; the Manhattan Project; defense and development; uses of isotopes and radiation; classification of wastes; spent fuels from nuclear reactors; storage of spent fuel; reprocessing, recycling, and resources; uranium mill tailings; low-level wastes; transportation; methods of handling high-level nuclear wastes; project salt vault; multiple barrier approach; research on waste isolation; legal requiremnts; the national waste management program; societal aspects of radioactive wastes; perspectives; glossary; appendix A (scientific American articles); appendix B (reference material on wastes). (ATT)

  1. Municipal Solid Waste Resources

    Energy Technology Data Exchange (ETDEWEB)

    None

    2016-06-01

    Municipal solid waste (MSW) is a source of biomass material that can be utilized for bioenergy production with minimal additional inputs. MSW resources include mixed commercial and residential garbage such as yard trimmings, paper and paperboard, plastics, rubber, leather, textiles, and food wastes. Waste resources such as landfill gas, mill residues, and waste grease are already being utilized for cost-effective renewable energy generation. MSW for bioenergy also represents an opportunity to divert greater volumes of residential and commercial waste from landfills.

  2. Influence of calcination temperature on Cd{sub 0.3}Co{sub 0.7}Fe{sub 2}O{sub 4} nanoparticles: Structural, thermal and magnetic properties

    Energy Technology Data Exchange (ETDEWEB)

    Reddy, Ch.Venkata, E-mail: cvrphy@gmail.com [School of Mechanical Engineering, Yeungnam University, 214-1, Dae-dong, Gyeongsan-si, Gyeongsangbuk-do 712-749 (Korea, Republic of); PrabhakarVattikuti, S.V. [School of Mechanical Engineering, Yeungnam University, 214-1, Dae-dong, Gyeongsan-si, Gyeongsangbuk-do 712-749 (Korea, Republic of); Ravikumar, R.V.S.S.N. [Department of Physics, Acharya Nagarjuna University, AP 522510 (India); Moon, Sang Jun, E-mail: nanobiomems@dgist.ac.kr [Cybernetics Laboratory, Daegu Gyeongbuk Institute of Science and Technology (DGIST) (Korea, Republic of); Shim, Jaesool, E-mail: jshim@ynu.ac.kr [School of Mechanical Engineering, Yeungnam University, 214-1, Dae-dong, Gyeongsan-si, Gyeongsangbuk-do 712-749 (Korea, Republic of)

    2015-11-15

    Cadmium substituted cobalt ferrite nanoparticles are synthesis using the chemical method. The as-prepared ferrite nanoparticles are calcinated at 300 °C and 600 °C respectively. The samples are studied using; Powder XRD, SEM with EDX, TEM, FT-IR, TG-DTA and vibrating sample magnetometer (VSM) in order to study the calcination temperature effect on structural, morphological and magnetic properties. The magnetic properties, like saturation magnetization and coercivity increases with increasing the calcination temperature. This enhancement is attributed to the transition from amulti-domain to a single-domain nature. The absorption bands observed at 588 cm{sup −1} (ν{sub 1}) and 440 cm{sup −1} (ν{sub 2}) are attributed to the vibrations of tetrahedral and octahedral complexes. The TG-DTA curves reveal the thermal stability of the prepared ferrite nanoparticles. The calcination temperature influences the magnetic properties, surface morphology and crystalline size. - Highlights: • Cd{sub 0.3}Co{sub 0.7}Fe{sub 2}O{sub 4} nanoparticles synthesized using the chemical co-precipitation. • The magnetization, coercivity values increases with increasing the calcination temperature. • The calcination temperature influences the magnetic properties and crystallite size. • The FTIR spectra results confirmed the vibrations of tetrahedral and octahedral complexes.

  3. Development of high-performance supercapacitor electrode derived from sugar industry spent wash waste.

    Science.gov (United States)

    Mahto, Ashesh; Gupta, Rajeev; Ghara, Krishna Kanta; Srivastava, Divesh N; Maiti, Pratyush; D, Kalpana; Rivera, Paul-Zavala; Meena, R; Nataraj, S K

    2017-10-15

    This study aims at developing supercapacitor materials from sugar and distillery industry wastes, thereby mediating waste disposal problem through reuse. In a two-step process, biomethanated spent wash (BMSW) was acid treated to produce solid waste sludge and waste water with significantly reduced total organic carbon (TOC) and biological oxygen demand (BOD) content. Further, waste sludge was directly calcined in presence of activating agent ZnCl2 in inert atmosphere resulting in high surface area (730-900m2g-1) carbon of unique hexagonal morphology. Present technique resulted in achieving two-faceted target of liquid-solid waste remediation and production of high-performance carbon material. The resulted high surface area carbon was tested in both three and two electrode systems. Electrochemical tests viz. cyclic voltammetry, galvanostatic charge-discharge and impedance measurement were carried out in aqueous KOH electrolyte yielding specific capacitance as high as 120Fg-1, whereas all solid supercapacitor devised using PVA/H3PO4 polyelectrolyte showed stable capacitance of 105Fg-1 at 0.2Ag-1. The presence of transition metal particles and hetero-atoms on carbon surface were confirmed by XPS, EDX and TEM analysis which enhanced the conductivity and imparted pseudocapacitance to some extent into the working electrode. The present study successfully demonstrated production of high-performance electrode material from dirtiest wastewater making process green, sustainable and economically viable. Copyright © 2017. Published by Elsevier B.V.

  4. Feasibility of disposing waste glyphosate neutralization liquor with cement rotary kiln

    Energy Technology Data Exchange (ETDEWEB)

    Bai, Y.; Bao, Y.B.; Cai, X.L.; Chen, C.H. [College of Materials Science and Engineering, Nanjing Tech University, Nanjing 210009 (China); State Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing Tech University, Nanjing 210009 (China); Ye, X.C., E-mail: yexuchu@njtech.edu.cn [College of Materials Science and Engineering, Nanjing Tech University, Nanjing 210009 (China); State Key Laboratory of Materials-Oriented Chemical Engineering, Nanjing Tech University, Nanjing 210009 (China)

    2014-08-15

    Highlights: • The waste neutralization liquor was injected directly into the kiln system. • No obvious effect on the quality of cement clinker. • The disposing method was a zero-discharge process. • The waste liquor can be used as an alternative fuel to reduce the coal consumption. - Abstract: The waste neutralization liquor generated during the glyphosate production using glycine-dimethylphosphit process is a severe pollution problem due to its high salinity and organic components. The cement rotary kiln was proposed as a zero discharge strategy of disposal. In this work, the waste liquor was calcinated and the mineralogical phases of residue were characterized by scanning electron microscope (SEM) and X-ray diffraction (XRD). The mineralogical phases and the strength of cement clinker were characterized to evaluate the influence to the products. The burnability of cement raw meal added with waste liquor and the calorific value of waste liquor were tested to evaluate the influence to the thermal state of the kiln system. The results showed that after the addition of this liquor, the differences of the main phases and the strength of cement clinker were negligible, the burnability of raw meal was improved; and the calorific value of this liquor was 6140 J/g, which made it could be considered as an alternative fuel during the actual production.

  5. CHARACTERIZATION AND DEVELOPMENT OF ECO-FRIENDLY CONCRETE USING INDUSTRIAL WASTE – A REVIEW

    Directory of Open Access Journals (Sweden)

    Rajesh Kumar

    2014-01-01

    Full Text Available At present in India, about 960 million metric tons of solid was te is being generated annually as byproducts during industrial, mining, municipal, agricultural and other processes. Advances in solid waste management resulted in alter native construction materials as a substitute to traditional materials like bricks, blocks, tiles, aggregates, ceramics, cement, lime, soil, timber and paint. To safeguard th e environment, efforts are being made for recycling different wastes and to utilize th em in value added applications. The cement industries have been making significan t progress in reducing carbon dioxide (CO 2 emissions through improvements in process technology and enhancements in process efficiency, but further improvements ar e limited because CO 2 production is inherent to the basic process of calcinations of limestone. In the past two decades, various investigations have been conducted on industri al wastes like flyash, blast furnace slag, Silica fume, rice husks and other industria l waste materials to act as cement replacements .This paper consist of a review extensively conducted on publications related to utilization of waste materials as cemen t replacement with an intention to develop a process so as to produce an eco-friendly concrete having similar or higher strength and thus simultaneously providing a remedy t o environmental hazards resulting from waste material disposal.

  6. Minimisation and utilisation of waste mineral sludge from sodium perborate production.

    Science.gov (United States)

    Grilc, Viktor; Jersan, Rok

    2002-10-01

    Various approaches to waste minimisation, waste treatment and recycling or safe disposal of the waste mineral sludge from sodium perborate production are presented and critically discussed. Some most promising actions for waste (or its harmful potential) reduction on the production level are identified. These include: a) use of better raw materials (richer boron ore), b) improvement of the ore leaching process, and c) intensification of sludge washing and dewatering. These source reduction measures have already resulted in 50% reduction of boron content in the sludge. Utilisation of the raw or treated (e.g. dried, compacted) waste sludge could be found in agriculture, civil engineering and construction material production. Agricultural use (as a lime substitute) is based on favourable content of calcium-magnesium minerals and alkali pH value of the sludge, and simultaneous absence of heavy metals. Application in civil engineering (as an aggregate) is possible after calcination, which is costly, or as a cement kiln additive. Stabilisation of sludge before disposal, when no utilisation is available, is possible by small addition of commercial binders (e.g. Portland cement) or larger amounts of pozzolanic wastes (e.g. coal fly ash).

  7. Calcium oxide derived from waste shells of mussel, cockle, and scallop as the heterogeneous catalyst for biodiesel production.

    Science.gov (United States)

    Buasri, Achanai; Chaiyut, Nattawut; Loryuenyong, Vorrada; Worawanitchaphong, Phatsakon; Trongyong, Sarinthip

    2013-01-01

    The waste shell was utilized as a bioresource of calcium oxide (CaO) in catalyzing a transesterification to produce biodiesel (methyl ester). The economic and environmen-friendly catalysts were prepared by a calcination method at 700-1,000°C for 4 h. The heterogeneous catalysts were characterized by X-ray diffraction (XRD), X-ray fluorescence (XRF), scanning electron microscopy (SEM), and the Brunauer-Emmett-Teller (BET) method. The effects of reaction variables such as reaction time, reaction temperature, methanol/oil molar ratio, and catalyst loading on the yield of biodiesel were investigated. Reusability of waste shell catalyst was also examined. The results indicated that the CaO catalysts derived from waste shell showed good reusability and had high potential to be used as biodiesel production catalysts in transesterification of palm oil with methanol.

  8. Calcium Oxide Derived from Waste Shells of Mussel, Cockle, and Scallop as the Heterogeneous Catalyst for Biodiesel Production

    Directory of Open Access Journals (Sweden)

    Achanai Buasri

    2013-01-01

    Full Text Available The waste shell was utilized as a bioresource of calcium oxide (CaO in catalyzing a transesterification to produce biodiesel (methyl ester. The economic and environmen-friendly catalysts were prepared by a calcination method at 700–1,000°C for 4 h. The heterogeneous catalysts were characterized by X-ray diffraction (XRD, X-ray fluorescence (XRF, scanning electron microscopy (SEM, and the Brunauer-Emmett-Teller (BET method. The effects of reaction variables such as reaction time, reaction temperature, methanol/oil molar ratio, and catalyst loading on the yield of biodiesel were investigated. Reusability of waste shell catalyst was also examined. The results indicated that the CaO catalysts derived from waste shell showed good reusability and had high potential to be used as biodiesel production catalysts in transesterification of palm oil with methanol.

  9. Determination of the Structure of Vitrified Hydroceramic/CBC Waste Form Glasses Manufactured from DOE Reprocessing Waste

    Energy Technology Data Exchange (ETDEWEB)

    Scheetz, B.E.; White, W. B.; Chesleigh, M.; Portanova, A.; Olanrewaju, J.

    2005-05-31

    The selection of a glass-making option for the solidification of nuclear waste has dominated DOE waste form programs since the early 1980's. Both West Valley and Savannah River are routinely manufacturing glass logs from the high level waste inventory in tank sludges. However, for some wastes, direct conversion to glass is clearly not the optimum strategy for immobilization. INEEL, for example, has approximately 4400 m{sup 3} of calcined high level waste with an activity that produces approximately 45 watts/m{sup 3}, a rather low concentration of radioactive constituents. For these wastes, there is value in seeking alternatives to glass. An alternative approach has been developed and the efficacy of the process demonstrated that offers a significant savings in both human health and safety exposures and also a lower cost relative to the vitrification option. The alternative approach utilizes the intrinsic chemical reactivity of the highly alkaline waste with the addition of aluminosilicate admixtures in the appropriate proportions to form zeolites. The process is one in which a chemically bonded ceramic is produced. The driving force for reaction is derived from the chemical system itself at very modest temperatures and yet forms predominantly crystalline phases. Because the chemically bonded ceramic requires an aqueous medium to serve as a vehicle for the chemical reaction, the proposed zeolite-containing waste form can more adequately be described as a hydroceramic. The hydrated crystalline materials are then subject to hot isostatic pressing (HIP) which partially melts the material to form a glass ceramic. The scientific advantages of the hydroceramic/CBC approach are: (1) Low temperature processing; (2) High waste loading and thus only modest volumetric bulking from the addition of admixtures; (3) Ability to immobilize sodium; (4) Ability to handle low levels of nitrate (2-3% NO{sub 3}{sup -}); (5) The flexibility of a vitrifiable waste; and (6) A process

  10. 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.

  11. Waste catalysts for waste polymer.

    Science.gov (United States)

    Salmiaton, A; Garforth, A

    2007-01-01

    Catalytic cracking of high-density polyethylene (HDPE) over fluid catalytic cracking (FCC) catalysts (1:6 ratio) was carried out using a laboratory fluidized bed reactor operating at 450 degrees C. Two fresh and two steam deactivated commercial FCC catalysts with different levels of rare earth oxide (REO) were compared as well as two used FCC catalysts (E-Cats) with different levels of metal poisoning. Also, inert microspheres (MS3) were used as a fluidizing agent to compare with thermal cracking process at BP pilot plant at Grangemouth, Scotland, which used sand as its fluidizing agent. The results of HDPE degradation in terms of yield of volatile hydrocarbon product are fresh FCC catalysts>steamed FCC catalysts approximately used FCC catalysts. The thermal cracking process using MS3 showed that at 450 degrees C, the product distribution gave 46 wt% wax, 14% hydrocarbon gases, 8% gasoline, 0.1% coke and 32% nonvolatile product. In general, the product yields from HDPE cracking showed that the level of metal contamination (nickel and vanadium) did not affect the product stream generated from polymer cracking. This study gives promising results as an alternative technique for the cracking and recycling of polymer waste.

  12. Hazardous Waste: Learn the Basics of Hazardous Waste

    Science.gov (United States)

    ... Agency Search Search Hazardous Waste Contact Us Share Learn the Basics of Hazardous Waste Hazardous waste that ... Regulations part 261 . Select a question below to learn more about each step in the hazardous waste ...

  13. Hanford Site annual dangerous waste report: Volume 1, Part 2, Generator dangerous waste report, dangerous waste

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1994-12-31

    This report contains information on hazardous materials at the Hanford Site. Information consists of shipment date, physical state, chemical nature, waste description, waste number, weight, and waste designation.

  14. 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.

  15. 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: CO3(2-)>SO4(2-)>H2PO4(-)>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.

  16. Highly enhanced photocatalytic reduction of Cr(VI) on AgI/TiO{sub 2} under visible light irradiation: Influence of calcination temperature

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Qi; Shi, Xiaodong; Xu, Jianjia [School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou 310018 (China); Crittenden, John C. [The Brook Byer Institute for Sustainable Systems and School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta,GA 30332 (United States); Liu, Enqin; Zhang, Yi [School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou 310018 (China); Cong, Yanqing, E-mail: yqcong@hotmail.com [School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou 310018 (China)

    2016-04-15

    Highlights: • β-AgI riched AgI/TiO2 was obtained after simple heat pretreatment at 350 °C. • Greatly enhanced visible light response was observed on AgI/TiO2-350. • AgI/TiO2-350 exhibited superior photocatalytic activity and stability. • 5 times rate constant for Cr(VI) reduction was achieved. • More efficient separation and easier transfer of e{sup −}–h{sup +} pairs were facilitated. - Abstract: AgI/TiO{sub 2} was prepared using a dissolution-precipitation method, followed by calcination at different temperatures (100–700 °C). The as-prepared AgI/TiO{sub 2} powders were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible diffuse reflectance spectroscopy (UV–Vis-DRS) and electrochemical impedance spectroscopy (EIS). The results revealed that calcination temperature significantly impacted the visible light absorption of AgI/TiO{sub 2} along with a shift from metastable γ-AgI to relatively stable β-AgI. We found that highest photocatalytic reduction rate of Cr(VI) and β-AgI content were obtained for a calcination temperature of 350 °C. Furthermore, the pseudo-first order rate constant was five times that for a photocatalyst calcined at 100 °C. The dramatically enhanced reduction rate of Cr(VI) was attributed to enhanced visible light absorption and greatly reduced charge transfer resistance, which eventually facilitates more efficient separation and easier transfer of photogenerated electron–hole pairs to the catalyst surface. Other experimental conditions were also carefully investigated and optimized with initial AgI loading percentage (5%), catalyst dosage (1.0 g/L), coexisting organics (1.0 mmol/L EDTA) and pH (1–2). The optimal AgI/TiO{sub 2} exhibited good stability with little change in activity after 5 cycles.

  17. Construction and Demolition Waste

    DEFF Research Database (Denmark)

    Christensen, Thomas Højlund; Andersen, L.

    2011-01-01

    Construction and demolition waste (C&D waste) is the waste generated during the building, repair, remodeling or removal of constructions. The constructions can be roads, residential housing and nonresidential buildings. C&D waste has traditionally been considered without any environmental problems...... and has just been landfilled. However, in recent years more focus has been put on C&D waste and data are starting to appear. One reason is that it has been recognized that C&D waste may include many materials that are contaminated either as part of their original design or through their use and therefore...... should be managed accordingly. Another reason is that it has been documented that a large fraction of C&D waste (about 90 %) can be easily recycled and thus can conserve landfill capacity. C&D waste may conveniently be divided into three subcategories: Buildings, roads and excavations. This chapter...

  18. Waste canister for storage of nuclear wastes

    Science.gov (United States)

    Duffy, James B.

    1977-01-01

    A waste canister for storage of nuclear wastes in the form of a solidified glass includes fins supported from the center with the tips of the fins spaced away from the wall to conduct heat away from the center without producing unacceptable hot spots in the canister wall.

  19. Business unusual - Waste Act implementation: solid waste

    CSIR Research Space (South Africa)

    Oelofse, Suzanna HH

    2013-08-01

    Full Text Available The preamble to the Waste Act (2008) is very clear that, as a result of this legislation, waste management in South Africa will never be the same again. This should send a clear message that ‘business as usual’ will no longer be sufficient....

  20. Biohazardous waste management plan.

    Energy Technology Data Exchange (ETDEWEB)

    Lane, Todd W.

    2004-01-01

    This plan describes the process for managing non-medical biohazardous waste at Sandia National Laboratories California. It applies to operations at the Chemical and Radiation Detection Laboratory (CRDL), Building 968, and other biosafety level 1 or 2 activities at the site. It addresses the accumulation, storage, treatment and disposal of biohazardous waste and sharps waste. It also describes the procedures to comply with regulatory requirements and SNL policies applicable to non-medical biohazardous waste.

  1. Medical waste management plan.

    Energy Technology Data Exchange (ETDEWEB)

    Lane, Todd W.; VanderNoot, Victoria A.

    2004-12-01

    This plan describes the process for managing research generated medical waste at Sandia National Laboratories/California. It applies to operations at the Chemical and Radiation Detection Laboratory (CRDL), Building 968, and other biosafety level 1 or 2 activities at the site. It addresses the accumulation, storage, treatment and disposal of medical waste and sharps waste. It also describes the procedures to comply with regulatory requirements and SNL policies applicable to medical waste.

  2. INTEGRATED WASTE MANAGEMENT SYSTEM

    OpenAIRE

    Truptimala Patanaik; Ambika Priyadarshini Mishra; Aishariya Durga; Gayatri Avipsa

    2016-01-01

    The towns and cities have become the centres of population growth and require three essential services viz., water supply, waste water treatment and solid wastes disposal. The tremendous increase in population accelerates the amount of municipal solid waste (MSW) generation. Hence, the solid waste management (SWM) is one of the essential municipal services, to protect the environment, safeguard public health services and improve productivity.   In this context the case study is c...

  3. Solid waste handling

    Energy Technology Data Exchange (ETDEWEB)

    Parazin, R.J.

    1995-05-31

    This study presents estimates of the solid radioactive waste quantities that will be generated in the Separations, Low-Level Waste Vitrification and High-Level Waste Vitrification facilities, collectively called the Tank Waste Remediation System Treatment Complex, over the life of these facilities. This study then considers previous estimates from other 200 Area generators and compares alternative methods of handling (segregation, packaging, assaying, shipping, etc.).

  4. Household food waste

    NARCIS (Netherlands)

    Wahlen, S.; Winkel, Thomas

    2017-01-01

    Food waste is debated not only in the light of sustainable consumption in research and policy, but also in the broader public. This article focuses on food waste in household contexts, what is widely believed the end of the food chain. However, household food waste is far more complex and intricate

  5. Nuclear wastes; Dechets nucleaires

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2004-07-01

    Here is made a general survey of the situation relative to radioactive wastes. The different kinds of radioactive wastes and the different way to store them are detailed. A comparative evaluation of the situation in France and in the world is made. The case of transport of radioactive wastes is tackled. (N.C.)

  6. Waste disposal package

    Science.gov (United States)

    Smith, M.J.

    1985-06-19

    This is a claim for a waste disposal package including an inner or primary canister for containing hazardous and/or radioactive wastes. The primary canister is encapsulated by an outer or secondary barrier formed of a porous ceramic material to control ingress of water to the canister and the release rate of wastes upon breach on the canister. 4 figs.

  7. Radioactive Wastes. Revised.

    Science.gov (United States)

    Fox, Charles H.

    This publication is one of a series of information booklets for the general public published by the United States Atomic Energy Commission. This booklet deals with the handling, processing and disposal of radioactive wastes. Among the topics discussed are: The Nature of Radioactive Wastes; Waste Management; and Research and Development. There are…

  8. Rock & Roll : Waste seperation

    NARCIS (Netherlands)

    Beunder, L.; Rem, P.C.; Van Den Berg, R.

    2000-01-01

    Five hundred tonnes of glass, 1 million tonnes of plastic,14 million tonnes of building and demolition waste, 7 million tonnes of household waste, 3 million tonnes of packaging, 3.5 million tonnes of paper and board, and 300,000 old cars. All part of the annual harvest of waste materials in the

  9. Waste vs Resource Management

    CSIR Research Space (South Africa)

    Oelofse, Suzanna HH

    2014-10-01

    Full Text Available Recent global waste statistics show that in the order of 70% of all municipal waste generated worldwide is disposed at landfill, 11% is treated in thermal and Waste-to-Energy (WtE) facilities and the rest (19%) is recycled or treated by mechanical...

  10. Green Biodiesel Synthesis Using Waste Shells as Sustainable Catalysts with Camelina sativa Oil

    Directory of Open Access Journals (Sweden)

    Yelda Hangun-Balkir

    2016-01-01

    Full Text Available Waste utilization is an essential component of sustainable development and waste shells are rarely used to generate practical products and processes. Most waste shells are CaCO3 rich, which are converted to CaO once calcined and can be employed as inexpensive and green catalysts for the synthesis of biodiesel. Herein, we utilized lobster and eggshells as green catalysts for the transesterification of Camelina sativa oil as feedstock into biodiesel. Camelina sativa oil is an appealing crop option as feedstock for biodiesel production because it has high tolerance of cold weather, drought, and low-quality soils and contains approximately 40% oil content. The catalysts from waste shells were characterized by X-ray powder diffraction, Fourier Transform Infrared Spectroscopy, and Scanning Electron Microscope. The product, biodiesel, was studied by 1H NMR and FTIR spectroscopy. The effects of methanol to oil ratio, reaction time, reaction temperature, and catalyst concentration were investigated. Optimum biodiesel yields were attained at a 12 : 1 (alcohol : oil molar ratio with 1 wt.% heterogeneous catalysts in 3 hours at 65°C. The experimental results exhibited a first-order kinetics and rate constants and activation energy were calculated for the transesterification reaction at different temperatures. The fuel properties of the biodiesel produced from Camelina sativa oil and waste shells were compared with those of the petroleum-based diesel by using American Society for Testing and Materials (ASTM standards.

  11. Influence of Zn/Fe Molar Ratio on Optical and Magnetic Properties of ZnO and ZnFe2O4 Nanocrystal as Calcined Products of Layered Double Hydroxides

    Directory of Open Access Journals (Sweden)

    Abdullah Ahmed Ali Ahmed

    2014-01-01

    Full Text Available The coprecipitation method has been used to synthesize layered double hydroxide (Zn-Fe-LDH nanostructure at different Zn2+/Fe3+ molar ratios. The structural properties of samples were studied using powder X-ray diffraction (PXRD. LDH samples were calcined at 600°C to produce mixed oxides (ZnO and ZnFe2O4. The crystallite size of mixed oxide was found in the nanometer scale (18.1 nm for ZnFe2O4 and 43.3 nm for ZnO. The photocatalytic activity of the calcination products was investigated using ultraviolet-visible-near infrared (UV-VIS-NIR diffuse reflectance spectroscopy. The magnetic properties of calcined LDHs were investigated using a vibrating sample magnetometer (VSM. The calcined samples showed a paramagnetic behavior for all Zn2+/Fe3+ molar ratios. The effect of molar ratio on magnetic susceptibility of the calcined samples was also studied.

  12. Spectroscopic properties of MgAl{sub 2−x}O{sub 4}:xCr{sup 3+} nanoparticles prepared by a high-temperature calcination method

    Energy Technology Data Exchange (ETDEWEB)

    Du, Xinhua [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004 (China); Tian, Hai [Science and Technology on Vacuum Technology and Physics Laboratory, Lanzhou 730000, Gansu (China); Yao, Shiyue [State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004 (China); Long, Yumei [College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Liang, Bo, E-mail: liangbo@ysu.edu.cn [State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004 (China); Li, Weifeng, E-mail: liweifeng@suda.edu.cn [State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004 (China)

    2015-12-01

    In this study, Cr{sup 3+}-doped MgAl{sub 2}O{sub 4} nanophosphors have been prepared via a facile high-temperature calcination route. The structure and morphology of the products were characterized by x-ray diffraction (XRD), scanning electron microscope (SEM) and transmission electron microscopy (TEM) techniques, which confirmed the typical spinel MgAl{sub 2}O{sub 4} phase and sphere-like shape with particle size distribution of 50–80 nm. It was found that the Cr{sup 3+}-doped MgAl{sub 2}O{sub 4} can be efficiently excited by visible light and exhibits intense red emission peaking at 695 nm, corresponding to the {sup 2}E{sub g}→{sup 4}A{sub 2g} transition of Cr{sup 3+} ions. The evolution of the luminescent properties on the Cr-doping concentration (0, 0.5, 1, 2, 3, 4 and 6 mol%) was then investigated and the optimal concentration was 3.0 mol%. It is believed that active intermediates and gases created in the calcining process play important roles not only on the formation of the monodispersed nanoparticles, but also on the homogeneous doping of Cr{sup 3+} at high concentration.

  13. SOx removal by calcined MgAlFe hydrotalcite-like materials: effect of the chemical composition and the cerium incorporation method.

    Science.gov (United States)

    Cantú, Manuel; López-Salinas, Esteban; Valente, Jaime S; Montiel, Ramon

    2005-12-15

    Sulfur oxides are one of the most hazardous atmospheric pollutants since they contribute directly to acid rain formation. Consequently, stringent environmental regulations limit atmospheric SOx emissions, motivating research on efficient ways to reduce them. To supply an alternative to reduce these emissions in fluid catalytic cracking units, this study discloses efficient SOx reducing materials based on calcined MgAlFe hydrotalcite-like compounds (HT's). Thus, HT materials were synthesized by several methods including cerium addition. The adsorption of SO2 was carried out by contacting the calcined solid with a mixture of SO2 (1%) in air at 650 degrees C. It was demonstrated that the isomorphic incorporation of iron increased its reduction capability which was reflected in higher reduction rates and metal sulfate reduction grade at 550 degrees C. Moreover, when cerium was present in the iron-containing materials the saturation rate was improved, because cerium oxide promotes the oxidation of SO2 to SO3. The way cerium is incorporated influences the SO2 adsorption capacity.

  14. Effect of calcination temperature on the activity of solid Ca/Al composite oxide-based alkaline catalyst for biodiesel production.

    Science.gov (United States)

    Meng, Yong-Lu; Wang, Bo-Yang; Li, Shu-Fen; Tian, Song-Jiang; Zhang, Min-Hua

    2013-01-01

    A solid Ca/Al composite oxide-based alkaline catalyst containing Ca(12)Al(14)O(33) and CaO was prepared by chemical synthesis and thermal activation from sodium aluminate solution and calcium hydroxide emulsion. The effect of calcination temperatures ranging from 120 °C to 1000 °C on activity of the catalyst was investigated. The catalyst calcined at 600 °C showed the highest activity with >94% yield of fatty acid methyl esters (i.e. biodiesel) when applied to the transesterification of rapeseed oil at a methanol:oil molar ratio of 15:1 at 65 °C for 3h. Structure and properties of the catalyst were studied and the characterizations with XRD, TGA, FTIR, BET, and SEM demonstrated that the performance of the catalyst was closely related to its specific surface area and crystalline structure. In particular, the generation of crystalline Ca(12)Al(14)O(33) improved the catalytic activity due its synergistic effect with CaO. Copyright © 2012 Elsevier Ltd. All rights reserved.

  15. 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.

  16. 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.

  17. 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.

  18. Technology development at the Pacific Northwest Laboratory high-level waste management history

    Energy Technology Data Exchange (ETDEWEB)

    McElroy, J.L. [Geosafe Corp., Richland, WA (United States); Platt, A.M.

    1996-12-31

    During WWII and the post-WWII years, until the late 1950`s, plutonium production was Hanford`s primary mission. This mission produced an enormous legacy of wastes that have themselves become the new mission at Hanford. Waste management, as practiced at Hanford, during the defense production years was in many ways unique to Hanford, taking advantage of the dry climate, distance from the Columbia river and depth to the water table. Near-surface storage in tanks, ion exchange in seepage trenches and cribs, and near surface burial were the norm. Isolation of the wastes by the high and dry nature of the 200 Area plateau, where reprocessing and waste management took place, was one of the reasons Hanford had been selected for it`s nuclear mission. Thus, location was a significant aspect of the initial waste management program at Hanford. Treatment, other than simple chemical steps such as neutralization and ion exchange, had not been considered necessary to the mission and was therefore not developed. To support the development of commercial nuclear power and to provide improved means of handling nuclear wastes, new waste management programs were initiated in the 1950`s by the Atomic Energy Commission. The programs focused on high level waste. They included `spray calcination/vitrification` at Hanford Laboratories. Hanford Labs later became Pacific Northwest Laboratories (PNL) when Battelle Memorial Institute became the Operating Contractor in 1965. In 1996, it was renamed Pacific Northwest National Laboratory (PNNL). The purpose of this paper is to describe the HLW projects and programs that followed from this early HLW R&D at PNNL.

  19. Mixed waste management options

    Energy Technology Data Exchange (ETDEWEB)

    Owens, C.B.; Kirner, N.P. [EG and G Idaho, Inc., Idaho Falls, ID (United States). Idaho National Engineering Lab.

    1991-12-31

    Disposal fees for mixed waste at proposed commercial disposal sites have been estimated to be $15,000 to $40,000 per cubit foot. If such high disposal fees are imposed, generators may be willing to apply extraordinary treatment or regulatory approaches to properly dispose of their mixed waste. This paper explores the feasibility of several waste management scenarios and attempts to answer the question: Can mixed waste be managed out of existence? Existing data on commercially generated mixed waste streams are used to identify the realm of mixed waste known to be generated. Each waste stream is evaluated from both a regulatory and technical perspective in order to convert the waste into a strictly low-level radioactive or a hazardous waste. Alternative regulatory approaches evaluated in this paper include a delisting petition, no migration petition, and a treatability variance. For each waste stream, potentially available treatment options are identified that could lead to these variances. Waste minimization methodology and storage for decay are also considered. Economic feasibility of each option is discussed broadly.

  20. Waste Management Technical Manual

    Energy Technology Data Exchange (ETDEWEB)

    Buckingham, J.S. [ed.

    1967-08-31

    This Manual has been prepared to provide a documented compendium of the technical bases and general physical features of Isochem Incorporated`s Waste Management Program. The manual is intended to be used as a means of training and as a reference handbook for use by personnel responsible for executing the Waste Management Program. The material in this manual was assembled by members of Isochem`s Chemical Processing Division, Battelle Northwest Laboratory, and Hanford Engineering Services between September 1965 and March 1967. The manual is divided into the following parts: Introduction, contains a summary of the overall Waste Management Program. It is written to provide the reader with a synoptic view and as an aid in understanding the subsequent parts; Feed Material, contains detailed discussion of the type and sources of feed material used in the Waste Management Program, including a chapter on nuclear reactions and the formation of fission products; Waste Fractionization Plant Processing, contains detailed discussions of the processes used in the Waste Fractionization Plant with supporting data and documentation of the technology employed; Waste Fractionization Plant Product and Waste Effluent Handling, contains detailed discussions of the methods of handling the product and waste material generated by the Waste Fractionization Plant; Plant and Equipment, describes the layout of the Waste Management facilities, arrangement of equipment, and individual equipment pieces; Process Control, describes the instruments and analytical methods used for process control; and Safety describes process hazards and the methods used to safeguard against them.

  1. Mixed waste: Proceedings

    Energy Technology Data Exchange (ETDEWEB)

    Moghissi, A.A.; Blauvelt, R.K.; Benda, G.A.; Rothermich, N.E. [eds.] [Temple Univ., Philadelphia, PA (United States). Dept. of Environmental Safety and Health

    1993-12-31

    This volume contains the peer-reviewed and edited versions of papers submitted for presentation a the Second International Mixed Waste Symposium. Following the tradition of the First International Mixed Waste Symposium, these proceedings were prepared in advance of the meeting for distribution to participants. The symposium was organized by the Mixed Waste Committee of the American Society of Mechanical Engineers. The topics discussed at the symposium include: stabilization technologies, alternative treatment technologies, regulatory issues, vitrification technologies, characterization of wastes, thermal technologies, laboratory and analytical issues, waste storage and disposal, organic treatment technologies, waste minimization, packaging and transportation, treatment of mercury contaminated wastes and bioprocessing, and environmental restoration. Individual abstracts are catalogued separately for the data base.

  2. Introduction to Waste Engineering

    DEFF Research Database (Denmark)

    Christensen, Thomas Højlund

    2011-01-01

    Solid waste management as introduced in Chapter 1.1 builds in many ways on engineering. Waste engineering here means the skills and ability to understand quantitatively how a waste management system works in such a detail that waste management can be planned, facilities can be designed and sited...... and systems can be operated in a way that is environmentally sound, technical feasible, economically efficient and socially acceptable. This applies to all scales of relevance: (1) national surveys of energy use and material flows determining the frame for politically setting goals in waste management, (2......) regional plans for waste management, including (3) the selection of main management technologies and siting of facilities, (4) the design of individual technological units and, for example, (5) the operation of recycling schemes within a municipality. This chapter gives an introduction to waste engineering...

  3. Cleaning Up Electronic Waste (E-Waste)

    Science.gov (United States)

    While accurate data on the amount of e-waste being exported from the U.S. are not available, the United States government is concerned that these exports are being mismanaged abroad, causing serious public health and environmental hazards.

  4. TSA waste stream and final waste form composition

    Energy Technology Data Exchange (ETDEWEB)

    Grandy, J.D.; Eddy, T.L.; Anderson, G.L.

    1993-01-01

    A final vitrified waste form composition, based upon the chemical compositions of the input waste streams, is recommended for the transuranic-contaminated waste stored at the Transuranic Storage Area of the Radioactive Waste Management Complex at the Idaho National Engineering Laboratory. The quantities of waste are large with a considerable uncertainty in the distribution of various waste materials. It is therefore impractical to mix the input waste streams into an ``average`` transuranic-contaminated waste. As a result, waste stream input to a melter could vary widely in composition, with the potential of affecting the composition and properties of the final waste form. This work examines the extent of the variation in the input waste streams, as well as the final waste form under conditions of adding different amounts of soil. Five prominent Rocky Flats Plant 740 waste streams are considered, as well as nonspecial metals and the ``average`` transuranic-contaminated waste streams. The metals waste stream is the most extreme variation and results indicate that if an average of approximately 60 wt% of the mixture is soil, the final waste form will be predominantly silica, alumina, alkaline earth oxides, and iron oxide. This composition will have consistent properties in the final waste form, including high leach resistance, irrespective of the variation in waste stream. For other waste streams, much less or no soil could be required to yield a leach resistant waste form but with varying properties.

  5. Solid Waste Management Plan. Revision 4

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-04-26

    The waste types discussed in this Solid Waste Management Plan are Municipal Solid Waste, Hazardous Waste, Low-Level Mixed Waste, Low-Level Radioactive Waste, and Transuranic Waste. The plan describes for each type of solid waste, the existing waste management facilities, the issues, and the assumptions used to develop the current management plan.

  6. Calculation of percent shrinkage in human fetal diaphyseal lengths from fresh bone to carbonized and calcined bone using Petersohn and Köhler's data.

    Science.gov (United States)

    Huxley, A K; Kósa, F

    1999-05-01

    Calculation of age from fetal and newborn remains may be problematic, and when these remains are altered by maceration, decomposition or burning, age may be more difficult to discern. When soft tissue indicators are transformed, then two techniques exist for accurate age determination; dental development, which may prove difficult given the degree of tissue alteration; and appearance, size and fusion of ossification centers, including diaphyseal length, which may yield inaccurate ages if shrinkage is not accounted for. This study is undertaken to facilitate age calculation by systematically re-evaluating diaphyseal shrinkage and determine shrinkage rates from wet to carbonized states and wet to calcined states using Petersohn and Köhler's data, originally published in German and then published in Fazekas and Kósa (1978:362-369). Average shrinkage, standard deviation, minimum and maximum values are calculated for each diaphysis and then for all diaphyses between 4-10 lunar months (LM) and for newborns. Associated values for carbonized diaphyses are: 4 LM--32.50% +/- 12.12%; 5 LM--14.04% +/- 4.44%; 6 LM--6.78% +/- 1.06%; 7 LM--4.18% +/- 0.31%; 8 LM--3.47% +/- 0.42%; 9 LM--3.05% +/- 0.18%; 10 LM--2.46% +/- 0.67%; and in newborns 2.16% +/- 0.29%. Similar values for calcined diaphyses are: 4 LM--40.11% +/- 17.51%; 5 LM--18.29% +/- 4.42%; 6 LM--9.84% +/- 1.27%; 7 LM--9.82% +/- 0.51%; 8 LM--9.42% +/- 0.72%; 9 LM--9.45% +/- 0.33%; 10 LM--8.94% +/- 0.37%; and in newborns 8.96% +/- 0.49%. These findings suggest that percent shrinkage due to carbonization and calcination is greatest in the earliest age groups, decreasing substantially with advancing age. The rates of shrinkage, however, vary by the burning process utilized and age group studied. These general findings are similar to those of Petersohn and Köhler, yet specific values for percent shrinkage vary greatly from values cited in this analysis. These data provide a means to assess the degree of shrinkage that

  7. 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}.

  8. Waste statistics 2004

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2006-04-07

    The 2004 reporting to the ISAG comprises 394 plants owned by 256 enterprises. In 2003, reports covered 403 plants owned by 273 enterprises. Waste generation in 2004 is compared to targets for 2008 in the government's Waste Strategy 2005-2008. The following summarises waste generation in 2004: 1) In 2004, total reported waste arisings amounted to 13,359,000 tonnes, which is 745,000 tonnes, or 6 per cent, more than in 2003. 2) If amounts of residues from coal-fired power plants are excluded from statistics, waste arisings in 2004 were 12,179,000 tonnes, which is a 9 per cent increase from 2003. 3) If amounts of residues from coal-fired power plants and waste from the building and construction sector are excluded from statistics, total waste generation in 2004 amounted to 7,684,000 tonnes, which is 328,000 tonnes, or 4 per cent, more than in 2002. In other words, there has been an increase in total waste arisings, if residues and waste from building and construction are excluded. Waste from the building and construction sector is more sensitive to economic change than most other waste. 4) The total rate of recycling was 65 per cent. The 2008 target for recycling is 65 per cent. The rate of recycling in 2003 was also 65 per cent. 5) The total amount of waste led to incineration amounted to 26 per cent, plus an additional 1 per cent left in temporary storage to be incinerated at a later time. The 2008 target for incineration is 26 per cent. These are the same percentage figures as applied to incineration and storage in 2003. 6) The total amount of waste led to landfills amounted to 8 per cent, which is one percentage point better than the overall landfill target of a maximum of 9 per cent landfilling in 2008. Also in 2003, 8 per cent of the waste was landfilled. 7) The targets for treatment of waste from individual sectors are still not being met: too little waste from households and the service sector is being recycled, and too much waste from industry is being

  9. Ceramics in nuclear waste management

    Energy Technology Data Exchange (ETDEWEB)

    Chikalla, T D; Mendel, J E [eds.

    1979-05-01

    Seventy-three papers are included, arranged under the following section headings: national programs for the disposal of radioactive wastes, waste from stability and characterization, glass processing, ceramic processing, ceramic and glass processing, leaching of waste materials, properties of nuclear waste forms, and immobilization of special radioactive wastes. Separate abstracts were prepared for all the papers. (DLC)

  10. Operational Waste Volume Projection

    Energy Technology Data Exchange (ETDEWEB)

    STRODE, J.N.

    1999-08-24

    Waste receipts to the double-shell tank system are analyzed and wastes through the year 2018 are projected based on assumption as of July 1999. A computer simulation of site operations is performed, which results in projections of tank fill schedules, tank transfers, evaporator operations, tank retrieval, and aging waste tank usage. This projection incorporates current budget planning and the clean-up schedule of the Tri-Party Agreement.

  11. Operational waste volume projection

    Energy Technology Data Exchange (ETDEWEB)

    Koreski, G.M.

    1996-09-20

    Waste receipts to the double-shell tank system are analyzed and wastes through the year 2015 are projected based on generation trends of the past 12 months. A computer simulation of site operations is performed, which results in projections of tank fill schedules, tank transfers, evaporator operations, tank retrieval, and aging waste tank usage. This projection incorporates current budget planning and the clean-up schedule of the Tri-Party Agreement. Assumptions were current as of June 1996.

  12. Waste inspection tomography (WIT)

    Energy Technology Data Exchange (ETDEWEB)

    Bernardi, R.T. [Bio-Imaging Research, Inc., Lincolnshire, IL (United States)

    1995-10-01

    Waste Inspection Tomography (WIT) provides mobile semi-trailer mounted nondestructive examination (NDE) and assay (NDA) for nuclear waste drum characterization. WIT uses various computed tomography (CT) methods for both NDE and NDA of nuclear waste drums. Low level waste (LLW), transuranic (TRU), and mixed radioactive waste can be inspected and characterized without opening the drums. With externally transmitted x-ray NDE techniques, WIT has the ability to identify high density waste materials like heavy metals, define drum contents in two- and three-dimensional space, quantify free liquid volumes through density and x-ray attenuation coefficient discrimination, and measure drum wall thickness. With waste emitting gamma-ray NDA techniques, WIT can locate gamma emitting radioactive sources in two- and three-dimensional space, identify gamma emitting, isotopic species, identify the external activity levels of emitting gamma-ray sources, correct for waste matrix attenuation, provide internal activity approximations, and provide the data needed for waste classification as LLW or TRU.

  13. WASTE PACKAGE TRANSPORTER DESIGN

    Energy Technology Data Exchange (ETDEWEB)

    D.C. Weddle; R. Novotny; J. Cron

    1998-09-23

    The purpose of this Design Analysis is to develop preliminary design of the waste package transporter used for waste package (WP) transport and related functions in the subsurface repository. This analysis refines the conceptual design that was started in Phase I of the Viability Assessment. This analysis supports the development of a reliable emplacement concept and a retrieval concept for license application design. The scope of this analysis includes the following activities: (1) Assess features of the transporter design and evaluate alternative design solutions for mechanical components. (2) Develop mechanical equipment details for the transporter. (3) Prepare a preliminary structural evaluation for the transporter. (4) Identify and recommend the equipment design for waste package transport and related functions. (5) Investigate transport equipment interface tolerances. This analysis supports the development of the waste package transporter for the transport, emplacement, and retrieval of packaged radioactive waste forms in the subsurface repository. Once the waste containers are closed and accepted, the packaged radioactive waste forms are termed waste packages (WP). This terminology was finalized as this analysis neared completion; therefore, the term disposal container is used in several references (i.e., the System Description Document (SDD)) (Ref. 5.6). In this analysis and the applicable reference documents, the term ''disposal container'' is synonymous with ''waste package''.

  14. On Value and Waste

    OpenAIRE

    Wallström, Peter

    2016-01-01

    Value and waste are concepts that are used in improvement projects. In lean the concepts are fairly simple. Reduce the waste and the value has increased. However, value is both multidimensional and differs over time. If the concepts value and waste are to be used, the concepts must be clearly defined and measured. Otherwise, value can be reduced for the customer/user and the cost increased for the producer/seller. The purpose in this thesis is to investigate how value and waste are perceived ...

  15. Disposal of radioactive waste

    Science.gov (United States)

    Van Dorp, Frits; Grogan, Helen; McCombie, Charles

    The aim of radioactive and non-radioactive waste management is to protect man and the environment from unacceptable risks. Protection criteria for both should therefore be based on similar considerations. From overall protection criteria, performance criteria for subsystems in waste management can be derived, for example for waste disposal. International developments in this field are summarized. A brief overview of radioactive waste sorts and disposal concepts is given. Currently being implemented are trench disposal and engineered near-surface facilities for low-level wastes. For low-and intermediate-level waste underground facilities are under construction. For high-level waste site selection and investigation is being carried out in several countries. In all countries with nuclear programmes, the predicted performance of waste disposal systems is being assessed in scenario and consequence analyses. The influences of variability and uncertainty of parameter values are increasingly being treated by probabilistic methods. Results of selected performance assessments show that radioactive waste disposal sites can be found and suitable repositories can be designed so that defined radioprotection limits are not exceeded.

  16. Avoidable waste management costs

    Energy Technology Data Exchange (ETDEWEB)

    Hsu, K.; Burns, M.; Priebe, S.; Robinson, P.

    1995-01-01

    This report describes the activity based costing method used to acquire variable (volume dependent or avoidable) waste management cost data for routine operations at Department of Energy (DOE) facilities. Waste volumes from environmental restoration, facility stabilization activities, and legacy waste were specifically excluded from this effort. A core team consisting of Idaho National Engineering Laboratory, Los Alamos National Laboratory, Rocky Flats Environmental Technology Site, and Oak Ridge Reservation developed and piloted the methodology, which can be used to determine avoidable waste management costs. The method developed to gather information was based on activity based costing, which is a common industrial engineering technique. Sites submitted separate flow diagrams that showed the progression of work from activity to activity for each waste type or treatability group. Each activity on a flow diagram was described in a narrative, which detailed the scope of the activity. Labor and material costs based on a unit quantity of waste being processed were then summed to generate a total cost for that flow diagram. Cross-complex values were calculated by determining a weighted average for each waste type or treatability group based on the volume generated. This study will provide DOE and contractors with a better understanding of waste management processes and their associated costs. Other potential benefits include providing cost data for sites to perform consistent cost/benefit analysis of waste minimization and pollution prevention (WMIN/PP) options identified during pollution prevention opportunity assessments and providing a means for prioritizing and allocating limited resources for WMIN/PP.

  17. 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

  18. Structural evolution during calcination and sintering of a (La0.6Sr0.4)0.99CoO3-δ nanofiber prepared by electrospinning

    Science.gov (United States)

    Simonsen, S. B.; Shao, J.; Zhang, W.

    2017-06-01

    Design of three-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 be widely applied to design metal oxide one-dimensional nanomaterials with precise control in both geometry (nanofiber, nanotube and nano-pearl string) and surface area (by varying grain size).

  19. Structure and photoluminescence property of Eu-doped SnO{sub 2} nanocrystalline powders fabricated by sol-gel calcination process

    Energy Technology Data Exchange (ETDEWEB)

    Chen Jiangtao; Wang Jun; Zhang Fei; Yan De; Zhang Guangan; Zhuo Renfu; Yan Pengxun [School of Physical Science and Technology, Lanzhou University, Lanzhou 730000 (China)], E-mail: pxyan@lzu.edu.cn

    2008-05-21

    Eu-doped SnO{sub 2} nanocrystalline powders were fabricated by the sol-gel calcination process. The effect of Eu doping concentrations on the structure and photoluminescence properties of Eu-doped SnO{sub 2} nanocrystalline powders was investigated. X-ray diffraction patterns, Fourier transformation infrared spectrum, field emission scanning electron microscope and high-resolution transmission electron microscope are employed to investigate the morphology and the structure of Eu-doped SnO{sub 2} nanocrystalline powders. The samples display reddish-orange light and red light when excited at indirect and direct excitation, respectively. Meanwhile, PL spectra indicate that the quenching concentrations are different when the excitation wavelength alters. Based on the analysis of the PL spectra, it is believed that Eu{sup 3+} ions located at different sites in the SnO{sub 2} host are selectively excited.

  20. Catalytic Pyrolysis of Wild Reed over a Zeolite-Based Waste Catalyst

    Directory of Open Access Journals (Sweden)

    Myung Lang Yoo

    2016-03-01

    Full Text Available Fast catalytic pyrolysis of wild reed was carried out at 500 °C. Waste fluidized catalytic cracking (FCC catalyst disposed from a petroleum refinery process was activated through acetone-washing and calcination and used as catalyst for pyrolysis. In order to evaluate the catalytic activity of waste FCC catalyst, commercial HY zeolite catalyst with a SiO2/Al2O3 ratio of 5.1 was also used. The bio-oil produced from pyrolysis was analyzed using gas chromatography/mass spectrometry (GC/MS. When the biomass-to-catalyst ratio was 1:1, the production of phenolics and aromatics was promoted considerably by catalysis, whereas the content of oxygenates was affected little. Significant conversion of oxygenates to furans and aromatics was observed when the biomass-to-catalyst ratio of 1:10 was used. Activated waste FCC catalyst showed comparable catalytic activity for biomass pyrolysis to HY in terms of the promotion of valuable chemicals, such as furans, phenolics and aromatics. The results of this study imply that waste FCC catalyst can be an important economical resource for producing high-value-added chemicals from biomass.

  1. Feasibility of disposing waste glyphosate neutralization liquor with cement rotary kiln.

    Science.gov (United States)

    Bai, Y; Bao, Y B; Cai, X L; Chen, C H; Ye, X C

    2014-08-15

    The waste neutralization liquor generated during the glyphosate production using glycine-dimethylphosphit process is a severe pollution problem due to its high salinity and organic components. The cement rotary kiln was proposed as a zero discharge strategy of disposal. In this work, the waste liquor was calcinated and the mineralogical phases of residue were characterized by scanning electron microscope (SEM) and X-ray diffraction (XRD). The mineralogical phases and the strength of cement clinker were characterized to evaluate the influence to the products. The burnability of cement raw meal added with waste liquor and the calorific value of waste liquor were tested to evaluate the influence to the thermal state of the kiln system. The results showed that after the addition of this liquor, the differences of the main phases and the strength of cement clinker were negligible, the burnability of raw meal was improved; and the calorific value of this liquor was 6140 J/g, which made it could be considered as an alternative fuel during the actual production. Copyright © 2014 Elsevier B.V. All rights reserved.

  2. Recovering Y and Eu from Waste Phosphors Using Chlorination Roasting—Water Leaching Process

    Directory of Open Access Journals (Sweden)

    Mingming Yu

    2016-10-01

    Full Text Available Recovering Y and Eu from waste phosphors using chlorination roasting followed by a water leaching process was investigated in this study. Firstly, by chlorination roasting and water leaching, Y and Eu elements present in waste phosphors were efficiently extracted into a leach solution. Secondly, the majority of the impurities in the solution can be removed by adjusting the pH to 4.5 using a Na2S and NH3·H2O solution. Thirdly, the rare earths can be precipitated afterwards by adding a H2C2O4 solution and adjusting the pH to 2.0. Then rare earth oxides (REOs can be obtained after calcining at 800 °C for 1 h. The characterization study of the waste phosphors and the rare earth oxide products was performed by XRD, XRF, and SEM-EDS analysis to determine the phase and morphological features. Influences of the factors, such as roasting temperatures and time, the addition of ammonium chloride on the roasting of waste phosphors, as well as the pH and the amount of oxalates on the precipitation of Y and Eu, were investigated. The maximum grade (99.84% of mixed rare earth oxides and recovery rate (87.35% of Y and Eu were obtained at the optimized conditions.

  3. 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.

  4. 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 

  5. Secondary Waste Cast Stone Waste Form Qualification Testing Plan

    Energy Technology Data Exchange (ETDEWEB)

    Westsik, Joseph H.; Serne, R. Jeffrey

    2012-09-26

    The Hanford Tank Waste Treatment and Immobilization Plant (WTP) is being constructed to treat the 56 million gallons of radioactive waste stored in 177 underground tanks at the Hanford Site. The WTP includes a pretreatment facility to separate the wastes into high-level waste (HLW) and low-activity waste (LAW) fractions for vitrification and disposal. The LAW will be converted to glass for final disposal at the Integrated Disposal Facility (IDF). Cast Stone – a cementitious waste form, has been selected for solidification of this secondary waste stream after treatment in the ETF. The secondary-waste Cast Stone waste form must be acceptable for disposal in the IDF. This secondary waste Cast Stone waste form qualification testing plan outlines the testing of the waste form and immobilization process to demonstrate that the Cast Stone waste form can comply with the disposal requirements. Specifications for the secondary-waste Cast Stone waste form have not been established. For this testing plan, Cast Stone specifications are derived from specifications for the immobilized LAW glass in the WTP contract, the waste acceptance criteria for the IDF, and the waste acceptance criteria in the IDF Permit issued by the State of Washington. This testing plan outlines the testing needed to demonstrate that the waste form can comply with these waste form specifications and acceptance criteria. The testing program must also demonstrate that the immobilization process can be controlled to consistently provide an acceptable waste form product. This testing plan also outlines the testing needed to provide the technical basis for understanding the long-term performance of the waste form in the disposal environment. These waste form performance data are needed to support performance assessment analyses of the long-term environmental impact of the secondary-waste Cast Stone waste form in the IDF

  6. 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.

  7. Waste Generation Overview, Course 23263

    Energy Technology Data Exchange (ETDEWEB)

    Simpson, Lewis Edward [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2016-11-28

    This course, Waste Generation Overview Live (COURSE 23263), provides an overview of federal and state waste management regulations, as well as Los Alamos National Laboratory (LANL) policies and procedures for waste management operations. The course covers the activities involved in the cradle-to-grave waste management process and focuses on waste characterization, waste compatibility determinations and classification, and the storage requirements for temporary waste accumulation areas at LANL. When you have completed this course, you will be able to recognize federal, state, and LANL environmental requirements and their impact on waste operations; recognize the importance of the cradle-to-grave waste management process; identify the roles and responsibilities of key LANL waste management personnel (e.g., Waste Generator, Waste Management Coordinator, Waste Stream Profile approver, and Waste Certification Official); characterize a waste stream to determine whether it meets the definition of a hazardous waste, as well as characterize the use and minimum requirements for use of acceptable knowledge (AK) for waste characterization and waste compatibility documentation requirements; and identify the requirements for setting up and managing temporary waste accumulation areas.

  8. Gas generation during waste treatment of acidic solutions from the dissolution of irradiated LEU targets for 99Mo production

    Energy Technology Data Exchange (ETDEWEB)

    Bakel, Allen J. [Argonne National Lab. (ANL), Argonne, IL (United States); Conner, Cliff [Argonne National Lab. (ANL), Argonne, IL (United States); Quigley, Kevin [Argonne National Lab. (ANL), Argonne, IL (United States); Vandegrift, George F. [Argonne National Lab. (ANL), Argonne, IL (United States)

    2017-01-01

    The goal of the Reduced Enrichment for Research and Test Reactors Program is to limit the use of high-enriched uranium (HEU) in research and test reactors by substituting low-enriched uranium (LEU) wherever possible. The work reported here documents our work to develop the calcining technologies and processes that will be needed for 99Mo production using LEU foil targets and the Modified Cintichem Process. The primary concern with the conversion to LEU from HEU targets is that it would result in a five- to six-fold increase in the total uranium. This increase results in more liquid waste from the process. We have been working to minimize the increase in liquid waste and to minimize the impact of any change in liquid waste. Direct calcination of uranium-rich nitric acid solutions generates NO2 gas and UO3 solid. We have proposed two processes for treating the liquid waste from a Modified Cintichem Process with a LEU foil. One is an optimized direct calcination process that is similar to the process currently in use. The other is a uranyl oxalate precipitation process. The specific goal of the work reported here was to characterize and compare the chemical reactions that occur during these two processes. In particular, the amounts and compositions of the gaseous and solid products were of interest. A series of experiments was carried out to show the effects of temperature and the redox potential of the reaction atmosphere. The primary products of the direct calcination process were mixtures of U3O8 and UO3 solids and NO2 gas. The primary products of the oxalate precipitation process were mixtures of U3O8 and UO2 solid and CO2 gas. Higher temperature and a reducing atmosphere tended to favor quadrivalent over hexavalent uranium in the solid product. These data will help producers to decide between the two processes. In addition, the data can be used

  9. Household Hazardous Waste and Demolition

    Science.gov (United States)

    Household wastes that are toxic, corrosive, ignitable, or reactive are known as Household Hazardous Waste (HHW). Household Hazardous Waste may be found during residential demolitions, and thus require special handling for disposal.

  10. Waste management and the workplace*

    African Journals Online (AJOL)

    User

    . 48 For instance, the City's Solid Waste Department argues that specialised, expensive recycling equipment is required at drop-off centres to recycle garden waste and building rubble. Also, the compactor trucks used for waste collection are ...

  11. Waste management and chemical inventories

    Energy Technology Data Exchange (ETDEWEB)

    Gleckler, B.P.

    1995-06-01

    This section of the 1994 Hanford Site Environmental Report summarizes the classification and handling of waste at the Hanford Site. Waste produced at the Hanford Site is classified as either radioactive, nonradioactive, or mixed waste. Radioactive wastes are further categorized as transuranic, high-level, and low-level. Mixed waste may contain both radioactive and hazardous nonradioactive substances. This section describes waste management practices and chemical inventories at the site.

  12. Synthesis of alumina powder with seeds by Pechini Method using O{sub 2} as calcination atmosphere; Sintese de pos de alumina com seeds pelo Metodo Pechini utilizando O{sub 2} como atmosfera de calcinacao

    Energy Technology Data Exchange (ETDEWEB)

    Salem, R.E.P.; Guilherme, K.A.; Chinelatto, A.S.A.; Chinelatto, A. L., E-mail: raphaelprestes@gmail.com [Universidade Estadual de Ponta Grossa (UEPG), PR (Brazil). Dept. de Engenharia de Materiais

    2012-07-01

    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{sub 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)

  13. Waste to energy

    CERN Document Server

    Syngellakis, S

    2014-01-01

    Waste to Energy deals with the very topical subject of converting the calorific content of waste material into useful forms of energy. Topics included cover: Biochemical Processes; Conversions by Thermochemical Processes; Computational Fluid Dynamics Modelling; Combustion; Pyrolysis; Gasification; Biofuels; Management and Policies.

  14. Radioactive waste storage issues

    Energy Technology Data Exchange (ETDEWEB)

    Kunz, Daniel E. [Colorado Christian Univ., Lakewood, CO (United States)

    1994-08-15

    In the United States we generate greater than 500 million tons of toxic waste per year which pose a threat to human health and the environment. Some of the most toxic of these wastes are those that are radioactively contaminated. This thesis explores the need for permanent disposal facilities to isolate radioactive waste materials that are being stored temporarily, and therefore potentially unsafely, at generating facilities. Because of current controversies involving the interstate transfer of toxic waste, more states are restricting the flow of wastes into - their borders with the resultant outcome of requiring the management (storage and disposal) of wastes generated solely within a state`s boundary to remain there. The purpose of this project is to study nuclear waste storage issues and public perceptions of this important matter. Temporary storage at generating facilities is a cause for safety concerns and underscores, the need for the opening of permanent disposal sites. Political controversies and public concern are forcing states to look within their own borders to find solutions to this difficult problem. Permanent disposal or retrievable storage for radioactive waste may become a necessity in the near future in Colorado. Suitable areas that could support - a nuclear storage/disposal site need to be explored to make certain the health, safety and environment of our citizens now, and that of future generations, will be protected.

  15. Food-Processing Wastes.

    Science.gov (United States)

    Frenkel, Val S; Cummings, Gregg A; Maillacheruvu, K Y; Tang, Walter Z

    2017-10-01

    Literature published in 2016 and early 2017 related to food processing wastes treatment for industrial applications are reviewed. This review is a subsection of the Treatment Systems section of the annual Water Environment Federation literature review and covers the following food processing industries and applications: general, meat and poultry, fruits and vegetables, dairy and beverage, and miscellaneous treatment of food wastes.

  16. Nuclear waste solutions

    Science.gov (United States)

    Walker, Darrel D.; Ebra, Martha A.

    1987-01-01

    High efficiency removal of technetium values from a nuclear waste stream is achieved by addition to the waste stream of a precipitant contributing tetraphenylphosphonium cation, such that a substantial portion of the technetium values are precipitated as an insoluble pertechnetate salt.

  17. Waste statistics 2001

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2004-07-01

    Reports to the ISAG (Information System for Waste and Recycling) for 2001 cover 402 Danish waste treatment plants owned by 295 enterprises. The total waste generation in 2001 amounted to 12,768,000 tonnes, which is 2% less than in 2000. Reductions are primarily due to the fact that sludge for mineralization is included with a dry matter content of 20% compared to 1,5% in previous statistics. This means that sludge amounts have been reduced by 808,886 tonnes. The overall rate of recycling amounted to 63%, which is 1% less than the overall recycling target of 64% for 2004. Since sludge has a high recycling rate, the reduction in sludge amounts of 808,886 tonnes has also caused the total recycling rate to fall. Waste amounts incinerated accounted for 25%, which is 1% more than the overall target of 24% for incineration in 2004. Waste going to landfill amounted to 10%, which is better than the overall landfill target for 2004 of a maximum of 12% for landfilling. Targets for treatment of waste from the different sectors, however, are still not complied with, since too little waste from households and the service sector is recycled, and too much waste from industry is led to landfill. (BA)

  18. Greening waste management

    CSIR Research Space (South Africa)

    Godfrey, Linda K

    2014-11-01

    Full Text Available The Waste Sector, as with many sectors of the economy, is responding to the call to transition to a Green Economy. Globally, waste management is changing from one of ‘collect-transport-dispose’, to one of ‘secondary resource management’, driven...

  19. Radioactive waste disposal package

    Science.gov (United States)

    Lampe, Robert F.

    1986-11-04

    A radioactive waste disposal package comprising a canister for containing vitrified radioactive waste material and a sealed outer shell encapsulating the canister. A solid block of filler material is supported in said shell and convertible into a liquid state for flow into the space between the canister and outer shell and subsequently hardened to form a solid, impervious layer occupying such space.

  20. Lyophilization -Solid Waste Treatment

    Science.gov (United States)

    Litwiller, Eric; Flynn, Michael; Fisher, John; Reinhard, Martin

    2004-01-01

    This paper discusses the development of a solid waste treatment system that has been designed for a Mars transit exploration mission. The technology described is an energy-efficient lyophilization technique that is designed to recover water from spacecraft solid wastes. Candidate wastes include feces, concentrated brines from water processors, and other solid wastes that contain free water. The system is designed to operate as a stand-alone process or to be integrated into the International Space Station Waste Collection System. In the lyophilization process, water in an aqueous waste is frozen and then sublimed, separating the waste into a dried solid material and liquid water. The sublimed water is then condensed in a solid ice phase and then melted to generate a liquid product. In the subject system the waste solids are contained within a 0.2 micron bio-guard bag and after drying are removed from the system and stored in a secondary container. This technology is ideally suited to applications such as the Mars Reference Mission, where water recovery rates approaching 100% are desirable but production of CO2 is not. The system is designed to minimize power consumption through the use of thermoelectric heat pumps. The results of preliminary testing of a prototype system and testing of the final configuration are provided. A mathematical model of the system is also described.

  1. Solid-Waste Management

    Science.gov (United States)

    Science Teacher, 1973

    1973-01-01

    Consists of excerpts from a forthcoming publication of the United States Environmental Protection Agency, Student's Guide to Solid-Waste Management.'' Discusses the sources of wastes from farms, mines, factories, and communities, the job of governments, ways to collect trash, methods of disposal, processing, and suggests possible student action.…

  2. FOUNDRY WASTE MANAGEMENT

    Directory of Open Access Journals (Sweden)

    Borut Kosec

    2008-06-01

    Full Text Available Waste management in foundries is gaining a higher ecological and economical importance. Waste is becoming an increasingly traded product, where excellent profits can be made. Due to the cost reduction and successful business operation in companies, waste has to be regenerated and used again as a material to the maximum possible extent. Such research is long lasting and expensive and is a great challenge for companies. In the frame of our research, a total waste management case study for the Slovenian foundry Feniks was carried out. From the sustainable development point of view, waste management is most suitable, since it ensures the material utilization of waste, reduces the consumption of natural renewable or non-renewable resources and makes efficient production capacity utilization possible. Properly treated ecologically safe waste with a suitable physical characteristic, long-term existence, is a substitute for natural materials. Sand, dust, slag and other mineral waste from foundries are increasingly being used as materials in other industries. The foundry Feniks was awarded with certification of the environmental management system according to the standard SIST EN ISO 14001 and confirmed its environmental credentials.

  3. Waste statistics 2003

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2005-07-01

    The 2003 reporting to the ISAG comprises 403 plants owned by 273 enterprises. In 2002, reports covered 407 plants owned by 296 enterprises. Waste generation in 2003 is compared to targets from 2008 in the government's Waste Strategy 2005-2008. The following can be said to summarise waste generation in 2003: 1) In 2003, total reported waste arisings amounted to 12,835,000 tonnes, which is 270,000 tonnes, or 2 per cent, less than in 2002. 2) If amounts of residues from coal-fired power plants are excluded from statistics, waste arisings in 2003 were 11,597,000 tonnes, which is a 2 per cent increase from 2002. 3) If amounts of residues from coal-fired power plants and waste from the building and construction sector are excluded from statistics, total waste generation in 2003 amounted to 7,814,000 tonnes, which is 19,000 tonnes, or 1 per cent, less than in 2002. In other words, there has been a fall in total waste arisings, if residues and waste from building and construction are excluded. 4) The overall rate of recycling amounted to 66 per cent, which is one percentage point above the overall recycling target of 65 per cent for 2008. In 2002 the total rate of recycling was 64 per cent. 5) The total amount of waste led to incineration amounted to 26 per cent, plus an additional 1 per cent left in temporary storage to be incinerated at a later time. The 2008 target for incineration is 26 per cent. These are the same percentage figures as applied to incineration and storage in 2002. 6) The total amount of waste led to landfills amounted to 8 per cent, which is one percentage point below the overall landfill target of a maximum of 9 per cent landfilling in 2008. In 2002, 9 per cent was led to landfill. 7) The targets for treatment of waste from individual sectors are still not being met: too little waste from households and the service sector is being recycled, and too much waste from industry is being led to landfill. (au)

  4. Heterogeneities in nuclear waste glass; Heterogeneites dans le verre de confinement industriel

    Energy Technology Data Exchange (ETDEWEB)

    Ladirat, Ch. [CEA Valrho, Dir. de l' Energie Nucleaire, DEN, 30 - Marcoule (France)

    1997-07-01

    The industrial vitrification of high level radioactive wastes is a 2 stage process. During the first stage, the concentrated solution is heated in a spinning resistance oven at the temperature of 400 Celsius degrees till evaporation and calcination. The second stage begins when the dry residue falls into a melting pot that is maintained at a temperature of 1100-1150 Celsius degrees. Glass fretting is added and the glass is elaborated through the fusion of the different elements present in the melting pot. Heterogeneities in the glass may be associated to: - the presence in the solution to vitrify of insoluble elements from the dissolution of the fuel (RuO{sub 2}, Rh, Pd), - the presence of minuscule metal scraps (Zr) that have been produced during the cutting of the fuel element, - the failures to conform to the technical specifications of the vitrification process, for instance, temperatures or flow rates when introducing the different elements in the melting pot. (A.C.)

  5. Modeling of NOx Destruction Options for INEEL Sodium-Bearing Waste Vitrification

    Energy Technology Data Exchange (ETDEWEB)

    Wood, Richard Arthur

    2001-09-01

    Off-gas NOx concentrations in the range of 1-5 mol% are expected as a result of the proposed vitrification of sodium-bearing waste at the Idaho National Engineering and Environmental Laboratory. An existing kinetic model for staged combustion (originally developed for NOx abatement from the calcination process) was updated for application to vitrification offgas. In addition, two new kinetic models were developed to assess the feasibility of using selective non-catalytic reduction (SNCR) or high-temperature alone for NOx abatement. Each of the models was developed using the Chemkin code. Results indicate that SNCR is a viable option, reducing NOx levels to below 1000 ppmv. In addition, SNCR may be capable of simultaneously reducing CO emissions to below 100 ppmv. Results for using high-temperature alone were not as promising, indicating that a minimum NOx concentration of 3950 ppmv is achievable at 3344°F.

  6. An Overview of Organic Waste in Composting

    OpenAIRE

    Kadir Aeslina Abdul; Azhari Nur Wahidah; Jamaludin Siti Noratifah

    2016-01-01

    This paper reviewed studies on the composting process of organic waste. Organic wastes are wastes that easily biodegradable. These wastes are produced from many sources such as agricultural waste, market waste, kitchen waste, urban solid food wastes and municipal solid waste. Without proper management, these waste could create several environment problem. Therefore, composting is the best low cost alternative solution to overcome this problem. Composting method can degrade all types of organi...

  7. Storing Waste in Ceramic

    Energy Technology Data Exchange (ETDEWEB)

    Bourcier, W L; Sickafus, K

    2004-07-20

    Not all the nuclear waste destined for Yucca Mountain is in the form of spent fuel. Some of it will be radioactive waste generated from the production of nuclear weapons. This so-called defense waste exists mainly as corrosive liquids and sludge in underground tanks. An essential task of the U.S. high-level radioactive waste program is to process these defense wastes into a solid material--called a waste form. An ideal waste form would be extremely durable and unreactive with other repository materials. It would be simple to fabricate remotely so that it could be safely transported to a repository for permanent storage. What's more, the material should be able to tolerate exposure to intense radiation without degradation. And to minimize waste volume, the material must be able to contain high concentrations of radionuclides. The material most likely to be used for immobilization of radioactive waste is glass. Glasses are produced by rapid cooling of high-temperature liquids such that the liquid-like non-periodic structure is preserved at lower temperatures. This rapid cooling does not allow enough time for thermodynamically stable crystalline phases (mineral species) to form. In spite of their thermodynamic instability, glasses can persist for millions of years. An alternate to glass is a ceramic waste form--an assemblage of mineral-like crystalline solids that incorporate radionuclides into their structures. The crystalline phases are thermodynamically stable at the temperature of their synthesis; ceramics therefore tend to be more durable than glasses. Ceramic waste forms are fabricated at temperatures below their melting points and so avoid the danger of handling molten radioactive liquid--a danger that exists with incorporation of waste in glasses. The waste form provides a repository's first line of defense against release of radionuclides. It, along with the canister, is the barrier in the repository over which we have the most control. When a waste

  8. Radioactive waste material disposal

    Science.gov (United States)

    Forsberg, Charles W.; Beahm, Edward C.; Parker, George W.

    1995-01-01

    The invention is a process for direct conversion of solid radioactive waste, particularly spent nuclear fuel and its cladding, if any, into a solidified waste glass. A sacrificial metal oxide, dissolved in a glass bath, is used to oxidize elemental metal and any carbon values present in the waste as they are fed to the bath. Two different modes of operation are possible, depending on the sacrificial metal oxide employed. In the first mode, a regenerable sacrificial oxide, e.g., PbO, is employed, while the second mode features use of disposable oxides such as ferric oxide.

  9. ZeroWaste

    DEFF Research Database (Denmark)

    Goltermann, Per; Ottosen, Lisbeth M.; Jensen, Pernille Erland

    2014-01-01

    The ZeroWaste research group at the Department of Civil Engineering at the Technical University of Denmark (DTU Byg) was established two years ago and covers the broad range of expertise, required for turning waste materials into attractive, new materials. Members of the group have, prior to that......, developed methods for removal of heavy metals and phosphorous from waste incineration, sewage sludge and other bio ashes, providing the basis of to make these ash types an attractive, new material for the building sector. Initial results for upgrading and using different types of ashes are presented...

  10. High-Level Radioactive Waste.

    Science.gov (United States)

    Hayden, Howard C.

    1995-01-01

    Presents a method to calculate the amount of high-level radioactive waste by taking into consideration the following factors: the fission process that yields the waste, identification of the waste, the energy required to run a 1-GWe plant for one year, and the uranium mass required to produce that energy. Briefly discusses waste disposal and…

  11. Methane generation from waste materials

    Science.gov (United States)

    Samani, Zohrab A.; Hanson, Adrian T.; Macias-Corral, Maritza

    2010-03-23

    An organic solid waste digester for producing methane from solid waste, the digester comprising a reactor vessel for holding solid waste, a sprinkler system for distributing water, bacteria, and nutrients over and through the solid waste, and a drainage system for capturing leachate that is then recirculated through the sprinkler system.

  12. Urban Wood Waste Resource Assessment

    Energy Technology Data Exchange (ETDEWEB)

    Wiltsee, G.

    1998-11-20

    This study collected and analyzed data on urban wood waste resources in 30 randomly selected metropolitan areas in the United States. Three major categories wood wastes disposed with, or recovered from, the municipal solid waste stream; industrial wood wastes such as wood scraps and sawdust from pallet recycling, woodworking shops, and lumberyards; and wood in construction/demolition and land clearing debris.

  13. Hanford Site Secondary Waste Roadmap

    Energy Technology Data Exchange (ETDEWEB)

    Westsik, Joseph H.

    2009-01-29

    Summary The U.S. Department of Energy (DOE) is making plans to dispose of 54 million gallons of radioactive tank wastes at the Hanford Site near Richland, Washington. The high-level wastes and low-activity wastes will be vitrified and placed in permanent disposal sites. Processing of the tank wastes will generate secondary wastes, including routine solid wastes and liquid process effluents, and these need to be processed and disposed of also. The Department of Energy Office of Waste Processing sponsored a meeting to develop a roadmap to outline the steps necessary to design the secondary waste forms. Representatives from DOE, the U.S. Environmental Protection Agency, the Washington State Department of Ecology, the Oregon Department of Energy, Nuclear Regulatory Commission, technical experts from the DOE national laboratories, academia, and private consultants convened in Richland, Washington, during the week of July 21-23, 2008, to participate in a workshop to identify the risks and uncertainties associated with the treatment and disposal of the secondary wastes and to develop a roadmap for addressing those risks and uncertainties. This report describes the results of the roadmap meeting in Richland. Processing of the tank wastes will generate secondary wastes, including routine solid wastes and liquid process effluents. The secondary waste roadmap workshop focused on the waste streams that contained the largest fractions of the 129I and 99Tc that the Integrated Disposal Facility risk assessment analyses were showing to have the largest contribution to the estimated IDF disposal impacts to groundwater. Thus, the roadmapping effort was to focus on the scrubber/off-gas treatment liquids with 99Tc to be sent to the Effluent Treatment Facility for treatment and solidification and the silver mordenite and carbon beds with the captured 129I to be packaged and sent to the IDF. At the highest level, the secondary waste roadmap includes elements addressing regulatory and

  14. Hazardous Waste Research Center

    Data.gov (United States)

    Federal Laboratory Consortium — The U.S. Army Engineer Waterways Experiment Station (WES) is playing a major role in development of technologies for cleanup of toxic and hazardous waste in military...

  15. Nuclear Waste and Ethics

    Energy Technology Data Exchange (ETDEWEB)

    Damveld, Herman [Groningen (Netherlands)

    2003-10-01

    In the past years in almost all conferences on storage of nuclear waste, ethics has been considered as an important theme. But what is ethics? We will first give a sketch of this branch of philosophy. We will then give a short explanation of the three principal ethical theories. In the discussion about storage of nuclear waste, the ethical theory of utilitarianism is often implicitly invoked. In this system future generations weigh less heavily than the present generation, so that people of the future are not considered as much as those now living. We reject this form of reasoning. The discussion about nuclear waste is also sometimes pursued from ethical points of departure such as equality and justice. But many loose ends remain in these arguments, which gives rise to the question of whether the production and storage of nuclear waste is responsible.

  16. Solid Waste Management Districts

    Data.gov (United States)

    Vermont Center for Geographic Information — The Solid waste management districts layer is part of a dataset that contains administrative boundaries for Vermont's Agency of Natural Resources. This dataset...

  17. Household Hazardous Waste

    Science.gov (United States)

    ... waste collection" near your zip code in the Earth 911 database Exit for more information. Contact your ... If your community doesn’t have a year-round collection system for HHW, see if there are ...

  18. Treatment of organic waste

    Science.gov (United States)

    Grantham, LeRoy F.

    1979-01-01

    An organic waste containing at least one element selected from the group consisting of strontium, cesium, iodine and ruthenium is treated to achieve a substantial reduction in the volume of the waste and provide for fixation of the selected element in an inert salt. The method of treatment comprises introducing the organic waste and a source of oxygen into a molten salt bath maintained at an elevated temperature to produce solid and gaseous reaction products. The gaseous reaction products comprise carbon dioxide and water vapor, and the solid reaction products comprise the inorganic ash constituents of the organic waste and the selected element which is retained in the molten salt. The molten salt bath comprises one or more alkali metal carbonates, and may optionally include from 1 to about 25 wt.% of an alkali metal sulfate.

  19. Nuclear waste and hazardous waste in the public perception

    Energy Technology Data Exchange (ETDEWEB)

    Kruetli, Pius; Seidl, Roman; Stauffacher, Michael [ETH Zurich (Switzerland). Inst. for Environmental Decisions

    2015-07-01

    The disposal of nuclear waste has gained attention of the public for decades. Accordingly, nuclear waste has been a prominent issue in natural, engineer and social science for many years. Although bearing risks for todays and future generations hazardous waste in contrast is much less an issue of public concern. In 2011, we conducted a postal survey among Swiss Germans (N = 3.082) to learn more about, how nuclear waste is perceived against hazardous waste. We created a questionnaire with two versions, nuclear waste and hazardous waste, respectively. Each version included an identical part with well-known explanatory factors for risk perception on each of the waste types separately and additional questions directly comparing the two waste types. Results show that basically both waste types are perceived similarly in terms of risk/benefit, emotion, trust, knowledge and responsibility. However, in the direct comparison of the two waste types a complete different pattern can be observed: Respondents perceive nuclear waste as more long-living, more dangerous, less controllable and it, furthermore, creates more negative emotions. On the other hand, respondents feel more responsible for hazardous waste and indicate to have more knowledge about this waste type. Moreover, nuclear waste is perceived as more carefully managed. We conclude that mechanisms driving risk perception are similar for both waste types but an overarching negative image of nuclear waste prevails. We propose that hazardous waste should be given more attention in the public as well as in science which may have implications on further management strategies of hazardous waste.

  20. Citrus Waste Biomass Program

    Energy Technology Data Exchange (ETDEWEB)

    Karel Grohman; Scott Stevenson

    2007-01-30

    Renewable Spirits is developing an innovative pilot plant bio-refinery to establish the commercial viability of ehtanol production utilizing a processing waste from citrus juice production. A novel process based on enzymatic hydrolysis of citrus processing waste and fermentation of resulting sugars to ethanol by yeasts was successfully developed in collaboration with a CRADA partner, USDA/ARS Citrus and Subtropical Products Laboratory. The process was also successfully scaled up from laboratory scale to 10,000 gal fermentor level.

  1. PLASTIC WASTE CONVERSION TO LIQUID FUELS OVER MODIFIED-RESIDUAL CATALYTIC CRACKING CATALYSTS: MODELING AND OPTIMIZATION USING HYBRID ARTIFICIAL NEURAL NETWORK – GENETIC ALGORITHM

    Directory of Open Access Journals (Sweden)

    Istadi Istadi

    2012-04-01

    Full Text Available The plastic waste utilization can be addressed toward different valuable products. A promising technology for the utilization is by converting it to fuels. Simultaneous modeling and optimization representing effect of reactor temperature, catalyst calcinations temperature, and plastic/catalyst weight ratio toward performance of liquid fuel production was studied over modified catalyst waste. The optimization was performed to find optimal operating conditions (reactor temperature, catalyst calcination temperature, and plastic/catalyst weight ratio that maximize the liquid fuel product. A Hybrid Artificial Neural Network-Genetic Algorithm (ANN-GA method was used for the modeling and optimization, respectively. The variable interaction between the reactor temperature, catalyst calcination temperature, as well as plastic/catalyst ratio is presented in surface plots. From the GC-MS characterization, the liquid fuels product was mainly composed of C4 to C13 hydrocarbons.KONVERSI LIMBAH PLASTIK MENJADI BAHAN BAKAR CAIR DENGAN METODE PERENGKAHAN KATALITIK MENGGUNAKAN KATALIS BEKAS YANG TERMODIFIKASI: PEMODELAN DAN OPTIMASI MENGGUNAKAN GABUNGAN METODE ARTIFICIAL NEURAL NETWORK DAN GENETIC ALGORITHM. Pemanfaatan limbah plastik dapat dilakukan untuk menghasilkan produk yang lebih bernilai tinggi. Salah satu teknologi yang menjanjikan adalah dengan mengkonversikannya menjadi bahan bakar. Permodelan, simulasi dan optimisasi simultan yang menggambarkan efek dari suhu reaktor, suhu kalsinasi katalis, dan rasio berat plastik/katalis terhadap kinerja produksi bahan bakar cair telah dipelajari menggunakan katalis bekas termodifikasi Optimisasi ini ditujukan untuk mencari kondisi operasi optimum (suhu reaktor, suhu kalsinasi katalis, dan rasio berat plastik/katalis yang memaksimalkan produk bahan bakar cair. Metode Hybrid Artificial Neural Network-Genetic Algorithm (ANN-GA telah digunakan untuk permodelan dan optimisasi simultan tersebut. Inetraksi antar variabel

  2. Photocatalytic efficiency of Fe2O3/TiO2for the degradation of typical dyes in textile industries: Effects of calcination temperature and UV-assisted thermal synthesis.

    Science.gov (United States)

    Nasirian, Mohsen; Bustillo-Lecompte, Ciro Fernando; Mehrvar, Mehrab

    2017-07-01

    The inadequate management practices in industrial textile effluents have a considerable negative impact on the environment and human health due to the indiscriminate release of dyes. Photocatalysis is one of the diverse advance oxidation processes (AOPs) and titanium dioxide (TiO 2 ) is recognized for its high oxidation and reduction power. A composite photocatalyst of Fe 2 O 3 /TiO 2 is synthesized using different mass ratios of Fe:TiO 2 to improve its photoactivity. The composite photocatalyst is calcined at 300-900 °C. Their photocatalytic activity for the degradation of Congo red (CR) and methyl orange (MO) is investigated by total organic carbon (TOC) analysis. The formation and characterization of the as-prepared composite are studied by scanning electron microscopy (SEM) coupled with energy dispersive X-ray spectroscopy (EDS). The effect of calcination temperature on the composite Fe 2 O 3 /TiO 2 photocatalyst is investigated using Fourier transform infrared spectroscopy (FTIR). The photocatalytic activity and the phase conversion are studied by X-ray diffraction (XRD). The specific surface area of photocatalysts at different calcination temperatures is investigated based on Brunauer-Emmett-Teller (BET) surface area analysis. Results show that at an optimum calcination temperature of 300 °C for the photocatalyst preparation, the specific surface area is maximum and the photocatalyst has the highest photoactivity. Thus, the degradation of organic materials reaches 62.0% for MO and 46.8% for CR in the presence of Fe 2 O 3 /TiO 2 (0.01 w:w Fe:TiO 2 ) calcined at 300 °C with the highest specific surface area (98.73 m 2 /g). The transformation of TiO 2 from anatase to rutile is facilitated by high temperature and high concentration of iron while high crystallization and particle size increase occur. An optimum calcination temperature of 300 °C is found at which the degradation of typical dyes in textile industries is maximum. Copyright © 2017 Elsevier

  3. Recovery of silica from electronic waste for the synthesis of cubic MCM-48 and its application in preparing ordered mesoporous carbon molecular sieves using a green approach

    Science.gov (United States)

    Liou, Tzong-Horng

    2012-07-01

    The electronics industry is one of the world's fastest growing manufacturing industries. However, e-waste has become a serious pollution problem. This study reports the recovery of e-waste for preparing valuable MCM-48 and ordered mesoporous carbon for the first time. Specifically, this study adopts an alkali-extracted method to obtain sodium silicate precursors from electronic packaging resin ash. The influence of synthesis variables such as gelation pH, neutral/cationic surfactant ratio, hydrothermal treatment temperature, and calcination temperature on the mesophase of MCM-48 materials is investigated. Experimental results confirm that well-ordered cubic MCM-48 materials were synthesized in strongly acidic and strongly basic media. The resulting mesoporous silica had a high surface area of 1,317 m2/g, mean pore size of about 3.0 nm, and a high purity of 99.87 wt%. Ordered mesoporous carbon with high surface area (1,715 m2/g) and uniform pore size of CMK-1 type was successfully prepared by impregnating MCM-48 template using the resin waste. The carbon structure was sensitive to the sulfuric acid concentration and carbonization temperature. Converting e-waste into MCM-48 materials not only eliminates the disposal problem of e-waste, but also transforms industrial waste into a useful nanomaterial.

  4. Processing of food wastes.

    Science.gov (United States)

    Kosseva, Maria R

    2009-01-01

    Every year almost 45 billion kg of fresh vegetables, fruits, milk, and grain products is lost to waste in the United States. According to the EPA, the disposal of this costs approximately $1 billion. In the United Kingdom, 20 million ton of food waste is produced annually. Every tonne of food waste means 4.5 ton of CO(2) emissions. The food wastes are generated largely by the fruit-and-vegetable/olive oil, fermentation, dairy, meat, and seafood industries. The aim of this chapter is to emphasize existing trends in the food waste processing technologies during the last 15 years. The chapter consists of three major parts, which distinguish recovery of added-value products (the upgrading concept), the food waste treatment technologies as well as the food chain management for sustainable food system development. The aim of the final part is to summarize recent research on user-oriented innovation in the food sector, emphasizing on circular structure of a sustainable economy.

  5. Classification of waste packages

    Energy Technology Data Exchange (ETDEWEB)

    Mueller, H.P.; Sauer, M.; Rojahn, T. [Versuchsatomkraftwerk GmbH, Kahl am Main (Germany)

    2001-07-01

    A barrel gamma scanning unit has been in use at the VAK for the classification of radioactive waste materials since 1998. The unit provides the facility operator with the data required for classification of waste barrels. Once these data have been entered into the AVK data processing system, the radiological status of raw waste as well as pre-treated and processed waste can be tracked from the point of origin to the point at which the waste is delivered to a final storage. Since the barrel gamma scanning unit was commissioned in 1998, approximately 900 barrels have been measured and the relevant data required for classification collected and analyzed. Based on the positive results of experience in the use of the mobile barrel gamma scanning unit, the VAK now offers the classification of barrels as a service to external users. Depending upon waste quantity accumulation, this measurement unit offers facility operators a reliable and time-saving and cost-effective means of identifying and documenting the radioactivity inventory of barrels scheduled for final storage. (orig.)

  6. Radioactive waste management; Gerencia de rejeitos radioativos

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2013-11-15

    This eighth chapter presents the radioactive wastes and waste disposal; classification of radioactive wastes; basis requests of the radioactive waste management; conditions for a radioactive waste disposal; registers and inventories; transport of radioactive wastes from a facility to another and the radioactive waste management plan.

  7. 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.

  8. 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.

  9. Ni/Fe and Mg/Fe layered double hydroxides and their calcined derivatives: preparation, characterization and application on textile dyes removal

    Directory of Open Access Journals (Sweden)

    Rachid Elmoubarki

    2017-07-01

    Full Text Available In this study, Mg/Fe and Ni/Fe layered double hydroxides (LDHs with molar ratio (M2+/Fe3+ of 3 and intercalated with carbonate ions were synthesized by co-precipitation method. The as-synthesized materials and their calcined products (CLDHs were characterized by X-ray diffraction (XRD, Fourier transform infrared spectroscopy (FT-IR, thermo-gravimetric and differential thermal analyses (TGA–DTA, transmission electron microscopy coupled with energy dispersive X-ray spectroscopy (TEM-EDX, inductively coupled plasma (ICP and elemental chemical analysis CHNSO. The materials were used as adsorbents for the removal availability of textile dyes from aqueous solution. Methylene blue (MB and malachite green (MG, representative of cationic dyes, and methyl orange (MO representative of anionic dyes were used as model molecules. Adsorption experiments were carried out under different parameters such as contact time, temperature, initial dyes concentration and solution pH. Experimental results indicate that CLDHs had much higher adsorption capacities compared to LDHs. Adsorption kinetic data fitted well the pseudo-second order kinetic model. The process was spontaneous, endothermic for cationic dyes and exothermic for the anionic dye. Equilibrium sorption data fitted the Langmuir model instead of Freundlich model.

  10. 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

  11. Effects of calcination temperatures on photocatalytic activity of SnO2/TiO2 composite films prepared by an EPD method.

    Science.gov (United States)

    Zhou, Minghua; Yu, Jiaguo; Liu, Shengwei; Zhai, Pengcheng; Jiang, Li

    2008-06-15

    SnO2/TiO2 composite films were fabricated on transparent electro-conductive glass substrates (F-doped SnO2-coated glass:FTO glass) via an electrophoretic deposition (EPD) method using Degussa P25 as raw materials, and were further characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscope (FESEM), UV-vis diffuse reflectance spectra and Photoluminescence spectra (PL). XRD and XPS results confirmed that the films were composed of TiO2 and SnO2. FESEM images indicated that the as-prepared TiO2 films had roughness surfaces, which consisted of nano-sized particles. The effects of calcination temperatures on the surface morphology, microstructures and photocatalytic activity of SnO2/TiO2 composite films were further investigated. All the prepared SnO2/TiO2 composite films exhibited high photocatalytic activities for photocatalytic decolorization of Rhodamine-B aqueous solution. At 400 degrees C, the SnO2/TiO2 composite films showed the highest photocatalytic activity due to synergetic effects of low sodium content, good crystallization, appropriate phase composition and slower recombination rate of photogenerated charge carriers.

  12. 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.

  13. Glass Formulation Development for INEEL Sodium-Bearing Waste

    Energy Technology Data Exchange (ETDEWEB)

    J.D. Vienna; M.J. Schweiger; D.E. Smith; H.D. Smith; J.V. Crum; D.K. Peeler; I.A. Reamer; C.A. Musick; R.D. Tillotson

    1999-08-03

    For about four decades, radioactive wastes have been collected and calcined from nuclear fuels reprocessing at the Idaho Nuclear Technology and Engineering Center (INTEC), formerly Idaho Chemical Processing Plant (ICPP). Over this time span, secondary radioactive wastes have also been collected and stored as liquid from decontamination, laboratory activities, and fuel-storage activities. These liquid wastes are collectively called sodium-bearing wastes (SBW). About 5.7 million liters of these wastes are temporarily stored in stainless steel tanks at the Idaho National Engineering and Environmental Laboratory (INEEL). Vitrification is being considered as an immobilization step for SBW with a number of treatment and disposal options. A systematic study was undertaken to develop a glass composition to demonstrate direct vitrification of INEEL's SBW. The objectives of this study were to show the feasibility of SBW vitrification, not a development of an optimum formulation. The waste composition is relatively high in sodium, aluminum, and sulfur. A specific composition and glass property restrictions, discussed in Section 2, were used as a basis for the development. Calculations based on first-order expansions of selected glass properties in composition and some general tenets of glass chemistry led to an additive (fit) composition (68.69 mass % SiO{sub 2}, 14.26 mass% B{sub 2}O{sub 3}, 11.31 mass% Fe{sub 2}O{sub 3}, 3.08 mass% TiO{sub 2}, and 2.67 mass % Li{sub 2}O) that meets all property restrictions when melted with 35 mass % of SBW on an oxide basis, The glass was prepared using oxides, carbonates, and boric acid and tested to confirm the acceptability of its properties. Glass was then made using waste simulant at three facilities, and limited testing was performed to test and optimize processing-related properties and confirm results of glass property testing. The measured glass properties are given in Section 4. The viscosity at 1150 C, 5 Pa{center_dot}s, is

  14. Hanford Waste Vitrification Plant Project Waste Form Qualification Program Plan

    Energy Technology Data Exchange (ETDEWEB)

    Randklev, E.H.

    1993-06-01

    The US Department of Energy has created a waste acceptance process to help guide the overall program for the disposal of high-level nuclear waste in a federal repository. This Waste Form Qualification Program Plan describes the hierarchy of strategies used by the Hanford Waste Vitrification Plant Project to satisfy the waste form qualification obligations of that waste acceptance process. A description of the functional relationship of the participants contributing to completing this objective is provided. The major activities, products, providers, and associated scheduling for implementing the strategies also are presented.

  15. SECONDARY WASTE MANAGEMENT STRATEGY FOR EARLY LOW ACTIVITY WASTE TREATMENT

    Energy Technology Data Exchange (ETDEWEB)

    TW, CRAWFORD

    2008-07-17

    This study evaluates parameters relevant to River Protection Project secondary waste streams generated during Early Low Activity Waste operations and recommends a strategy for secondary waste management that considers groundwater impact, cost, and programmatic risk. The recommended strategy for managing River Protection Project secondary waste is focused on improvements in the Effiuent Treatment Facility. Baseline plans to build a Solidification Treatment Unit adjacent to Effluent Treatment Facility should be enhanced to improve solid waste performance and mitigate corrosion of tanks and piping supporting the Effiuent Treatment Facility evaporator. This approach provides a life-cycle benefit to solid waste performance and reduction of groundwater contaminants.

  16. Densified waste form and method for forming

    Science.gov (United States)

    Garino, Terry J.; Nenoff, Tina M.; Sava Gallis, Dorina Florentina

    2015-08-25

    Materials and methods of making densified waste forms for temperature sensitive waste material, such as nuclear waste, formed with low temperature processing using metallic powder that forms the matrix that encapsulates the temperature sensitive waste material. The densified waste form includes a temperature sensitive waste material in a physically densified matrix, the matrix is a compacted metallic powder. The method for forming the densified waste form includes mixing a metallic powder and a temperature sensitive waste material to form a waste form precursor. The waste form precursor is compacted with sufficient pressure to densify the waste precursor and encapsulate the temperature sensitive waste material in a physically densified matrix.

  17. Waste Tax 1987-1996

    DEFF Research Database (Denmark)

    Andersen, M. S.; Dengsøe, N.; Brendstrup, S.

    The report gives an ex-post evaluation of the Danish waste tax from 1987 to 1996. The evaluation shows that the waste tax has had a significant impact on the reductions in taxable waste. The tax has been decisive for the reduction in construction and demolition waste, while for the heavier fracti...... fractions under 'household waste', it has provided an important incentive for separate collection.......The report gives an ex-post evaluation of the Danish waste tax from 1987 to 1996. The evaluation shows that the waste tax has had a significant impact on the reductions in taxable waste. The tax has been decisive for the reduction in construction and demolition waste, while for the heavier...

  18. Perspectives on sustainable waste management.

    Science.gov (United States)

    Castaldi, Marco J

    2014-01-01

    Sustainable waste management is a goal that all societies must strive to maintain. Currently nearly 80% of global wastes are sent to landfill, with a significant amount lacking proper design or containment. The increased attention to environmental impacts of human activities and the increasing demand for energy and materials have resulted in a new perspective on waste streams. Use of waste streams for energy and materials recovery is becoming more prevalent, especially in developed regions of the world, such as Europe, the United States, and Japan. Although currently these efforts have a small impact on waste disposal, use of waste streams to extract value very likely will increase as society becomes more aware of the options available. This review presents an overview of waste management with a focus on following an expanded waste hierarchy to extract value specifically from municipal solid waste streams.

  19. Hazardous waste management.

    Science.gov (United States)

    Schaefer, M E

    1991-04-01

    The management of waste in the dental office is dictated by the federal, state, and local ordinances in force in the locale in which the office is located. The dentist must first determine what the laws require and then implement the changes in waste management into the office setting. The local component society of the ADA often provides such information; otherwise, the health department of the government branch having jurisdiction over the office locale will either have the information or know where to find it. Once it has been established what constitutes hazardous waste, the next steps are to contain it, store it, and finally dispose of it according to the information gained from the authorities. Storage of sharps should be accomplished in "hard-walled, leak-proof containers," usually red, which can be closed securely when they have been filled, and which are located as close to the point of use as possible. Solid waste should usually be contained in red bags, which are then bagged in a second bag when full or in a hard-walled container. Waste may then be hauled away for disposal by a qualified company that keeps the required records of the waste from the time it leaves the office until final disposal by incineration or burial in an approved landfill. The company chosen to do the hauling should be able to demonstrate that they have appropriate insurance to indemnify your office in the event of a problem while they have the waste in their possession.(ABSTRACT TRUNCATED AT 250 WORDS)

  20. Amelioration of acidic soil using various renewable waste resources.

    Science.gov (United States)

    Moon, Deok Hyun; Chang, Yoon-Young; Ok, Yong Sik; Cheong, Kyung Hoon; Koutsospyros, Agamemnon; Park, Jeong-Hun

    2014-01-01

    In this study, improvement of acidic soil with respect to soil pH and exchangeable cations was attempted for sample with an initial pH of approximately 5. Acidic soil was amended with various waste resources in the range of 1 to 5 wt.% including waste oyster shells (WOS), calcined oyster shells (COS), Class C fly ash (FA), and cement kiln dust (CKD) to improve soil pH and exchangeable cations. Upon treatment, the soil pH was monitored for periods up to 3 months. The exchangeable cations were measured after 1 month of curing. After a curing period of 1 month, a maize growth experiment was conducted with selected-treated samples to evaluate the effectiveness of treatment. The treatment results indicate that in order to increase the soil pH to a value of 7, 1 wt.% of WOS, 3 wt.% of FA, and 1 wt.% of CKD are required. In the case of COS, 1 wt.% was more than enough to increase the soil pH value to 7 because of COS's strong alkalinity. Moreover, the soil pH increases after a curing period of 7 days and remains virtually unchanged thereafter up to 1 month of curing. Upon treatment, the summation of cations (Ca, Mg, K, and Na) significantly increased. The growth of maize is superior in the treated samples rather than the untreated one, indicating that the amelioration of acidic soil is beneficial to plant growth, since soil pH was improved and nutrients were replenished.

  1. Mg Al{sub 2} O{sub 4}-Si C composites. Influence of the calcination atmosphere; Compositos Mg Al{sub 2} O{sub 4} -Si C. Influencia de la atmosfera de calcinacion

    Energy Technology Data Exchange (ETDEWEB)

    Mazzoni, A.D.; Aglietti, E.F. [Centro de Tecnologia de Recursos Minerales y Ceramicas, Buenos Aires (Argentina); Sainz, M.A.; Caballero, A.C. [Instituto de Ceramica y Vidro, Madrid (Spain)

    1997-12-31

    Alumina-magnesia spinel is a ceramic material with excellent physicochemical properties. The addition of a second phase like silicon carbide is with the objective of enhance its thermochemical properties. The preparation and sintering of spinel with Si C is studied. The samples were isostatically pressed at 200 Mpa. Calcination were performed under different atmospheres: air, Ar, CO and N{sub 2}. Compacts after calcination were studied using XRD and Hg-density. Chemical interactions between Si C and spinel were observed depending on the atmosphere employed. Under Ar, spinel is partially reduced by the Si C producing the weight loss of the samples. Under N{sub 2} nitrogenous phases of the system Si-Al-O-N are formed and densities are near 90%. The reactions that takes place are explained taking into to account the atmosphere use. (author) 9 refs., 3 figs., 3 tabs.

  2. FY-97 operations of the pilot-scale glass melter to vitrify simulated ICPP high activity sodium-bearing waste

    Energy Technology Data Exchange (ETDEWEB)

    Musick, C.A.

    1997-11-01

    A 3.5 liter refractory-lined joule-heated glass melter was built to test the applicability of electric melting to vitrify simulated high activity waste (HAW). The HAW streams result from dissolution and separation of Idaho Chemical Processing Plant (ICPP) calcines and/or radioactive liquid waste. Pilot scale melter operations will establish selection criteria needed to evaluate the application of joule heating to immobilize ICPP high activity waste streams. The melter was fabricated with K-3 refractory walls and Inconel 690 electrodes. It is designed to be continuously operated at 1,150 C with a maximum glass output rate of 10 lbs/hr. The first set of tests were completed using surrogate HAW-sodium bearing waste (SBW). The melter operated for 57 hours and was shut down due to excessive melt temperatures resulting in low glass viscosity (< 30 Poise). Due to the high melt temperature and low viscosity the molten glass breached the melt chamber. The melter has been dismantled and examined to identify required process improvement areas and successes of the first melter run. The melter has been redesigned and is currently being fabricated for the second run, which is scheduled to begin in December 1997.

  3. Liquid secondary waste: Waste form formulation and qualification

    Energy Technology Data Exchange (ETDEWEB)

    Cozzi, A. D. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Dixon, K. L. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Hill, K. A. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Nichols, R. L. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2017-07-31

    The Hanford Site Effluent Treatment Facility (ETF) currently treats aqueous waste streams generated during site cleanup activities. When the Hanford Tank Waste Treatment and Immobilization Plant (WTP) begins operations, including Direct Feed Low Activity Waste (DFLAW) vitrification, a liquid secondary waste (LSW) stream from the WTP will need to be treated. The volume of effluent for treatment at the ETF will increase significantly. The powdered salt waste form produced by the ETF will be replaced by a stabilized solidified waste form for disposal in Hanford’s Integrated Disposal Facility (IDF). Washington River Protection Solutions is implementing a Secondary Liquid Waste Immobilization Technology Development Plan to address the technology needs for a waste form and solidification process to treat the increased volume of waste planned for disposal at the IDF. Waste form testing to support this plan is composed of work in the near term to provide data as input to a performance assessment (PA) for Hanford’s IDF. In 2015, three Hanford Liquid Secondary Waste simulants were developed based on existing and projected waste streams. Using these waste simulants, fourteen mixes of Hanford Liquid Secondary Waste were prepared and tested varying the waste simulant, the water-to-dry materials ratio, and the dry materials blend composition.1 In FY16, testing was performed using a simulant of the EMF process condensate blended with the caustic scrubber—from the Low Activity Waste (LAW) melter—, processed through the ETF. The initial EMF-16 simulant will be based on modeling efforts performed to determine the mass balance of the ETF for the DFLAW.2 The compressive strength of all of the mixes exceeded the target of 3.4 MPa (500 psi) to meet the requirements identified as potential IDF Waste Acceptance Criteria in Table 1 of the Secondary Liquid Waste Immobilization Technology Development Plan.3 The hydraulic properties of the waste forms tested (hydraulic conductivity

  4. Effect of calcination temperature on the structure and performance of CeO{sub x}–MnO{sub x}/TiO{sub 2} nanoparticles for the catalytic combustion of chlorobenzene

    Energy Technology Data Exchange (ETDEWEB)

    He, Fei; Chen, Yong; Zhao, Pei; Liu, Shantang, E-mail: anliu123@hotmail.com [Wuhan Institute of Technology, Key Laboratory for Green Chemical Process of Ministry of Education, School of Chemistry and Environmental Engineering (China)

    2016-05-15

    In this study, MnO{sub x}/TiO{sub 2}, CeO{sub x}/TiO{sub 2}, and CeO{sub x}–MnO{sub x}/TiO{sub 2} catalysts were prepared by the homogeneous precipitation method. The effect of calcination temperature on the structure and catalytic performance of CeO{sub x}–MnO{sub x}/TiO{sub 2} mixed oxide catalyst in the catalytic combustion of chlorobenzene was investigated. The samples were characterized by X-ray diffraction, nitrogen adsorption–desorption, transmission electron microscopy, Raman spectra, hydrogen temperature-programmed reduction, and X-ray photoelectron spectroscopy. The results indicate that calcination significantly affect the activity of the prepared catalysts. When calcined at a low temperature such as 400 °C, Ce, and Mn species form a solid solution of MnCeO{sub x} in the catalyst, thus locating the O atoms in a perturbed chemical surrounding in the catalysts. This increases the mobility of the O atoms during the reaction, probably contributing to the highest catalytic activity of CeO{sub x}–MnO{sub x}/TiO{sub 2} among all the tested catalysts. However, a further increase in the calcination temperature decreased the performance of the catalyst for the catalytic combustion of chlorobenzene. This is probably because of a reduction in surface chemisorbed oxygen concentration, a decrease in the interface area between metal oxides and MnCeO{sub x} caused by the isolation of MnO{sub x} or CeO{sub 2} from MnCeO{sub x}, and a decrease in the specific surface area of CeO{sub x}–MnO{sub x}/TiO{sub 2} catalyst due to the sintering of catalyst.Graphical Abstract.

  5. 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%).

  6. Classification of dimension stone wastes.

    Science.gov (United States)

    Karaca, Zeki; Pekin, Abdülkerim; Deliormanlı, Ahmet Hamdi

    2012-07-01

    For countries in which the stone industry is well developed, opposition to quarry and plant waste is gradually increasing. The primary step for waste control and environmental management is to define the problem of concern. In this study, natural building stone wastes were classified for the first time in the literature. Following on-site physical observations and research at more than 50 quarries and 20 plants, stone wastes were classified as (1) solid, (2) dust and (3) semi-slurry, slurry and cake. As a result of this study, the characteristics of wastes, their main environmental threats and the industries in which wastes could be used were defined for each group.

  7. Radioactive waste study released

    Science.gov (United States)

    Dowhaluk, Bohdan

    A National Research Council (NRC) panel has concluded that the technology for safely storing radioactive waste is ready for confirmation in a test facility. At the same time, the panel proposed safety standards that are more stringent than standards currently proposed by some government agencies. The report, Study of the Isolation System for the Geologic Disposal of Radioactive Wastes, was funded by the Department of Energy as part of its effort to comply with a Congressional mandate to open a national radioactive waste storage facility by the end of the century.The Waste Isolation Panel of the NRC's Board on Radioactive Waste Management did not choose a specific site for the first U.S. repository because the state of current technology does not allow the U.S. to design, construct, and safely operate a full-fledged site. However, the panel's chairman, Thomas H. Pigford, of the University of California at Berkeley, believes that the goal established by Congress can be met.

  8. Effect of Calcination Temperatures on Ratio of Atomic Weight of Al/O in Sol-Gel Method for Synthesis γ Al2O3 as a Buffer Catalyst

    Science.gov (United States)

    Suastiyanti, Dwita; Handayani, Sri; Manawan, Maykel T. E.

    2017-07-01

    The aim of this research was to determine the effect of calcination temperatures on the ratio of atomic weight of Al/O that could affect the formation of γ-Al2O3 phase. The novelty of this research is how to produce γ-Al2O3 in single phase and nanosize by simple method (sol-gel method).The calcination process was performed at a temperature which varied of 190°C, 275°C and 320°C for 4 hours respectively and sinter process carried out at a temperature of 420°C for 6 hours. Calcination process at temperature of 320°C for 4 hours produces powder with the ratio of atomic weight of Al/O in accordance with the ratio of atomic weight of Al/O in Al2O3 compound, 0.6667 (2/3). This ratio is as expected for a compound according to formula of Al2O3. This condition also produces alumina powder with the smallest particle size on the nanometer scale of 84.5 nm. SEM test results show that the grain is still heterogenous in size and shape. The results also show that the grain is still agglomerated.

  9. Liquid secondary waste. Waste form formulation and qualification

    Energy Technology Data Exchange (ETDEWEB)

    Cozzi, A. D. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Dixon, K. L. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Hill, K. A. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); King, W. D. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Nichols, R. L. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2016-03-01

    The Hanford Site Effluent Treatment Facility (ETF) currently treats aqueous waste streams generated during Site cleanup activities. When the Hanford Tank Waste Treatment and Immobilization Plant (WTP) begins operations, a liquid secondary waste (LSW) stream from the WTP will need to be treated. The volume of effluent for treatment at the ETF will increase significantly. Washington River Protection Solutions is implementing a Secondary Liquid Waste Immobilization Technology Development Plan to address the technology needs for a waste form and solidification process to treat the increased volume of waste planned for disposal at the Integrated Disposal Facility IDF). Waste form testing to support this plan is composed of work in the near term to demonstrate the waste form will provide data as input to a performance assessment (PA) for Hanford’s IDF.

  10. WasteWise Resource Management: Innovative Solid Waste Contracting Methods

    Science.gov (United States)

    Resource management is an innovative contractual partnership between a waste-generating organization and a qualified contractor that changes the nature of current disposal services to support waste minimization and recycling.

  11. DOE Waste Treatability Group Guidance

    Energy Technology Data Exchange (ETDEWEB)

    Kirkpatrick, T.D.

    1995-01-01

    This guidance presents a method and definitions for aggregating U.S. Department of Energy (DOE) waste into streams and treatability groups based on characteristic parameters that influence waste management technology needs. Adaptable to all DOE waste types (i.e., radioactive waste, hazardous waste, mixed waste, sanitary waste), the guidance establishes categories and definitions that reflect variations within the radiological, matrix (e.g., bulk physical/chemical form), and regulated contaminant characteristics of DOE waste. Beginning at the waste container level, the guidance presents a logical approach to implementing the characteristic parameter categories as part of the basis for defining waste streams and as the sole basis for assigning streams to treatability groups. Implementation of this guidance at each DOE site will facilitate the development of technically defined, site-specific waste stream data sets to support waste management planning and reporting activities. Consistent implementation at all of the sites will enable aggregation of the site-specific waste stream data sets into comparable national data sets to support these activities at a DOE complex-wide level.

  12. Waste generator services implementation plan

    Energy Technology Data Exchange (ETDEWEB)

    Mousseau, J.; Magleby, M.; Litus, M.

    1998-04-01

    Recurring waste management noncompliance problems have spurred a fundamental site-wide process revision to characterize and disposition wastes at the Idaho National Engineering and Environmental Laboratory. The reengineered method, termed Waste Generator Services, will streamline the waste acceptance process and provide waste generators comprehensive waste management services through a single, accountable organization to manage and disposition wastes in a timely, cost-effective, and compliant manner. This report outlines the strategy for implementing Waste Generator Services across the INEEL. It documents the culmination of efforts worked by the LMITCO Environmental Management Compliance Reengineering project team since October 1997. These efforts have included defining problems associated with the INEEL waste management process; identifying commercial best management practices; completing a review of DOE Complex-wide waste management training requirements; and involving others through an Integrated Process Team approach to provide recommendations on process flow, funding/charging mechanisms, and WGS organization. The report defines the work that will be performed by Waste Generator Services, the organization and resources, the waste acceptance process flow, the funding approach, methods for measuring performance, and the implementation schedule and approach. Field deployment will occur first at the Idaho Chemical Processing Plant in June 1998. Beginning in Fiscal Year 1999, Waste Generator Services will be deployed at the other major INEEL facilities in a phased approach, with implementation completed by March 1999.

  13. Swedish nuclear waste efforts

    Energy Technology Data Exchange (ETDEWEB)

    Rydberg, J.

    1981-09-01

    After the introduction of a law prohibiting the start-up of any new nuclear power plant until the utility had shown that the waste produced by the plant could be taken care of in an absolutely safe way, the Swedish nuclear utilities in December 1976 embarked on the Nuclear Fuel Safety Project, which in November 1977 presented a first report, Handling of Spent Nuclear Fuel and Final Storage of Vitrified Waste (KBS-I), and in November 1978 a second report, Handling and Final Storage of Unreprocessed Spent Nuclear Fuel (KBS II). These summary reports were supported by 120 technical reports prepared by 450 experts. The project engaged 70 private and governmental institutions at a total cost of US $15 million. The KBS-I and KBS-II reports are summarized in this document, as are also continued waste research efforts carried out by KBS, SKBF, PRAV, ASEA and other Swedish organizations. The KBS reports describe all steps (except reprocessing) in handling chain from removal from a reactor of spent fuel elements until their radioactive waste products are finally disposed of, in canisters, in an underground granite depository. The KBS concept relies on engineered multibarrier systems in combination with final storage in thoroughly investigated stable geologic formations. This report also briefly describes other activities carried out by the nuclear industry, namely, the construction of a central storage facility for spent fuel elements (to be in operation by 1985), a repository for reactor waste (to be in operation by 1988), and an intermediate storage facility for vitrified high-level waste (to be in operation by 1990). The R and D activities are updated to September 1981.

  14. Biomedical dental waste management and awareness of waste ...

    African Journals Online (AJOL)

    Biomedical dental waste management and awareness of waste management policy among private dental practitioners in Mangalore city, India. ... services within the city, 44.8% contacted the certified waste carrier services, 42.7% discarded blood soaked swabs and gauze in specific colour coded plastics during disposal.

  15. Waste management of ENM-containing solid waste in Europe

    DEFF Research Database (Denmark)

    Heggelund, Laura Roverskov; Boldrin, Alessio; Hansen, Steffen Foss

    2015-01-01

    waste fractions with waste treatment statistics for Europe, and 4. illustrating the general distribution of ENM into incineration, recycling and landfilling. Our results indicate that ╲plastic from used product containers╡ is the most abundant and diverse waste fraction, comprising a variety of both...

  16. Solid medical waste

    DEFF Research Database (Denmark)

    Udofia, Emilia Asuquo; Gulis, Gabriel; Fobil, Julius

    2017-01-01

    BACKGROUND: Solid medical waste (SMW) in households is perceived to pose minimal risks to the public compared to SMW generated from healthcare facilities. While waste from healthcare facilities is subject to recommended safety measures to minimize risks to human health and the environment, similar......-demographic characteristics, medication related practices, the belief that one is at risk of diseases associated with SMW, SMW disposal practices and reported harm associated with SMW at home and in the community. RESULTS: Eighty percent and 89% of respondents discarded unwanted medicines and sharps in household refuse bins...

  17. 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)

  18. Micro-structural characterization of the hydration products of bauxite-calcination-method red mud-coal gangue based cementitious materials.

    Science.gov (United States)

    Liu, Xiaoming; Zhang, Na; Yao, Yuan; Sun, Henghu; Feng, Huan

    2013-11-15

    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 [AlO4] to [AlO6] and inhibits the combination between [AlO4] and [SiO4] to form C-A-S-H gel. Meanwhile, the polymerization degree of [SiO4] in the hydration products declines. Published by Elsevier B.V.

  19. Waste Isolation Pilot Plant Overview

    Energy Technology Data Exchange (ETDEWEB)

    Weaver, Douglas James [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2017-03-27

    The mission of Waste Isolation Pilot Plant (WIPP) is to demonstrate the safe, environmentally sound, cost effective, permanent disposal of Transuranic (TRU) waste left from production of nuclear weapons.

  20. Biotoxin Safety and Waste Management

    Science.gov (United States)

    The General Safety and Waste Management page offers section-specific safety and waste management details for the biotoxins included in EPA's Selected Analytical Methods for Environmental Remediation and Recovery (SAM).