Density of biogas digestate depending on temperature and composition.

Science.gov (United States)

Gerber, Mandy; Schneider, Nico

2015-09-01

Density is one of the most important physical properties of biogas digestate to ensure an optimal dimensioning and a precise design of biogas plant components like stirring devices, pumps and heat exchangers. In this study the density of biogas digestates with different compositions was measured using pycnometers at ambient pressure in a temperature range from 293.15 to 313.15K. The biogas digestates were taken from semi-continuous experiments, in which the marine microalga Nannochloropsis salina, corn silage and a mixture of both were used as feedstocks. The results show an increase of density with increasing total solid content and a decrease with increasing temperature. Three equations to calculate the density of biogas digestate were set up depending on temperature as well as on the total solid content, organic composition and elemental composition, respectively. All correlations show a relative deviation below 1% compared to experimental data. Copyright © 2015. Published by Elsevier Ltd.

Gas diffusion, non-Darcy air permeability, and computed tomography images of a clay subsoil affected by compaction

DEFF Research Database (Denmark)

Schjønning, Per; Lamandé, Mathieu; Berisso, Feto Esimo

2013-01-01

Soil productivity and other soil functions are dependent on processes in the untilled subsoil. Undisturbed soil cores were collected at the 0.3- to 0.4-m depth from a heavy clay soil in Finland subjected to a single heavy traffic event by agricultural machinery three decades before sampling....... Untrafficked control plots were used as a reference. Computed tomography (CT) scanning was performed on soil cores at a field-sampled field capacity water content. Gas diffusion and air permeability were measured when the soil cores were drained to −1000 hPa matric potential (air permeability also at −100...... and −300 hPa). The air-filled pore space was measured with an air pycnometer and also calculated from mass balance and CT data. Gas diffusion and air permeability were also measured on a straight model tube and on autoclaved aerated concrete. The compaction treatment had not influenced soil total porosity...

Characterisation of the physico-mechanical parameters of MSW.

Science.gov (United States)

Stoltz, Guillaume; Gourc, Jean-Pierre; Oxarango, Laurent

2010-01-01

Following the basics of soil mechanics, the physico-mechanical behaviour of municipal solid waste (MSW) can be defined through constitutive relationships which are expressed with respect to three physical parameters: the dry density, the porosity and the gravimetric liquid content. In order to take into account the complexity of MSW (grain size distribution and heterogeneity larger than for conventional soils), a special oedometer was designed to carry out laboratory experiments. This apparatus allowed a coupled measurement of physical parameters for MSW settlement under stress. The studied material was a typical sample of fresh MSW from a French landfill. The relevant physical parameters were measured using a gas pycnometer. Moreover, the compressibility of MSW was studied with respect to the initial gravimetric liquid content. Proposed methods to assess the set of three physical parameters allow a relevant understanding of the physico-mechanical behaviour of MSW under compression, specifically, the evolution of the limit liquid content. The present method can be extended to any type of MSW. 2010 Elsevier Ltd. All rights reserved.

The evaluation of chosen properties of ashes created by thermal utilization of hazardous and communal wastes

Directory of Open Access Journals (Sweden)

Damian Krawczykowski

2005-11-01

Full Text Available One of methods of the waste neutralization is their thermal transformation in suitable installations or devices in order to achieve the state, which is no longer dangerous for the human health and life or for the environment. In effect of the thermal transformation the “new” wastes are created, which, by law are suppose a to be utilized first. These wastes may be utilized if their properties are suitable. In the paper, the process of thermal utilization of hazardous and municipal wastes is presented, together with the investigation results of the grain composition, surface area, density and of the initial chemical analysis of the created ashes. The research of the grain composition was conducted by using the “Fritsch” apparatus. On the base of the grain composition, the surface area of ashes under investigation was determined, whereas the density was determined by using the helium pycnometer. The purpose of the research was to determine how the properties of ashes are changed and if the differences allow to use these ashes in future.

Radio-frequency (RF) studies of the magneto-dielectric composites: Cr{sub 0.75}Fe{sub 1.25}O{sub 3} (CRFO)-Fe{sub 0.5}Cu{sub 0.75}Ti{sub 0.75}O{sub 3} (FCTO)

Energy Technology Data Exchange (ETDEWEB)

Rocha, H.H.B. [Departamento de Engenharia de Teleinformatica (DETI), Universidade Federal do Ceara, Caixa Postal 6007, CEP 60755-640, Fortaleza, CE (Brazil); Laboratorio de Telecomunicacoes e Ciencia e Engenharia dos Materiais (LOCEM), Departamento de Fisica, Universidade Federal do Ceara, Caixa Postal 6030, CEP 60455-760, Fortaleza, CE (Brazil); Freire, F.N.A. [Departamento de Quimica Organica e Inorganica, Universidade Federal do Ceara, CEP 60455-760, Fortaleza, CE (Brazil); Santos, M.R.P.; Sasaki, J.M. [Laboratorio de Telecomunicacoes e Ciencia e Engenharia dos Materiais (LOCEM), Departamento de Fisica, Universidade Federal do Ceara, Caixa Postal 6030, CEP 60455-760, Fortaleza, CE (Brazil); Cordaro, T. [Celestica do Brasil Ltda, Rod Sp 340 km 128.7-Cp 151, CEP 13820-000, Jaguariuna, SP (Brazil); Sombra, A.S.B. [Laboratorio de Telecomunicacoes e Ciencia e Engenharia dos Materiais (LOCEM), Departamento de Fisica, Universidade Federal do Ceara, Caixa Postal 6030, CEP 60455-760, Fortaleza, CE (Brazil)], E-mail: sombra@fisica.ufc.br

2008-08-01

This paper concerns a study about the electrical properties of Cr{sub 0.75}Fe{sub 1.25}O{sub 3} (CRFO)/Fe{sub 0.5}Cu{sub 0.75}Ti{sub 0.75}O{sub 3} (FCTO) magneto-dielectric composites. These compounds were prepared by the conventional solid-state reaction synthesis. The samples synthesized, as well their two-phase composites [Cr{sub 0.75}Fe{sub 1.25}O{sub 3}]{sub Z}-[Fe{sub 0.5}Cu{sub 0.75}Ti{sub 0.75}O{sub 3}]{sub 100-Z} (Z=17, 34, 50, 66, 83), were characterized by X-ray powder diffraction technique (XRD). Rietveld's method was employed to verify the quantitative phase abundances in the composites' and their theoretical densities, which were compared with the experimental densities (pycnometer method). To predict the effect of the phases in the composites effective dielectric function ({kappa}), traditional dielectric mixing models such as parallel, series, and Lichtenecker's model were observed. An alternative approach, a sigmoidal fitting function based on the Boltzmann equation, was proposed to fit the experimental data.

Laboratory characterization of shale pores

Science.gov (United States)

Nur Listiyowati, Lina

2018-02-01

To estimate the potential of shale gas reservoir, one needs to understand the characteristics of pore structures. Characterization of shale gas reservoir microstructure is still a challenge due to ultra-fine grained micro-fabric and micro level heterogeneity of these sedimentary rocks. The sample used in the analysis is a small portion of any reservoir. Thus, each measurement technique has a different result. It raises the question which methods are suitable for characterizing pore shale. The goal of this paper is to summarize some of the microstructure analysis tools of shale rock to get near-real results. The two analyzing pore structure methods are indirect measurement (MIP, He, NMR, LTNA) and direct observation (SEM, TEM, Xray CT). Shale rocks have a high heterogeneity; thus, it needs multiscale quantification techniques to understand their pore structures. To describe the complex pore system of shale, several measurement techniques are needed to characterize the surface area and pore size distribution (LTNA, MIP), shapes, size and distribution of pore (FIB-SEM, TEM, Xray CT), and total porosity (He pycnometer, NMR). The choice of techniques and methods should take into account the purpose of the analysis and also the time and budget.

Basic and Morphological Properties of Bukit Goh Bauxite

Science.gov (United States)

Hasan, Muzamir; Nor Azmi, Ahmad Amirul Faez Ahmad; Tam, Weng Long; Phang, Biao Yu; Azizul Moqsud, M.

2018-03-01

Investigation conducted by International Maritime Organization (IMO) concluded that the loss of the Bulk Jupiter that carrying bauxite from Kuantan has uncovered evidence to suggest liquefaction led to loss of stability. This research analysed Bukit Goh bauxite and comparison was made with International Maritime Solid Bulk Cargoes (IMSBC Code) standard. To analyse these characteristics of the bauxite, four samples were selected at Bukit Goh, Kuantan ; two of the samples from the Bukit Goh mine and two samples from the stock piles were tested to identify the bauxite basic and morphological properties by referring to GEOSPEC 3 : Model Specification for Soil Testing ; particle size distribution, moisture content and specific gravity and its morphological properties. Laboratory tests involved including Hydrometer test, Small Pycnometer test, Dry Sieve test and Field Emission Scanning Electron Microscop (FESEM) test. The results show that the average moisture content of raw Bukit Goh bauxite is 20.64% which exceeded the recomended value of maximum 10%. Average fine material for raw bauxite is 37.75% which should not be greater than 30% per IMSBC standard. By that, the bauxite from Bukit Goh mine do not achieved the minimum requirements and standards of the IMSBC standard and need to undergo beneficiation process for better quality and safety.

Properties, structure and machnining capabilities sintered corundum abrasives

Directory of Open Access Journals (Sweden)

Cz.J. Niżankowski

2010-07-01

Full Text Available The diversity of sintered corundum abrasives used in both bonded and in the embankment of abrasive tools currently poses substantialproblems for their choice of technology to specific tasks. Therefore performed a comparative study of ownership structures and capacitiesof elected representatives machnining sintered corundum abrasives of different generations, and this is normal sintered alumina,submicrocrystalline alumina sintered and nanocrystalline alumina sintered. Were studied some properties of a set of abrasive particles,physicochemical properties and structural and mechanical and technological properties. The studies used the method of microscopicmeasurement to determine the shape of abrasive particles, the pycnometer to determine the density of abrasive, a spectrometer todetermine the chemical composition of the magnetic analyzer for determining the magnetic fraction, scanning electron microscope toanalysis of abrasive grains and a special position to designate the machining capacity abrasive grains. The results showed a significantincrease in machining capacity sintered corundum abrasives with increasing degree of fragmentation of the crystallites sintered corundum abrasives and distinctive bands in the emerging microchip. The originality of the development provides a comparative summary ofproperties of sintered corundum abrasives of different generations and functions obtained by the author making the change in value indexof machininhcapacity grit from cutting speeds for different generations of sintered corundum.

Herbal mouthwash based on Libidibia ferrea: microbiological control, sensory characteristics, sedimentation, pH and density

Directory of Open Access Journals (Sweden)

Gisely Naura Venâncio

Full Text Available Introduction Phytotherapy is the study of herbal medicines and their applicability to cure diseases in general, being a therapeutic method which can be used for the prevention and treatment of mouth diseases. Among the herbal studied, the Libidibia ferrea, known as jucá or ironwood, is widely used in folk medicine by presenting anti-inflammatory, analgesic, antimicrobial and antipyretic therapeutic properties. Objective To evaluate in vitro pharmacological stability of the Libidibia ferrea extract’s mouthwash (INPA - 228 022. Material and method It was held the mouthwash microbiological control by determining the total number of microorganisms and Salmonella sp, Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus; stability characteristics (color, odor, brightness and consistency, sedimentation test (centrifuge, the pH measurement (pH meter and density evaluation (pycnometer were analyzed. Result The mouthwash showed to be absent from microorganisms and no changes were observed in the organoleptics and sedimentation characteristics. The average pH values were 6.21, 6.15 and 5.85 at 0, 30 and 60 days, respectively, and 1.029, 1.033 and 1.035 g/ mL density values, respectively, without interfering with the final characteristic of the formulation. Conclusion The mouthwash presented pharmacological stability and quality conditions.

Characterization of glass filter micromodels used for polymer EOR flooding experiments

Energy Technology Data Exchange (ETDEWEB)

Foedisch, H.; Wegner, J.; Hincapie-Reina, R.; Ganzer, L. [Technische Univ. Clausthal, Clausthal-Zellerfeld (Germany). ITE

2013-08-01

This work is conducted as part of the research project DGMK 746 - ''Experimental and Numerical Analysis of Polymer Flooding Processes Using Micromodels - From Pore Scale to Continuum Scale''. The industry standard to assess polymer flood performance is through flooding experiments with cores or plugs. A complement to flooding experiments in cores is represented by micromodels such as glass filters, which resemble real porous media through their porous structures. In this way, an almost unlimited number of equivalent samples can be produced. Moreover, compared to cores the micromodels enable visual access to the flooding process enabling a detailed process description. The sintered glass filters used in this work represent one way to make displacement processes inside artificial structures visible. However, challenges exist to transfer the results obtained from models composed of glass to real plugs or rock sections. Therefore, this study focuses on the comparison of glass filter micromodels and real rock samples composed of Bentheimer sandstone. We determine water permeability and oil-water relative permeability endpoints with flooding experiments, compare capillary pressure functions of the glass models obtained from mercury porosimetry analysis with results from Bentheimer sandstone, and characterize the glass filter with respect of connate water saturation using NMR-spectroscopy and porosity obtained from pycnometer measurements. (orig.)

RF and microwave dielectric properties of stored-grain insects and their implications for potential insect control

International Nuclear Information System (INIS)

Nelson, S.O.; Bartley, P.G. Jr.; Lawrence, K.C.

1998-01-01

The permittivities of bulk samples of adult insects of the rice weevil, red flour beetle, sawtoothed grain beetle, and lesser grain borer were measured at single frequencies of 9.4 and 11.7 Ghz in X-band waveguide at about 23 degrees C, and permittivities of homogenized samples of the same species were measured from 0.2 to 20 GHz at temperatures from 10 to 70 degrees C with an open-ended coaxial-line probe and network analyzer. Sample densities for the coaxial-line probe measurements were determined from the X-band measurements with a linear relationship between the cube root of the dielectric constant and sample bulk density determined from permittivity measurements on bulk samples of the adult insects in a waveguide sample holder taken with the short-circuited line technique. Since linearity of the cube root of the dielectric constant with bulk density is consistent with the Landau and Lifshitz, Looyenga dielectric mixture equation, this equation was used to calculate estimated dielectric constants and loss factors of the insects from measured permittivities and volume fractions determined from measured bulk density and adult insect density determined by air-comparison pycnometer measurements. Estimated dielectric constants and loss factors of the insects are presented graphically for temperatures from 10 to 70 degrees C, and tabulated data are provided for range information and comparative purposes

Influence of the composition and agglomeration pressure on the compaction level of the fertilizers based on biomass ash and digestate

Directory of Open Access Journals (Sweden)

Wróbel Marek

2018-01-01

Full Text Available The paper presents the results of research aimed at determining the influence of the composition of the fertilizer mixtures and the compaction pressure on the specific density and density index of fertilizer granules. Investigated mixtures were prepared from fly ash from power plant fuelled by biomass and digestate from biogas plant. The urea, sulfur and phosphorite were also added as enhancing additives. For granule samples made on a strength machine, their specific density was determined on a quasifluid-pycnometer. To determine the effect of agglomerate pressure on the compaction process, the absolute density of the materials was omitted. In such case it was needed to introduce a density index AI. Such a presentation of the results obtained has made it possible to clearly determine how the density of the test mixture results in the applied agglomeration pressure. The specific density of the resulting granules was in the range of 0.85-1.27 g/cm3. The determined density index for the given pressure was in the following ranges: 0.44-0.49 g/cm3 (pressure 100MPa, 0.47-0.51 g/cm3 (pressure 150MPa 0.51 - 0.59 g/cm3 (200MPa pressure. This means that, regardless of the contribution of components to the mixture at the given pressure, a similar degree of compaction was obtained.

Review of intermediate and final product characterization on coated particles preparation

International Nuclear Information System (INIS)

Sukarsono; Kristanti Nurwidyaningrum

2015-01-01

Review of the intermediate and final product characterization on preparation of coated particles was done. Product characterization included a tool to measure the character of raw materials, intermediate product and the final product of the process, which affects the success of getting the high temperature reactor fuel are eligible. Equipment's for the characterization of such materials were pH meter, viscometer, microbalance, turbidity meter, tab density measurement, true density measurement and auto pycnometer. Being for the measurement of particles there are two types destructive testing and non destructive. Destructive testing was done by polished the particles then cross sectional imaging of particle observed using an optical microscope. In this way contains errors due to polishing treatment that could not be right on the equator section so it needs correction. Destructive testing also create waste that must be processed from the remnants of the polishing process. By using non-destructive testing, waste was not formed but the imaging results are often unclear due to lack of contrast. Development of non-destructive test equipment has been made using radiographic method and automated microscopy. The overall activity is still much needed additional tools for measurement and for processing, so that the results obtained will not rejected as the specification of nuclear fuel. Similarly, in the case of a sampling test method and limits to a product accepted or rejected, it should be determined based on statistical methods. (author)

A rapid method for measuring soil water content in the field with a areometer

Directory of Open Access Journals (Sweden)

Calbo Adonai Gimenez

2002-01-01

Full Text Available The availability of a rapid method to evaluate the soil water content (U can be an important tool to determine the moment to irrigate. The soil areometer consists of an elongated hydrostatic balance with a weighing pan, a graduated neck, a float and a pynometric flask. In this work an areometer was adapted to rapidly measure soil water content without the need of drying the soil. The expression U = (M A - M AD/(M M -M A was used to calculate the soil water content. In this equation M M is the mass to level the areometer with the pycnometric flask filled with water, M A the mass to level the areometer with a mass M M of soil in the pycnometer, the volume being completed with water, and similarly M AD the mass added to the pan to level the areometer with a mass M M of dried soil in the pycnometric flask. The convenience of this method is that the values M M and M AD are known. Consequently, the decision on irrigation can be made after a measurement that takes, about, ten minutes. The procedure involves only stirring the soil with water for at least 2 minutes to remove the adhered air. The soil water content data obtained with the areometric method were similar to those obtained weighing the soil before and after drying to constant weight, in an oven at 105º C.

Characterization and surface treatment effects on topography of a glass-infiltrated alumina/zirconia-reinforced ceramic.

Science.gov (United States)

Della Bona, Alvaro; Donassollo, Tiago A; Demarco, Flávio F; Barrett, Allyson A; Mecholsky, John J

2007-06-01

Characterize the microstructure, composition and some physical properties of a glass-infiltrated alumina/zirconia-reinforced ceramic (IZ) and the effect of surface treatment on topography. IZ ceramic specimens were fabricated according to ISO6872 instructions and polished through 1 microm alumina abrasive. Quantitative and qualitative analyses were performed using scanning electron microscopy (SEM), backscattered imaging (BSI), electron dispersive spectroscopy (EDS) and stereology. The elastic modulus (E) and Poisson's ratio (nu) were determined using ultrasonic waves, and the density (rho) using a helium pycnometer. The following ceramic surface treatments were used: AP-as-polished; HF-etching with 9.5% hydrofluoric acid for 90 s; SB-sandblasting with 25 microm aluminum oxide particles for 15s and SC-blasting with 30 microm aluminum oxide particles modified by silica (silica coating) for 15s. An optical profilometer was used to examine the surface roughness (Ra) and SEM-EDS were used to measure the amount of silica after all treatments. The IZ mean property values were as follows: rho=4.45+/-0.01 g/cm(3); nu=0.26 and E=245 GPa. Mean Ra values were similar for AP- and HF-treated IZ but significantly increased after either SC or SB treatment (p

The Influence of Uranium Content and PVA/U Ratio on Physical Propertiesof PVA-U Gel and Its Oxide

International Nuclear Information System (INIS)

Damunir; W, Bangun; Indra-Suryawan; Endang-Nawangsih

2000-01-01

The influence of uranium content and PVA/U ratio on physical propertiesof PVA-U gel and its oxide has been investigated. Fifty milliliters of uranylnitrate solution containing 100 g U/l was neutralized using 1M NH 4 0H. Thesolution was converted into PVA-U sol by adding 9.18 % PVA while mixed andheated at 80 o C for 20 minutes. In order to find spherical gel, the solsolution was dropped into a 5 M NH 4 0H solution at room temperature. Theshape formed of the gels small spherical, shape of the formed gels werefiltered, washed and heated at 120 o C. After that the gels were calcined at800 o C for 4 hours. The formed U 3 O 8 particles. Under a similar method, theinfluence of uranium content from 150-400 g/l and the influence of PVA/Uratio of 6.5-12.5 % in 100 g U/l were studied. Characterization of the resultwas obtained from physical properties of the gel and its oxide in the form ofdensity using pycnometer, surface area using surface areameter with N 2 asabsorbent and particle size/ shape using a loop and optical microscope. Theexperimental results showed that both uranium content and PVA/U ratioaffected the physical properties of the kernel properties. The best resultoccurred at uranium content of 100 g/l and PVA/U 9.18 %. The resulted gelwith solid content of 89.17 %, density of 3.36 g/l and size of 124 μm. Theresulted oxide U 3 0 8 had density of 7.98 g U/l, surface area of specific of0.449 m 2 /g and grain size of 810 μm. (author)

The Influence of Oxidation on the Quality of U3O8 Kernels

International Nuclear Information System (INIS)

Damunir; Sukarsono; Indra Suryawan

2002-01-01

The influence of oxidation on quality of U 3 O 8 kernels have been studied. The investigated the influence was changed of time and temperature oxidation of Uranyl-4(ammonia)-2(polyvinyl alcohol) gel on surface area, pore radius, pore volume, porosity and diameter size of U 3 O 8 kernel. The spherical of uranyl-4(ammonia)-2(polyvinyl alcohol) containing 150g U/l were oxidized at 200-800 o C temperature for 2-24 hours, formed U 3 O 8 kernel. After that, the quality of U 3 O 8 kernel were measured by their physical properties i.e. the surface area and pore radius using Surface areameter with N 2 gas as absorbent. The pore volume and porosity using pycnometer with aquabidest of water as a solvent, diameter size using a optical microscope. The experiment results, showed that the time and temperature oxidation of uranyl-4(ammonia)-2(polyvinyl alcohol) grain the influence to quality of U 3 O 8 in formed the surface area of specific, pore radius, pore volume of specific, porosity, and diameter size of U 3 O 8 kernel. The best accurred at 600-800 o C oxidation temperature and oxidation time was 2-5 hours. The resulted quality of U 3 O 8 kernel i.e surface area of specific was 10.84 - 5.99 m 2 /g, pore volume of specific was 10.35x10 -2 - 3.23x10 -2 cc/g, pore radius was 21.05 - 24.62 Angstrom, diameter size was 1264 - 1456 μm and porosity was 49.49 - 21.36 % Vol with Cumulative analysis error was 8.55 % Vol. (author)

The precursors effects on biomimetic hydroxyapatite ceramic powders.

Science.gov (United States)

Yoruç, Afife Binnaz Hazar; Aydınoğlu, Aysu

2017-06-01

In this study, effects of the starting material on chemical, physical, and biological properties of biomimetic hydroxyapatite ceramic powders (BHA) were investigated. Characterization and chemical analysis of BHA powders were performed by using XRD, FT-IR, and ICP-AES. Microstructural features such as size and morphology of the resulting BHA powders were characterized by using BET, nano particle sizer, pycnometer, and SEM. Additionally, biological properties of the BHA ceramic powders were also investigated by using water-soluble tetrazolium salts test (WST-1). According to the chemical analysis of BHA ceramic powders, chemical structures of ceramics which are prepared under different conditions and by using different starting materials show differences. Ceramic powders which are produced at 80°C are mainly composed of hydroxyapatite, dental hydroxyapatite (contain Na and Mg elements in addition to Ca), and calcium phosphate sulfide. However, these structures are altered at high temperatures such as 900°C depending on the features of starting materials and form various calcium phosphate ceramics and/or their mixtures such as Na-Mg-hydroxyapatite, hydroxyapatite, Mg-Whitlockit, and chloroapatite. In vitro cytotoxicity studies showed that amorphous ceramics produced at 80°C and ceramics containing chloroapatite structure as main or secondary phases were found to be extremely cytotoxic. Furthermore, cell culture studies showed that highly crystalline pure hydroxyapatite structures were extremely cytotoxic due to their high crystallinity values. Consequently, the current study indicates that the selection of starting materials which can be used in the production of calcium phosphate ceramics is very important. It is possible to produce calcium phosphate ceramics which have sufficient biocompatibility at physiological pH values and by using appropriate starting materials. Copyright © 2017 Elsevier B.V. All rights reserved.

A simple method to estimate restoration volume as a possible predictor for tooth fracture.

Science.gov (United States)

Sturdevant, J R; Bader, J D; Shugars, D A; Steet, T C

2003-08-01

Many dentists cite the fracture risk posed by a large existing restoration as a primary reason for their decision to place a full-coverage restoration. However, there is poor agreement among dentists as to when restoration placement is necessary because of the inability to make objective measurements of restoration size. The purpose of this study was to compare a new method to estimate restoration volumes in posterior teeth with analytically determined volumes. True restoration volume proportion (RVP) was determined for 96 melamine typodont teeth: 24 each of maxillary second premolar, mandibular second premolar, maxillary first molar, and mandibular first molar. Each group of 24 was subdivided into 3 groups to receive an O, MO, or MOD amalgam preparation design. Each preparation design was further subdivided into 4 groups of increasingly larger size. The density of amalgam used was calculated according to ANSI/ADA Specification 1. The teeth were weighed before and after restoration with amalgam. Restoration weight was calculated, and the density of amalgam was used to calculate restoration volume. A liquid pycnometer was used to calculate coronal volume after sectioning the anatomic crown from the root horizontally at the cementoenamel junction. True RVP was calculated by dividing restoration volume by coronal volume. An occlusal photograph and a bitewing radiograph were made of each restored tooth to provide 2 perpendicular views. Each image was digitized, and software was used to measure the percentage of the anatomic crown restored with amalgam. Estimated RVP was calculated by multiplying the percentage of the anatomic crown restored from the 2 views together. Pearson correlation coefficients were used to compare estimated RVP with true RVP. The Pearson correlation coefficient of true RVP with estimated RVP was 0.97 overall (Pvolume of restorative material in coronal tooth structure. The fact that it can be done in a nondestructive manner makes it attractive for

Field studies at the Apache Leap Research Site in support of alternative conceptual models

Energy Technology Data Exchange (ETDEWEB)

Woodhouse, E.G.; Davidson, G.R.; Theis, C. [eds.] [and others

1997-08-01

This is a final technical report for a project of the U.S Nuclear Regulatory Commission (sponsored contract NRC-04-090-51) with the University of Arizona. The contract was an optional extension that was initiated on July 21, 1994 and that expired on May 31, 1995. The project manager was Thomas J. Nicholson, Office of Nuclear Regulatory Research. The objectives of this contract were to examine hypotheses and conceptual models concerning unsaturated flow and transport through fractured rock, and to design and execute confirmatory field and laboratory experiments to test these hypotheses and conceptual models at the Apache Leap Research Site near Superior, Arizona. The results discussed here are products of specific tasks that address a broad spectrum of issues related to flow and transport through fractures. Each chapter in this final report summarizes research related to a specific set of objectives and can be read and interpreted as a separate entity. The tasks include detection and characterization of historical rapid fluid flow through fractured rock and the relationship to perched water systems using environmental isotopic tracers of {sup 3}H and {sup 14}C, fluid- and rock-derived {sup 2343}U/{sup 238}U measurements, and geophysical data. The water balance in a small watershed at the ALRS demonstrates the methods of acounting for ET, and estimating the quantity of water available for infiltration through fracture networks. Grain density measurements were made for core-sized samples using a newly designed gas pycnometer. The distribution and magnitude of air permeability measurements have been measured in a three-dimensional setting; the subsequent geostatistical analysis is presented. Electronic versions of the data presented here are available from authors; more detailed discussions and analyses are available in technical publications referenced herein, or soon to appear in the professional literature.

Pycnometric and Spectroscopic Studies of Red Phosphors Ca{sub (1-1.5x)}{sup 2+} WO{sub 4}:Eu{sub x}{sup 3+} Ca{sub (1}-{sub 2x)}{sup 2+} WO{sub 4}:Eu{sub x}{sup 3+},Na{sub x}{sup +}

Energy Technology Data Exchange (ETDEWEB)

Cho, Seonwoog [Silla Univ., Busan (Korea, Republic of)

2013-09-15

Red phosphors Ca{sub (1-1.5x)}Eu{sub x}WO{sub 4} and Ca{sub (1-2x)}Eu{sub x}Na{sub x}WO{sub 4} were synthesized with various concentrations x of Eu{sup 3+} ions by using a solid-state reaction method. The crystal structure of the red phosphors were found to be a tetragonal scheelite structure with space group I4{sub 1}/a. X-ray diffraction (XRD) results show the (112) main diffraction peak centered at 2θ = 28.71 .deg., and indicate that there is no basic structural deformation caused by the vacancies V{sub Ca}'' or the Eu{sup 3+} (and Na{sup +}) ions in the host crystals. Densities of Ca{sub (1.1.5x)}Eu{sub x}WO{sub 4} were measured on a (helium) gas pycnometer. Comparative results between the experimental and theoretical densities reveal that Eu{sup 3+} (and Na{sup +}) ions replace the Ca{sup 2+} ions in the host CaWO{sub 4}. Also, the photoluminescence (PL) emission and photoluminescence excitation (PLE) spectra show the optical properties of trivalent Eu{sup 3+} ions, not of divalent Eu{sup 2+}. Raman spectra exhibit that, without showing any difference before and after the doping of activators to the host material CaWO{sub 4}, all the gerade normal modes occur at the identical frequencies with the same shapes and weaker intensities after the substitution. However, the FT-IR spectra show that some of the ungerade normal modes have shifted positions and different shapes, caused by different masses of Eu{sup 3+} ions (or Na{sup +} ions, or V{sub Ca}'' vacancies) from Ca2{sup +}.

Field studies at the Apache Leap Research Site in support of alternative conceptual models

International Nuclear Information System (INIS)

Woodhouse, E.G.; Davidson, G.R.; Theis, C.

1997-08-01

This is a final technical report for a project of the U.S Nuclear Regulatory Commission (sponsored contract NRC-04-090-51) with the University of Arizona. The contract was an optional extension that was initiated on July 21, 1994 and that expired on May 31, 1995. The project manager was Thomas J. Nicholson, Office of Nuclear Regulatory Research. The objectives of this contract were to examine hypotheses and conceptual models concerning unsaturated flow and transport through fractured rock, and to design and execute confirmatory field and laboratory experiments to test these hypotheses and conceptual models at the Apache Leap Research Site near Superior, Arizona. The results discussed here are products of specific tasks that address a broad spectrum of issues related to flow and transport through fractures. Each chapter in this final report summarizes research related to a specific set of objectives and can be read and interpreted as a separate entity. The tasks include detection and characterization of historical rapid fluid flow through fractured rock and the relationship to perched water systems using environmental isotopic tracers of 3 H and 14 C, fluid- and rock-derived 2343 U/ 238 U measurements, and geophysical data. The water balance in a small watershed at the ALRS demonstrates the methods of acounting for ET, and estimating the quantity of water available for infiltration through fracture networks. Grain density measurements were made for core-sized samples using a newly designed gas pycnometer. The distribution and magnitude of air permeability measurements have been measured in a three-dimensional setting; the subsequent geostatistical analysis is presented. Electronic versions of the data presented here are available from authors; more detailed discussions and analyses are available in technical publications referenced herein, or soon to appear in the professional literature

Assessment of Methods to Consolidate Iodine-Loaded Silver-Functionalized Silica Aerogel

Energy Technology Data Exchange (ETDEWEB)

Matyas, Josef; Engler, Robert K.

2013-09-01

The U.S. Department of Energy is currently investigating alternative sorbents for the removal and immobilization of radioiodine from the gas streams in a nuclear fuel reprocessing plant. One of these new sorbents, Ag0-functionalized silica aerogels, shows great promise as a potential replacement for Ag-bearing mordenites because of its high selectivity and sorption capacity for iodine. Moreover, a feasible consolidation of iodine-loaded Ag0-functionalized silica aerogels to a durable SiO2-based waste form makes this aerogel an attractive choice for sequestering radioiodine. This report provides a preliminary assessment of the methods that can be used to consolidate iodine-loaded Ag0-functionalized silica aerogels into a final waste form. In particular, it focuses on experimental investigation of densification of as prepared Ag0-functionalized silica aerogels powders, with or without organic moiety and with or without sintering additive (colloidal silica), with three commercially available techniques: 1) hot uniaxial pressing (HUP), 2) hot isostatic pressing (HIP), and 3) spark plasma sintering (SPS). The densified products were evaluated with helium gas pycnometer for apparent density, with the Archimedes method for apparent density and open porosity, and with high-resolution scanning electron microscopy and energy dispersive spectroscopy (SEM-EDS) for the extent of densification and distribution of individual elements. The preliminary investigation of HUP, HIP, and SPS showed that these sintering methods can effectively consolidate powders of Ag0-functionalized silica aerogel into products of near-theoretical density. Also, removal of organic moiety and adding 5.6 mass% of colloidal silica to Ag0-functionalized silica aerogel powders before processing provided denser products. Furthermore, the ram travel data for SPS indicated that rapid consolidation of powders can be performed at temperatures below 950°C.

ANALISA KADAR ALKOHOL PADA SUSU FERMENTASI BERDASARKAN LAMA PENYIMPANAN LEMARI ES

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Siti Mardiyah

2015-02-01

Abstract Fermented milk is one of dairy products, obtained by fermentation of milk by certain microbes to produce lactic acid. In general, fermented milk stored at a temperature of 50C cooler cupboard to inhibit acid formation by bacteria is still alive, so as to avoid excessive formation of a sour taste. During storage of fermented milk pH decreased continuously. At a temperature of 100C, the damage began to emerge after 3-4 days of storage, which is a sour, watery, and the accompanying changes in the original tender texture and cause contamination between certain bacteria that cause alcohol. Based on the above formulation of the problem can be taken "Is there any effect of fermented milk storage time in the freezer for alcohol content? ". The purpose of this study was to investigate the effect of storage time of fermented milk in the fridge for alcohol content. This research is a type of observational analytic studies because there is no treatment of the researchers aimed to determine the effect of long storage of fermented milk in the fridge for alcohol content. The sampling technique used is random sampling, totaling 5 samples at each storage time. Research variables consisting of the independent variable storage time, and the dependent variable is the alcohol content. The level of alcohol is done in fermented milk after being stored for 1 week, 2 weeks, 3 weeks, and 4 weeks using the method five times Pycnometer with replication. From the results of this study the mean increase in the alcohol content of fermented milk on each storage time is 1 week, 2 weeks, 3 weeks and 4 weeks. Having performed using ANOVA statistical test obtained p = 0.000 (p <0.05 can be summed Ha Ho is rejected or accepted, which means there is the influence of storage time of fermented milk in the fridge for alcohol content.   Keyword : fermented milk, alchohol level

Metrological evaluation of characterization methods applied to nuclear fuels

International Nuclear Information System (INIS)

Faeda, Kelly Cristina Martins; Lameiras, Fernando Soares; Camarano, Denise das Merces; Ferreira, Ricardo Alberto Neto; Migliorini, Fabricio Lima; Carneiro, Luciana Capanema Silva; Silva, Egonn Hendrigo Carvalho

2010-01-01

In manufacturing the nuclear fuel, characterizations are performed in order to assure the minimization of harmful effects. The uranium dioxide is the most used substance as nuclear reactor fuel because of many advantages, such as: high stability even when it is in contact with water at high temperatures, high fusion point, and high capacity to retain fission products. Several methods are used for characterization of nuclear fuels, such as thermogravimetric analysis for the ratio O / U, penetration-immersion method, helium pycnometer and mercury porosimetry for the density and porosity, BET method for the specific surface, chemical analyses for relevant impurities, and the laser flash method for thermophysical properties. Specific tools are needed to control the diameter and the sphericity of the microspheres and the properties of the coating layers (thickness, density, and degree of anisotropy). Other methods can also give information, such as scanning and transmission electron microscopy, X-ray diffraction, microanalysis, and mass spectroscopy of secondary ions for chemical analysis. The accuracy of measurement and level of uncertainty of the resulting data are important. This work describes a general metrological characterization of some techniques applied to the characterization of nuclear fuel. Sources of measurement uncertainty were analyzed. The purpose is to summarize selected properties of UO 2 that have been studied by CDTN in a program of fuel development for Pressurized Water Reactors (PWR). The selected properties are crucial for thermalhydraulic codes to study basic design accidents. The thermal characterization (thermal diffusivity and thermal conductivity) and the penetration immersion method (density and open porosity) of UO 2 samples were focused. The thermal characterization of UO 2 samples was determined by the laser flash method between room temperature and 448 K. The adaptive Monte Carlo Method was used to obtain the endpoints of the

Making of U3O8 Microsphere as a Preliminary Material for Manufacturing UO2 Kernel of HTR

International Nuclear Information System (INIS)

Hidayati; Triyono; Endang Nawangsih

2007-01-01

The making of U 3 O 8 microsphere as a preliminary material for manufacturing UO 2 kernel of HTR on various feed solution with internal gelation method use of paraffin gelation medium has been done. The aim of this research is to make U 3 O 8 microsphere as preliminary material for making UO 2 kernel which has good characteristic and for knowing to some extent the feed solution influence on U 3 O 8 microsphere. Uranyl nitrate solution was used as a feed solution with acidity 1 M and some various of ADUN solution. ADUN solution was made by adding various of ammonia solution on the solution of uranyl nitrate. Each of the feed solution was added urea + HMTA solution and then it was dropped to a column containing hot paraffin solution at the temperature 95°Celsius in order to get UO 3 gel. UO 3 gel was dipped and washed with NH 4 OH, dried and calcined at the temperature of 800°Celsius . The obtained product was analyzed its surface area, radius of pore, total volume of pore and distribution of pore size of Surface Area Analyzer NOVA-1000. The density was analyzed with pycnometer and the form of microsphere was analyzed with SEM. The obtained product shows that U 3 O 8 microsphere with less ammonium nitrate gave U 3 O 8 much better and vice versa. The best U 3 O 8 obtained from the with ratio mole nitrate/uranium = 1.9, namely uranyl nitrate solution with the feed acidity of 1 N which was added by the lest amount of NH 4 OH. U 3 O 8 microsphere has density 7.06 g/cc (85.62% theoretical density), specific surface area = 6.77 m 2 /g, mean pore radius 20.52 Å, and also total pore volume 6.91x10 -3 cc/g. (author)

Geological constraints for muon tomography: The world beyond standard rock

Science.gov (United States)

Lechmann, Alessandro; Mair, David; Ariga, Akitaka; Ariga, Tomoko; Ereditato, Antonio; Käser, Samuel; Nishiyama, Ryuichi; Scampoli, Paola; Vladymyrov, Mykhailo; Schlunegger, Fritz

2017-04-01

In present day muon tomography practice, one often encounters an experimental setup in which muons propagate several tens to a few hundreds of meters through a material to the detector. The goal of such an undertaking is usually centred on an attempt to make inferences from the measured muon flux to an anticipated subsurface structure. This can either be an underground interface geometry or a spatial material distribution. Inferences in this direction have until now mostly been done, thereby using the so called "standard rock" approximation. This includes a set of empirically determined parameters from several rocks found in the vicinity of physicist's laboratories. While this approach is reasonable to account for the effects of the tens of meters of soil/rock around a particle accelerator, we show, that for material thicknesses beyond that dimension, the elementary composition of the material (average atomic weight and atomic number) has a noticeable effect on the measured muon flux. Accordingly, the consecutive use of this approximation could potentially lead into a serious model bias, which in turn, might invalidate any tomographic inference, that base on this standard rock approximation. The parameters for standard rock are naturally close to a granitic (SiO2-rich) composition and thus can be safely used in such environments. As geophysical surveys are not restricted to any particular lithology, we investigated the effect of alternative rock compositions (carbonatic, basaltic and even ultramafic) and consequentially prefer to replace the standard rock approach with a dedicated geological investigation. Structural field data and laboratory measurements of density (He-Pycnometer) and composition (XRD) can be merged into an integrative geological model that can be used as an a priori constraint for the rock parameters of interest (density & composition) in the geophysical inversion. Modelling results show that when facing a non-granitic lithology the measured muon

Metrological evaluation of characterization methods applied to nuclear fuels

Energy Technology Data Exchange (ETDEWEB)

Faeda, Kelly Cristina Martins; Lameiras, Fernando Soares; Camarano, Denise das Merces; Ferreira, Ricardo Alberto Neto; Migliorini, Fabricio Lima; Carneiro, Luciana Capanema Silva; Silva, Egonn Hendrigo Carvalho, E-mail: kellyfisica@gmail.co, E-mail: fernando.lameiras@pq.cnpq.b, E-mail: dmc@cdtn.b, E-mail: ranf@cdtn.b, E-mail: flmigliorini@hotmail.co, E-mail: lucsc@hotmail.co, E-mail: egonn@ufmg.b [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

2010-07-01

In manufacturing the nuclear fuel, characterizations are performed in order to assure the minimization of harmful effects. The uranium dioxide is the most used substance as nuclear reactor fuel because of many advantages, such as: high stability even when it is in contact with water at high temperatures, high fusion point, and high capacity to retain fission products. Several methods are used for characterization of nuclear fuels, such as thermogravimetric analysis for the ratio O / U, penetration-immersion method, helium pycnometer and mercury porosimetry for the density and porosity, BET method for the specific surface, chemical analyses for relevant impurities, and the laser flash method for thermophysical properties. Specific tools are needed to control the diameter and the sphericity of the microspheres and the properties of the coating layers (thickness, density, and degree of anisotropy). Other methods can also give information, such as scanning and transmission electron microscopy, X-ray diffraction, microanalysis, and mass spectroscopy of secondary ions for chemical analysis. The accuracy of measurement and level of uncertainty of the resulting data are important. This work describes a general metrological characterization of some techniques applied to the characterization of nuclear fuel. Sources of measurement uncertainty were analyzed. The purpose is to summarize selected properties of UO{sub 2} that have been studied by CDTN in a program of fuel development for Pressurized Water Reactors (PWR). The selected properties are crucial for thermalhydraulic codes to study basic design accidents. The thermal characterization (thermal diffusivity and thermal conductivity) and the penetration immersion method (density and open porosity) of UO{sub 2} samples were focused. The thermal characterization of UO{sub 2} samples was determined by the laser flash method between room temperature and 448 K. The adaptive Monte Carlo Method was used to obtain the endpoints of

Efecto de la concentración de sulfato de sodio en la viscosidad y difusividad térmica de barbotinas de arcillas rojas

Directory of Open Access Journals (Sweden)

Victor Useche

2009-01-01

Full Text Available We reports the thermal diffusivity (αand kinematic viscosity (σ of red-clay suspensions used by Ceramica Italia SA. company in the productions of spraydried clay powders, in function of sodium sulphate concentration. The samples are formed in percentage in weight of a 64% of clay (solid and a 36% of water (liquid. It is made an addition curve of Na2SO4 from 0,018% to 0,153% in weight, in order to maintain similar density conditions (1.689 ± 0.007 g/cm3 and only change the viscosity of the sample. The dynamic viscosity (μ is measured using the viscosimeter BROOKFIELD-DV-II+Pro. Density (ρ is determined by a metallic pycnometer at 100 cm3. The thermal diffusivity is found by a SH-2 Sensor of the KD2-Pro System, which consists of 2 stainless steel needles 6mm separated, one is functioning as a source of heat and the other one is as a sensor of temperature. X-Rays fluorescence is used to found the chemical composition it reports the presence of SiO2 (64,4%, Al2O3 (21,8% y Fe2O3 (5,4% mainly. The rheological results indicate that the viscosity increases when the concentration of sodium sulfate increases in the sample, appearing a change in the state of dispersion of particles; since the suspensions demonstrate a behavior from fluid to reach a higher viscosity. The thermal diffusivity depends on the concentration of Na2SO4 that showed an average deviation of 3.5% and reported a minimum value of 0.00330 cm2/s and a maximum value of 0.00375 cm2/s. The Prandtl Numbers ( found for each concentration of Na2SO4 used, which were very much greater that one (Pr>> 1, which indicates the thermal boundary layer ismuch smaller than the hydrodynamic boundary layer.

The heating of UO_2 kernels in argon gas medium on the physical properties of sintered UO_2 kernels

International Nuclear Information System (INIS)

Damunir; Sri Rinanti Susilowati; Ariyani Kusuma Dewi

2015-01-01

The heating of UO_2 kernels in argon gas medium on the physical properties of sinter UO_2 kernels was conducted. The heated of the UO_2 kernels was conducted in a sinter reactor of a bed type. The sample used was the UO_2 kernels resulted from the reduction results at 800 °C temperature for 3 hours that had the density of 8.13 g/cm"3; porosity of 0.26; O/U ratio of 2.05; diameter of 1146 μm and sphericity of 1.05. The sample was put into a sinter reactor, then it was vacuumed by flowing the argon gas at 180 mmHg pressure to drain the air from the reactor. After that, the cooling water and argon gas were continuously flowed with the pressure of 5 mPa with 1.5 liter/minutes velocity. The reactor temperature was increased and variated at 1200-1500 °C temperature and for 1-4 hours. The sinters UO_2 kernels resulted from the study were analyzed in term of their physical properties including the density, porosity, diameter, sphericity, and specific surface area. The density was analyzed using pycnometer with CCl_4 solution. The porosity was determined using Haynes equation. The diameters and sphericity were showed using the Dino-lite microscope. The specific surface area was determined using surface area meter Nova-1000. The obtained products showed the the heating of UO_2 kernel in argon gas medium were influenced on the physical properties of sinters UO_2 kernel. The condition of best relatively at 1400 °C temperature and 2 hours time. The product resulted from the study was relatively at its best when heating was conducted at 1400 °C temperature and 2 hours time, produced sinters UO_2 kernel with density of 10.14 gr/ml; porosity of 7 %; diameters of 893 μm; sphericity of 1.07 and specific surface area of 4.68 m"2/g with solidify shrinkage of 22 %. (author)

Determination of degradation rates of organic substances in the unsaturated soil zone depending on the grain size fractions of various soil types

Science.gov (United States)

Fichtner, Thomas; Stefan, Catalin; Goersmeyer, Nora

2015-04-01

respectively pore sizes in the soil samples occurred by air pycnometer measurement and determination of soil moisture characteristic by evaporation method according to Wind/Schindler. The present study results can be useful to find a correlation between various soil types with different grain size distributions and the suitability of these soils for example for the infiltration of treated wastewater in the context of managed aquifer recharge (MAR) measures.

Effect of roughness and porosity on geometry and kinematics of lock-exchange gravity currents

Science.gov (United States)

Gatto, Elena; Adduce, Claudia; Ferreira, Rui M. L.

2017-04-01

Gravity currents generated by lock-exchange are an important research tool to understand key features of flows driven by a density may be naturally caused by interaction of geophysical nature but may also be triggered by adverse anthropic actions, from oil spills to pollution related turbidity. Research on the fundamental geometrical and kinematic features of these currents is still necessary, especially when they propagate on complex geometries. The purpose of this work is to investigate the shape and the velocity of propagation of gravity currents over rough beds and over rough-porous beds. To attain this objective, different initial conditions were specified, namely smooth bed, rough bed composed of a single layer of 2 mm glass beads and rough and porous bed composed of 4 layers of the same beads. The dimensions of the channel are 300 × 19,6 × 40 cm in which a steel gate is inserted to define the lock. Two initial mixtures were tested: 1015 and 1030 kgm-3. The density is measured with a pycnometer on a high precision balance. The mixture is composed of fresh water, salt and rhodamine, to allow for visualization and measurements based on image analysis. A high-speed video system camera was used to record the motion of the current. The camera has a 50 mm lens and a sampling frequency of 100 fps. Gray-level images were obtained with 8 bit depth. Calibration of gray-levels was performed pixel by pixel to mixture concentrations. The current is examined in three positions: immediately after the gate ((x-x0)/x0 = 0 to 3), in the middle ((x-x0)/x0 = 5 to 8) and at the end of the channel((x - x0)/x0 = 10 to 13). It is shown that the celerity of the gravity current wave front varies with the different boundary conditions. Indeed, the current is faster for the smooth bed and slower for the rough bed conditions. No appreciable effects of porosity were registered on the wave celerity. The shape of the current varied slightly between the rough and the porous-rough tests

Caracterização termofísica de polpas de bacuri Thermophysical characterization of bacuri pulp

Directory of Open Access Journals (Sweden)

Marcelo B. Muniz

2006-06-01

Full Text Available Foram estudadas as propriedades termofísicas calor específico, massa específica, difusividade térmica e condutividade térmica de polpas de bacuri em diferentes concentrações. O calor específico foi determinado pelo método do calorímetro de mistura; a massa específica foi determinada em picnômetro; a difusividade térmica foi obtida utilizando-se o método do cilindro infinito; a condutividade térmica foi determinada a partir dos resultados experimentais obtidos para massa específica, calor específico e difusividade térmica. Todas as propriedades também foram estimadas teoricamente com o uso de equações propostas em literatura e por meio de regressões dependentes da concentração. Entre os resultados experimentais o calor específico situou-se entre 3,616 a 2,986 kJ/kgºC; a massa específica variou de 1.008,40 a 1.048,36 kg/m³; a difusividade térmica variou de 1,637x10-7 a 1,787x10-7 m²/s; a condutividade térmica variou de 0,50 a 0,64 W/mºC. Exceto a massa específica, o valor de todas as propriedades diminuiu com o aumento da concentração. A condutividade térmica foi melhor representada por equação do tipo exponencial. As demais propriedades foram bem ajustadas por equações do tipo quadrática.Thermophysical properties, specific heat, density, thermal diffusivity and thermal conductivity of bacuri pulps at different concentrations were studied. The specific heat was determined by the mixture calorimeter method; the density was determined by the pycnometer; the thermal diffusivity was obtained by using the infinite cylinder method; the thermal conductivity was determined from the experimental results obtained for density, specific heat and thermal diffusivity. All the properties were also theoretically determined using proposals equations and regressions. Among the experimental results the specific heat varied from 3.616 to 2.986 kJ/kgºC; the density varied from 1,008.40 to 1,048.36 kg/m³; the thermal

Influence of the metakaolin on porous structure of matrixes based in mk/cement

Directory of Open Access Journals (Sweden)

Frías, M.

2000-09-01

Full Text Available The incorporation of pozzolanic materials in the manufacturing of blended cement has a positive effect on the improvement of blended mortar and concretes performances. These active additions modify porous structure, impeding or delaying the access of aggressive solutions and, therefore materials more durable are possible of obtaining. An increase or decrease on the durability of blended pastes, mortars and concretes will depend on chemical and mineralogical compositions, fineness and reaction kinetics of these pozzolans. The current work shows the results of a research carried out in blended pastes to know the effect of activated material (metakaolin on the microporosity of pastes elaborated with different amounts of mk (0-25%. A water/ binder ratio of 0,55 was used. Samples were cured at 20ºC for 360 days. The evolution of total, capilary and gel porosity as well as average pore size were carried out through mercury intrusion porosimeter (MIP. Also, the helium pycnometer as alternative method to obtain additional information about porosity above 1,4 Å was used. A good correlation between both methods has been obtained. In addition, it is proposed the best mk content for the elaboration of mk-blended pastes.

La incorporación de materiales puzolánicos presenta un efecto positivo en la mejora de las prestaciones de los morteros y hormigones mixtos. Estos modifican la estructura porosa, impidiendo o retrasando el acceso de los medios agresivos y, por lo tanto, contribución a la obtención de materiales mixtos más durables. La mayor o menor durabilidad de las pastas, morteros y hormigones mixtos dependerá de la composición química, mineralógica, finura y de la cinética de reacción de estas adiciones activas. En el presente trabajo se recogen los resultados de una investigación llevada a cabo para conocer el efecto de un material activado (metacaolin en la microporosidad de pastas, elaboradas con diferentes contenidos de

Effect of freezing conditions on β-Tricalcium Phosphate /Camphene scaffold with micro sized particles fabricated by freeze casting.

Science.gov (United States)

Singh, Gurdev; Soundarapandian, S

2018-03-01

The long standing need of the implant manufacturing industries is to fabricate multi-matrix, customized porous scaffold as cost-effectively. In recent years, freeze casting has shown greater opportunity in the fabrication of porous scaffolds (tricalcium phosphate, hydroxyapatite, bioglass, alumina, etc.) such as at ease and good control over pore size, porosity, a range of materials and economic feasibility. In particular, tricalcium phosphate (TCP) has proved as it possesses good biocompatible (osteoinduction, osteoconduction, etc.) and biodegradability hence beta-tricalcium phosphate (β-TCP, particle size of 10µm) was used as base material and camphene was used as a freezing vehicle in this study. Both freezing conditions such as constant freezing temperature (CFT) and constant freezing rate (CFR) were used for six different conditional samples (CFT: 30, 35 and 40vol% solid loading; similarly CFR: 30, 35 and 40vol% solid loading) to study and understand the effect of various properties (pore size, porosity and compressive strength) of the freeze-cast porous scaffold. It was observed that the average size of the pore was varying linearly as from lower to higher when the solid loading was varying higher to lower. With the help of scanning electron micrographs (SEM), it was observed that the average size of pore during CFR (9.7/ 6.5/ 4.9µm) was comparatively higher than the process of CFT (6.0/ 4.8/ 2.6µm) with respect to the same solid loading (30/ 35/ 40vol%) conditions. From the Gas pycnometer analysis, it was found that the porosity in both freezing conditions (CFT, CFR) were almost near values such as 32.8% and 28.5%. Further to be observed that with the increase in solid loading, the total porosity value has decreased due to the reduction in the concentration of the freezing vehicle. Hence, the freezing vehicle was found as responsible for the formation of appropriate size and orientation of pores during freeze casting. The compressive strength (CS

Compaction of PDMS due to proton beam irradiation

International Nuclear Information System (INIS)

Szilasi, S.Z.; Huszank, R.; Rajta, I.; Kokavecz, J.

2011-01-01

Complete text of publication follows. This work is about the detailed investigation of the changes of the surface topography, the degree of compaction/shrinkage and its relation to the irradiation fluence and the structure spacing in poly(dimethylsiloxane) (PDMS) patterned with 2 MeV proton microbeam. Sylgard 184 kit (Dow-Corning) was used to create the PDMS samples. The density of the PDMS samples was determined with pycnometer. The penetration depth for 2 MeV protons is ∼85 μm, the PDMS layer was ∼95 μm thick, so the incident protons stop in the PDMS, they do not reach the substrate. The irradiations have been performed at the nuclear microprobe facility at ATOMKI. The irradiated periodic structures consisted of parallel lines with different widths and spacing. To achieve different degrees of compaction, each structure was irradiated with five different fluences. The surface topography, the phase modification of the surface, and the connection between them were revealed using an atomic force microscope (AFM PSIA XE 100). The shrinkage data were obtained from the topography images. The structures with different line widths and spacing show different degrees of compaction as a function of irradiation fluence. By plotting them in the same graph (Fig. 1) it is clearly seen that the degree of compaction depends on both the irradiation fluence and the distance of the structures. The fluence dependence of the compaction can be explained with the chemical changes of PDMS. When an energetic ion penetrates through the material it scissions the polymer chain, whereupon among other things volatile products form. In the case of PDMS, these are mainly hydrogen, methane and ethane gases that can be released from PDMS. The irradiated volume shrinks due to significant structural change during which silicate derivatives (SiO x ) are formed. The phase change and the corresponding surface topography was compared and studied at all applied irradiation fluences. It was concluded

Hydrogen storage of catalyst-containing activated carbon fibers and effect of surface modification

International Nuclear Information System (INIS)

Ikpyo Hong; Seong Young Lee; Kyung Hee Lee; Sei Min Park

2005-01-01

thermogravimetric analyzer under pressure range from vacuum to 10 Mpa. Sample was pretreated by degassing at 250 C for 5 hours and cooling overnight under 10 -3 torr vacuum and measurement of hydrogen adsorption was performed under pressure ranged 10 -3 torr - 10 MPa. The hydrogen storage amount is calculated from measurement weight change with respect to pressure by subtracted buoyancy measured by reference test which performed measurement of weight reading change of volume-known glassy carbon with respect to the pressure. The sample volume was calculated from density measured with Micromeritics Accupyc 1330 automatic helium pycnometer. Surface modification of adsorbents was performed by physical and chemical treatment such as hall milling or acid treatment and also analyzed as mentioned above. Results and discussion: Prepared ACFs with various catalysts were obtained with form of web which filament diameter is ranged 1-5 μ but spinnability of pitch solution was relatively decreased comparing with pure pitch solution owing to decrease of viscosity. The optimum conditions were 30-40 wt.% pitch/solvent concentration, 13-30 kV for spinning voltage and 13-17 cm for tip to collector distance. Specific surface area measured by nitrogen adsorption isotherm of ACFs was ranged 700 - 3000 m 2 /g and pore size distribution of ACFs were varied with respect to species and contents of catalyst which indicated similar result by catalyst dispersed melt spun ACFs. Hydrogen storage capacities of ACFs showed ranged 0.3 - 1.0% in weight at 10 MPa in room temperature and shows effect of hydrogen storage by surface modification. Hydrogen storage capacity was decreased by ball milling and increased by acid treatment. It is assumed that pore structure deforms by ball milling but effective hydrogen storage capacity increases with edge exposure by acid treatment. But this result was obtained by mild treatments and still requires farther in-depth study about relationship between hydrogen storage and

Volumetric Properties and Molecular Interactions of Binary Mixtures Imidazolium Acetates-ethanol at 293.15 K%293.15 K时咪唑醋酸盐-乙醇二元体系的体积性质及分子间相互作用

Institute of Scientific and Technical Information of China (English)

侯海云; 黄银蓉; 白博峰; 杨靖

2014-01-01

用比重瓶法测定了293.15 K时1-甲基咪唑醋酸盐([Mim]Ac)/1,3-二甲基咪唑醋酸盐([Mmim]Ac)/1-乙基-3-甲基咪唑醋酸盐([Emim]Ac)-乙醇(EtOH)二元体系在全组成范围内的密度.计算出[Mim]Ac/[ Mmim] Ac/[ Emim] Ac和EtOH的表观摩尔体积和体系的超额摩尔体积.用三参数多项式关联拟合了表观摩尔体积与摩尔分数的关系,外推出组分的极限偏摩尔体积和摩尔体积.[ Mim] Ac/[ Mmim] Ac/[ Emim] Ac和EtOH的摩尔体积的外推值与实验值分别在±0.07和±0.04 cm3/mol范围内相一致.计算出了[ Mim] Ac/[ Mmim] Ac/[ Emim] Ac和EtOH分别在无限稀溶液中的溶剂化系数.用Redlich-Kister 方程关联拟合了超额摩尔体积与摩尔分数的关系.分别根据极限偏摩尔体积、摩尔体积与极限偏摩尔体积的差值、溶剂化系数和超额摩尔体积对照讨论了分子间相互作用的强弱.结果显示,在[ Mim] Ac/[ Mmim] Ac/[ Emim] Ac的浓度无限稀溶液中,[ Mim] Ac/[ Mmim] Ac/[ Emim] Ac-EtOH 分子对间相互作用的强弱顺序为[ Mim] Ac-EtOH>[Mmim]Ac-EtOH>[Emim] Ac-EtOH；在 EtOH 的浓度无限稀溶液中,以及体系中[ Mim] Ac/[ Mmim] Ac/[ Emim] Ac的摩尔分数在0.15~0.95间时,[ Mim] Ac/[ Mmim] Ac/[ Emim] Ac-EtOH分子对间相互作用的强弱顺序都为[ Emim] Ac-EtOH>[ Mmim] Ac-EtOH>[ Mim] Ac-EtOH.%Over the full molar fraction range and at 293.15 K, the densities of binary systems 1-methylimi-dazolium acetate ( [ Mim ] Ac )/1 , 3-dimethylimidazolium acetate ( [ Mmim ] Ac )/1-ethyl-3-methylimidazolium acetate([Emim]Ac)(1)-ethanol(EtOH)(2) were measured by pycnometer method. The apparent molar volumes of [ Mim] Ac/[ Mmim] Ac/[ Emim] Ac and EtOH, and the excess molar volumes of the binary mix-tures were calculated. The relations of apparent molar volumes and molar fractions were fitted by three-parame-ter polynomials, from which, the limiting partial molar volumes and molar volumes were extrapolated. For [ Mim] Ac/[ Mmim] Ac/[ Emim

The Effect of Compost and the Ripe Fruit Waste of Fig on some Physical Properties of Surface Soil

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zahra dianat maharluei

2017-02-01

Full Text Available Introduction: In arid and semi-arid soils, low organic matter is one of the barriers to achieving optimal performance. The soils with more organic matter have a better structure and are more resistant to erosive factors such as water and wind. Soil organic matter has a particular importance and has significant impact on the stability of soil aggregates, the extension of plant root system, carbon and water cycles and soil resistance to erosion. This substance acts as a cementing agent and plays an important role in soil flocculation and formation of resistant aggregates.Also, the addition of organic matter to the soil increases soil porosity and decreases soil bulk density. Materials and Methods: In this research, the effect of the two types of organic matter (compost and the ripe fruit waste of fig on some soil physical properties was studied. A factorial experiment based on completely randomized design, including the four levels of compost and the ripe fruit waste of fig (0, 1, 2 and 4 by weight % and three soil types (loamy sand, loam and silty clay loam with three replications was carried out. The soil samples were collected from the three territories of Fars Province: loamy sand soil from Shiraz, loamy soil from Maharlu and Silty clay loam soil from Zarghan area. The soil samples were air dried and passed through a 2 mm sieve. The physical properties including the bulk density, particle density, porosity, moisture content and soil crust strength was measured. In this research, the soil texture by hydrometer method, Electrical conductivity of the soil saturated paste extract by electrical conductivity meter, saturated paste pH by pH meter, seedling emergence test, soil crust strength by a pocket penetrometer (HUMBOLDT MFG.CO. bulk density by cylindrical sample and particle density by pycnometer method were measured. The fig fruit treatments were prepared by thoroughly mixing the dried powder of ripe fig fruit passed through a 2 mm sieve (with

Rapid Solidification of AB{sub 5} Hydrogen Storage Alloys

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Gulbrandsen-Dahl, Sverre

2002-01-01

thesis the changes of the crystal structure and the grain structure of La{sub 0.60}Ce{sub 0.29}Pr{sub 0.04}Nd{sub 0.07}Ni{sub 3.37}Co{sub 0.79}Mn{sub 0.25}Al{sub 0.7}= cooling rate during chill-block melt spinning are described. Totally, the material was rapidly solidified at 9 different cooling rates. The grain structure, crystallographic texture and the lattice parameters were studied by means of electron microscopy and powder X-ray diffraction. Additionally, the density of the rapidly solidified materials was measured by a gas pycnometer. All these properties were found to change with increasing cooling rate. The grain size decreased continuously with increasing cooling rate and was in the range of 1-5 {mu}m. The strength of the crystallographic texture first increased and then decreased with increasing cooling rate. Transmission electron microscopy studies revealed that the grains contained a large amount of crystallographic twins and that the solidification morphology changed from cellular to plane front at a cooling rate during solidification of approximately 6*10{sup 4} Ks{sup -1}. The unit cell volume and the density followed the same pattern with increasing cooling rate and decreased within each solidification morphology, but at the cooling rate from which the morphology changed, both these parameters suddenly increased. The identical variations in the unit cell volume and the density is explained by formation of excess lattice vacancies during rapid solidification. In Part IV of the thesis rapid solidification of the materials La{sub 0.60}Ce{sub 0.27}Pr{sub 0.04}Nd{sub 0.09}Ni{sub 4.76}Sn{sub 0.24} and LaNi{sub 4.76}Sn different cooling rates are described. The materials were analysed by means of electron microscopy and powder X-ray diffraction. The grain structures of both alloys were found to be in the nanometer range, and the grain sizes were almost invariant with increasing cooling rate. Furthermore, the lattice parameters of these materials were almost

Modeling moisture absorption kinetics of barley grain using viscoelastic model and neural networks

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M Kamali

2015-09-01

containers having 200 mg of distilled water. Grains were weighed after a predetermined period of elapsed time (5, 10, 15, 30, 60, 120, etc. minutes. The experiments were conducted with three replications and moisture absorption rates were determined by the equations presented by McWatters et al., 2002. The experiments were conducted on a time table based on which the time for the dissolving of grains was reached. In this case, the moisture content of the grains reaches the saturation point. According to equations presented by Peleg, as water density increases as much as 0.01 gram due to grains dissolving in water, the saturation point has been reached (Peleg, 1988. For this reason, distilled water density was measured and controlled before and after each experiment by a pycnometer. Neural network was designed according to the two methods of multi-layer perceptron (MLP and radial basis function (RBF with three neuron layers. The first layer, i.e. input layer, is independent variables of temperature and time.The second layer, i.e. hidden layers, is the networks hidden layer and the third layer, i.e. output layer, is the dependent variable of moisture content which was selected. In each case, the nonlinear reduced gradient, combined gradient and BFGS algorithm, and Trigonometric, Logarithmic, Gaussian, and Logical functions were used to train, test and evaluate the network. To evaluate the predicting viscoelastic model and the network, we used statistical indices maximum value of coefficient of determination (R2 and minimum value of mean square error (RMSE. Results and Discussion: Moisture absorption curves showed that as the temperature increases, moisture absorption rate increases as well. Higher equilibrium moisture levels are obtained in water with higher temperatures. This phenomenon is the result of increased moisture diffusion in grains due to higher temperature levels. Higher water temperatures causes grain internal material which is mainly starch to gelatinize and