Science.gov

Sample records for xvi calorimetric determination

  1. Thermochemistry of uranium compounds: XVI, Calorimetric determination of the standard molar enthalpy of formation at 298.15 K, low-temperature heat capacity, and high-temperature enthalpy increments of UO{sub 2}(OH){sub 2} {center_dot} H{sub 2}O (schoepite)

    SciTech Connect

    Tasker, I.R.; O`Hare, P.A.G.; Lewis, B.M.; Johnson, G.K.; Cordfunke, E.H.P.

    1987-08-01

    Three precise calorimetric methods, viz., low-temperature adiabatic, high-temperatuare drop, and solution-reaction, have been used to determine as a function of temperature the key chemical thermodynamic properties of a pure sample of schoepite, UO{sub 2}(OH){sub 2} {center_dot} H{sub 2}O. The following results have been obtained at the standard reference temperature T = 298.15 K:standard molar enthalpy of formation {Delta}/sub f/H/sub m/{sup 0}(T) = {minus}1825.4 +- 2.1 kJ mol/sup {minus}1/; molar heat capacity C/sub p,m/{sup 0}(T) = 172.07 +- 0.34 JK/sup {minus}1/; and the standard molar entropy S/sub m/{sup 0}(T) = 188.54 +- 0.38 JK/sup {minus}1/ mol/sup {minus}1/. The molar enthalpy increments relative to 298.15 K and the molar heat capacity are given by the polynomials: {H{sub m}{sup 0}(T) {minus} H{sub m}{sup 0}(298.15 K)}/(J mol/sup {minus}1/) = {minus}38209.0 + 84.2375 (T/K) + 0.1472958 (T/K){sup 2} and C/sub p,m/{sup 0}(T)/(JK/sup {minus}1/ mol/sup {minus}1/) = 84.238 + 0.294592 (T/K), where 298.15 K < T < 400 K. The present result for {Delta}/sup f/H/sub m/{sup 0} at 298.15 K has been combined with three other closely-agreeing values from the literature to give a recommended weighted mean {Delta}/sub f/H/sub m/{sup 0} = {minus}1826.4 +- 1.7 kJ mol/sup {minus}1/, from which is calculated the standard Gibbs energy of formation {Delta}/sub f/G/sub m/{sup 0} = {minus}1637.0 +- 1.7 kJ mol/sup {minus}1/ at 298.15 K. Complete thermodynamic properties of schoepite are tabulated from 298.15 to 423.15 K. 19 refs., 6 tabs.

  2. Calorimetric determination of the enthalpy of formation for pyrophyllite

    NASA Astrophysics Data System (ADS)

    Ogorodova, L. P.; Kiseleva, I. A.; Mel'Chakova, L. V.; Vigasina, M. F.; Spiridonov, E. M.

    2011-09-01

    A calorimetric study of the natural pyrophyllite was performed by high-temperature melt calorimetry on a Tian-Calvet calorimeter. Based on experimentally determined in this work for pyrophyllite and gibbsite, as well as previously obtained for corundum and quartz, the total value of the enthalpy increment for the sample heated from room temperature to 973 K and the enthalpy of dissolution at 973 K by Hess's law, the enthalpy of formation of pyrophyllite of Al2[(OH)2/Si4O10] composed of elements was calculated at 298.15 K: Δf H {el/o}(298.15 K) = -5639.8 ± 5.7 kJ/mol.

  3. Calorimetric method for determination of {sup 51}Cr neutrino source activity

    SciTech Connect

    Veretenkin, E. P. Gavrin, V. N.; Danshin, S. N.; Ibragimova, T. V.; Kozlova, Yu. P.; Mirmov, I. N.

    2015-12-15

    Experimental study of nonstandard neutrino properties using high-intensity artificial neutrino sources requires the activity of the sources to be determined with high accuracy. In the BEST project, a calorimetric system for measurement of the activity of high-intensity (a few MCi) neutrino sources based on {sup 51}Cr with an accuracy of 0.5–1% is created. In the paper, the main factors affecting the accuracy of determining the neutrino source activity are discussed. The calorimetric system design and the calibration results using a thermal simulator of the source are presented.

  4. Calorimetric determinations and theoretical calculations of polymorphs of thalidomide

    NASA Astrophysics Data System (ADS)

    Lara-Ochoa, F.; Pérez, G. Espinosa; Mijangos-Santiago, F.

    2007-09-01

    The analysis of the thermograms of thalidomide obtained for the two reported polymorphs α and β by differential scanning calorimetry (DSC) shows some inconsistencies that are discussed in the present work. The conception of a new polymorph form, named β ∗, allowed us to explain the observed thermal behavior more satisfactorily. This new polymorph shows enantiotropy with both α and β polymorphs, reflected in the unique endotherm obtained in the DSC-thermograms, when a heating rate of 10 °C/min is applied. Several additional experiments, such as re-melting of both polymorph forms, showed that there is indeed a new polymorph with an endotherm located between the endotherms of α and β. IR, Raman, and powder X-ray permit us to characterize the isolated compound, resulting from the re-melting of both polymorph forms. Mechanical calculations were performed to elucidate the conformations of each polymorph, and ab initio quantum chemical calculations were performed to determine the energy of the more stable conformers and the spatial cell energy for both polymorphs α and β. These results suggested a possible conformation for the newly discovered polymorph β ∗.

  5. Thermodynamic Properties of Liquid Silver-Antimony-Tin Alloys Determined from Electrochemical and Calorimetric Measurements

    NASA Astrophysics Data System (ADS)

    Łapsa, Joanna; Onderka, Bogusław

    2016-08-01

    The thermodynamic properties of liquid Ag-Sb-Sn alloys were obtained through use of the drop solution calorimetric method and electromotive force (emf) measurements of galvanic cells with a yttria stabilized zirconia (YSZ) solid electrolyte. The experiments were carried out along Ag0.25Sb0.75, Ag0.5Sb0.5 and Ag0.75Sb0.25 sections of the ternary system in the temperature range from 973 K to 1223 K. From the measured emf, the tin activity in liquid solutions of Ag-Sb-Sn was determined for the first time. The partial and integral enthalpy of mixing were determined from calorimetric measurements at two temperatures. These measurements were performed along two cross-sections: Sb0.5Sn0.5 at 912 K and 1075 K, and Ag0.75Sb0.25 at 1075 K. Both experimental data sets were used to find ternary interaction parameters by applying the Redlich-Kister-Muggianu model of the substitutional solution. Consequently, the set of parameters describing the thermodynamic properties of the liquid phase was derived.

  6. Calorimetric Determinations of the Heat and Products of Detonation for Explosives: October 1961 to April 1982

    NASA Astrophysics Data System (ADS)

    Ornellas, D. L.

    1982-04-01

    This report is a compilation of heat-of-detonation and product-composition data obtained at Lawrence Livermore National Laboratory during the last 21 years. In each determination, a 25-g high-explosive charge was detonated in a bomb calorimeter; a complete calorimetric measurement was made in 1 to 2 h with a precision of 0.3%. Data were interpreted using thermodynamic and hydrodynamic computer calculations. For unconfined or lightly confined charges, the released energy is largely retained in the products, which are subsequently shocked considerably off the Chapman-Jouguet isentrope by reflections from the bomb wall. For heavily confined charges, the detonation energy is largely converted to kinetic and internal energy of the confining case, and the products expand with minimal reshock along the Chapman-Jouguet isentrope.

  7. Device for calorimetric measurement

    DOEpatents

    King, William P; Lee, Jungchul

    2015-01-13

    In one aspect, provided herein is a single crystal silicon microcalorimeter, for example useful for high temperature operation and long-term stability of calorimetric measurements. Microcalorimeters described herein include microcalorimeter embodiments having a suspended structure and comprising single crystal silicon. Also provided herein are methods for making calorimetric measurements, for example, on small quantities of materials or for determining the energy content of combustible material having an unknown composition.

  8. First calorimetric determination of heat of extraction of 248Cm in a bi-phasic system

    SciTech Connect

    Leigh R. Martin; Peter R. Zalupski

    2011-06-01

    This report presents a summary of the work performed to meet FCR&D level 2 milestone M21SW050201, 'Complete the first calorimetric determination of heat of extraction of 248Cm in a bi-phasic system'. This work was carried out under the auspices of the Thermodynamics and Kinetics FCR&D work package. To complement previous work undertaken under this work package we have extended out heat of extraction studies by di-2-ethyl-hexyl-phosphoric acid to curium. This report also details the heat of extraction of samarium in the same system. This work was performed to not only test the methodology but also to check for consistency with the heats of extraction obtained with those in the prior literature. The heat of extraction for samarium that was obtained in this study was -9.6 kJ mol-1, which is in reasonable agreement with the previously obtained value of -10.9 kJ mol-1. The curium heat of extraction was performed under two sets of conditions and the obtained heats of extraction were in reasonable agreement with each other at -16.0 {+-} 1.1 and -16.8 {+-} 1.5 kJ mol-1.

  9. Calorimetric determination of thermal parameters for the Li/BrCl in SOCl2 (BCX) chemistry

    NASA Technical Reports Server (NTRS)

    Darcy, Eric C.; Kalu, Eric E.; White, Ralph E.

    1990-01-01

    The heat capacity of a Li-BCX DD-cell was found to be dependent on its state of charge by drop calorimetry measurements. The method of drop calorimetry involves measuring the energy (joules) gained or lost from a sample that is transferred from a bath at temperature A to one at temperature B. The thermoneutral potential is defined as the cell potential where the cell electrochemical reactions are neither exothermic nor endothermic. A Hart scientific calorimeter system, Model No. S77XX, designed for heat conduction calorimetry and drop calorimetry was used. Calorimetric analysis yielded a thermoneutral potential of 4.14 volts and a cell heat capacity dependent on the state of charge.

  10. Thermodynamic study of rhodamine 123-calf thymus DNA interaction: determination of calorimetric enthalpy by optical melting study.

    PubMed

    Masum, Abdulla Al; Chakraborty, Maharudra; Pandya, Prateek; Halder, Umesh Chandra; Islam, Md Maidul; Mukhopadhyay, Subrata

    2014-11-20

    In this paper, the interaction of rhodamine123 (R123) with calf thymus DNA has been studied using molecular modeling and other biophysical methods like UV-vis spectroscopy, fluoremetry, optical melting, isothermal titration calorimetry, and circular dichroic studies. Results showed that the binding energy is about -6 to -8 kcal/mol, and the binding process is favored by both negative enthalpy change and positive entropy change. A new method to determine different thermodynamic properties like calorimetric enthalpy and heat capacity change has been introduced in this paper. The obtained data has been crossed-checked by other methods. After dissecting the free-energy contribution, it was observed that the binding was favored by both negative hydrophobic free energy and negative molecular free energy which compensated for the positive free energies due to the conformational change loss of rotational and transitional freedom of the DNA helix.

  11. Thermodynamic study of rhodamine 123-calf thymus DNA interaction: determination of calorimetric enthalpy by optical melting study.

    PubMed

    Masum, Abdulla Al; Chakraborty, Maharudra; Pandya, Prateek; Halder, Umesh Chandra; Islam, Md Maidul; Mukhopadhyay, Subrata

    2014-11-20

    In this paper, the interaction of rhodamine123 (R123) with calf thymus DNA has been studied using molecular modeling and other biophysical methods like UV-vis spectroscopy, fluoremetry, optical melting, isothermal titration calorimetry, and circular dichroic studies. Results showed that the binding energy is about -6 to -8 kcal/mol, and the binding process is favored by both negative enthalpy change and positive entropy change. A new method to determine different thermodynamic properties like calorimetric enthalpy and heat capacity change has been introduced in this paper. The obtained data has been crossed-checked by other methods. After dissecting the free-energy contribution, it was observed that the binding was favored by both negative hydrophobic free energy and negative molecular free energy which compensated for the positive free energies due to the conformational change loss of rotational and transitional freedom of the DNA helix. PMID:25383921

  12. Determination of Nuclear Charge Distributions of Fission Fragments from ^{235}U (n_th, f) with Calorimetric Low Temperature Detectors

    NASA Astrophysics Data System (ADS)

    Grabitz, P.; Andrianov, V.; Bishop, S.; Blanc, A.; Dubey, S.; Echler, A.; Egelhof, P.; Faust, H.; Gönnenwein, F.; Gomez-Guzman, J. M.; Köster, U.; Kraft-Bermuth, S.; Mutterer, M.; Scholz, P.; Stolte, S.

    2016-08-01

    Calorimetric low temperature detectors (CLTD's) for heavy-ion detection have been combined with the LOHENGRIN recoil separator at the ILL Grenoble for the determination of nuclear charge distributions of fission fragments produced by thermal neutron-induced fission of ^{235}U. The LOHENGRIN spectrometer separates fission fragments according to their mass-to-ionic-charge ratio and their kinetic energy, but has no selectivity with respect to nuclear charges Z. For the separation of the nuclear charges, one can exploit the nuclear charge-dependent energy loss of the fragments passing through an energy degrader foil (absorber method). This separation requires detector systems with high energy resolution and negligible pulse height defect, as well as degrader foils which are optimized with respect to thickness, homogeneity, and energy loss straggling. In the present, contribution results of test measurements at the Maier Leibnitz tandem accelerator facility in Munich with ^{109}Ag and ^{127}I beams with the aim to determine the most suitable degrader material, as well as measurements at the Institut Laue-Langevin will be presented. These include a systematic study of the quality of Z-separation of fission fragments in the mass range 82le A le 132 and a systematic measurement of ^{92}Rb fission yields, as well as investigations of fission yields toward the symmetry region.

  13. Calorimetric determination of the enthalpy change for the alpha-helix to coil transition of an alanine peptide in water.

    PubMed Central

    Scholtz, J M; Marqusee, S; Baldwin, R L; York, E J; Stewart, J M; Santoro, M; Bolen, D W

    1991-01-01

    The enthalpy change (delta H) accompanying the alpha-helix to random coil transition in water has been determined calorimetrically for a 50-residue peptide of defined sequence that contains primarily alanine. The enthalpy of helix formation is one of the basic parameters needed to predict thermal unfolding curves for peptide helices and it provides a starting point for analysis of the peptide hydrogen bond. The experimental uncertainty in delta H reflects the fact that the transition curve is too broad to measure in its entirety, which precludes fitting the baselines directly. A lower limit for delta H of unfolding, 0.9 kcal/mol per residue, is given by assuming that the change in heat capacity (delta Cp) is zero, and allowing the baseline to intersect the transition curve at the lowest measured Cp value. Use of the van't Hoff equation plus least-squares fitting to determine a more probable baseline gives delta H = 1.3 kcal/mol per residue. Earlier studies of poly(L-lysine) and poly(L-glutamate) have given 1.1 kcal/mol per residue. Those investigations, along with our present result, suggest that the side chain has little effect on delta H. The possibility that the peptide hydrogen bond shows a correspondingly large delta H, and the implications for protein stability, are discussed. PMID:2011594

  14. The Silver-Nickel Interfacial Enthalpy Determined by Magnetic and Calorimetric Measurements.

    NASA Astrophysics Data System (ADS)

    Zolla, Howard Gordon

    1995-01-01

    A new method for the determination of the average interfacial enthalpy, sigma_sp{A -B}{H}, between unlike phases is presented. A differential scanning calorimeter is used to measure the heat released during precipitation of a superparamagnetic phase from a supersaturated solid solution. The volume fraction distribution of the precipitated phase is determined by maximum entropy modeling of the magnetization, measured to ultra-high fields, as a linear superposition of Langevin functions. Transmission electron microscopy is used to determine the aspect ratios of the precipitates, which is combined with the volume fraction distributions to calculate the total interfacial area in each specimen. The saturation magnetization is used to determine the total amount of the precipitated phase in each sample. The changes in enthalpy, interfacial area, and amount precipitated are used in a thermodynamic and kinetic model to calculate the interfacial enthalpy and heat of mixing. This method is applied to Ag-(5-10)at.% Ni alloys, produced in thin-film form by electron-beam co-evaporation. The average interfacial enthalpy between Ag and Ni, sigma_sp {Ag-Ni} {H}, and the heat of mixing are found to be, respectively, 0.779 +/- 0.076 J/m^2 and 3.59 +/- 0.03 kJ/mol for the average alloy composition of 6.89 at.% Ni.

  15. Calorimetric determination of the enthalpy of formation of partheite, a calcium zeolite

    NASA Astrophysics Data System (ADS)

    Ogorodova, L. P.; Kiseleva, I. A.; Mel'Chakova, L. V.

    2007-02-01

    A thermochemical study of partheite of composition (Ca1.96Mg0.04Na0.01K0.01) · [(Al4.04Fe{0.01/3+})Si3.95O14.97(OH)2.03] · 4.2H2O, a natural calcium zeolite extracted from gabbro pegmatites of the Denezhkin Kamen’ deposit (North Ural, Russia), was performed. The enthalpies of formation of partheite from the constituent oxides, (Δf H°ox(298.15 K) = -359 ± 21), and elements, (Δf H°el(298.15 K) = -10108 ± 21), were determined by means of high-temperature in-melt-dissolution calorimetry. On the basis of the experimental data obtained, the enthalpy of formation of partheite of theoretical composition Ca2[Al4Si4O15(OH)2] · 4H2O from the elements was evaluated, -10052 ± 21 kJ/mol.

  16. Determination of the Temperature Change by Means of an Outcoming Signal of Electric Resistance in an Isoperibolic Calorimetric Cell. Obtainment of Heat Solution

    PubMed Central

    Giraldo-Gutierréz, Liliana; Moreno-Piraján, Juan Carlos

    2005-01-01

    An isoperibolic calorimetric cell is built with glass surrounded by plastic insulation. The cell has a lid on which a thermistor thermometer, an electric resistance to provide the cell with definite quantities of electric work and a container for a glass ampoule, are placed. For measuring the thermal changes, an NTC thermistor, which provides an electric resistance signal that varies with temperature, is used. Calibration curves of the thermistor and of the stabilization of the system signal in thermal equilibrium are shown, which enable the observation of a good insulation. The calorific capacity of the system with water, with a value of 206.7 ±0.7 J °C-1 is determined; the solution enthalpy for propanol-water and KCl-water systems is obtained, which shows the behavior of the cell before exothermic and endothermic effects, respectively.

  17. Isothermal titration calorimetric procedure to determine protein-metal ion binding parameters in the presence of excess metal ion or chelator.

    PubMed

    Nielsen, Anders D; Fuglsang, Claus C; Westh, Peter

    2003-03-15

    Determination of binding parameters for metal ion binding to proteins usually requires preceding steps to remove protein-bound metal ions. Removal of bound metal ions from protein is often associated with decreased stability and inactivation. We present two simple isothermal titration calorimetric procedures that eliminate separate metal ion removal steps and directly monitor the exchange of metal ions between buffer, protein, and chelator. The concept is to add either excess chelator or metal ion to the protein under investigation and subsequently titrate with metal ion or chelator, respectively. It is thereby possible in the same experimental trial to obtain both chelator-metal ion and protein-metal ion binding parameters due to the different thermodynamic "fingerprints" of chelator and protein. The binding models and regression routines necessary to analyze the corresponding binding isotherms have been constructed. Verifications of the models have been done by titrations of mixtures of calcium chelators (BAPTA, HEDTA, and EGTA) and calcium ions and they were both able to account satisfactorily for the observed binding isotherms. Therefore, it was possible to determine stoichiometric and thermodynamic binding parameters. In addition, the concept has been tested on a recombinant alpha-amylase from Bacillus halmapalus where it proved to be a consistent procedure to obtain calcium binding parameters.

  18. Prototype of calorimetric flow microsensor

    NASA Astrophysics Data System (ADS)

    Sazhin, Oleg

    2012-11-01

    An analytical model of calorimetric flow sensor has been developed. The results of the application of this model are utilized to develop a calorimetric flow microsensor with optimal functional characteristics. The technology to manufacture the microsensor is described. A prototype of the microsensor suitable to be used in the mass air flow meter has been designed. The basic characteristics of the microsensor are presented.

  19. Calorimetric studies on viroids.

    PubMed Central

    Klump, H; Riesner, D; Sänger, H L

    1978-01-01

    Thermodynamic studies on highly purified viroid preparations were carried out with the help of a very sensitive adiabatic microcalorimeter. Parallel to the change of UV-absorption at 260 nm as a function of temperature, the additional heat capacity of the dilute viroid solution rises sharply within the melting interval, reaches a maximum at T = Tm and declines to a baseline again when the temperature is increased further. From the peak area the molar transition enthalpy can be calculated. The transition enthalpies of citrus exocortis viroid and cucumber pale fruit viroid are 4200 kJ/mol and 3930 kJ/mol, respectively. The calorimetric results are compared to the results obtained from melting studies using UV-absorption. PMID:662694

  20. Transient calorimetric diagnostics for plasma processing

    NASA Astrophysics Data System (ADS)

    Bornholdt, Sven; Kersten, Holger

    2013-08-01

    This paper reports on an improvement of the calorimetric method for the determination of energy fluxes from plasma towards substrates by using a transient technique. It provides a short overview of the traditional method used for characterization of plasma-wall-interactions during plasma processing. The mathematical framework of the method and possible implications are discussed. It is shown how the method can be improved to obtain additional and detailed information about the energy influx in a shorter measurement time. For this purpose, the probe bias (if applied), which has commonly been kept constant is varied like in Langmuir probe measurements. The experimental validation of the theoretical considerations emphasizes the potential of the method for control in plasma processing. The possibility how the passive calorimetric probe can be used in continuous measurements for process monitoring without any feedback loops used by other probes, is finally discussed.

  1. Calorimetric gas sensor

    DOEpatents

    Ricco, Antonio J.; Hughes, Robert C.; Smith, James H.; Moreno, Daniel J.; Manginell, Ronald P.; Senturia, Stephen D.; Huber, Robert J.

    1998-01-01

    A combustible gas sensor that uses a resistively heated, noble metal-coated, micromachined polycrystalline Si filament to calorimetrically detect the presence and concentration of combustible gases. The filaments tested to date are 2 .mu.m thick.times.10 .mu.m wide.times.100, 250, 500, or 1000 .mu.m-long polycrystalline Si; some are overcoated with a 0.25 .mu.m-thick protective CVD Si.sub.3 N.sub.4 layer. A thin catalytic Pt film was deposited by CVD from the precursor Pt(acac).sub.2 onto microfilaments resistively heated to approximately 500.degree. C.; Pt deposits only on the hot filament. Using a constant-resistance-mode feedback circuit, Pt-coated filaments operating at ca. 300.degree. C. (35 mW input power) respond linearly, in terms of the change in supply current required to maintain constant resistance (temperature), to H.sub.2 concentrations between 100 ppm and 1% in an 80/20 N.sub.2 /O.sub.2 mixture. Other catalytic materials can also be used.

  2. Calorimetric gas sensor

    DOEpatents

    Ricco, A.J.; Hughes, R.C.; Smith, J.H.; Moreno, D.J.; Manginell, R.P.; Senturia, S.D.; Huber, R.J.

    1998-11-10

    A combustible gas sensor is described that uses a resistively heated, noble metal-coated, micromachined polycrystalline Si filament to calorimetrically detect the presence and concentration of combustible gases. The filaments tested to date are 2 {micro}m thick {times} 10{micro}m wide {times} 100, 250, 500, or 1000 {micro}m-long polycrystalline Si; some are overcoated with a 0.25 {micro}m-thick protective CVD Si{sub 3}N{sub 4} layer. A thin catalytic Pt film was deposited by CVD from the precursor Pt(acac){sub 2} onto microfilaments resistively heated to approximately 500 C; Pt deposits only on the hot filament. Using a constant-resistance-mode feedback circuit, Pt-coated filaments operating at ca. 300 C (35 mW input power) respond linearly, in terms of the change in supply current required to maintain constant resistance (temperature), to H{sub 2} concentrations between 100 ppm and 1% in an 80/20 N{sub 2}/O{sub 2} mixture. Other catalytic materials can also be used. 11 figs.

  3. Calorimetric system and method

    DOEpatents

    Gschneidner, K.A. Jr.; Pecharsky, V.K.; Moorman, J.O.

    1998-09-15

    Apparatus is described for measuring heat capacity of a sample where a series of measurements are taken in succession comprises a sample holder in which a sample to be measured is disposed, a temperature sensor and sample heater for providing a heat pulse thermally connected to the sample, and an adiabatic heat shield in which the sample holder is positioned and including an electrical heater. An electrical power supply device provides an electrical power output to the sample heater to generate a heat pulse. The electrical power from a power source to the heat shield heater is adjusted by a control device, if necessary, from one measurement to the next in response to a sample temperature-versus-time change determined before and after a previous heat pulse to provide a subsequent sample temperature-versus-time change that is substantially linear before and after the subsequent heat pulse. A temperature sensor is used and operable over a range of temperatures ranging from approximately 3K to 350K depending upon the refrigerant used. The sample optionally can be subjected to dc magnetic fields such as from 0 to 12 Tesla (0 to 120 kOe). 18 figs.

  4. Calorimetric system and method

    DOEpatents

    Gschneidner, Jr., Karl A.; Pecharsky, Vitalij K.; Moorman, Jack O.

    1998-09-15

    Apparatus for measuring heat capacity of a sample where a series of measurements are taken in succession comprises a sample holder in which a sample to be measured is disposed, a temperature sensor and sample heater for providing a heat pulse thermally connected to the sample, and an adiabatic heat shield in which the sample holder is positioned and including an electrical heater. An electrical power supply device provides an electrical power output to the sample heater to generate a heat pulse. The electrical power from a power source to the heat shield heater is adjusted by a control device, if necessary, from one measurement to the next in response to a sample temperature-versus-time change determined before and after a previous heat pulse to provide a subsequent sample temperature-versus-time change that is substantially linear before and after the subsequent heat pulse. A temperature sensor is used and operable over a range of temperatures ranging from approximately 3K to 350K depending upon the refrigerant used. The sample optionally can be subjected to dc magnetic fields such as from 0 to 12 Tesla (0 to 120 kOe).

  5. PREFACE: Symmetries in Science XVI

    NASA Astrophysics Data System (ADS)

    2014-10-01

    This volume of the proceedings ''Symmetries in Science XVI'' is dedicated to the memory of Miguel Lorente and Allan Solomon who both participated several times in these Symposia. We lost not only two great scientists and colleagues, but also two wonderful persons of high esteem whom we will always remember. Dieter Schuch, Michael Ramek There is a German saying ''all good things come in threes'' and ''Symmetries in Science XVI'', convened July 20-26, 2013 at the Mehrerau Monastery, was our third in the sequel of these symposia since taking it over from founder Bruno Gruber who instigated it in 1988 (then in Lochau). Not only the time seemed to have been perfect (one week of beautiful sunshine), but also the medley of participants could hardly have been better. This time, 34 scientists from 16 countries (more than half outside the European Union) came together to report and discuss their latest results in various fields of science, all related to symmetries. The now customary grouping of renowned experts and talented newcomers was very rewarding and stimulating for all. The informal, yet intense, discussions at ''Gasthof Lamm'' occurred (progressively later) each evening till well after midnight and finally till almost daybreak! However, prior to the opening ceremony and during the conference, respectively, we were informed that Miguel Lorente and Allan Solomon had recently passed away. Both attended the SIS Symposia several times and had many friends among present and former participants. Professor Peter Kramer, himself a long-standing participant and whose 80th birthday commemoration prevented him from attending SIS XVI, kindly agreed to write the obituary for Miguel Lorente. Professors Richard Kerner and Carol Penson (both also former attendees) penned, at very short notice, the tribute to Allan Solomon. The obituaries are included in these Proceedings and further tributes have been posted to our conference website. In 28 lectures and an evening poster

  6. Radiation beam calorimetric power measurement system

    DOEpatents

    Baker, John; Collins, Leland F.; Kuklo, Thomas C.; Micali, James V.

    1992-01-01

    A radiation beam calorimetric power measurement system for measuring the average power of a beam such as a laser beam, including a calorimeter configured to operate over a wide range of coolant flow rates and being cooled by continuously flowing coolant for absorbing light from a laser beam to convert the laser beam energy into heat. The system further includes a flow meter for measuring the coolant flow in the calorimeter and a pair of thermistors for measuring the temperature difference between the coolant inputs and outputs to the calorimeter. The system also includes a microprocessor for processing the measured coolant flow rate and the measured temperature difference to determine the average power of the laser beam.

  7. Automated analysis of calorimetric demicellization titrations.

    PubMed

    Textor, Martin; Keller, Sandro

    2015-09-15

    Determination of the critical micellar concentration of surfactants and of the heat of demicellization by means of isothermal titration calorimetry usually involves either calculation of the first derivative of the heat of demicellization with respect to surfactant concentration or application of a generic sigmoidal fit to the demicellization isotherm. Here, we show that a combination of both approaches provides an unbiased and reproducible data analysis strategy without the need for user input other than the calorimetric data proper. The approach is explained and exemplified using demicellization isotherms of the fluorinated surfactant F6OPC (3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-n-octylphosphocholine) and the zwitterionic detergent CHAPSO (3-([3-cholamidopropyl]dimethylammonio)-2-hydroxy-1-propanesulfonate).

  8. PREFACE: Symmetries in Science XVI

    NASA Astrophysics Data System (ADS)

    2014-10-01

    This volume of the proceedings ''Symmetries in Science XVI'' is dedicated to the memory of Miguel Lorente and Allan Solomon who both participated several times in these Symposia. We lost not only two great scientists and colleagues, but also two wonderful persons of high esteem whom we will always remember. Dieter Schuch, Michael Ramek There is a German saying ''all good things come in threes'' and ''Symmetries in Science XVI'', convened July 20-26, 2013 at the Mehrerau Monastery, was our third in the sequel of these symposia since taking it over from founder Bruno Gruber who instigated it in 1988 (then in Lochau). Not only the time seemed to have been perfect (one week of beautiful sunshine), but also the medley of participants could hardly have been better. This time, 34 scientists from 16 countries (more than half outside the European Union) came together to report and discuss their latest results in various fields of science, all related to symmetries. The now customary grouping of renowned experts and talented newcomers was very rewarding and stimulating for all. The informal, yet intense, discussions at ''Gasthof Lamm'' occurred (progressively later) each evening till well after midnight and finally till almost daybreak! However, prior to the opening ceremony and during the conference, respectively, we were informed that Miguel Lorente and Allan Solomon had recently passed away. Both attended the SIS Symposia several times and had many friends among present and former participants. Professor Peter Kramer, himself a long-standing participant and whose 80th birthday commemoration prevented him from attending SIS XVI, kindly agreed to write the obituary for Miguel Lorente. Professors Richard Kerner and Carol Penson (both also former attendees) penned, at very short notice, the tribute to Allan Solomon. The obituaries are included in these Proceedings and further tributes have been posted to our conference website. In 28 lectures and an evening poster

  9. The VLT-FLAMES Tarantula Survey. XVI. The optical and NIR extinction laws in 30 Doradus and the photometric determination of the effective temperatures of OB stars

    NASA Astrophysics Data System (ADS)

    Maíz Apellániz, J.; Evans, C. J.; Barbá, R. H.; Gräfener, G.; Bestenlehner, J. M.; Crowther, P. A.; García, M.; Herrero, A.; Sana, H.; Simón-Díaz, S.; Taylor, W. D.; van Loon, J. Th.; Vink, J. S.; Walborn, N. R.

    2014-04-01

    Context. The commonly used extinction laws of Cardelli et al. (1989, ApJ, 345, 245) have limitations that, among other issues, hamper the determination of the effective temperatures of O and early B stars from optical and near-infrared (NIR) photometry. Aims: We aim to develop a new family of extinction laws for 30 Doradus, check their general applicability within that region and elsewhere, and apply them to test the feasibility of using optical and NIR photometry to determine the effective temperature of OB stars. Methods: We use spectroscopy and NIR photometry from the VLT-FLAMES Tarantula Survey and optical photometry from HST/WFC3 of 30 Doradus and we analyze them with the software code CHORIZOS using different assumptions, such as the family of extinction laws. Results: We derive a new family of optical and NIR extinction laws for 30 Doradus and confirm its applicability to extinguished Galactic O-type systems. We conclude that by using the new extinction laws it is possible to measure the effective temperatures of OB stars with moderate uncertainties and only a small bias, at least up to E(4405-5495) ~ 1.5 mag. Appendices are available in electronic form at http://www.aanda.org

  10. Thermodynamic properties by non-calorimetric methods. Final report

    SciTech Connect

    Steele, W.V.; Chirico, R.D.; Collier, W.B.; Strube, M.M.; Klots, T.D. |

    1992-12-31

    This research program provided a valuable complement to the experimental programs currently in progress at NIPER for the Advanced Research and Technology Development (AR and TD) and Advanced Exploration and Process Technology (AEPT) divisions of the Department of Energy. These experimental programs are focused on the calorimetric determination of thermodynamic properties of key polynuclear heteroatom-containing aromatic molecules. The project for the Office of Energy Research focused on the non-calorimetric determination of thermodynamic properties through the extension of existing correlation methodologies and through molecular spectroscopy with statistical mechanics. The paper discusses the following studies: Group-contribution approach for polycyclic aromatic hydrocarbons (naphthalene, phenanthrene, anthracene, pyrene, 3-methylphenanthrene, benzoquinolines, biphenyl/hydrogen system); Group-contribution approach for key monocyclic organic compounds; Molecular spectroscopy and statistical mechanics; and Thermophysical property correlations.

  11. Calorimetric Power Measurements of the DIII-D Gyrotron System

    NASA Astrophysics Data System (ADS)

    Gorelov, I.; Lohr, J.; Callis, R. W.; Cary, W. P.; Ponce, D.; Pinsker, R. I.; Chiu, H.; Baity, F. W.

    2001-10-01

    Gyrotron power measurements are an integral part of rf experiments on DIII-D. The ECH complex at General Atomics is built up from four 110 GHz, 1 MW gyrotrons, one from Communication and Power Industry (CPI) and three from Russia's Gyrotron Company (Gycom). Power measurements are made calorimetrically using the temperature and flow measurements of the gyrotron cooling circuits. Three such circuits are measured on the Gycom gyrotrons: window, MOU and dummy load. Interior cooling circuits are additionally measured on the CPI gyrotron that are very useful when tuning for maximum power and efficiency. Calorimetric signals from each cooling circuit are acquired by computer, where the dissipated energy is calculated with a LabView program. From these calculations, total rf power and efficiency were determined. Thus, calorimetry measurements were effectuated during gyrotron operations to provide the average power of each pulse.

  12. Calorimetric Measurements of Liquid Al-Zn Alloys

    NASA Astrophysics Data System (ADS)

    Dębski, Adam; Gąsior, Władysław; Szmit, Katarzyna

    2016-10-01

    The integral molar enthalpies of mixing were determined by the drop calorimetric method for binary AL-Zn liquid solutions and compared with the Miedema model as well as the earlier experimental data. The measurements were conducted at two temperatures: 957 K and 1001 K (684 °C and 728 °C), in the entire concentration range. Based on the experimental calorimetric data of this study as well as those available in the literature and the results of the activity studies, the interaction parameters of the Redlich-Kister equation for the liquid Al-Zn phase were worked out with the use of the least square method. The partial and integral Gibbs energies, entropies and enthalpies were calculated and presented in tables and figures. Additionally, the concentration-concentration partial structure factors for the ideal and real Al-Zn solutions were calculated and graphically presented.

  13. Melting enthalpies of mantle peridotite: calorimetric determinations in the system CaO-MgO-Al 2O 3-SiO 2 and application to magma generation

    NASA Astrophysics Data System (ADS)

    Kojitani, Hiroshi; Akaogi, Masaki

    1997-12-01

    High-temperature drop calorimetry in the temperature range of 1398-1785 K was performed for the samples of mixtures of synthetic anorthite (An), diopside (Di), enstatite (En) and forsterite (Fo) with the same compositions as those of primary melts generated at 1.1, 3 and 4 GPa at most 10° above the solidus of anhydrous mantle peridotite in the CaO-MgO-Al 2O 3-SiO 2 system. From the differences between the heat contents ( H T-H 298) of liquid and that of crystal mixture at the liquidus temperature, melting enthalpies of the samples of 1.1, 3 and 4 GPa-primary melt compositions were determined at 1 atm to be 531 ± 39 J · g -1 at 1583 K, 604 ± 21 J · g -1 at 1703 K, 646 ± 21 J · g -1 at 1753 K, respectively. These heat of fusion values suggest that mixing enthalpy of the melt in the An-Di-En-Fo system is approximately zero within the experimental errors when we use the heat of fusion of Fo by Richet et al. (P. Richet, F. Leclerc, L. Benoist, Melting of forsterite and spinel, with implications for the glass transition of Mg 2SiO 4 liquid, Geophys. Res. Lett. 20 (1993) 1675-1678). The measured enthalpies of melting at 1 atm were converted into those for melting reactions which occur under high pressures by correcting enthalpy changes associated with solid-state mineral reactions. Correcting the effects of pressure, temperature and FeO and Na 2O components on the melting enthalpies at 1 atm, heat of fusion values of a representative mantle peridotite just above the solidus under high pressure were estimated to be 590 J at 1.1 GPa and 1523 K, 692 J at 3 GPa and 1773 K, and 807 J at 4 GPa and 1923 K for melting reactions producing liquid of 1 g, with uncertainties of 50 J. By applying these melting enthalpies to a mantle diapir model which generates present MORBs, a potential mantle temperature of 1533 K has been estimated, assuming an eruption temperature of magma of 1473 K.

  14. A calorimetric probe for plasma diagnostics

    SciTech Connect

    Stahl, Marc; Trottenberg, Thomas; Kersten, Holger

    2010-02-15

    A calorimetric probe for plasma diagnostics is presented, which allows measurements of the power taken by a test substrate. The substrate can be biased and used as an electric probe in order to obtain information about the composition of the total heating power. A new calibration technique for calorimetric probes, which uses monoenergetic electrons at low pressure, has been developed for an improved accuracy. The use of the probe is exemplified with an experiment where both energetic neutral atoms and ions heat the test substrate.

  15. Measurement of the calorimetric energy scale in MINOS

    SciTech Connect

    Hartnell, Jeffrey J.

    2005-01-01

    MINOS is a long-baseline neutrino oscillation experiment. A neutrino beam is created at the Fermi National Accelerator Laboratory in Illinois and fired down through the Earth. Measurements of the energy spectra and composition of the neutrino beam are made both at the source using the Near detector and 735 km away at the Soudan Underground Laboratory in Minnesota using the Far detector. By comparing the spectrum and flavour composition of the neutrino beam between the two detectors neutrino oscillations can be observed. Such a comparison depends on the accuracy of the relative calorimetric energy scale. This thesis details a precise measurement of the calorimetric energy scale of the MINOS Far detector and Calibration detector using stopping muons with a new ''track window'' technique. These measurements are used to perform the relative calibration between the two detectors. This calibration has been accomplished to 1.7% in data and to significantly better than 2% in the Monte Carlo simulation, thus achieving the MINOS relative calibration target of 2%. A number of cross-checks have been performed to ensure the robustness of the calorimetric energy scale measurements. At the Calibration detector the test-beam energy between run periods is found to be consistent with the detector response to better than 2% after the relative calibration is applied. The muon energy loss in the MINOS detectors determined from Bethe-Bloch predictions, data and Monte Carlo are compared and understood. To estimate the systematic error on the measurement of the neutrino oscillation parameters caused by a relative miscalibration a study is performed. A 2% relative miscalibration is shown to cause a 0.6% bias in the values of Δm2 and sin2(2θ).

  16. Adiabatic calorimetric decomposition studies of 50 wt.% hydroxylamine/water.

    PubMed

    Cisneros, L O; Rogers, W J; Mannan, M S

    2001-03-19

    Calorimetric data can provide a basis for determining potential hazards in reactions, storage, and transportation of process chemicals. This work provides calorimetric data for the thermal decomposition behavior in air of 50wt.% hydroxylamine/water (HA), both with and without added stabilizers, which was measured in closed cells with an automatic pressure tracking adiabatic calorimeter (APTAC). Among the data provided are onset temperatures, reaction order, activation energies, pressures of noncondensable products, thermal stability at 100 degrees C, and the effect of HA storage time. Discussed also are the catalytic effects of carbon steel, stainless steel, stainless steel with silica coating, inconel, titanium, and titanium with silica coating on the reaction self-heat rates and onset temperatures. In borosilicate glass cells, HA was relatively stable at temperatures up to 133 degrees C, where the HA decomposition self-heat rate reached 0.05 degrees C/min. The added stabilizers appeared to reduce HA decomposition rates in glass cells and at ambient temperatures. The tested metals and metal surfaces coated with silica acted as catalysts to lower the onset temperatures and increase the self-heat rates. PMID:11165058

  17. Adiabatic calorimetric decomposition studies of 50 wt.% hydroxylamine/water.

    PubMed

    Cisneros, L O; Rogers, W J; Mannan, M S

    2001-03-19

    Calorimetric data can provide a basis for determining potential hazards in reactions, storage, and transportation of process chemicals. This work provides calorimetric data for the thermal decomposition behavior in air of 50wt.% hydroxylamine/water (HA), both with and without added stabilizers, which was measured in closed cells with an automatic pressure tracking adiabatic calorimeter (APTAC). Among the data provided are onset temperatures, reaction order, activation energies, pressures of noncondensable products, thermal stability at 100 degrees C, and the effect of HA storage time. Discussed also are the catalytic effects of carbon steel, stainless steel, stainless steel with silica coating, inconel, titanium, and titanium with silica coating on the reaction self-heat rates and onset temperatures. In borosilicate glass cells, HA was relatively stable at temperatures up to 133 degrees C, where the HA decomposition self-heat rate reached 0.05 degrees C/min. The added stabilizers appeared to reduce HA decomposition rates in glass cells and at ambient temperatures. The tested metals and metal surfaces coated with silica acted as catalysts to lower the onset temperatures and increase the self-heat rates.

  18. Calorimetric thermobarometry of experimentally shocked quartz

    NASA Technical Reports Server (NTRS)

    Ocker, Katherine D.; Gooding, James L.; Hoerz, Friedrich

    1994-01-01

    Structural damage in experimentally shock-metamorphosed, granular quartz is quantitatively measurable by differential scanning calorimetry (DSC). Shock-induced loss of crystallinity is witnessed by disappearance of the alpha/beta phase transformation and evolution of a broad endoenthalpic strain peak at 650-900 K. The strain-energy peak grows rapidly at less than 10 GPa but declines with increasing shock pressure; it approaches zero at 32 GPa where vitrification is extensive. Effects of grain size and post-shock thermal history must be better understood before calorimetric thermobarometry of naturally shocked samples becomes possible.

  19. PIXE analysis of Italian ink drawings of the XVI century

    NASA Astrophysics Data System (ADS)

    Zucchiatti, A.; Climent-Font, A.; Enguita, O.; Fernandez-Jimenez, M. T.; Finaldi, G.; Garrido, C.; Matillas, J. M.

    2005-10-01

    The composition of inks in a group of 24 drawings of ten XVI century Italian painters, has been determined by PIXE at the external micro-beam line of the Centro de Micro Análisis de Materiales of the Universidad Autónoma de Madrid. Ink elemental thicknesses have been determined by comparison with a set of certified thin standards. A comprehensive comparison of inks has also been performed by renormalisation of spectra and definition of an ink-to-ink distance. The elemental compositions and the ink-to-ink distances give consistent results that are generally in line with the appearance of the drawings and add relevant instrumental information to the stylistic observation, revealing for example the presence of retouches and additions in different parts of a drawing. Cluster analysis performed on a subgroup of 13 artefacts from the Genoese painter Luca Cambiaso and his school has revealed a partition that separates neatly the work of the master from that of his followers.

  20. Nanoclay modified polycarbonate blend nanocomposites: Calorimetric and mechanical properties

    NASA Astrophysics Data System (ADS)

    Zicans, Janis; Meri, Remo Merijs; Ivanova, Tatjana; Berzina, Rita; Kalnins, Martins; Maksimovs, Roberts

    2014-05-01

    The research is devoted to characterization of polycarbonate (PC)/acrylonitrile-butadiene styrene (ABS) blend nanocomposites in respects to it mechanical and calorimetric properties. It is shown that PC blend with 10wt% of ABS is more suitable for development of polymer-clay nanocomposites than PC blend with 40wt.% of ABS. It is revealed that the greatest modulus and strength increment is observed for PC/10wt.%ABS blend nanocomposites, containing aromatic organomodifier treated clay (Dellite 43B). It is also determined that optimal nanofiller content for the investigated PC/10%ABS blend is 1.5 wt.%. Increase of mechanical characteristics of PC/10wt.%ABS blend nanocomposites is accompanied with the rise of glass transition temperatures of both polymeric phases, particularly that of PC.

  1. Calorimetric study of tellurium rich Se-Te-Sn glasses

    NASA Astrophysics Data System (ADS)

    Heera, Pawan; Kumar, Anup; Jharwal, Manish; Sharma, Raman

    2016-05-01

    We report the calorimetric study of amorphous Se30Te70-x Snx alloys for x= 0, 1.5, 2.5, 4.5 in terms of kinetic parameters. The DSC curves recorded at four different heating rates are analyzed to determine the transition temperatures, activation energy, thermal stability, glass forming ability. The crystallization process has been investigated using Kissinger, Matusita, Augis and Bennett, and Gao and Wang models. Various kinetic parameters have been calculated for a better understanding of the growth mechanism. The glass transition temperatures Tg, onset crystallization Tc, peak crystallization Tp, and melting temperature Tm are found to increase with the increase in Sn content. The system under investigation is found to be thermally stable for at lower at% of Sn. The values of parameters HR, Hw, and S indicate that Glass forming ability (GFA) decays with an increase in Sn content.

  2. Calorimetric and Magnetic Study of the Holmium

    NASA Astrophysics Data System (ADS)

    Henry, Laurence L.

    Calorimetric measurements have been performed on a series of cubic Laves phase compounds Ho(Co _{rm 1-x}Rh_ {rm x})_2 for x = 0.02, 0.05, 0.08, 0.12, 0.16, and 0.25. The heat capacity data show first-order type peaks at the ferromagnetic transition temperature T_{rm c} for concentrations with x- values between 0.02 and 0.08. For larger concentrations, the peaks at T_{rm c} are much broader and more suggestive of a second-order transition. Utilizing the "s-d" model in conjunction with the specific heat data suggests that the change from first- to second-order in the ferromagnetic transition for x _sp{ ~}{>} 0.10 is due to a reduction in the magnetic exchange interactions between the Ho 4f moments and the cobalt 3d electrons. In addition, the calorimetric data for x <=q 0.16 show another first-order peak at a lower temperature T _{rm sf} which can be associated with a change in the easy magnetization direction of the Ho moments.

  3. New calorimetric all-particle energy spectrum

    NASA Technical Reports Server (NTRS)

    Linsley, J.

    1985-01-01

    Both the maximum size N sub m and the sea level muon size N sub mu have been used separately to find the all-particle energy spectrum in the air shower domain. However the conversion required, whether from N sub m to E or from N sub mu to E, has customarily been carried out by means of calculations based on an assumed cascase model. It is shown here that by combining present data on N sub m and N sub mu spectra with data on: (1); the energy spectrum of air shower muons and (2) the average width of the electron profile, one can obtain empirical values of the N sub m to E and N sub mu to E conversion factors, and an empirical calorimetric all-particle spectrum, in the energy range 2 x 10 to the 6th power E 2 x 10 to the 9th power GeV.

  4. Calorimetric sensors for energy deposition measurements

    SciTech Connect

    Langenbrunner, J.; Cooper, R.; Morgan, G.

    1998-12-31

    A calorimetric sensor with several novel design features has been developed. These sensors will provide an accurate sampling of thermal power density and energy deposition from proton beams incident on target components of accelerator-based systems, such as the Accelerator Production of Tritium Project (APT) and the Spallation Neutron Source (SNS). A small, solid slug (volume = 0.347 cc) of target material is suspended by kevlar fibers and surrounded by an adiabatic enclosure in an insulating vacuum canister of stainless steel construction. The slug is in thermal contact with a low-mass, calibrated, 100-k{Omega} thermistor. Power deposition caused by the passage of radiation through the slug is calculated from the rate of temperature rise of the slug. The authors have chosen slugs composed of Pb, Al, and LiAl.

  5. 25 CFR 36.43 - Standard XVI-Student activities.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 25 Indians 1 2012-04-01 2011-04-01 true Standard XVI-Student activities. 36.43 Section 36.43 Indians BUREAU OF INDIAN AFFAIRS, DEPARTMENT OF THE INTERIOR EDUCATION MINIMUM ACADEMIC STANDARDS FOR THE BASIC EDUCATION OF INDIAN CHILDREN AND NATIONAL CRITERIA FOR DORMITORY SITUATIONS Instructional Support § 36.43 Standard XVI—Student activities....

  6. An Improved Formulation for Calorimetric Emittance Testing of Spacecraft Thermal Control Coatings

    NASA Technical Reports Server (NTRS)

    Kauder, Lonny R.

    2008-01-01

    Spacecraft often really heavily on passive thermal control to maintain operating temperature. An important parameter in the spacecraft heat balance equation is the emittance of thermal control coatings as a function of coating temperature. One method for determining the emittance of spacecraft thermal control from elevated temperature to cryogenic temperatures relies on a calorimetric technique. The fundamental equation governing this test method can be found in numerous places in the literature and although it generally provides reasonable results, its formulation is based on a conceptual flaw that only becomes apparent when the sample temperature approaches the wall temperature during testing. This paper investigates the cause for this error and develops the correct formulation for calorimetric emittance testing. Experimental data will also be presented that illustrates the difference between the two formulations and the resulting difference in the calculated emittance.

  7. Adaptive measurement control for calorimetric assay

    SciTech Connect

    Glosup, J.G.; Axelrod, M.C.

    1994-10-01

    The performance of a calorimeter is usually evaluated by constructing a Shewhart control chart of its measurement errors for a collection of reference standards. However, Shewhart control charts were developed in a manufacturing setting where observations occur in batches. Additionally, the Shewhart control chart expects the variance of the charted variable to be known or at least well estimated from previous experimentation. For calorimetric assay, observations are collected singly in a time sequence with a (possibly) changing mean, and extensive experimentation to calculate the variance of the measurement errors is seldom feasible. These facts pose problems in constructing a control chart. In this paper, the authors propose using the mean squared successive difference to estimate the variance of measurement errors based solely on prior observations. This procedure reduces or eliminates estimation bias due to a changing mean. However, the use of this estimator requires an adjustment to the definition of the alarm and warning limits for the Shewhart control chart. The authors propose adjusted limits based on an approximate Student`s t-distribution for the measurement errors and discuss the limitations of this approximation. Suggestions for the practical implementation of this method are provided also.

  8. The CALorimetric Electron Telescope, CALET, Mission

    NASA Astrophysics Data System (ADS)

    Torii, Shoji

    We are developing the CALorimetric Electron Telescope, CALET, mission for the Japanese Experiment Module Exposed Facility, JEM-EF, of the International Space Station. Major scientific objectives are to search for nearby cosmic ray sources and dark matter by carrying out a precise measurement of the electrons in GeV 20 TeV and the gamma-rays in 20 MeV TeV. CALET has a unique capability to observe electrons and gamma-rays over 1 TeV since the hadron rejection power is more than 105 and the energy resolution better than a few percent over 100 GeV. The detector consists of an Imaging Calorimeter (IMC) with scintillating fiber belts and tungsten plates, a Total Absorption Calorimeter (TASC) with BGO logs, a Silicon Pixel Array (SIA) and a Scintillator Anti-Coincidence System (SACS). CALET has also a capability to measure protons and nuclei in 10 GeV 1000 TeV, and will have a function to monitor solar activity and gamma-ray bursts with additional instruments. The phase A study has started on a schedule of launch in 2013 by H-II Transfer Vehicle (HTV) for 5 years observation.

  9. A calorimetric investigation of spessartine: Vibrational and magnetic heat capacity

    NASA Astrophysics Data System (ADS)

    Dachs, Edgar; Geiger, Charles A.; Withers, Anthony C.; Essene, Eric J.

    2009-06-01

    The heat capacity ( Cp) of two synthetic spessartine samples (Sps) was measured on 20-30 mg-size samples in the temperature range 2-864 K by relaxation calorimetry (RC) and differential scanning calorimetry (DSC). The polycrystalline spessartine samples were synthesized in two different laboratories at high pressures and temperatures from glass and oxide-mixture starting materials and characterized by X-ray powder diffraction and electron-microprobe analysis. The low-temperature heat capacity data show a prominent lambda transition with a peak at 6.2 K, which is interpreted to be the result of a paramagnetic-antiferromagnetic phase transition. The DSC data around ambient T agree excellently with the RC data and can be represented by the Cp polynomial for T > 250 K: CpSps=610-3060·T-0.5-1.45·107·T-2+1.82·109·T-3. Integration of the low temperature Cp data yields a calorimetric standard entropy for the two different samples of So = 334.6 ± 2.7 J/mol · K and 336.0 ± 2.7 J/mol · K. The preferred standard third-law entropy for spessartine is So = 335.3 ± 3.8 J/mol · K, which is the mean value from the two separate determinations. The lattice (vibrational) heat capacity of spessartine was calculated using the single-parameter phonon dispersion model of Komada and Westrum. The lattice entropy at 298.15 K is Svib298.15=297.7J/mol·K, which represents 89% of the calorimetric entropy. The magnetic heat capacity and entropy of spessartine, Smag, at 298.15 K were also calculated. The Smag of the two samples is 38.7 and 37.4 J/mol · K, which is 87% and 83% of the maximum possible magnetic entropy given by 3Rln6 = 44.7 J/mol · K. Published model-dependent lattice-dynamic calculations of Svib298.15 are analyzed and compared to the experimental data. Using the calorimetrically determined So and the Cp polynomial for spessartine, together with high P- T experimental phase-equilibrium data on Mn 2+-Mg partitioning between garnet and olivine, allows calculation of the

  10. Adiabatic Heat of Hydration Calorimetric Measurements for Reference Saltstone Waste

    SciTech Connect

    Bollinger, James

    2006-01-12

    The production of nuclear materials for weapons, medical, and space applications from the mid-1950's through the late-1980's at the Savannah River Site (SRS) generated approximately 35 million gallons of liquid high-level radioactive waste, which is currently being processed into vitrified glass for long-term storage. Upstream of the vitrification process, the waste is separated into three components: high activity insoluble sludge, high activity insoluble salt, and very low activity soluble salts. The soluble salt represents 90% of the 35 million gallons of overall waste and is processed at the SRS Saltstone Facility, where it mixed with cement, blast furnace slag, and flyash, creating a grout-like mixture. The resulting grout is pumped into aboveground storage vaults, where it hydrates into concrete monoliths, called saltstone, thus immobilizing the low-level radioactive salt waste. As the saltstone hydrates, it generates heat that slowly diffuses out of the poured material. To ensure acceptable grout properties for disposal and immobilization of the salt waste, the grout temperature must not exceed 95 C during hydration. Adiabatic calorimetric measurements of the heat generated for a representative sample of saltstone were made to determine the time-dependent heat source term. These measurements subsequently were utilized as input to a numerical conjugate heat transfer model to determine the expected peak temperatures for the saltstone vaults.

  11. Calorimetric versus Growth Microbial Analysis of Cellulase Enzymes Acting on Cellulose

    PubMed Central

    Lovrien, Rex E.; Williams, Karl K.; Ferrey, Mark L.; Ammend, David A.

    1987-01-01

    Assay of cellulase enzymology on cellulose was investigated by two methods: (i) plate colony counting to determine microbial growth and (ii) microbial calorimetry. These methods were chosen because they accept raw samples and have the potential to be far more specific than spectrophotometric reducing sugar assays. Microbial calorimetry requires ca. 0.5 to 1 h and 10 to 100 μM concentrations of cellulolytic lower sugars (glucose and cellobiose). Growth assay (liquid culture, plating, colony counting) requires 15 to 20 h and ca. 0.5 mM sugars. Microbial calorimetry requires simply aerobic metabolism, whereas growth assay requires completion of the cell cycle. A stripping technique is described for use in conjunction with the calorimetric method to enable separate analysis of the two sugars. Mixtures of glucose and cellobiose are equilibrated with Escherichia coli and spun out to remove glucose. The supernatant is calorimetrically combusted with Klebsiella sp. to quantitate cellobiose, and the same organism combusting the nonstripped mixture gives heat proportional to the sum of the two sugars. Calorimetry of cellulolysis products from individual exo- and endocellulases, and from their reconstituted mixture, was carried out to develop a microbial calorimetric means for demonstrating enzyme synergism. PMID:16347508

  12. Neutrino mass calorimetric searches in the MARE experiment

    NASA Astrophysics Data System (ADS)

    Nucciotti, A.; MARE Collaboration

    2012-08-01

    The international project "Microcalorimeter Arrays for a Rhenium Experiment" (MARE) aims at the direct and calorimetric measurement of the electron neutrino mass with sub-electronvolt sensitivity. Calorimetric neutrino mass experiments measure all the energy released in a beta decay except for the energy carried away by the neutrino, therefore removing the most severe systematic uncertainties which have plagued the traditional and, so far, more sensitive spectrometers. Calorimetric measurements are best realized exploiting the thermal detection technique. This approach uses thermal microcalorimeters whose absorbers contain a low transition energy Q beta decaying isotope. To date the two best options are 187Re and 163Ho. While the first beta decays, the latter decays via electron capture, but both have a Q value around 2.5 keV. The potential of using 187Re for a calorimetric neutrino mass experiment has been already demonstrated. On the contrary, no calorimetric spectrum of 163Ho has been so far measured with the precision required to set a useful limit on the neutrino mass. In this talk we present the status and the perspectives of the MARE project activities for the active isotope selection and the single channel development. We also discuss the neutrino mass statistical sensitivity achievable with both isotopes.

  13. EDITORIAL: Special issue: CAMOP MOLEC XVI

    NASA Astrophysics Data System (ADS)

    Ascenzi, Daniela; Franceschi, Pietro; Tosi, Paolo

    2007-09-01

    In this special issue of CAMOP/Physica Scripta we would like to present a picture of the state-of-the-art in the field of the dynamics of molecular systems. It contains a collection of papers submitted in association with the most recent MOLEC meeting (MOLEC XVI), which was held in September 2006 in Levico Terme (Italy) to celebrate the 30th anniversary of the MOLEC conference series. The series of biennial European Conferences on the Dynamics of Molecular Systems (MOLEC) started in 1976, when the first meeting was held in Trento (Italy). Successive conferences were organized in Brandbjerg Højskole (Denmark, 1978), Oxford (UK, 1980), Nijmegen (The Netherlands, 1982), Jerusalem (Israel, 1984), Aussois (France, 1986), Assisi (Italy, 1988), Bernkastel-Kues (Germany, 1990), Prague (Czech Republic, 1992), Salamanca (Spain, 1994), Nyborg Strand (Denmark, 1996), Bristol (UK, 1998), Jerusalem (Israel, 2000), Istanbul (Turkey, 2002) and Nunspeet (The Netherlands, 2004). This is the second time that Physica Scripta has hosted a special issue dedicated to MOLEC. The previous issue ( Physica Scripta (2006) 73 C1-C89) was edited by Steven Stolte and Harold Linnartz following the MOLEC 2004 conference. Following the philosophy of CAMOP, we have asked invited speakers to summarize important problems in their research area, with the objective of setting forth the current thinking of leading researchers in atomic, molecular and optical physics. This comprises discussions of open questions, important new applications, new theoretical and experimental approaches and also predictions of where the field is heading. In addition to being authoritative contributions of acknowledged experts, we hope that the papers also appeal to non-specialists as each work contains a clear and broad introduction and references to the accessible literature. The present special issue comprises 17 papers, which are arranged according to the following topics: theoretical and experimental studies of

  14. Absolute calorimetric calibration of low energy brachytherapy sources

    NASA Astrophysics Data System (ADS)

    Stump, Kurt E.

    In the past decade there has been a dramatic increase in the use of permanent radioactive source implants in the treatment of prostate cancer. A small radioactive source encapsulated in a titanium shell is used in this type of treatment. The radioisotopes used are generally 125I or 103Pd. Both of these isotopes have relatively short half-lives, 59.4 days and 16.99 days, respectively, and have low-energy emissions and a low dose rate. These factors make these sources well suited for this application, but the calibration of these sources poses significant metrological challenges. The current standard calibration technique involves the measurement of ionization in air to determine the source air-kerma strength. While this has proved to be an improvement over previous techniques, the method has been shown to be metrologically impure and may not be the ideal means of calbrating these sources. Calorimetric methods have long been viewed to be the most fundamental means of determining source strength for a radiation source. This is because calorimetry provides a direct measurement of source energy. However, due to the low energy and low power of the sources described above, current calorimetric methods are inadequate. This thesis presents work oriented toward developing novel methods to provide direct and absolute measurements of source power for low-energy low dose rate brachytherapy sources. The method is the first use of an actively temperature-controlled radiation absorber using the electrical substitution method to determine total contained source power of these sources. The instrument described operates at cryogenic temperatures. The method employed provides a direct measurement of source power. The work presented here is focused upon building a metrological foundation upon which to establish power-based calibrations of clinical-strength sources. To that end instrument performance has been assessed for these source strengths. The intent is to establish the limits of

  15. Calorimetric determination of kQ factors for NE 2561 and NE 2571 ionization chambers in 5 cm × 5 cm and 10 cm × 10 cm radiotherapy beams of 8 MV and 16 MV photons

    NASA Astrophysics Data System (ADS)

    Krauss, Achim; Kapsch, Ralf-Peter

    2007-10-01

    The relative uncertainty of the ionometric determination of the absorbed dose to water, Dw, in the reference dosimetry of high-energy photon beams is in the order of 1.5% and is dominated by the uncertainty of the calculated chamber- and energy-dependent correction factors kQ. In the present investigation, kQ values were determined experimentally in 5 cm × 5 cm and 10 cm × 10 cm radiotherapy beams of 8 MV and 16 MV bremsstrahlung by means of a water calorimeter operated at 4 °C. Ionization chambers of the types NE 2561 and NE 2571 were calibrated directly in the water phantom of the calorimeter. The measurements were carried out at the linear accelerator of the Physikalisch-Technische Bundesanstalt. It is shown that the kQ factor of a single ionization chamber can be measured with a standard uncertainty of less than 0.3%. No significant variations of kQ were found for the different lateral sizes of the radiation fields used in this investigation.

  16. A calorimetric determination of the standard enthalpies of formation of huntite, CaMg3 (CO3)4 , and artinite, Mg2(OH)2 CO3 * 3H2O, and their standard Gibbs free energies of formation

    USGS Publications Warehouse

    Hemingway, Bruce S.; Robie, Richard A.

    1973-01-01

    The enthalpies of formation, ΔH°f, of huntite, CaMg3(CO3)4 , and artinite, Mg2(OH)2CO3 * 3H2O, have been determined by HCl solution calorimetry using a constant-volume isoperibol reaction calorimeter. For the reaction CaO(c) + 3MgO(c) + 4CO2 (g) = CaMg3(CO3)4 (c), the enthalpy change at 298.15 K, ΔH°298 , is -123,203±145 cal mol-1. For the reaction 2MgO(c) + 4H2O(l) + CO2(g)=Mg2(OH)2CO3 * 3H2O(c), we obtained -45,132±100 cal mol-1. These results combined with the standard enthalpies of formation of CaO, MgO, H2O, and CO2 lead to ΔH°298 (huntite) = -1,082,600±375 cal mol-1 and ΔH°298  (artinite) = -698,043±170 cal mol-1. Using recently determined values for the standard entropies of huntite, CaMg3(CO3)4, and artinite, Mg2(OH)2CO3 * 3H2O, and of Mg, Ca, C, O2 , and H2 , we calculate ΔG°f,298 (huntite) = -1,004,707±390 cal mol-1 and ΔG°f,298 (artinite) = -613,924±180 cal mol-1.

  17. Calorimetric and computational study of the thermochemistry of phenoxyphenols.

    PubMed

    Ribeiro da Silva, Manuel A V; Lobo Ferreira, Ana I M C; Cimas, Álvaro

    2011-05-20

    Thermodynamic properties of 3- and 4-phenoxyphenol have been determined by using a combination of calorimetric and effusion techniques as well as by high-level ab initio molecular orbital calculations. The standard (p° = 0.1 MPa) molar enthalpies of formation in the condensed and gas states, Δ(f)H(m)°(cr or l) and Δ(f)H(m)°(g), at T = 298.15 K, of 3- and 4-phenoxyphenol were derived from their energies of combustion in oxygen, measured by a static bomb calorimeter, and from the enthalpies of vaporization or sublimation derived respectively by Calvet microcalorimetry for the 3-phenoxyphenol and by Knudsen effusion technique for the 4-phenoxyphenol. The theoretically estimated gas-phase enthalpies of formation were calculated from high-level ab initio molecular orbital calculations at the G3(MP2)//B3LYP level of theory. Furthermore, this composite approach was also used to obtain information about the gas-phase acidities, gas-phase basicities, proton and electron affinities, adiabatic ionization enthalpies, and, finally, O−H bond dissociation enthalpies. The good agreement between the G3MP2B3-derived values and the experimental gas-phase enthalpies of formation for the 3- and 4-phenoxyphenol gives confidence to the estimate concerning the 2-phenoxyphenol isomer, which was not experimentally studied, and to the estimates concerning the radical and the anion. Additionally, the experimental values of gas-phase enthalpies of formation were also compared with estimates based on the empirical scheme developed by Cox. PMID:21486007

  18. Calorimetric measurements of energy transfer efficiency and melting efficiency in CO sub 2 laser beam welding

    SciTech Connect

    Fuerschbach, P.W.

    1990-01-01

    Our previous calorimetric studies of weld melting efficiency and arc efficiency in the GTAW and PAW processes have naturally led us to speculate as to the magnitude of the efficiencies in the LBW process which to data have also not been adequately investigated. Most welding engineers that have had experience with the LBW process are acutely aware that the metals' absorptivity, the surface finish, and the laser wavelength, all play an important role in affecting the energy transfer efficiency, but the extent of their influence and our understanding of the influence of other process variables is not well understood. In addition, it is widely thought that only the LBW or EBW processes can be selected for applications where thermal damage and distortion from the welding process must be kept to a minimum. For these reasons, we have looked forward to performing these calorimetric experiments since they potentially can answer such important questions as: whether or not the melting efficiency of the LBW process is superior to that obtainable with conventional GTAW and PAW welding processes This study was prompted by poor production yields on switching device due to cracking of the ceramic header after final closure welding with the CO{sub 2} LBW process. This calorimetric study was begun in hopes of determining if allowed variations in production process control variables were responsible for increases in heat input and the resulting thermal stresses. By measuring the net heat input to the workpiece with the calorimeter and by measuring the laser output energy and the weld fusion zone size it was possible to determine the magnitudes of both the energy transfer efficiency and the melting efficiency as well as observe their dependence on the process variables. 3 refs.

  19. A Calorimetric Method for Determination of Heat Capacity of Ceramics for Concentrated Solar Thermal Systems / Skenējošās Kalorimetrijas Metode Siltumietilpības Noteikšanai Saules Kolektoru Keramikā

    NASA Astrophysics Data System (ADS)

    Kalnačs, J.; Grehovs, V.; Mežinskis, G.; Bidermanis, L.

    2013-10-01

    Differential scanning calorimetry was carried out to determine the heat capacity (Cp) of the high temperature resistant ceramic materials to be used as protective coatings for stainless steel tubes of parabolic trough solar collectors in concentrated solar power (CSP) systems. The Ср(Т) measurements and calculations were performed at continuous scanning in the temperature range 20-800 °С. In the work, calibration curves have been derived for conversion of measuring units from mcV into mW. To achieve a better repeatability of measurements, methods for stabilization of the thermal contact between the sample-containing vessel and the probe have been developed. The Ср(Т) dependence was obtained for different ceramic materials. Rakstā izklāstīta izstrādātā metodika keramikas un emalju siltumietilpības noteikšanai pēc diferenciālās skenējošās kalorimetrijas mērījumiem. Parādīta virkne traucējošo faktoru kalibrēšanas līknes un mērījumu veikšanai, piedāvātas metodes to samazināšanai vai novēršanai, precīzāku rezultātu ieguvei. Noteikta siltumietilpības atkarība no temperatūras virknei emalju, kas var tikt izmantotas saules siltuma kolektoros, kā aizsargpārklājumi. Parādīta siltumietilpības noteikšanas atkārtojamības atkarība no siltuma kontakta. Izstrādāta metode termiskā kontakta stabilizācijai. Virknei emalju noteikta siltumietilpības atkarība no temperatūras diapazonā 20 - 800°С.

  20. Calorimetric and relaxation properties of xylitol-water mixtures.

    PubMed

    Elamin, Khalid; Sjöström, Johan; Jansson, Helén; Swenson, Jan

    2012-03-14

    We present the first broadband dielectric spectroscopy (BDS) and differential scanning calorimetry study of supercooled xylitol-water mixtures in the whole concentration range and in wide frequency (10(-2)-10(6) Hz) and temperature (120-365 K) ranges. The calorimetric glass transition, T(g), decreases from 247 K for pure xylitol to about 181 K at a water concentration of approximately 37 wt. %. At water concentrations in the range 29-35 wt. % a plentiful calorimetric behaviour is observed. In addition to the glass transition, almost simultaneous crystallization and melting events occurring around 230-240 K. At higher water concentrations ice is formed during cooling and the glass transition temperature increases to a steady value of about 200 K for all higher water concentrations. This T(g) corresponds to an unfrozen xylitol-water solution containing 20 wt. % water. In addition to the true glass transition we also observed a glass transition-like feature at 220 K for all the ice containing samples. However, this feature is more likely due to ice dissolution [A. Inaba and O. Andersson, Thermochim. Acta, 461, 44 (2007)]. In the case of the BDS measurements the presence of water clearly has an effect on both the cooperative α-relaxation and the secondary β-relaxation. The α-relaxation shows a non-Arrhenius temperature dependence and becomes faster with increasing concentration of water. The fragility of the solutions, determined by the temperature dependence of the α-relaxation close to the dynamic glass transition, decreases with increasing water content up to about 26 wt. % water, where ice starts to form. This decrease in fragility with increasing water content is most likely caused by the increasing density of hydrogen bonds, forming a network-like structure in the deeply supercooled regime. The intensity of the secondary β-relaxation of xylitol decreases noticeably already at a water content of 2 wt. %, and at a water content above 5 wt. % it has been

  1. Molecular energetics of alkyl pyrrolecarboxylates: calorimetric and computational study.

    PubMed

    Santos, Ana Filipa L O M; Ribeiro da Silva, Manuel A V

    2013-06-20

    The pyrrole subunit plays an important role in material science as the building block of polypyrroles, an important representative class of conducting polymers, which found widely applications in the area of new materials due to their chemical, thermal, and electrical properties associated with their easiness and low cost of production, making them especially promising for commercial applications. The energetic characterization of this kind of molecules provides information concerning stability, reactivity, and biodegrability of chemical compounds in environment being, for example, helpful in choosing the most adequate method for their elimination by converting the waste into harmless compounds or even decreasing the production of toxic substances in industrial processes. This work reports a combination of calorimetric and computational determinations of several alkyl pyrrolecarboxylates (alkyl = methyl or ethyl) whose main purpose is the calculation of their standard (p° = 0.1 MPa) molar enthalpies of formation, in the gaseous phase, at T = 298.15 K. Experimentally, for methyl 1-pyrrolecarboxylate (M1PC), methyl 2-pyrrolecarboxylate (M2PC), and ethyl 2-pyrrolecarboxylate (E2PC), these values were derived from the standard (p° = 0.1 MPa) molar enthalpies of formation, in the condensed phase, ΔfHm° (cr,l), at T = 298.15 K, obtained by static bomb combustion calorimetry, and from the standard molar enthalpies of phase transition, Δcr,l(g)Hm°, at T = 298.15 K, determined by high-temperature Calvet microcalorimetry. Standard ab initio molecular calculations, at the G3(MP2)//B3LYP level, were performed, and the standard enthalpies of formation of these three compounds were estimated. A very good agreement between the calculated and the experimental data was obtained. Thereby, we have extended these calculations to other alkyl pyrrolecarboxylates, namely, ethyl 1-pyrrolecarboxylate (E1PC), methyl 3-pyrrolecarboxylate (M3PC), and ethyl 3-pyrrolecarboxylate (E3PC

  2. Molecular energetics of alkyl pyrrolecarboxylates: calorimetric and computational study.

    PubMed

    Santos, Ana Filipa L O M; Ribeiro da Silva, Manuel A V

    2013-06-20

    The pyrrole subunit plays an important role in material science as the building block of polypyrroles, an important representative class of conducting polymers, which found widely applications in the area of new materials due to their chemical, thermal, and electrical properties associated with their easiness and low cost of production, making them especially promising for commercial applications. The energetic characterization of this kind of molecules provides information concerning stability, reactivity, and biodegrability of chemical compounds in environment being, for example, helpful in choosing the most adequate method for their elimination by converting the waste into harmless compounds or even decreasing the production of toxic substances in industrial processes. This work reports a combination of calorimetric and computational determinations of several alkyl pyrrolecarboxylates (alkyl = methyl or ethyl) whose main purpose is the calculation of their standard (p° = 0.1 MPa) molar enthalpies of formation, in the gaseous phase, at T = 298.15 K. Experimentally, for methyl 1-pyrrolecarboxylate (M1PC), methyl 2-pyrrolecarboxylate (M2PC), and ethyl 2-pyrrolecarboxylate (E2PC), these values were derived from the standard (p° = 0.1 MPa) molar enthalpies of formation, in the condensed phase, ΔfHm° (cr,l), at T = 298.15 K, obtained by static bomb combustion calorimetry, and from the standard molar enthalpies of phase transition, Δcr,l(g)Hm°, at T = 298.15 K, determined by high-temperature Calvet microcalorimetry. Standard ab initio molecular calculations, at the G3(MP2)//B3LYP level, were performed, and the standard enthalpies of formation of these three compounds were estimated. A very good agreement between the calculated and the experimental data was obtained. Thereby, we have extended these calculations to other alkyl pyrrolecarboxylates, namely, ethyl 1-pyrrolecarboxylate (E1PC), methyl 3-pyrrolecarboxylate (M3PC), and ethyl 3-pyrrolecarboxylate (E3PC

  3. Comparison of the calorimetric and kinematic methods of neutrino energy reconstruction in disappearance experiments

    DOE PAGESBeta

    Ankowski, Artur M.; Benhar, Omar; Coloma, Pilar; Huber, Patrick; Jen, Chun -Min; Mariani, Camillo; Meloni, Davide; Vagnoni, Erica

    2015-10-22

    To be able to achieve their physics goals, future neutrino-oscillation experiments will need to reconstruct the neutrino energy with very high accuracy. In this work, we analyze how the energy reconstruction may be affected by realistic detection capabilities, such as energy resolutions, efficiencies, and thresholds. This allows us to estimate how well the detector performance needs to be determined a priori in order to avoid a sizable bias in the measurement of the relevant oscillation parameters. We compare the kinematic and calorimetric methods of energy reconstruction in the context of two νμ → νμ disappearance experiments operating in different energymore » regimes. For the calorimetric reconstruction method, we find that the detector performance has to be estimated with an O(10%) accuracy to avoid a significant bias in the extracted oscillation parameters. Thus, in the case of kinematic energy reconstruction, we observe that the results exhibit less sensitivity to an overestimation of the detector capabilities.« less

  4. Calorimetric Investigation of Hydrogen Bonding of Formamide and Its Methyl Derivatives in Organic Solvents and Water

    NASA Astrophysics Data System (ADS)

    Varfolomeev, Mikhail A.; Rakipov, Ilnaz T.; Solomonov, Boris N.

    2013-04-01

    Formamide and its derivatives have a large number of practical applications; also they are structural fragments of many biomolecules. Hydrogen bonds strongly affect their physicochemical properties. In the present work a calorimetric study of formamide and its methyl derivatives was carried out. Enthalpies of solution at infinite dilution of formamide, N-methylformamide, and N, N-dimethylformamide in organic solvents at 298.15 K were measured. The relationships between the obtained enthalpies of solvation and the structure of the studied compounds were observed. Hydrogen-bond enthalpies of amides with chlorinated alkanes, ethers, ketones, esters, nitriles, amines, alcohols, and water were determined. The strength of hydrogen bonds of formamide, N-methylformamide, and N, N-dimethylformamide with proton donor solvents is practically equal. Enthalpies of hydrogen bonds of formamide with the proton acceptor solvents are two times larger in magnitude than the enthalpies of N-methylformamide. The process of hydrogen bonding of amides in aliphatic alcohols and water is complicated. The obtained enthalpies of hydrogen bonding in aliphatic alcohols vary considerably from the amide structure due to the competition between solute-solvent and solvent-solvent hydrogen bonds. Fourier transform infrared spectroscopic measurements were carried out to explain the calorimetric data. Hydration enthalpies of methyl derivatives of formamides contain a contribution of the hydrophobic effect. New thermochemical data on the hydrogen bonding of formamides may be useful for predicting the properties of biomacromolecules.

  5. Comparison of the calorimetric and kinematic methods of neutrino energy reconstruction in disappearance experiments

    SciTech Connect

    Ankowski, Artur M.; Benhar, Omar; Coloma, Pilar; Huber, Patrick; Jen, Chun -Min; Mariani, Camillo; Meloni, Davide; Vagnoni, Erica

    2015-10-22

    To be able to achieve their physics goals, future neutrino-oscillation experiments will need to reconstruct the neutrino energy with very high accuracy. In this work, we analyze how the energy reconstruction may be affected by realistic detection capabilities, such as energy resolutions, efficiencies, and thresholds. This allows us to estimate how well the detector performance needs to be determined a priori in order to avoid a sizable bias in the measurement of the relevant oscillation parameters. We compare the kinematic and calorimetric methods of energy reconstruction in the context of two νμ → νμ disappearance experiments operating in different energy regimes. For the calorimetric reconstruction method, we find that the detector performance has to be estimated with an O(10%) accuracy to avoid a significant bias in the extracted oscillation parameters. Thus, in the case of kinematic energy reconstruction, we observe that the results exhibit less sensitivity to an overestimation of the detector capabilities.

  6. Calorimetric low temperature detectors for low-energetic heavy ions and their application in accelerator mass spectrometry

    NASA Astrophysics Data System (ADS)

    Kraft-Bermuth, S.; Andrianov, V. A.; Bleile, A.; Echler, A.; Egelhof, P.; Kiseleva, A.; Kiselev, O.; Meier, H. J.; Meier, J. P.; Shrivastava, A.; Weber, M.; Golser, R.; Kutschera, W.; Priller, A.; Steier, P.; Vockenhuber, C.

    2009-10-01

    The energy-sensitive detection of heavy ions with calorimetric low temperature detectors was investigated in the energy range of E =0.1-1 MeV/amu, commonly used for accelerator mass spectrometry (AMS). The detectors used consist of sapphire absorbers and superconducting aluminum transition edge thermometers operated at T ˜1.5 K. They were irradiated with various ion beams (C13,A197u,U238) provided by the VERA tandem accelerator in Vienna, Austria. The relative energy resolution obtained was ΔE /E=(5-9)×10-3, even for the heaviest ions such as U238. In addition, no evidence for a pulse height defect was observed. This performance allowed for the first time to apply a calorimetric low temperature detector in an AMS experiment. The aim was to precisely determine the isotope ratio of U236/U238 for several samples of natural uranium, U236 being known as a sensitive monitor for neutron fluxes. Replacing a conventionally used detection system at VERA by the calorimetric detector enabled to substantially reduce background from neighboring isotopes and to increase the detection efficiency. Due to the high sensitivity achieved, a value of U236/U238=6.1×10-12 could be obtained, representing the smallest U236/U238 ratio measured at the time. In addition, we contributed to establishing an improved material standard of U236/U238, which can be used as a reference for future AMS measurements.

  7. A no-calorimetric method for measuring SAR in MRI

    NASA Astrophysics Data System (ADS)

    Romano, Rocco; Acernese, Fausto; Barone, Fabrizio

    2011-04-01

    During an MR procedure, the patient absorbs a portion of the transmitted RF energy, which may result in tissue heating and other adverse effects, such as alterations in visual, auditory and neural functions. The Specific Absorption Rate (SAR), in W/kg, is the RF power absorbed per unit mass of tissue and is one of the most important parameters related with thermal effects and acts as a guideline for MRI safety. Strict limits to the SAR levels are imposed by patient safety international regulations (CEI - EN 60601 - 2 - 33) and SAR measurements are required in order to verify its respect. The recommended methods for mean SAR measurement are quite problematic and often require a maintenance man intervention and long stop machine. For example, in the CEI recommended pulse energy method, the presence of a maintenance man is required in order to correctly connect the required instrumentation; furthermore, the procedure is complex and requires remarkable processing and calculus. Simpler are the calorimetric methods, also if in this case long acquisition times are required in order to have significant temperature variations and accurate heat capacity knowledge (CEI - EN 60601 - 2 - 33). The phase transition method is a new no-calorimetric method to measure SAR in MRI which has the advantages to be very simple and to overcome all the typical calorimetric method problems. It does not require in gantry temperature measurements, any specific heat or heat capacity knowledge, but only mass and time measurement. On the other hand, it is necessary to establish if all deposited power SAR can be considered acquired and measured. In this paper, that will be shown.

  8. A calorimetric study on interactions of colchicine with human serum albumin

    NASA Astrophysics Data System (ADS)

    Zhao, Qiang; Xu, Xiang-Yu; Sun, Xiang-Jun; Liu, Min; Sun, De-Zhi; Li, Lin-Wei

    2009-08-01

    Interaction of colchicine (COL) with human serum albumin (HSA) in buffer solutions (pH 7.2) has been investigated by isothermal titration calorimetry (ITC) combined with circular dichroism (CD) and UV-vis spectra. Heats of the interactions have been determined at 298.15 K. Based on the calorimetric data and reasonable suppositions for the bio-macromolecule - ligand binding process, the equilibrium constants, standard changes of enthalpy, entropy and Gibbs free energy of the processes are obtained. The results show that there are two classes of ligand binding sites. The first-class binding is mainly driven by entropy, while the second-class binding is synergistically driven by entropy and enthalpy. Circular dichroism (CD) and UV-vis spectra show that COL can change the secondary structure of HSA molecule.

  9. Novel micro-calorimetric spectroscopy for mine detection

    SciTech Connect

    Datskos, P.G. |; Rajic, S.; Egert, C.M.; Datskou, I.

    1998-03-01

    The authors have developed a novel micro-calorimetric spectroscopy technique that can be used in mine detection applications. In this technique target molecules are allowed to adsorb on the surface of sub-femtojoule sensitive micromechanical thermal detectors. The adsorption of molecules on the thermal detector surface causes a differential surface stress resulting in an initial trigger. By exposing each element in an array of thermal detectors to different photon wavelengths, an extremely sensitive and unique photothermal signature response can be obtained. The authors present their results on target chemicals adsorbed on the detector surface at sub-monolayer coverage levels. They will present infrared photothermal spectra for trace concentrations of diisopropyl methylphosphonate (DIMP), and trinitrotoluene (TNT) over the wavelength region 2.5 to 14.5 microns. They found that in the wavelength region 2.5 to 14.5 microns the photothermal spectra of DIMP and TNT exhibit a number of peaks and are in excellent agreement with infrared absorption spectra found in the literature. Chemical detectors based on micro-calorimetric spectroscopy can be used to sensitively sense small number of molecules adsorbed on a thermal detector surface. The photothermal signature resulting from photon irradiation can be used for improved chemical characterization.

  10. 76 FR 45309 - Social Security Ruling 11-1p; Titles II and XVI: Procedures for Handling Requests To File...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-28

    ... ADMINISTRATION Social Security Ruling 11-1p; Titles II and XVI: Procedures for Handling Requests To File... title and benefit type in our administrative review process. This change will allow us to more... Titles II and XVI: Procedures for Handling Requests To File Subsequent Applications for...

  11. Remote calorimetric detection of urea via flow injection analysis.

    PubMed

    Gaddes, David E; Demirel, Melik C; Reeves, W Brian; Tadigadapa, Srinivas

    2015-12-01

    The design and development of a calorimetric biosensing system enabling relatively high throughput sample analysis are reported. The calorimetric biosensor system consists of a thin (∼20 μm) micromachined Y-cut quartz crystal resonator (QCR) as a temperature sensor placed in close proximity to a fluidic chamber packed with an immobilized enzyme. Layer by layer enzyme immobilization of urease is demonstrated and its activity as a function of the number of layers, pH, and time has been evaluated. This configuration enables a sensing system where a transducer element is physically separated from the analyte solution of interest and is thereby free from fouling effects typically associated with biochemical reactions occuring on the sensor surface. The performance of this biosensing system is demonstrated by detection of 1-200 mM urea in phosphate buffer via a flow injection analysis (FIA) technique. Miniaturized fluidic systems were used to provide continuous flow through a reaction column. Under this configuration the biosensor has an ultimate resolution of less than 1 mM urea and showed a linear response between 0-50 mM. This work demonstrates a sensing modality in which the sensor itself is not fouled or contaminated by the solution of interest and the enzyme immobilized Kapton® fluidic reaction column can be used as a disposable cartridge. Such a system enables reuse and reliability for long term sampling measurements. Based on this concept a biosensing system is envisioned which can perform rapid measurements to detect biomarkers such as glucose, creatinine, cholesterol, urea and lactate in urine and blood continuously over extended periods of time. PMID:26479269

  12. 1H NMR and calorimetric measurements on rabbit eye lenses.

    PubMed

    Gutsze, A; Bodurka, J; Olechnowicz, R; Buntkowsky, G; Limbach, H H

    1995-01-01

    The dynamic properties of water molecules in the rabbit lens were studied by proton nuclear magnetic resonance line shape analysis, measurements of relaxation times as a function of temperature and calorimetric measurements. The experiments prove, as already suggested by other authors, that there are two types of water in the lens of rabbit eyes, namely bound unfreezable hydration water and bulk freezable water. Line shape analysis and relaxometry showed, that this two types of water exist in two different environments, which may be identified as the nucleus and the cortex of the lens. The line shape analysis showed furthermore that water molecules in the rabbit lens has a common spin lattice relaxation time (T1), but two different transverse relaxation times (T2A and T2B). The tentative model of fast water exchange on the T1 time scale and slow water exchange on the T2 time scale, was used to explain experimental proton relaxation data of the rabbit lens. An estimation for this exchange rate kex by comparing it to the relaxation times is given (T1(-1) < kex < T1(-1)). It has also been shown by a calorimetric measurements, that the lenses can be easily under-cooled to temperatures well below the freezing point of water. The achievable maximum undercooling temperature of the lens is a function of the cooling rate KC, therefore it has to be considered as an experimentally adjustable parameter which is not characteristic for the investigated sample. Thus it must be noted that any previous discussions about the specific value of the temperature of water crystallisation in biological systems need to be carefully reconsidered.

  13. A TEMPORAL MAP IN GEOSTATIONARY ORBIT: THE COVER ETCHING ON THE EchoStar XVI ARTIFACT

    SciTech Connect

    Weisberg, Joel M.; Paglen, Trevor

    2012-10-01

    Geostationary satellites are unique among orbital spacecraft in that they experience no appreciable atmospheric drag. After concluding their respective missions, geostationary spacecraft remain in orbit virtually in perpetuity. As such, they represent some of human civilization's longest lasting artifacts. With this in mind, the EchoStar XVI satellite, to be launched in fall 2012, will play host to a time capsule intended as a message for the deep future. Inspired in part by the Pioneer Plaque and Voyager Golden Records, the EchoStar XVI Artifact is a pair of gold-plated aluminum jackets housing a small silicon disk containing 100 photographs. The Cover Etching, the subject of this paper, is etched onto one of the two jackets. It is a temporal map consisting of a star chart, pulsar timings, and other information describing the epoch from which EchoStar XVI came. The pulsar sample consists of 13 rapidly rotating objects, 5 of which are especially stable, having spin periods <10 ms and extremely small spin-down rates. In this paper, we discuss our approach to the time map etched onto the cover and the scientific data shown on it, and we speculate on the uses that future scientists may have for its data. The other portions of the EchoStar XVI Artifact will be discussed elsewhere.

  14. 20 CFR 416.1535 - Services in a proceeding under title XVI of the Act.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 20 Employees' Benefits 2 2010-04-01 2010-04-01 false Services in a proceeding under title XVI of the Act. 416.1535 Section 416.1535 Employees' Benefits SOCIAL SECURITY ADMINISTRATION SUPPLEMENTAL SECURITY INCOME FOR THE AGED, BLIND, AND DISABLED Representation of Parties § 416.1535 Services in...

  15. 20 CFR 416.1535 - Services in a proceeding under title XVI of the Act.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 20 Employees' Benefits 2 2011-04-01 2011-04-01 false Services in a proceeding under title XVI of the Act. 416.1535 Section 416.1535 Employees' Benefits SOCIAL SECURITY ADMINISTRATION SUPPLEMENTAL SECURITY INCOME FOR THE AGED, BLIND, AND DISABLED Representation of Parties § 416.1535 Services in...

  16. A Temporal Map in Geostationary Orbit: The Cover Etching on the EchoStar XVI Artifact

    NASA Astrophysics Data System (ADS)

    Weisberg, Joel M.; Paglen, Trevor

    2012-10-01

    Geostationary satellites are unique among orbital spacecraft in that they experience no appreciable atmospheric drag. After concluding their respective missions, geostationary spacecraft remain in orbit virtually in perpetuity. As such, they represent some of human civilization's longest lasting artifacts. With this in mind, the EchoStar XVI satellite, to be launched in fall 2012, will play host to a time capsule intended as a message for the deep future. Inspired in part by the Pioneer Plaque and Voyager Golden Records, the EchoStar XVI Artifact is a pair of gold-plated aluminum jackets housing a small silicon disk containing 100 photographs. The Cover Etching, the subject of this paper, is etched onto one of the two jackets. It is a temporal map consisting of a star chart, pulsar timings, and other information describing the epoch from which EchoStar XVI came. The pulsar sample consists of 13 rapidly rotating objects, 5 of which are especially stable, having spin periods <10 ms and extremely small spin-down rates. In this paper, we discuss our approach to the time map etched onto the cover and the scientific data shown on it, and we speculate on the uses that future scientists may have for its data. The other portions of the EchoStar XVI Artifact will be discussed elsewhere.

  17. Estimation of the diversity between DNA calorimetric profiles, differential melting curves and corresponding melting temperatures.

    PubMed

    Chang, Chun-Ling; Fridman, Alexander S; Grigoryan, Inessa E; Galyuk, Elena N; Murashko, Oleg N; Hu, Chin-Kun; Lando, Dmitri Y

    2016-11-01

    The Poland-Fixman-Freire formalism was adapted for modeling of calorimetric DNA melting profiles, and applied to plasmid pBR 322 and long random sequences. We studied the influence of the difference (HGC -HAT ) between the helix-coil transition enthalpies of AT and GC base pairs on the calorimetric melting profile and on normalized calorimetric melting profile. A strong alteration of DNA calorimetrical profile with HGC -HAT was demonstrated. In contrast, there is a relatively slight change in the normalized profiles and in corresponding ordinary (optical) normalized differential melting curves (DMCs). For fixed HGC -HAT , the average relative deviation (S) between DMC and normalized calorimetric profile, and the difference between their melting temperatures (Tcal -Tm ) are weakly dependent on peculiarities of the multipeak fine structure of DMCs. At the same time, both the deviation S and difference (Tcal -Tm ) enlarge with the temperature melting range of the helix-coil transition. It is shown that the local deviation between DMC and normalized calorimetric profile increases in regions of narrow peaks distant from the melting temperature. PMID:27422497

  18. The ISLANDS Project. I. Andromeda XVI, An Extremely Low Mass Galaxy Not Quenched by Reionization

    NASA Astrophysics Data System (ADS)

    Monelli, Matteo; Martínez-Vázquez, Clara E.; Bernard, Edouard J.; Gallart, Carme; Skillman, Evan D.; Weisz, Daniel R.; Dolphin, Andrew E.; Hidalgo, Sebastian L.; Cole, Andrew A.; Martin, Nicolas F.; Aparicio, Antonio; Cassisi, Santi; Boylan-Kolchin, Michael; Mayer, Lucio; McConnachie, Alan; McQuinn, Kristen B. W.; Navarro, Julio F.

    2016-03-01

    Based on data aquired in 13 orbits of Hubble Space Telescope time, we present a detailed evolutionary history of the M31 dSph satellite Andromeda XVI, including its lifetime star formation history (SFH), the spatial distribution of its stellar populations, and the properties of its variable stars. And XVI is characterized by prolonged star formation activity from the oldest epochs until star formation was quenched ˜6 Gyr ago, and, notably, only half of the mass in stars of And XVI was in place 10 Gyr ago. And XVI appears to be a low-mass galaxy for which the early quenching by either reionization or starburst feedback seems highly unlikely, and thus it is most likely due to an environmental effect (e.g., an interaction), possibly connected to a late infall in the densest regions of the Local Group. Studying the SFH as a function of galactocentric radius, we detect a mild gradient in the SFH: the star formation activity between 6 and 8 Gyr ago is significantly stronger in the central regions than in the external regions, although the quenching age appears to be the same, within 1 Gyr. We also report the discovery of nine RR Lyrae (RRL) stars, eight of which belong to And XVI. The RRL stars allow a new estimate of the distance, (m - M)0 = 23.72 ± 0.09 mag, which is marginally larger than previous estimates based on the tip of the red giant branch. Based on observations made with the NASA/ESA Hubble Space Telescope, obtained at the Space Telescope Science Institute, which is operated by the Association of Universities for Research in Astronomy, Inc., under NASA contract NAS 5-26555. These observations are associated with program #13028.

  19. Neutron induced capture and fission discrimination using calorimetric shape decomposition

    NASA Astrophysics Data System (ADS)

    Carrapiço, C.; Berthoumieux, E.; Dridi, W.; Gonçalves, I. F.; Gunsing, F.; Lampoudis, C.; Vaz, P.; n TOF Collaboration

    2013-03-01

    The neutron capture and fission cross-sections of 233U have been measured at the neutron time-of-flight facility n_TOF at CERN in the energy range from 1 eV to 1 keV using a high performance 4π BaF2 Total Absorption Calorimeter (TAC) as a detection device. In order to separate the contributions of neutron capture and neutron induced fission in the TAC, a methodology called Calorimetric Shape Decomposition (CSD) was developed. The CSD methodology is based on the study of the TAC's energy response for all competing reactions, allowing to discriminate between γ s originating from neutron induced fission and those from neutron capture reactions without the need for fission tagging or any additional detection system. In this article, the concept behind the CSD is explained in detail together with the necessary analysis to obtain the TAC's response to neutron capture and neutron induced fission. The discrimination between capture and fission contributions is shown for several neutron energies. A comparison between the 233U neutron capture and fission yield extraction with ENDF/B-VII v1. library data is also provided.

  20. Calorimetric measurements of energetics of defect interactions in fluorite oxides.

    PubMed

    Navrotsky, Alexandra; Simoncic, Petra; Yokokawa, Harumi; Chen, Weiqun; Lee, Theresa

    2007-01-01

    Direct measurement by oxide melt solution calorimetry of energetics of mixing in rare earth and yttrium doped zirconia, hafnia, and ceria systems provides support for spectroscopic and computational studies of the location and clustering of vacancies in these systems. Strongly negative heats of mixing are seen when the vacancy is transferred from being nearest neighbor to Y or RE in the sesquioxide to being nearest neighbor to Zr or Hf in the cubic solid solution. In the absence of such redistribution, small positive enthalpies of mixing are seen in CeO2-YO1.5 and CeO2-REO.15 systems. Strongly positive enthalpies of mixing are seen in CeO2-ZrO2, which has a large difference in cation sizes and no vacancy formation. The system Ce0.8Y0.2O1.9-Zr0.8Y0.2O1.9 shows small positive heats of formation with less destabilization in the Ce-rich region, suggestive of "scavenging" of oxygen vacancies by Zr. The calorimetric data obtained in these studies offer direct comparison with the results of computations on defect clusters and their binding energies. PMID:17326568

  1. Formation and properties of ice XVI obtained by emptying a type sII clathrate hydrate

    NASA Astrophysics Data System (ADS)

    Falenty, Andrzej; Hansen, Thomas C.; Kuhs, Werner F.

    2014-12-01

    Gas hydrates are ice-like solids, in which guest molecules or atoms are trapped inside cages formed within a crystalline host framework (clathrate) of hydrogen-bonded water molecules. They are naturally present in large quantities on the deep ocean floor and as permafrost, can form in and block gas pipelines, and are thought to occur widely on Earth and beyond. A natural point of reference for this large and ubiquitous family of inclusion compounds is the empty hydrate lattice, which is usually regarded as experimentally inaccessible because the guest species stabilize the host framework. However, it has been suggested that sufficiently small guests may be removed to leave behind metastable empty clathrates, and guest-free Si- and Ge-clathrates have indeed been obtained. Here we show that this strategy can also be applied to water-based clathrates: five days of continuous vacuum pumping on small particles of neon hydrate (of structure sII) removes all guests, allowing us to determine the crystal structure, thermal expansivity and limit of metastability of the empty hydrate. It is the seventeenth experimentally established crystalline ice phase, ice XVI according to the current ice nomenclature, has a density of 0.81 grams per cubic centimetre (making it the least dense of all known crystalline water phases) and is expected to be the stable low-temperature phase of water at negative pressures (that is, under tension). We find that the empty hydrate structure exhibits negative thermal expansion below about 55 kelvin, and that it is mechanically more stable and has at low temperatures larger lattice constants than the filled hydrate. These observations attest to the importance of kinetic effects and host-guest interactions in clathrate hydrates, with further characterization of the empty hydrate expected to improve our understanding of the structure, properties and behaviour of these unique materials.

  2. Formation and properties of ice XVI obtained by emptying a type sII clathrate hydrate.

    PubMed

    Falenty, Andrzej; Hansen, Thomas C; Kuhs, Werner F

    2014-12-11

    Gas hydrates are ice-like solids, in which guest molecules or atoms are trapped inside cages formed within a crystalline host framework (clathrate) of hydrogen-bonded water molecules. They are naturally present in large quantities on the deep ocean floor and as permafrost, can form in and block gas pipelines, and are thought to occur widely on Earth and beyond. A natural point of reference for this large and ubiquitous family of inclusion compounds is the empty hydrate lattice, which is usually regarded as experimentally inaccessible because the guest species stabilize the host framework. However, it has been suggested that sufficiently small guests may be removed to leave behind metastable empty clathrates, and guest-free Si- and Ge-clathrates have indeed been obtained. Here we show that this strategy can also be applied to water-based clathrates: five days of continuous vacuum pumping on small particles of neon hydrate (of structure sII) removes all guests, allowing us to determine the crystal structure, thermal expansivity and limit of metastability of the empty hydrate. It is the seventeenth experimentally established crystalline ice phase, ice XVI according to the current ice nomenclature, has a density of 0.81 grams per cubic centimetre (making it the least dense of all known crystalline water phases) and is expected to be the stable low-temperature phase of water at negative pressures (that is, under tension). We find that the empty hydrate structure exhibits negative thermal expansion below about 55 kelvin, and that it is mechanically more stable and has at low temperatures larger lattice constants than the filled hydrate. These observations attest to the importance of kinetic effects and host-guest interactions in clathrate hydrates, with further characterization of the empty hydrate expected to improve our understanding of the structure, properties and behaviour of these unique materials. PMID:25503235

  3. Formation and properties of ice XVI obtained by emptying a type sII clathrate hydrate.

    PubMed

    Falenty, Andrzej; Hansen, Thomas C; Kuhs, Werner F

    2014-12-11

    Gas hydrates are ice-like solids, in which guest molecules or atoms are trapped inside cages formed within a crystalline host framework (clathrate) of hydrogen-bonded water molecules. They are naturally present in large quantities on the deep ocean floor and as permafrost, can form in and block gas pipelines, and are thought to occur widely on Earth and beyond. A natural point of reference for this large and ubiquitous family of inclusion compounds is the empty hydrate lattice, which is usually regarded as experimentally inaccessible because the guest species stabilize the host framework. However, it has been suggested that sufficiently small guests may be removed to leave behind metastable empty clathrates, and guest-free Si- and Ge-clathrates have indeed been obtained. Here we show that this strategy can also be applied to water-based clathrates: five days of continuous vacuum pumping on small particles of neon hydrate (of structure sII) removes all guests, allowing us to determine the crystal structure, thermal expansivity and limit of metastability of the empty hydrate. It is the seventeenth experimentally established crystalline ice phase, ice XVI according to the current ice nomenclature, has a density of 0.81 grams per cubic centimetre (making it the least dense of all known crystalline water phases) and is expected to be the stable low-temperature phase of water at negative pressures (that is, under tension). We find that the empty hydrate structure exhibits negative thermal expansion below about 55 kelvin, and that it is mechanically more stable and has at low temperatures larger lattice constants than the filled hydrate. These observations attest to the importance of kinetic effects and host-guest interactions in clathrate hydrates, with further characterization of the empty hydrate expected to improve our understanding of the structure, properties and behaviour of these unique materials.

  4. A calorimetric investigation of the growth of the luminescent bacteria Beneckea harveyi and Photobacterium leiognathi.

    PubMed Central

    McIlvaine, P; Langerman, N

    1977-01-01

    Direct calorimetric determinations of the rate of heat production along with simultaneous determinations of the rate of photon emission and the number of viable cells have provided insight into the growth of Beneckea harveyi and Photobacterium leiognathi. These experiments were performed with a Tronac isothermal microcalorimeter modified with a fiber optic light guide to allow in situ detection of light. Escherichia coli and a dark variant of P. leiognathi were also examined to provide points of reference. It is demonstrated that B. harveyi seems to pause in the rate of metabolic heat production at the same point in time that the enzyme luciferase begins to be synthesized. This effect is not removed if B. harveyi is grown in conditioned medium. The thermograms for all species are correlated with cell generation time. The heat production per cell indicates that uncrowded cultures produce more heat than older, more crowded cultures, supporting the original observation of Bayne-Jones and Rhees (1929). These observations reopen for examination the suggestion that living systems tend toward a state of minimum metabolism per unit mass. PMID:401656

  5. Huwentoxin-XVI, an analgesic, highly reversible mammalian N-type calcium channel antagonist from Chinese tarantula Ornithoctonus huwena.

    PubMed

    Deng, Meichun; Luo, Xuan; Xiao, Yucheng; Sun, Zhenghua; Jiang, Liping; Liu, Zhonghua; Zeng, Xiongzhi; Chen, Hanchun; Tang, Jianhua; Zeng, Weimin; Songping Liang

    2014-04-01

    N-type calcium channels play important roles in the control of neurotransmission release and transmission of pain signals to the central nervous system. Their selective inhibitors are believed to be potential drugs for treating chronic pain. In this study, a novel neurotoxin named Huwentoxin-XVI (HWTX-XVI) specific for N-type calcium channels was purified and characterized from the venom of Chinese tarantula Ornithoctonus huwena. HWTX-XVI is composed of 39 amino acid residues including six cysteines that constitute three disulfide bridges. HWTX-XVI could almost completely block the twitch response of rat vas deferens to low-frequency electrical stimulation. Electrophysiological assay indicated that HWTX-XVI specifically inhibited N-type calcium channels in rat dorsal root ganglion cells (IC50 ∼60 nM). The inhibitory effect of HWTX-XVI on N-type calcium channel currents was dose-dependent and similar to that of CTx-GVIA and CTx-MVIIA. However, the three peptides exhibited markedly different degrees of reversibility after block. The toxin had no effect on voltage-gated T-type calcium channels, potassium channels or sodium channels. Intraperitoneal injection of the toxin HWTX-XVI to rats elicited significant analgesic responses to formalin-induced inflammation pain. Toxin treatment also changed withdrawal latency in hot plate tests. Intriguingly, we found that intramuscular injection of the toxin reduced mechanical allodynia induced by incisional injury in Von Frey test. Thus, our findings suggest that the analgesic potency of HWTX-XVI and its greater reversibility could contribute to the design of a novel potential analgesic agent with high potency and low side effects. PMID:24467846

  6. Huwentoxin-XVI, an analgesic, highly reversible mammalian N-type calcium channel antagonist from Chinese tarantula Ornithoctonus huwena.

    PubMed

    Deng, Meichun; Luo, Xuan; Xiao, Yucheng; Sun, Zhenghua; Jiang, Liping; Liu, Zhonghua; Zeng, Xiongzhi; Chen, Hanchun; Tang, Jianhua; Zeng, Weimin; Songping Liang

    2014-04-01

    N-type calcium channels play important roles in the control of neurotransmission release and transmission of pain signals to the central nervous system. Their selective inhibitors are believed to be potential drugs for treating chronic pain. In this study, a novel neurotoxin named Huwentoxin-XVI (HWTX-XVI) specific for N-type calcium channels was purified and characterized from the venom of Chinese tarantula Ornithoctonus huwena. HWTX-XVI is composed of 39 amino acid residues including six cysteines that constitute three disulfide bridges. HWTX-XVI could almost completely block the twitch response of rat vas deferens to low-frequency electrical stimulation. Electrophysiological assay indicated that HWTX-XVI specifically inhibited N-type calcium channels in rat dorsal root ganglion cells (IC50 ∼60 nM). The inhibitory effect of HWTX-XVI on N-type calcium channel currents was dose-dependent and similar to that of CTx-GVIA and CTx-MVIIA. However, the three peptides exhibited markedly different degrees of reversibility after block. The toxin had no effect on voltage-gated T-type calcium channels, potassium channels or sodium channels. Intraperitoneal injection of the toxin HWTX-XVI to rats elicited significant analgesic responses to formalin-induced inflammation pain. Toxin treatment also changed withdrawal latency in hot plate tests. Intriguingly, we found that intramuscular injection of the toxin reduced mechanical allodynia induced by incisional injury in Von Frey test. Thus, our findings suggest that the analgesic potency of HWTX-XVI and its greater reversibility could contribute to the design of a novel potential analgesic agent with high potency and low side effects.

  7. Calorimetric low temperature detectors for mass identification of heavy ions

    NASA Astrophysics Data System (ADS)

    Kraft, S.; Bleile, A.; Egelhof, P.; Golser, R.; Kisselev, O.; Kutschera, W.; Liechtenstein, V.; Meier, H. J.; Priller, A.; Shrivastava, A.; Steier, P.; Vockenhuber, C.; Weber, M.

    2002-02-01

    The energy sensitive detection of heavy ions with calorimetric low temperature detectors (CLTDs) is investigated for the energy range E=0.1-1 MeV/u, commonly used for accelerator mass spectrometry (AMS). Such measurements complement earlier investigations [1, 2] at higher energies (E=5-300 MeV/u) where an energy resolution of ΔE/E=1-2×10-3 was obtained for various ion species. The detectors used consist of sapphire absorbers and superconducting transition edge thermometers operated at T~1.5 K. They were irradiated with various heavy ion beams (13C, 197Au, 238U) provided by the VERA tandem accelerator in Vienna, Austria. An energy resolution of ΔE/E=5-6×10-3 has been obtained even for heaviest ions like 197Au and 238U at E=0.1-0.3 MeV/u, thereby exceeding the resolution of conventional semiconductor detectors in this energy range by at least one order of magnitude. In addition, no evidence for pulse height defects has been observed. With the achieved performance, the present CLTDs bear a large potential for applications in various fields of heavy ion research. Of special interest is isotope mass identification via combined energy and time-of-flight (TOF) measurement. In present test measurements, including a standard TOF spectrometer, a clear separation of the isotopes 206Pb and 208Pb at E~0.1 MeV/u has been obtained. Such a detection scheme may in future provide substantial background suppression for AMS measurements. .

  8. Higher order inclusion complexes and secondary interactions studied by global analysis of calorimetric titrations.

    PubMed

    Schönbeck, Christian; Holm, René; Westh, Peter

    2012-03-01

    This paper investigates the use of isothermal titration calorimetry (ITC) as a tool for studying molecular systems in which weaker secondary interactions are present in addition to a dominant primary interaction. Such systems are challenging since the signal pertaining to the stronger primary interaction tends to overshadow the signal from the secondary interaction. The methodology presented here enables a complete and precise thermodynamic characterization of both the primary and the weaker secondary interaction, exemplified by the binding of β-cyclodextrin to the primary and secondary binding sites of the bile salt glycodeoxycholate. Global regression analysis of calorimetric experiments at various concentrations and temperatures provide a precise determination of ΔH, ΔG°, and ΔC(p) for both binding sites in glycodeoxycholate (K1 = 5.67 ± 0.05 × 10(3) M(-1), K2 = 0.31 ± 0.02 × 10(3) M(-1)). The results are validated by a (13)C NMR titration and negative controls with a bile salt with no secondary binding site (glycocholate) (K = 2.96 ± 0.01 × 10(3) M(-1)). The method proved useful for detailed analysis of ITC data and may strengthen its use as a tool for studying molecular systems by advanced binding models.

  9. Calorimetric method for adjusting the mass of culture fluid in a bioreactor

    NASA Astrophysics Data System (ADS)

    Kotelnikov, G. V.; Moiseyeva, S. P.; Krayev, V. P.

    1998-05-01

    A new calorimetric method for adjusting the mass of culture fluid in a bioreactor and the results of its experimental testing are described. The method is based on constant heat capacity of liquids in the presence of disturbing factors accompanying biotechnology processes. A new measuring parameter independent of thermal noise induced by the stirrer, the flow of fluids, chemical and physical interactions of substances in the bioreactor was used for adjusting the mass of culture fluid. This parameter is Ph, the power increment in the heater under steady-state conditions of heating the bioreactor. The scanning calorimetry principle was used to make the measurements. It was shown that it is necessary to provide a constant heating rate V for the bioreactor and a high-speed response of the automated control system (ACS) for bioreactor temperature. The ACS developed on the base of the dynamic error and transient response h(t) calculated by the inverse Laplace transform with the use of the closed-loop transfer function gives V=const and the control time of about several seconds. The experimental data reported show the adjustment of the mass of culture fluid in a 3 l bioreactor with an error of no more than 10 g. This enables an accurate evaluation of the biomass amount in the bioreactor, specific growth rate, and other growth parameters determined using specific growth rate.

  10. Adsorption of methylene blue on raw and MTZ/imogolite hybrid surfaces: effect of concentration and calorimetric investigation.

    PubMed

    Guerra, Denis L; Batista, Adriano C; Viana, Rúbia R; Airoldi, Claudio

    2010-11-15

    The synthetic imogolite sample was used for organofunctionalization process with 2-mercaptothiazoline (MTZ). The compound 2-mercaptothiazoline was anchored onto imogolite surface by heterogeneous route. Due to the increment of basic centers attached to the pendant chains the dye adsorption capability of the final chelating material, was found to be higher than is precursor. The ability of these materials to remove methylene blue from aqueous solution was followed by a series of adsorption isotherms at room temperature and pH 4.0. The maximum number of moles adsorbed was determined to be 40.32×10(-2) and 65.13×10(-2) mmol g(-1) for IMO and IMO(MTZ), respectively. The energetic effects caused by dye cations adsorption were determined through calorimetric titrations. Thermodynamics indicated the existence of favorable conditions for such methylene blue-nitrogen and sulfur interactions.

  11. Genomic analysis of the blood attributed to Louis XVI (1754-1793), king of France.

    PubMed

    Olalde, Iñigo; Sánchez-Quinto, Federico; Datta, Debayan; Marigorta, Urko M; Chiang, Charleston W K; Rodríguez, Juan Antonio; Fernández-Callejo, Marcos; González, Irene; Montfort, Magda; Matas-Lalueza, Laura; Civit, Sergi; Luiselli, Donata; Charlier, Philippe; Pettener, Davide; Ramírez, Oscar; Navarro, Arcadi; Himmelbauer, Heinz; Marquès-Bonet, Tomàs; Lalueza-Fox, Carles

    2014-01-01

    A pyrographically decorated gourd, dated to the French Revolution period, has been alleged to contain a handkerchief dipped into the blood of the French king Louis XVI (1754-1793) after his beheading but recent analyses of living males from two Bourbon branches cast doubts on its authenticity. We sequenced the complete genome of the DNA contained in the gourd at low coverage (~2.5×) with coding sequences enriched at a higher ~7.3× coverage. We found that the ancestry of the gourd's genome does not seem compatible with Louis XVI's known ancestry. From a functional perspective, we did not find an excess of alleles contributing to height despite being described as the tallest person in Court. In addition, the eye colour prediction supported brown eyes, while Louis XVI had blue eyes. This is the first draft genome generated from a person who lived in a recent historical period; however, our results suggest that this sample may not correspond to the alleged king. PMID:24763138

  12. Modeling protein density of states: additive hydrophobic effects are insufficient for calorimetric two-state cooperativity.

    PubMed

    Chan, H S

    2000-09-01

    A well-established experimental criterion for two-state thermodynamic cooperativity in protein folding is that the van't Hoff enthalpy DeltaH(vH) around the transition midpoint is equal, or very nearly so, to the calorimetric enthalpy DeltaH(cal) of the entire transition. This condition is satisfied by many small proteins. We use simple lattice models to provide a statistical mechanical framework to elucidate how this calorimetric two-state picture may be reconciled with the hierarchical multistate scenario emerging from recent hydrogen exchange experiments. We investigate the feasibility of using inverse Laplace transforms to recover the underlying density of states (i.e., enthalpy distribution) from calorimetric data. We find that the constraint imposed by DeltaH(vH)/DeltaH(cal) approximately 1 on densities of states of proteins is often more stringent than other "two-state" criteria proposed in recent theoretical studies. In conjunction with reasonable assumptions, the calorimetric two-state condition implies a narrow distribution of denatured-state enthalpies relative to the overall enthalpy difference between the native and the denatured conformations. This requirement does not always correlate with simple definitions of "sharpness" of a transition and has important ramifications for theoretical modeling. We find that protein models that assume capillarity cooperativity can exhibit overall calorimetric two-state-like behaviors. However, common heteropolymer models based on additive hydrophobic-like interactions, including highly specific two-dimensional Gō models, fail to produce proteinlike DeltaH(vH)/DeltaH(cal) approximately 1. A simple model is constructed to illustrate a proposed scenario in which physically plausible local and nonlocal cooperative terms, which mimic helical cooperativity and environment-dependent hydrogen bonding strength, can lead to thermodynamic behaviors closer to experiment. Our results suggest that proteinlike thermodynamic

  13. Heat capacty, relative enthalpy, and calorimetric entropy of silicate minerals: an empirical method of prediction.

    USGS Publications Warehouse

    Robinson, G.R.; Haas, J.L.

    1983-01-01

    Through the evaluation of experimental calorimetric data and estimates of the molar isobaric heat capacities, relative enthalpies and entropies of constituent oxides, a procedure for predicting the thermodynamic properties of silicates is developed. Estimates of the accuracy and precision of the technique and examples of its application are also presented. -J.A.Z.

  14. Comparing M31 and Milky Way satellites: The extended star formation histories of Andromeda II and Andromeda XVI

    SciTech Connect

    Weisz, Daniel R.; Skillman, Evan D.; McQuinn, Kristen B. W.; Hidalgo, Sebastian L.; Monelli, Matteo; Gallart, Carme; Aparicio, Antonio; McConnachie, Alan; Stetson, Peter B.; Bernard, Edouard J.; Boylan-Kolchin, Michael; Cassisi, Santi; Cole, Andrew A.; Ferguson, Henry C.; Irwin, Mike; Martin, Nicolas F.; Mayer, Lucio; Navarro, Julio F.

    2014-07-01

    We present the first comparison between the lifetime star formation histories (SFHs) of M31 and Milky Way (MW) satellites. Using the Advanced Camera for Surveys on board the Hubble Space Telescope, we obtained deep optical imaging of Andromeda II (And II; M{sub V} = –12.0; log(M {sub *}/M {sub ☉}) ∼ 6.7) and Andromeda XVI (And XVI; M{sub V} = –7.5; log(M {sub *}/M {sub ☉}) ∼ 4.9) yielding color-magnitude diagrams that extend at least 1 mag below the oldest main-sequence turnoff, and are similar in quality to those available for the MW companions. And II and And XVI show strikingly similar SFHs: both formed 50%-70% of their total stellar mass between 12.5 and 5 Gyr ago (z ∼ 5-0.5) and both were abruptly quenched ∼5 Gyr ago (z ∼ 0.5). The predominance of intermediate age populations in And XVI makes it qualitatively different from faint companions of the MW and clearly not a pre-reionization fossil. Neither And II nor And XVI appears to have a clear analog among MW companions, and the degree of similarity in the SFHs of And II and And XVI is not seen among comparably faint-luminous pairs of MW satellites. These findings provide hints that satellite galaxy evolution may vary substantially among hosts of similar stellar mass. Although comparably deep observations of more M31 satellites are needed to further explore this hypothesis, our results underline the need for caution when interpreting satellite galaxies of an individual system in a broader cosmological context.

  15. A Calorimetric Study of Almandine: Are the Thermodynamic Properties of the End-Member Aluminosilicate Garnets Finally Known Quantitatively?

    NASA Astrophysics Data System (ADS)

    Dachs, E.; Geiger, C. A.; Benisek, A.

    2012-12-01

    The aluminosilicate garnets (E3Al2Si3O12 with E = Fe2+, Mn2+, Ca, Mg) form an important rock-forming mineral group. Much study has been directed toward determining their thermodynamic properties. The iron end-member almandine (Fe3Al2Si3O12) is a key phase in many petrologic investigations. As part of an ongoing calorimetric and thermodynamic study of the aluminosilicate garnets, the heat capacity of three synthetic well-characterized polycrystalline almandine garnets and one natural almandine-rich single crystal was measured. The various garnets were characterized by optical microscopy, electron-microprobe analysis, X-ray powder diffraction and 57Fe Mössbauer spectroscopy. Heat capacity measurements were performed in the temperature range 3 to 300 K using relaxation calorimetry and between 282 and 764 K using DSC methods. From the former, So values between 336.7 ± 0.8 and 337.8 ± 0.8 J/molK are calculated for the different samples. The smaller value is considered the best So for end-member stoichiometric almandine, because it derives from the "best" Fe3+-free synthetic sample. The Cp behavior for almandine at T > 298 K is given by the polynomial (in J/molK): Cp = 649.06(±4) - 3837.57(±122)T-0.5 - 1.44682(±0.06)107T-2 + 1.94834(±0.09)109T-3, which is calculated using DSC data together with one published heat-content datum determined by transposed-drop calorimetry along with a new determination that gives H1181K - H302K = 415.0 ± 3.2 kJ/mole. Almandine shows a λ-type heat-capacity anomaly at low temperatures resulting from a paramagnetic-antiferromagnetic phase transition at about 9 K. The lattice heat capacity was calculated using the single-parameter phonon dispersion model of Komada and Westrum (1997), which allows the non-lattice heat capacity (Cex) behavior to be modelled. An analysis shows the presence of an electronic heat-capacity contribution (Cel - Schottky anomaly) around 17 K that is superimposed on a larger magnetic heat-capacity effect (Cmag

  16. Genetic analysis of the presumptive blood from Louis XVI, King of France.

    PubMed

    Lalueza-Fox, Carles; Gigli, Elena; Bini, Carla; Calafell, Francesc; Luiselli, Donata; Pelotti, Susi; Pettener, Davide

    2011-11-01

    A text on a pyrographically decorated gourd dated to 1793 explains that it contains a handkerchief dipped with the blood of Louis XVI, king of France, after his execution. Biochemical analyses confirmed that the material contained within the gourd was blood. The mitochondrial DNA (mtDNA) hypervariable region 1 (HVR1) and 2 (HVR2), the Y-chromosome STR profile, some autosomal STR markers and a SNP in HERC2 gene associated to blue eyes, were retrieved, and some results independently replicated in two different laboratories. The uncommon mtDNA sequence retrieved can be attributed to a N1b haplotype, while the novel Y-chromosome haplotype belongs to haplogroup G2a. The HERC2 gene showed that the subject analyzed was a heterozygote, which is compatible with a blue-eyed person, as king Louis XVI was. To confirm the identity of the subject, an analysis of the dried heart of his son, Louis XVII, could be undertaken. PMID:20940110

  17. Calorimetric analysis of lambda cI repressor binding to DNA operator sites.

    PubMed

    Merabet, E; Ackers, G K

    1995-07-11

    Enthalpies and heat capacities were determined by isothermal titration calorimetry for bacteriophage lambda cI repressor binding to DNA containing various combinations of the three operator sites OR1, OR2, and OR3 (each comprising a consensus half-site and a specific nonconsensus half-site). Differential scanning calorimetry was employed to evaluate the effects of specific DNA binding on thermal melting of the N-terminal and C-terminal repressor domains. Principal findings of this study are as follows: (1) Binding of repressor to each of the DNA operators is dominated by a large negative enthalpy, in agreement with earlier van't Hoff analyses of quantitative footprint titration data [Koblan & Ackers (1992) Biochemistry 31, 57-65]. The calorimetric data also revealed negative heat capacities for cI binding that are of comparable magnitude with many other systems [Spolar & Record (1994) Science 263, 777-784]. However, this feature in combination with the large negative values of binding enthalpies leads to an enthalpic dominance throughout the physiological temperature range. The resulting thermodynamic profile is opposite to the entropically dominated binding observed for many systems, including lambda cro repressor which binds to the same sites as cI and also employs a helix-turn-helix binding domain [Takeda et al. (1992) Proc. Natl. Acad. Sci. U.S.A. 89, 8180-8184]. It is suggested that these thermodynamic differences may arise from interactions of the cI repressor's N-terminal "arm" with the DNA. (2) Repressor monomers do not bind significantly to DNA containing either a consensus half-site or a nonconsensus half-site. Binding affinity to the double-consensus operator is much weaker than to any of the natural full-site operators. The same was found with other combinations of half-sites. A mutant repressor (PT158) which is severely defective in dimerization [Burz et al. (1994) Biochemistry 33, 8399-8405] was also found to bind only full-site operators and showed

  18. The calorimetric spectrum of the electron-capture decay of 163Ho. The spectral endpoint region

    NASA Astrophysics Data System (ADS)

    De Rújula, A.; Lusignoli, M.

    2016-05-01

    The electron-neutrino mass (or masses and mixing angles) may be directly measurable in weak electron-capture decays. The favoured experimental technique is "calorimetric". The optimal nuclide is 163Ho, and several experiments (ECHo, HOLMES and NuMECS) are currently studying its decay. The most relevant range of the calorimetric-energy spectrum extends for the last few hundred eV below its endpoint. It has not yet been well measured. We explore the theory, mainly in the cited range, of electron capture in 163Ho decay. A so far neglected process turns out to be most relevant: electron-capture accompanied by the shake-off of a second electron. Our two main conclusions are very encouraging: the counting rate close to the endpoint may be more than an order of magnitude larger than previously expected; the "pile-up" problem may be significantly reduced.

  19. Kinetics of Solid-State Reactions in Al-Li-Cu-Mg-Zr Alloys from Calorimetric Studies

    NASA Astrophysics Data System (ADS)

    Ghosh, K. S.; Das, K.; Chatterjee, U. K.

    2007-09-01

    Differential scanning calorimetric (DSC) studies at different heating rates have been carried out to examine the solid-state reactions in 1441 and 8090 Al-Li-Cu-Mg-Zr alloys of water-quenched (WQ) and retrogressed tempers. The DSC peaks indicating the reactions sequence such as formation of GPB zones, precipitations of δ' phase, dissolution of GPB zones and δ' precipitates, and precipitations of S', T 1, T 2, and δ phases have been identified. From the heat flow associated with the peaks of the thermograms, the fraction transformation ( Y), the rate of transformation ( dY/ dt), the activation energy ( Q*), the frequency factor ( k 0), and the transformation function f( Y) for all the reactions of the 1441 and 8090 alloys have been determined. The appearance of separate peaks of GPB zone formation and δ' precipitation in the 1441 alloy of retrogressed tempers has enabled determination of the kinetic parameters, which is otherwise not possible from the thermograms of the WQ state due to peak overlapping, by varying heating rate method. The kinetic parameters determined from the DSC data of all the reactions of the alloys are in good agreement with the previously published data.

  20. 77 FR 43640 - Social Security Ruling, SSR 12-2p; Titles II and XVI: Evaluation of Fibromyalgia

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-07-25

    ... From the Federal Register Online via the Government Publishing Office SOCIAL SECURITY ADMINISTRATION Social Security Ruling, SSR 12-2p; Titles II and XVI: Evaluation of Fibromyalgia AGENCY: Social Security Administration. ACTION: Notice of Social Security Ruling (SSR). SUMMARY: In accordance with 20...

  1. 78 FR 17744 - Social Security Ruling, SSR 13-2p; Titles II and XVI: Evaluating Cases Involving Drug Addiction...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-03-22

    ... Federal Register on February 20, 2013. (78 FR 11939). On page 11940, in the first column, under the... From the Federal Register Online via the Government Publishing Office SOCIAL SECURITY ADMINISTRATION Social Security Ruling, SSR 13-2p; Titles II and XVI: Evaluating Cases Involving Drug...

  2. Use of calorimetric assay for operational and accountability measurements of pure plutonium metal

    SciTech Connect

    Cremers, Teresa L; Sampson, Thomas E

    2010-01-01

    Plutonium pure metal products (PMP) are high purity plutonium metal items produced by electrorefining. The plutonium metal is produced as an approximately 3-kg ring. Accountability measurements for the electro-refining runs are typically balance/weight factor (incoming impure metal), chemistry (pure metal rings), and calorimetric assay or neutron counting of the crucibles and other wastes. The PMP items are qualified for their end use by extensive chemical assay. After PMP materials are made they are often sent to the vault for storage before being sent to the casting process, the next step in the production chain. The chemical assay of PMP items often takes a few weeks; however, before the metal items are allowed into the vault they must be measured. Non-destructive assay personnel measure the metals either by multiplicity neutron counting or calorimetric assay, depending on which instrument is available, thus generating comparisons between non-destructive assay and chemical assay. The suite of measurements, calorimetric assay, chemical assay, and neutron mUltiplicity counting is compared for a large group of PMP items.

  3. Ultra-Responsive Thermal Sensors for the Detection of Explosives Using Calorimetric Spectroscopy (CalSpec)

    SciTech Connect

    Datskos, P.G.; Datskou, I.; Marlar, T.A.; Rajic, S.

    1999-04-05

    We have developed a novel chemical detection technique based on infrared micro-calorimetric spectroscopy that can be used to identify the presence of trace amounts of very low vapor pressure target compounds. Unlike numerous recently developed low-cost sensor approaches, the selectivity is derived from the unique differential temperature spectrum and does not require the questionable reliability of highly selective coatings to achieve the required specificity. This is accomplished by obtaining the infrared micro-calorimetric absorption spectrum of a small number of molecules absorbed on the surface of a thermal detector after illumination through a scanning monochromator. We have obtained infrared micro-calorimetric spectra for explosives such as TNT over the wavelength region 2.5 to 14.5 Mu-m. Thus both sophisticated and relatively crude explosive compounds and components are detectable with these ultra-sensitive thermal-mechanical micro-structures. In addition to the above mentioned spectroscopy technique and associated data, the development of these advanced thermal detectors is also presented in detail.

  4. Calorimetric and spectroscopic studies of aminoglycoside binding to AT-rich DNA triple helices

    PubMed Central

    Xi, Hongjuan; Kumar, Sunil; Dosen-Micovic, Ljiljana; Arya, Dev P.

    2013-01-01

    Calorimetric and fluorescence techniques were used to characterize the binding of aminoglycosides-neomycin, paromomycin, and ribostamycin, with 5′-dA12-x-dT12-x-dT12-3′ intramolecular DNA triplex (x = hexaethylene glycol) and poly(dA).2poly(dT) triplex. Our results demonstrate the following features: (1) UV thermal analysis reveals that the Tm for triplex decreases with increasing pH value in the presence of neomycin, while the Tm for the duplex remains unchanged. (2) The binding affinity of neomycin decreases with increased pH, although there is an increase in observed binding enthalpy. (3) ITC studies conducted in two buffers (sodium cacodylate and MOPS) yield the number of protonated drug amino groups (Δn) as 0.29 and 0.40 for neomycin and paromomycin interaction with 5′-dA12-x-dT12-x-dT12-3′, respectively. (4) The specific heat capacity change (ΔCp) determined by ITC studies is negative, with more negative values at lower salt concentrations. From 100 mM to 250 mM KCl, the ΔCp ranges from −402 to −60 cal/(mol K) for neomycin. At pH 5.5, a more positive ΔCp is observed, with a value of −98 cal/(mol K) at 100 mM KCl. ΔCp is not significantly affected by ionic strength. (5) Salt dependence studies reveal that there are at least three amino groups of neomycin participating in the electrostatic interactions with the triplex. (6) FID studies using thiazole orange were used to derive the AC50 (aminoglycoside concentration needed to displace 50% of the dye from the triplex) values. Neomycin shows a seven fold higher affinity than paromomycin and eleven fold higher affinity than ribostamycin at pH 6.8. (7) Modeling studies, consistent with UV and ITC results, show the importance of an additional positive charge in triplex recognition by neomycin. The modeling and thermodynamic studies indicate that neomycin binding to the DNA triplex depends upon significant contributions from charge as well as shape complementarity of the drug to the DNA triplex

  5. Direct calorimetric measurement of enthalpy of adsorption of carbon dioxide on CD-MOF-2, a green metal-organic framework.

    PubMed

    Wu, Di; Gassensmith, Jeremiah J; Gouvêa, Douglas; Ushakov, Sergey; Stoddart, J Fraser; Navrotsky, Alexandra

    2013-05-01

    The enthalpy of adsorption of CO2 on an environmentally friendly metal-organic framework, CD-MOF-2, has been determined directly for the first time using adsorption calorimetry at 25 °C. This calorimetric methodology provides a much more accurate and model-independent measurement of adsorption enthalpy than that obtained by calculation from the adsorption isotherms, especially for systems showing complex and strongly exothermic adsorption behavior. The differential enthalpy of CO2 adsorption shows enthalpy values in line with chemisorption behavior. At near-zero coverage, an irreversible binding event with an enthalpy of -113.5 kJ/mol CO2 is observed, which is followed by a reversible -65.4 kJ/mol binding event. These enthalpies are assigned to adsorption on more and less reactive hydroxyl groups, respectively. Further, a second plateau shows an enthalpy of -40.1 kJ/mol and is indicative of physisorbed CO2. The calorimetric data confirm the presence of at least two energetically distinct binding sites for chemisorbed CO2 on CD-MOF-2.

  6. Investigation of the accuracy of MV radiation isocentre calculations in the Elekta cone-beam CT software XVI.

    PubMed

    Riis, Hans L; Moltke, Lars N; Zimmermann, Sune J; Ebert, Martin A; Rowshanfarzad, Pejman

    2016-06-01

    Accurate determination of the megavoltage (MV) radiation isocentre of a linear accelerator (linac) is an important task in radiotherapy. The localization of the MV radiation isocentre is crucial for correct calibration of the in-room lasers and the cone-beam CT scanner used for patient positioning prior to treatment. Linac manufacturers offer tools for MV radiation isocentre localization. As a user, there is no access to the documentation for the underlying method and calculation algorithm used in the commercial software. The idea of this work was to evaluate the accuracy of the software tool for MV radiation isocentre calculation as delivered by Elekta using independent software. The image acquisition was based on the scheme designed by the manufacturer. Eight MV images were acquired in each series of a ball-bearing (BB) phantom attached to the treatment couch. The images were recorded at cardinal angles of the gantry using the electronic portal imaging device (EPID). Eight Elekta linacs with three different types of multileaf collimators (MLCs) were included in the test. The influence of MLC orientation, x-ray energy, and phantom modifications were examined. The acquired images were analysed using the Elekta x-ray volume imaging (XVI) software and in-house developed (IHD) MATLAB code. Results from the two different software were compared. A discrepancy in the longitudinal direction of the isocentre localization was found averaging 0.23 mm up to a maximum of 0.75 mm. The MLC orientation or the phantom asymmetry in the longitudinal direction do not appear to cause the discrepancy. The main cause of the differences could not be clearly identified. However, it is our opinion that the commercial software delivered by the linac manufacturer should be improved to reach better stability and precise results in the MV radiation isocentre calculations. PMID:27183466

  7. Investigation of the accuracy of MV radiation isocentre calculations in the Elekta cone-beam CT software XVI

    NASA Astrophysics Data System (ADS)

    Riis, Hans L.; Moltke, Lars N.; Zimmermann, Sune J.; Ebert, Martin A.; Rowshanfarzad, Pejman

    2016-06-01

    Accurate determination of the megavoltage (MV) radiation isocentre of a linear accelerator (linac) is an important task in radiotherapy. The localization of the MV radiation isocentre is crucial for correct calibration of the in-room lasers and the cone-beam CT scanner used for patient positioning prior to treatment. Linac manufacturers offer tools for MV radiation isocentre localization. As a user, there is no access to the documentation for the underlying method and calculation algorithm used in the commercial software. The idea of this work was to evaluate the accuracy of the software tool for MV radiation isocentre calculation as delivered by Elekta using independent software. The image acquisition was based on the scheme designed by the manufacturer. Eight MV images were acquired in each series of a ball-bearing (BB) phantom attached to the treatment couch. The images were recorded at cardinal angles of the gantry using the electronic portal imaging device (EPID). Eight Elekta linacs with three different types of multileaf collimators (MLCs) were included in the test. The influence of MLC orientation, x-ray energy, and phantom modifications were examined. The acquired images were analysed using the Elekta x-ray volume imaging (XVI) software and in-house developed (IHD) MATLAB code. Results from the two different software were compared. A discrepancy in the longitudinal direction of the isocentre localization was found averaging 0.23 mm up to a maximum of 0.75 mm. The MLC orientation or the phantom asymmetry in the longitudinal direction do not appear to cause the discrepancy. The main cause of the differences could not be clearly identified. However, it is our opinion that the commercial software delivered by the linac manufacturer should be improved to reach better stability and precise results in the MV radiation isocentre calculations.

  8. Calorimetric evaluation of commercial Ni-MH cells and charges

    NASA Technical Reports Server (NTRS)

    Darcy, Eric C.; Hughes, Brent M.

    1995-01-01

    The test objectives are to evaluate the electrical and thermal performance of commercial Ni-MH cells and to evaluate the effectiveness of commercial charge control circuits. The ultimate design objectives are to determine which cell designs are most suitable for scale-up and to guide the design of future Shuttle and Station based battery chargers.

  9. Calorimetric studies of natural talc: Enthalpy of dehydroxylation

    NASA Astrophysics Data System (ADS)

    Ogorodova, L. P.; Kiseleva, I. A.

    2011-10-01

    The standard dehydroxylation enthalpy of natural talc Mg3[Si4O10](OH)2 (87.8 ± 9.0 kJ/mol at 298.15 K) and the enthalpy of formation of dehydrated talc from the elements (Δf H {el/o} (298.15 K) = -5527.0 ± 9.0 kJ/mol) were determined for the first time using Hess's law, based on the total values of the enthalpy increments in heating a sample from room temperature to 973 K and the enthalpies of dissolution at 973 K for dehydrated talc measured in this work and those previously determined for talc and corresponding oxides.

  10. Non-destructive testing of an original XVI century painting on wood by ESPI system

    NASA Astrophysics Data System (ADS)

    Arena, G.; Paturzo, M.; Fatigati, G.; Grilli, M.; Pezzati, L.; Ferraro, P.

    2015-03-01

    Electronic Speckle Pattern Interferometry (ESPI), a non-contact and non-destructive optical techniques, was employed for assessing the conservation state of a XVI Century painting on wood (72x88x1,9 cm). By a long term analysis, the whole structure alterations, induced by the room temperature and relative humidity variations, were evaluated. Measurement of the whole painting structural bends was achieved. Local flaws and hidden detachments of pictorial layers from the support, which cannot be recognized by traditional art-restorer methods, were also revealed. This work was prevalently aimed at achieving a simple approach, in the laboratory practice, to get an intuitively user-friendly method for art conservators, not accustomed to high-tech or math based methods. The results demonstrate that ESPI can largely improve the traditional art conservation survey techniques.

  11. PREFACE: XVI International Youth Scientific School 'Actual Problems of Magnetic Resonance and its Applications'

    NASA Astrophysics Data System (ADS)

    Salakhov, M. Kh; Tagirov, M. S.; Dooglav, A. V.

    2013-12-01

    In 1997, A S Borovik-Romanov, the Academician of RAS, and A V Aganov, the head of the Physics Department of Kazan State University, suggested that the 'School of Magnetic Resonance', well known in the Soviet Union, should recommence and be regularly held in Kazan. This school was created in 1968 by G V Scrotskii, the prominent scientist in the field of magnetic resonance and the editor of many famous books on magnetic resonance (authored by A Abragam, B. Bleaney, C. Slichter, and many others) translated and edited in the Soviet Union. In 1991 the last, the 12th School, was held under the supervision of G V Scrotskii. Since 1997, more than 600 young scientists, 'schoolboys', have taken part in the School meetings, made their oral reports and participated in heated discussions. Every year a competition among the young scientist takes place and the Program Committee members name the best reports, the authors of which are invited to prepare full-scale scientific papers. The XVI International Youth Scientific School 'Actual problems of the magnetic resonance and its application' in its themes is slightly different from previous ones. A new section has been opened this year: Coherent Optics and Optical Spectroscopy. Many young people have submitted interesting reports on optical research, many of the reports are devoted to the implementation of nanotechnology in optical studies. The XVI International Youth Scientific School has been supported by the Program of development of Kazan Federal University. It is a pleasure to thank the sponsors (BRUKER Ltd, Moscow, the Russian Academy of Science, the Dynasty foundation of Dmitrii Zimin, Russia, Russian Foundation for Basic Research) and all the participants and contributors for making the International School meeting possible and interesting. A V Dooglav, M Kh Salakhov and M S Tagirov The Editors

  12. Calorimetric Low Temperature Detectors for High Resolution X-ray Spectroscopy on Stored Highly Stripped Heavy Ions

    SciTech Connect

    Bleile, A.; Egelhof, P.; Kluge, H.J.; Liebisch, U.; McCammon, D.; Meier, H.J.; Sebastian, O.; Stahle, C.K.; Stoehlker, T.; Weber, M.

    2000-12-31

    The precise determination of the Lamb shift in heavy hydrogen-like ions provides a sensitive test of QED in very strong Coulomb fields, not accessible otherwise, and has also the potential to deduce nuclear charge radii. A brief overview on the present status of such experiments, performed at the storage ring ESR at GSI Darmstadt, is given. For the investigation of the Lyman-{alpha} transitions in Au{sup 78+} or U{sup 91+} ions with improved accuracy, a high-resolution calorimetric low-temperature detector for hard x-rays (E {le} 100 keV) has been recently developed. The detector modules consist of arrays of silicon thermistors and of x-ray absorbers made of high-Z material to optimize the absorption efficiency. The detectors are housed in a specially designed {sup 3}He/{sup 4}He dilution refrigerator which fits to the geometry of the ESR target. The detector performance presently achieved is already close to fulfilling the demands of the Lamb shift experiment. For a prototype detector an energy resolution of {Delta}E{sub FWHM} = 75 eV is obtained for 60-keV x-rays.

  13. Calorimetric evaluation of antennas used for microwave interstitial hyperthermia.

    PubMed

    Wilkinson, D A; Saylor, T K; Shrivastava, P N; Werts, E D

    1990-01-01

    Several quasi-adiabatic calorimeters have been constructed for determining the heating efficiency of microwave antennas. The absorber is 0.9% saline which is stirred continuously, making equilibration times short (several seconds). Depth of insertion data have been obtained for standard BSD and CTC antennas at 915 MHz. Efficiency varies only slightly with insertion depth in the range 7-16 cm and can be as high as 65%. At shallower depths efficiency drops off, while reflected power and leakage fields increase. Data obtained in site visits conducted by the Hyperthermia Physics Center show that antenna efficiency of the BSD and CTC models can vary by as much as 35% within sets of functional 'identical' antennas.

  14. Calorimetric Study of Kinetic Glass Transition in Metallic Glasses

    SciTech Connect

    Hiki, Y.; Takahashi, H.

    2008-02-21

    Differential scanning calorimetry (DSC) experiments were carried out for a bulk metallic glass (BMG), Zr{sub 41.2}Ti{sub 13.8}Cu{sub 12.5}Ni{sub 10.0}Be{sub 22.5}, below and above the glass transition temperature T{sub g}. The T{sub g} values were determined from the DSC curves. A wide range of heating rate, q = dT/dt = 0.1-100 K/min, was adopted for the experiment, and the q dependence of the apparent T{sub g} was investigated. As q was decreased, the value of T{sub g} decreased rapidly, then more slowly, and seemed to approach a constant value at low q. The experimental result of this kinetic glass transition phenomenon was analyzed on the basis of the relaxation process occurring in the transition temperature range.

  15. Development of a new type of high pressure calorimetric cell, mechanically agitated and equipped with a dynamic pressure control system: Application to the characterization of gas hydrates

    SciTech Connect

    Plantier, F. Missima, D.; Torré, J.-P.; Marlin, L.

    2013-12-15

    A novel prototype of calorimetric cell has been developed allowing experiments under pressure with an in situ agitation system and a dynamic control of the pressure inside the cell. The use of such a system opens a wide range of potential practical applications for determining properties of complex fluids in both pressurized and agitated conditions. The technical details of this prototype and its calibration procedure are described, and an application devoted to the determination of phase equilibrium and phase change enthalpy of gas hydrates is presented. Our results, obtained with a good precision and reproducibility, were found in fairly good agreement with those found in literature, illustrate the various interests to use this novel apparatus.

  16. Calorimetric detection of influenza virus induced membrane fusion.

    PubMed

    Nebel, S; Bartoldus, I; Stegmann, T

    1995-05-01

    Membrane fusion induced by the hemagglutinin glycoprotein of influenza virus has been extensively characterized, but the mechanism whereby the protein achieves the merger of the viral and target membrane lipids remains enigmatic. Various lipid intermediate structures have been proposed, and the energies required for their formation predicted. Here, we have analyzed the enthalpies of fusion of influenza with liposomes by titration calorimetry. If a small sample of virus in a weak neutral pH buffer was added to an excess of liposomes at low pH, a two-component reaction was seen, composed of an exothermic reaction and a slower endothermic reaction. The exothermic reaction was the result of acid-base reactions between the neutral pH virus sample and low pH buffer and low-pH-induced changes in the virus. The endothermic reaction was not observed in the absence of liposomes and much reduced if acid-inactivated virus, which had lost its fusion but not its binding activity, was added to liposomes. The endothermic reaction was more temperature dependent than the exothermic reaction; its pH dependence corresponded with that of fusion and its enthalpy was higher if fusion was more extensive. These data indicate that most of the endothermic reaction was due to membrane fusion. The experimentally determined enthalpy of fusion, 0.6-0.7 kcal per mol of viral phospholipids, is much higher than expected on the basis of current theories about the formation of lipid intermediates during membrane fusion.

  17. Calorimetric glass transition explained by hierarchical dynamic facilitation

    PubMed Central

    Keys, Aaron S.; Garrahan, Juan P.; Chandler, David

    2013-01-01

    The glass transition refers to the nonequilibrium process by which an equilibrium liquid is transformed to a nonequilibrium disordered solid, or vice versa. Associated response functions, such as heat capacities, are markedly different on cooling than on heating, and the response to melting a glass depends markedly on the cooling protocol by which the glass was formed. This paper shows how this irreversible behavior can be interpreted quantitatively in terms of an East-model picture of localized excitations (or soft spots) in which molecules can move with a specific direction, and from which excitations with the same directionality of motion can appear or disappear in adjacent regions. As a result of these facilitated dynamics, excitations become correlated in a hierarchical fashion. These correlations are manifested in the dynamic heterogeneity of the supercooled liquid phase. Although equilibrium thermodynamics is virtually featureless, a nonequilibrium glass phase emerges when the model is driven out of equilibrium with a finite cooling rate. The correlation length of this emergent phase is large and increases with decreasing cooling rate. A spatially and temporally resolved fictive temperature encodes memory of its preparation. Parameters characterizing the model can be determined from reversible transport data, and with these parameters, predictions of the model agree well with irreversible differential scanning calorimetry.

  18. Relativistic electron precipitation at International Space Station: Space weather monitoring by Calorimetric Electron Telescope

    NASA Astrophysics Data System (ADS)

    Kataoka, Ryuho; Asaoka, Yoichi; Torii, Shoji; Terasawa, Toshio; Ozawa, Shunsuke; Tamura, Tadahisa; Shimizu, Yuki; Akaike, Yosui; Mori, Masaki

    2016-05-01

    The charge detector (CHD) of the Calorimetric Electron Telescope (CALET) on board the International Space Station (ISS) has a huge geometric factor for detecting MeV electrons and is sensitive to relativistic electron precipitation (REP) events. During the first 4 months, CALET CHD observed REP events mainly at the dusk to midnight sector near the plasmapause, where the trapped radiation belt electrons can be efficiently scattered by electromagnetic ion cyclotron (EMIC) waves. Here we show that interesting 5-20 s periodicity regularly exists during the REP events at ISS, which is useful to diagnose the wave-particle interactions associated with the nonlinear wave growth of EMIC-triggered emissions.

  19. Nanowell-patterned TiO{sub 2} microcantilevers for calorimetric chemical sensing

    SciTech Connect

    Lee, Dongkyu Chae, Inseok; Thundat, Thomas; Kim, Seonghwan; Jeon, Sangmin

    2014-04-07

    A sensitive calorimetric sensor using a TiO{sub 2} microcantilever with nanowells patterned on one of its sides is described. This single material cantilever is sensitive to temperature change without relying on the metal deposition-based bimetallic effect. The thermomechanical sensitivity originates from the structure dependent variations in both the elastic modulus and thermal expansion coefficient due to the presence of ordered nanowells. These cantilever beams offer an alternate and efficient chemical sensing route for vapor phase analytes using photothermal spectroscopy. Selective and sensitive detection of organophosphorus compounds, as well as their photocatalytic decomposition under ultraviolet light exposure are demonstrated.

  20. Method for measurement of diffusivity: Calorimetric studies of Fe/Ni multilayer thin films

    SciTech Connect

    Liu, JX; Barmak, K

    2015-07-15

    A calorimetric method for the measurement of diffusivity in thin film multilayers is introduced and applied to the Fe Ni system. Using this method, the diffusivity in [Fe (25 nm)/Ni (25 nm)](20) multilayer thin films is measured as 4 x 10(-3)exp(-1.6 +/- 0.1 eV/ k(B)T) cm(2)/s, respectively. The diffusion mechanism in the multilayers and its relevance to laboratory synthesis of L1(0) ordered FeNi are discussed. (C) 2015 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

  1. Calorimetric determination of the heat of combustion of spent Green River shale at 978 K

    SciTech Connect

    Mraw, S.C.; Keweshan, C.F.

    1987-08-01

    A Calvet-type calorimeter was used to measure heats of combustion of spent Colorado oil shales. For Green River shale, the samples were members of a sink-float series spanning oil yields from 87 to 340 L . tonne/sup -1/. Shale samples (30-200 mg) are dropped into the calorimeter at high temperature, and a peak in the thermopile signal records the total enthalpy change of the sample between room temperature and the final temperature. Duplicate samples from the above sink-float series were first retorted at 773 K and then dropped separately into nitrogen and oxygen at 978 K. The resulting heats are subtracted to give the heat of combustion, and the results are compared to values from classical bomb calorimetry. The agreement shows that the heats of combustion of the organic component are well understood but that question remain on the reactions of the mineral components.

  2. Calorimetric method for the determination of Curie temperatures of magnetic nanoparticles in dispersion.

    PubMed

    Nica, V; Sauer, H M; Embs, J; Hempelmann, R

    2008-05-21

    Mn(x)Zn(1-x)Fe(2)O(4)-based magnetic fluids with x = 0.1-0.9 are synthesized by coprecipitation. The samples are heated in a radio frequency (rf) magnetic field using an rf generator at different powers, and the temperature is measured as function of time using an optical thermometer. The heating effect of the dispersed magnetic nanoparticles is proportional to the imaginary part of the dynamic magnetic susceptibility of the ferrofluid, a quantity that depends on the temperature through the magnetization of the ferrite nanoparticles and the Néel or Brownian relaxation times, respectively. We propose an extrapolation method to actuate the Curie temperatures of the dispersed magnetic nanoparticles. By means of appropriate fitting functions for (dT/dt) versus T for both the heating and the cooling process, we deduce the Curie temperature of the samples under investigation. For Mn(x)Zn(1-x)Fe(2)O(4)-based magnetic nanoparticles the Curie temperatures decrease with increasing Zn content. They turn out to be lower than the literature values for bulk Mn(x)Zn(1-x)Fe(2)O(4), a phenomenon which is generally observed for phase transitions of nanocrystalline materials.

  3. Chemical trends of the luminescence in wide band gap II 1-xMn xVI semimagnetic semiconductors

    NASA Astrophysics Data System (ADS)

    Benecke, C.; Busse, W.; Gumlich, H.-E.

    1990-04-01

    Time resolved emission and excitation spectroscopy is used to investigate the Mn correlated luminescence in wide band gap II-VI compounds, i.e. Zn 1-xMn xS, Cd 1-xMn xSe, Zn 1-xMn xTe and Cd 1-xMn xTe. Additional Information has been obtained with CdxZnyMnzTe( x+ y+ z=1) in checking the luminescence by variation of the ratio of the cations Cd and Zn. Generally speaking, at least two distinct emissions bands can be observed for each II 1- xMn xVI compound. One emissions band is attributed to the internal transition 4T 1(G)→ 6A 1(S) of the 3d 5 electron of the Mn 2+ on regular metal sites with energies of about ≈2 eV. The other emission band is found to occur in the near infrared range of about ≈1.3 eV. This emission band is tentatively interpreted as a transition of Mn 2+ ions on interstitial sites or in small Mn chalcogenide clusters, both interpretations assuming cubic symmetry. This model is supported by the existence of low energy excitation bands and by the great similarity of the shape of the two emission bands which lead to comparable Huang-Rhys factors and effective phonon energies. Also the established trend in the experimental data of the II-VI compounds under consideration confirm this interpretation. For both the IR and the yellow Mn 2+ center, the Racah parameters B and C and the crystal field parameter Dq are determined on the basis of experimental data. As a result, the energy of both the emission and the excitation bands is predominantly determined by the sorrounding anions. These bands shift to higher energies when the anions are changed in the fixed order: Te→Se→S. Regularly, there is also a spectral shift when Zn is replaced by Cd, which is smaller than the shift due to the variation of onions.

  4. Genetic comparison of the head of Henri IV and the presumptive blood from Louis XVI (both Kings of France).

    PubMed

    Charlier, Philippe; Olalde, Iñigo; Solé, Neus; Ramírez, Oscar; Babelon, Jean-Pierre; Galland, Bruno; Calafell, Francesc; Lalueza-Fox, Carles

    2013-03-10

    A mummified head was identified in 2010 as belonging to Henri IV, King of France. A putative blood sample from the King Louis XVI preserved into a pyrographically decorated gourd was analyzed in 2011. Both kings are in a direct male-line descent, separated by seven generations. We have retrieved the hypervariable region 1 of the mitochondrial DNA as well as a partial Y-chromosome profile from Henri IV. Five STR loci match the alleles found in Louis XVI, while another locus shows an allele that is just one mutation step apart. Taking into consideration that the partial Y-chromosome profile is extremely rare in modern human databases, we concluded that both males could be paternally related. The likelihood ratio of the two samples belonging to males separated by seven generations (as opposed to unrelated males) was estimated as 246.3, with a 95% confidence interval between 44.2 and 9729. Historically speaking, this forensic DNA data would confirm the identity of the previous Louis XVI sample, and give another positive argument for the authenticity of the head of Henri IV.

  5. Genetic comparison of the head of Henri IV and the presumptive blood from Louis XVI (both Kings of France).

    PubMed

    Charlier, Philippe; Olalde, Iñigo; Solé, Neus; Ramírez, Oscar; Babelon, Jean-Pierre; Galland, Bruno; Calafell, Francesc; Lalueza-Fox, Carles

    2013-03-10

    A mummified head was identified in 2010 as belonging to Henri IV, King of France. A putative blood sample from the King Louis XVI preserved into a pyrographically decorated gourd was analyzed in 2011. Both kings are in a direct male-line descent, separated by seven generations. We have retrieved the hypervariable region 1 of the mitochondrial DNA as well as a partial Y-chromosome profile from Henri IV. Five STR loci match the alleles found in Louis XVI, while another locus shows an allele that is just one mutation step apart. Taking into consideration that the partial Y-chromosome profile is extremely rare in modern human databases, we concluded that both males could be paternally related. The likelihood ratio of the two samples belonging to males separated by seven generations (as opposed to unrelated males) was estimated as 246.3, with a 95% confidence interval between 44.2 and 9729. Historically speaking, this forensic DNA data would confirm the identity of the previous Louis XVI sample, and give another positive argument for the authenticity of the head of Henri IV. PMID:23283403

  6. Calorimetric Thermoelectric Gas Sensor for the Detection of Hydrogen, Methane and Mixed Gases

    PubMed Central

    Park, Nam-Hee; Akamatsu, Takafumi; Itoh, Toshio; Izu, Noriya; Shin, Woosuck

    2014-01-01

    A novel miniaturized calorimeter-type sensor device with a dual-catalyst structure was fabricated by integrating different catalysts on the hot (Pd/θ-Al2O3) and cold (Pt/α-Al2O3) ends of the device. The device comprises a calorimeter with a thermoelectric gas sensor (calorimetric-TGS), combining catalytic combustion and thermoelectric technologies. Its response for a model fuel gas of hydrogen and methane was investigated with various combustor catalyst compositions. The calorimetric-TGS devices detected H2, CH4, and a mixture of the two with concentrations ranging between 200 and 2000 ppm at temperatures of 100–400 °C, in terms of the calorie content of the gases. It was necessary to reduce the much higher response voltage of the TGS to H2 compared to CH4. We enhanced the H2 combustion on the cold side so that the temperature differences and response voltages to H2 were reduced. The device response to H2 combustion was reduced by 50% by controlling the Pt concentration in the Pt/α-Al2O3 catalyst on the cold side to 3 wt%. PMID:24818660

  7. Calorimetric thermoelectric gas sensor for the detection of hydrogen, methane and mixed gases.

    PubMed

    Park, Nam-Hee; Akamatsu, Takafumi; Itoh, Toshio; Izu, Noriya; Shin, Woosuck

    2014-01-01

    A novel miniaturized calorimeter-type sensor device with a dual-catalyst structure was fabricated by integrating different catalysts on the hot (Pd/θ-Al2O3) and cold (Pt/α-Al2O3) ends of the device. The device comprises a calorimeter with a thermoelectric gas sensor (calorimetric-TGS), combining catalytic combustion and thermoelectric technologies. Its response for a model fuel gas of hydrogen and methane was investigated with various combustor catalyst compositions. The calorimetric-TGS devices detected H2, CH4, and a mixture of the two with concentrations ranging between 200 and 2000 ppm at temperatures of 100-400 °C, in terms of the calorie content of the gases. It was necessary to reduce the much higher response voltage of the TGS to H2 compared to CH4. We enhanced the H2 combustion on the cold side so that the temperature differences and response voltages to H2 were reduced. The device response to H2 combustion was reduced by 50% by controlling the Pt concentration in the Pt/α-Al2O3 catalyst on the cold side to 3 wt%. PMID:24818660

  8. Calorimetric thermoelectric gas sensor for the detection of hydrogen, methane and mixed gases.

    PubMed

    Park, Nam-Hee; Akamatsu, Takafumi; Itoh, Toshio; Izu, Noriya; Shin, Woosuck

    2014-05-09

    A novel miniaturized calorimeter-type sensor device with a dual-catalyst structure was fabricated by integrating different catalysts on the hot (Pd/θ-Al2O3) and cold (Pt/α-Al2O3) ends of the device. The device comprises a calorimeter with a thermoelectric gas sensor (calorimetric-TGS), combining catalytic combustion and thermoelectric technologies. Its response for a model fuel gas of hydrogen and methane was investigated with various combustor catalyst compositions. The calorimetric-TGS devices detected H2, CH4, and a mixture of the two with concentrations ranging between 200 and 2000 ppm at temperatures of 100-400 °C, in terms of the calorie content of the gases. It was necessary to reduce the much higher response voltage of the TGS to H2 compared to CH4. We enhanced the H2 combustion on the cold side so that the temperature differences and response voltages to H2 were reduced. The device response to H2 combustion was reduced by 50% by controlling the Pt concentration in the Pt/α-Al2O3 catalyst on the cold side to 3 wt%.

  9. Estimating free-energy barrier heights for an ultrafast folding protein from calorimetric and kinetic data.

    PubMed

    Godoy-Ruiz, Raquel; Henry, Eric R; Kubelka, Jan; Hofrichter, James; Muñoz, Victor; Sanchez-Ruiz, Jose M; Eaton, William A

    2008-05-15

    Differential scanning calorimetry was used to measure the temperature dependence of the absolute heat capacity of the 35-residue subdomain of the villin headpiece, a protein that folds in 5 mus and is therefore assumed to have a small free-energy barrier separating folded and unfolded states. To obtain an estimate of the barrier height from the calorimetric data, two models, a variable-barrier model and an Ising-like model, were used to fit the heat capacity in excess of the folded state over the temperature range 15-125 degrees C. The variable-barrier model is based on an empirical mathematical form for the density of states, with four adjustable parameters and the enthalpy (H) as a reaction coordinate. The Ising-like model is based on the inter-residue contact map of the X-ray structure with exact enumeration of approximately 10(5) possible conformations, with two adjustable parameters in the partition function, and either the fraction of native contacts (Q) or the number of ordered residues (P) as reaction coordinates. The variable-barrier model provides an excellent fit to the data and yields a barrier height at the folding temperature ranging from 0.4 to 1.1 kcal mol(-1), while the Ising-like model provides a less good fit and yields barrier heights of 2.3 +/- 0.1 kcal mol(-1) and 2.1 +/- 0.1 kcal mol(-1) for the Q and P reaction coordinates, respectively. In both models, the barrier to folding increases with increasing temperature. Assuming a sufficiently large activation energy for diffusion on the free-energy surfaces, both models are consistent with the observation of a temperature-independent folding rate in previously published laser temperature-jump experiments. Analysis of this kinetic data, using an approximate form for the pre-exponential factor of Kramers theory and the 70 ns relaxation time for the fast phase that precedes the unfolding/refolding relaxation to determine the diffusion coefficient, results in a barrier height of 1.6 +/- 0.3 kcal mol

  10. XVI European Charcot Foundation Lecture: Nutrition and environment, can MS be prevented?

    PubMed Central

    Simon, Kelly Claire; Munger, Kassandra L; Ascherio, Alberto

    2012-01-01

    Multiple sclerosis is a relatively common debilitating neurologic disease that affects people in early adulthood. While the characteristic pathology of MS has been well described, the etiology of the disease is not well understood, despite decades of research and the identification of strong genetic and environmental candidates for susceptibility. A question central to all diseases, but posed specifically for MS at the XVI European Charcot Foundation Lecture, was ‘Can MS be prevented?’ To address this question, we have evaluated the available data regarding nutritional and environmental factors that may be related to MS susceptibility and suggest the extent to which a potential intervention may reduce disease burden. It is our opinion that intervention, particularly supplementation with vitamin D, could have a dramatic impact on disease prevalence. Understanding that any intervention or behavioral modification will surely act in the context of genetic susceptibility and unidentified stochastic events, it is likely that not all MS is ‘preventable’. Epidemiologic observation has provided key insights into environmental and nutritional factors that may alter one’s susceptibility to MS, however, there are still many questions in unraveling the etiology of this complex disease. PMID:21975017

  11. Rapid discrimination of DNA strands using an opto-calorimetric microcantilever sensor.

    PubMed

    Lee, Dongkyu; Hwang, Kyo Seon; Kim, Seonghwan; Thundat, Thomas

    2014-12-21

    A rapid technique for quantitative detection and discrimination of DNA strands without using immobilized probe molecules is demonstrated using an opto-calorimetric, self-powered sensor based on a Pb(Zr(0.52)Ti(0.48))O3 (PZT) microcantilever. Microcalorimetric infrared (IR) spectroscopy provides excellent chemical selectivity based on the unique molecular vibrational characteristics of each nucleotide in the mid IR region. The piezoelectric and pyroelectric properties of the PZT microcantilever were exploited in the quantitative detection and discrimination of adsorbed DNA strands with their spectral characteristics. We report the unique spectral characteristics of different DNA nucleotides that are monitored by wavelength-dependent temperature variations for different relative molar ratio of each nucleotide. This approach offers a fast, label-free technique which is highly sensitive and selective for the detection of single nucleotide differences in DNA strands and has the potential to be used as a rapid prescreening biosensor for various biomolecules.

  12. Calorimetric Observation of Single He_2^* Excimers in a 100-mK He Bath

    NASA Astrophysics Data System (ADS)

    Carter, F. W.; Hertel, S. A.; Rooks, M. J.; McClintock, P. V. E.; McKinsey, D. N.; Prober, D. E.

    2016-10-01

    We report the first calorimetric detection of individual He_2^* excimers within a bath of superfluid ^4He. The detector used in this work is a single superconducting titanium transition edge sensor (TES) with an energy resolution of {˜ }1 eV, immersed directly in the helium bath. He_2^* excimers are produced in the surrounding bath using an external gamma-ray source. These excimers exist either as short-lived singlet or long-lived triplet states. We demonstrate detection (and discrimination) of both states: In the singlet case the calorimeter records the absorption of a prompt {≈ }15 eV photon, and in the triplet case the calorimeter records a direct interaction of the molecule with the TES surface, which deposits a distinct fraction of the {≈ }15 eV, released upon decay, into the surface. We also briefly discuss the detector fabrication and characterization.

  13. Isothermal calorimetric titrations on charge-assisted halogen bonds: role of entropy, counterions, solvent, and temperature.

    PubMed

    Walter, Sebastian M; Kniep, Florian; Rout, Laxmidhar; Schmidtchen, Franz P; Herdtweck, Eberhardt; Huber, Stefan M

    2012-05-23

    We have conducted isothermal calorimetric titrations to investigate the halogen-bond strength of cationic bidentate halogen-bond donors toward halides, using bis(iodoimidazolium) compounds as probes. These data are intended to aid the rational design of halogen-bond donors as well as the development of halogen-bond-based applications in solution. In all cases examined, the entropic contribution to the overall free energy of binding was found to be very important. The binding affinities showed little dependency on the weakly coordinating counteranions of the halogen-bond donors but became slightly stronger with higher temperatures. We also found a marked influence of different solvents on the interaction strength. The highest binding constant detected in this study was 3.3 × 10(6) M(-1).

  14. Direct calorimetric verification of thermodynamic instability of lead halide hybrid perovskites.

    PubMed

    Nagabhushana, G P; Shivaramaiah, Radha; Navrotsky, Alexandra

    2016-07-12

    Hybrid perovskites, especially methylammonium lead iodide (MAPbI3), exhibit excellent solar power conversion efficiencies. However, their application is plagued by poor chemical and structural stability. Using direct calorimetric measurement of heats of formation, MAPbI3 is shown to be thermodynamically unstable with respect to decomposition to lead iodide and methylammonium iodide, even in the absence of ambient air or light or heat-induced defects, thus limiting its long-term use in devices. The formation enthalpy from binary halide components becomes less favorable in the order MAPbCl3, MAPbBr3, MAPbI3, with only the chloride having a negative heat of formation. Optimizing the geometric match of constituents as measured by the Goldschmidt tolerance factor provides a potentially quantifiable thermodynamic guide for seeking chemical substitutions to enhance stability. PMID:27357677

  15. Evidence of secondary electron emission during PIII pulses as measured by calorimetric probe

    NASA Astrophysics Data System (ADS)

    Haase, Fabian; Manova, Darina; Mändl, Stephan; Kersten, Holger

    2016-09-01

    Secondary electrons are an ubiquitous nuisance during plasma immersion ion implantation (PIII) necessitating excessive current supplies and shielding for X-rays generated by them. However, additional effects - especially at low pulse voltages - can include interactions with the plasma and transient increases in the plasma density. Here, it is shown that the transient thermal flux associated with secondary electrons emitted from the pulsed substrate can be directly measured using a passive calorimetric probe mounted near the chamber wall away from the pulsed substrate holder. A small increase of a directed energy flux from the substrate towards the probe is consistently observed on top of the isotropic flux from the plasma surrounding the probe, scaling with pulse frequency, pulse voltage, pulse length - as well as depending on gas and substrate material. A strong correlation between voltage and substrate-probe distance is observed, which should allow further investigation of low energy electrons with the plasma itself.

  16. Calorimetric quantification of linked equilibria in cyclodextrin/lipid/detergent mixtures for membrane-protein reconstitution.

    PubMed

    Textor, Martin; Vargas, Carolyn; Keller, Sandro

    2015-04-01

    Reconstitution from detergent micelles into lipid bilayer membranes is a prerequisite for many in vitro studies on purified membrane proteins. Complexation by cyclodextrins offers an efficient and tightly controllable way of removing detergents for membrane-protein reconstitution, since cyclodextrins sequester detergents at defined stoichiometries and with tuneable affinities. To fully exploit the potential advantages of cyclodextrin for membrane-protein reconstitution, we establish a quantitative model for predicting the supramolecular transition from mixed micelles to vesicles during cyclodextrin-mediated detergent extraction. The model is based on a set of linked equilibria among all pseudophases present in the course of the reconstitution process. Various isothermal titration-calorimetric protocols are used for quantifying a detergent's self-association as well as its colloidal and stoichiometric interactions with lipid and cyclodextrin, respectively. The detergent's critical micellar concentration, the phase boundaries in the lipid/detergent phase diagram, and the dissociation constant of the cyclodextrin/detergent complex thus obtained provide all thermodynamic parameters necessary for a quantitative prediction of the transition from micelles to bilayer membranes during cyclodextrin-driven reconstitution. This is exemplified and validated by stepwise complexation of the detergent lauryldimethylamine N-oxide in mixtures with the phospholipid 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine upon titration with 2-hydroxypropyl-β-cyclodextrin, both in the presence and in the absence of the membrane protein Mistic. The calorimetric approach presented herein quantitatively predicts the onset and completion of the reconstitution process, thus obviating cumbersome trial-and-error efforts and facilitating the rational optimisation of reconstitution protocols, and can be adapted to different cyclodextrin/lipid/detergent combinations.

  17. Soluble expression and sodium channel activity of lt16a, a novel framework XVI conotoxin from the M-superfamily.

    PubMed

    Zhou, Maojun; Wang, Lei; Wu, Yun; Liu, Junliang; Sun, Dandan; Zhu, Xiaoyan; Feng, Yuchao; Qin, Mengying; Chen, Shangwu; Xu, Anlong

    2015-05-01

    A peptide toxin, lt16a, from the venom of the worm-hunting Conus litteratus, shares the typical signal peptide sequences of M-superfamily conotoxins, which usually contain six cysteine residues that are arranged in a CC-C-C-CC pattern. Interestingly, lt16a comprises 21 amino acid residues in its mature region and has a cysteine framework XVI, which is arranged in a C-C-CC pattern. The coding region of lt16a was cloned into the pTRX vector and the fusion protein was overexpressed in Escherichia coli. After cleaving the fusion protein and purifying the protein lt16a using chromatography, the mass of lt16a was found by mass spectrometry to be consistent with the expected mass of 2357.7 Da. Whole-cell patch clamp experiments demonstrated that lt16a could inhibit both the TTX-sensitive and TTX-resistant sodium currents in adult rat dorsal root ganglion neurons. The inhibition of lt16a on TTX-resistant sodium currents was stronger than on TTX-sensitive sodium currents. To our knowledge, this is the first report of a framework XVI conotoxin that can inhibit voltage-gated sodium channel currents in mammalian sensory neurons. This report helps facilitates an understanding of the sequence diversity of conotoxins.

  18. Differential scanning calorimetric evaluation of human meibomian gland secretions and model lipid mixtures: transition temperatures and cooperativity of melting

    PubMed Central

    Lu, Hua; Wojtowicz, Jadwiga C.; Butovich, Igor A.

    2013-01-01

    Meibomian gland secretions (or meibum) are produced by holocrine meibomian glands and are secreted in melted form onto the ocular surface of humans and animals to form a protective tear film lipid layer (TFLL). Its protective effect strongly depends on the composition and, hence, thermotropic behavior of meibum. The goal of our study was to quantitatively evaluate the melting characteristics of human meibum and model lipid mixtures using differential scanning microcalorimetry. Standard calorimetric parameters, e.g. changes in calorimetric enthalpy, transition temperatures T(m), cooperativity of melting etc. were assessed. We found that thermotropic behavior of meibum resembled that of relatively simple mixtures of unsaturated wax esters, but showed a lower change in calorimetric enthalpy, which can be indicative of a looser packing of lipids in meibum compared with pure standards and their simple mixtures. The cooperativity of melting of meibomian lipids was comparable to that of an equimolar mixture of four oleic-acid based wax esters. We demonstrated that the phase transitions in meibum start at about 10 to 15 °C and end at 35-36 °C, with T(m) being about 30 °C. The highly asymmetrical shape of the thermotropic peak of meibum is important for the physiology and biophysics of TFLL. PMID:23578711

  19. Effect of Temperature on Xylanase II from Trichoderma reesei QM 9414: A Calorimetric, Catalytic, and Conformational Study

    PubMed Central

    López, Gloria

    2014-01-01

    The secondary structure of xylanase II from Trichoderma reesei is lost in an apparent irreversible cooperative process as temperature is increased with a midpoint transition of 58.8 ± 0.1°C. The shift of the spectral centre of mass above 50°C is also apparently cooperative with midpoint transition of 56.3 ± 0.2°C, but the existence of two isofluorescent points in the fluorescence emission spectra suggests a non-two-state process. Further corroboration comes from differential scanning calorimetry experiments. At protein concentrations ≤0.56 mg·mL−1 the calorimetric transition is reversible and the data were fitted to a non-two-state model and deconvoluted into six transitions, whereas at concentrations greater than 0.56 mg·mL−1 the calorimetric transition is irreversible with an exothermic contribution to the thermogram. The apparent Tm increased linearly with the scan rate according to first order inactivation kinetics. The effect of additives on the calorimetric transition of xylanase is dependent on their nature. The addition of sorbitol transforms reversible transitions into irreversible transitions while stabilizing the protein as the apparent Tm increases linearly with sorbitol concentration. d-Glucono-1,5-lactone, a noncompetitive inhibitor in xylanase kinetics, and soluble xylan change irreversible processes into reversible processes at high protein concentration. PMID:25276420

  20. 20 CFR 416.573 - How much will we withhold from your title II and title VIII benefits to recover a title XVI...

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 20 Employees' Benefits 2 2010-04-01 2010-04-01 false How much will we withhold from your title II and title VIII benefits to recover a title XVI overpayment? 416.573 Section 416.573 Employees... Payment of Benefits, Overpayments, and Underpayments § 416.573 How much will we withhold from your...

  1. 20 CFR 416.573 - How much will we withhold from your title II and title VIII benefits to recover a title XVI...

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 20 Employees' Benefits 2 2011-04-01 2011-04-01 false How much will we withhold from your title II and title VIII benefits to recover a title XVI overpayment? 416.573 Section 416.573 Employees... Payment of Benefits, Overpayments, and Underpayments § 416.573 How much will we withhold from your...

  2. The Bayer Facts of Science Education XVI: "US STEM Workforce Shortage--Myth or Reality? Fortune 1000 Talent Recruiters on the Debate"

    ERIC Educational Resources Information Center

    Journal of Science Education and Technology, 2014

    2014-01-01

    A major debate is currently underway in the USA about whether there is, in fact, a science, technology, engineering and mathematics (STEM) workforce shortage in the country or not. This is the subject of the "Bayer Facts of Science Education XVI: US STEM Workforce Shortage--Myth or Reality? Fortune 1000 Talent Recruiters on the Debate."…

  3. The CALorimetric Electron Telescope (CALET) for high-energy astroparticle physics on the International Space Station

    NASA Astrophysics Data System (ADS)

    Adriani, O.; Akaike, Y.; Asano, K.; Asaoka, Y.; Bagliesi, M. G.; Bigongiari, G.; Binns, W. R.; Bonechi, S.; Bongi, M.; Buckley, J. H.; Castellini, G.; Cherry, M. L.; Collazuol, G.; Ebisawa, K.; Di Felice, V.; Fuke, H.; Guzik, T. G.; Hams, T.; Hareyama, M.; Hasebe, N.; Hibino, K.; Ichimura, M.; Ioka, K.; Israel, M. H.; Javaid, A.; Kamioka, E.; Kasahara, K.; Kataoka, J.; Kataoka, R.; Katayose, Y.; Kawanaka, N.; Kitamura, H.; Kotani, T.; Krawczynski, H. S.; Krizmanic, J. F.; Kubota, A.; Kuramata, S.; Lomtadze, T.; Maestro, P.; Marcelli, L.; Marrocchesi, P. S.; Mitchell, J. W.; Miyake, S.; Mizutani, K.; Moiseev, A. A.; Mori, K.; Mori, M.; Mori, N.; Motz, H. M.; Munakata, K.; Murakami, H.; Nakagawa, Y. E.; Nakahira, S.; Nishimura, J.; Okuno, S.; Ormes, J. F.; Ozawa, S.; Palma, F.; Papini, P.; Rauch, B. F.; Ricciarini, S. B.; Sakamoto, T.; Sasaki, M.; Shibata, M.; Shimizu, Y.; Shiomi, A.; Sparvoli, R.; Spillantini, P.; Takahashi, I.; Takayanagi, M.; Takita, M.; Tamura, T.; Tateyama, N.; Terasawa, T.; Tomida, H.; Torii, S.; Tunesada, Y.; Uchihori, Y.; Ueno, S.; Vannuccini, E.; Wefel, J. P.; Yamaoka, K.; Yanagita, S.; Yoshida, A.; Yoshida, K.; Yuda, T.

    2015-05-01

    The CALorimetric Electron Telescope (CALET) is a space experiment, currently under development by Japan in collaboration with Italy and the United States, which will measure the flux of cosmic-ray electrons (and positrons) up to 20 TeV energy, of gamma rays up to 10 TeV, of nuclei with Z from 1 to 40 up to 1 PeV energy, and will detect gamma-ray bursts in the 7 keV to 20 MeV energy range during a 5 year mission. These measurements are essential to investigate possible nearby astrophysical sources of high energy electrons, study the details of galactic particle propagation and search for dark matter signatures. The main detector of CALET, the Calorimeter, consists of a module to identify the particle charge, followed by a thin imaging calorimeter (3 radiation lengths) with tungsten plates interleaving scintillating fibre planes, and a thick energy measuring calorimeter (27 radiation lengths) composed of lead tungstate logs. The Calorimeter has the depth, imaging capabilities and energy resolution necessary for excellent separation between hadrons, electrons and gamma rays. The instrument is currently being prepared for launch (expected in 2015) to the International Space Station ISS, for installation on the Japanese Experiment Module - Exposure Facility (JEM-EF).

  4. The CALorimetric Electron Telescope (CALET) for high-energy astroparticle physics on the International Space Station

    NASA Astrophysics Data System (ADS)

    Adriani, O.; Akaike, Y.; Asano, K.; Asaoka, Y.; Bagliesi, M. G.; Bigongiari, G.; Binns, W. R.; Bonechi, S.; Bongi, M.; Buckley, J. H.; Castellini, G.; Cherry, M. L.; Collazuol, G.; Ebisawa, K.; Di Felice, V.; Fuke, H.; Guzik, T. G.; Hams, T.; Hareyama, M.; Hasebe, N.; Hibino, K.; Ichimura, M.; Ioka, K.; Israel, M. H.; Javaid, A.; Kamioka, E.; Kasahara, K.; Kataoka, J.; Kataoka, R.; Katayose, Y.; Kawanaka, N.; Kitamura, H.; Kotani, T.; Krawczynski, H. S.; Krizmanic, J. F.; Kubota, A.; Kuramata, S.; Lomtadze, T.; Maestro, P.; Marcelli, L.; Marrocchesi, P. S.; Mitchell, J. W.; Miyake, S.; Mizutani, K.; Moiseev, A. A.; Mori, K.; Mori, M.; Mori, N.; Motz, H. M.; Munakata, K.; Murakami, H.; Nakagawa, Y. E.; Nakahira, S.; Nishimura, J.; Okuno, S.; Ormes, J. F.; Ozawa, S.; Palma, F.; Papini, P.; Rauch, B. F.; Ricciarini, S. B.; Sakamoto, T.; Sasaki, M.; Shibata, M.; Shimizu, Y.; Shiomi, A.; Sparvoli, R.; Spillantini, P.; Takahashi, I.; Takayanagi, M.; Takita, M.; Tamura, T.; Tateyama, N.; Terasawa, T.; Tomida, H.; Torii, S.; Tunesada, Y.; Uchihori, Y.; Ueno, S.; Vannuccini, E.; Wefel, J. P.; Yamaoka, K.; Yanagita, S.; Yoshida, A.; Yoshida, K.; Yuda, T.

    2015-08-01

    The CALorimetric Electron Telescope (CALET) is a space experiment, currently under development by Japan in collaboration with Italy and the United States, which will measure the flux of cosmic-ray electrons (and positrons) up to 20 TeV energy, of gamma rays up to 10 TeV, of nuclei with Z from 1 to 40 up to 1 PeV energy, and will detect gamma-ray bursts in the 7 keV to 20 MeV energy range during a 5 year mission. These measurements are essential to investigate possible nearby astrophysical sources of high energy electrons, study the details of galactic particle propagation and search for dark matter signatures. The main detector of CALET, the Calorimeter, consists of a module to identify the particle charge, followed by a thin imaging calorimeter (3 radiation lengths) with tungsten plates interleaving scintillating fibre planes, and a thick energy measuring calorimeter (27 radiation lengths) composed of lead tungstate logs. The Calorimeter has the depth, imaging capabilities and energy resolution necessary for excellent separation between hadrons, electrons and gamma rays. The instrument is currently being prepared for launch (expected in 2015) to the International Space Station ISS, for installation on the Japanese Experiment Module - Exposure Facility (JEM-EF).

  5. Binding of the anticancer alkaloid sanguinarine with tRNA(phe): spectroscopic and calorimetric studies.

    PubMed

    Hossain, Maidul; Kabir, Ayesha; Suresh Kumar, Gopinatha

    2012-01-01

    The interaction of the natural plant alkaloid and anticancer agent sanguinarine with tRNA(phe) has been investigated by spectroscopic and calorimetric techniques. Sanguinarine iminium binds to tRNA(phe) cooperatively; alkanolamine does not bind but in presence of large tRNA(phe) concentration, a conversion from alkanolamine to iminium occurs resulting in concomitant binding of the latter. The binding affinity of the iminium to tRNA(phe) obtained from isothermal titration calorimetry was of the order of 10(5) M(-1), which is close to that evaluated from spectroscopy. The binding was driven largely by negative enthalpy and a smaller but favourable positive entropy change. The binding was dependent on the [Na(+)] concentration, but had a larger non-electrostatic contribution to the Gibbs energy. A small heat capacity value and the enthalpy-entropy compensation in the energetics of the interaction characterized the binding of the iminium form to tRNA(phe). This study confirms that the tRNA(phe) binding moiety is the iminium form of sanguinarine. PMID:22702734

  6. Electron energy and charge albedos - calorimetric measurement vs Monte Carlo theory

    SciTech Connect

    Lockwood, G.J.; Ruggles, L.E.; Miller, G.H.; Halbleib, J.A.

    1981-11-01

    A new calorimetric method has been employed to obtain saturated electron energy albedos for Be, C, Al, Ti, Mo, Ta, U, and UO/sub 2/ over the range of incident energies from 0.1 to 1.0 MeV. The technique was so designed to permit the simultaneous measurement of saturated charge albedos. In the cases of C, Al, Ta, and U the measurements were extended down to about 0.025 MeV. The angle of incidence was varied from 0/sup 0/ (normal) to 75/sup 0/ in steps of 15/sup 0/, with selected measurements at 82.5/sup 0/ in Be and C. In each case, state-of-the-art predictions were obtained from a Monte Carlo model. The generally good agreement between theory and experiment over this extensive parameter space represents a strong validation of both the theoretical model and the new experimental method. Nevertheless, certain discrepancies at low incident energies, especially in high-atomic-number materials, and at all energies in the case of the U energy albedos are not completely understood.

  7. Status and performance of the CALorimetric Electron Telescope (CALET) on the International Space Station

    NASA Astrophysics Data System (ADS)

    Adriani, O.; Akaike, Y.; Asaoka, Y.; Asano, K.; Bagliesi, M. G.; Bigongiari, G.; Binns, W. R.; Bongi, M.; Buckley, J. H.; Cassese, A.; Castellini, G.; Cherry, M. L.; Collazuol, G.; Ebisawa, K.; Di Felice, V.; Fuke, H.; Guzik, T. G.; Hams, T.; Hasebe, N.; Hareyama, M.; Hibino, K.; Ichimura, M.; Ioka, K.; Israel, M. H.; Javaid, A.; Kamioka, E.; Kasahara, K.; Katayose, Y.; Kataoka, J.; Kataoka, R.; Kawanaka, N.; Kitamura, H.; Kotani, T.; Krawczynski, H. S.; Krizmanic, J. F.; Kubota, A.; Kuramata, S.; Lomtadze, T.; Maestro, P.; Marcelli, L.; Marrocchesi, P. S.; Mitchell, J. W.; Miyake, S.; Mizutani, K.; Motz, H. M.; Moiseev, A. A.; Mori, K.; Mori, M.; Mori, N.; Munakata, K.; Murakami, H.; Nakagawa, Y. E.; Nakahira, S.; Nishimura, J.; Okuno, S.; Ormes, J. F.; Ozawa, S.; Palma, F.; Papini, P.; Rauch, B. F.; Ricciarini, S.; Sakamoto, T.; Sasaki, M.; Shibata, M.; Shimizu, Y.; Shiomi, A.; Sparvoli, R.; Spillantini, P.; Takahashi, I.; Takayanagi, M.; Takita, M.; Tamura, T.; Tateyama, N.; Terasawa, T.; Tomida, H.; Torii, S.; Tunesada, Y.; Uchihori, Y.; Ueno, S.; Vannuccini, E.; Wefel, J. P.; Yamaoka, K.; Yanagita, S.; Yoshida, A.; Yoshida, K.; Yuda, T.

    2014-11-01

    The CALorimetric Electron Telescope (CALET) space experiment, currently under development by Japan in collaboration with Italy and the United States, will measure the flux of cosmic-ray electrons (including positrons) to 20 TeV, gamma rays to 10 TeV and nuclei with Z=1 to 40 up to 1,000 TeV during a two-year mission on the International Space Station (ISS), extendable to five years. These measurements are essential to search for dark matter signatures, investigate the mechanism of cosmic-ray acceleration and propagation in the Galaxy and discover possible astrophysical sources of high-energy electrons nearby the Earth. The instrument consists of two layers of segmented plastic scintillators for the cosmic-ray charge identification (CHD), a 3 radiation length thick tungsten-scintillating fiber imaging calorimeter (IMC) and a 27 radiation length thick lead-tungstate calorimeter (TASC). CALET has sufficient depth, imaging capabilities and excellent energy resolution to allow for a clear separation between hadrons and electrons and between charged particles and gamma rays. The instrument will be launched to the ISS within 2014 Japanese Fiscal Year (by the end of March 2015) and installed on the Japanese Experiment Module-Exposed Facility (JEM-EF). In this paper, we will review the status and main science goals of the mission and describe the instrument configuration and performance.

  8. Calorimetric studies of the ammonia-water system with application to the outer solar system

    NASA Astrophysics Data System (ADS)

    Yarger, J.; Lunine, J. I.; Burke, M.

    1993-07-01

    A series of heating experiments was performed on the condensed ammonia-water system using a differential scanning calorimeter (DSC). The water-rich samples were cooled quickly to below 130 K, then heated at a variety of rates. Rather than a single peritectic melt at 176 K, expected for the equilibrium system of water ice and ammonia dihydrate, four enthalpic transitions were repeatedly seen in the temperature range 150-176 K. These transitions are generally consistent with the earlier calorimetric results of Van Kasteren (1973), who interpreted the lowest temperature exotherm as crystallization of an amorphous ammonia-water compound formed during cooling. We propose that both sets of experiments are seeing the crystallization of ammonia monohydrate, which is metastable relative to the dihydrate, followed by partial remelting and crystallization of dihydrate upon further heating. The apparent stability of the monohydrate in the dihydrate equilibrium field implies a potentially complex behavior of ammonia-water ices in satellites. Possible self-heating of the mixture by several tens of degrees up to the 170 K eutectic could make mobilization of ammonia-water liquids in icy satellite interiors energetically easier than previously thought.

  9. The Calorimetric Electron Telescope (CALET) for High Energy Astroparticle Physics on the International Space Station

    NASA Astrophysics Data System (ADS)

    Torii, Shoji

    The Calorimetric Electron Telescope, CALET, space experiment, currently under development by Japan in collaboration with Italy and the United States, will measure the flux of Cosmic Ray electrons (and positrons) t o 20 TeV, gamma rays to 10 TeV , nuclei with Z=1 to 40 up to 1,000 TeV, and Gamma-ray bursts in the 7 keV- 10 MeV energy range during a five year mission. These measurements are essential to investigate possible nearby astrophysical sources of high energy electrons, study the details of galactic particle propagation and search for dark matter signatures. The main detector of Calet, the Calorimeter, consists of a module to identify the particle charge, followed by a thin imaging calorimeter (3 radiation lengths) with tungsten plates interleaving scintillating fiber planes, and a thick energy measuring calorimeter (27 radiation lengths) composed of lead tungstate logs. The Calorimeter has the depth, imaging capabilities and energy resolution necessary for excellent separation between hadrons, electrons and gamma rays. The instrument is currently being prepared for launch, during the Japan Fiscal Year (April, 2014- March, 2015) time frame, to the International Space Station (ISS) for installation on the Japanese Experiment Module - Exposure Facility (JEM-EF).

  10. Effect of sulfoxides on the thermal denaturation of hen lysozyme: A calorimetric and Raman study

    NASA Astrophysics Data System (ADS)

    Torreggiani, A.; Di Foggia, M.; Manco, I.; De Maio, A.; Markarian, S. A.; Bonora, S.

    2008-11-01

    A multidisciplinary study of the thermal denaturation of lysozyme in the presence of three sulfoxides with different length in hydrocarbon chain (DMSO, DESO, and DPSO) was carried out by means of DSC, Raman spectroscopy, and SDS-PAGE techniques. In particular, the Td and Δ H values obtained from the calorimetric measurements showed that lysozyme is partially unfolded by sulfoxides but most of the conformation holds native state. The sulfoxide denaturing ability increases in the order DPSO > DESO > DMSO. Moreover, only DMSO and DESO have a real effect in preventing the heat-induced inactivation of the protein and their maximum heat-protective ability is reached when the DMSO and DESO amount is ⩾25% w/w. The sulfoxide ability to act as effective protective agents against the heat-induced inactivation was confirmed by the protein analysis. The enzymatic activity, as well as the SDS-PAGE analysis, suggested that DESO, having a low hydrophobic character and a great ability to stabilise the three-dimensional water structure, is the most heat-protective sulfoxide. An accurate evaluation of the heat-induced conformational changes of the lysozyme structure before and after sulfoxide addition was obtained by the analysis of the Raman spectra. The addition of DMSO or DESO in low concentration resulted to sensitively decrease the heat-induced structural modifications of the protein.

  11. Optical and Calorimetric Studies of Cholesterol-Rich Filamentous, Helical Ribbon and Crystal Microstructures (abstract)

    NASA Astrophysics Data System (ADS)

    Miroshnikova, Y. A.; Elsenbeck, M.; Kashuri, K.; Iannacchione, G. S.; Zastavker, Y. V.

    2009-04-01

    Formation of biological self-assemblies at all scales is a focus of studies in fields ranging from biology to physics to biomimetics. Understanding the physico-chemical properties of these self-assemblies may lead to the design of bio-inspired structures and technological applications. Here we examine self-assembled filamentous, helical ribbon, and crystal microstructures formed in chemically defined lipid concentrate (CDLC), a model system for cholesterol crystallization in gallbladder bile. CDLC consists of cholesterol, bilayer-forming amphiphiles, micelle-forming amphiphiles, and water. Phase contrast and differential interference contrast (DIC) microscopy indicate the presence of three microstructure types in all samples studied, and allow for an investigation of the structures' unique geometries. Additionally, confocal microscopy is used for qualitative assessment of surface and internal composition. To complement optical observations, calorimetric (differential-scanning and modulation) experiments, provide the basis for an in-depth understanding of collective and individual thermal behavior. Observed ``transition'' features indicate clustering and ``straightening'' of helical ribbons into short, increasingly thickening, filaments that dissolve with increasing temperature. These results suggest that all microstructures formed in CDLC may coexist in a metastable chemical equilibrium. Further investigation of the CDLC thermal profile should uncover the process of cholesterol crystallization as well as the unique design and function of microstructures formed in this system.

  12. Optical and Calorimetric Studies of Cholesterol-Rich Filamentous, Helical Ribbon and Crystal Microstructures

    SciTech Connect

    Miroshnikova, Y. A.; Elsenbeck, M.; Zastavker, Y. V.; Kashuri, K; Iannacchione, G. S.

    2009-04-19

    Formation of biological self-assemblies at all scales is a focus of studies in fields ranging from biology to physics to biomimetics. Understanding the physico-chemical properties of these self-assemblies may lead to the design of bio-inspired structures and technological applications. Here we examine self-assembled filamentous, helical ribbon, and crystal microstructures formed in chemically defined lipid concentrate (CDLC), a model system for cholesterol crystallization in gallbladder bile. CDLC consists of cholesterol, bilayer-forming amphiphiles, micelle-forming amphiphiles, and water. Phase contrast and differential interference contrast (DIC) microscopy indicate the presence of three microstructure types in all samples studied, and allow for an investigation of the structures' unique geometries. Additionally, confocal microscopy is used for qualitative assessment of surface and internal composition. To complement optical observations, calorimetric (differential-scanning and modulation) experiments, provide the basis for an in-depth understanding of collective and individual thermal behavior. Observed ''transition'' features indicate clustering and ''straightening'' of helical ribbons into short, increasingly thickening, filaments that dissolve with increasing temperature. These results suggest that all microstructures formed in CDLC may coexist in a metastable chemical equilibrium. Further investigation of the CDLC thermal profile should uncover the process of cholesterol crystallization as well as the unique design and function of microstructures formed in this system.

  13. Algorithms for Identification of Nearly-Coincident Events in Calorimetric Sensors

    NASA Astrophysics Data System (ADS)

    Alpert, B.; Ferri, E.; Bennett, D.; Faverzani, M.; Fowler, J.; Giachero, A.; Hays-Wehle, J.; Maino, M.; Nucciotti, A.; Puiu, A.; Swetz, D.; Ullom, J.

    2016-07-01

    For experiments with high arrival rates, reliable identification of nearly-coincident events can be crucial. For calorimetric measurements to directly measure the neutrino mass such as HOLMES, unidentified pulse pile-ups are expected to be a leading source of experimental error. Although Wiener filtering can be used to recognize pile-up, it suffers from errors due to pulse shape variation from detector nonlinearity, readout dependence on subsample arrival times, and stability issues from the ill-posed deconvolution problem of recovering Dirac delta-functions from smooth data. Due to these factors, we have developed a processing method that exploits singular value decomposition to (1) separate single-pulse records from piled-up records in training data and (2) construct a model of single-pulse records that accounts for varying pulse shape with amplitude, arrival time, and baseline level, suitable for detecting nearly-coincident events. We show that the resulting processing advances can reduce the required performance specifications of the detectors and readout system or, equivalently, enable larger sensor arrays and better constraints on the neutrino mass.

  14. Calorimetric studies of the ammonia-water system with application to the outer solar system

    NASA Technical Reports Server (NTRS)

    Yarger, Jeffery; Lunine, Jonathan I.; Burke, Michael

    1993-01-01

    A series of heating experiments was performed on the condensed ammonia-water system using a differential scanning calorimeter (DSC). The water-rich samples were cooled quickly to below 130 K, then heated at a variety of rates. Rather than a single peritectic melt at 176 K, expected for the equilibrium system of water ice and ammonia dihydrate, four enthalpic transitions were repeatedly seen in the temperature range 150-176 K. These transitions are generally consistent with the earlier calorimetric results of Van Kasteren (1973), who interpreted the lowest temperature exotherm as crystallization of an amorphous ammonia-water compound formed during cooling. We propose that both sets of experiments are seeing the crystallization of ammonia monohydrate, which is metastable relative to the dihydrate, followed by partial remelting and crystallization of dihydrate upon further heating. The apparent stability of the monohydrate in the dihydrate equilibrium field implies a potentially complex behavior of ammonia-water ices in satellites. Possible self-heating of the mixture by several tens of degrees up to the 170 K eutectic could make mobilization of ammonia-water liquids in icy satellite interiors energetically easier than previously thought.

  15. Characterization of commercial Li-ion batteries using electrochemical-calorimetric measurements

    NASA Astrophysics Data System (ADS)

    Al Hallaj, S.; Prakash, J.; Selman, J. R.

    Commercial Li-ion cells of Type 18650 dimensions and prismatic designs from different manufacturers have been tested to evaluate their performance and to study their thermal behavior using electrochemical-calorimetric methods. All cells tested in this work showed good performance and cyclability under normal operating conditions. The measured heat effect for the cells were exothermic during discharge and partially endothermic during charge. Cell impedance was measured for selected cells and showed some dependence on the state of charge or depth of discharge, with significant increase at the end of discharge due to concentration polarization. The entropy coefficient (d Eeq/d T) for the A&T (18650) and Panasonic (CGR 18650) cells were measured using potentiometric methods at different depths of discharge (DOD). The measured values for both cells showed some dependence on the DOD with some perturbation near 4.0 V, where the measured d Eeq/d T for Panasonic cell had an unexpected positive value. This was found to be consistent with the measured endothermic heat effect during discharge for the Panasonic cell near Eeq=4.0 V. This may be related to a phase change in the LiCoO 2 cathode material, as reported in the literature, and to structural transformation in the graphite used as anode material, in the Panasonic cell.

  16. Calorimetric and acoustic emission study of martensitic transformation in single-crystalline Ni2MnGa alloys

    NASA Astrophysics Data System (ADS)

    Tóth, László Z.; Szabó, Sándor; Daróczi, Lajos; Beke, Dezső L.

    2014-12-01

    The jerky character of austenite-martensite phase transformation in Ni2MnGa single crystals (with 10M martensite structure) has been investigated by thermal cycling using a differential scanning calorimeter (DSC) and by detection of acoustic emissions (AEs) at low cooling and heating rates (0.1 K/min and below). It is illustrated that, besides the low cooling and heating rate, mass and surface roughness are also important parameters in optimizing the best signal/noise ratio in order to obtain individual peaks suitable for statistical analysis. Three types of samples, differing in the twin structure and twin boundary behavior, were investigated with and without surface roughening made by electro-erosion. The statistical analysis, carried out for both (thermal and acoustic) types of signals, provided power-law behavior. In calorimetric measurements the energy exponents, obtained in cooling, were the same within the experimental errors (ɛ =1.7 ±0.2 ) for the three samples investigated. In acoustic emission experiments the energy and amplitude, α , exponents were determined both for cooling and heating. The exponents for cooling and heating runs are slightly different. They are larger for heating for both α and ɛ , in accordance with the asymmetric acoustic activity: we observed higher acoustic activity (higher number of hits) during cooling. The effect of the surface roughness is negligible in the exponents (but higher acoustic activity corresponds to higher roughness) and the following values were obtained: ɛ =1.5 ±0.1 and α =2.1 ±0.1 for cooling as well as ɛ =1.8 ±0.1 and α =2.6 ±0.1 for heating. Our results are in accordance with the results of Gallardo et al. [Phys. Rev. B 81, 174102 (2010), 10.1103/PhysRevB.81.174102] obtained in Cu based alloys: the exponents of the energy distributions, for both DSC and AE signals, were the same within the experimental errors. Furthermore, our exponents obtained from the AE measurements are close to the values

  17. 34 CFR 361.42 - Assessment for determining eligibility and priority for services.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... services due to the severity of the applicant's disability. (3) Presumption of eligibility for Social Security recipients and beneficiaries. (i) Any applicant who has been determined eligible for Social Security benefits under Title II or Title XVI of the Social Security Act is— (A) Presumed eligible...

  18. 34 CFR 361.42 - Assessment for determining eligibility and priority for services.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... services due to the severity of the applicant's disability. (3) Presumption of eligibility for Social Security recipients and beneficiaries. (i) Any applicant who has been determined eligible for Social Security benefits under Title II or Title XVI of the Social Security Act is— (A) Presumed eligible...

  19. 34 CFR 361.42 - Assessment for determining eligibility and priority for services.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... services due to the severity of the applicant's disability. (3) Presumption of eligibility for Social Security recipients and beneficiaries. (i) Any applicant who has been determined eligible for Social Security benefits under Title II or Title XVI of the Social Security Act is— (A) Presumed eligible...

  20. An IR and Calorimetric Investigation of the Structural, Crystal-Chemical and Thermodynamic Properties of Hydrogrossular

    NASA Astrophysics Data System (ADS)

    Geiger, C. A.; Dachs, E.

    2012-04-01

    their collective interactions measurably affect the lattice dynamic (i.e. thermodynamic) behavior. The low temperature heat capacity behavior was investigated with a commercially designed relaxation calorimeter between 5 and 300 K on a mg-sized sample. The heat capacity data are well behaved at T < 300 K and show a monotonic decrease in magnitude with decreasing temperature. A standard third-law entropy value of So = 421.7 ± 1.6 J/mol·K was calculated. Using this new calorimetric-based So value and published standard enthalpy of formation data for katoite, a calorimetric-based Gibbs free energy of formation at 298 K can be obtained as ΔG°f = -5021.2 kJ/mol. The Cp data show no evidence for any phase transition as possibly expected by the change in OH-mode behavior with decreasing temperature. We have no explanation for the appearance of the additional modes. It is worth noting that the katoite crystal structure in terms of lattice dynamic or thermodynamic behavior should be thought of having OH groups and not O4H4 clusters or polyhedral units as is often written in the literature. The single crystallographic OH group in katoite shows very weak, if any, hydrogen bonding and the H atoms have large amplitudes of vibration. The weak H bonding controls the nature of low energy OH-related vibrations and this leads to its large So value.

  1. Seasonal Variability in Calorimetric Energy Content of Two Caribbean Mesophotic Corals

    PubMed Central

    Brandtneris, Viktor W.; Brandt, Marilyn E.; Glynn, Peter W.; Gyory, Joanna; Smith, Tyler B.

    2016-01-01

    Energetic responses of zooxanthellate reef corals along depth gradients have relevance to the refugia potential of mesophotic coral ecosystems (MCEs). Previous observations suggested that MCEs in the Caribbean are thermally buffered during the warmest parts of the year and occur within or just below the chlorophyll maximum, suggesting abundant trophic resources. However, it is not known if mesophotic corals can maintain constant energy needs throughout the year with changing environmental and biological conditions. The energetic content of tissues from the stony coral species Orbicella faveolata and Agaricia lamarcki was measured on the southern insular shelf of St. Thomas, US Virgin Islands (USVI), using micro-bomb calorimetry. Three sites for each species, at depths of 6m, 25m, 38m and 63m, were selected to capture energetic differences across the major vertical range extent of both species in the USVI—and sampled over five periods from April 2013 to April 2014. Mesophotic colonies of O. faveolata exhibited a significant reduction in energetic content during the month of September 2013 compared to mid-depth and shallow colonies (p = 0.032), whereas A. lamarcki experienced similar energetic variability, but with a significant reduction in energy content that occurred in July 2013 for colonies at sites deeper than 25m (p = 0.014). The results of calorimetric analyses indicate that O. faveolata may be at risk during late summer stress events, possibly due to the timing of reproductive activities. The low-point of A. lamarcki energy content, which may also coincide with reproduction, occurs prior to seasonal stress events, indicating contrasting, species-specific responses to environmental variability on MCEs. PMID:27050430

  2. Thermodynamic model for calorimetric and phase coexistence properties of coal derived fluids. Final technical report

    SciTech Connect

    Kabadi, V.N.

    1992-10-01

    The work on this project was initiated on September 1, 1989. The project consisted of three different tasks. 1. A thermodynamic model to predict VLE and calorimetric properties of coal liquids. 2. VLE measurements at high temperature and high pressure for coal model compounds and 3. Chromatographic characterization of coal liquids for distribution of heteroatoms. The thermodynamic model developed is an extension of the previous model developed for VLE of coal derived fluids (DOE Grant no. FG22-86PC90541). The model uses the modified UNIFAC correlation for the liquid phase. Some unavailable UNIFAC interactions parameters have been regressed from experimental VLE and excess enthalpy data. The model is successful in predicting binary VLE and excess enthalpy data. Further refinements of the model are suggested. An apparatus for the high pressure high temperature VLE data measurements has been built and tested. Tetralin-Quinoline is the first binary system selected for data measurements. The equipment was tested by measuring 325{degree}C isotherm for this system and comparing it with literature data. Additional isotherms at 350{degree}C and 370{degree}C have been measured. The framework for a characterization procedure for coal derived liquids has been developed. A coal liquid is defined by a true molecular weight distribution and distribution of heteroatoms as a function of molecular weights. Size exclusions liquid chromatography, elemental analysis and FTIR spectroscopy methods are used to obtain the molecular weight and hetroatom distributions. Further work in this area should include refinements of the characterization procedure, high temperature high pressure VLE data measurements for selective model compound binary systems, and improvement of the thermodynamic model using the new measured data and consistent with the developments in the characterization procedure.

  3. High-resolution differential scanning calorimetric analysis of the subunits of Escherichia coli aspartate transcarbamoylase.

    PubMed

    Edge, V; Allewell, N M; Sturtevant, J M

    1985-10-01

    The thermal denaturation of the catalytic (c3) and regulatory (r2) subunits of Escherichia coli aspartate transcarbamoylase (c6r6) in the absence and presence of various ligands has been studied by means of highly sensitive differential scanning calorimetry. The denaturation of both types of subunit is irreversible as judged by the facts that the proteins coagulate when heated and that no endotherm is observed when previously scanned protein is rescanned. Despite this apparent irreversibility, there is empirical justification for analyzing the calorimetric data in terms of equilibrium thermodynamics as embodied in the van't Hoff equation. The observed curves of excess apparent specific heat vs. temperature are asymmetric and can be expressed within experimental uncertainty as the sums of sequential two-state steps, a minimum of two steps being required for r2 and three for c3. As previously reported [Vickers, K. P., Donovan, J. W., & Schachman, H. K. (1978) J. Biol. Chem. 253, 8493-8498], the addition of the effectors ATP and CTP raises the denaturation temperature of r2 and lowers that of c3 while the addition of the bisubstrate analogue N-(phosphonoacetyl)-L-aspartate raises the denaturation temperature of c3 and lowers that of r2. These effects vary with ligand concentration in the manner expected from the van't Hoff equation, indicating that they are simply manifestations of Le Chatelier's principle rather than being due to "stabilization" or "destabilization" of the proteins. The denaturational enthalpy is increased in those cases of ligand binding in which the denaturation temperature is increased, because of the contribution from the enthalpy of dissociation of the ligand. PMID:3910085

  4. Calorimetric and spectroscopic studies on solvation energetics for H₂ storage in the CO₂/HCOOH system.

    PubMed

    Fink, Cornel; Katsyuba, Sergey; Laurenczy, Gabor

    2016-04-28

    Solvents playing a crucial role in many chemical reactions and additives can be used to shift the reaction equilibrium. Herein we study the enthalpy of mixing for selected solvents (aqueous, organic) and basic additives (amines, aqueous KOH) when mixed with formic acid with the aim to optimize hydrogen storage/delivery in the CO2/HCOOH system. Formic acid, resulting from carbon dioxide hydrogenation, reaches highest yields when effectively "removed" from the reaction equilibrium. In terms of energy efficiency, any heat released during CO2 hydrogenation has to be reused in the reverse reaction, during the production of hydrogen. In any scenario, the usage of basic chemicals, non-innocent solvents, causes higher energy release in CO2 hydrogenation, which has to be reused in the hydrogen delivery process. Therefore, the enthalpy of mixing is a valuable parameter for designing hydrogen storage devices since it allows the estimation of energy balance for the CO2 hydrogenation/H2 liberation cycle. The highest formic acid concentrations in direct catalytic CO2 hydrogenation under acidic conditions were reached in DMSO. DMSO exhibits considerably stronger interactions with formic acid compared to water as was observed in calorimetric measurements. This difference can be ascribed, at least partly, to stronger hydrogen bonding of FA to DMSO than to water in the corresponding solutions, examined by a combination of IR spectroscopic and quantum chemical studies. Furthermore, the investigation of DMSO/FA- and water/FA systems by (1)H- and (13)C-NMR spectroscopy revealed that only 1 : 1 aggregates are formed in the DMSO solutions of FA in a broad concentration range, while the stoichiometry and the number of the FA-water aggregates essentially depend on the concentration of aqueous solutions.

  5. Seasonal Variability in Calorimetric Energy Content of Two Caribbean Mesophotic Corals.

    PubMed

    Brandtneris, Viktor W; Brandt, Marilyn E; Glynn, Peter W; Gyory, Joanna; Smith, Tyler B

    2016-01-01

    Energetic responses of zooxanthellate reef corals along depth gradients have relevance to the refugia potential of mesophotic coral ecosystems (MCEs). Previous observations suggested that MCEs in the Caribbean are thermally buffered during the warmest parts of the year and occur within or just below the chlorophyll maximum, suggesting abundant trophic resources. However, it is not known if mesophotic corals can maintain constant energy needs throughout the year with changing environmental and biological conditions. The energetic content of tissues from the stony coral species Orbicella faveolata and Agaricia lamarcki was measured on the southern insular shelf of St. Thomas, US Virgin Islands (USVI), using micro-bomb calorimetry. Three sites for each species, at depths of 6m, 25m, 38m and 63m, were selected to capture energetic differences across the major vertical range extent of both species in the USVI-and sampled over five periods from April 2013 to April 2014. Mesophotic colonies of O. faveolata exhibited a significant reduction in energetic content during the month of September 2013 compared to mid-depth and shallow colonies (p = 0.032), whereas A. lamarcki experienced similar energetic variability, but with a significant reduction in energy content that occurred in July 2013 for colonies at sites deeper than 25m (p = 0.014). The results of calorimetric analyses indicate that O. faveolata may be at risk during late summer stress events, possibly due to the timing of reproductive activities. The low-point of A. lamarcki energy content, which may also coincide with reproduction, occurs prior to seasonal stress events, indicating contrasting, species-specific responses to environmental variability on MCEs. PMID:27050430

  6. Characterization of hidden defects of an original XVI century painting on wood by Electronic Speckle Pattern Interferometry

    NASA Astrophysics Data System (ADS)

    Arena, G.

    2015-03-01

    Electronic Speckle Pattern Interferometry, a non-contact and non-destructive optical diagnostic technique, was employed for evaluating the conservation state of a XVI century painting on wood. The whole structure alterations, induced by the laboratory temperature and relative humidity variations, were evaluated. Long-term analysis, by sequential recording and subsequent off-line processing of the fringes progression, was carried out. Local flaws and hidden detachments of pictorial layers from the support, which could not be recognized by traditional art-restorer survey methods, were also easily revealed. In such a case, a simple measurement approach was utilized, with the aim to get a user-friendly method for art conservators. The results demonstrate that the interferometry method can largely improve the traditional art conservation survey techniques.

  7. Mitochondrial DNA analysis on remains of a putative son of Louis XVI, King of France and Marie-Antoinette.

    PubMed

    Jehaes, E; Decorte, R; Peneau, A; Petrie, J H; Boiry, P A; Gilissen, A; Moisan, J P; Van den Berghe, H; Pascal, O; Cassiman, J J

    1998-01-01

    Carl Wilhelm Naundorff was buried in 1845 in Delft as Louis Charles, Duc de Normandie, 'Louis XVII'. However, the son of Louis XVI and Marie-Antoinette-Louis XVII--officially died in the Temple of Paris in 1795. In order to resolve the identity of Naundorff, mitochondrial DNA (mtDNA) D-loop sequences of his remains were compared with the sequences obtained from the hairs of two sisters of Marie-Antoinette, Marie-Antoinette herself, and with the sequences obtained from DNA samples of two living maternal relatives. The mtDNA sequence of a bone sample from Naundorff showed two nucleotide differences from the sequences of the three sisters and four differences from the sequences of living maternal relatives. Based on this evidence it becomes very unlikely that Naundroff is the son of Marie-Antoinette. PMID:9781047

  8. Notable Stabilization of α-Chymotrypsin by the Protic Ionic Additive, [ch][dhp]: Calorimetric Evidence for a Fine Enthalpy/Entropy Balance.

    PubMed

    Uchaneishvili, Sophio; Makharadze, Maya; Shushanyan, Mikhael; van Eldik, Rudi; Khoshtariya, Dimitri E

    2014-01-01

    An impact of 0.5 to 3 M choline dihydrogen phosphate, [ch][dhp], the biotechnologically relevant ionic substance, on the thermal stability of a model globular protein, α-chymotrypsin (α-CT), has been studied exploiting the highly sensitive differential scanning calorimetry (DSC) technique. The notable overall stabilizing effect of 11 ± 2 K regarding the thermal transition (melting) temperature, T m , has been detected. For this kind of series, for the first time, the calorimetric melting enthalpy (ΔH cal) and transition entropy (ΔS m ) parameters have been determined simultaneously throughout. The first analysis indicated a two-phase impact implying (a) the initial, dramatic drop in both ΔH cal and ΔS m , obviously connected to specific, direct interaction between the [ch][dhp] components and α-CT's charged groups (within 0 to 1 mol/L [ch][dhp]), leading to the essential rearrangement of the interfacial hydrogen-bonded (HB) network; and (b) the follow-up (within 1 to 3.0 mol/L [ch][dhp]), modest changes in ΔH cal and lack of changes in ΔS m , seemingly connected with a subsequent steady strengthening of already reformed HB network, respectively. These changes, presumably, are primarily facilitated by Coulombic interactions between the [dhp] anions and solvent-exposed positively charged amino groups of α-CT.

  9. Analbite - Sanidine Thermodynamic Mixing Properties: Highly Precise HF Solution Calorimetric Data Across A Twenty-Member Crystalline Solution Series

    NASA Astrophysics Data System (ADS)

    Hovis, G. L.

    2013-12-01

    Enthalpies of K-Na mixing for the analbite - sanidine feldspar series were investigated by Hovis (1988, J. Petrology) in the early 80's. That work was based on data at a limited number of compositions, owing to the large sample sizes required for HF solution calorimetric measurements at the time. Thermodynamic mixing properties for mineral series, especially those exhibiting compositionally asymmetric mixing quantities, are best defined when samples at a large number of compositions are utilized. Enabled by the small sample sizes now possible for HF solution calorimetric dissolutions (Hovis et al., 1998, Amer. Mineral.), we revisit feldspar thermodynamic properties, having synthesized an analbite - sanidine series consisting of samples at 20 compositions. Solution calorimetric experiments on these samples at 50 °C in 20.1 wt% HF under isoperibolic conditions have resulted in highly precise calorimetric data (standard deviation per sample averaging 0.06 % of the heat of solution). Although enthalpies of K-Na mixing based on the new data display some degree of compositional asymmetry, with a maximum value of 4.8 kJ/mol at a mole fraction potassium of 0.47, the distribution of enthalpy-of-mixing values remains nearly symmetric with respect to K content. This contrasts significantly with data for Al-Si ordered low albite - microcline crystalline solutions, reinvestigated via synthesis of a 21-member series, which show significantly higher mixing magnitudes and considerably greater asymmetry with respect to composition. The maximization of enthalpies of K-Na mixing at sodic compositions correlates well with the sodic critical compositions for both solvi. The lower mixing magnitudes for analbite - sanidine are consistent with the comparatively lower critical temperature of the analbite - sanidine solvus (e.g., Smith & Parsons, 1974, Mineral. Mag.) relative to that for low albite - microcline (Bachinski & Müller, 1971, J. Petrology). Entropies of K-Na mixing for

  10. Analbite - Sanidine Thermodynamic Mixing Properties: Highly Precise HF Solution Calorimetric Data Across A Twenty-Member Crystalline Solution Series

    NASA Astrophysics Data System (ADS)

    Hovis, G. L.

    2012-12-01

    Enthalpies of K-Na mixing for the analbite - sanidine feldspar series were investigated by Hovis (1988, J. Petrology) in the early 80's. That work was based on data at a limited number of compositions, owing to the large sample sizes required for HF solution calorimetric measurements at the time. Thermodynamic mixing properties for mineral series, especially those exhibiting compositionally asymmetric mixing quantities, are best defined when samples at a large number of compositions are utilized. Enabled by the small sample sizes now possible for HF solution calorimetric dissolutions (Hovis et al., 1998, Amer. Mineral.), we revisit feldspar thermodynamic properties, having synthesized an analbite - sanidine series consisting of samples at 20 compositions. Solution calorimetric experiments on these samples at 50 °C in 20.1 wt% HF under isoperibolic conditions have resulted in highly precise calorimetric data (standard deviation per sample averaging 0.06 % of the heat of solution). Although enthalpies of K-Na mixing based on the new data display some degree of compositional asymmetry, with a maximum value of 4.8 kJ/mol at a mole fraction potassium of 0.47, the distribution of enthalpy-of-mixing values remains nearly symmetric with respect to K content. This contrasts significantly with data for Al-Si ordered low albite - microcline crystalline solutions, reinvestigated via synthesis of a 21-member series, which show significantly higher mixing magnitudes and considerably greater asymmetry with respect to composition. The maximization of enthalpies of K-Na mixing at sodic compositions correlates well with the sodic critical compositions for both solvi. The lower mixing magnitudes for analbite - sanidine are consistent with the comparatively lower critical temperature of the analbite - sanidine solvus (e.g., Smith & Parsons, 1974, Mineral. Mag.) relative to that for low albite - microcline (Bachinski & Müller, 1971, J. Petrology). Entropies of K-Na mixing for

  11. Measurement and Modeling of Inner-Shell Satellites of Na-like Fe XVI between 14.5 Å and 18 Å

    SciTech Connect

    Graf, A; Beiersdorfer, P; Brown, G V; Gu, M F

    2007-09-10

    We have used the University of California Lawrence Livermore National Laboratory's EBIT-I electron beam ion trap to perform measurements of the wavelengths and relative intensities of the X-ray lines from inner-shell satellite transitions in sodium-like Fe XVI. The measurements were carried out with high-resolution crystal and grating spectrometers and covered the 14.5-18 {angstrom} wavelength band. Contrary to predicted line strengths and positions found in the literature, our results show that the strongest inner-shell satellites of Fe XVI are located near 15.2 {angstrom}. This is near the location of the 3d {yields} 2p intercombination line in Fe XVII. Calculations using the Flexible Atomic Code are presented, which agree well with the EBIT-I measurements.

  12. Development of Metallic Magnetic Calorimeters for High Precision Measurements of Calorimetric Re-187 and Ho-163 Spectra

    NASA Technical Reports Server (NTRS)

    Ranitzsch, P. C.-O.; Porst, J.-P.; Kempf, S.; Pies, C.; Schafer, S.; Hengstler, D.; Fleischmann, A.; Enss, C.; Gastaldo, L.

    2012-01-01

    The measurement of calorimetric spectra following atomic weak decays, beta (b) and electron capture (EC), of nuclides having a very low Q-value, can provide an impressively high sensitivity to a non-vanishing neutrino mass. The achievable sensitivity in this kind of experiments is directly connected to the performance of the used detectors. In particular an energy resolution of a few eV and a pulse formation time well below 1 microsecond are required. Low temperature Metallic Magnetic Calorimeters (MMCs) for soft X-rays have already shown an energy resolution of 2.0 eV FWHM and a pulse rise-time of about 90 ns for fully micro-fabricated detectors. We present the use of MMCs for high precision measurements of calorimetric spectra following the beta-decay of Re-187 and the EC of Ho-163. We show results obtained with detectors optimized for Re-187 and for Ho-163 experiments respectively. While the detectors equipped with superconducting Re absorbers have not yet reached the aimed performance, a first detector prototype with a Au absorber having implanted Ho-163 ions already shows excellent results. An energy resolution of 12 eV FWHM and a rise time of 90 ns were measured.

  13. Calorimetric measurements of emittance of pipe surfaces: influence of enclosure diameter, test pipe length, and an argon atmosphere

    SciTech Connect

    Reitter, T.A.

    1981-10-01

    Additional results using a calorimetric technique for measuring the total hemispherical emittance of pipe surfaces from 400 to 600 K are described. Two different Pyrex pipe enclosures were used, one of 15 cm i.d. and the other of 30 cm i.d. An error analysis showed that the larger diameter Pyrex pipe should have a smaller error, but the difference was negligible for the 4.4-cm test pipe diameter used. Measurements on a short length of a previously-measured pipe agreed with earlier measurements, but only over the temperature range of the measurements. While the technique normally uses a vacuum to minimize nonradiative heat transfer, measurements were done succesfully with an argon atmosphere in a closed system. A nickel-plated pipe, measured first in a vacuum and then in an argon atmosphere, allowed calculation of an effective convective heat-transfer coefficient for use with test pipes of unknown emittances. Measurements done with an atmosphere have larger uncertainties than those done in vacuum. Measurements using this technique agreed with measurements made using a reflectance technique. It is believed that within the range of temperatures measured, emittance measurements made using the calorimetric technique have a relative error of no more than 10% when done in vacuum.

  14. Low-temperature heat capacity of diopside glass (CaMgSi2O6): A calorimetric test of the configurational-entropy theory applied to the viscosity of liquid silicates

    USGS Publications Warehouse

    Richet, P.; Robie, R.A.; Hemingway, B.S.

    1986-01-01

    Heat-capacity measurements have been made between 8 and 370 K on an annealed and a rapidly quenched diopside glass. Between 15 and 200 K, Cp does not depend significantly on the thermal history of the glass. Below 15 K Cp is larger for the quenched than for the annealed specimen. The opposite is true above 200 K as a result of what is interpreted as a secondary relaxation around room temperature. The magnitude of these effects, however, is small enough that the relative entropies S(298)-S(0) of the glasses differ by only 0.5 J/mol K, i.e., a figure within the combined experimental uncertainties. The insensitivity of relative entropies to thermal history supports the assumption that the configurational heat capacity of the liquid may be taken as the heat capacity difference between the liquid and the glass (??Cp). Furthermore, this insensitivity allows calculation of the residual entropies at 0 K of diopside glasses as a function of the fictive temperature from the entropy of fusion of diopside and the heat capacities of the crystalline, glassy and liquid phases. For a glass with a fictive temperature of 1005 K, for example, this calorimetric residual entropy is 24.3 ?? 3 J/mol K, in agreement with the prediction made by RICHET (1984) from an analysis of the viscosity data with the configurational-entropy theory of relaxation processes of Adam and Gibbs (1965). In turn, all the viscosity measurements for liquid diopside, which span the range 0.5-4?? 1013 poise, can be quantitatively reproduced through this theory with the calorimetrically determined entropies and ??Cp data. Finally, the unclear significance of "activation energies" for structural interpretations of viscosity data is emphasized, and the importance of ??Cp and glass-transition temperature systematics for determining the composition and temperature dependences of the viscosity is pointed out. ?? 1986.

  15. Determination by the enzyme thermistor of cellobiose formed on degradation of cellulose

    SciTech Connect

    Danielsson, B.; Rieke, E.; Mattiasson, B.; Winquist, F.; Mosbach, K.

    1981-01-01

    A calorimetric assay procedure for the determination of cellobiose was developed. The cellobiose is hydrolyzed by beta-glucosidase and the glucose formed is measured calorimetrically by an enzyme thermistor containing coimmobilized glucose oxidase and catalase. The system was optimized with regard to the arrangement of the enzymes, the pH-dependence of the separated enzymic steps, and of the total system. By placing the Beta-glucosidase in a precolumn that could be switched in and out of the flow through the enzyme thermistor, both cellobiose and glucose present in the sample could be determined. The performance with saturated solutions and crude samples from cellulose degradation experiments was investigated.

  16. Thermogravimetric and calorimetric characteristics during co-pyrolysis of municipal solid waste components.

    PubMed

    Ansah, Emmanuel; Wang, Lijun; Shahbazi, Abolghasem

    2016-10-01

    The thermogravimetric and calorimetric characteristics during pyrolysis of wood, paper, textile and polyethylene terephthalate (PET) plastic in municipal solid wastes (MSW), and co-pyrolysis of biomass-derived and plastic components with and without torrefaction were investigated. The active pyrolysis of the PET plastic occurred at a much higher temperature range between 360°C and 480°C than 220-380°C for the biomass derived components. The plastic pyrolyzed at a heating rate of 10°C/min had the highest maximum weight loss rate of 18.5wt%/min occurred at 420°C, followed by 10.8wt%/min at 340°C for both paper and textile, and 9.9wt%/min at 360°C for wood. At the end of the active pyrolysis stage, the final mass of paper, wood, textile and PET was 28.77%, 26.78%, 21.62% and 18.31%, respectively. During pyrolysis of individual MSW components at 500°C, the wood required the least amount of heat at 665.2J/g, compared to 2483.2J/g for textile, 2059.4J/g for paper and 2256.1J/g for PET plastic. The PET plastic had much higher activation energy of 181.86kJ/mol, compared to 41.47kJ/mol for wood, 50.01kJ/mol for paper and 36.65kJ/mol for textile during pyrolysis at a heating rate of 10°C/min. H2O and H2 peaks were observed on the MS curves for the pyrolysis of three biomass-derived materials but there was no obvious H2O and H2 peaks on the MS curves of PET plastic. There was a significant interaction between biomass and PET plastic during co-pyrolysis if the biomass fraction was dominant. The amount of heat required for the co-pyrolysis of the biomass and plastic mixture increased with the increase of plastic mass fraction in the mixture. Torrefaction at a proper temperature and time could improve the grindability of PET plastic. The increase of torrefaction temperature and time did not affect the temperature where the maximum pyrolytic rates occurred for both biomass and plastic but decreased the maximum pyrolysis rate of biomass and increased the maximum pyrolysis

  17. Thermogravimetric and calorimetric characteristics during co-pyrolysis of municipal solid waste components.

    PubMed

    Ansah, Emmanuel; Wang, Lijun; Shahbazi, Abolghasem

    2016-10-01

    The thermogravimetric and calorimetric characteristics during pyrolysis of wood, paper, textile and polyethylene terephthalate (PET) plastic in municipal solid wastes (MSW), and co-pyrolysis of biomass-derived and plastic components with and without torrefaction were investigated. The active pyrolysis of the PET plastic occurred at a much higher temperature range between 360°C and 480°C than 220-380°C for the biomass derived components. The plastic pyrolyzed at a heating rate of 10°C/min had the highest maximum weight loss rate of 18.5wt%/min occurred at 420°C, followed by 10.8wt%/min at 340°C for both paper and textile, and 9.9wt%/min at 360°C for wood. At the end of the active pyrolysis stage, the final mass of paper, wood, textile and PET was 28.77%, 26.78%, 21.62% and 18.31%, respectively. During pyrolysis of individual MSW components at 500°C, the wood required the least amount of heat at 665.2J/g, compared to 2483.2J/g for textile, 2059.4J/g for paper and 2256.1J/g for PET plastic. The PET plastic had much higher activation energy of 181.86kJ/mol, compared to 41.47kJ/mol for wood, 50.01kJ/mol for paper and 36.65kJ/mol for textile during pyrolysis at a heating rate of 10°C/min. H2O and H2 peaks were observed on the MS curves for the pyrolysis of three biomass-derived materials but there was no obvious H2O and H2 peaks on the MS curves of PET plastic. There was a significant interaction between biomass and PET plastic during co-pyrolysis if the biomass fraction was dominant. The amount of heat required for the co-pyrolysis of the biomass and plastic mixture increased with the increase of plastic mass fraction in the mixture. Torrefaction at a proper temperature and time could improve the grindability of PET plastic. The increase of torrefaction temperature and time did not affect the temperature where the maximum pyrolytic rates occurred for both biomass and plastic but decreased the maximum pyrolysis rate of biomass and increased the maximum pyrolysis

  18. Gibbs free energies of formation of RuO 2, IrO 2, and OsO 2: A high-temperature electrochemical and calorimetric study

    NASA Astrophysics Data System (ADS)

    O'Neill, Hugh St. C.; Nell, Johan

    1997-12-01

    The Gibbs free energies of formation of RuO 2, OsO 2 and IrO 2 have been determined by measuring the chemical potentials of oxygen (μO 2) defined by the reactions M + O 2 = MO 2, where M = Ru, Os. or Ir, using an electrochemical method with calcia-stabilized zirconia (CSZ) solid electrolytes. Measurements were attempted in the temperature ranges from ˜870 K to 1620, 1270, and 1415 K for the Ru, Os, and Ir equilibria, respectively, but inspection of the results reveals that equilibrium could not be established below ˜930 K for all three reactions. For Ru + RuO 2, the highest temperature data (above 1520 K) may be systematically affected by the onset of significant electronic conduction in the CSZ electrolyte, while the attempted measurements of the Os + OsO 2 equilibrium above 1190 K are obscured by the disproportionation of OsO 2 to gaseous Os oxides. The high temperature heat capacities at constant pressure ( Cp) of RuO 2 and IrO 2 were determined from 370 to 1070 K by differential scanning calorimetry. These data were combined with heat content measurements and low-temperature heat capacities from the literature, and fitted to an extended Maier-Kelley equation. The calorimetric data for RuO 2 and IrO 2, together with assessed data for Ru, Os, and Ir metals and estimated data for OsO 2, were used in a third law analysis of the electrochemical measurements. The values of μO 2 of the three equilibria were smoothed and filtered by the third-law analysis to yield the following equations which can be extrapolated to lower and higher temperatures as indicated: μO 2 ( Ru + RuO 2) = -324563 + 344.151 T-22.1155 T ln T (700 ⩽ T ⩽ 1800) μO 2 ( Os + OsO 2) = -300399 + 307.639 T-17.4819 T ln T (700 ⩽ T ⩽ 1500) μO 2 ( Ir + IrO 2) = -256518 + 295.854 T-15.2368 T ln T (700 ⩽ T ⩽ 1500) where μO 2 is in J mol -1, T is in K, the reference pressure for O 2 is 1 bar (10 5 Pa), and estimated accuracies are approximately 200 to 400 J mol -1. For Ru + RuO 2, the drift

  19. Thermal stability of extracellular hemoglobin of Glossoscolex paulistus: determination of activation parameters by optical spectroscopic and differential scanning calorimetric studies.

    PubMed

    Santiago, Patrícia S; Carvalho, José Wilson P; Domingues, Marco M; Santos, Nuno C; Tabak, Marcel

    2010-11-01

    Glossoscolex paulistus hemoglobin (HbGp) was studied by dynamic light scattering (DLS), optical absorption spectroscopy (UV-VIS) and differential scanning calorimetry (DSC). At pH 7.0, cyanomet-HbGp is very stable, no oligomeric dissociation is observed, while denaturation occurs at 56°C, 4°C higher as compared to oxy-HbGp. The oligomeric dissociation of HbGp occurs simultaneously with some protein aggregation. Kinetic studies for oxy-HbGp using UV-VIS and DLS allowed to obtain activation energy (E(a)) values of 278-262 kJ/mol (DLS) and 333 kJ/mol (UV-VIS). Complimentary DSC studies indicate that the denaturation is irreversible, giving endotherms strongly dependent upon the heating scan rates, suggesting a kinetically controlled process. Dependence on protein concentration suggests that the two components in the endotherms are due to oligomeric dissociation effect upon denaturation. Activation energies are in the range 200-560 kJ/mol. The mid-point transition temperatures were in the range 50-65 °C. Cyanomet-HbGp shows higher mid-point temperatures as well as activation energies, consistent with its higher stability. DSC data are reported for the first time for an extracellular hemoglobin. PMID:20875698

  20. X-ray fluorescence analysis of yellow pigments in altarpieces by Valencian artists of the XV and XVI centuries

    NASA Astrophysics Data System (ADS)

    Ferrero, J. L.; Roldán, C.; Ardid, M.; Navarro, E.

    1999-02-01

    XRF analysis has allowed a quick and precise detection and identification of the inorganic elements that compose the yellow pigments in altarpieces of the XV and XVI centuries painted by the Valencian artists Miguel Alcañiz, Vicente Macip, Juan de Juanes, Hernando Yáñez de la Almedina and Hernando Llanos. The analyses have been carried out with an XRF portable system that consists of a tube of X-rays and detectors of Si(Li) and cadmium zinc telluride. This system has enabled a non-aggressive and non-destructive analysis of many pieces at the Museo de Bellas Artes of Valencia (Spain). Among the yellow pigments we have identified a pigment composed by lead and tin oxides named lead-tin yellow (Pb 2SnO 4), frequently used in European paintings from the XIV century until the first half of the XVIII century. This fact demonstrates the influence of elements and pictorial techniques from Europe to the region of Valencia.

  1. Crop changes from the XVI century to the present in a hill/mountain area of eastern Liguria (Italy)

    PubMed Central

    Gentili, Rodolfo; Gentili, Elio; Sgorbati, Sergio

    2009-01-01

    Background Chronological information on the composition and structure of agrocenoses and detailed features of land cover referring to specific areas are uncommon in ethnobotanical studies, especially for periods before the XIX century. The aim of this study was to analyse the type of crop or the characteristics of soil cover from the XVI century to the present. Methods This diachronic analysis was accomplished through archival research on the inventories of the Parish of St. Mary and those of the Municipality of Pignone and from recent surveys conducted in an area of eastern Liguria (Italy). Results Archival data revealed that in study area the primary means of subsistence during the last five centuries, until the first half of the XX century, was chestnuts. In the XVIII and XIX centuries, crop diversification strongly increased in comparison with previous and subsequent periods. In more recent times, the abandonment of agricultural practices has favoured the re-colonisation of mixed woodland or cluster-pine woodland. Conclusion Ancient documents in the ecclesiastic or municipal inventories can be a very useful tool for enhancing the knowledge of agricultural practice, as well as of subsistence methods favoured by local populations during a particular time and for reconstructing land use change over time. PMID:19361339

  2. Winter temperatures in the second half of the XVI century in the central area of the Iberian Peninsula

    NASA Astrophysics Data System (ADS)

    Bullón, T.

    2008-06-01

    This paper studies the winter temperatures of the second part of the XVI century in the central area of the Iberian Peninsula. A large number of historical documents that are stored in many different Spanish archives were consulted in order to carry out this research. The data was first arranged and weighted according to the intensity and significance of the meteorological phenomena described and, subsequently, these values were assigned an ordinal index ranging from +4 to -4. The statistical treatment applied is based on the reconstruction of temperatures equivalent to this ordinal index, expressed as anomalies of the 1961-1990 period, belonging to a reference station located at the approximate geographical center of the area under study. The results show winter thermal conditions different from current ones that, for the most part, stay below the reference average and that occurred with a wide range of variability. The influence that thermal conditions had on the evolution of some environmental aspects are considered based on the forest exploitation problem information and on the wine harvest production.

  3. Thyroid hormone-induced differential synthesis of water-insoluble proteins in epidermal cell cultures from the hind limb of Rana catesbeiana tadpoles in stages XII-XV and XVI-XIX.

    PubMed

    Ketola-Pirie, C A; Atkinson, B G

    1990-08-01

    Hind limb epidermal cell cultures from stage XII-XV and XVI-XIX tadpoles of the American bullfrog Rana catesbeiana were maintained for 36 and 120 hr in medium containing either fetal calf serum or thyroid hormone (3,3',5-triiodothyronine, T3; 3 x 10(-10) mol/ml). T3 induces the precocious synthesis (within the first 36 hr) of a 59-kDa keratin associated with epidermal stratification in cultures from stages XII-XV. In epidermal cell cultures from stages XVI-XIX, T3 produces an overall pattern of water-insoluble proteins, including keratins, which is strikingly similar to temporally differentiated cultures (120 hr). A 73-kDa protein is among the water-insoluble proteins precociously synthesized by 36-hr-old cultures from stages XVI-XIX treated with T3. This protein, which is not immunoprecipitated by antibodies raised against keratins, corresponds in Mr and pI to a mammalian differentiation-specific desmosomal plaque protein. Immunoprecipitation of keratins from 120-hr-old cultures shows that many of the water-insoluble proteins synthesized are, indeed, keratins. Further, quantitation, by laser densitometry, of immunoprecipitated keratins from 120-hr cultures demonstrates that greater amounts of keratins, particularly the 65 and 59 kDa which are associated with a differentiated epidermis, are present in stages XVI-XIX. This study indicates that epidermal cell cultures from stages XVI-XIX respond more quickly to the differentiating effects of T3.

  4. Non-exponential nature of calorimetric and other relaxations: effects of 2 nm-size solutes, loss of translational diffusion, isomer specificity, and sample size.

    PubMed

    Johari, G P; Khouri, J

    2013-03-28

    Certain distributions of relaxation times can be described in terms of a non-exponential response parameter, β, of value between 0 and 1. Both β and the relaxation time, τ0, of a material depend upon the probe used for studying its dynamics and the value of β is qualitatively related to the non-Arrhenius variation of viscosity and τ0. A solute adds to the diversity of an intermolecular environment and is therefore expected to reduce β, i.e., to increase the distribution and to change τ0. We argue that the calorimetric value β(cal) determined from the specific heat [Cp = T(dS∕dT)p] data is a more appropriate measure of the distribution of relaxation times arising from configurational fluctuations than β determined from other properties, and report a study of β(cal) of two sets of binary mixtures, each containing a different molecule of ∼2 nm size. We find that β(cal) changes monotonically with the composition, i.e., solute molecules modify the nano-scale composition and may increase or decrease τ0, but do not always decrease β(cal). (Plots of β(cal) against the composition do not show a minimum.) We also analyze the data from the literature, and find that (i) β(cal) of an orientationally disordered crystal is less than that of its liquid, (ii) β(cal) varies with the isomer's nature, and chiral centers in a molecule decrease β(cal), and (iii) β(cal) decreases when a sample's thickness is decreased to the nm-scale. After examining the difference between β(cal) and β determined from other properties we discuss the consequences of our findings for theories of non-exponential response, and suggest that studies of β(cal) may be more revealing of structure-freezing than studies of the non-Arrhenius behavior. On the basis of previous reports that β → 1 for dielectric relaxation of liquids of centiPoise viscosity observed at GHz frequencies, we argue that its molecular mechanism is the same as that of the Johari-Goldstein (JG) relaxation. Its

  5. Non-exponential nature of calorimetric and other relaxations: Effects of 2 nm-size solutes, loss of translational diffusion, isomer specificity, and sample size

    NASA Astrophysics Data System (ADS)

    Johari, G. P.; Khouri, J.

    2013-03-01

    Certain distributions of relaxation times can be described in terms of a non-exponential response parameter, β, of value between 0 and 1. Both β and the relaxation time, τ0, of a material depend upon the probe used for studying its dynamics and the value of β is qualitatively related to the non-Arrhenius variation of viscosity and τ0. A solute adds to the diversity of an intermolecular environment and is therefore expected to reduce β, i.e., to increase the distribution and to change τ0. We argue that the calorimetric value βcal determined from the specific heat [Cp = T(dS/dT)p] data is a more appropriate measure of the distribution of relaxation times arising from configurational fluctuations than β determined from other properties, and report a study of βcal of two sets of binary mixtures, each containing a different molecule of ˜2 nm size. We find that βcal changes monotonically with the composition, i.e., solute molecules modify the nano-scale composition and may increase or decrease τ0, but do not always decrease βcal. (Plots of βcal against the composition do not show a minimum.) We also analyze the data from the literature, and find that (i) βcal of an orientationally disordered crystal is less than that of its liquid, (ii) βcal varies with the isomer's nature, and chiral centers in a molecule decrease βcal, and (iii) βcal decreases when a sample's thickness is decreased to the nm-scale. After examining the difference between βcal and β determined from other properties we discuss the consequences of our findings for theories of non-exponential response, and suggest that studies of βcal may be more revealing of structure-freezing than studies of the non-Arrhenius behavior. On the basis of previous reports that β → 1 for dielectric relaxation of liquids of centiPoise viscosity observed at GHz frequencies, we argue that its molecular mechanism is the same as that of the Johari-Goldstein (JG) relaxation. Its spectrum becomes broader on

  6. Protonation and Complexation of Isosaccharinic Acid with U(VI) and Fe(III) in Acidic Solutions: Potentiometric and Calorimetric Studies

    SciTech Connect

    Rao, Linfeng; Garnov, A Y.; Rai, Dhanpat; Xia, Yuanxian; Moore, R C.

    2004-12-01

    Protonation and complexation of {alpha}-isosaccharinic acid with U(VI) and Fe(III) have been studied in acidic solutions at t=25 C and I=1.0 mol dm{sup -3} NaClO{sub 4}. From the potentiometric titrations, the protonation constant of the carboxylate group is calculated to be 3.65 {+-} 0.05 and the data are consistent with the presence of three and four successive mononuclear complexes for U(VI) and Fe(III), respectively. The formation constants of the complexes, log {beta}{sub j}for the reactions of M+L=ML{sub j} where j=1-3 for U(VI), j=1-4 for Fe(III) and L stands for isosaccharinate, are determined to be 2.91 {+-} 0.15 (UO{sub 2}L), 5.37 {+-} 0.07 (UO{sub 2}L{sub 2}), 7.25 {+-} 0.18 (UO{sub 2}L{sub 3}), 5.06 {+-} 0.17 (FeL), 8.51 {+-} 0.15 (FeL{sub 2}), 11.00 {+-} 0.16 (FeL{sub 3}), and 12.99 {+-} 0.17 (FeL{sub 4}). From the calorimetric titrations, the enthalpy of protonation of the carboxylate group is determined to be -(7.94 {+-} 0.03)kJ mol{sup -1}, similar to that of other ?-hydroxycarboxylates. The enthalpies of complexation between U(VI) and isosaccharinate are quite small: {Delta} H{sub 1} = -(1.0 {+-} 1.0)kJ mol{sup -1}, {Delta} H{sub 2}=1.4 {+-} 1.8 kJ mol{sup -1} and {Delta} H{sub 3}=-(6.2 {+-} 3.0)kJ mol{sup -1}, typical of the interactions between carboxylates and hard-acid cations. The complexation between U(VI) and isosaccharinate is mainly entropy-driven. In comparison, the enthalpies of complexation for FeL{sub 3} and FeL{sub 4} are large and exothermic, contributing significantly to the stability of the complexes.

  7. Magnetic structure in cool stars. XVI - Emissions from the outer atmosphere of M-type dwarfs

    NASA Technical Reports Server (NTRS)

    Rutten, R. G. M.; Zwaan, C.; Schrijver, C. J.; Duncan, D. K.; Mewe, R.

    1989-01-01

    Consideration is given to emission from the outer atmospheres of M-type dwarfs in several spectral lines originating from the chromosphere, the transition-region, and the soft X-ray emission from the corona. It is shown that M-type dwarfs systematically deviate from relations between flux densities in soft X-rays and chromospheric and transition-region emission lines. The quantitative relation between the equivalent width of H-alpha and the Ca II, H, and K emission index is determined. It is suggested that the emission in the Balmer spectrum may result from back heating by coronal soft X-rays.

  8. Comparative dose evaluations between XVI and OBI cone beam CT systems using Gafchromic XRQA2 film and nanoDot optical stimulated luminescence dosimeters

    SciTech Connect

    Giaddui, Tawfik; Cui Yunfeng; Galvin, James; Yu Yan; Xiao Ying

    2013-06-15

    Purpose: To investigate the effect of energy (kVp) and filters (no filter, half Bowtie, and full Bowtie) on the dose response curves of the Gafchromic XRQA2 film and nanoDot optical stimulated luminescence dosimeters (OSLDs) in CBCT dose fields. To measure surface and internal doses received during x-ray volume imager (XVI) (Version R4.5) and on board imager (OBI) (Version 1.5) CBCT imaging protocols using these two types of dosimeters. Methods: Gafchromic XRQA2 film and nanoDot OSLD dose response curves were generated at different kV imaging settings used by XVI (software version R4.5) and OBI (software version 1.5) CBCT systems. The settings for the XVI system were: 100 kVp/F0 (no filter), 120 kVp/F0, and 120 kVp/F1 (Bowtie filter), and for the OBI system were: 100 kVp/full fan, 125 kVp/full fan, and 125 kVp/half fan. XRQA2 film was calibrated in air to air kerma levels between 0 and 11 cGy and scanned using reflection scanning mode with the Epson Expression 10000 XL flat-bed document scanner. NanoDot OSLDs were calibrated on phantom to surface dose levels between 0 and 14 cGy and read using the inLight{sup TM} MicroStar reader. Both dosimeters were used to measure in field surface and internal doses in a male Alderson Rando Phantom. Results: Dose response curves of XRQA2 film and nanoDot OSLDs at different XVI and OBI CBCT settings were reported. For XVI system, the surface dose ranged between 0.02 cGy in head region during fast head and neck scan and 4.99 cGy in the chest region during symmetry scan. On the other hand, the internal dose ranged between 0.02 cGy in the head region during fast head and neck scan and 3.17 cGy in the chest region during chest M20 scan. The average (internal and external) dose ranged between 0.05 cGy in the head region during fast head and neck scan and 2.41 cGy in the chest region during chest M20 scan. For OBI system, the surface dose ranged between 0.19 cGy in head region during head scan and 4.55 cGy in the pelvis region during

  9. Representative payment under titles II, VIII and XVI of the Social Security Act. Final rule.

    PubMed

    2008-11-10

    We are amending our rules governing how we investigate representative payee applicants. Under these rules, any payee who previously satisfied the payee investigation criteria, including a face-to-face interview, and currently serves as a payee generally need not appear for another face-to-face interview when subsequently applying to become a payee unless we determine within our discretion, that a new face-to-face interview is necessary. The payee applicant would still be required to satisfy the rest of the investigation process as set forth in the regulations. Reducing the number of subsequent face-to-face interviews of payee applicants will streamline our representative payee application process, allowing payee applicants to become qualified more quickly when they already serve as a payee. This rule also will expedite payment of benefits in certain representative payee situations and reduce the burden on our field office employees by eliminating the necessity of interviewing such payee applicants.

  10. Calorimetric Low-Temperature Detectors for X-Ray Spectroscopy on Trapped Highly-Charged Heavy Ions

    NASA Technical Reports Server (NTRS)

    Kilbourne, Caroline; Kraft-Bermuth, S.; Andrianov, V.; Bleile, A.; Echler, A.; Egelhof, P.; Ilieva, S.; Kilbourne, C.; McCammon, D.

    2012-01-01

    The application of Calorimetric Low-Temperature Detectors (CLTDs) has been proposed at the Heavy-Ion TRAP facility HITRAP which is currently being installed at the Helmholtz Research Center for Heavy Ion Research GSI. This cold ion trap setup will allow the investigation of X-rays from ions practically at rest, for which the excellent energy resolution of CLTDs can be used to its full advantage. However, the relatively low intensities at HITRAP demand larger solid angles and an optimized cryogenic setup. The influence of external magnetic fields has to be taken into account. CLTDs will also be a substantial part of the instrumental equipment at the future Facility for Antiproton and Heavy Ion Research (FAIR), for which a wide variety of high-precision X-ray spectroscopy experiments has been proposed. This contribution will give an overview on the chances and challenges for the application of CLTDs at HITRAP as well as perspectives for future experiments at the FAIR facility.

  11. pH-tuneable binding of 2′-phospho-ADP-ribose to ketopantoate reductase: a structural and calorimetric study

    SciTech Connect

    Ciulli, Alessio; Lobley, Carina M. C.; Tuck, Kellie L.; Smith, Alison G.; Blundell, Tom L.; Abell, Chris

    2007-02-01

    A combined crystallographic, calorimetric and mutagenic study has been used to show how changes in pH give rise to two distinct binding modes of 2′-phospho-ADP-ribose to ketopantoate reductase. The crystal structure of Escherichia coli ketopantoate reductase in complex with 2′-monophosphoadenosine 5′-diphosphoribose, a fragment of NADP{sup +} that lacks the nicotinamide ring, is reported. The ligand is bound at the enzyme active site in the opposite orientation to that observed for NADP{sup +}, with the adenine ring occupying the lipophilic nicotinamide pocket. Isothermal titration calorimetry with R31A and N98A mutants of the enzyme is used to show that the unusual ‘reversed binding mode’ observed in the crystal is triggered by changes in the protonation of binding groups at low pH. This research has important implications for fragment-based approaches to drug design, namely that the crystallization conditions and the chemical modification of ligands can have unexpected effects on the binding modes.

  12. Surfactants induced release of a red emitting dye from the nanocavity of a molecular container: A spectroscopic and calorimetric study.

    PubMed

    Ahmed, Sayeed Ashique; Chatterjee, Aninda; Maity, Banibrata; Seth, Debabrata

    2016-08-01

    Supramolecular interaction of a red emitting dye Nile blue A (NBA) with Cucurbit[7]uril (CB7) in aqueous solution was studied and the release of the dye from the hydrophobic cavity of CB7 was reported. To investigate the supramolecular host-guest complex formation and release of dye, we have used the steady state absorption, fluorescence and time resolved fluorescence emission spectroscopy, (1)H NMR spectroscopy and isothermal titration calorimetry (ITC). The spectral properties of NBA were changed in the presence of CB7. The change in spectral features of NBA in presence of CB7 indicates the formation of supramolecular host-guest complexes. By using the SED equation the diameter of the complex was estimated. The complex formation further affirmed by the (1)H NMR study. Upfield and downfield shifts of the protons of NBA was observed in both the aliphatic and aromatic region. From the ITC measurement, we have drawn up the forces involved for the complexation of NBA with CB7. We have studied the release of NBA from the hydrophobic cavity of CB7 by using ionic, neutral surfactants and ionic liquid with the help of spectroscopic and calorimetric techniques. It is observed that on addition of SDS and ionic liquid (

  13. Design and performance tests of the calorimetric tract of a Compton Camera for small-animals imaging

    NASA Astrophysics Data System (ADS)

    Rossi, P.; Baldazzi, G.; Battistella, A.; Bello, M.; Bollini, D.; Bonvicini, V.; Fontana, C. L.; Gennaro, G.; Moschini, G.; Navarria, F.; Rashevsky, A.; Uzunov, N.; Zampa, G.; Zampa, N.; Vacchi, A.

    2011-02-01

    The bio-distribution and targeting capability of pharmaceuticals may be assessed in small animals by imaging gamma-rays emitted from radio-isotope markers. Detectors that exploit the Compton concept allow higher gamma-ray efficiency compared to conventional Anger cameras employing collimators, and feature sub-millimeter spatial resolution and compact geometry. We are developing a Compton Camera that has to address several requirements: the high rates typical of the Compton concept; detection of gamma-rays of different energies that may range from 140 keV ( 99 mTc) to 511 keV ( β+ emitters); presence of gamma and beta radiation with energies up to 2 MeV in case of 188Re. The camera consists of a thin position-sensitive Tracker that scatters the gamma ray, and a second position-sensitive detection system to totally absorb the energy of the scattered photons (Calorimeter). In this paper we present the design and discuss the realization of the calorimetric tract, including the choice of scintillator crystal, pixel size, and detector geometry. Simulations of the gamma-ray trajectories from source to detectors have helped to assess the accuracy of the system and decide on camera design. Crystals of different materials, such as LaBr 3 GSO and YAP, and of different size, in continuous or segmented geometry, have been optically coupled to a multi-anode Hamamatsu H8500 detector, allowing measurements of spatial resolution and efficiency.

  14. High-resolution calorimetric study of the nematic to smectic- A transition in aligned liquid crystal-aerosil gels

    NASA Astrophysics Data System (ADS)

    Cruceanu, F.; Liang, D.; Leheny, R. L.; Garland, C. W.; Iannacchione, G. S.

    2009-01-01

    High-resolution ac calorimetry has been used to study the nematic to smectic- A (N-SmA) phase transition in the liquid crystal octylcyanobiphenyl (8CB) confined in aligned colloidal aerosil gels. A stable and robust nematic alignment was achieved by repeated thermal cycling of the samples in the presence of a strong uniform magnetic field. In some ways (such as transition temperature and integrated enthalpy), the dependence of the specific heat peak associated with the N-SmA transition on the aerosil density for aligned gels is consistent with that observed in unaligned (random) gel samples. However, a power-law analysis reveals that the behavior of the critical exponent α is quite different. For random gels, α varies gradually with aerosil density, whereas we find that α for aligned gels shifts abruptly to an XY -like value for the lowest aerosil density studied and remains essentially constant as the sil density increases. This aerosil density independence of α is consistent with the critical behavior of the smectic correlation lengths obtained from an x-ray scattering study of 8CB in aligned aerosil gels. The combined calorimetric and x-ray results indicate that the role of quenched randomness in aligned gels of 8CB+sils differs significantly from that in random gels.

  15. Spectroscopic and calorimetric investigations on the binding of phenazinium dyes safranine-O and phenosafranine to double stranded RNA polynucleotides.

    PubMed

    Saha, Baishakhi; Kumar, Gopinatha Suresh

    2016-08-01

    RNA targeting through small molecules that can selectively bind specific RNA structures is an important current strategy in therapeutic drug development. Towards this strategy a comparative study on the interaction of two phenazinium dyes, safranine-O and phenosafranine to double stranded RNAs, poly(I).poly(C), poly(A).poly(U) and poly(C).poly(G) was performed. Spectrophotometric and spectrofluorimetric studies revealed non-cooperative binding of the dyes to the duplex RNA with binding constants of the order 10(5)M(-1) with a higher affinity of safranine-O to poly(I).poly(C) followed by poly(A).poly(U) and poly(C).poly(G). Anisotropy and fluorescence quenching results confirmed an intercalation mode of binding for the dyes on these RNAs. Binding induced conformational changes in the RNA polynucleotides were revealed from circular dichroism data. Thermal melting study and DSC experiments demonstrated stabilization of dye-RNA complexes. Calorimetric studies revealed that the binding was accompanied by a large positive entropy term with a small negative enthalpy contributions. Significant hydrophobic forces in the complexation of the double stranded RNAs with the dyes were confirmed from the negative heat capacity changes. Enthalpy-entropy compensation was also observed in the binding. Parsing of the Gibbs energy suggested a larger non-electrostatic contribution in all the cases. The results presented here may be helpful to design new types of RNA-based therapeutic agents. PMID:27236048

  16. Oral Histories in Meteoritics and Planetary Science--XVI: Grenville Turner

    NASA Astrophysics Data System (ADS)

    Sears, Derek W. G.

    2012-03-01

    In this interview, Grenville Turner (Fig. 1) recounts how he became interested in meteorites during postdoctoral research with John Reynolds at the University of California, Berkeley, after completing a DPhil with Ken Mayne at the University of Oxford. At Berkeley, he worked on xenon isotopes with fellow students Bob Pepin and Craig Merrihue, but Reynolds' insistence that they analyze all the inert gases in their samples meant that they also made important contributions to Ne isotope studies and potassium-argon dating leading to the Ar-Ar technique. In 1964, Grenville obtained a teaching position at the University of Sheffield where he developed his own laboratory for inert gas isotope measurements. After the return of samples from the Moon by the Apollo program, he became involved in determining the chronology of volcanism and major impacts on the Moon. In 1988, Grenville and his team moved to the University of Manchester as part of a national reorganization of earth science departments. During the post Apollo years, Grenville's interest turned to the development of new instrumentation (resonance ionization mass spectrometry and the ion microprobe), and to problems in terrestrial isotope geochemistry, particularly the source of inert gases in fluid inclusions. He received the Leonard Medal of the Meteoritical Society in 1999, and he has also received awards from the Royal Society, the European Association of Geochemistry, and the Royal Astronomical Society.

  17. Studies of molybdena-alumina catalysts XVI. Effect of high-temperature sulfiding

    SciTech Connect

    Miciukiewicz, J. ); Massoth, F.E. )

    1989-10-01

    Candia et. al. recently reported an increase in hydrodesulfurization (HDS) activity of CoMo/Al{sub 2}O{sub 3} catalysts sulfided at 600 C. They attributed the increase in activity to a more active CoMoS phase (Type II) compared to the regular Type I CoMoS phase found in catalysts sulfided at 400 C. Breysse et. al. found a similar effect with NiW/Al{sub 2}O{sub 3} catalysts. Prada Silvy et. al., however, reported no change in HDS activity in sulfiding CoMo/Al{sub 2}O{sub 3} catalysts up to 700 C. In these studies, sintering of the support occurred due to the higher sulfiding temperatures employed compared with the original calcining temperature of the catalyst ({approximately}500 C). The authors decided to determine the effect of sulfiding temperature on the HDS and hydrogenation (HYD) activity of Mo and CoMo catalysts on an alumina support stabilized by calcining at a higher temperature than that used in the sulfiding treatments in order to avoid the complications due to support sintering during sulfiding. The catalysts were sulfided at 400, 550, or 700 C. Sulfided catalysts were characterized by CO{sub 2} and NO chemisorption using a pulse technique. At least duplicate measurements were made on each sample. Catalytic activities for HDS of thiophene and HYD of hexene were carried out at 350 C and under atmospheric pressure in a fixed-bed reactor. Pseudo first-order rate constants were calculated from conversions.

  18. Measurement of the absorption coefficient of scattering liquid media by the calorimetric method

    NASA Astrophysics Data System (ADS)

    Butenin, A. V.; Kogan, B. Ya.

    2012-02-01

    Using the example of a number of hydrosols (gold nanorods and nanoshells, silver nanoshells, zinc phthalocyanine nanoparticles), we show that the absorption coefficient of a scattering liquid medium can be measured from its heating by a short-time laser irradiation. The degree of heating was determined from expansion of the liquid in an ampoule with a capillary (the principle of liquid thermometer). Irradiation was performed at a wavelength of 671 or 1069 nm. From the transmission of samples of hydrosols at these wave-lengths, the sum of the absorption and scattering coefficients has been determined. To measure the absorption spectra of scattering liquids by this method, a laser with a tunable radiation wavelength is required. In the case of monodisperse colloidal solutions, the method ensures the measurement of the absorption and scattering cross-section ratio of particles.

  19. The ruthenium-yttrium system: An experimental calorimetric study with a phase diagram optimization

    SciTech Connect

    Selhaoui, N.; Bouirden, L.; Charles, J.; Gachon, J.C.; Kleppa, O.J.

    1998-07-01

    After an experimental determination of the standard enthalpies of formation of Ru{sub 0.67}Y{sub 0.33} and Ru{sub 0.286}Y{sub 0.714}, the Ru-Y system was numerically assessed with help of NANCYUN software to check the consistency between the experimental results and the phase diagram proposed in the literature.

  20. Introduction of Differential Scanning Calorimetry in a General Chemistry Laboratory Course: Determination of Thermal Properties of Organic Hydrocarbons

    ERIC Educational Resources Information Center

    D'Amelia, Ronald; Franks, Thomas; Nirode, William F.

    2007-01-01

    In first-year general chemistry undergraduate courses, thermodynamics and thermal properties such as melting points and changes in enthalpy ([Delta]H) and entropy ([Delta]S) of phase changes are frequently discussed. Typically, classical calorimetric methods of analysis are used to determine [Delta]H of reactions. Differential scanning calorimetry…

  1. SU-E-J-50: An Evaluation of the Stability of Image Quality Parameters of the Elekta XVI and IView Imaging Systems

    SciTech Connect

    Stanley, D; Papanikolaou, N; Gutierrez, A

    2015-06-15

    Introduction Quality assurance of the image quality for image guided localization systems is crucial to ensure accurate visualization and localization of target volumes. In this study, the long term stability of selected image parameters was assessed and evaluated for CBCT mode, planar radiographic kV mode and MV mode. Methods and Materials: The CATPHAN, QckV-1 and QC-3 phantoms were used to evaluate the image quality parameters. The planar radiographic images were analyzed in PIPSpro™ with spatial resolution (f30, f40, f50) being recorded. For XVI CBCT, Head and Neck Small20 (S20) and Pelvis Medium20 (M20) standard acquisition modes were evaluated for Uniformity, Noise, Spatial Resolution and HU constancy. Dose and kVp for the XVI were recorded using the Unfors RaySafe Xi system with the R/F Low Detector for the kV planar radiographic mode. Results A total of 20 and 10 measurements were acquired for the planar radiographic and CBCT systems respectively over a two month period. Values were normalized to the mean and the standard deviations (STD) were recorded. For the planar radiographic spatial resolution, the STD for f30, f40, f50 were 0.004, 0.002, 0.002 and 0.005, 0.007, 0.008 for the kV and MV, respectively. The average recorded dose for kV was 38.7±2.7 μGy. The STD of the evaluated metrics for the S20 acquisition were: 0.444(f30), 0.067(f40), 0.062(f50), 0.018(Water/poly-HU constancy), 0.028(uniformity) and 0.106(noise). The standard deviations for the M20 acquisition were: 0.108(f30), 0.073(f40), 0.091(f50), 0.008(Water/poly-HU constancy), 0.005(uniformity) and 0.005(noise). Using these, tolerances can be reported as a warning and action threshold of 1σ and 2σ. Conclusion A study was performed to assess the stability of the basic image quality parameters recommended by TG-142 for the Elekta XVI and iView imaging systems. Consistent imaging and dosimetric properties over the evaluated time frame were noted. This work was funded in part by the Cancer

  2. β-Lactoglobulin interactions with local anaesthetic drugs – Crystallographic and calorimetric studies.

    PubMed

    Loch, Joanna I; Bonarek, Piotr; Polit, Agnieszka; Jabłoński, Mateusz; Czub, Mateusz; Ye, Xinxia; Lewiński, Krzysztof

    2015-09-01

    Interactions between bovine and goat β-lactoglobulin and tetracaine and pramocaine were investigated with isothermal titration calorimetry, X-ray crystallography and molecular modelling. Tetracaine and pramocaine binding to lactoglobulin is an entropy driven endothermic reaction. In this work, we found that determined association constants and thermodynamic parameters indicate that pramocaine has a higher affinity to lactoglobulin than tetracaine. Crystal structures that were determined with resolutions in the range from 1.90 to 2.30 Å revealed in each case the presence of a single drug molecule bound in the β-barrel in a mode similar to that observed for 14- and 16-carbon fatty acids. The position of the ligand in the β-barrel indicates the optimal fit of 6-carbon aromatic rings to the binding pocket and the major role of hydrophobic interactions in ligand binding. Calculations of tetracaine and pramocaine docking to lactoglobulin revealed that molecular modelling overestimated the role of polar protein-drug interactions. PMID:26092174

  3. Localized Recrystallization in Cast Al-Si-Mg Alloy during Solution Heat Treatment: Dilatometric and Calorimetric Studies

    NASA Astrophysics Data System (ADS)

    Chaudhury, S. K.; Warke, V.; Shankar, S.; Apelian, D.

    2011-10-01

    During heat treatment, the work piece experiences a range of heating rates depending upon the sizes and types of furnace. When the Al-Si-Mg cast alloy is heated to the solutionizing temperature, recrystallization takes place during the ramp-up stage. The effect of heating rate on recrystallization in the A356 (Al-Si-Mg) alloy was studied using dilatometric and calorimetric methods. Recrystallization in as-cast Al-Si alloys is a localized event and is confined to the elasto-plastic zone surrounding the eutectic Si phase; there is no evidence of recrystallization in the center of the primary Al dendritic region. The size of the elasto-plastic zone is of the same order of magnitude as the Si particles, and recrystallized grains are observed in the elasto-plastic region near the Si particles. The coefficient of thermal expansion of Al is an order of magnitude greater than Si, and thermal stresses are generated due to the thermal mismatch between the Al phase and Si particles providing the driving force for recrystallization. In contrast, recrystallization in Al wrought alloy (7075) occurs uniformly throughout the matrix, stored energy due to cold work being the driving force for recrystallization in wrought alloys. The activation energy for recrystallization in as-cast A356 alloy is 127 KJ/mole. At a slow heating rate of 4.3 K/min, creep occurs during the heating stage of solution heat treatment. However, creep does not occur in samples heated at higher heating rates, namely, 520, 130, and 17.3 K/min.

  4. Kinetic and calorimetric evidence for two distinct scaffolding protein binding populations within the bacteriophage P22 procapsid.

    PubMed

    Parker, M H; Brouillette, C G; Prevelige, P E

    2001-07-31

    A wide variety of viruses require the transient presence of scaffolding proteins to direct capsid assembly. In the case of bacteriophage P22, a model in which the scaffolding protein selectively stabilizes on-pathway growing intermediates has been proposed. The stoichiometry and thermodynamics of binding of the bacteriophage P22 scaffolding protein within the procapsid were analyzed by light scattering and isothermal titration calorimetry. Calorimetric experiments carried out between 10 and 37 degrees C were consistent with the presence of at least two distinct populations of binding sites, in agreement with kinetic evidence obtained by a light scattering assay. Binding to the high-affinity sites occurred at 20 degrees C with a stoichiometry of approximately 60 scaffolding molecules per procapsid and an apparent K(d) of approximately 100-300 nM and was almost completely enthalpy-driven. For the second binding population, precise fitting of the data was impossible due to small heats of binding, but the thermodynamics of binding were clearly distinct from the high-affinity phase. The heat capacity change (DeltaC(p)()) of binding was large for the high-affinity sites and negative for both sets of sites. Addition of sodium chloride (1 M) greatly reduced the magnitude of the apparent DeltaH, in agreement with previous evidence that electrostatic interactions play a major role in binding. A mutant scaffolding protein that forms covalent dimers (R74C/L177I) bound only to the high-affinity sites. These data comprise the first quantitative measurements of the energetics of the coat protein/scaffolding protein interaction.

  5. Energetics of the binding of phototoxic and cytotoxic plant alkaloid sanguinarine to DNA: Isothermal titration calorimetric studies

    NASA Astrophysics Data System (ADS)

    Adhikari, Anupam; Hossain, Maidul; Maiti, Motilal; Suresh Kumar, Gopinatha

    2008-10-01

    Sanguinarine is a medically important plant alkaloid with remarkable pharmacological and biological activities. DNA binding is considered to be an important aspect in its mode of action. Isothermal titration calorimetric technique was used for the first time to derive the thermodynamic aspects of the interaction of the phototoxic and cytotoxic plant alkaloid sanguinarine with natural calf thymus DNA and four synthetic DNAs of differing base pair sequences under various environmental conditions The affinity of binding of sanguinarine (iminium form) was found to be in the order of 10 5 M -1 to calf thymus DNA. The binding affinity to calf thymus DNA decreased with increase of ionic strength and temperature. The salt dependence of the binding data showed that release of 0.55 U of the cations per bound alkaloid. The binding of the iminium form was exothermic under all conditions, but the uncharged alkanolamine form showed no binding to DNA. The heat capacity changes obtained from the temperature dependence of enthalpy indicated a value of -140 cal/mol K. Sanguinarine showed high specificity to alternating purine-pyrimidine sequences with affinity of the order 10 6 M -1 and the affinity to the polynucleotides varied in the order poly(dG-dC)·poly(dG-dC) > poly(dA-dT)·poly(dA-dT) > poly(dA)·poly(dT) > poly(dG)·poly(dC). The binding to alternating GC polymer was exothermic and enthalpy driven, to the homo GC polymer was exothermic and favoured by both negative enthalpy and positive entropy changes, to the alternating AT polymer was exothermic and enthalpy driven while to the homo AT polymer was endothermic and entropy driven.

  6. Comparative spectroscopic, calorimetric, and computational studies of nucleic acid complexes with 2',5"-versus 3',5"-phosphodiester linkages.

    PubMed Central

    Jin, R; Chapman, W H; Srinivasan, A R; Olson, W K; Breslow, R; Breslauer, K J

    1993-01-01

    We have used a combination of spectroscopic, calorimetric, and computational techniques to characterize the properties of nucleic acid complexes with 2',5''- and 3',5''-phosphodiester linkages. Specifically, we have compared the properties of complexes formed by the association of 3',5'' single-stranded 16-mers of adenylic acid (A16) and thymidylic acid (T16) with the complexes formed by the corresponding single-stranded 16-mers with 2',5''-phosphodiester linkages (A*16 and T*16). Our results reveal the following differential features: (i) the 3',5'' strands form either a duplex or a triplex, depending on the sodium ion concentration, whereas the 2',5'' strands form either a triplex or no complex at all; (ii) the 2',5'' and 3',5'' triplexes exhibit significantly different CD spectra, suggesting that the two triplex states are conformationally nonequivalent; (iii) the 2',5'' triplex has a lower charge density than the 3',5'' triplex; (iv) the thermal stability of the 3',5'' triplex, as expected, is concentration dependent, whereas the thermal stability of the 2',5'' triplex is concentration independent; (v) relative to their component single strands, the 2',5'' triplex is thermodynamically much less stable than the 3',5'' triplex, despite being thermally more stable; (vi) the reduced thermodynamic stability of the 2',5'' triplex relative to the 3',5'' triplex is overwhelmingly enthalpic in origin. In the aggregate, our results reveal and characterize significant differences in the properties of complexes formed by the association of strands with identical base sequences but different phosphodiester linkages. We describe a structural model that is consistent with many of the differential properties observed. We also speculate on how these differential properties may have provided an evolutionary advantage for 3',5'' linkages and how the properties of 2',5'' complexes might be exploited in antisense strategies. Images Fig. 3 PMID:8248146

  7. Composite bone cements loaded with a bioactive and ferrimagnetic glass-ceramic. Part I: Morphological, mechanical and calorimetric characterization.

    PubMed

    Bruno, Matteo; Miola, Marta; Bretcanu, Oana; Vitale-Brovarone, Chiara; Gerbaldo, Roberto; Laviano, Francesco; Verné, Enrica

    2014-02-01

    Hyperthermia is a technique for destroying cancer cells which involves the exposition of body's tissue to a controlled heat, normally between 41℃ and 46℃. It has been reported that ferro- or ferrimagnetic materials can heat locally, if they are placed (after being implanted) under an alternating magnetic field, damaging only tumoral cells and not the healthy ones. The power loss produced by the magnetic materials can be dissipated in the form of heat. This phenomenon has to be regulated in order to obtain a controlled temperature inside the tissues. The material that was produced and characterized in this work is composed of two phases: a polymethylmethacrylate (PMMA) matrix in which a ferrimagnetic biocompatible/bioactive glass ceramic is dispersed. This composite material is intended to be applied as bone filler for the hyperthermic treatment of bone tumors. The ferrimagnetic bioactive glass-ceramic belongs to the system SiO2-Na2O-CaO-P2O5-FeO-Fe2O3 and contains magnetite (FeO*Fe2O3) inside an amorphous bioactive residual phase. The composite material possesses structural, magnetic and bioactivity properties. The structural ones are conferred by PMMA which acts as filler for the bone defect or its damaged area. Bioactivity is conferred by the composition of the residual amorphous phase of the glass-ceramic and magnetic properties are conferred by magnetite crystals embedded in the bioactive glass-ceramic. The characterization involved the following tests: morphological and chemical characterization (scanning electron microscopy-energy dispersion spectrometry-micro computed tomography analysis), calorimetric tests and mechanical test (compression and flexural four point test). In vitro assessment of biological behavior will be the object of the part II of this work.

  8. Thermochemistry of 2- and 3-thiopheneacetic acids: calorimetric and computational study.

    PubMed

    Temprado, Manuel; Roux, María Victoria; Jiménez, Pilar; Foces-Foces, Concepción; Notario, Rafael

    2008-10-16

    The enthalpies of formation in the condensed and gas states, Delta f H m degrees (cd) and Delta f H m degrees (g), of 2- and 3-thiopheneacetic acids were derived from their respective enthalpies of combustion in oxygen, measured by a rotating bomb calorimeter, and the variation of vapor pressure with temperature determined by the Knudsen effusion technique. Theoretical calculations at the G3 level were performed, and a study on molecular and electronic structure of the compounds has been carried out. Calculated Delta f H m degrees (g) values using atomization and isodesmic reactions are compared with the experimental data. Experimental and theoretical results show that the 3-thiopheneacetic acid is thermodynamically more stable than the 2-isomer. PMID:18816026

  9. Calorimetric study of the entropy relation in the NaCl–KCl system

    PubMed Central

    Benisek, Artur; Dachs, Edgar

    2013-01-01

    The heat capacity of one Na-rich and two K-rich samples of the NaCl–KCl (halite–sylvite) crystalline solution was investigated between 5 and 300 K. It deviated positively from ideal behaviour with a maximum at 40 K. The thereby produced excess entropy at 298.15 K was described by a symmetric Margules mixing model yielding WmS = 8.73 J/mol/K. Using enthalpy of mixing data from the literature and our data on the entropy, the solvus was calculated for a pressure of 105 Pa and compared with the directly determined solvus. The difference between them can be attributed to the effect of Na–K short range ordering (clustering). PMID:24926102

  10. Calorimetric study of the entropy relation in the NaCl-KCl system.

    PubMed

    Benisek, Artur; Dachs, Edgar

    2013-07-01

    The heat capacity of one Na-rich and two K-rich samples of the NaCl-KCl (halite-sylvite) crystalline solution was investigated between 5 and 300 K. It deviated positively from ideal behaviour with a maximum at 40 K. The thereby produced excess entropy at 298.15 K was described by a symmetric Margules mixing model yielding [Formula: see text] = 8.73 J/mol/K. Using enthalpy of mixing data from the literature and our data on the entropy, the solvus was calculated for a pressure of 10(5) Pa and compared with the directly determined solvus. The difference between them can be attributed to the effect of Na-K short range ordering (clustering).

  11. Calorimetric and transport properties of Zircalloy 2, Zircalloy 4, and Inconel 625

    NASA Astrophysics Data System (ADS)

    Maglić, K. D.; Perović, N. Lj.; Stanimirović, A. M.

    1994-07-01

    This paper presents the measurements and the results on thermal and electrical transport properties of three nuclear reactor cladding materials: Zircalloy 2, Zircalloy 4, and Inconel 625. Study of these materials constituted a part of the IAEA coordinated research program aimed at the generation and establishment of a reliable and complete database of the thermal properties of reactor materials. Measured properties include thermal diffusivity, specific heat, and electrical resistivity. Thermal diffusivity was measured by the laser pulse technique. Specific heat and electrical resistivity were measured using a millisecond-resolution direct electrical pulse heating technique. Thermal conductivity was computed from the experimentally determined thermal difusivity and specific heat functions and the room temperature density values. Measurements were performed in the 20 to 1500°C temperature range, depending on the material and property concerned.

  12. Introduction: Invertebrate Neuropeptides XVI

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This publication represents an introduction to the sixteenth in a series of special issues of the Peptides journal dedicated to invertebrate neuropeptides. The issue addresses a number of aspects of invertebrate neuropeptide research including identification of novel invertebrate neuropeptide seque...

  13. Structure-energy relationship in barbituric acid: a calorimetric, computational, and crystallographic study.

    PubMed

    Roux, María Victoria; Temprado, Manuel; Notario, Rafael; Foces-Foces, Concepción; Emel'yanenko, Vladimir N; Verevkin, Sergey P

    2008-08-14

    This paper reports the value of the standard (p(o) = 0.1 MPa) molar enthalpy of formation in the gas phase at T = 298.15 K for barbituric acid. The enthalpies of combustion and sublimation were measured by static bomb combustion calorimetry and transference (transpiration) method in a saturated N2 stream and a gas-phase enthalpy of formation value of -(534.3 +/- 1.7) kJ x mol(-1) was determined at T = 298.15 K. G3-calculated enthalpies of formation are in very good agreement with the experimental value. The behavior of the sample as a function of the temperature was studied by differential scanning calorimetry, and a new polymorph of barbituric acid at high temperature was found. In the solid state, two anhydrous forms are known displaying two out of the six hydrogen-bonding patterns observed in the alkyl/alkenyl derivatives retrieved from the Cambridge Crystallographic Database. The stability of these motifs has been analyzed by theoretical calculations. X-ray powder diffraction technique was used to establish to which polymorphic form corresponds to the commercial sample used in this study and to characterize the new form at high temperature. PMID:18646743

  14. Calorimetric studies of the heat capacity and relaxation of amorphous Si prepared by electron beam evaporation

    NASA Astrophysics Data System (ADS)

    Tsang, K. H.; Kui, H. W.; Chik, K. P.

    1993-10-01

    The heat capacity of a-Si thin film prepared by electron beam evaporation method was measured from 360 to 820 K by a differential scanning calorimeter. For the as-prepared a-Si specimen, two novel irreversible endothermic processes and one irreversible broad exothermic reaction were found. The origins of the endothermic reactions were not known. It is suggested that they may be caused by a change in the number and distribution of voids that occurs at approximately 465 K and the creation of dangling bonds at the higher temperature regime (≳620 K). The exothermic reaction is attributed to heat release during structural relaxation. When measuring the heat capacity of a-Si, Ca-Sip, these irreversible reactions were first eliminated by annealing the specimens at high temperatures. The heat capacity of crystalline Si, Cc-Sip, was also measured and the difference, ΔCSip=Ca-Sip -Cc-Sip, was used to evaluate the thermodynamic melting temperature of the a-Si, Tal, which is determined to be 1400 K.

  15. Calorimetric and computational study of 1,3- and 1,4-oxathiane sulfones.

    PubMed

    Roux, María Victoria; Temprado, Manuel; Jiménez, Pilar; Notario, Rafael; Guzman-Mejía, Ramón; Juaristi, Eusebio

    2007-02-16

    The enthalpies of formation in the condensed and gas states, DeltafH degrees m(cd) and DeltafH degrees m(g), of 1,3- and 1,4-oxathiane sulfones were derived from their respective enthalpies of combustion in oxygen, measured by a rotating bomb calorimeter and the variation of vapor pressures with temperatures determined by the Knudsen effusion technique. Standard ab initio molecular orbital calculations at the G2(MP2) and G3 levels were performed, and a theoretical study on molecular and electronic structure of the compounds has been carried out. Calculated DeltafH degrees m(g) values at the G3 level using atomization reactions agree well with the experimental ones. These experimental and theoretical studies support that the destabilization found in 1,3-oxathiane sulfone, 11.2 kJ mol-1 respecting to 1,4-oxathiane sulfone, is due to the electrostatic repulsion between the negative charges of the axial oxygen of the sulfone and the oxygen of the ring and apparently masks any stabilization originating from the hyperconjugative nO --> sigma*C-SO2 stereoelectronic interaction. PMID:17288369

  16. Structure-energy relationship in barbituric acid: a calorimetric, computational, and crystallographic study.

    PubMed

    Roux, María Victoria; Temprado, Manuel; Notario, Rafael; Foces-Foces, Concepción; Emel'yanenko, Vladimir N; Verevkin, Sergey P

    2008-08-14

    This paper reports the value of the standard (p(o) = 0.1 MPa) molar enthalpy of formation in the gas phase at T = 298.15 K for barbituric acid. The enthalpies of combustion and sublimation were measured by static bomb combustion calorimetry and transference (transpiration) method in a saturated N2 stream and a gas-phase enthalpy of formation value of -(534.3 +/- 1.7) kJ x mol(-1) was determined at T = 298.15 K. G3-calculated enthalpies of formation are in very good agreement with the experimental value. The behavior of the sample as a function of the temperature was studied by differential scanning calorimetry, and a new polymorph of barbituric acid at high temperature was found. In the solid state, two anhydrous forms are known displaying two out of the six hydrogen-bonding patterns observed in the alkyl/alkenyl derivatives retrieved from the Cambridge Crystallographic Database. The stability of these motifs has been analyzed by theoretical calculations. X-ray powder diffraction technique was used to establish to which polymorphic form corresponds to the commercial sample used in this study and to characterize the new form at high temperature.

  17. Differential Scanning Calorimetric (DSC) Analysis of Rotary Nickel-Titanium (NiTi) Endodontic File (RNEF)

    NASA Astrophysics Data System (ADS)

    Wu, Ray Chun Tung; Chung, C. Y.

    2012-12-01

    To determine the variation of A f along the axial length of rotary nickel-titanium endodontic files (RNEF). Three commercial brands of 4% taper RNEF: GTX (#20, 25 mm, Dentsply Tulsa Dental Specialties, Tulsa, OK, USA), K3 (#25, 25 mm) and TF (Twisted File #25, 27 mm) (Sybron Kerr, Orange, CA, USA) were cut into segments at 4 mm increment from the working tip. Regional specimens were measured for differential heat-flow over thermal cycling, generally with continuous heating or cooling (5 °C/min) and 5 min hold at set temperatures (start, finish temperatures): GTX: -55, 90 °C; K3: -55, 45 °C; TF: -55, 60 °C; using differential scanning calorimeter. This experiment demonstrated regional differences in A f along the axial length of GTX and K3 files. Similar variation was not obvious in the TF samples. A contributory effect of regional difference in strain-hardening due to grinding and machining during manufacturing is proposed.

  18. Calorimetric studies of Cu-Li, Li-Sn, and Cu-Li-Sn.

    PubMed

    Fürtauer, S; Tserenjav, E; Yakymovych, A; Flandorfer, H

    2013-06-01

    Integral molar enthalpies of mixing were determined by drop calorimetry for Cu-Li-Sn at 1073 K along five sections xCu/xSn ≈ 1:1, xCu/xSn ≈ 2:3, xCu/xSn ≈ 1:4, xLi/xSn ≈ 1:1, and xLi/xSn ≈ 1:4. The integral and partial molar mixing enthalpies of Cu-Li and Li-Sn were measured at the same temperature, for Li-Sn in addition at 773 K. All binary data could be described by Redlich-Kister-polynomials. Cu-Li shows an endothermic mixing effect with a maximum in the integral molar mixing enthalpy of ∼5300 J · mol(-1) at xCu = 0.5, Li-Sn an exothermic minimum of ∼ -37,000 J · mol(-1) at xSn ∼ 0.2. For Li-Sn no significant temperature dependence between 773 K and 1073 K could be deduced. Our measured ternary data were fitted on the basis of an extended Redlich-Kister-Muggianu model for substitutional solutions. Additionally, a comparison of these results to the extrapolation model of Chou is given.

  19. Calorimetric studies of Cu–Li, Li–Sn, and Cu–Li–Sn

    PubMed Central

    Fürtauer, S.; Tserenjav, E.; Yakymovych, A.; Flandorfer, H.

    2013-01-01

    Integral molar enthalpies of mixing were determined by drop calorimetry for Cu–Li–Sn at 1073 K along five sections xCu/xSn ≈ 1:1, xCu/xSn ≈ 2:3, xCu/xSn ≈ 1:4, xLi/xSn ≈ 1:1, and xLi/xSn ≈ 1:4. The integral and partial molar mixing enthalpies of Cu–Li and Li–Sn were measured at the same temperature, for Li–Sn in addition at 773 K. All binary data could be described by Redlich–Kister-polynomials. Cu–Li shows an endothermic mixing effect with a maximum in the integral molar mixing enthalpy of ∼5300 J · mol−1 at xCu = 0.5, Li–Sn an exothermic minimum of ∼ −37,000 J · mol−1 at xSn ∼ 0.2. For Li–Sn no significant temperature dependence between 773 K and 1073 K could be deduced. Our measured ternary data were fitted on the basis of an extended Redlich–Kister–Muggianu model for substitutional solutions. Additionally, a comparison of these results to the extrapolation model of Chou is given. PMID:23814314

  20. Structural and binding properties of laminarin revealed by analytical ultracentrifugation and calorimetric analyses.

    PubMed

    Oda, Masayuki; Tanabe, Yoichi; Noda, Masanori; Inaba, Satomi; Krayukhina, Elena; Fukada, Harumi; Uchiyama, Susumu

    2016-08-01

    One of the β-1,3-glucans, laminarin, has been widely used as a substrate for enzymes including endo-1,3-β-glucanase. To obtain quantitative information about the molecular interaction between laminarin and endo-1,3-β-glucanase, the structural properties of laminarin should be determined. The results from pioneering work using analytical ultracentrifugation for carbohydrate analysis showed that laminarin from Laminaria digitata predominantly exists as a single-chain species with approximately 5% of triple-helical species. Differential scanning calorimetry experiments did not show a peak assignable to the transition from triple-helix to single-chain, supporting the notion that a large proportion of laminarin is the single-chain species. The interaction of laminarin with an inactive variant of endo-1,3-β-glucanase from Cellulosimicrobium cellulans, E119A, was quantitatively analyzed using isothermal titration calorimetry. The binding was enthalpically driven and the binding affinity was approximately 10(6) M(-1). The results from binding stoichiometric analysis indicated that on average, E119A binds to laminarin in a 2:1 ratio. This seems to be reasonable, because laminarin mainly exists as a monomer, the apparent molecular mass of laminarin is 3.6 kDa, and E119A would have substrate-binding subsites corresponding to 6 glucose units. The analytical ultracentrifugation experiments could detect different complex species of laminarin and endo-1,3-β-glucanase. PMID:27267066

  1. Exploring the comparative binding aspects of benzophenanthridine plant alkaloid chelerythrine with RNA triple and double helices: a spectroscopic and calorimetric approach.

    PubMed

    Haque, Lucy; Pradhan, Ankur Bikash; Bhuiya, Sutanwi; Das, Suman

    2015-07-14

    A comparative study on the interaction of a benzophenanthridine alkaloid chelerythrine (CHL) with RNA triplex poly(U).poly(A)*poly(U) (hereafter U.A*U, .(dot) and *(asterisk) represent Watson-Crick and Hoogsteen base pairing respectively) and its parent duplex poly(A).poly(U) (A.U) was carried out by using a combination of various spectroscopic, viscometric and calorimetric techniques. The interaction was characterized by hypochromic and bathochromic effects in the absorption spectrum, the increase of thermal melting temperature, enhancement in solution viscosity, and perturbation in the circular dichroic spectrum. The binding constant calculated by using spectrophotometric data was in the order of 10(5) for both forms of RNA, but it was greater for triplex RNA (30.2 × 10(5) M(-1)) than duplex RNA (3.6 × 10(5) M(-1)). Isothermal titration calorimetric data are in good agreement with the spectrophotometric data. The data indicated stronger binding of CHL to the triplex structure of RNA compared to the native duplex structure. Thermal melting studies indicated greater stabilization of the Hoogsteen base paired third strand of the RNA triplex compared to its Watson-Crick strands. The mode of binding of CHL to both U.A*U and A.U was intercalation as revealed from fluorescence quenching, viscosity measurements and sensitization of the fluorescence experiment. Thermodynamic data obtained from isothermal calorimetric measurements revealed that association was favoured by both a negative enthalpy change and a positive entropy change. Taken together, our results suggest that chelerythrine binds and stabilizes the RNA triplex more strongly than its respective parent duplex. The results presented here may be useful for formulating effective antigene strategies involving benzophenanthridine alkaloids and the RNA triplex. PMID:26073991

  2. Synthesis, calorimetric, structural and conductivity studies in a new thallium selenate tellurate adduct compound

    SciTech Connect

    Ktari, L.; Abdelhedi, M.; Bouhlel, N.; Dammak, M.; Cousson, A.

    2009-08-05

    The crystal structure of the thallium selenate tellurate Tl{sub 2}SeO{sub 4}.Te(OH){sub 6} (TlSeTe) was determined by X-ray diffraction method. The title compound crystallizes in the monoclinic system with P2{sub 1}/c space group. The following parameters are: a = 12.358(3) A; b = 7.231(1) A; c = 11.986(2) A; {beta} = 111.092(2){sup o}; Z = 4. The structure can be regarded as being built of isolated TeO{sub 6} octahedra and SeO{sub 4} tetrahedra. The Tl{sup +} cations are intercalated between these kinds of polyhedra. The main feature of this structure is the coexistence of two different and independent anions (SeO{sub 4}{sup 2-} and TeO{sub 6}{sup 6-}) in the same unit cell. The structure is stable due to O-H...O hydrogen bonds which link tetrahedral and octahedral groups. Crystals of Tl{sub 2}SeO{sub 4}.Te(OH){sub 6} undergo three endothermal transitions at 373, 395 and 437 K. These transitions are detected by DSC and analyzed by dielectric measurements with impedance spectroscopy. The evolution of conductivity versus temperature showed the presence of a protonic conduction phase transition at 437 K. The phase transition at 373 K can be related to a structural phase transition, whereas the one at 395 K is ascribed as likely due to a ferroelectric-paraelectric phase transition.

  3. Thermodynamic properties of autunite, uranyl hydrogen phosphate, and uranyl orthophosphate from solubility and calorimetric measurements

    SciTech Connect

    Gorman-Lewis, Drew; Shareva, Tatiana; kubatko, Karrie-Ann; burns, Peter; Wellman, Dawn M.; McNamara, Bruce K.; szymanowski, jennifer; Navrotsky, Alexandra; Fein, Jeremy B.

    2009-10-01

    In this study, we use solubility and oxide melt solution calorimetry measurements to determine the thermodynamic properties of the uranyl phosphate phases autunite (abbreviated: CaUP), uranyl hydrogen phosphate (HUP), and uranyl orthophosphate (UP). Solubility measurements from both supersaturated and undersaturated conditions, as well as under different pH conditions, rigorously demonstrate attainment of equilibrium and yield well-constrained solubility product values of -48.36 (-0.03 /+ 0.03), -13.17 (-0.11 / +0.07), and -49.36 (-0.04 / +0.02) for CaUP, HUP, and UP, respectively. We use the solubility data to calculate standard state Gibbs free energies of formation for all phases (-7630.61 ± 9.69, -3072.27 ± 4.76, and -6138.95 ± 12.24 kJ mol-1 for CaUP, HUP, and UP, respectively), and calorimetry data to calculate standard state enthalpies of formation of -3223.22 ± 4.00 and -7001.01 ± 15.10 kJ mol-1 for HUP and UP, respectively. Combining these results allows us also to calculate the standard state entropies of formation of -506.54 ± 10.48 and -2893.12 ± 19.44 kJ mol-1 K-1 for HUP and UP phases, respectively. The results from this study are part of a combined effort to develop reliable and internally consistent thermodynamic data for environmentally relevant uranyl minerals. Data such as these are required in order to optimize and quantitatively assess the effect of phosphate amendment remediation technologies for uranium contaminated systems.

  4. Comparative Study of the Phenomena of Precipitation in Al-Zn-Mg Alloy by the Differential Scanning Calorimetric and the Dilatometry and Interpretation of Dilatometric Effects

    NASA Astrophysics Data System (ADS)

    Hadjadj, L.; Amira, R.; Bouchear, M.

    2012-07-01

    Our aim is to contribute to comprehension of the phenomena of precipitation in the Al-Zn-Mg alloys. For this, we have made a comparative study of the transformations of phases using the differential scanning calorimetric and the dilatometry. This last technique is relatively new in the case of Al-Zn-Mg alloys. It consists of two opposite effects (contraction and expansion) observed on the dilatometric curves. These effects translate two opposite metallurgical phenomena which are generally the precipitation and the dissolution.

  5. Calorimetric studies of the interactions of metalloenzyme active site mimetics with zinc-binding inhibitors.

    PubMed

    Robinson, Sophia G; Burns, Philip T; Miceli, Amanda M; Grice, Kyle A; Karver, Caitlin E; Jin, Lihua

    2016-07-19

    The binding of drugs to metalloenzymes is an intricate process that involves several interactions, including binding of the drug to the enzyme active site metal, as well as multiple interactions between the drug and the enzyme residues. In order to determine the free energy contribution of Zn(2+) binding by known metalloenzyme inhibitors without the other interactions, valid active site zinc structural mimetics must be formed and binding studies need to be performed in biologically relevant conditions. The potential of each of five ligands to form a structural mimetic with Zn(2+) was investigated in buffer using Isothermal Titration Calorimetry (ITC). All five ligands formed strong 1 : 1 (ligand : Zn(2+)) binary complexes. The complexes were used in further ITC experiments to study their interaction with 8-hydroxyquinoline (8-HQ) and/or acetohydroxamic acid (AHA), two bidentate anionic zinc-chelating enzyme inhibitors. It was found that tetradentate ligands were not suitable for creating zinc structural mimetics for inhibitor binding in solution due to insufficient coordination sites remaining on Zn(2+). A stable binary complex, [Zn(BPA)](2+), which was formed by a tridentate ligand, bis(2-pyridylmethyl)amine (BPA), was found to bind one AHA in buffer or a methanol : buffer mixture (60 : 40 by volume) at pH 7.25 or one 8-HQ in the methanol : buffer mixture at pH 6.80, making it an effective structural mimetic for the active site of zinc metalloenzymes. These results are consistent with the observation that metalloenzyme active site zinc ions have three residues coordinated to them, leaving one or two sites open for inhibitors to bind. Our findings indicate that Zn(BPA)X2 can be used as an active site structural mimetic for zinc metalloenzymes for estimating the free energy contribution of zinc binding to the overall inhibitor active site interactions. Such use will help aid in the rational design of inhibitors to a variety of zinc metalloenzymes

  6. Ground calorimetric studies using the REMS ground temperature sensor and the Curiosity rover

    NASA Astrophysics Data System (ADS)

    Zorzano, María-Paz; Martín-Torres, Francisco Javier; Newman, Claire; de la Torre, Manuel; Hamilton, Victoria; Sebastian, Eduardo; Javier Gómez-Elvira, REMS Team; the MSL Science Team

    2013-04-01

    The REMS instrument, on board the Curiosity rover, has an infrared ground temperature sensor that allows monitoring the diurnal evolution of the ground temperature every day at the different sites visited by the rover during its operation on Gale crater. The amplitude of the diurnal ground temperature oscillation depends on the local column of dust, as well as on the thermal inertia (I) of the ground. The rover has a hot Radiosotope Thermal Generator (RTG) of which the temperature is monitored by engineering sensors. This element is an unavoidable extra source of heat that irradiates the ground where the rover stands. Whenever the rover moves and samples a new site the sensed temperature shows a significant drop that ranges between 3 and 15 K depending on the location and time of the day. This drop is the increment of temperature (ΔT) caused by the heat (q) emited by the RTG source alone, and thus the soil heat capacity (C) can be obtained by rating these magnitudes and allowing the rover to perform in situ ground calorimetry in a simple way: - The heat emited by the RTG can be evaluated using the Stefan Boltzman law (q=σT4) - The soil heat capacity scales with the square of the termal inertial ( C ~ I2) Orbitally determined inertias in the region of the rover [Fergason et al., 2012 ] range from 250 (J/m2K s1/2 ) to 410 (J/m2K s1/2). Thus in the area explored by the rover I may vary a factor 2, which leads to a factor 4 increment in C and thus the final ground offset induced by the RTG extra heating is expected to be significantly greater for soils of higher thermal inertia. Once the rover stands at a fixed position the ground is heated up as the ground responses in time to the irradiated heat until a new equilibrium temperature is reached. Soils with low thermal inertia respond faster to the RTG heating source (around 40 minutes) whereas high thermal inertia soils respond more slowly (around 75 minutes). This method shall be improved for future calorimetry

  7. Trophic relay and prey switching - A stomach contents and calorimetric investigation of an ambassid fish and their saltmarsh prey

    NASA Astrophysics Data System (ADS)

    McPhee, Jack J.; Platell, Margaret E.; Schreider, Maria J.

    2015-12-01

    Trophic relay is an ecological model that involves the movement of biomass and energy from vegetation, such as saltmarshes, within estuaries to the open sea via a series of predator-prey relationships. Any potential for trophic relay is therefore affected by water movements within an estuary and by the ability of a predator to "switch" prey in response to fluctuating abundances of those prey. Saltmarsh-dwelling grapsid crabs, which feed on saltmarsh-derived detritus and microphytobenthos, release zoeae into ebbing tides that inundate saltmarshes during spring-tide cycles within tidally-dominated estuaries, such as Brisbane Water Estuary, therefore providing an opportunity to examine whether prey-switching and/or trophic relay may occur in fish that feed on those zoeae (such as the highly abundant estuarine ambassid, Ambassis jacksoniensis). This model was examined by sampling A. jacksoniensis near saltmarshes in a large, temperate south-eastern Australian estuary during flood and ebb tides on days of saltmarsh inundation and non-inundation over four spring-tide events in 2012. Stomach fullnesses of A. jacksoniensis were generally highest during ebb tides on days of saltmarsh inundation, implying that feeding was most marked at these times. Caridean decapods dominated diets during flood tides and on days of no saltmarsh inundation, while crab zoeae dominated diets during ebb tides and on days of inundation, suggesting that, when saltmarsh-derived zoeae became abundant, A. jacksoniensis switched to feeding on those prey. Three potential zooplankton prey (calanoid copepods, caridean decapods and crab zoeae) did not differ calorimetrically, indicating that switching of prey by A. jacksoniensis is not directly related to their preying on energetically greater prey, but reflects opportunistic feeding on more abundant and/or less elusive prey. As A. jacksoniensis is able to switch prey from estuarine caridean decapods to saltmarsh-derived crab zoeae, this very abundant

  8. Introduction of Differential Scanning Calorimetry in a General Chemistry Laboratory Course: Determination of Heat Capacity of Metals and Demonstration of Law of Dulong and Petit

    ERIC Educational Resources Information Center

    D'Amelia, Ronald P.; Stracuzzi, Vincent; Nirode, William F.

    2008-01-01

    Today's general chemistry students are introduced to many of the principles and concepts of thermodynamics. In first-year general chemistry undergraduate courses, thermodynamic properties such as heat capacity are frequently discussed. Classical calorimetric methods of analysis and thermal equilibrium experiments are used to determine heat…

  9. Acyclic diterpene glycosides, capsianosides VIII, IX, X, XIII, XV and XVI from the fruits of Paprika Capsicum annuum L. var. grossum BAILEY and Jalapeño Capsicum annuum L. var. annuum.

    PubMed

    Lee, Jong-Hyun; Kiyota, Naoko; Ikeda, Tsuyoshi; Nohara, Toshihiro

    2006-10-01

    Paprika and Jalapeño are used as vegetables and spices. We have obtained six new acyclic diterpene glycosides, called capsianosides XIII (2), XV (3), IX (4), XVI (5), X (6) and VIII (7) together with known capsianoside II (1) from the fruits of the Paprika and Jalapeño. The structures of these compounds have been elucidated by the (1)H- and (13)C-NMR spectra and two-dimensional NMR methods.

  10. Micromechanical calorimetric sensor

    DOEpatents

    Thundat, Thomas G.; Doktycz, Mitchel J.

    2000-01-01

    A calorimeter sensor apparatus is developed utilizing microcantilevered spring elements for detecting thermal changes within a sample containing biomolecules which undergo chemical and biochemical reactions. The spring element includes a bimaterial layer of chemicals on a coated region on at least one surface of the microcantilever. The chemicals generate a differential thermal stress across the surface upon reaction of the chemicals with an analyte or biomolecules within the sample due to the heat of chemical reactions in the sample placed on the coated region. The thermal stress across the spring element surface creates mechanical bending of the microcantilever. The spring element has a low thermal mass to allow detection and measuring of heat transfers associated with chemical and biochemical reactions within a sample placed on or near the coated region. A second surface may have a different material, or the second surface and body of microcantilever may be of an inert composition. The differential thermal stress between the surfaces of the microcantilever create bending of the cantilever. Deflections of the cantilever are detected by a variety of detection techniques. The microcantilever may be approximately 1 to 200 .mu.m long, approximately 1 to 50 .mu.m wide, and approximately 0.3 to 3.0 .mu.m thick. A sensitivity for detection of deflections is in the range of 0.01 nanometers. The microcantilever is extremely sensitive to thermal changes in samples as small as 30 microliters.

  11. 78 FR 11939 - Social Security Ruling, SSR 13-2p.; Titles II and XVI: Evaluating Cases Involving Drug Addiction...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-02-20

    ... determination or decision that explains the rationale supporting their determination of the materiality of DAA... understand the basis for the materiality finding and the determination of whether the claimant is disabled... requires a finding of the materiality of DAA to the determination that the claimant is disabled. List...

  12. Calorimetric and computational study of thiacyclohexane 1-oxide and thiacyclohexane 1,1-dioxide (thiane sulfoxide and thiane sulfone). Enthalpies of formation and the energy of the S=O bond.

    PubMed

    Roux, María Victoria; Temprado, Manuel; Jiménez, Pilar; Dávalos, Juan Zenón; Notario, Rafael; Guzmán-Mejía, Ramón; Juaristi, Eusebio

    2003-03-01

    A rotating-bomb combustion calorimeter specifically designed for the study of sulfur-containing compounds [J. Chem. Thermodyn. 1999, 31, 635] has been used for the determination of the enthalpy of formation of thiane sulfone, 4, Delta(f)H(o) m(g) = -394.8 +/- 1.5 kJ x mol(-1). This value stands in stark contrast with the enthalpy of formation reported for thiane itself, Delta(f)H(o) m(g) = -63.5 +/- 1.0 kJ x mol(-1), and gives evidence of the increased electronegativity of the sulfur atom in the sulfonyl group, which leads to significantly stronger C-SO2 bonds. Given the known enthalpy of formation of atomic oxygen in the gas phase, Delta(f)H(o) m(O,g) = +249.18 kJ x mol(-1), and the reported bond dissociation energy for the S=O bond in alkyl sulfones, BDE(S=O) = +470.0 kJ x mol(-1), it was possible to estimate the enthalpy of formation of thiane sulfoxide, 5, a hygroscopic compound not easy to use in experimental calorimetric measurements, Delta(f)H(o) m(5) = -174.0 kJ x mol(-1). The experimental enthalpy of formation of both 4 and 5 were closely reproduced by theoretical calculations at the G2(MP2)+ level, Delta(f)H(o) m(4) = -395.0 kJ x mol(-1) and Delta(f)H(o) m(5) = -178.0 kJ x mol(-1). Finally, calculated G2(MP2)+ values for the bond dissociation energy of the S=O bond in cyclic sulfoxide 5 and sulfone 4 are +363.7 and +466.2 kJ x mol(-1), respectively. PMID:12608789

  13. Calorimetric and computational study of thiacyclohexane 1-oxide and thiacyclohexane 1,1-dioxide (thiane sulfoxide and thiane sulfone). Enthalpies of formation and the energy of the S=O bond.

    PubMed

    Roux, María Victoria; Temprado, Manuel; Jiménez, Pilar; Dávalos, Juan Zenón; Notario, Rafael; Guzmán-Mejía, Ramón; Juaristi, Eusebio

    2003-03-01

    A rotating-bomb combustion calorimeter specifically designed for the study of sulfur-containing compounds [J. Chem. Thermodyn. 1999, 31, 635] has been used for the determination of the enthalpy of formation of thiane sulfone, 4, Delta(f)H(o) m(g) = -394.8 +/- 1.5 kJ x mol(-1). This value stands in stark contrast with the enthalpy of formation reported for thiane itself, Delta(f)H(o) m(g) = -63.5 +/- 1.0 kJ x mol(-1), and gives evidence of the increased electronegativity of the sulfur atom in the sulfonyl group, which leads to significantly stronger C-SO2 bonds. Given the known enthalpy of formation of atomic oxygen in the gas phase, Delta(f)H(o) m(O,g) = +249.18 kJ x mol(-1), and the reported bond dissociation energy for the S=O bond in alkyl sulfones, BDE(S=O) = +470.0 kJ x mol(-1), it was possible to estimate the enthalpy of formation of thiane sulfoxide, 5, a hygroscopic compound not easy to use in experimental calorimetric measurements, Delta(f)H(o) m(5) = -174.0 kJ x mol(-1). The experimental enthalpy of formation of both 4 and 5 were closely reproduced by theoretical calculations at the G2(MP2)+ level, Delta(f)H(o) m(4) = -395.0 kJ x mol(-1) and Delta(f)H(o) m(5) = -178.0 kJ x mol(-1). Finally, calculated G2(MP2)+ values for the bond dissociation energy of the S=O bond in cyclic sulfoxide 5 and sulfone 4 are +363.7 and +466.2 kJ x mol(-1), respectively.

  14. Calorimetric Studies of the Energetics of Order-Disorder in the System Mg(1-x)Fe(x)Ca(CO(3))(2)

    SciTech Connect

    Brady, P.; Dooley, D.; Navrotsky, A.; Reeder, R.

    1999-02-10

    Calorimetric studies by Chai and Navrotsky (1996) on dolomite-ankerite energetic have been extended by including two additional types of samples: a very disordered stoichiometric MgCa(CO{sub 3}){sub 2} prepared from low temperature aqueous solution and three largely ordered natural samples of intermediate iron content. Combining these data with previous work, three distinct trends of energetic can be seen: those for samples with nearly complete order, nearly complete disorder, and intermediate order. From these trends, the enthalpy of complete disordering is estimated to be 33 {+-} 6 kJ/mol for MgCa(CO{sub 3}){sub 2} and 18 {+-} 5 kJ/mol for FeCa(CO{sub 3}){sub 2}.

  15. Spectroscopic and calorimetric studies of formation of the supramolecular complexes of PAMAM G5-NH₂ and G5-OH dendrimers with 5-fluorouracil in aqueous solution.

    PubMed

    Buczkowski, Adam; Olesinski, Tomasz; Zbicinska, Elzbieta; Urbaniak, Pawel; Palecz, Bartlomiej

    2015-07-25

    The results of spectroscopic measurements (increase in solubility, equilibrium dialysis, (1)H NMR titration) and calorimetric measurements (isothermal titration ITC) indicate exothermic (ΔH<0) and spontaneous (ΔG < 0) combination of an antitumor drug, 5-fluorouracil, by both cationic PAMAM G5-NH2 dendrimer and its hydroxyl analog PAMAM G5-OH in aqueous solutions at room temperature. PAMAM G5-NH2 dendrimer combines about 70 molecules of the drug with equilibrium constant K ≅ 300, which is accompanied by an increase in the system order (ΔS < 0). Hydroxyl dendrimer, PAMAM G5-OH, combines about 14 molecules of 5-fluorouracil with equilibrium constant K ≅ 100. This process is accompanied by an increase in the system disorder (ΔS > 0).

  16. A Search for Low-Mass Weakly Interacting Massive Particles Using Voltage-Assisted Calorimetric Ionization Detection in the SuperCDMS Experiment

    SciTech Connect

    Agnese, R.; Anderson, A. J.; Asai, M.; Balakishiyeva, D.; Basu Thakur, R.; Bauer, D. A.; Billard, J.; Borgland, A.; Bowles, M. A.; Brandt, D.; Brink, P. L.; Bunker, R.; Cabrera, B.; Caldwell, D. O.; Cerdeno, D. G.; Chagani, H.; Cooley, J.; Cornell, B.; Crewdson, C. H.; Cushman, Priscilla B.; Daal, M.; Di Stefano, P. C.; Doughty, T.; Esteban, L.; Fallows, S.; Figueroa-Feliciano, E.; Godfrey, G. L.; Golwala, S. R.; Hall, Jeter C.; Harris, H. R.; Hertel, S. A.; Hofer, T.; Holmgren, D.; Hsu, L.; Huber, M. E.; Jastram, A.; Kamaev, O.; Kara, B.; Kelsey, M. H.; Kennedy, A.; Kiveni, M.; Koch, K.; Loer, B.; Lopez Asamar, E.; Mahapatra, R.; Mandic, V.; Martinez, C.; McCarthy, K. A.; Mirabolfathi, N.; Moffatt, R. A.; Moore, D. C.; Nadeau, P.; Nelson, R. H.; Page, K.; Partridge, R.; Pepin, M.; Phipps, A.; Prasad, K.; Pyle, M.; Qiu, H.; Rau, W.; Redi, P.; Reisetter, A.; Ricci, Y.; Saab, T.; Sadoulet, B.; Sander, J.; Schneck, K.; Schnee, Richard; Scorza, S.; Serfass, B.; Shank, B.; Speller, D.; Villano, A. N.; Welliver, B.; Wright, D. H.; Yellin, S.; Yen, J. J.; Young, B. A.; Zhang, J.

    2014-01-27

    SuperCDMS is an experiment designed to directly detect weakly interacting massive particles (WIMPs), a favored candidate for dark matter ubiquitous in the Universe. In this Letter, we present WIMP-search results using a calorimetric technique we call CDMSlite, which relies on voltage-assisted Luke-Neganov amplification of the ionization energy deposited by particle interactions. The data were collected with a single 0.6 kg germanium detector running for ten live days at the Soudan Underground Laboratory. A low energy threshold of (electron equivalent) was obtained, which allows us to constrain new WIMP-nucleon spin-independent parameter space for WIMP masses below 6 GeV/c2.

  17. Search for Low-Mass Weakly Interacting Massive Particles Using Voltage-Assisted Calorimetric Ionization Detection in the SuperCDMS Experiment

    NASA Astrophysics Data System (ADS)

    Agnese, R.; Anderson, A. J.; Asai, M.; Balakishiyeva, D.; Basu Thakur, R.; Bauer, D. A.; Billard, J.; Borgland, A.; Bowles, M. A.; Brandt, D.; Brink, P. L.; Bunker, R.; Cabrera, B.; Caldwell, D. O.; Cerdeno, D. G.; Chagani, H.; Cooley, J.; Cornell, B.; Crewdson, C. H.; Cushman, P.; Daal, M.; Di Stefano, P. C. F.; Doughty, T.; Esteban, L.; Fallows, S.; Figueroa-Feliciano, E.; Godfrey, G. L.; Golwala, S. R.; Hall, J.; Harris, H. R.; Hertel, S. A.; Hofer, T.; Holmgren, D.; Hsu, L.; Huber, M. E.; Jastram, A.; Kamaev, O.; Kara, B.; Kelsey, M. H.; Kennedy, A.; Kiveni, M.; Koch, K.; Loer, B.; Lopez Asamar, E.; Mahapatra, R.; Mandic, V.; Martinez, C.; McCarthy, K. A.; Mirabolfathi, N.; Moffatt, R. A.; Moore, D. C.; Nadeau, P.; Nelson, R. H.; Page, K.; Partridge, R.; Pepin, M.; Phipps, A.; Prasad, K.; Pyle, M.; Qiu, H.; Rau, W.; Redl, P.; Reisetter, A.; Ricci, Y.; Saab, T.; Sadoulet, B.; Sander, J.; Schneck, K.; Schnee, R. W.; Scorza, S.; Serfass, B.; Shank, B.; Speller, D.; Villano, A. N.; Welliver, B.; Wright, D. H.; Yellin, S.; Yen, J. J.; Young, B. A.; Zhang, J.; SuperCDMS Collaboration

    2014-01-01

    SuperCDMS is an experiment designed to directly detect weakly interacting massive particles (WIMPs), a favored candidate for dark matter ubiquitous in the Universe. In this Letter, we present WIMP-search results using a calorimetric technique we call CDMSlite, which relies on voltage-assisted Luke-Neganov amplification of the ionization energy deposited by particle interactions. The data were collected with a single 0.6 kg germanium detector running for ten live days at the Soudan Underground Laboratory. A low energy threshold of 170 eVee (electron equivalent) was obtained, which allows us to constrain new WIMP-nucleon spin-independent parameter space for WIMP masses below 6 GeV /c2.

  18. Photopyroelectric ac calorimetric study of the nematic-smectic-A phase-transition line in binary liquid crystal mixtures with injected smectic-A phases.

    PubMed

    Caerels, J; Glorieux, C; Thoen, J

    2002-03-01

    Using a recently developed photopyroelectric ac calorimetric technique we investigate two binary liquid crystal mixtures with so-called injected smectic-A phases. Characteristic of these systems is the occurrence of nematic-to-smectic-A transition lines in the phase diagram of mixtures of pure compounds having only a nematic phase. The two binary systems are pentylcyanobiphenyl with either 4-n-propylcyclohexyl-carboxylate or 4-n-pentylphenyl 4(')-n-pentyloxybenzoate. Both these systems have domelike smectic-A ranges with narrow nematic ranges at the top. Near the top the N-SmA transitions are of first order and are crossing over to second order at a tricritical point on either side of the top with the increasing width of the nematic range. The obtained critical exponents are almost completely Fisher renormalized because of the strong concentration dependence of the nematic-to-smectic-A transition temperatures.

  19. Calorimetric measurements of the effect of nickel and stabrite coatings and resistive cores on AC loss in accelerator cables under fixed pressure

    SciTech Connect

    Sumption, M.D.; Collings, E.W.; Scanlan, R.M.

    1997-06-01

    Calorimetric measurements of AC loss on long three- and four-layer stacks of Rutherford cable have been made with the applied field both normal to (face-on, FO, orientation) and parallel to the plane of the cable. Cables studied had bare-Cu, Ni-plated, and stabrite-coated strands; the latter were provided with metallic or insulating interlayers (cores) of, respectively, unalloyed Ti, stainless steel, and kapton ribbon. The cable packs were clamped in a fixture to a pressure of 75 MPa and heat treated for several hours at temperatures of 185 to 250{degrees}C. After cooling, the clamped cables were transferred to the calorimeter and measured without releasing the pressure. From the field-ramp-rate dependence of coupling loss the interlayer and intralayer interstrand contact resistances, R{sub {perpendicular}} and R{sub {parallel}} were deduced. The results were interpreted against a background of earlier {open_quotes}cure-release-repressurize{close_quotes} calorimetric measurements of cable loss as well as direct measurements of contact resistance. Depending on the curing temperature the bare-Cu cable exhibited the highest (T{sub cure} = 250{degrees}C) and the lowest (T{sub cure} = 185{degrees}C) FO losses. Nickel plating resulted in a cable that was much less sensitive to curing temperature. All the core-type cables (T{sub cure} = 185 and 200{degrees}C) exhibited FO loss that was mid-way between those of bare Cu (T{sub cure} = 185{degrees}C) and Ni-plated (T{sub cure} = 200{degrees}C) cables.

  20. Thermodynamic properties of illite, smectite and beidellite by calorimetric methods: Enthalpies of formation, heat capacities, entropies and Gibbs free energies of formation

    NASA Astrophysics Data System (ADS)

    Gailhanou, H.; Blanc, P.; Rogez, J.; Mikaelian, G.; Kawaji, H.; Olives, J.; Amouric, M.; Denoyel, R.; Bourrelly, S.; Montouillout, V.; Vieillard, P.; Fialips, C. I.; Michau, N.; Gaucher, E. C.

    2012-07-01

    The thermodynamic properties of three aluminous 2:1 clay minerals were acquired at 1.013 bars and at temperatures between 5 and 500 K using various calorimetric methods. Calorimetric measurements were performed on hydrated and dehydrated <2 μm clay fractions of smectite MX-80 (Wyoming), illite IMt-2 (Silver Hill) and beidellite SBId-1 (Black Jack Mine). After purification, the mineralogical analyses gave the following structural formulae: Na0.409K0.024Ca0.009 (Si3.738Al0.262) (Al1.598Mg0.214Fe 0.173 3 + Fe 0.035 2 +)O10(OH)2,K0.762Na0.044 (Si3.387Al0.613) (Al1.427Mg0.241Fe 0.292 3 + Fe 0.084 2 +)O10(OH)2 and Ca0.185K0.104 (Si3.574Al0.426) (Al1.812Mg0.09Fe 0.112 3 +)O10(OH)2 for smectite MX-80, illite IMt-2 and beidellite SBId-1, respectively. Heat capacities were measured by low temperature adiabatic calorimetry and differential scanning calorimetry, from 5 to 500 K. Standard enthalpies of formation were obtained from solution-reaction calorimetry at 298.15 K. The standard Gibbs free energies of formation of the clay minerals were also calculated, together with the equilibrium constants at 25 °C, for anhydrous and hydrated minerals. A comparison between these experimental data and estimated values obtained from prediction models available in the literature, enabled the calculation method that appears to be the most relevant to be selected, at least for aluminous 2:1 clay minerals.

  1. [Microcalorimetric determination of thermochemical parameters of the phosphofructokinase reaction].

    PubMed

    Böhme, H J; Schellenberger, W; Hofmann, E

    1975-01-01

    A calorimetric procedure for determining deltaH, deltaG, deltaS and Keq of a bimolecular reaction with two or more products is described. By using this method the thermodynamic parameters of the phosphofructokinase reaction are determined. At pH 7.0 and 25 degrees C a reaction enthalpy of-6.96kcal/mole was found after correction for the neutralization enthalpy of the buffer and of the enthalpy difference of the magnesium complexes of ATP and ADP, respectively. The free energy of the phosphofructokinase reaction has been found under these conditions to be -3.96kcal/mole.

  2. The Bayer Facts of Science Education XVI: US STEM Workforce Shortage— Myth or Reality? Fortune 1000 Talent Recruiters on the Debate

    NASA Astrophysics Data System (ADS)

    Bayer Corporation

    2014-10-01

    A major debate is currently underway in the USA about whether there is, in fact, a science, technology, engineering and mathematics (STEM) workforce shortage in the country or not. This is the subject of the Bayer Facts of Science Education XVI: US STEM Workforce Shortage—Myth or Reality? Fortune 1000 Talent Recruiters on the Debate. An ongoing public opinion research project commissioned by Bayer Corporation, the Bayer Facts surveys examine US STEM education, diversity and workforce issues. The 16th in the series, the newest survey asks talent recruiters at some of the country's largest employers—those included in the Fortune 1000—to weigh in on current and future demand for new hires with 2- and 4-year STEM degrees. As professionals responsible for scouting, recruiting and hiring talent at Fortune 1000 companies, both STEM and non-STEM alike, these individuals are on the frontlines, tasked with assessing and filling their companies' workforce needs. The survey asks the recruiters whether new hires with 2- and 4-year STEM degrees are as, more or less in demand than their peers without STEM degrees? Are more new STEM jobs being created at their companies than non-STEM jobs? Can they find adequate numbers of qualified candidates in a timely manner and how fierce is the competition for STEM degree holders? To answer these and other questions, the survey polled 150 talent recruiters at Fortune 1000 companies, both STEM and non-STEM alike. The survey also asks the recruiters about diversion in STEM, workforce diversity in the pipeline, the role of community colleges in developing the STEM pipeline and the desired skills and competencies of new hires.

  3. A calorimetric determination of the enthalpy of formation and a description of the defect structure of the ordered beta-phase /Ni, Cu/ /1-x/ Al/x/

    NASA Technical Reports Server (NTRS)

    Henig, E. T.; Lukas, H. L.

    1988-01-01

    In order to describe thermodynamically the defect structure of an ordered B-Hume-Rothery phase, the heat of formation of (Ni,Cu)(1-x)Al(x) was measured at 1100 K as a function of concentration in the range x (sub Al) = 0.4 and 0.55 for three substitution rations x (sub Ni)/x (sub Cu) = infinity; 11; 5. The heat of formation of the NiAl beta-phase is strongly negative. For the stoichiometric composition it is -72.2 kJ/g-atom. On both the nickel-rich side and the aluminum-rich side the magnitude of the enthalpy of formation decreases linearly with concentration. Substitution of nickel for copper decreases the magnitude of the enthalpy of formation over the entire homogeneity range for the phase (Ni,Cu)(1-x)Al(x). The curve for the enthalpy of formation as well as the literature values for the chemical potential of aluminum are described with great accuracy by the disorder model of Wagner-Schottky.

  4. Calorimetric and spectroscopic studies of the thermotropic phase behavior of lipid bilayer model membranes composed of a homologous series of linear saturated phosphatidylserines.

    PubMed Central

    Lewis, R N; McElhaney, R N

    2000-01-01

    The thermotropic phase behavior of lipid bilayer model membranes composed of the even-numbered, N-saturated 1,2-diacyl phosphatidylserines was studied by differential scanning calorimetry and by Fourier-transform infrared and (31)P-nuclear magnetic resonance spectroscopy. At pH 7.0, 0.1 M NaCl and in the absence of divalent cations, aqueous dispersions of these lipids, which have not been incubated at low temperature, exhibit a single calorimetrically detectable phase transition that is fully reversible, highly cooperative, and relatively energetic, and the transition temperatures and enthalpies increase progressively with increases in hydrocarbon chain length. Our spectroscopic observations confirm that this thermal event is a lamellar gel (L(beta))-to-lamellar liquid crystalline (L(alpha)) phase transition. However, after low temperature incubation, the L(beta)/L(alpha) phase transition of dilauroyl phosphatidylserine is replaced by a higher temperature, more enthalpic, and less cooperative phase transition, and an additional lower temperature, less enthalpic, and less cooperative phase transition appears in the longer chain phosphatidylserines. Our spectroscopic results indicate that this change in thermotropic phase behavior when incubated at low temperatures results from the conversion of the L(beta) phase to a highly ordered lamellar crystalline (L(c)) phase. Upon heating, the L(c) phase of dilauroyl phosphatidylserine converts directly to the L(alpha) phase at a temperature slightly higher than that of its original L(beta)/L(alpha) phase transition. Calorimetrically, this process is manifested by a less cooperative but considerably more energetic, higher-temperature phase transition, which replaces the weaker L(beta)/L(alpha) phase transition alluded to above. However, with the longer chain compounds, the L(c) phase first converts to the L(beta) phase at temperatures some 10-25 degrees C below that at which the L(beta) phase converts to the L(alpha) phase

  5. Label-Free Determination of the Dissociation Constant of Small Molecule-Aptamer Interaction by Isothermal Titration Calorimetry.

    PubMed

    Vogel, Marc; Suess, Beatrix

    2016-01-01

    Isothermal titration calorimetry (ITC) is a powerful label-free technique to determine the binding constant as well as thermodynamic parameters of a binding reaction and is therefore well suited for the analysis of small molecule-RNA aptamer interaction. We will introduce you to the method and present a protocol for sample preparation and the calorimetric measurement. A detailed note section will point out useful tips and pitfalls.

  6. An active thermal control surfaces experiment. [spacecraft temperature determination

    NASA Technical Reports Server (NTRS)

    Wilkes, D. R.; Brown, M. J.

    1979-01-01

    An active flight experiment is described that has the objectives to determine the effects of the low earth natural environment and the Shuttle induced environment on selected thermal control and optical surfaces. The optical and thermal properties of test samples will be measured in-situ using an integrating sphere reflectrometer and using calorimetric methods. This experiment has been selected for the Long Duration Exposure Facility (LDEF) flight which will be carried to orbit by the NASA Space Shuttle. The LDEF will remain in orbit to be picked up by a later Shuttle mission and returned for postflight evaluation.

  7. Ferric ion (hydr)oxo clusters in the "Venus flytrap" cleft of FbpA: Mössbauer, calorimetric and mass spectrometric studies.

    PubMed

    Mukherjee, Arindam; Bilton, Paul R; Mackay, Logan; Janoschka, Adam; Zhu, Haizhong; Rea, Dean; Langridge-Smith, Pat R R; Campopiano, Dominic J; Teschner, Thomas; Trautwein, Alfred X; Schünemann, Volker; Sadler, Peter J

    2012-04-01

    Isothermal calorimetric studies of the binding of iron(III) citrate to ferric ion binding protein from Neisseria gonorrhoeae suggested the complexation of a tetranuclear iron(III) cluster as a single step binding event (apparent binding constant K(app) (ITC) = 6.0(5) × 10(5) M(-1)). High-resolution Fourier transform ion cyclotron resonance mass spectrometric data supported the binding of a tetranuclear oxo(hydroxo) iron(III) cluster of formula [Fe(4)O(2)(OH)(4)(H(2)O)(cit)](+) in the interdomain binding cleft of FbpA. The mutant H9Y-nFbpA showed a twofold increase in the apparent binding constant [K(app) (ITC) = 1.1(7) × 10(6) M(-1)] for the tetranuclear iron(III) cluster compared to the wild-type protein. Mössbauer spectra of Escherichia coli cells overexpressing FbpA and cultured in the presence of added (57)Fe citrate were indicative of the presence of dinuclear and polynuclear clusters. FbpA therefore appears to have a strong affinity for iron clusters in iron-rich environments, a property which might endow the protein with new biological functions. PMID:22349975

  8. Calorimetric and Light Scattering Investigations of the Transition from Spherical to Wormlike Micelles of C₁₄TAB Triggered by Salicylate.

    PubMed

    Ito, Thiago Heiji; Rodrigues, Roberta Kamei; Loh, Watson; Sabadini, Edvaldo

    2015-06-01

    Although wormlike micelles (WLM) were first described more than 30 years ago, many aspects of their formation process are still unclear. Herein, a systematic experimental investigation of the process for wormlike micelle (WLM) formation in mixtures of tetradecyltrimethylammonium bromide (C14TAB) and salicylate (2-hydroxybenzoate) was carried out. This system was used as a model to investigate the conditions for the formation of the giant aggregate. For comparison, the other two isomers of salicylate (3- and 4-hydroxybenzoate) were also investigated, once in these cases wormlike micelles are not formed. The studies were based on calorimetric titration, static light scattering, and rheological measurements. Enthalpy changes upon titration of C14TAB into 2-hydroxybenzoate solutions revealed a highly cooperative and exothermic process that was associated with micelle growth. The size of the aggregates, obtained by static light scattering measurements, confirms the shape transition. In addition, the correlation of these two sets of results with measurements of micelle charge surface indicates that this transition occurs around the point of charge neutralization.

  9. A chip-calorimetric approach to the analysis of Ag nanoparticle caused inhibition and inactivation of beads-grown bacterial biofilms.

    PubMed

    Hartmann, Tom; Mühling, Martin; Wolf, Antje; Mariana, Frida; Maskow, Thomas; Mertens, Florian; Neu, Thomas R; Lerchner, Johannes

    2013-11-01

    With the increasing complexity of model systems for the investigation of antibacterial effects of nanoparticles, the demands on appropriate analysis methods are rising. In case of biofilms grown on small particles, the high inhomogeneity of the samples represents a major challenge for traditional biofilm analysis. For this purpose, we developed a new calorimetric method which allows non-invasive and real-time investigation of the effects of nanoparticles on beads-grown biofilms which meets the requirements for an increased sample throughput. The method employs a newly developed chip calorimeter that is able to detect changes in the metabolic activity of biofilm samples within minutes. Using this novel device, the antibacterial effect of silver nanoparticles on Pseudomonas putida biofilms grown on agarose beads was investigated. The superparamagnetic properties of the embedded particles within the agarose beads allow an automated sample throughput. Growth inhibition and inactivation effects of silver nanoparticles (AgNPs) on biofilm bacteria were quantified by analyzing the metabolic heat production rate. As a result, a concentration dependent manner of growth inhibition and inactivation was found demonstrating the suitability and sensitivity of the methodology.

  10. Calorimetric study of the nematic to smectic- A and smectic- A to smectic- C phase transitions in liquid-crystal-aerosil dispersions

    NASA Astrophysics Data System (ADS)

    Roshi, A.; Iannacchione, G. S.; Clegg, P. S.; Birgeneau, R. J.; Neubert, M. E.

    2005-11-01

    A high-resolution calorimetric study has been carried out on nanocolloidal dispersions of aerosils in the liquid crystal 4-n -pentylphenylthiol- 4'-n -octyloxybenzoate (8¯S5) as a function of aerosil concentration and temperature spanning the smectic- C to nematic phases. Over this temperature range, this liquid crystal possesses two continuous XY phase transitions: a fluctuation-dominated nematic to smectic- A transition with α≈αXY=-0.013 and a mean-field smectic- A to smectic- C transition. The effective critical character of the N-SmA transition remains unchanged over the entire range of the introduced quenched random disorder while the peak height and enthalpy can be well described by considering a cutoff length scale to the quasicritical fluctuations. The robust nature of the N-SmA transition in this system contrasts with cyanobiphenyl-aerosil systems and may be due to the mesogens being nonpolar and having a long nematic range. The character of the SmA-SmC transition changes gradually with increasing disorder but remains mean field like. The heat capacity maximum at the SmA-SmC transition scales as ρS-0.5 with an apparent evolution from tricritical to a simple mean-field step behavior. These results may be generally understood as a stiffening of the liquid crystal (both the nematic elasticity as well as the smectic layer compression modulus B ) with silica density.

  11. Thermodynamic property determination in low gravity

    NASA Technical Reports Server (NTRS)

    Margrave, J. L.

    1977-01-01

    Techniques for determining heat capacities and other properties of molten metals were investigated and critically evaluated. Precisely determining heat capacities calorimetrically in space poses several problems. The weight of a drop calorimeter block along with the necessity of obtaining a large number of data points tend to make traditional approaches appear infeasible. However, for many substances exhibiting sufficiently high thermal conductivities and with known emissivities, it appears possible to investigate their properties by observing the rate of cooling of a levitated sphere which is initially at a uniform temperature above the melting point. A special advantage of the levitation method is that considerable supercooling is expected, making the study of the heat capacities of molten metals both above and below their melting points possible.

  12. Calorimetric and computational study of 2H-1, 4-benzoxazin-3(4H)-one and of related species

    NASA Astrophysics Data System (ADS)

    Agostinha, M.; Matos, R.; Miranda, Margarida S.; Morais, Victor M. F.; Liebman, Joel F.

    The standard molar enthalpy of formation in the gas phase of 2H-1,4-benzoxazin-3(4H)-one was derived from the standard energy of combustion determined by static bomb combustion calorimetry in oxygen atmosphere and from the standard sublimation enthalpy determined by Calvet microcalorimetry. In addition, we report the results of a systematic theoretical study of the keto and enol tautomers in benzoxazinones and diones using density functional theory. The keto tautomers are computed to be more stable than the enols. Tautomerization energies are reported.

  13. Spectrophotometric and Calorimetric Studies of Np(V) Complexation with Acetate at Variable Temperatures (T = 283 - 343 K)

    SciTech Connect

    Rao, Linfeng; Tian, Guoxin; Srinivasan, Thandankorai G.; Zanonato, PierLuigi; Di Bernardo, Plinio

    2009-12-21

    Spectrophotometric titrations were performed to identify the Np(V)/acetate complex and determine the equilibrium constants at variable temperatures (T = 283 - 343 K) and at the ionic strength of 1.05 mol {center_dot} kg{sup -1}. The enthalpy of complexation at corresponding temperatures was determined by microcalorimetric titrations. Results show that the complexation of Np(V) with acetate is weak but strengthened as the temperature is increased. The complexation is endothermic and is entropy-driven. The enhancement of the complexation at elevated temperatures is primarily due to the increasingly larger entropy gain when the solvent molecules are released from the highly-ordered solvation spheres of NpO{sub 2}{sup +} and acetate to the bulk solvent where the degree of disorder is higher at higher temperatures.

  14. Interaction of pyrophosphate ion with di-, tri- and tetra-amines in aqueous solution: a potentiometric and calorimetric study.

    PubMed

    Labadi, I; Jenei, E; Lahti, R; Lönnberg, H

    1991-11-01

    Successive macroscopic pKa values have been determined potentiometrically for the conjugate acids of spermidine (4-azaoctane-1,8-diamine), spermine (4,9-diazadodecane-1,12-diamine) and some acylic diamines at various ionic strengths in the absence and presence of tetrasodium pyrophosphate. The stability of the amine/pyrophosphate adducts have been estimated on the basis of effects of the pyrophosphate ion on the apparent acidity constants of the amines. Stoichiometry and thermodynamics of adduct formation have been elucidated from microcalorimetric measurements.

  15. Effects of methoxy and formyl substituents on the energetics and reactivity of α-naphthalenes: a calorimetric and computational study.

    PubMed

    Silva, Ana L R; Freitas, Vera L S; Ribeiro da Silva, Maria D M C

    2014-07-01

    A combined experimental and computational study was developed to evaluate and understand the energetics and reactivity of formyl and methoxy α-naphthalene derivatives. Static bomb combustion calorimetry and the Calvet microcalorimetry were the experimental techniques used to determine the standard (p(o)=0.1 MPa) molar enthalpies of formation, in the liquid phase, ΔfHm(o)(l), and of vaporization, Δl(g)Hm(o), at T=298.15K, respectively, of the two liquid naphthalene derivatives. Those experimental values were used to derive the values of the experimental standard molar enthalpies of formation, in the gaseous phase, ΔfHm(o)(g), of 1-methoxynaphthalene, (-3.0 ± 3.1)kJmol(-1), and of 1-formylnaphthalene, (36.3 ± 4.1)kJ mol(-1). High-level quantum chemical calculations at the composite G3(MP2)//B3LYP level were performed to estimate the values of the ΔfHm(o)(g) of the two compounds studied resulting in values in very good agreement with experimental ones. Natural bond orbital (NBO) calculations were also performed to determine more about the structure and reactivity of this class of compounds. PMID:24444416

  16. Effects of methoxy and formyl substituents on the energetics and reactivity of α-naphthalenes: a calorimetric and computational study.

    PubMed

    Silva, Ana L R; Freitas, Vera L S; Ribeiro da Silva, Maria D M C

    2014-07-01

    A combined experimental and computational study was developed to evaluate and understand the energetics and reactivity of formyl and methoxy α-naphthalene derivatives. Static bomb combustion calorimetry and the Calvet microcalorimetry were the experimental techniques used to determine the standard (p(o)=0.1 MPa) molar enthalpies of formation, in the liquid phase, ΔfHm(o)(l), and of vaporization, Δl(g)Hm(o), at T=298.15K, respectively, of the two liquid naphthalene derivatives. Those experimental values were used to derive the values of the experimental standard molar enthalpies of formation, in the gaseous phase, ΔfHm(o)(g), of 1-methoxynaphthalene, (-3.0 ± 3.1)kJmol(-1), and of 1-formylnaphthalene, (36.3 ± 4.1)kJ mol(-1). High-level quantum chemical calculations at the composite G3(MP2)//B3LYP level were performed to estimate the values of the ΔfHm(o)(g) of the two compounds studied resulting in values in very good agreement with experimental ones. Natural bond orbital (NBO) calculations were also performed to determine more about the structure and reactivity of this class of compounds.

  17. Interaction of cationic dodecyl-trimethyl-ammonium bromide with oxy-HbGp by isothermal titration and differential scanning calorimetric studies: Effect of proximity of isoelectric point.

    PubMed

    Alves, Fernanda Rosa; Carvalho, Francisco Adriano O; Carvalho, José Wilson P; Tabak, Marcel

    2016-04-01

    In this work, isothermal titration and differential scanning calorimetric methods, in combination with pyrene fluorescence emission and dynamic light scattering have been used to investigate the interaction of dodecyltrimethylammonium bromide (DTAB) with the giant extracellular Glossoscolex paulistus hemoglobin (HbGp) in the oxy-form, at pH values around the isoelectric point (pI ≈ 5.5). Our ITC results have shown that the interaction of DTAB with the hemoglobin is more intense at pH 7.0, with a smaller cac (critical aggregation concentration) value. The increase of protein concentration does not influence the cac value of the interaction, at both pH values. Therefore, the beginning of the DTAB-oxy-HbGp premicellar aggregates formation, in the cac region, is not affected by the increase of protein concentration. HSDSC studies show higher Tm values at pH 5.0, in the absence and presence of DTAB, when compared with pH 7.0. Furthermore, at pH 7.0, an aggregation process is observed with DTAB in the range from 0.75 to 1.5 mmol/L, noticed by the exothermic peak, and similar to that observed for pure oxy-HbGp, at pH 5.0, and in the presence of DTAB. DLS melting curves show a decrease on the hemoglobin thermal stability for the oxy-HbGp-DTAB mixtures and formation of larger aggregates, at pH 7.0. Our present data, together with previous results, support the observation that the protein structural changes, at pH 7.0, occur at smaller DTAB concentrations, as compared with pH 5.0, due to the acidic pI of protein that favors the oxy-HbGp-cationic surfactant interaction at neutral pH.

  18. In vitro activity of gallium maltolate against Staphylococci in logarithmic, stationary, and biofilm growth phases: comparison of conventional and calorimetric susceptibility testing methods.

    PubMed

    Baldoni, Daniela; Steinhuber, Andrea; Zimmerli, Werner; Trampuz, Andrej

    2010-01-01

    Ga(3+) is a semimetal element that competes for the iron-binding sites of transporters and enzymes. We investigated the activity of gallium maltolate (GaM), an organic gallium salt with high solubility, against laboratory and clinical strains of methicillin-susceptible Staphylococcus aureus (MSSA), methicillin-resistant S. aureus (MRSA), methicillin-susceptible Staphylococcus epidermidis (MSSE), and methicillin-resistant S. epidermidis (MRSE) in logarithmic or stationary phase and in biofilms. The MICs of GaM were higher for S. aureus (375 to 2000 microg/ml) than S. epidermidis (94 to 200 microg/ml). Minimal biofilm inhibitory concentrations were 3,000 to >or=6,000 microg/ml (S. aureus) and 94 to 3,000 microg/ml (S. epidermidis). In time-kill studies, GaM exhibited a slow and dose-dependent killing, with maximal action at 24 h against S. aureus of 1.9 log(10) CFU/ml (MSSA) and 3.3 log(10) CFU/ml (MRSA) at 3x MIC and 2.9 log(10) CFU/ml (MSSE) and 4.0 log(10) CFU/ml (MRSE) against S. epidermidis at 10x MIC. In calorimetric studies, growth-related heat production was inhibited by GaM at subinhibitory concentrations; and the minimal heat inhibition concentrations were 188 to 4,500 microg/ml (MSSA), 94 to 1,500 microg/ml (MRSA), and 94 to 375 microg/ml (MSSE and MRSE), which correlated well with the MICs. Thus, calorimetry was a fast, accurate, and simple method useful for investigation of antimicrobial activity at subinhibitory concentrations. In conclusion, GaM exhibited activity against staphylococci in different growth phases, including in stationary phase and biofilms, but high concentrations were required. These data support the potential topical use of GaM, including its use for the treatment of wound infections, MRSA decolonization, and coating of implants.

  19. Calorimetric study of the effect of bent-shaped dopant molecules on the critical behavior at the nematic-smectic-Ad phase transition.

    PubMed

    Sasaki, Y; Ema, K; Le, K V; Takezoe, H; Dhara, S; Sadashiva, B K

    2011-06-01

    We report results of calorimetric studies for the binary mixture of rodlike host n-alkyloxy-cyanobiphenyl (nOCB, n=8,9) and bent-shaped guest 1,3-phenylene-bis[4-(3-methylbenzoyloxy)]-4'-n-dodecylbiphenyl-4'-carboxylate (BC12). The effect of bent-shaped dopant molecules on the critical behavior associated with the nematic-smectic-A(d) phase transition has been studied in detail. The transition temperature for the nematic-smectic-A(d) phase sharply decreases as the increase of the mole fraction of the dopant concentration (denoted X for the BC12/9OCB mixture and Y for the BC12/8OCB mixture). The dependence of the critical exponent α on X and Y is well explained in terms of the McMillan ratio. A nearly tricritical exponent has been obtained for the X=0.01 mixture. X=0.02-0.03 mixtures, pure 8OCB, and Y=0.01-0.03 mixtures exhibit nonuniversal behaviors with effective exponents lying between the 3D-XY and tricritical exponents. The heat capacity anomaly for Y=0.05 has been well described with the 3D-XY exponent. The critical amplitude ratio A(-)/A(+) is close to 1 and insensitive to the dopant concentration. No Fisher renormalization of the critical exponent has been observed even for nearly tricritical compositions, which indicates the smallness of the concentration plays a decisive role rather than the steepness of the N-SmA(d) phase boundary.

  20. Calorimetric and computational study of 1,4-dithiacyclohexane 1,1-dioxide (1,4-dithiane sulfone).

    PubMed

    Roux, María Victoria; Temprado, Manuel; Jiménez, Pilar; Notario, Rafael; Guzman-Mejía, Ramón; Juaristi, Eusebio

    2006-03-31

    This work reports the enthalpies of formation in the condensed and gas state of 1,4-dithiacyclohexane 1,1-dioxide (1,4-dithiane sulfone, 5), derived from the enthalpy of combustion in oxygen, measured by a rotating bomb calorimeter and the variation of vapor pressures with temperatures determined by the Knudsen effusion technique. The theoretically estimated enthalpy of formation was calculated from high-level ab initio molecular orbital calculations at the G2(MP2) level. The theoretical calculations appear to be in very good agreement with experiment. A comparison of the conversion of thiane sulfone 3 to 1,3-dithiane sulfone 4 and 1,4-dithiane sulfone 5 clearly shows the 1,3 isomer to be 6.7 kJ mol(-1) less stable, probably owing to diminished electrostatic repulsion between the sulfur heteroatoms in 1,4-sulfone 5. PMID:16555808

  1. Spectrophotometric and Calorimetric Studies of Np(V) Complexation with Sulfate at 10-70oC

    SciTech Connect

    Rao, Linfeng; Tian, Guoxin; Xia, Yuanxian; Friese, Judah I.

    2008-06-16

    Sulfate, one of the inorganic constituents in the groundwater of nuclear waste repository, could affect the migration of radioactive materials by forming complexes. Spectrophotometric and microcalorimetric titrations were performed to identify the Np(V)/sulfate complex and determine the equilibrium constants and enthalpy of complexation at 10-70 C. Results show that the complexation of Np(V) with sulfate is weak but slightly enhanced by the increase in temperature. The complexation is endothermic and becomes more endothermic with the increase in temperature. The enhanced complexation at elevated temperatures is due to the increasingly larger entropy of complexation that exceeds the increase in enthalpy, suggesting that the complexation of Np(V) with sulfate is entropy-driven.

  2. Calorimetric and computational study of 1,3-dithiacyclohexane 1,1-dioxide (1,3-dithiane sulfone).

    PubMed

    Roux, María Victoria; Temprado, Manuel; Jiménez, Pilar; Notario, Rafael; Guzmán-Mejía, Ramón; Juaristi, Eusebio

    2004-03-01

    The enthalpies of combustion and sublimation of 1,3-dithiacyclohexane 1,1-dioxide (1,3-dithiane sulfone) were measured by a rotating-bomb combustion calorimeter and the Knudsen effusion technique, and the gas-phase enthalpy of formation was determined, Delta(f)H(m)*(g) = -326.3 +/- 2.0 kJ mol(-1). Standard ab initio molecular orbital calculations at the G2(MP2) level were performed, and a theoretical study on molecular and electronic structure of the compound has been carried out. Calculated Delta(f)H(m)*(g) values agree very well with the experimental one. These experimental and theoretical studies support the relevance of the repulsive electrostatic interaction between sulfur atoms in 1,3-dithiane sulfone, that apparently counterbalances any n(S) --> rho(C-SO2)* stabilizing hyperconjugative interaction. PMID:14987027

  3. Simultaneous calorimetric and polarization microscopy investigations of light induced changes over phase transitions in a liquid crystal-napthopyran mixture

    NASA Astrophysics Data System (ADS)

    Paoloni, S.; Mercuri, F.; Marinelli, M.; Pizzoferrato, R.; Zammit, U.; Kosa, T.; Sukhomlinova, L.; Taheri, B.

    2015-10-01

    We have studied the specific heat and the thermal conductivity in a 4-(n-octyl)-4'-cyanobiphenyl liquid crystal (LC)-photochromic molecules mixture, before, during, and after the photo-activation of the dispersed photochromic molecules, over both the smectic A-nematic and the nematic-isotropic phase transitions. The evaluation of the specific heat has enabled the determination of the changes of the phase transition characteristics induced by the photochromic molecules photoisomerization, while that of the thermal conductivity could be used to monitor the modifications induced in the average LC molecular orientation. The polarization microscopy imaging of the sample texture constituted a valuable support for the interpretation of the obtained thermal conductivity results.

  4. SU-E-J-39: Comparison of PTV Margins Determined by In-Room Stereoscopic Image Guidance and by On-Board Cone Beam Computed Tomography Technique for Brain Radiotherapy Patients

    SciTech Connect

    Ganesh, T; Paul, S; Munshi, A; Sarkar, B; Krishnankutty, S; Sathya, J; George, S; Jassal, K; Roy, S; Mohanti, B

    2014-06-01

    Purpose: Stereoscopic in room kV image guidance is a faster tool in daily monitoring of patient positioning. Our centre, for the first time in the world, has integrated such a solution from BrainLAB (ExacTrac) with Elekta's volumetric cone beam computed tomography (XVI). Using van Herk's formula, we compared the planning target volume (PTV) margins calculated by both these systems for patients treated with brain radiotherapy. Methods: For a total of 24 patients who received partial or whole brain radiotherapy, verification images were acquired for 524 treatment sessions by XVI and for 334 sessions by ExacTrac out of the total 547 sessions. Systematic and random errors were calculated in cranio-caudal, lateral and antero-posterior directions for both techniques. PTV margins were then determined using van Herk formula. Results: In the cranio-caudal direction, systematic error, random error and the calculated PTV margin were found to be 0.13 cm, 0.12 cm and 0.41 cm with XVI and 0.14 cm, 0.13 cm and 0.44 cm with ExacTrac. The corresponding values in lateral direction were 0.13 cm 0.1 cm and 0.4 cm with XVI and 0.13 cm, 0.12 cm and 0.42 cm with ExacTrac imaging. The same parameters for antero-posterior were for 0.1 cm, 0.11 cm and 0.34 cm with XVI and 0.13 cm, 0.16 cm and 0.43 cm with ExacTrac imaging. The margins estimated with the two imaging modalities were comparable within ± 1 mm limit. Conclusion: Verification of setup errors in the major axes by two independent imaging systems showed the results are comparable and within ± 1 mm. This implies that planar imaging based ExacTrac can yield equal accuracy in setup error determination as the time consuming volumetric imaging which is considered as the gold standard. Accordingly PTV margins estimated by this faster imaging technique can be confidently used in clinical setup.

  5. PREFACE: Sensors & their Applications XVI

    NASA Astrophysics Data System (ADS)

    Kyriacou, Panicos; O'Riordan, Alan

    2011-08-01

    This volume records the Proceedings of the sixteenth conference in the biennial Sensors and Their Applications series which took place at the Clarion Hotel, Cork, Ireland between 12-14 September 2011. The conference is organized by the Instrument Science and Technology Group of the Institute of Physics. On this occasion, the conference was hosted by Tyndall National Institute at University College Cork. This year the conference returns to Ireland, having last been held in Limerick in 2003. The conference proceedings record the continuing growth of the sensors community nationally and internationally. The conferences bring together contributions from scientists and engineers from academia, research institutes and industrial establishments, and therefore provide an excellent opportunity for these communities to present and discuss the latest results in the field of sensors, instrumentation and measurement. Amongst the more traditional themes, such as optical sensing, there is growth in new areas such as biomedical sensing and instrumentation, and nanosensing, which is reflected in this volume. Similarly the contribution of modelling and simulation techniques in sensor and instrumentation design and their applications is acknowledged by a session in this area. The sessions across the conference are supported by notable contributions from invited speakers. We would like to thank all of our colleagues in the sensor and instrumentation community who have supported this event by contributing manuscripts. Our thanks also go to Tyndall National Institute for hosting this conference and all the sponsors who, with their generous financial and in-kind contributions, enabled the better organization of this conference. We would also like to thank all the members of the Instrument Science and Technology Group for their support, and in particular for refereeing the submitted manuscripts. We are also pleased to express our thanks to the Conference Department of the Institute of Physics for their invaluable support in organising this event. We are especially grateful to Dawn Stewart for her responsive and efficient day-to-day handling of this event, as well as to Claire Garland for her planning and management of this event. We hope that the conference authors, participants and a wider audience will find these proceedings to be of interest and to serve as a useful reference text. Panicos KyriacouConference ChairmanAlan O'RiordanConference Local Chairman

  6. Spectrophotometric and Calorimetric Studies of U(VI) Complexation with Sulfate at 25-70oC

    SciTech Connect

    Tian, Guoxin; Rao, Linfeng

    2008-10-30

    Sulfate, one of the inorganic constituents in the groundwater of nuclear waste repository, could affect the migration of radioactive materials by forming complexes. Spectrophotometric and microcalorimetric titrations were performed to identify the U(VI)/sulfate complexes and determine the equilibrium constants and enthalpy of complexation at 25-70 C. Results show that U(VI) forms moderately strong complexes with sulfate, i.e., UO{sub 2}SO{sub 4}(aq) and UO{sub 2}(SO{sub 4}){sub 2}{sup 2-}, in this temperature range and the complexes become stronger as the temperature is increased: 2-fold and 10-fold increases in the stability constants of UO{sub 2}SO{sub 4}(aq) and UO{sub 2}(SO{sub 4}{sub 2}{sup 2-}), respectively, when the temperature is increased from 25 C to 70 C. The complexation is endothermic and entropy-driven, showing typical characteristics of inner-sphere complexation and 'hard acid'/'hard base' interactions. The thermodynamic trends are discussed in terms of dehydration of both the cation (UO{sub 2}{sup 2+}) and the anion (SO{sub 4}{sup 2-}) as well as the effect of temperature on the structure of water.

  7. Thermochemistry of 1,3-dithiacyclohexane 1-oxide (1,3-dithiane sulfoxide): calorimetric and computational study.

    PubMed

    Roux, María Victoria; Temprado, Manuel; Jiménez, Pilar; Dávalos, Juan Z; Notario, Rafael; Martín-Valcárcel, Gloria; Garrido, Leoncio; Guzmán-Mejía, Ramón; Juaristi, Eusebio

    2004-08-01

    The enthalpies of combustion and sublimation of 1,3-dithiacyclohexane 1-oxide (1,3-dithiane sulfoxide, 2) were measured by a rotating-bomb combustion calorimeter and the Knudsen effusion technique, and the gas-phase enthalpy of formation was determined, DeltafH degrees m(g) = -98.0 +/- 1.9 kJ mol(-1). This value is not as large (negative) as could have been expected from comparison with thermochemical data available for the thiane/thiane oxide reference system. High-level ab initio molecular orbital calculations at the MP2(FULL)/6-31G(3df,2p) level were performed, and the optimized molecular and electronic structures of 2 afforded valuable information on (1) the relative conformational energies of 2-axial and 2-equatorial--the latter being 7.1 kJ mol(-1) more stable than 2-axial, (2) the possible involvement of nS --> sigma*(C-S(O)) hyperconjugation in 2-equatorial, (3) the lack of computational evidence for sigma(S-C) --> sigma*(S-O) stereoelectronic interaction in 2-equatorial, and (4) the relevance of a repulsive electrostatic interaction between sulfur atoms in 1,3-dithiane sulfoxide, which apparently counterbalances any nS --> sigma*(C-S(O)) stabilizing hyperconjugative interaction and accounts for the lower than expected enthalpy of formation for sulfoxide 2. PMID:15287796

  8. Entropy-Driven Folding of an RNA Helical Junction: An Isothermal Titration Calorimetric Analysis of the Hammerhead Ribozyme†

    PubMed Central

    Mikulecky, Peter J.; Takach, Jennifer C.; Feig, Andrew L.

    2008-01-01

    Helical junctions are extremely common motifs in naturally occurring RNAs, but little is known about the thermodynamics that drive their folding. Studies of junction folding face several challenges: non-two-state folding behavior, superposition of secondary and tertiary structural energetics, and drastically opposing enthalpic and entropic contributions to folding. Here we describe a thermodynamic dissection of the folding of the hammerhead ribozyme, a three-way RNA helical junction, by using isothermal titration calorimetry of bimolecular RNA constructs. By using this method, we show that tertiary folding of the hammerhead core occurs with a highly unfavorable enthalpy change, and is therefore entropically driven. Furthermore, the enthalpies and heat capacities of core folding are the same whether supported by monovalent or divalent ions. These properties appear to be general to the core sequence of bimolecular hammerhead constructs. We present a model for the ion-induced folding of the hammerhead core that is similar to those advanced for the folding of much larger RNAs, involving ion-induced collapse to a structured, non-native state accompanied by rearrangement of core residues to produce the native fold. In agreement with previous enzymological and structural studies, our thermodynamic data suggest that the hammerhead structure is stabilized in vitro predominantly by diffusely bound ions. Our approach addresses several significant challenges that accompany the study of junction folding, and should prove useful in defining the thermodynamic determinants of stability in these important RNA motifs. PMID:15134461

  9. Isothermal Calorimetric Observations of the Affect of Welding on Compatibility of Stainless Steels with High-Test Hydrogen Peroxide Propellant

    NASA Technical Reports Server (NTRS)

    Gostowski, Rudy C.

    2002-01-01

    Compatibility is determined by the surface area, the chemical constituency and the surface finish of a material. In this investigation exposed area is obviously not a factor as the welded samples had a slightly smaller surface than the unwelded, but were more reactive. The chemical makeup of welded CRES 316L and welded CRES 304L have been observed in the literature to change from the parent material as chromium and iron are segregated in zones. In particular, the ratio of chromium to iron in CRES 316L increased from 0.260 to 0.79 in the heat affected zone (HAZ) of the weld and to 1.52 in the weld bead itself. In CRES 304L the ratio of chromium to iron increased from 0.280 to 0.44 in the HAZ and to 0.33 in the weld bead. It is possible that the increased reactivity of the welded samples and of those welded without purge gas is due to this segregation phenomenon. Likewise the reactivity increased in keeping with the greater roughness of the welded and welded without purge gas samples. Therefore enhanced roughness may also be responsible for the increased reactivity.

  10. Calorimetric studies of solvates of C{sub 60} and C{sub 70} with aromatic solvents

    SciTech Connect

    Korobov, M.V.; Mirakyan, A.L.; Avramenko, N.V.; Olofsson, G.; Smith, A.L.; Ruoff, R.S.

    1999-02-25

    To improve the understanding of the solution properties of C{sub 60} and C{sub 70} in aromatic solvents, binary systems of C{sub 60} and C{sub 70} with benzene, toluene, 1,2- and 1,3-dimethylbenzene, 1,2,4,- and 1,3,5-trimethylbenzene, bromobenzene, and 1,2- and 1,3-dichlorobenzene were studied using differential scanning calorimetry, solution calorimetry, and thermogravimetry. Solid solvates with different compositions were identified in many of the systems. The solvates were characterized by composition and by the temperature and the enthalpy of the incongruent melting transition. Enthalpies of solution of C{sub 60} in toluene, 1,2-dimethylbenzene, 1,2- and 1,3-dichlorobenzene, and 1,2,4-trimethylbenzene and of C{sub 70} in 1,2-dimethylbenzene and in 1,2- and 1,3-dichlorobenzene were determined. The formation-incongruent melting of solid solvates causes maxima in the temperature-solubility curves of fullerenes in aromatic solvents. Trends in solubility behavior of fullerenes were discussed in terms of thermodynamics of solution and solvate formation.

  11. A calorimetric study of energy conversion efficiency of a sonochemical reactor at 500 kHz for organic solvents.

    PubMed

    Toma, Maricela; Fukutomi, Satoshi; Asakura, Yoshiyuki; Koda, Shinobu

    2011-01-01

    It would seem that the economic viability is yet to be established for a great number of sonochemical processes, owning to their perfectible ultrasonic equipments. Industrial scale sonoreactors may become more important as a result of mastering the parameters with influence on their energy balance. This work related the solvent type to the energy efficiency as the first step of a complex study aiming to assess the energy balance of sonochemical reactors at 500 kHz. Quantitative measurements of ultrasonic power for water and 10 pure organic solvents were performed by calorimetry for a cylindrically shaped sonochemical reactor with a bottom mounted vibrating plate. It was found that the ultrasonic power is strongly related to the solvent, the energy conversion for organic liquids is half from that of water and there is a drop in energy efficiency for filling levels up to 250 mm organic solvents. Surface tension, viscosity and vapor pressure influence the energy conversion for organic solvents, but it is difficult explain these findings based on physical properties of solvents alone. The apparent intensity of the atomization process shows a good agreement with the experimentally determined values for energy conversion for water and the solvent group studied here. This study revealed that to attain the same ultrasonic power level, more electrical energy is need for organic solvents as compared to water. The energy balance equation has been defined based on these findings by considering an energy term for atomization. PMID:20655791

  12. Combined Spectroscopic and Calorimetric Studies to Reveal Absorption Mechanisms and Conformational Changes of Protein on Nanoporous Biomaterials

    PubMed Central

    Ahmadi, Saharnaz; Farokhi, Maryam; Padidar, Parisa; Falahati, Mojtaba

    2015-01-01

    In this study the effect of surface modification of mesoporous silica nanoparticles (MSNs) on its adsorption capacities and protein stability after immobilization of beta-lactoglobulin B (BLG-B) was investigated. For this purpose, non-functionalized (KIT-6) and aminopropyl-functionalized cubic Ia3d mesoporous silica ([n-PrNH2-KIT-6]) nanoparticles were used as nanoporous supports. Aminopropyl-functionalized mesoporous nanoparticles exhibited more potential candidates for BLG-B adsorption and minimum BLG leaching than non-functionalized nanoparticles. It was observed that the amount of adsorbed BLG is dependent on the initial BLG concentration for both KIT-6 and [n-PrNH2-KIT-6] mesoporous nanoparticles. Also larger amounts of BLG-B on KIT-6 was immobilized upon raising the temperature of the medium from 4 to 55 °C while such increase was undetectable in the case of immobilization of BLG-B on the [n-PrNH2-KIT-6]. At temperatures above 55 °C the amounts of adsorbed BLG on both studied nanomaterials decreased significantly. By Differential scanning calorimetry or DSC analysis the heterogeneity of the protein solution and increase in Tm may indicate that immobilization of BLG-B onto the modified KIT-6 results in higher thermal stability compared to unmodified one. The obtained results provide several crucial factors in determining the mechanism(s) of protein adsorption and stability on the nanostructured solid supports and the development of engineered nano-biomaterials for controlled drug-delivery systems and biomimetic interfaces for the immobilization of living cells. PMID:26230687

  13. Micro-machined calorimetric biosensors

    DOEpatents

    Doktycz, Mitchel J.; Britton, Jr., Charles L.; Smith, Stephen F.; Oden, Patrick I.; Bryan, William L.; Moore, James A.; Thundat, Thomas G.; Warmack, Robert J.

    2002-01-01

    A method and apparatus are provided for detecting and monitoring micro-volumetric enthalpic changes caused by molecular reactions. Micro-machining techniques are used to create very small thermally isolated masses incorporating temperature-sensitive circuitry. The thermally isolated masses are provided with a molecular layer or coating, and the temperature-sensitive circuitry provides an indication when the molecules of the coating are involved in an enthalpic reaction. The thermally isolated masses may be provided singly or in arrays and, in the latter case, the molecular coatings may differ to provide qualitative and/or quantitative assays of a substance.

  14. Calorimetric study of cationic photopolymerization

    NASA Astrophysics Data System (ADS)

    Czajlik, I.; Hedvig, P.; Ille, A.; Dobó, J.

    1996-03-01

    The photopolymerization of penta-erythritol tetra-glycidyl ether (initiator Degacure KI-85) was studied by a du Pont 910 type DSC. From our experimental results the following conclusions can be drawn: (1) During the cationic polymerization reaction the lifetime of the initiating centers are long compared to the lifetime of free radicals in case of radical polymerization. (2) The rate of deactivation of the initiating centers increases with increasing temperature.

  15. Silicon photomultipliers in calorimetric applications

    NASA Astrophysics Data System (ADS)

    Berra, A.; Bolognini, D.; Bonvicini, V.; Cauz, D.; Driutti, A.; Hasan, S.; Iugovaz, D.; Lietti, D.; Mascagna, Y.; Mattera, A.; Pauletta, G.; Penzo, A.; Prest, M.; Rashevskaya, I.; Reia, S.; Scarpino, F.; Vallazza, E.

    2010-04-01

    In recent years Silicon Photomultipliers (SiPMs) have been proposed as a new type of readout system for scintillating detectors in many experiments. SiPMs consist of a matrix of parallel-connected silicon micro-pixels, which are independent photon counters working in limited Geiger mode with very high gain (~106). This contribution presents the use of an array of SiPMs (manufactured by FBK-irst) for the readout of a shashlik calorimeter composed by lead and scintillator tiles for a total of ~23 X0; the scintillator light is carried out by 64 WLS fibers (4 fibers per SiPM). The performances of the calorimeter in terms of linearity and energy resolution have been tested in a beam test with charged particles (e±, muons and pions) with a momentum up to 6 GeV/c at the CERN PS T10 line.

  16. Steps Toward Determination of the Size and Structure of the Broad-Line Region in Active Galactic Nuclei XVI: A 13 Year Study of Spectral Variability in NGC 5548

    NASA Technical Reports Server (NTRS)

    Peterson, B. M.; Berlind, P.; Bertram, R.; Bischoff, K.; Bochkarev, N. G.; Burenkov, A. N.; Calkins, M.; Carrasco, L.; Chavushyan, V. H.

    2002-01-01

    We present the final installment of an intensive 13 year study of variations of the optical continuum and broad H beta emission line in the Seyfert 1 galaxy NGC 5548. The database consists of 1530 optical continuum measurements and 1248 H beta measurements. The H beta variations follow the continuum variations closely, with a typical time delay of about 20 days. However, a year-by-year analysis shows that the magnitude of emission-line time delay is correlated with the mean continuum flux. We argue that the data are consistent with the simple model prediction between the size of the broad-line region and the ionizing luminosity, r is proportional to L(sup 1/2)(sub ion). Moreover, the apparently linear nature of the correlation between the H beta response time and the nonstellar optical continuum F(sub opt) arises as a consequence of the changing shape of the continuum as it varies, specifically F(sub opt) is proportional to F(sup 0.56)(sub UV).

  17. Surfactant loss control in chemical flooding: Spectroscopic and calorimetric study of adsorption and precipitation on reservoir minerals. Quarterly technical progress report, January 1, 1993--March 31, 1993

    SciTech Connect

    Somasundaran, P.

    1993-05-01

    The aim of this project is to elucidate the mechanisms of adsorption and surface precipitation of flooding surfactants on reservoir minerals. Effect of surfactant structure, surfactant combinations and other inorganic and polymeric species will be determined using solids of relevant mineralogy. A multi-pronged approach consisting of micro & nano spectroscopy, microcalorimetry, electrokinetics, surface tension and wettability win be used to achieve the goals. The results of this study should help in controlling surfactant loss in chemical flooding and also in developing optimum structures and conditions for efficient chemical flooding processes. Adsorption of selected individual surfactants on oxide minerals was studied. The aim was to determine the effect of structure on surfactant adsorption at the solid-liquid as well as at the liquid-air interface. Nonionic polyethoxylated alkyl phenols and anionic meta xylene sulfonates (MXS) were the surfactants studied. Electrokinetic behavior was also determined along with adsorption in order to determine the role of electrostatic forces in determining the adsorption. In addition, the effect of varying the number of ethylene oxide groups on the adsorption of polyethoxylated alkyl phenols on silica was determined since the ethoxyl groups offer unique opportunities to control adsorption as well as wettability. Effect of pH was studied both because it is a parameter with first order effect and also because pH effects can help in developing mechanisms.

  18. State of water at 136 K determined by its relaxation time.

    PubMed

    Johari, G P

    2005-03-21

    Dielectric relaxation time of pure bulk water has been determined from the dielectric loss tangent scans against temperature at two frequencies. After calculating the frequency-independent background loss, the relaxation loss was obtained, and the relaxation time determined. The dielectric relaxation time of water is 35 +/- 13 s at 136 +/- 1 K, which is comparable with its structural relaxation time of ca. 33 s estimated from its T(g) endotherm (G. P. Johari, A. Hallbrucker and E. Mayer, Nature, 1987, 330, 552). Therefore, water is an ultraviscous liquid at 136 K, and this removes the basis for a comparison-based inference that water is a rigid glass up to a temperature of 165 K or higher (Y. Yue and C. A. Angell, Nature, 2004, 427, 717). The method yields satisfactory values for the relaxation time of stable glasses at their known calorimetric T(g). PMID:19791317

  19. First stars. XVI. HST/STIS abundances of heavy elements in the uranium-rich metal-poor star CS 31082-001

    NASA Astrophysics Data System (ADS)

    Siqueira Mello, C.; Spite, M.; Barbuy, B.; Spite, F.; Caffau, E.; Hill, V.; Wanajo, S.; Primas, F.; Plez, B.; Cayrel, R.; Andersen, J.; Nordström, B.; Sneden, C.; Beers, T. C.; Bonifacio, P.; François, P.; Molaro, P.

    2013-02-01

    Context. The origin and site(s) of the r-process nucleosynthesis is(are) still not known with certainty, but complete, detailed r-element abundances offer our best clues. The few extremely metal-poor (EMP) stars with large r-element excesses allow us to study the r-process signatures in great detail, with minimal interference from later stages of Galactic evolution. CS 31082-001 is an outstanding example of the information that can be gathered from these exceptional stars. Aims: Here we aim to complement our previous abundance determinations for third-peak r-process elements with new and improved results for elements of the first and second r-process peaks from near-UV HST/STIS and optical UVES spectra. These results should provide new insight into the nucleosynthesis of the elements beyond iron. Methods: The spectra were analyzed by a consistent approach based on an OSMARCS LTE model atmosphere and the Turbospectrum spectrum synthesis code to derive abundances of heavy elements in CS 31082-001, and using updated oscillator strengths from the recent literature. Synthetic spectra were computed for all lines of the elements of interest to check for proper line intensities and possible blends in these crowded spectra. Our new abundances were combined with the best previous results to provide reliable mean abundances for the first and second-peak r-process elements. Results: We present new abundances for 23 neutron-capture elements, 6 of which - Ge, Mo, Lu, Ta, W, and Re - have not been reported before. This makes CS 31082-001 the most completely studied r-II star, with abundances for a total of 37 neutron-capture elements. We also present the first NLTE+3D abundance of lead in this star, further constraining the nature of the r-process. Based on observations made with the NASA/ESA Hubble Space Telescope (HST) through the Space Telescope Science Institute, operated by the Association of Universities for Research in Astronomy, Inc., under NASA contract NAS5-26555; and

  20. A calorimetric and spectroscopic comparison of the effects of cholesterol and its sulfur-containing analogs thiocholesterol and cholesterol sulfate on the thermotropic phase behavior and organization of dipalmitoylphosphatidylcholine bilayer membranes.

    PubMed

    Benesch, Matthew G K; Lewis, Ruthven N A H; McElhaney, Ronald N

    2016-02-01

    We performed differential scanning calorimetric (DSC) and Fourier transform infrared (FTIR) spectroscopic studies of the effects of cholesterol (Chol), thiocholesterol (tChol) and cholesterol sulfate (CholS) on the thermotropic phase behavior and organization of dipalmitoylphosphatidylcholine (DPPC) bilayer membranes. Our DSC results indicate that Chol and tChol incorporation produce small temperature increases in the main phase transition broad component while CholS markedly decreases it, but Chol decreases cooperativity and enthalpy more strongly than CholS and especially tChol. Hence, Chol and tChol thermally stabilize fluid DPPC bilayer sterol-rich domains while CholS markedly destabilizes them, and CholS and particularly tChol are less miscible in such domains. Our FTIR spectroscopic results indicate that Chol incorporation increases the rotational conformational order of fluid DPPC bilayers to a slightly and somewhat greater degree than tChol and CholS, respectively, consistent with our DSC findings. Also, Chol and CholS produce comparable degrees of H-bonding (hydration) of the DPPC ester carbonyls in fluid bilayers, whereas tChol increases H-bonding. At low temperatures, Chol is fully soluble in gel-state DPPC bilayers, whereas tChol and CholS are not. Thus tChol and CholS incorporation can produce considerably different effects on DPPC bilayers. In particular, the tChol thiol group markedly reduces its lateral miscibility and increases DPPC carbonyl H-bonding without significantly affecting the other characteristic effects of Chol itself, while the CholS sulfate group significantly reduces its ability to thermally stabilize and order fluid DPPC membranes. This latter result suggests that the molecular basis for the purported ability of CholS to "stabilize" various biological membranes should be re-examined.

  1. Characterizing the secondary hydration shell on hydrated myoglobin, hemoglobin, and lysozyme powders by its vitrification behavior on cooling and its calorimetric glass-->liquid transition and crystallization behavior on reheating.

    PubMed Central

    Sartor, G; Hallbrucker, A; Mayer, E

    1995-01-01

    For hydrated metmyoglobin, methemoglobin, and lysozyme powders, the freezable water fraction of between approximately 0.3-0.4 g water/g protein up to approximately 0.7-0.8 g water/g protein has been fully vitrified by cooling at rates up to approximately 1500 K min-1 and the influence of cooling rate characterized by x-ray diffractograms. This vitreous but freezable water fraction started to crystallize at approximately 210 K to cubic ice and at approximately 240 K to hexagonal ice. Measurements by differential scanning calorimetry have shown that this vitreous but freezable water fraction undergoes, on reheating at a rate of 30 K min-1, a glass-->liquid transition with an onset temperature of between approximately 164 and approximately 174 K, with a width of between approximately 9 and approximately 16 degrees and an increase in heat capacity of between approximately 20 and approximately 40 J K-1 (mol of freezable water)-1 but that the glass transition disappears upon crystallization of the freezable water. These calorimetric features are similar to those of water imbibed in the pores of a synthetic hydrogel but very different from those of glassy bulk water. The difference to glassy bulk water's properties is attributed to hydrophilic interaction and H-bonding of the macromolecules' segments with the freezable water fraction, which thereby becomes dynamically modified. Abrupt increase in minimal or critical cooling rate necessary for complete vitrification is observed at approximately 0.7-0.8 g water/g protein, which is attributed to an abrupt increase of water's mobility, and it is remarkably close to the threshold value of water's mobility on a hydrated protein reported by Kimmich et al. (1990, Biophys. J. 58:1183). The hydration level of approximately 0.7-0.8 g water/g protein is approximately that necessary for completing the secondary hydration shell. PMID:8599674

  2. Numerical Modeling and Experimental Validation by Calorimetric Detection of Energetic Materials Using Thermal Bimorph Microcantilever Array: A Case Study on Sensing Vapors of Volatile Organic Compounds (VOCs).

    PubMed

    Kang, Seok-Won; Fragala, Joe; Banerjee, Debjyoti

    2015-01-01

    Bi-layer (Au-Si₃N₄) microcantilevers fabricated in an array were used to detect vapors of energetic materials such as explosives under ambient conditions. The changes in the bending response of each thermal bimorph (i.e., microcantilever) with changes in actuation currents were experimentally monitored by measuring the angle of the reflected ray from a laser source used to illuminate the gold nanocoating on the surface of silicon nitride microcantilevers in the absence and presence of a designated combustible species. Experiments were performed to determine the signature response of this nano-calorimeter platform for each explosive material considered for this study. Numerical modeling was performed to predict the bending response of the microcantilevers for various explosive materials, species concentrations, and actuation currents. The experimental validation of the numerical predictions demonstrated that in the presence of different explosive or combustible materials, the microcantilevers exhibited unique trends in their bending responses with increasing values of the actuation current. PMID:26334276

  3. Role of an invariant lysine residue in folate binding on Escherichia coli thymidylate synthase: calorimetric and crystallographic analysis of the K48Q mutant

    PubMed Central

    Arvizu-Flores, Aldo A.; Sugich-Miranda, Rocio; Arreola, Rodrigo; Garcia-Orozco, Karina D.; Velazquez-Contreras, Enrique F.; Montfort, William R.; Maley, Frank; Sotelo-Mundo, Rogerio R.

    2008-01-01

    Thymidylate synthase (TS) catalyzes the reductive methylation of deoxyuridine monophosphate (dUMP) using methylene tetrahydrofolate (CH2THF) as cofactor, the glutamate tail of which forms a water-mediated hydrogen-bond with an invariant lysine residue of this enzyme. To understand the role of this interaction, we studied the K48Q mutant of Escherichia coli TS using structural and biophysical methods. The kcat of the K48Q mutant was 430 fold lower than wild-type TS in activity, while the the Km for the (R)-stereoisomer of CH2THF was 300 µM, about 30 fold larger than Km from the wild-type TS. Affinity constants were determined using isothermal titration calorimetry, which showed that binding was reduced by one order of magnitude for folate-like TS inhibitors, such as propargyl-dideaza folate (PDDF) or compounds that distort the TS active site like BW1843U89 (U89). The crystal structure of the K48Q-dUMP complex revealed that dUMP binding is not impaired in the mutamt, and that U89 in a ternary complex of K48Q-nucleotide-U89 was bound in the active site with subtle differences relative to comparable wild type complexes. PDDF failed to form ternary complexes with K48Q and dUMP. Thermodynamic data correlated with the structural determinations, since PDDF binding was dominated by enthalpic effects while U89 had an important entropic component. In conclusion, K48 is critical for catalysis since it leads to a productive CH2THF binding, while mutation at this residue does not affect much the binding of inhibitors that do not make contact with this group. PMID:18403248

  4. Effect of temperature on the protonation of N-(2-hydroxyethyl)ethylenediamine-N,N',N'-triacetic acid in aqueous solutions: Potentiometric and calorimetric studies

    SciTech Connect

    Li, Xingliang; Zhang, Zhicheng; Endrizzi, Francesco; Martin, Leigh R.; Luo, Shunzhong; Rao, Linfeng

    2015-06-01

    The TALSPEAK process (Trivalent Actinide Lanthanide Separations by Phosphorus-reagent Extraction from Aqueous Komplexes) has been demonstrated in several pilot-scale operations to be effective at separating trivalent actinides (An3+) from trivalent lanthanides (Ln3+). However, fundamental studies have revealed undesired aspects of TALSPEAK, such as the significant partitioning of Na+, lactic acid, and water into the organic phase, thermodynamically unpredictable pH dependence, and the slow extraction kinetics. In the modified TALSPEAK process, the combination of the aqueous holdback complexant HEDTA (N-(2-hydroxyethyl)ethylenediamine-N,N',N'-triacetic acid) with the extractant HEH[EHP] (2-ethyl(hexyl) phosphonic acid mono-2-ethylhexyl ester) in the organic phase has been found to exhibit a nearly flat pH dependence between 2.5 and 4.5 and more rapid phase transfer kinetics for the heavier lanthanides. To help understand the speciation of Ln3+ and An3+ in the modified TALSPEAK, systematic studies are underway on the thermodynamics of major reactions in the HEDTA system under conditions relevant to the process (e.g., higher temperatures). Thermodynamics of the protonation and complexation of HEDTA with Ln3+ were studied at variable temperatures. Equilibrium constants and enthalpies were determined by a combination of techniques including potentiometry and calorimetry. This paper presents the protonation constants of HEDTA at T = (25 to 70) °C. The potentiometric titrations have demonstrated that, stepwise, the first two protonation constants decrease and the third one slightly increases with the increase of temperature. This trend is in good agreement with the enthalpy of protonation directly determined by calorimetry. The results of NMR analysis further confirm that the first two protonation reactions occur on the diamine nitrogen atoms, while the third protonation reaction occurs on the oxygen of a

  5. Surfactant loss control in chemical flooding: Spectroscopic and calorimetric study of adsorption and precipitation on reservoir minerals. Annual report, September 30, 1992--September 30, 1993

    SciTech Connect

    Somasundaran, P.

    1994-07-01

    The aim of this research project is to investigate mechanisms underlying adsorption and surface precipitation of flooding surfactants on reservoir minerals. Effects of surfactant structure, surfactant combinations, various inorganic and polymeric species, and solids mineralogy will be determined. A multi-pronged approach consisting of micro & nano spectroscopy, microcalorimetry, electrokinetics, surface tension and wettability; is used in this study. The results obtained should help in controlling surfactant loss in chemical flooding and in developing optimum structures and conditions for efficient chemical flooding processes. During the first year of this three year contract, adsorption of single surfactants and select surfactant mixtures was studied at the solid-liquid and gas-liquid interfaces. Surfactants studied include alkyl xylene sulfonates, polyethoxylated alkyl phenols, octaethylene glycol mono n-decyl ether, and tetradecyl trimethyl ammonium chloride. Adsorption of surfactant mixtures of varying composition was also investigated. The microstructure of the adsorbed layer was characterized using fluorescence spectroscopy. Changes interfacial properties such as wettability, electrokinetics and stability of reservoir minerals were correlated with the amount of reagent adsorbed. Strong effects of the structure of the surfactant and position of functional groups were revealed.

  6. Surfactant loss control in chemical flooding spectroscopic and calorimetric study of adsorption and precipitation on reservoir minerals. Annual report, September 30, 1992--September 30 1995

    SciTech Connect

    Casteel, J.

    1996-07-01

    The aim of this research project was to investigate mechanisms governing adsorption and surface precipitation of flooding surfactants on reservoir minerals. Effects of surfactant structure, surfactant combinations, various inorganic and polymeric species, and solids mineralogy have been determined. A multi-pronged approach consisting of micro & nano spectroscopy, electrokinetics, surface tension and wettability is used in this study. The results obtained should help in controlling surfactant loss in chemical flooding and in developing optimum structures and conditions for efficient chemical flooding processes. During the three years contract period, adsorption of single surfactants and select surfactant mixtures was studied at the solid-liquid and gas-liquid interfaces. Alkyl xylene sulfonates, polyethoxylated alkyl phenols, octaethylene glycol mono n-decyl ether, and tetradecyl trimethyl ammonium chloride were the surfactants studied. Adsorption of surfactant mixtures of varying composition was also investigated. The microstructure of the adsorbed layer was characterized using fluorescence spectroscopy. Changes in interfacial properties such as wettability, electrokinetics and stability of reservoir minerals were correlated with the amounts of reagent adsorbed. Strong effects of the structure of the surfactant and position of functional groups were revealed. Changes of microstructure upon dilution (desorption) were also studied. Presence of the nonionic surfactants in mixed aggregate leads to shielding of the charge of ionic surfactants which in turn promotes aggregation but reduced electrostatic attraction between the charged surfactant and the mineral surface. Strong consequences of surfactant interactions in solution on adsorption as well as correlations between monomer concentration in mixtures and adsorption were revealed.

  7. Biophysical studies on the interactions of a classic mitochondrial uncoupler with bovine serum albumin by spectroscopic, isothermal titration calorimetric and molecular modeling methods.

    PubMed

    Zhang, Yue; Li, Jia-Han; Ge, Yu-Shu; Liu, Xiao-Rong; Jiang, Feng-Lei; Liu, Yi

    2011-03-01

    The interaction between a classic uncoupler (2,4-dinitrophenol, DNP) and bovine serum albumin (BSA) was investigated by fluorescence spectroscopy under the physiological conditions. The fluorescence quenching constants were calculated by the Stern-Volmer equation, and based upon the temperature dependence of quenching constants, it was proved that DNP caused a static quenching of the intrinsic fluorescence of BSA. Owing to the static quenching mechanism, different associative binding constants at various temperatures were determined and thus the thermodynamic parameters, namely enthalpy (ΔH=-21.12 kJ mol(-1)) and entropy changes (ΔS=23.51 J mol(-1) K(-1)) could be calculated based on the binding constants. Moreover, the enthalpy and entropy changes are consistent with the "Enthalpy-Entropy Compensation" equation obtained from our previous work. The negative enthalpy and positive entropy indicated that the electrostatic interactions played a major role in DNP-BSA binding process. Site marker competitive displacement experiments were carried out by using fluorescence and isothermal titration calorimetry (ITC) methods. These results showed that DNP bound with high affinity to Sudlow's site I (subdomain IIA) of BSA. The distance (r=3.78 nm) between donor (BSA) and acceptor (DNP) was obtained according to the mechanism of fluorescence resonance energy transfer (FRET). Furthermore, the results of synchronous fluorescence and circular dichroism (CD) spectroscopic studies indicated that the microenvironment and the secondary conformation of BSA were altered. The above results were supported by theoretical molecular modeling methods.

  8. Numerical Modeling and Experimental Validation by Calorimetric Detection of Energetic Materials Using Thermal Bimorph Microcantilever Array: A Case Study on Sensing Vapors of Volatile Organic Compounds (VOCs)

    PubMed Central

    Kang, Seok-Won; Fragala, Joe; Banerjee, Debjyoti

    2015-01-01

    Bi-layer (Au-Si3N4) microcantilevers fabricated in an array were used to detect vapors of energetic materials such as explosives under ambient conditions. The changes in the bending response of each thermal bimorph (i.e., microcantilever) with changes in actuation currents were experimentally monitored by measuring the angle of the reflected ray from a laser source used to illuminate the gold nanocoating on the surface of silicon nitride microcantilevers in the absence and presence of a designated combustible species. Experiments were performed to determine the signature response of this nano-calorimeter platform for each explosive material considered for this study. Numerical modeling was performed to predict the bending response of the microcantilevers for various explosive materials, species concentrations, and actuation currents. The experimental validation of the numerical predictions demonstrated that in the presence of different explosive or combustible materials, the microcantilevers exhibited unique trends in their bending responses with increasing values of the actuation current. PMID:26334276

  9. Structural and calorimetric studies demonstrate that the hepatocyte nuclear factor 1β (HNF1β) transcription factor is imported into the nucleus via a monopartite NLS sequence.

    PubMed

    Wiedmann, Mareike M; Aibara, Shintaro; Spring, David R; Stewart, Murray; Brenton, James D

    2016-09-01

    The transcription factor hepatocyte nuclear factor 1β (HNF1β) is ubiquitously overexpressed in ovarian clear cell carcinoma (CCC) and is a potential therapeutic target. To explore potential approaches that block HNF1β transcription we have identified and characterised extensively the nuclear localisation signal (NLS) for HNF1β and its interactions with the nuclear protein import receptor, Importin-α. Pull-down assays demonstrated that the DNA binding domain of HNF1β interacted with a spectrum of Importin-α isoforms and deletion constructs tagged with eGFP confirmed that the HNF1β (229)KKMRRNR(235) sequence was essential for nuclear localisation. We further characterised the interaction between the NLS and Importin-α using complementary biophysical techniques and have determined the 2.4Å resolution crystal structure of the HNF1β NLS peptide bound to Importin-α. The functional, biochemical, and structural characterisation of the nuclear localisation signal present on HNF1β and its interaction with the nuclear import protein Importin-α provide the basis for the development of compounds targeting transcription factor HNF1β via its nuclear import pathway.

  10. Structural and Calorimetric Studies Demonstrate that Xeroderma Pigmentosum Type G (XPG) Can Be Imported to the Nucleus by a Classical Nuclear Import Pathway via a Monopartite NLS Sequence.

    PubMed

    Barros, Andrea C de; Takeda, Agnes A S; Dreyer, Thiago R; Velazquez-Campoy, Adrian; Kobe, Bostjan; Fontes, Marcos R M

    2016-05-22

    Xeroderma pigmentosum type G (XPG) proteins are involved in DNA lesion recognition and promotion of nucleotide excision repair. Specific mutations in these proteins may lead to Cockayne syndrome, in which the patients may display severe developmental retardation and neurological abnormalities. No structural information is available for their spacer region or the C-terminal domain, which are important, respectively, for specific nucleotide excision repair activity and substrate specificity, as well as nuclear translocation. Immunofluorescence studies suggested two specific regions of the XPG C-terminus as potential bipartite nuclear localization sequences, which would be responsible for its translocation to the nucleus by the classical nuclear import pathway mediated by the importin-α (Impα). Thus, in order to test these hypotheses and gain insight into the structural basis for the nuclear import process for the XPG protein, we solved the crystal structures of complexes formed by the Impα and peptides corresponding to both putative nuclear localization signal (NLS) sequences (XPG1 and XPG2) and performed isothermal titration calorimetry assays to determine their binding affinities. Structural experiments confirm the binding of both NLS peptides to Impα but, unexpectedly, they bind to the receptor as monopartite NLSs. The isothermal titration calorimetry assays demonstrated that XPG1 and XPG2 peptides bind to two separate binding sites, but with high affinity to the major NLS-binding site of the Impα, resembling classical monopartite SV40 TAg NLS. The results lead to insights about what distinguishes monopartite and bipartite NLSs, as well as the differential roles of XPG1 and XPG2 NLSs in the nuclear localization of XPG.

  11. Determination of plutonium isotopic composition by gamma-ray spectroscopy

    SciTech Connect

    Sampson, T.E.; Hsue, S.T.; Parker, J.L.; Johnson, S.S.; Bowersox, D.F.

    1981-01-01

    We discuss the general approach, computerized data analysis methods, and results of measurements used to determine the isotopic composition of plutonium by gamma-ray spectroscopy. The simple techniques are designed to be applicable to samples of arbitrary size, geometry, age, chemical, and isotopic composition. The combination of the gamma spectroscopic measurement of isotopic composition coupled with calorimetric measurement of total sample power is shown to give a totally nondestructive determination of sample plutonium mass with a precision of 0.6% for 1000-g samples of PuO/sub 2/ with 12% /sup 240/Pu content. The precision of isotopic measurements depends upon many factors, including sample size, sample geometry, and isotopic content. Typical ranges are found to be /sup 238/Pu, 1 to 10%; /sup 239/Pu, 0.1 to 0.5%; /sup 240/Pu, 2 to 5%; /sup 241/Pu, 0.3 to 0.7%; /sup 242/Pu (determined by isotopic correlation); and /sup 241/Am, 0.2 to 10%.

  12. A calorimetric study on the low temperature dynamics of doped ice V and its reversible phase transition to hydrogen ordered ice XIII.

    PubMed

    Salzmann, Christoph G; Radaelli, Paolo G; Finney, John L; Mayer, Erwin

    2008-11-01

    Doped ice V samples made from solutions containing 0.01 M HCl (DCl), HF (DF), or KOH (KOD) in H(2)O (D(2)O) were slow-cooled from 250 to 77 K at 0.5 GPa. The effect of the dopant on the hydrogen disorder --> order transition and formation of hydrogen ordered ice XIII was studied by differential scanning calorimetry (DSC) with samples recovered at 77 K. DSC scans of acid-doped samples are consistent with a reversible ice XIII <--> ice V phase transition at ambient pressure, showing an endothermic peak on heating due to the hydrogen ordered ice XIII --> disordered ice V phase transition, and an exothermic peak on subsequent cooling due to the ice V --> ice XIII phase transition. The equilibrium temperature (T(o)) for the ice V <--> ice XIII phase transition is 112 K for both HCl doped H(2)O and DCl doped D(2)O. From the maximal enthalpy change of 250 J mol(-1) on the ice XIII --> ice V phase transition and T(o) of 112 K, the change in configurational entropy for the ice XIII --> ice V transition is calculated as 2.23 J mol(-1) K(-1) which is 66% of the Pauling entropy. For HCl, the most effective dopant, the influence of HCl concentration on the formation of ice XIII was determined: on decreasing the concentration of HCl from 0.01 to 0.001 M, its effectiveness is only slightly lowered. However, further HCl decrease to 0.0001 M drastically lowered its effectiveness. HF (DF) doping is less effective in inducing formation of ice XIII than HCl (DCl) doping. On heating at a rate of 5 K min(-1), kinetic unfreezing starts in pure ice V at approximately 132 K, whereas in acid doped ice XIII it starts at about 105 K due to acceleration of reorientation of water molecules. KOH doping does not lead to formation of hydrogen ordered ice XIII, a result which is consistent with our powder neutron diffraction study (C. G. Salzmann, P. G. Radaelli, A. Hallbrucker, E. Mayer, J. L. Finney, Science, 2006, 311, 1758). We further conjecture whether or not ice XIII has a stable region in

  13. Nanobridge SQUIDs as calorimetric inductive particle detectors

    NASA Astrophysics Data System (ADS)

    Gallop, John; Cox, David; Hao, Ling

    2015-08-01

    Superconducting transition edge sensors (TESs) have made dramatic progress since their invention some 65 years ago (Andrews et al 1949 Phys. Rev. 76 154-155 Irwin and Hilton 2005 Topics Appl. Phys. 99 63-149) until now there are major imaging arrays of TESs with as many as 7588 separate sensors. These are extensively used by astronomers for some ground-breaking observations (Hattori et al 2013 Nucl. Instrum. Methods Phys. Res. A 732 299-302). The great success of TES systems has tended to overshadow other superconducting sensor developments. However there are other types (Sobolewski et al 2003 IEEE Trans. Appl. Supercond. 13 1151-7 Hadfield 2009 Nat. Photonics 3 696-705) which are discussed in papers within this special edition of the journal. Here we describe a quite different type of detector, also applicable to single photon detection but possessing possible advantages (higher sensitivity, higher operating temperature) over the conventional TES, at least for single detectors.

  14. Calorimetric and computational study of indanones.

    PubMed

    Matos, M Agostinha R; Miranda, Margarida S; Monte, Manuel J S; Santos, Luís M N B F; Morais, Victor M F; Chickos, James S; Umnahanant, Patamaporn; Liebman, Joel F

    2007-11-01

    Condensed phase standard (p degrees = 0.1 MPa) molar enthalpies of formation for 1-indanone, 2-indanone, and 1,3-indandione were derived from the standard molar enthalpies of combustion, in oxygen, at T = 298.15 K, measured by static bomb combustion calorimetry. The standard molar enthalpies of sublimation for 1-indanone and 2-indanone, at T = 298.15 K, were measured both by correlation-gas chromatography and by Calvet microcalorimetry leading to a mean value for each compound. For 1,3-indandione, the standard molar enthalpy of sublimation was derived from the vapor pressure dependence on temperature. The following enthalpies of formation in gas phase, at T = 298.15 K, were then derived: 1-indanone, -64.0 +/- 3.8 kJ mol(-1); 2-indanone, -56.6 +/- 4.8 kJ mol(-1); 1,3-indandione, -165.0 +/- 2.6 kJ mol(-1). The vaporization and fusion enthalpies of the indanones studied are also reported. In addition, theoretical calculations using the density functional theory with the B3LYP and MPW1B95 energy functionals and the 6-311G** and cc-pVTZ basis sets have been performed for these molecules and the corresponding one-ring species to obtain the most stable geometries and to access their energetic stabilities. PMID:17929782

  15. The CDF level 2 calorimetric trigger upgrade

    SciTech Connect

    Bhatti, A.; Canepa, A.; Casarsa, M.; Convery, M.; Cortiana, G.; Dell'Orso, M.; Donati, S.; Flanagan, G.; Frisch, H.; Fukun, T.; Krop, D.; /Chicago U., EFI /INFN, Pisa /Pisa U. /Pisa, Scuola Normale Superiore

    2009-01-01

    CDF II upgraded the calorimeter trigger to cope with the higher detector occupancy due to the increased Tevatron instantaneous luminosity ({approx} 2.8 x 10{sup 32} cm{sup -2} s{sup -1}). While the original system was implemented in custom hardware and provided to the L2 trigger a limited-quality jet clustering performed using a reduced resolution measurement of the transverse energy in the calorimeter trigger towers, the upgraded system provides offline-quality jet reconstruction of the full resolution calorimeter data. This allows to keep better under control the dependence of the trigger rates on the instantaneous luminosity and to improve the efficiency and purity of the trigger selections. The upgraded calorimeter trigger uses the general purpose VME board Pulsar, developed at CDF II and already widely used to upgrade the L2 tracking and L2 decision systems. A battery of Pulsars is used to merge and send the calorimeter data to the L2 CPUs, where software-implemented algorithms perform offline-like clustering. In this paper we review the design and the performance of the upgraded system.

  16. Calorimetric measurement of energy of ultrasonic cleaners

    SciTech Connect

    Harding, W.B.

    1994-11-01

    The development of a calorimeter that measured the power within an ultrasonic cleaning tank is presented. The principle involved is explained. Several types of calorimeter that were tested are described. Measurement of the power in an ultrasonic cleaner permits: (1) comparing different ultrasonic cleaners; (2) monitoring the performance of a specific cleaner; (3) measuring the distribution of power in a cleaning tank, and (4) evaluating the effects of process variables on the power.

  17. Use of flow calorimetry for determining enthalpies of absorption and the solubility of CO{sub 2} in aqueous monoethanolamine solutions

    SciTech Connect

    Mathonat, C.; Majer, V.; Grolier, J.P.E.

    1998-10-01

    A flow mixing unit adapted to a Setaram C-80 calorimeter was used for measuring enthalpies of absorption of carbon dioxide in a 30 wt% aqueous solution of monoethanolamine (MEA) at three temperatures (313.15, 353.15, and 393.15 K) and three pressures (2.0, 5.0, and 10.0 MPa). Determinations were performed both in the region where the gas is fully absorbed in the solvent and also in the region of concentrations above the saturation. Experimental data served to obtain the integral enthalpies of absorption and for indirect determination of solubility limits. Where comparison was possible, the presented results derived from calorimetric determinations were in reasonable agreement with those obtained from phase equilibria measurements.

  18. Inhibition of beta-amylase activity by calcium, magnesium and zinc ions determined by spectrophotometry and isothermal titration calorimetry.

    PubMed

    Dahot, M Umar; Saboury, A A; Moosavi-Movahedi, A A

    2004-04-01

    The inhibition effect of metal ions on beta amylase activity was studied. The inhibitor-binding constant (Ki) was determined by spectrophotometric and isothermal titration calorimetric (ITC) methods. The binding of calcium, magnesium and zinc ion as inhibitors at the active site of barley beta amylase was studied at pH = 4.8 (sodium acetate 16 mM) and T = 300K. The Ki and enthalpy of binding for calcium (13.4, 13.1 mM and -14.3 kJ/mol), magnesium (18.6, 17.8mM and -17.7 kJ/mol) and zinc (17.5, 17.7 mM and -20.0 kJ/mol) were found by spectrophotometric and ITC methods respectively.

  19. An oxygen flow calorimeter for determining the heating value of kilogram size samples of municipal solid waste

    NASA Astrophysics Data System (ADS)

    Domalski, E. S.; Churney, K. L.; Ledford, A. E.; Ryan, R. V.; Reilly, M. L.

    1982-02-01

    A calorimeter to determine the enthalpies of combustion of kilogram size samples of minimally processed municipal solid municipal waste (MSW) in flowing oxygen near atmospheric pressure is discussed. The organic fraction of 25 gram pellets of highly processed MSW was burned in pure oxygen to CO2 and H2O in a small prototype calorimeter. The carbon content of the ash and the uncertainty in the amount of CO in the combustion products contribute calorimetric errors of 0.1 percent or less to the enthalpy of combustion. Large pellets of relatively unprocessed MSW have been successfully burned in a prototype kilogram size combustor at a rate of 15 minutes per kilogram with CO/CO2 ratios not greater than 0.1 percent. The design of the kilogram size calorimeter was completed and construction was begun.

  20. Stochastic determination of matrix determinants.

    PubMed

    Dorn, Sebastian; Ensslin, Torsten A

    2015-07-01

    Matrix determinants play an important role in data analysis, in particular when Gaussian processes are involved. Due to currently exploding data volumes, linear operations-matrices-acting on the data are often not accessible directly but are only represented indirectly in form of a computer routine. Such a routine implements the transformation a data vector undergoes under matrix multiplication. While efficient probing routines to estimate a matrix's diagonal or trace, based solely on such computationally affordable matrix-vector multiplications, are well known and frequently used in signal inference, there is no stochastic estimate for its determinant. We introduce a probing method for the logarithm of a determinant of a linear operator. Our method rests upon a reformulation of the log-determinant by an integral representation and the transformation of the involved terms into stochastic expressions. This stochastic determinant determination enables large-size applications in Bayesian inference, in particular evidence calculations, model comparison, and posterior determination.

  1. Virulence Determination

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This chapter reviews the in vitro and in vivo assays that are available for determination of pathogenic potential of Listeria monocytogenes bacteria, highlighting the value of using multiplex PCR for rapid and accurate assessment of listerial virulence....

  2. Climate determinism or Geomagnetic determinism?

    NASA Astrophysics Data System (ADS)

    Gallet, Y.; Genevey, A.; Le Goff, M.; Fluteau, F.; Courtillot, V.

    2006-12-01

    A number of episodes of sharp geomagnetic field variations (in both intensity and direction), lasting on the order of a century, have been identified in archeomagnetic records from Western Eurasia and have been called "archeomagnetic jerks". These seem to correlate well with multi-decadal cooling episodes detected in the North Atlantic Ocean and Western Europe, suggesting a causal link between both phenomena. A possible mechanism could be a geomagnetic modulation of the cosmic ray flux that would control the nucleation rate of clouds. We wish to underline the remarkable coincidence between archeomagnetic jerks, cooling events in Western Europe and drought periods in tropical and sub-tropical regions of the northern hemisphere. The latter two can be interpreted in terms of global teleconnections among regional climates. It has been suggested that these climatic variations had caused major changes in the history of ancient civilizations, such as in Mesopotamia, which were critically dependent on water supply and particularly vulnerable to lower rainfall amounts. This is one of the foundations of "climate determinism". Our studies, which suggest a geomagnetic origin for at least some of the inferred climatic events, lead us to propose the idea of a "geomagnetic determinism" in the history of humanity.

  3. Determination of ideal-gas enthalpies of formation for key compounds: The 1989 project results

    NASA Astrophysics Data System (ADS)

    Steele, W. V.; Chirico, R. D.; Nguyen, A.; Hossenlopp, I. A.; Smith, N. K.

    1991-10-01

    The results of a study aimed at improvement of group-contribution methodology for estimation of thermodynamic properties of organic and organosilicon substances are reported. Specific weaknesses where particular group-contribution terms were unknown, or estimated because of lack of experimental data, are addressed by experimental studies of enthalpies of combustion in the condensed phase, vapor pressure measurements, and differential scanning calorimetric (dsc) heat capacity measurements. Ideal gas enthalpies of formation of (+ or -) butan-2-ol, tetradecan-1-ol, hexan-1,6-diol, methacrylamide, benzoyl formic acid, naphthalene 2,6-dicarboxylic acid dimethyl ester, and tetraethylsilane are reported. A crystalline-phase enthalpy of formation at 298.15 K was determined for naphthalene-2,6-dicarboxylic acid, which decomposed at 695 K before melting. The combustion calorimetry of tetraethylsilane used the proven fluorine-additivity methodology. Critical temperature and critical density were determined for tetraethylsilane with differential scanning calorimeter and the critical pressure was derived. Group additivity parameters useful in the application of group contribution correlations are derived.

  4. Determination of ideal-gas enthalpies of formation for key compounds:

    SciTech Connect

    Steele, W.V.; Chirico, R.D.; Nguyen, A.; Hossenlopp, I.A.; Smith, N.K.

    1991-10-01

    The results of a study aimed at improvement of group-contribution methodology for estimation of thermodynamic properties of organic and organosilicon substances are reported. Specific weaknesses where particular group-contribution terms were unknown, or estimated because of lack of experimental data, are addressed by experimental studies of enthalpies of combustion in the condensed phase, vapor-pressure measurements, and differential scanning calorimetric (d.s.c.) heat-capacity measurements. Ideal-gas enthalpies of formation of ({plus minus})-butan-2-ol, tetradecan-1-ol, hexan-1,6-diol, methacrylamide, benzoyl formic acid, naphthalene-2,6-dicarboxylic acid dimethyl ester, and tetraethylsilane are reported. A crystalline-phase enthalpy of formation at 298.15 K was determined for naphthalene-2,6-dicarboxylic acid, which decomposed at 695 K before melting. The combustion calorimetry of tetraethylsilane used the proven fluorine-additivity methodology. Critical temperature and critical density were determined for tetraethylsilane with differential scanning calorimeter and the critical pressure was derived. Group-additivity parameters useful in the application of group- contribution correlations are derived. 112 refs., 13 figs., 19 tabs.

  5. 34 CFR 361.42 - Assessment for determining eligibility and priority for services.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... applicant is incapable of benefiting in terms of an employment outcome from vocational rehabilitation... rehabilitation services asserts that he or she is eligible for Social Security benefits under Title II or Title XVI of the Social Security Act (and, therefore, is presumed eligible for vocational...

  6. 34 CFR 361.42 - Assessment for determining eligibility and priority for services.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... applicant is incapable of benefiting in terms of an employment outcome from vocational rehabilitation... rehabilitation services asserts that he or she is eligible for Social Security benefits under Title II or Title XVI of the Social Security Act (and, therefore, is presumed eligible for vocational...

  7. Determination of test methods for the prediction of the behavior of mass concrete

    NASA Astrophysics Data System (ADS)

    Ferraro, Christopher C.

    Hydration at early ages results from chemical and physical processes that take place between Portland cement and water, and is an exothermic process. The resultant heat evolution and temperature rise for massive concrete placements can be so great that the temperature differentials between the internal concrete core and outer concrete stratum can cause cracking due to thermal gradients. Accurate prediction of temperature distribution and stresses in mass concrete is needed to determine if a given concrete mixture design may have problems in the field, so that adjustments to the design can be made prior to its use. This research examines calorimetric, strength, and physical testing methods in an effort to predict the thermal and physical behavior of mass concrete. Four groups of concrete mixture types containing different cementitious materials are examined. One group contains Portland cement, while the other three groups incorporate large replacements of supplementary cementitious materials: granulated blast furnace slag, fly ash, and a ternary blend (combining Portland cement, fly ash, and slag).

  8. DIPPER project 871 determination of ideal-gas enthalpies of formation for key compounds, The 1991 project results

    SciTech Connect

    Steele, W.V.; Chirico, R.D.; Knipmeyer, S.E.; Nguyen, A.; Tasker, I.R.

    1993-09-01

    Results of a study aimed at improving group-contribution methodology for estimating thermodynamic properties of organic substances are reported. Specific weaknesses where particular group-contribution terms were unknown, or estimated because of lack of experimental data, are addressed by experimental studies of enthalpies of combustion in condensed phase, vapor-pressure measurements, and differential scanning calorimetric (d.s.c.) heat-capacity measurements. Ideal-gas enthalpies of formation of cyclohexene, phthalan (2,5-dihydrobenzo-3,4-furan), isoxazole, n-octylamine, di-n-octylamine, tri-n-octylamine, phenyl isocyanate, and 1,4,5,6-tetrahydropyrimidine are reported. Two-phase (liquid + vapor) heat capacities were determined for phthalan, isoxazole, the three octylamines, and phenyl isocyanate. Liquid-phase densities along the saturation line were measured for phthalan and isoxazole at 298 to 425 K. The critical temperature and critical density of n-octylamine were determined from d.s.c. results and critical pressure derived from the fitting procedures. Fitting procedures were used to derive critical temperatures, pressures, and densities for cyclohexene (pressure and density only), phthalan, isoxazole, di-n-octylamine, and phenyl isocyanate. Group-additivity parameters or ring-correction terms are derived.

  9. Determination of the Crystallinity of Semicrystalline Poly(3-hexyl thiophene) by Means of Wide Angle X-Ray Scattering

    NASA Astrophysics Data System (ADS)

    Balko, Jens; Lohwasser, Ruth; Thelakkat, Mukundan; Sommer, Michael; Pascui, Ovidiu; Saalwaechter, Kay; Thurn-Albrecht, Thomas

    2013-03-01

    Poly(3-hexyl thiophene) (P3HT) is a common polymer semiconductor, often used as material or component in organic field effect transistors or solar cells. The crystallinity of this semicrystalline material is among other parameters governing the electronic mobility. However, at present there is no routine method available to determine an absolute value for the crystallinity, and the values given in the literature e.g. for the enthalpy of melting vary by a factor of three. Wide Angle X-Ray Scattering (WAXS) probes the crystals as well the amorphous parts of the sample. We present an approach for the determination of the crystallinity based on the evaluation of WAXS intensities at low scattering vectors emanating from the amorphous regions. The result is used for a calibration of the melting enthalpy (34 J/g) that can serve as a reference value for more convenient calorimetric techniques and compared to the results of recent NMR investigations. We discuss the crystallinity for a number of chemically well-defined samples, with different molecular weight and a typical commercial sample with broad molecular weight distribution. Despite the high crystallinities of 60 to 80% the crystallites exhibit a large amount of disorder.

  10. Twist, tilt, and orientational order at the nematic to twist-bend nematic phase transition of 1″,9″-bis(4-cyanobiphenyl-4'-yl) nonane: A dielectric, 2H NMR, and calorimetric study

    NASA Astrophysics Data System (ADS)

    Robles-Hernández, Beatriz; Sebastián, Nerea; de la Fuente, M. Rosario; López, David O.; Diez-Berart, Sergio; Salud, Josep; Ros, M. Blanca; Dunmur, David A.; Luckhurst, Geoffrey R.; Timimi, Bakir A.

    2015-12-01

    The nature of the nematic-nematic phase transition in the liquid crystal dimer 1″,9″-bis(4-cyanobiphenyl-4'-yl) nonane (CB9CB) has been investigated using techniques of calorimetry, dynamic dielectric response measurements, and 2H NMR spectroscopy. The experimental results for CB9CB show that, like the shorter homologue CB7CB, the studied material exhibits a normal nematic phase, which on cooling undergoes a transition to the twist-bend nematic phase (NTB), a uniaxial nematic phase, promoted by the average bent molecular shape, in which the director tilts and precesses describing a conical helix. Modulated differential scanning calorimetry has been used to analyze the nature of the NTB-N phase transition, which is found to be weakly first order, but close to tricritical. Additionally broadband dielectric spectroscopy and 2H magnetic resonance studies have revealed information on the structural characteristics of the recently discovered twist-bend nematic phase. Analysis of the dynamic dielectric response in both nematic phases has provided an estimate of the conical angle of the heliconical structure for the NTB phase. Capacitance measurements of the electric-field realignment of the director in initially planar aligned cells have yielded values for the splay and bend elastic constants in the high temperature nematic phase. The bend elastic constant is small and decreases with decreasing temperature as the twist-bend phase is approached. This behavior is expected theoretically and has been observed in materials that form the twist-bend nematic phase. 2H NMR measurements characterize the chiral helical twist identified in the twist-bend nematic phase and also allow the determination of the temperature dependence of the conical angle and the orientational order parameter with respect to the director.

  11. Twist, tilt, and orientational order at the nematic to twist-bend nematic phase transition of 1″,9″-bis(4-cyanobiphenyl-4'-yl) nonane: A dielectric, (2)H NMR, and calorimetric study.

    PubMed

    Robles-Hernández, Beatriz; Sebastián, Nerea; de la Fuente, M Rosario; López, David O; Diez-Berart, Sergio; Salud, Josep; Ros, M Blanca; Dunmur, David A; Luckhurst, Geoffrey R; Timimi, Bakir A

    2015-12-01

    The nature of the nematic-nematic phase transition in the liquid crystal dimer 1″,9″-bis(4-cyanobiphenyl-4'-yl) nonane (CB9CB) has been investigated using techniques of calorimetry, dynamic dielectric response measurements, and (2)H NMR spectroscopy. The experimental results for CB9CB show that, like the shorter homologue CB7CB, the studied material exhibits a normal nematic phase, which on cooling undergoes a transition to the twist-bend nematic phase (N(TB)), a uniaxial nematic phase, promoted by the average bent molecular shape, in which the director tilts and precesses describing a conical helix. Modulated differential scanning calorimetry has been used to analyze the nature of the N(TB)-N phase transition, which is found to be weakly first order, but close to tricritical. Additionally broadband dielectric spectroscopy and (2)H magnetic resonance studies have revealed information on the structural characteristics of the recently discovered twist-bend nematic phase. Analysis of the dynamic dielectric response in both nematic phases has provided an estimate of the conical angle of the heliconical structure for the N(TB) phase. Capacitance measurements of the electric-field realignment of the director in initially planar aligned cells have yielded values for the splay and bend elastic constants in the high temperature nematic phase. The bend elastic constant is small and decreases with decreasing temperature as the twist-bend phase is approached. This behavior is expected theoretically and has been observed in materials that form the twist-bend nematic phase. (2)H NMR measurements characterize the chiral helical twist identified in the twist-bend nematic phase and also allow the determination of the temperature dependence of the conical angle and the orientational order parameter with respect to the director.

  12. a GIS of SARDINIA'S Coastal Defense System (xvi - XVIII Century)

    NASA Astrophysics Data System (ADS)

    Deidda, M.; Musa, C.; Vacca, G.

    2015-06-01

    The use of GIS as a tool for archival, analysis and representation of geographic information has become significantly popular in many scientific fields that are directly concerned with the "territory" as their object of study. The field of application of GIS, however, has expanded also in other areas, such as those related to humanities and architecture, in which the territory is studied in an "indirect" mode because it constitutes a kind of substrate on which to develop a specific spatial analysis for particular purposes. Among these areas are to be included certainly archeology and restoration, fields in which the GIS has become a useful tool for historical studies. In this work we present a GIS developed for the study of the historical and territorial coastal defense system of Sardinia (16th - 18th century), in order to respond to the need to store, analyze and efficiently manage the information regarding cultural heritage and landscape heritage such as that consisting of the coastal defensive towers of Sardinia. This defensive system, in fact, was composed by over 100 towers positioned around the entire coastal perimeter of Sardinia, of which more than 90 still exist today. Their position was planned on the basis of the following criteria: - Warning the neighboring towers about the sighting of enemy ships - Protecting coasts located near the towns - Monitoring the water sources near the coast - Allowing for the full visibility of the coasts of any morphology With this study we also verified, through the use of high resolution and high accuracy DTM (LiDAR) and the topographic databases, whether the positioning criteria specified in the design of the system were respected and effective.

  13. 25 CFR 36.43 - Standard XVI-Student activities.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... activities program based on assessment of both student and program needs. Each activity program shall help... activities that include special interest clubs, physical activities, student government, and cultural affairs. The activity program shall be an integral part of the overall educational program. (a) All...

  14. Higher Education: Handbook of Theory and Research, Volume XVI.

    ERIC Educational Resources Information Center

    Smart, John C., Ed.

    This volume contains essays related to various aspects of higher education, focusing on both educational theory and research. The chapters are: (1) "Apologia pro Vita Mia" (Robert Berdahl); (2) "Varieties of Validity: Quality in Qualitative Research" (Yvonna S. Lincoln); (3) "Academic Freedom and Federal Courts in the 1990s: The Legitimation of…

  15. 25 CFR 36.43 - Standard XVI-Student activities.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... school board shall approve the overall activity plan. A qualified sponsor is a professional staff member... with other schools in setting up a schedule of sports and games. Schools that participate in state... CFR 31.7. All student activity accounts shall be audited annually. (h) The school shall provide...

  16. 25 CFR 36.43 - Standard XVI-Student activities.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... school board shall approve the overall activity plan. A qualified sponsor is a professional staff member... with other schools in setting up a schedule of sports and games. Schools that participate in state... CFR 31.7. All student activity accounts shall be audited annually. (h) The school shall provide...

  17. 25 CFR 36.43 - Standard XVI-Student activities.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ..., and planned types of fund-raising activities. (c) School may participate in interscholastic sports and... with other schools in setting up a schedule of sports and games. Schools that participate in state... participation in interscholastic competition in noncontact sports except on the basis of individual merit....

  18. Planck 2015 results. XVI. Isotropy and statistics of the CMB

    NASA Astrophysics Data System (ADS)

    Planck Collaboration; Ade, P. A. R.; Aghanim, N.; Akrami, Y.; Aluri, P. K.; Arnaud, M.; Ashdown, M.; Aumont, J.; Baccigalupi, C.; Banday, A. J.; Barreiro, R. B.; Bartolo, N.; Basak, S.; Battaner, E.; Benabed, K.; Benoît, A.; Benoit-Lévy, A.; Bernard, J.-P.; Bersanelli, M.; Bielewicz, P.; Bock, J. J.; Bonaldi, A.; Bonavera, L.; Bond, J. R.; Borrill, J.; Bouchet, F. R.; Boulanger, F.; Bucher, M.; Burigana, C.; Butler, R. C.; Calabrese, E.; Cardoso, J.-F.; Casaponsa, B.; Catalano, A.; Challinor, A.; Chamballu, A.; Chiang, H. C.; Christensen, P. R.; Church, S.; Clements, D. L.; Colombi, S.; Colombo, L. P. L.; Combet, C.; Contreras, D.; Couchot, F.; Coulais, A.; Crill, B. P.; Cruz, M.; Curto, A.; Cuttaia, F.; Danese, L.; Davies, R. D.; Davis, R. J.; de Bernardis, P.; de Rosa, A.; de Zotti, G.; Delabrouille, J.; Désert, F.-X.; Diego, J. M.; Dole, H.; Donzelli, S.; Doré, O.; Douspis, M.; Ducout, A.; Dupac, X.; Efstathiou, G.; Elsner, F.; Enßlin, T. A.; Eriksen, H. K.; Fantaye, Y.; Fergusson, J.; Fernandez-Cobos, R.; Finelli, F.; Forni, O.; Frailis, M.; Fraisse, A. A.; Franceschi, E.; Frejsel, A.; Frolov, A.; Galeotta, S.; Galli, S.; Ganga, K.; Gauthier, C.; Ghosh, T.; Giard, M.; Giraud-Héraud, Y.; Gjerløw, E.; González-Nuevo, J.; Górski, K. M.; Gratton, S.; Gregorio, A.; Gruppuso, A.; Gudmundsson, J. E.; Hansen, F. K.; Hanson, D.; Harrison, D. L.; Henrot-Versillé, S.; Hernández-Monteagudo, C.; Herranz, D.; Hildebrandt, S. R.; Hivon, E.; Hobson, M.; Holmes, W. A.; Hornstrup, A.; Hovest, W.; Huang, Z.; Huffenberger, K. M.; Hurier, G.; Jaffe, A. H.; Jaffe, T. R.; Jones, W. C.; Juvela, M.; Keihänen, E.; Keskitalo, R.; Kim, J.; Kisner, T. S.; Knoche, J.; Kunz, M.; Kurki-Suonio, H.; Lagache, G.; Lähteenmäki, A.; Lamarre, J.-M.; Lasenby, A.; Lattanzi, M.; Lawrence, C. R.; Leonardi, R.; Lesgourgues, J.; Levrier, F.; Liguori, M.; Lilje, P. B.; Linden-Vørnle, M.; Liu, H.; López-Caniego, M.; Lubin, P. M.; Macías-Pérez, J. F.; Maggio, G.; Maino, D.; Mandolesi, N.; Mangilli, A.; Marinucci, D.; Maris, M.; Martin, P. G.; Martínez-González, E.; Masi, S.; Matarrese, S.; McGehee, P.; Meinhold, P. R.; Melchiorri, A.; Mendes, L.; Mennella, A.; Migliaccio, M.; Mikkelsen, K.; Mitra, S.; Miville-Deschênes, M.-A.; Molinari, D.; Moneti, A.; Montier, L.; Morgante, G.; Mortlock, D.; Moss, A.; Munshi, D.; Murphy, J. A.; Naselsky, P.; Nati, F.; Natoli, P.; Netterfield, C. B.; Nørgaard-Nielsen, H. U.; Noviello, F.; Novikov, D.; Novikov, I.; Oxborrow, C. A.; Paci, F.; Pagano, L.; Pajot, F.; Pant, N.; Paoletti, D.; Pasian, F.; Patanchon, G.; Pearson, T. J.; Perdereau, O.; Perotto, L.; Perrotta, F.; Pettorino, V.; Piacentini, F.; Piat, M.; Pierpaoli, E.; Pietrobon, D.; Plaszczynski, S.; Pointecouteau, E.; Polenta, G.; Popa, L.; Pratt, G. W.; Prézeau, G.; Prunet, S.; Puget, J.-L.; Rachen, J. P.; Rebolo, R.; Reinecke, M.; Remazeilles, M.; Renault, C.; Renzi, A.; Ristorcelli, I.; Rocha, G.; Rosset, C.; Rossetti, M.; Rotti, A.; Roudier, G.; Rubiño-Martín, J. A.; Rusholme, B.; Sandri, M.; Santos, D.; Savelainen, M.; Savini, G.; Scott, D.; Seiffert, M. D.; Shellard, E. P. S.; Souradeep, T.; Spencer, L. D.; Stolyarov, V.; Stompor, R.; Sudiwala, R.; Sunyaev, R.; Sutton, D.; Suur-Uski, A.-S.; Sygnet, J.-F.; Tauber, J. A.; Terenzi, L.; Toffolatti, L.; Tomasi, M.; Tristram, M.; Trombetti, T.; Tucci, M.; Tuovinen, J.; Valenziano, L.; Valiviita, J.; Van Tent, B.; Vielva, P.; Villa, F.; Wade, L. A.; Wandelt, B. D.; Wehus, I. K.; Yvon, D.; Zacchei, A.; Zibin, J. P.; Zonca, A.

    2016-08-01

    We test the statistical isotropy and Gaussianity of the cosmic microwave background (CMB) anisotropies using observations made by the Planck satellite. Our results are based mainly on the full Planck mission for temperature, but also include some polarization measurements. In particular, we consider the CMB anisotropy maps derived from the multi-frequency Planck data by several component-separation methods. For the temperature anisotropies, we find excellent agreement between results based on these sky maps over both a very large fraction of the sky and a broad range of angular scales, establishing that potential foreground residuals do not affect our studies. Tests of skewness, kurtosis, multi-normality, N-point functions, and Minkowski functionals indicate consistency with Gaussianity, while a power deficit at large angular scales is manifested in several ways, for example low map variance. The results of a peak statistics analysis are consistent with the expectations of a Gaussian random field. The "Cold Spot" is detected with several methods, including map kurtosis, peak statistics, and mean temperature profile. We thoroughly probe the large-scale dipolar power asymmetry, detecting it with several independent tests, and address the subject of a posteriori correction. Tests of directionality suggest the presence of angular clustering from large to small scales, but at a significance that is dependent on the details of the approach. We perform the first examination of polarization data, finding the morphology of stacked peaks to be consistent with the expectations of statistically isotropic simulations. Where they overlap, these results are consistent with the Planck 2013 analysis based on the nominal mission data and provide our most thorough view of the statistics of the CMB fluctuations to date.

  19. 20 CFR 641.510 - What types of income are included and excluded for participant eligibility determinations?

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... under title XVI of the Social Security Act (42 U.S.C. 1381 et seq.), a payment made to or on behalf of... Affairs, or 25 percent of a benefit received under title II of the Social Security Act (42 U.S.C. 401...

  20. Application of In-Line Mid-Infrared (MIR) Spectroscopy Coupled with Calorimetry for the Determination of the Molar Enthalpy of Reaction between Ammonium Chloride and Sodium Nitrite.

    PubMed

    Kartnaller, Vinicius; Mariano, Danielly C O; Cajaiba, João

    2016-03-01

    The reaction between ammonium chloride and sodium nitrite has been known for its application as a source of heat because of its large enthalpy of reaction, for which it has been used by the oil industry. There have been no known calorimetric studies for the experimental determination of its molar enthalpy of reaction, which is necessary in order to predict the limits achieved for up-scale applications. Attenuated total reflection Fourier transform infrared spectroscopy (ATR FT-IR) and reaction calorimetry were used to determine this value by using a simple methodology. Both techniques were used concomitantly as a source of information regarding the time-dependent moles converted (Δn) and the amount of exchanged heat (ΔH). The molar enthalpy of reaction was calculated to be -74 ± 4 kcal mol(-1). The percentage between the confidence interval and the calculated value was 5.4%, which shows that the methodology was precise. After the determination of the molar enthalpy of reaction, it was proved that the ATR FT-IR alone was able to be used as a substitute for the reaction calorimetry technique, in which the IR signal is converted to the heat information, presenting as an easier technique for the monitoring of the heat released by this system for future applications. PMID:26798078

  1. Application of In-Line Mid-Infrared (MIR) Spectroscopy Coupled with Calorimetry for the Determination of the Molar Enthalpy of Reaction between Ammonium Chloride and Sodium Nitrite.

    PubMed

    Kartnaller, Vinicius; Mariano, Danielly C O; Cajaiba, João

    2016-03-01

    The reaction between ammonium chloride and sodium nitrite has been known for its application as a source of heat because of its large enthalpy of reaction, for which it has been used by the oil industry. There have been no known calorimetric studies for the experimental determination of its molar enthalpy of reaction, which is necessary in order to predict the limits achieved for up-scale applications. Attenuated total reflection Fourier transform infrared spectroscopy (ATR FT-IR) and reaction calorimetry were used to determine this value by using a simple methodology. Both techniques were used concomitantly as a source of information regarding the time-dependent moles converted (Δn) and the amount of exchanged heat (ΔH). The molar enthalpy of reaction was calculated to be -74 ± 4 kcal mol(-1). The percentage between the confidence interval and the calculated value was 5.4%, which shows that the methodology was precise. After the determination of the molar enthalpy of reaction, it was proved that the ATR FT-IR alone was able to be used as a substitute for the reaction calorimetry technique, in which the IR signal is converted to the heat information, presenting as an easier technique for the monitoring of the heat released by this system for future applications.

  2. Optimized structure and thermochemical properties of flavonoids determined by the CHIH(medium) DFT model chemistry versus experimental techniques

    NASA Astrophysics Data System (ADS)

    Mendoza-Wilson, Ana María.; Lardizabal-Gutiérrez, Daniel; Torres-Moye, Enrique; Fuentes-Cobas, Luis; Balandrán-Quintana, René R.; Camacho-Dávila, Alejandro; Quintero-Ramos, Armando; Glossman-Mitnik, Daniel

    2007-12-01

    The purpose of this work was to evaluate the accuracy of the CHIH(medium)-DFT model chemistry (PBEg/CBSB2 ∗∗//PBEg/CBSB4) in the determination of the optimized structure and thermochemical properties of heterocyclic systems of medium size such as flavonoids, wherefore were selected three of the most abundant flavonoids in vegetable tissues, and which posses the higher antioxidant activity: quercetin, (+)-catechin and cyanidin. As reference systems were employed three cyclic compounds: phenol, catechol and resorcinol. The thermochemical properties evaluated were enthalpy of formation, bond dissociation enthalpy (BDE) and ionization potential (IP), following the scheme of isodesmic reactions. The theoretical results were compared with experimental data generated by X-ray diffraction and calorimetric techniques realized in part by us, whereas other data were taken from the literature. The results obtained in this work reveal that the CHIH(medium)-DFT model chemistry represents an accurate computational tool to calculate structural and thermochemical properties in the studied flavonoid and reference compounds. The average absolute deviation of enthalpy of formation for reference compounds was 3.0 kcal/mol, 2.64 kcal/mol for BDE, and 2.97 kcal/mol for IP.

  3. Binding of nucleotides to nucleoside diphosphate kinase: a calorimetric study.

    PubMed

    Cervoni, L; Lascu, I; Xu, Y; Gonin, P; Morr, M; Merouani, M; Janin, J; Giartosio, A

    2001-04-17

    The source of affinity for substrates of human nucleoside diphosphate (NDP) kinases is particularly important in that its knowledge could be used to design more effective antiviral nucleoside drugs (e.g., AZT). We carried out a microcalorimetric study of the binding of enzymes from two organisms to various nucleotides. Isothermal titration calorimetry has been used to characterize the binding in terms of Delta G degrees, Delta H degrees and Delta S degrees. Thermodynamic parameters of the interaction of ADP with the hexameric NDP kinase from Dictyostelium discoideum and with the tetrameric enzyme from Myxococcus xanthus, at 20 degrees C, were similar and, in both cases, binding was enthalpy-driven. The interactions of ADP, 2'deoxyADP, GDP, and IDP with the eukaryotic enzyme differed in enthalpic and entropic terms, whereas the Delta G degrees values obtained were similar due to enthalpy--entropy compensation. The binding of the enzyme to nonphysiological nucleotides, such as AMP--PNP, 3'deoxyADP, and 3'-deoxy-3'-amino-ADP, appears to differ in several respects. Crystallography of the protein bound to 3'-deoxy-3'-amino-ADP showed that the drug was in a distorted position, and was unable to interact correctly with active site side chains. The interaction of pyrimidine nucleoside diphosphates with the hexameric enzyme is characterized by a lower affinity than that with purine nucleotides. Titration showed the stoichiometry of the interaction to be abnormal, with 9--12 binding sites/hexamer. The presence of supplementary binding sites might have physiological implications. PMID:11294625

  4. Superconducting calorimetric alpha particle sensors for nuclear nonproliferation applications

    SciTech Connect

    Horansky, Robert D.; Ullom, Joel N.; Beall, James A.; Hilton, Gene C.; Irwin, Kent D.; Dry, Donald E.; Hastings, Elizabeth P.; Lamont, Stephen P.; Rudy, Clifford R.; Rabin, Michael W.

    2008-09-22

    Identification of trace nuclear materials is usually accomplished by alpha spectrometry. Current detectors cannot distinguish critical elements and isotopes. We have developed a detector called a microcalorimeter, which achieves a resolution of 1.06 keV for 5.3 MeV alphas, the highest resolving power of any energy dispersive measurement. With this exquisite resolution, we can unambiguously identify the {sup 240}Pu/{sup 239}Pu ratio in Pu, a critical measurement for ascertaining the intended use of nuclear material. Furthermore, we have made a direct measurement of the {sup 209}Po ground state decay.

  5. Two Calorimetrically Distinct States of Liquid Water Below 150 Kelvin

    PubMed

    Johari; Hallbrucker; Mayer

    1996-07-01

    Vapor-deposited amorphous solid and hyperquenched glassy water were found to irreversibly transform, on compression at 77 kelvin, to a high-density amorphous solid. On heating at atmospheric pressure, this solid became viscous water (water B), with a reversible glass-liquid transition onset at 129 +/- 2 kelvin. A different form of viscous water (water A) was formed by heating the uncompressed vapor-deposited amorphous solid and hyperquenched liquid water. On thermal cycling up to 148 kelvin, water B remained kinetically and thermodynamically distinct from water A. The occurrence of these two states, which do not interconvert, helps explain both the configurational relaxation of water and stress-induced amorphization. PMID:8688057

  6. A calorimetric and computational study of aminomethoxybenzoic acids.

    PubMed

    Almeida, Ana R R P; Matos, M Agostinha R; Morais, Victor M F; Monte, Manuel J S

    2010-09-01

    The standard (p(0) = 0.1 MPa) molar enthalpies of formation, in the crystalline phase, of five aminomethoxybenzoic acids, at T = 298.15 K, were derived from the standard molar energies of combustion in oxygen, measured by static-bomb combustion calorimetry. Combining these results with literature results of the standard molar enthalpies of sublimation, at T = 298.15 K, the standard molar enthalpies of formation, in the gaseous phase, were derived. Additionally, the enthalpies of formation of the ten possible isomers of aminomethoxybenzoic acid were estimated using accurate Double Hybrid Density Functional Theory (DHDFT) computational methods. The good agreement between the experimental and estimated values of the enthalpies of formation of the five isomers studied experimentally allows us to be confident on the estimated values for the other five isomers. A quantitative evaluation and analysis of the aromatic character of all the studied isomers based on the calculation of Nucleus Independent Chemical Shifts (NICS) was also conducted. PMID:20718458

  7. Calorimetric thermometry of meteoritic troilite: A feasibility study

    NASA Technical Reports Server (NTRS)

    Allton, J. H.; Gooding, J. L.

    1993-01-01

    Two solid-state phase transitions in troilite (FeS) can be readily measured by differential scanning calorimetry (DSC) on samples of only a few milligrams. Troilite from the Mundrabilla iron meteorite displays a DSC fingerprint which is distinct from that of terrestrial troilite from Del Norte Co., California; their response to subsequent heating also differ significantly. Further work may establish whether troilite thermometry of meteorites is possible using DSC.

  8. Calorimetric thermometry of meteoritic troilite: Preliminary thermometer relationships

    NASA Technical Reports Server (NTRS)

    Allton, Judith H.; Wentworth, Susan J.; Gooding, James L.

    1994-01-01

    Thermodynamic properties of the alpha/beta phase transformation in terrestrial troilite (FeS), as measured by differential scanning calorimetry (DSC), vary systematically with prior thermal history of the troilite, as imposed under laboratory conditions. Both the transition temperature and enthalpy change for the alpha/beta transformation decrease with increasing maximum temperature of prior heat treatment. DSC measurements on troilite from various meteorites indicate clear differences in the alpha/beta thermodynamic properties that are consistent with differences in the natural thermal histories of the meteorites.

  9. Thermodynamics of the lysozyme--salt interaction from calorimetric titrations.

    PubMed

    Boncina, Matjaz; Lah, Jurij; Rescic, Jurij; Vlachy, Vojko

    2010-04-01

    It is well-known that the addition of salts influences the properties of proteins in solution. The essential nature of this phenomenon is far from being fully understood, partly due to the absence of the relevant thermodynamic information. To help fill this gap, in this work isothermal titration calorimetry (ITC) was employed to study the ion-lysozyme association in aqueous buffer solutions at pH = 4.0. ITC curves measured for NaCl, NaBr, NaI, NaNO3, NaSCN, KCl, CaCl2, and BaCl2 salts at three different temperatures were described by a model assuming two sets of independent binding sites on the lysozyme. The resulting thermodynamic parameters of binding of anions (counterions) to the first class of sites (N approximately 7) indicate that the binding constant (K approximately 102 M-1) increases in the order Cl- < Br- < I- < NO3- < SCN-. The anion-lysozyme association is entropy driven, accompanied by a small favorable enthalpy contribution and a positive change in heat capacity. It seems that the entropy and heat capacity increase is due to the water released upon binding, while the net exothermic effect originates from the anion-NH3+ pair formation. Moreover, the results reveal that the nature of the cation has little effect on the thermodynamics of the anion-lysozyme association under the given experimental conditions. Taken together, it seems that the observed thermodynamics of association is a result of a combination of both electrostatic and short-range interactions. The anion ordering reflects the strength of water mediated interactions between anions and lysozyme.

  10. Calorimetric study of Skyrmionic chiral magnet MnSi

    NASA Astrophysics Data System (ADS)

    Samatham, S. Shanmukharao; Ganesan, V.

    2014-04-01

    We present the analysis of specific internal energy as a function of magnetic fields in ordered, intermediate and paramagnetic phases of MnSi. Signatures of the formation of Skyrmion lattice, in conical order region, is identified by a hump-like structure in region-I. Gradual melting of blue phase, with magnetic fields, is demonstrated.

  11. Calorimetric studies of the growth of anaerobic microbes.

    PubMed

    Miyake, Hideo; Maeda, Yukiko; Ishikawa, Takashi; Tanaka, Akiyoshi

    2016-09-01

    This article aims to validate the use of calorimetry to measure the growth of anaerobic microbes. It has been difficult to monitor the growth of strict anaerobes while maintaining optimal growth conditions. Traditionally, optical density and ATP concentration are usually used as measures of the growth of anaerobic microbes. However, to take these measurements it is necessary to extract an aliquot of the culture, which can be difficult while maintaining anaerobic conditions. In this study, calorimetry was used to continuously and nondestructively measure the heat generated by the growth of anaerobic microbes as a function of time. Clostridium acetobutylicum, Clostridium beijerinckii, and Clostridium cellulovorans were used as representative anaerobic microbes. Using a multiplex isothermal calorimeter, we observed that peak time (tp) of C. acetobutylicum heat evolution increased as the inoculation rate decreased. This strong correlation between the inoculation rate and tp showed that it was possible to measure the growth rate of anaerobic microbes by calorimetry. Overall, our results showed that there is a very good correlation between heat evolution and optical density/ATP concentration, validating the use of the method. PMID:27012376

  12. Calorimetric analysis of cryopreservation and freeze-drying formulations.

    PubMed

    Sun, Wendell Q

    2015-01-01

    Differential scanning calorimetry (DSC) is a commonly used thermal analysis technique in cryopreservation and freeze-drying research. It has been used to investigate crystallization, eutectic formation, glass transition, devitrification, recrystallization, melting, polymorphism, molecular relaxation, phase separation, water transport, thermochemistry, and kinetics of complex reactions (e.g., protein denaturation). Such information can be used for the optimization of protective formulations and process protocols. This chapter gives an introduction to beginners who are less familiar with this technique. It covers the instrument and its basic principles, followed by a discussion of the methods as well as examples of specific applications.

  13. Calorimetric studies of the growth of anaerobic microbes.

    PubMed

    Miyake, Hideo; Maeda, Yukiko; Ishikawa, Takashi; Tanaka, Akiyoshi

    2016-09-01

    This article aims to validate the use of calorimetry to measure the growth of anaerobic microbes. It has been difficult to monitor the growth of strict anaerobes while maintaining optimal growth conditions. Traditionally, optical density and ATP concentration are usually used as measures of the growth of anaerobic microbes. However, to take these measurements it is necessary to extract an aliquot of the culture, which can be difficult while maintaining anaerobic conditions. In this study, calorimetry was used to continuously and nondestructively measure the heat generated by the growth of anaerobic microbes as a function of time. Clostridium acetobutylicum, Clostridium beijerinckii, and Clostridium cellulovorans were used as representative anaerobic microbes. Using a multiplex isothermal calorimeter, we observed that peak time (tp) of C. acetobutylicum heat evolution increased as the inoculation rate decreased. This strong correlation between the inoculation rate and tp showed that it was possible to measure the growth rate of anaerobic microbes by calorimetry. Overall, our results showed that there is a very good correlation between heat evolution and optical density/ATP concentration, validating the use of the method.

  14. Calorimetric studies of phase transitions in imidazolium perchlorate crystal

    NASA Astrophysics Data System (ADS)

    Przeslawski, J.; Czapla, Z.

    2006-06-01

    The first precise measurements of specific heat changes have been performed for a C3N2H5ClO4 crystal using an ac calorimeter. Phase transitions at about 373 and 219 K were revealed. The continuous second-order phase transition at 373 K to the ferroelectric phase is described by the Landau model using specific heat and linear birefringence data. The Landau expansion coefficients B and C are of the same order of magnitude as those obtained for hard ferroelectric materials. Thermal parameters (such as the excess enthalpy, ΔH, and the excess entropy, ΔS) of the continuous transition were estimated and discussed. During the first cooling, a distinct (~2 K) supercooling effect was observed at the discontinuous transition at about 219 K.

  15. Calorimetric studies of the in vitro polymerization of brain tubulin.

    PubMed Central

    Sutherland, J W; Sturtevant, J M

    1976-01-01

    The enthalpy change for chain propagation in the polymerization of bovine tubulin has been studied directly by stopped-flow microcalorimetry at 17 degrees and 25 degrees, and found to be 0 +/- 1 kcal per mol of 6S tubulin dimer at both temperatures. Substantial heat evolution with a half-time of decay of approximately 1 hr was observed w-en tubulin was injected into the calorimeter. This heat was shown to result from contamination of the tublin by small amounts of some material from the crude brain homogenate from which the tubulin was prepared, and to be totally unconnected with microtubule assembly. Model calculations of nucleated polymerization processes reveal that the van't Hoff enthalpy calculated from the temperature dependence of the critical polymerization concentration is a complicated function of the separate enthalpy changes for nucleation and chain propagation. The published values of this quantity for tubulin probably pertain primarily to the nucleation process. It is shown that our observation of a propagation enthalpy change of vanishingly small size is not necessarily inconsistent with the reported van't Hoff enthalpies. PMID:1068468

  16. Calorimetric validation of the Caltrac accelerometer during level walking.

    PubMed

    Balogun, J A; Martin, D A; Clendenin, M A

    1989-06-01

    The primary purpose of this study was to compare the Caltrac accelerometer output with measured energy expenditure (Ee). Twenty-five volunteers (10 men, 15 women) walked on a level motor-driven treadmill at four different speeds (54, 81, 104, and 130 m.min-1) with the Caltrac device affixed to the waistline. Each of the four experimental trials lasted eight minutes, and the testing was completed within an hour. During the test, oxygen consumption (VO2) (in L.min-1 and in mL.kg-1.min-1) and nonprotein respiratory exchange ratio were monitored by the Beckman Horizon metabolic cart. The accelerometer output at the end of each exercise bout was also monitored and subsequently divided by 8 to convert the readings to counts.min-1. The mean VO2 (L.min-1) at steady state (ie, 6th-8th minutes of exercise) was converted to a caloric value. We obtained a moderate correlation coefficient (r) of .76 between the accelerometer output and the VO2 (mL.kg-1.min-1) and a high correlation coefficient of .92 between the Ee and the accelerometer readings. The Caltrac accelerometer output (counts.min-1) was significantly higher (p less than .01) than the Ee (kcal.min-1) at the four walking speeds. The difference between the accelerometer output and the Ee ranged from 13.3% to 52.9%. The data were further analyzed with linear, polynomial, multiple, and stepwise regression models. The results of the analyses revealed that the Caltrac accelerometer output is a valid predictor of Ee during level walking when the appropriate regression equation is used to adjust the values.(ABSTRACT TRUNCATED AT 250 WORDS)

  17. RAPID COMMUNICATION: Calorimetric radar absorptivity measurement using a microwave oven

    NASA Astrophysics Data System (ADS)

    Lorenz, Ralph D.

    1999-06-01

    The measurement of the microwave absorptivity of materials typically requires expensive and arcane equipment and methods. I show that, for moderately absorbing materials (loss tangent icons/Journals/Common/delta" ALT="delta" ALIGN="TOP"/>icons/Journals/Common/simeq" ALT="simeq" ALIGN="TOP"/>0.005 or higher), useful measurements can be easily made using a thermometer and a normal domestic microwave oven: the heat absorbed for suitably designed sample size and geometry relates directly to the absorptivity. This technique, although not supremely accurate, is quick and inexpensive and may be useful for rapid investigations, educational projects and situations in which samples are awkward to handle. I show that water ice spiked with even only 0.2% ammonia is about three orders of magnitude more absorbing than is pure ice at -80 °C.

  18. Calorimetric studies of the state of water in seed tissues

    PubMed Central

    Vertucci, Christina W.

    1990-01-01

    To understand the physical state of water in hydrating biological tissues, thermodynamic properties of water in cotyledons of pea and soybean with moisture contents ranging from 0.01 g H2O/g dw to 1.0 g H2O/g dw were studied using differential scanning calorimetry. The heat capacity of the tissues increased abruptly at moisture contents above 0.08 and 0.12 g H2O/g dw for soybean and pea cotyledons, respectively. Melting transitions of water were observed at moisture contents >0.23 and 0.26 g H2O/g dw for soybean and pea. However, freezing of water was not observed unless moisture contents exceeded 0.33-0.35 g H2O/g dw. In both seed tissues, the temperatures of the freezing and melting varied with moisture content and showed hysterisis. The energy of the transition also varied with moisture content and was similar to the heats of fusion and crystallization of pure water only at moisture contents >0.54 and 0.58 gH2O/g dw for soybean and pea seeds, respectively. The thermal properties of water change distinctly as seed moisture content changes: at least five states or water can be identified. PMID:19431782

  19. Thermal characterization of Li-ion cells using calorimetric techniques

    SciTech Connect

    ROTH,EMANUEL P.

    2000-05-31

    The thermal stability of Li-ion cells with intercalating carbon anodes and metal oxide cathodes was measured as a function of state of charge and temperature for two advanced cell chemistries. Cells of the 18650 design with Li{sub x}CoO{sub 2} cathodes (commercial Sony cells) and Li{sub x}Ni{sub 0.8}Co{sub 0.2}O{sub 2} cathodes were measured for thermal reactivity. Accelerating rate calorimetry (ARC) was used to measure cell thermal runaway as a function of state of charge (SOC), microcalorimetry was used to measure the time dependence of thermal output, and differential scanning calorimetry (DSC) was used to study the thermal reactivity of the individual components. Thermal decomposition of the anode solid electrolyte interphase (SEI) layer occurred at low temperatures and contributes to the initiation of thermal runaway. Low temperature reactions from 40 C--70 C were observed during the ARC runs that were SOC dependent. These reactions measured in the microcalorimeter decayed over time with power-law dependence and were highly sensitive to SOC and temperature. ARC runs of aged and cycled cells showed complete absence of these low-temperature reactions but showed abrupt exothermic spikes between 105--135 C. These results suggest that during aging the anode SEI layer is decomposing from a metastable state to a stable composition that is breaking down at elevated temperatures.

  20. Short arcs at low current determination of the power lost by conduction into anode

    SciTech Connect

    Abbaoui, M.; Salihou, H.

    1995-12-31

    The mechanisms occurring at the anode of an electric arc are less important compared to that at the cathode, Many studies have been carried out to get a better understanding of anode phenomena in welding, but few of them have been reported on sham am in gases then last years. In general, for short arcs, the major problem encouraged in experiment was the instability of the arc voltage. This instability depends on the phenomena associated with the existence of the arc, the erosion, the nature and surface state of the electrode materials mainly for low currents arcs. Thus, for short arcs operating in gases at low current, experimental investigations are complicated because of their inherent instability and the metal gas interaction. Moreover, because of this instability, there are less data available. In this paper, we are concerned with low arc current (2-5A) and small electrode separation (0.4-1mm). For short arcs in gases at low-current, it is known from literature that one of the important tool is the energy balance which enables to deal with the power lost by conduction into electrodes and the current density. Calorimetric observations show that about 80% of the electrical power input is lost into both electrodes mainly by conduction. In the following analysis, a simple method of determining the power lost by conduction into different anode materials using a wall stabilised arc is presented. The experimental method consists in measuring the temperature reached in steady state at different points distributed along the electrode axis, fitting the values obtained and calculating the power supplied P{sub cd} to the anode surface facing the column.

  1. [Comparison of resting energy expenditure determined by indirect calorimetry and estimated by predictive formulas in women with obesity degrees I to III].

    PubMed

    Parra-Carriedo, Alicia; Cherem-Cherem, Loren; Galindo-De Noriega, Daniela; Díaz-Gutiérrez, Mary Carmen; Pérez-Lizaur, Ana Bertha; Hernández-Guerrero, César

    2013-01-01

    Introducción: La determinación del gasto energético en reposo (GER) se calcula cotidianamente a partir de fórmulas predictivas aunque el resultado varía dependiendo de la población. Objetivo: Comparar la determinación del GER mediante calorimetría indirecta y mediante las ecuaciones Harris-Benedict (HB), Mifflin (MF), Organización Mundial de la Salud (OMS), «Institute of Medicine» (IOM), Fórmula Rápida (FR) y Valencia (VA) en mujeres con grados de obesidad I a III. Métodos: Mujeres adultas mestizas mexicanas se incluyeron en el estudio y formaron 3 grupos a partir del índice de masa corporal (IMC). Obesidad grado I (IMC 30,0-34,9; n = 42), grado II (IMC 35,0-39,9; n = 38) y grado III (IMC > 40; n = 41). Se determinó el GER mediante calorimetría indirecta y mediante las ecuaciones antes señaladas. ANOVA de Kruskal-Wallis y la prueba de Dunn se emplearon para el análisis estadístico (p < 0,05 se aceptó como diferencia). Resultados: No se observó diferencia estadística entre los valores de las fórmulas HB, OMS y VA respecto a la CI. La concordancia obtenida de dichas fórmulas fue 63%, 67% y 64%, respectivamente, al analizar los datos en un solo grupo de obesidad. Asimismo, las fórmulas IOM, ER y MF mostraron diferencia estadística significativa versus la CI, siendo la concordancia 58%, 53% y 54%, respectivamente. En el grado III de obesidad la concordancia de VA (78%) y FR (71%) fue la mayor obtenida. Discusión: Las fórmulas HB, OMS y VA fueron las mejores para estimar el GER en mujeres mexicanas con IMC>30. En el grado III VA y FR muestran el mejor desempeño.

  2. Rethinking the Category 'Determiner'

    ERIC Educational Resources Information Center

    Spangler, Wayne E.

    1975-01-01

    The 'determiner' category was originally set up by structuralists for identifying nouns. The rewrite rule for 'determiners' in transformational generative grammar is inadequate for showing correspondences between type and token. An appraisal of quantity terms might eliminate the concept of the 'determiner,' and replace that category with one of…

  3. CALORIMETER-BASED ADJUSTMENT OF MULTIPLICITY DETERMINED 240PU EFF KNOWN-A ANALYSIS FOR THE ASSAY OF PLUTONIUM

    SciTech Connect

    Dubose, F.

    2012-02-21

    In nuclear material processing facilities, it is often necessary to balance the competing demands of accuracy and throughput. While passive neutron multiplicity counting is the preferred method for relatively fast assays of plutonium, the presence of low-Z impurities (fluorine, beryllium, etc.) rapidly erodes the assay precision of passive neutron counting techniques, frequently resulting in unacceptably large total measurement uncertainties. Conversely, while calorimeters are immune to these impurity effects, the long count times required for high accuracy can be a hindrance to efficiency. The higher uncertainties in passive neutron measurements of impure material are driven by the resulting large (>>2) {alpha}-values, defined as the ({alpha},n):spontaneous fission neutron emission ratio. To counter impurity impacts for high-{alpha} materials, a known-{alpha} approach may be adopted. In this method, {alpha} is determined for a single item using a combination of gamma-ray and calorimetric measurements. Because calorimetry is based on heat output, rather than a statistical distribution of emitted neutrons, an {alpha}-value determined in this way is far more accurate than one determined from passive neutron counts. This fixed {alpha} value can be used in conventional multiplicity analysis for any plutonium-bearing item having the same chemical composition and isotopic distribution as the original. With the results of single calorimeter/passive neutron/gamma-ray measurement, these subsequent items can then be assayed with high precision and accuracy in a relatively short time, despite the presence of impurities. A calorimeter-based known-{alpha} multiplicity analysis technique is especially useful when requiring rapid, high accuracy, high precision measurements of multiple plutonium bearing items having a common source. The technique has therefore found numerous applications at the Savannah River Site. In each case, a plutonium (or mixed U/Pu) bearing item is divided

  4. Nephelometric determination of fluorine

    USGS Publications Warehouse

    Stevens, R.E.

    1936-01-01

    Fluorine in minerals may be determined with the nephelometer to about 1 per cent of the fluorine. The determination is made on an aliquot of the sodium chloride solution of the fluorine, obtained by the Berzelius method of extraction. The fluorine is precipitated as colloidal calcium fluoride in alcoholic solution, gelatin serving as a protective colloid. Arsenates, sulfates, and phosphates, which interfere with the determination, must be removed.

  5. Temperature determination using pyrometry

    DOEpatents

    Breiland, William G.; Gurary, Alexander I.; Boguslavskiy, Vadim

    2002-01-01

    A method for determining the temperature of a surface upon which a coating is grown using optical pyrometry by correcting Kirchhoff's law for errors in the emissivity or reflectance measurements associated with the growth of the coating and subsequent changes in the surface thermal emission and heat transfer characteristics. By a calibration process that can be carried out in situ in the chamber where the coating process occurs, an error calibration parameter can be determined that allows more precise determination of the temperature of the surface using optical pyrometry systems. The calibration process needs only to be carried out when the physical characteristics of the coating chamber change.

  6. Spacecraft Attitude Determination Methods

    NASA Technical Reports Server (NTRS)

    Markley, F. Landis; Bauer, Frank H. (Technical Monitor)

    2000-01-01

    This document is presentation in viewgraph form, which outlines the methods of determining spacecraft attitude. The presentation reviews several parameterizations relating to spacecraft attitude, such as Euler's Theorem, Rodriques parameters, and Euler-Rodriques parameters or Quaternion. Onboard attitude determination is the norm, using either single frame or filtering methods. The presentation reviews several mathematical representations of attitude. The mechanisms for determining attitude on board the Hubble Space Telescope, the Tropical Rainfall and Measuring Mission and the Solar Anomalous and Magnetospheric Particle Explorer are reviewed. Wahba's problem, Procrustes Problem, and some solutions are also summarized.

  7. Synthesis of crystalline americium hydroxide, Am(OH){sub 3}, and determination of its enthalpy of formation; estimation of the solubility-product constants of actinide(III) hydroxides

    SciTech Connect

    Morss, L.R.; Williams, C.W.

    1993-12-31

    This paper reports a new synthesis of pure, microcrystalline Am(OH){sub 3}, its characterization by x-ray powder diffraction and infrared spectroscopy, and the calorimetric determination of its enthalpy of solution in dilute hydrochloric acid. From the enthalpy of solution the enthalpy of formation of Am(OH){sub 3} has been calculated to be {minus}1371.2{plus_minus}7.9 kj{center_dot}mol{sup {minus}1}, which represents the first experimental determination of an enthalpy of formation of any actinide hydroxide. The free energy of formation and solubility product constant of Am(OH){sub 3} (K{sub sp} = 7 {times} 10{sup {minus}31}) have been calculated from our enthalpy of formation and entropy estimates and are compared with literature measurements under near-equilibrium conditions. Since many properties of the tripositive lanthanide and actinide ions (e.g., hydrolysis, complex-ion formation, and thermochemistry) change in a regular manner, these properties can be interpreted systematically in terms of ionic size. This paper compares the thermochemistry of Am(OH){sub 3} with thermochemical studies of lanthanide hydroxides. A combined structural and acid-base model is used to explain the systematic differences in enthalpies of solution between the oxides and hydroxides of the 4f{sup n} and 5f{sup n} subgroups and to predict solubility-product constants for the actinide(III) hydroxides of Pu through Cf.

  8. Salinity determination using NIRA

    SciTech Connect

    Hirschfeld, T.

    1985-07-01

    The determination of salinity of water by near infrared spectroscopic techniques is discussed. The concept of 'spectral shift reagents' is used and sufficiently rapid computer calculations yield the concentrations of Naci from measured absorbances at selected wavelengths. (AIP)

  9. Autonomous attitude determination systems

    NASA Technical Reports Server (NTRS)

    Lowrie, J. W.

    1979-01-01

    A summary of autonomous attitude determination systems is presented by separating it into four areas: types of attitude determination systems which can be automated, a description of the attitude determination problem and its solution, specific types of sensors, and the processor requirements of two automated systems. The sensors used in attitude determination have been characteristically carried on-board the spacecraft in the past, so the major development requirement of automated systems is in the area of on-board processors. It is concluded that standardization of computers is not as beneficial as the standardization of computer architecture and the basic components which go into making them. It is also concluded that charge-coupled devices (CCD) or other solid state star tracking devices offer considerable advantages over the image-dissector type of star tracker.

  10. Structural Determination of Circulation.

    ERIC Educational Resources Information Center

    Blankenburg, William B.

    1981-01-01

    Analyzes the effects of both structural factors (demographics, economic conditions, and competition) and discretionary factors (content, design, and marketing techniques) and concludes that it is the former that determine a newspaper's circulation. (FL)

  11. Solids mass flow determination

    DOEpatents

    Macko, Joseph E.

    1981-01-01

    Method and apparatus for determining the mass flow rate of solids mixed with a transport fluid to form a flowing mixture. A temperature differential is established between the solids and fluid. The temperature of the transport fluid prior to mixing, the temperature of the solids prior to mixing, and the equilibrium temperature of the mixture are monitored and correlated in a heat balance with the heat capacities of the solids and fluid to determine the solids mass flow rate.

  12. Determining postural stability

    NASA Technical Reports Server (NTRS)

    Lieberman, Erez (Inventor); Forth, Katharine E. (Inventor); Paloski, William H. (Inventor)

    2011-01-01

    A method for determining postural stability of a person can include acquiring a plurality of pressure data points over a period of time from at least one pressure sensor. The method can also include the step of identifying a postural state for each pressure data point to generate a plurality of postural states. The method can include the step of determining a postural state of the person at a point in time based on at least the plurality of postural states.

  13. Metal hydride differential scanning calorimetry as an approach to compositional determination of mixtures of hydrogen isotopologues and helium

    DOE PAGESBeta

    Robinson, David B.; Luo, Weifang; Cai, Trevor Y.; Stewart, Kenneth D.

    2015-09-26

    Gaseous mixtures of diatomic hydrogen isotopologues and helium are often encountered in the nuclear energy industry and in analytical chemistry. Compositions of stored mixtures can vary due to interactions with storage and handling materials. When tritium is present, it decays to form ions and helium-3, both of which can lead to further compositional variation. Monitoring of composition is typically achieved by mass spectrometry, a method that is bulky and energy-intensive. Mass spectrometers disperse sample material through vacuum pumps, which is especially troublesome if tritium is present. Moreover, our ultimate goal is to create a compact, fast, low-power sensor that canmore » determine composition with minimal gas consumption and waste generation, as a complement to mass spectrometry that can be instantiated more widely. We propose calorimetry of metal hydrides as an approach to this, due to the strong isotope effect on gas absorption, and demonstrate the sensitivity of measured heat flow to atomic composition of the gas. Peak shifts are discernible when mole fractions change by at least 1%. A mass flow restriction results in a unique dependence of the measurement on helium concentration. We present a mathematical model as a first step toward prediction of the peak shapes and positions. The model includes a useful method to compute estimates of phase diagrams for palladium in the presence of arbitrary mixtures of hydrogen isotopologues. As a result, we expect that this approach can be used to deduce unknown atomic compositions from measured calorimetric data over a useful range of partial pressures of each component.« less

  14. Metal hydride differential scanning calorimetry as an approach to compositional determination of mixtures of hydrogen isotopologues and helium

    SciTech Connect

    Robinson, David B.; Luo, Weifang; Cai, Trevor Y.; Stewart, Kenneth D.

    2015-09-26

    Gaseous mixtures of diatomic hydrogen isotopologues and helium are often encountered in the nuclear energy industry and in analytical chemistry. Compositions of stored mixtures can vary due to interactions with storage and handling materials. When tritium is present, it decays to form ions and helium-3, both of which can lead to further compositional variation. Monitoring of composition is typically achieved by mass spectrometry, a method that is bulky and energy-intensive. Mass spectrometers disperse sample material through vacuum pumps, which is especially troublesome if tritium is present. Moreover, our ultimate goal is to create a compact, fast, low-power sensor that can determine composition with minimal gas consumption and waste generation, as a complement to mass spectrometry that can be instantiated more widely. We propose calorimetry of metal hydrides as an approach to this, due to the strong isotope effect on gas absorption, and demonstrate the sensitivity of measured heat flow to atomic composition of the gas. Peak shifts are discernible when mole fractions change by at least 1%. A mass flow restriction results in a unique dependence of the measurement on helium concentration. We present a mathematical model as a first step toward prediction of the peak shapes and positions. The model includes a useful method to compute estimates of phase diagrams for palladium in the presence of arbitrary mixtures of hydrogen isotopologues. As a result, we expect that this approach can be used to deduce unknown atomic compositions from measured calorimetric data over a useful range of partial pressures of each component.

  15. [Thermal analysis on water components in brain tissue--quantitative determination of free and bound water fractions].

    PubMed

    Furuse, M; Gonda, T; Inao, S; Kuchiwaki, H; Hirai, N; Kageyama, N

    1987-08-01

    In the living system, tissue water is considered to be composed of both free and bound water. Bound water encompasses the structural water of the cell wall and of various biological substances of high molecular weight, such as proteins and polypeptides. The present study was designed to measure thermoanalytically free and bound water on a quantitative basis in fresh brain of rats using differential scanning calorimetry (DSC). Our intention was to determine the fraction of freezable water in tissue. Freezable water in a tissue represents the fraction of free water. In the present study, freezing was conducted at a constant rate of -10 degrees C/min from room temperature to -75 degrees C by a SSC/560 S (Seiko Electronics). The system allows for calculation of the amount of free water from the differential scanning calorimetry curve employing a coloric constant of 79.4 cal/mg. Aluminium oxide was used as calorimetric reference. The fraction of bound water was calculated by subtraction of the amount of free water from that of total tissue water. Water binding to solid tissue component was estimated from tissue dry weight and the bound water fraction. Mean water content of normal gray matter in adult Wistar rats was 76.9 +/- 1.4% (SD). 88.9% of total tissue water was free whereas 11.1 +/- 2.8% (SD) was bound. Bound water of brain parenchyma amounted to 0.44 +/- 0.12 mg/mg dry weight. As compared to other tissues such as cardiac muscle and liver, brain parenchyma obviously exceeded in free water content. The total water content of serum was 94.4 +/- 1.2%; 90.7 +/- 2.6% was free and 9.3 +/- 2.6% (SD) was bound.(ABSTRACT TRUNCATED AT 250 WORDS) PMID:3426861

  16. Implementation of water calorimetry in a 180 MeV scanned pulsed proton beam including an experimental determination of kQ for a Farmer chamber

    NASA Astrophysics Data System (ADS)

    Medin, Joakim

    2010-06-01

    Water calorimetric measurements have been performed in a 180 MeV scanned pulsed proton beam and the absorbed dose determined has been compared with the results obtained using two NE2571 Farmer chambers and the IAEA TRS-398 code of practice. The depth of measurement in water corresponded to a residual range of Rres = 16.5 cm, corresponding to a mean energy of about 150 MeV. Ionization chambers were calibrated in terms of the absorbed dose to water in 60Co at the Swedish Secondary Standard Dosimetry Laboratory, directly traceable to Bureau International des Poids et Mesures. The present experimental investigation has shown that water calorimetry is feasible in a high-energy scanned pulsed proton beam. When comparing the results obtained with water calorimetry and ionometry, the beam quality correction factor, kQ, could be determined for the two NE2571 ionization chambers used. The kQ-factor was found to be 1.032 ± 0.013, which is in good agreement with the factor tabulated in IAEA TRS-398 for this chamber type (1.039 ± 0.018). The present result has also been compared with a previously obtained result in a passively scattered proton beam having similar energy. This comparison yielded a 1.1% deviation, which is not significant considering the combined uncertainties of the two experimental determinations of kQ. The dominating contribution to the combined uncertainty stems from the correction factor for ion recombination in the scanned proton beam (1%), and further studies are required in order to reduce this uncertainty and reveal any possible differences in the kQ-factor between these two proton beam delivery techniques.

  17. HEU age determination

    SciTech Connect

    Moorthy, A.R.; Kato, W.Y.

    1997-07-01

    A new technique has been developed to determine the age of highly enriched uranium (HEU) in solids. Uranium age is defined as the time since the uranium-containing material was last subjected to a process capable of separating uranium from its radioactive-decay daughters. [Most chemical processing, uranium enrichment, volatilization processes, and phase transformations (especially relevant for uranium hexafluoride) can result in separation of the uranium parent material from the decay-product daughters.] Determination of the uranium age, as defined here, may be relevant in verifying arms-control agreements involving uranium-containing nuclear weapons. The HEU age is determined from the ratios of relevant uranium daughter isotopes and their parents, viz {sup 230}Th/{sup 234}U and {sup 231}Pa/{sup 235}U. Uranium isotopes are quantitatively measured by their characteristic gamma rays and their daughters by alpha spectroscopy. In some of the samples, where HEU is enriched more than 99%, the only mode of HEU age determination is by the measurement of {sup 231}Pa since there is negligible quantity of {sup 230}Th due to very low atom concentrations of {sup 234}U in the samples. In this report the methodology and the data for determining the age of two HEU samples are presented.

  18. Determinants of marriage dissolution

    NASA Astrophysics Data System (ADS)

    Rahim, Mohd Amirul Rafiq Abu; Shafie, Siti Aishah Mohd; Hadi, Az'lina Abdul; Razali, Nornadiah Mohd; Azid @ Maarof, Nur Niswah Naslina

    2015-10-01

    Nowadays, the number of divorce cases among Muslim couples is very worrisome whereby the total cases reported in 2013 increased by half of the total cases reported in the previous year. The questions on the true key factors of dissolution of marriage continue to arise. Thus, the objective of this study is to reveal the factors that contribute to the dissolution of marriage. A total of 181 cases and ten potential determinants were included in this study. The potential determinants considered were age at marriage of husband and wife, educational level of husband and wife, employment status of husband and wife, income of husband and wife, the number of children and the presence at a counseling session. Logistic regression analysis was used to analyze the data. The findings revealed that four determinants, namely the income of husband and wife, number of children and the presence at a counselling session were significant in predicting the likelihood of divorce among Muslim couples.

  19. HEU age determination

    SciTech Connect

    Moorthy, A.R.; Kato, W.Y.

    1995-08-01

    A technique has been developed to determine the Highly Enriched Uranium (HEU) Age which is defined as the time since the HEU was produced in an enrichment process. The HEU age is determined from the ratios of relevant uranium parents and their daughters viz {sup 230}Th/{sup 234}U and {sup 231}Pa/{sup 235}U. Uranium isotopes are quantitatively measured by their characteristic gammas and their daughters by alpha spectroscopy. In some of the samples where HEU is enriched more than 99%, the only mode of HEU age determination is by the measurement of {sup 231}Pa since there is negligible quantity of {sup 230}Th due to very low atom concentrations of {sup 234}U in the sample. In this paper we have presented data and methodology of finding the age of two HEU samples.

  20. Sex determination in amphibians.

    PubMed

    Nakamura, Masahisa

    2009-05-01

    The heterogametic sex is male in all mammals, whereas it is female in almost all birds. By contrast, there are two heterogametic types (XX/XY and ZZ/ZW) for genetic sex determination in amphibians. Though the original heterogametic sex was female in amphibians, the two heterogametic types were probably interchangeable, suggesting that sex chromosomes evolved several times in this lineage. Indeed, the frog Rana rugosa has the XX/XY and ZZ/ZW sex-determining systems within a single species, depending on the local population in Japan. The XY and ZW geographic forms with differentiated sex chromosomes probably have a common origin as undifferentiated sex chromosomes resulted from the hybridization between the primary populations of West Japan and Kanto forms. It is clear that the sex chromosomes are still undergoing evolution in this species group. Regardless of the presence of a sex-determining gene in amphibians, the gonadal sex of some species can be changed by sex steroids. Namely, sex steroids can induce the sex reversal, with estrogens inducing the male-to-female sex reversal, whereas androgens have the opposite effect. In R. rugosa, gonadal activity of CYP19 (P450 aromatase) is correlated with the feminization of gonads. Of particular interest is that high levels of CYP19 expression are observed in indifferent gonads at time before sex determination. Increases in the expression of CYP19 in female gonads and CYP17 (P450 17alpha-hydroxylase/C17-20 lyase) in male gonads suggest that the former plays an important role in phenotypic female determination, whereas the latter is needed for male determination. Thus, steroids could be the key factor for sex determination in R. rugosa. In addition to the role of sex steroids in gonadal sex determination in this species, Foxl2 and Sox3 are capable of promoting CYP19 expression. Since both the genes are autosomal, another factor up-regulating CYP19 expression must be recruited. The factor, which may be located on the X or W

  1. Ultrasonic determination of recrystallization

    NASA Technical Reports Server (NTRS)

    Generazio, E. R.

    1986-01-01

    Ultrasonic attenuation was measured for cold worked Nickel 200 samples annealed at increasing temperatures. Localized dislocation density variations, crystalline order and colume percent of recrystallized phase were determined over the anneal temperature range using transmission electron microscopy, X-ray diffraction, and metallurgy. The exponent of the frequency dependence of the attenuation was found to be a key variable relating ultrasonic attenuation to the thermal kinetics of the recrystallization process. Identification of this key variable allows for the ultrasonic determination of onset, degree, and completion of recrystallization.

  2. Determinants of Disciplinary Discontent.

    ERIC Educational Resources Information Center

    Hargens, Lowell L.; Kelly-Wilson, Lisa

    1994-01-01

    Data from the 1984 Carnegie survey of faculty at U.S. universities show substantial disciplinary variation in pessimism that one's field is stagnant. Field-level variations in both anomie and consensus exert strong effects on average levels of scholarly pessimism within fields and are stronger determinants of scholarly pessimism than individual…

  3. Determinants of project success

    NASA Technical Reports Server (NTRS)

    Murphy, D. C.; Baker, B. N.; Fisher, D.

    1974-01-01

    The interactions of numerous project characteristics, with particular reference to project performance, were studied. Determinants of success are identified along with the accompanying implications for client organization, parent organization, project organization, and future research. Variables are selected which are found to have the greatest impact on project outcome, and the methodology and analytic techniques to be employed in identification of those variables are discussed.

  4. Determination of Fat Content

    NASA Astrophysics Data System (ADS)

    Carpenter, Charles

    The term "lipid" refers to a group of compounds that are sparingly soluble in water, but show variable solubility in a number of organic solvents (e.g., ethyl ether, petroleum ether, acetone, ethanol, methanol, benzene). The lipid content of a food determined by extraction with one solvent may be quite different from the lipid content as determined with another solvent of different polarity. Fat content is determined often by solvent extraction methods (e.g., Soxhlet, Goldfish, Mojonnier), but it also can be determined by nonsolvent wet extraction methods (e.g., Babcock, Gerber), and by instrumental methods that rely on the physical and chemical properties of lipids (e.g., infrared, density, X-ray absorption). The method of choice depends on a variety of factors, including the nature of the sample (e.g., dry versus moist), the purpose of the analysis (e.g., official nutrition labeling or rapid quality control), and instrumentation available (e.g., Babcock uses simple glassware and equipment; infrared requires an expensive instrument).

  5. Determination of Alpha

    NASA Astrophysics Data System (ADS)

    Chmeissani, Mokhtar Abdallah

    The determination of the strong coupling constant alpha_ s, using Energy-Energy Correlation Asymmetry and jet mass difference with Mark II data at SLC (91 GeV) is presented. In Energy-Energy Correlation Asymmetry (EECA), we used the same systematic procedure used to determine alpha_ s with MARK II data at PEP (29 GeV). The chi^2 fit suggests that alpha_ s = 0.119 +/- 0.007(stat.) +/- 0.007(syst.). In addition, we used the EECA method to determine the QCD scale parameter Lambda_{LLA}. The chi^2 fit suggests that Lambda _{LLA} = 420 +/- 90(stat.) MeV. In the jet mass difference method, the determination of alpha_ s is based on QCD calculations up to 2nd order. We showed that in this method we are able to reproduce the value of alpha _ s from a Monte Carlo sample to a very high accuracy. The result with this method is alpha _ s = 0.134 +/- 0.085(stat.) +/- 0.004(syst.). The two values of alpha_ s presented in this work are in agreement within the error bars and in a good agreement with recent results of alpha_ s published from other e^+e^- experiments.

  6. Determining TOC in Waters

    ERIC Educational Resources Information Center

    Kehoe, Thomas J.

    1977-01-01

    The instrumental method for detecting total organic carbon (TOC) in water samples is detailed. The method's limitations are discussed and certain precautions that must be taken are emphasized. The subject of TOC versus COD and BOD is investigated and TOC is determined to be a valid indication of biological demand. (BT)

  7. Ultrasonic Determination Of Recrystallization

    NASA Technical Reports Server (NTRS)

    Generazio, Edward R.

    1988-01-01

    State of recrystallization identified. Measurement of ultrasonic attenuation shows promise as means of detecting recrystallization in metal. Technique applicable to real-time acoustic monitoring of thermomechanical treatments. Starting with work-hardened material, one ultrasonically determines effect of annealing, using correlation between ultrasonic attenuation and temperature.

  8. Gender determination in populus

    SciTech Connect

    McLetchie, D.N.; Tuskan, G.A.

    1994-12-31

    Gender, the expression of maleness or femaleness, in dioecious plants has been associated with changes in morphology, physiology, ecological position, and commercial importance of several species, including members of the Salicaceae family. Various mechanisms have been proposed to explain the expression of gender in Salicaceae, including sex chromosomes, simple Mendelian genes, quantitative genes, environment, and genotype-by-environment interactions. Published reports would favor a genetic basis for gender. The objective of this study was to identify molecular markers associated with gender in a segregating family of hybrid poplars. Bulked segregant analysis and chi-squared analysis were used to test for the occurrence of sex chromosomes, individual loci, and chromosome ratios (i.e., ploidy levels) as the mechanisms for gender determination. Examination of 2488 PCR based RAPD markers from 1219 primers revealed nine polymorphic bands between male and female bulked samples. However, linkage analysis indicated that none of these markers were significantly associated with gender. Chisquared results for difference in male-to-female ratios between diploid and triploid genotypes also revealed no significant differences. These findings suggest gender is not controlled via sex chromosomes, simple Mendelian loci or ratios of autosome to gender-determining loci. It is possible that gender is determined genetically by regions of the genome not sampled by the tested markers or by a complex of loci operating in an additive threshold manner or in an epistatic manner. It is also possible that gender is determined environmentally at an early zygote stage, canalizing gender expression.

  9. Waste Determination Equivalency - 12172

    SciTech Connect

    Freeman, Rebecca D.

    2012-07-01

    The Savannah River Site (SRS) is a Department of Energy (DOE) facility encompassing approximately 800 square kilometers near Aiken, South Carolina which began operations in the 1950's with the mission to produce nuclear materials. The SRS contains fifty-one tanks (2 stabilized, 49 yet to be closed) distributed between two liquid radioactive waste storage facilities at SRS containing carbon steel underground tanks with storage capacities ranging from 2,800,000 to 4,900,000 liters. Treatment of the liquid waste from these tanks is essential both to closing older tanks and to maintaining space needed to treat the waste that is eventually vitrified or disposed of onsite. Section 3116 of the Ronald W. Reagan National Defense Authorization Act of Fiscal Year 2005 (NDAA) provides the Secretary of Energy, in consultation with the Nuclear Regulatory Commission (NRC), a methodology to determine that certain waste resulting from prior reprocessing of spent nuclear fuel are not high-level radioactive waste if it can be demonstrated that the waste meets the criteria set forth in Section 3116(a) of the NDAA. The Secretary of Energy, in consultation with the NRC, signed a determination in January 2006, pursuant to Section 3116(a) of the NDAA, for salt waste disposal at the SRS Saltstone Disposal Facility. This determination is based, in part, on the Basis for Section 3116 Determination for Salt Waste Disposal at the Savannah River Site and supporting references, a document that describes the planned methods of liquid waste treatment and the resulting waste streams. The document provides descriptions of the proposed methods for processing salt waste, dividing them into 'Interim Salt Processing' and later processing through the Salt Waste Processing Facility (SWPF). Interim Salt Processing is separated into Deliquification, Dissolution, and Adjustment (DDA) and Actinide Removal Process/Caustic Side Solvent Extraction Unit (ARP/MCU). The Waste Determination was signed by the

  10. Microcalorimetric and SAXS determination of PEO-SDS interactions: the effect of cosolutes formed by ions.

    PubMed

    Barbosa, Aparecida Mageste; Santos, Igor José Boggione; Ferreira, Guilherme Max Dias; da Silva, Maria do Carmo Hespanhol; Teixeira, Alvaro Vianna Novaes de Carvalho; da Silva, Luis Henrique Mendes

    2010-09-23

    The effect of different ionic cosolutes (NaCl, Na(2)SO(4), Li(2)SO(4), NaSCN, Na(2)[Fe(CN)(5)NO], and Na(3)[Co(NO)(6)]) on the interaction between sodium dodecyl sulfate (SDS) and poly(ethylene oxide) (PEO) was examined by small-angle X-ray scattering (SAXS) and isothermal titration calorimetric techniques. The critical aggregation concentration values (cac), the saturation concentration (C(2)), the integral enthalpy change for aggregate formation (ΔH(agg)(int)) and the standard free energy change of micelle adsorption on the macromolecule chain (ΔΔG(agg)) were derived from the calorimetric titration curves. In the presence of 1.00 mmol L(-1) cosolute, no changes in the parameters were observed when compared with those obtained for SDS-PEO interactions in pure water. For NaCl, Na(2)SO(4), Li(2)SO(4), and NaSCN at 10.0 and 100 mmol L(-1), the cosolute presence lowered cac, increased C(2), and the PEO-SDS aggregate became more stable. In the presence of Na(2)[Fe(CN)(5)NO], the calorimetric titration curves changed drastically, showing a possible reduction in the PEO-SDS degree of interaction, possibility disrupting the formed nanostructure; however, the SAXS data confirmed, independent of the small energy observed, the presence of aggregates adsorbed on the polymer chain.

  11. 29 CFR 2590.606-1 - General notice of continuation coverage.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... administrator of a determination by the Social Security Administration, under title II or XVI of the Social... of this chapter, including paragraph (c) of that section relating to the use of electronic media....

  12. 29 CFR 2590.606-1 - General notice of continuation coverage.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... administrator of a determination by the Social Security Administration, under title II or XVI of the Social... of this chapter, including paragraph (c) of that section relating to the use of electronic media....

  13. 29 CFR 2590.606-1 - General notice of continuation coverage.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... administrator of a determination by the Social Security Administration, under title II or XVI of the Social... of this chapter, including paragraph (c) of that section relating to the use of electronic media....

  14. 29 CFR 2590.606-1 - General notice of continuation coverage.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... administrator of a determination by the Social Security Administration, under title II or XVI of the Social... of this chapter, including paragraph (c) of that section relating to the use of electronic media....

  15. Stepwise shockwave velocity determinator

    NASA Technical Reports Server (NTRS)

    Roth, Timothy E.; Beeson, Harold

    1992-01-01

    To provide an uncomplicated and inexpensive method for measuring the far-field velocity of a surface shockwave produced by an explosion, a stepwise shockwave velocity determinator (SSVD) was developed. The velocity determinator is constructed of readily available materials and works on the principle of breaking discrete sensors composed of aluminum foil contacts. The discrete sensors have an average breaking threshold of approximately 7 kPa. An incremental output step of 250 mV is created with each foil contact breakage and is logged by analog-to-digital instrumentation. Velocity data obtained from the SSVD is within approximately 11 percent of the calculated surface shockwave velocity of a muzzle blast from a 30.06 rifle.

  16. Determination of intracellular nitrate.

    PubMed Central

    Romero, J M; Lara, C; Guerrero, M G

    1989-01-01

    A sensitive procedure has been developed for the determination of intracellular nitrate. The method includes: (i) preparation of cell lysates in 2 M-H3PO4 after separation of cells from the outer medium by rapid centrifugation through a layer of silicone oil, and (ii) subsequent nitrate analysis by ion-exchange h.p.l.c. with, as mobile phase, a solution containing 50 mM-H3PO4 and 2% (v/v) tetrahydrofuran, adjusted to pH 1.9 with NaOH. The determination of nitrate is subjected to interference by chloride and sulphate when present in the samples at high concentrations. Nitrite also interferes, but it is easily eliminated by treatment of the samples with sulphamic acid. The method has been successfully applied to the study of nitrate transport in the unicellular cyanobacterium Anacystis nidulans. PMID:2497740

  17. Determination of nickel-63

    SciTech Connect

    Poletiko, C.

    1988-01-01

    The research of activation products in the environment is often centered on cobalt-60 or other gamma emitters, since pure beta emitters require time consuming separations to be counted. However, some beta emitters must be checked because they have a build up in the environment, leading to potential hazards. Among these nuclides, there is nickel-63 which is a pure, soft beta emitter (67 keV) with a long half-life (100 years). A chemical separation, providing good results, was developed. Such a separation is based upon nickel carrier addition in the sample than DMG complex formation and isolation; after elimination of solvent. DMG complex is destroyed. Chemical yield is determined by flame atomic absorption measurement and nickel-63 counted by liquid scintillation. The described procedure allows the determination of low-level activities in different samples (soils, effluents, etc.). Detection limits are close to 0.1 Bq per sample.

  18. [Determination of dental age].

    PubMed

    Willems, Guy

    2005-01-01

    A review of the most commonly used dental age estimating techniques is generated. The most important issue for the forensic odontologist involved in dental age estimation is to employ as many of these methods as possible by performing repetitive measurements and calculations of different age-related parameters. That is the only way in order to try and establish reliable dental age estimations. In particular, a special chapter is attributed to the complex problem of determining the age of majority. PMID:16370435

  19. Determination of Epsomite-Hexahydrite Equilibria by the Humidity-Buffer Technique at 0.1 MPa with Implications for Phase Equilibria in the System MgSO4-H2O

    NASA Astrophysics Data System (ADS)

    Chou, I.-Ming; Seal, Robert R.

    2003-11-01

    Epsomite (MgSO4.7H2O) and hexahydrite (MgSO4.6H2O) are common minerals found in marine evaporite deposits, in saline lakes as precipitates, in weathering zones of coal and metallic deposits, in some soils and their efflorescences, and possibly on the surface of Europa as evaporite deposits. Thermodynamic properties of these two minerals reported in the literature are in poor agreement. In this study, epsomite-hexahydrite equilibria were determined along four humidity-buffer curves at 0.1 MPa and between 25 and 45°C. Results obtained for the reaction epsomite = hexahydrite + H2O, as demonstrated by very tight reversals along each humidity buffer, can be represented by ln K(+/- 0.012) = 20.001 - 7182.07/T, where K is the equilibrium constant, and T is temperature in Kelvin. The derived standard Gibbs free energy of reaction is 10.13 +/- 0.07 kJ/mol, which is essentially the same value as that calculated from vapor pressure measurements reported in the literature. However, this value is at least 0.8 kJ/mol lower than those calculated from the data derived mostly from calorimetric measurements.

  20. Determination of epsomite-hexahydrite equilibria by the humidity-buffer technique at 0.1 MPa with implications for phase equilibria in the system MgSO4-H2O.

    USGS Publications Warehouse

    Chou, I.-Ming; Seal, R.R.

    2003-01-01

    Epsomite (MgSO(4).7H(2)O) and hexahydrite (MgSO(4).6H(2)O) are common minerals found in marine evaporite deposits, in saline lakes as precipitates, in weathering zones of coal and metallic deposits, in some soils and their efflorescences, and possibly on the surface of Europa as evaporite deposits. Thermodynamic properties of these two minerals reported in the literature are in poor agreement. In this study, epsomite-hexahydrite equilibria were determined along four humidity-buffer curves at 0.1 MPa and between 25 and 45 degrees C. Results obtained for the reaction epsomite = hexahydrite + H(2)O, as demonstrated by very tight reversals along each humidity buffer, can be represented by ln K(+/- 0.012) = 20.001 - 7182.07/T, where K is the equilibrium constant, and T is temperature in Kelvin. The derived standard Gibbs free energy of reaction is 10.13 +/- 0.07 kJ/mol, which is essentially the same value as that calculated from vapor pressure measurements reported in the literature. However, this value is at least 0.8 kJ/mol lower than those calculated from the data derived mostly from calorimetric measurements.

  1. Gender determination using cheiloscopy

    PubMed Central

    Padmavathi, B. N.; Makkad, Ramanpal Singh; Rajan, S. Y.; Kolli, Gopi Krishna

    2013-01-01

    Background: Although lip prints have been used as an evidence for human identification in forensic science, there exists a doubt about its role in gender determination. Aims: The present study was designed for documenting common patterns, as well as their variation in the study population, with objective of evaluating uniqueness of the lip print pattern among the study population, as well as to evaluate the possibility of gender determination. Study Design: Two hundred and thirty five lip prints were collected from volunteers among out patients of Darshan Dental College and Hospital, as well as community dental care camps of rural areas around Udaipur. Materials and Methods: Lip prints were recorded with transparent overlay and transferred on to a bond paper. It was then photographed using a Canon EOS 55OD 16 mega pixel digital camera. Software Picasa 3.6 and Microsoft Picture Manager were used to digitally enhance the quality and magnify the image bearing the groove pattern. Lip prints were later analyzed. Statistical Analysis: Pearson chi square test was adopted for statistical analysis and probability (P value) was calculated. Conclusion: In our study, none of the lip prints were identical, thus confirming the role of lip prints in individual identification. Dots, reticular and complex patterns were significant in gender determination. PMID:24255561

  2. Determination of the Structure and Catalytic Mechanism of Sorghum bicolor Caffeic Acid O-Methyltransferase and the Structural Impact of Three brown midrib12 Mutations1[W

    PubMed Central

    Green, Abigail R.; Lewis, Kevin M.; Barr, John T.; Jones, Jeffrey P.; Lu, Fachuang; Ralph, John; Vermerris, Wilfred; Sattler, Scott E.; Kang, ChulHee

    2014-01-01

    Using S-adenosyl-methionine as the methyl donor, caffeic acid O-methyltransferase from sorghum (Sorghum bicolor; SbCOMT) methylates the 5-hydroxyl group of its preferred substrate, 5-hydroxyconiferaldehyde. In order to determine the mechanism of SbCOMT and understand the observed reduction in the lignin syringyl-to-guaiacyl ratio of three brown midrib12 mutants that carry COMT gene missense mutations, we determined the apo-form and S-adenosyl-methionine binary complex SbCOMT crystal structures and established the ternary complex structure with 5-hydroxyconiferaldehyde by molecular modeling. These structures revealed many features shared with monocot ryegrass (Lolium perenne) and dicot alfalfa (Medicago sativa) COMTs. SbCOMT steady-state kinetic and calorimetric data suggest a random bi-bi mechanism. Based on our structural, kinetic, and thermodynamic results, we propose that the observed reactivity hierarchy among 4,5-dihydroxy-3-methoxycinnamyl (and 3,4-dihydroxycinnamyl) aldehyde, alcohol, and acid substrates arises from the ability of the aldehyde to stabilize the anionic intermediate that results from deprotonation of the 5-hydroxyl group by histidine-267. Additionally, despite the presence of other phenylpropanoid substrates in vivo, sinapaldehyde is the preferential product, as demonstrated by its low Km for 5-hydroxyconiferaldehyde. Unlike its acid and alcohol substrates, the aldehydes exhibit product inhibition, and we propose that this is due to nonproductive binding of the S-cis-form of the aldehydes inhibiting productive binding of the S-trans-form. The S-cis-aldehydes most likely act only as inhibitors, because the high rotational energy barrier around the 2-propenyl bond prevents S-trans-conversion, unlike alcohol substrates, whose low 2-propenyl bond rotational energy barrier enables rapid S-cis/S-trans-interconversion. PMID:24948836

  3. HEU age determination

    SciTech Connect

    Moorthy, A.R.; Kato, W.Y.

    1994-12-31

    A criteria that a sample of highly enriched uranium (HEU) had come from a weapons stockpile and not newly produced in an enrichment plant is to show that the HEU had been produced a significant time in the past. The time since the HEU has produced in an enrichment plant is defined as the age of the HEU in this paper. The HEU age is determined by measuring quantitatively the daughter products {sup 230}Th and {sup 231}Pa of {sup 234}U and {sup 235}U, respectively, by first chemical separation of the thorium and protactinium and then conducting alpha spectrometry of the daughter products.

  4. Mass determination of neutrinos

    NASA Technical Reports Server (NTRS)

    Chiu, Hong-Yee

    1988-01-01

    A time-energy correlation method has been developed to determine the signature of a nonzero neutrino mass in a small sample of neutrinos detected from a distant source. The method is applied to the Kamiokande II (Hirata et al., 1987) and IMB (Bionta et al., 1987) observations of neutrino bursts from SN 1987A. Using the Kamiokande II data, the neutrino rest mass is estimated at 2.8 + 2.0, - 1.4 eV and the initial neutrino pulse is found to be less than 0.3 sec full width, followed by an emission tail lasting at least 10 sec.

  5. Satellite altitude determination uncertainties

    NASA Technical Reports Server (NTRS)

    Siry, J. W.

    1972-01-01

    Satellite altitude determination uncertainties will be discussed from the standpoint of the GEOS-C satellite, from the longer range viewpoint afforded by the Geopause concept. Data are focused on methods for short-arc tracking which are essentially geometric in nature. One uses combinations of lasers and collocated cameras. The other method relies only on lasers, using three or more to obtain the position fix. Two typical locales are looked at, the Caribbean area, and a region associated with tracking sites at Goddard, Bermuda and Canada which encompasses a portion of the Gulf Stream in which meanders develop.

  6. Determination of Survivable Fires

    NASA Technical Reports Server (NTRS)

    Dietrich, D. L.; Niehaus, J. E.; Ruff, G. A.; Urban, D. L.; Takahashi, F.; Easton, J. W.; Abbott, A. A.; Graf, J. C.

    2012-01-01

    At NASA, there exists no standardized design or testing protocol for spacecraft fire suppression systems (either handheld or total flooding designs). An extinguisher's efficacy in safely suppressing any reasonable or conceivable fire is the primary benchmark. That concept, however, leads to the question of what a reasonable or conceivable fire is. While there exists the temptation to over-size' the fire extinguisher, weight and volume considerations on spacecraft will always (justifiably) push for the minimum size extinguisher required. This paper attempts to address the question of extinguisher size by examining how large a fire a crew member could successfully survive and extinguish in the confines of a spacecraft. The hazards to the crew and equipment during an accidental fire include excessive pressure rise resulting in a catastrophic rupture of the vehicle skin, excessive temperatures that burn or incapacitate the crew (due to hyperthermia), carbon dioxide build-up or other accumulation of other combustion products (e.g. carbon monoxide). Estimates of these quantities are determined as a function of fire size and mass of material burned. This then becomes the basis for determining the maximum size of a target fire for future fire extinguisher testing.

  7. Determination of radar MTF

    SciTech Connect

    Chambers, D.

    1994-11-15

    The ultimate goal of the Current Meter Array (CMA) is to be able to compare the current patterns detected with the array with radar images of the water surface. The internal wave current patterns modulate the waves on the water surface giving a detectable modulation of the radar cross-section (RCS). The function relating the RCS modulations to the current patterns is the Modulation Transfer Function (MTF). By comparing radar images directly with co-located CMA measurements the MTF can be determined. In this talk radar images and CMA measurements from a recent experiment at Loch Linnhe, Scotland, will be used to make the first direct determination of MTF for an X and S band radar at low grazing angles. The technical problems associated with comparing radar images to CMA data will be explained and the solution method discussed. The results suggest the both current and strain rate contribute equally to the radar modulation for X band. For S band, the strain rate contributes more than the current. The magnitude of the MTF and the RCS modulations are consistent with previous estimates when the wind is blowing perpendicular to the radar look direction.

  8. Environment. Two biggest determinants.

    PubMed

    Zhang, Y

    1994-03-01

    In China, the chair of the Environmental Protection Committee of the National People's Congress, who was the director of the National Environmental Protection Agency for 10 years, notes that population growth puts much pressure on the environment. The Chinese extensively use agricultural and natural resources to meet their basic needs: food, clothing, and shelter. Population control is needed to preserve the environment. In fact, population control and environmental protection are the 2 most significant determinants of sustainable economic growth, social stability, and balanced development in China. The Chinese government allocates 0.8% of its annual gross national product to control of environmental pollution. As a result, urban pollution has been reduced. China takes part in international cooperative efforts.

  9. [Bromatometric determination of oxprenolol].

    PubMed

    Novákné Pékli, M

    1990-07-01

    A bromatometric method was elaborated for the quantitative determination of oxprenolol. 15 to 150 mg of oxprenolol dissolved in 10 cm3 of water is brominated by adding 20.00-40.00 cm3 of 0.02 or 0.1 N potassium bromate solution followed by 0.5-3 g of potassium bromide and 1-10 cm3 of 10% w/w hydrochloric acid. After a reaction time of 15 min. 2-10 cm3 of 10% w/w potassium iodide solution is added followed by 20-40 cm3 of chloroform. The liberated iodine is titrated with standard 0.1 N or 0.01 N sodium thiosulphate solution. A blank titration is also performed and the oxprenolol content is calculated from the difference of the two titrations. Under these conditions one oxprenolol molecule reacts with six bromine atoms. The relative standard deviation is 1.31%.

  10. Complexometric Determination of Calcium

    NASA Astrophysics Data System (ADS)

    Nielsen, S. Suzanne

    Ethylenediaminetetraacetate (EDTA) complexes with numerous mineral ions, including calcium and magnesium. This reaction can be used to determine the amount of these minerals in a sample by a complexometric titration. Endpoints in the titration are detected using indicators that change color when they complex with mineral ions. Calmagite and eriochrome black T (EBT) are such indicators that change from blue to pink when they complex with calcium and magnesium. In the titration of a mineral-containing solution with EDTA, the solution turns from pink to blue at the endpoint with either indicator. The pH affects a complexometric EDTA titration in several ways, and must be carefully controlled. A major application of EDTA titration is testing the hardness of water, for which the method described is an official one (Standard Methods for the Examination of Water and Wastewater, Method 2340C; AOAC Method 920.196).

  11. Sex determination using PCR.

    PubMed

    Kima, Peter E; Rasche, Madeline E

    2004-03-01

    PCR has revolutionized many aspects of biochemistry and molecular biology research. In the following exercise, students learn PCR by isolating their own DNA, amplifying specific segments of the X and Y chromosomes, and estimating the sizes of the PCR products using agarose gel electrophoresis. Based on the pattern of PCR products, students can distinguish between male and female samples and determine the gender of an unknown DNA donor. The exercise is presented for upper division undergraduate majors in microbiology, biochemistry, and molecular biology, but can be adapted to different academic levels and disciplines. The use of student samples in the exercise can enhance learning of these techniques by making PCR and agarose gel electrophoresis directly relevant to the students.

  12. Determinants of Food Allergy

    PubMed Central

    Masilamani, Madhan; Commins, Scott; Shreffler, Wayne

    2012-01-01

    SUMMARY Much has been learned by identifying the molecules that can be recognized by IgE from patients with allergies. Increasingly, by correlating patterns of sensitization with clinical features, it has become possible to distinguish molecules responsible for primary sensitization (complete allergens) from those that are more likely cross-reactive targets. In the case of animal allergens, evolutionary distance seems to be an important factor in determining allergenicity. However, until more is understood regarding the mechanistic details of primary sensitization, including the participation of molecules that stimulate innate immune responses and the repertoire of T-cell antigens, molecules that may or may not themselves be important B-cell antigens, we will not be able to explain fundamental questions, such as why peanut allergy is more severe than soy allergy or why tick exposure is associated with clinically relevant sensitization to a carbohydrate epitope. PMID:22244230

  13. Dietary determinants of obesity.

    PubMed

    Du, Huaidong; Feskens, Edith

    2010-08-01

    Obesity has become a serious public health problem worldwide, and dietary composition can play a role in its prevention and treatment. However, available literature on the impacts of different dietary factors on weight change is inconsistent, or even conflicting. In this review, we briefly summarized the mechanisms and influences of several major dietary determinants of weight change, with a focus on their potential in the prevention of weight gain or regain. We discussed the intake of fat, protein, total carbohydrates, fruits and vegetables, fibre, free sugars, fructose and sugar sweetened beverages, dietary energy density, portion size, eating outside home, glycaemic index and glycaemic load. Popular weight loss diets, including the Atkins diet, Weight Watchers, Ornish diet and Zone diet, are also briefly discussed for their safety and efficacy in the maintenance of weight loss.

  14. Automatic Bayesian polarity determination

    NASA Astrophysics Data System (ADS)

    Pugh, D. J.; White, R. S.; Christie, P. A. F.

    2016-07-01

    The polarity of the first motion of a seismic signal from an earthquake is an important constraint in earthquake source inversion. Microseismic events often have low signal-to-noise ratios, which may lead to difficulties estimating the correct first-motion polarities of the arrivals. This paper describes a probabilistic approach to polarity picking that can be both automated and combined with manual picking. This approach includes a quantitative estimate of the uncertainty of the polarity, improving calculation of the polarity probability density function for source inversion. It is sufficiently fast to be incorporated into an automatic processing workflow. When used in source inversion, the results are consistent with those from manual observations. In some cases, they produce a clearer constraint on the range of high-probability source mechanisms, and are better constrained than source mechanisms determined using a uniform probability of an incorrect polarity pick.

  15. Tracer for circulation determinations

    SciTech Connect

    Moore, H.; Santos, S.; Wysong, R. D.

    1985-03-19

    An improved tracer particle is described comprising an ion exchange core having a polymer coating thereon, the coated ion exchange core having a reaction site capable of reacting with a compound containing an oxirane group, said coated ion exchange core having been treated with a compound containing an oxirane group to react with said coated ion exchange core causing an increase in mass of the tracer particle. Preferably, the ion exchange core is labelled with a radionuclide. These particles have improved characteristics including improved stability against leaching and improved handling properties. Such particles are useful in circulatory determinations involving the injection of the particles as a suspension in a physiologically acceptable carrier or medium into the circulatory system of animals.

  16. Orbit Determination Toolbox

    NASA Technical Reports Server (NTRS)

    Carpenter, James R.; Berry, Kevin; Gregpru. Late; Speckman, Keith; Hur-Diaz, Sun; Surka, Derek; Gaylor, Dave

    2010-01-01

    The Orbit Determination Toolbox is an orbit determination (OD) analysis tool based on MATLAB and Java that provides a flexible way to do early mission analysis. The toolbox is primarily intended for advanced mission analysis such as might be performed in concept exploration, proposal, early design phase, or rapid design center environments. The emphasis is on flexibility, but it has enough fidelity to produce credible results. Insight into all flight dynamics source code is provided. MATLAB is the primary user interface and is used for piecing together measurement and dynamic models. The Java Astrodynamics Toolbox is used as an engine for things that might be slow or inefficient in MATLAB, such as high-fidelity trajectory propagation, lunar and planetary ephemeris look-ups, precession, nutation, polar motion calculations, ephemeris file parsing, and the like. The primary analysis functions are sequential filter/smoother and batch least-squares commands that incorporate Monte-Carlo data simulation, linear covariance analysis, measurement processing, and plotting capabilities at the generic level. These functions have a user interface that is based on that of the MATLAB ODE suite. To perform a specific analysis, users write MATLAB functions that implement truth and design system models. The user provides his or her models as inputs to the filter commands. The software provides a capability to publish and subscribe to a software bus that is compliant with the NASA Goddard Mission Services Evolution Center (GMSEC) standards, to exchange data with other flight dynamics tools to simplify the flight dynamics design cycle. Using the publish and subscribe approach allows for analysts in a rapid design center environment to seamlessly incorporate changes in spacecraft and mission design into navigation analysis and vice versa.

  17. The spectrophotometric determination of streptomycins.

    PubMed

    Wahbi, A M; Abdine, H; Rafik, A; Sadek, H

    1977-11-01

    The spectra produced by the acid treatment and alkaline treatment of streptomycin and dihydrostreptomycin have been investigated to obtain suitable methods for their determination. Mixtures of the two antibiotics have been successfully determined in the UV region. Thus, using the orthogonal function method, dihydrostreptomycin has been determined after acid treatment whereas streptomycin has been determined after alkaline treatment followed by immediate neutralization.

  18. Age determination of raccoons

    USGS Publications Warehouse

    Grau, G.A.; Sanderson, G.C.; Rogers, J.P.

    1970-01-01

    Age criteria, based on 61 skulls and eye lenses from 103 known-age captives, are described for separating raccoons (Procyon lotor) into eight age-classes as follows: young-of-the-year, 1, 2, 3, 4, 5, 6-7, > 7 years. Criteria studied were eye lens nitrogen, cranial suture closure, tooth wear and incisor cementum layers. Lens nitrogen increased rapidly up to 12 months of age, but at much reduced rate thereafter. Total lens nitrogen was useful only in separating young-of-the-year from adults. The closure sequence for five cranial sutures accurately divided the total known-age sample of males into seven groups, and the adults into five groups. The tooth wear criteria divided the known-age sample into five relative age groups, but aging of individuals by this method was inaccurate. Histological sectioning of known-age teeth was the best method of observing layering in the cementum tissue. The technique of basing estimation of age on cementum ring counts, although subjective, was accurate for aging individuals through their fourth year but tended to underestimate the age of animals over 4 years old. However, suture closure or tooth wear can be used to identify males over 4 years old. In field studies, technical difficulties limit the utility of age estimation by cementum layers. Maximum root thickness of the lower canine was accurate in determining the sex of individuals from 5 months to ,at least 48 months of age.

  19. Determining activated carbon performance

    SciTech Connect

    Naylor, W.F.; Rester, D.O.

    1995-07-01

    This article discusses the key elements involved in evaluating a system`s performance. Empty bed contact time (EBCT) is a term used to describe the length of time a liquid stream being treated is in contact with a granular activated carbon bed. The EBCT is the time required for a fluid to pass through the volume equivalent of the media bed, without the media being present. In a bed of granular activated carbon, the void volume or space between particles is usually about 45 percent. Therefore, the EBCT is about twice the true or actual time of contact between the fluid being treated and the GAC particles. The EBCT plays an important role in determining the effectiveness and longevity of granular activated carbon (GAC) used to treat liquids in a fixed-bed adsorber. Factors that influence and are influenced by EBCT, and their relationship to GAC performance in a treatment scheme include: adsorption, mass transfer zone, impurity concentration, adsorption affinity, flow rate and system design considerations.

  20. Perceived positions determine crowding.

    PubMed

    Maus, Gerrit W; Fischer, Jason; Whitney, David

    2011-01-01

    Crowding is a fundamental bottleneck in object recognition. In crowding, an object in the periphery becomes unrecognizable when surrounded by clutter or distractor objects. Crowding depends on the positions of target and distractors, both their eccentricity and their relative spacing. In all previous studies, position has been expressed in terms of retinal position. However, in a number of situations retinal and perceived positions can be dissociated. Does retinal or perceived position determine the magnitude of crowding? Here observers performed an orientation judgment on a target Gabor patch surrounded by distractors that drifted toward or away from the target, causing an illusory motion-induced position shift. Distractors in identical physical positions led to worse performance when they drifted towards the target (appearing closer) versus away from the target (appearing further). This difference in crowding corresponded to the difference in perceived positions. Further, the perceptual mislocalization was necessary for the change in crowding, and both the mislocalization and crowding scaled with drift speed. The results show that crowding occurs after perceived positions have been assigned by the visual system. Crowding does not operate in a purely retinal coordinate system; perceived positions need to be taken into account.

  1. Cryogenic Laser Calorimetry for Impurity Analysis

    NASA Technical Reports Server (NTRS)

    Swimm, R. T.

    1985-01-01

    The results of a one-year effort to determine the applicability of laser-calorimetric spectroscopy to the study of deep-level impurities in silicon are presented. Critical considerations for impurity analysis by laser-calorimetric spectroscopy are discussed, the design and performance of a cryogenic laser calorimeter is described, and measurements of background absorption in high-purity silicon are presented.

  2. Determinants of lemming outbreaks.

    PubMed

    Ims, Rolf A; Yoccoz, Nigel G; Killengreen, Siw T

    2011-02-01

    Population outbreaks in tundra rodents have intrigued scientists for a century as a result of their spectacular appearances and their general lessons in ecology. One outstanding question that has led to competing hypotheses is why sympatric lemmings and voles differ in regularity and shape of their outbreaks. Lemming outbreaks may be lost for decades while vole populations maintain regular population cycles. Moreover, when lemming populations eventually irrupt, they do so more steeply than the vole populations. Norwegian lemmings exhibited a large-scale outbreak synchronously with gray-sided voles in Finnmark, northern Fennoscandia, during 2006 to 2007 for the first time in two decades. Analyses of spatial variability of this outbreak across altitudinal gradients allowed us to identify determinants of the contrasting lemming and vole dynamics. The steeper lemming outbreak trajectories were caused by breeding and population growth during winter, when nonbreeding vole populations consistently declined. The differently shaped lemming and vole outbreaks appear to result from a particular demographic tactic of lemmings that evolved as an adaptation to the long and cold Arctic-Alpine winters. The lemming outbreak amplitude increased with altitude and vole density, indicating that lemming outbreaks are jointly facilitated by low temperatures and apparent mutualism with voles mediated by shared predators. High sensitivity to variation in climate and predation is likely to be the reasons why lemmings have more erratic population dynamics than sympatric voles. The combination of continued climatic warming and dampened vole cycles is expected to further decrease the frequency, amplitude, and geographic range of lemming outbreaks in tundra ecosystems.

  3. Determination of grave disability.

    PubMed

    Wilbert, D E; Jorstad, V; Loren, J D; Wirrer, B

    1976-01-01

    There is a historical dilemma concerning the civil rights of psychiatric patients who are believed to need a protected status because of incompetency. California's Lanterman-Petris-Short Act provides a mechanism for putting the patient under the care of a conservator if the patient is unable to provide for his own personal needs of food, clothing, and shelter. If successful, this legislation will likely be the model for the country. Fifty-one patients for whom the clinical staff desired to initiate conservatorship proceedings were given a test consisting of behavioral tasks specifically designed to be appropriate to the legal definition of grave disability. The natural groupings were: chronic organic brain syndrome, chronic schizophrenia, and other. We found that the grave disability of the organic brain syndrome patients was fairly predictable from their mental status examination, while the grave disability of the chronic schizophrenic patients was unpredictable from their mental status examination and required the application of the behavioral test for an appropriate determination of their ability to perform the functions specified in the law: The Lanterman-Petris-Short Act to provide for personal needs of food, clothing, and shelter. When the method or the proceedings were applied to patients of other diagnostic categories, they were found to be inappropriate. At this writing, our method of evaluation is being recognized and requested by public and legal agencies in our area. It has been used as evidence in court. The procedure is clear, relevant, and easily taught to new workers. The results, given in plain English and in essay form, are readily understood by physician, social worker, judge, and jury alike. We began our study with vexation, ambiguous criteria, and a chronic medical and legal problem; we conclude with a practical and relevant answer.

  4. The kinetics of the thermal denaturation of collagen in unrestrained rat tail tendon determined by differential scanning calorimetry.

    PubMed

    Miles, C A; Burjanadze, T V; Bailey, A J

    1995-01-27

    This paper shows that the position and shape of the denaturation endothem of collagen fibrils are governed by the kinetics of an irreversible rate process. This was proved by measuring the rate of denaturation in rat tail tendons held isothermally at different temperatures, thereby determining rate constant characteristics such as the activation enthalpy and entropy and predicting endotherm position and shape therefrom. Comparison with actual scanning results showed good correspondence. Isothermal measurements of the rate of collagen denaturation, measured continuously using a calorimetric method, were used to determine rate constants for collagen denaturation in tendons immersed in water and 0.5 M acetic acid. The temperature dependence of the rate constants were fitted to the three rate process models, previously examined theoretically: the D and z formulation, the Arrhenius equation and the absolute rate theory. For example, in water the activation enthalpy was 0.518 (+/- 0.016) Mj mol-1 and the activation entropy 1.485 (+/- 0.049) kj mol-1 K-1, while in acetic acid the corresponding figures were 1.306 (+/- 0.099) Mj mol-1 and 4.142 (+/- 0.323) kj mol-1 K-1. These characteristics are discussed in terms of the thermal activation of a region of the molecule, the co-operative unit. The ratio of the activation enthalpy to the calorimetry enthalpy of denaturation indicated a co-operative unit that was 66 (+/- 5) residues long when fibrils were swollen in acetic and the collagen molecules acted essentially independently. On the other hand the intact fibrils in water gave a co-operative unit of 26 (+/- 1) residues long. The reason for the reduction in size of the co-operative unit is that it is surrounded, and therefore stabilized by other molecules in the fibre. It is interesting to note that the suggested co-operative unit lies almost entirely within the "gap" zone of the collagen fibril in its quarter-staggered arrangement of molecules. We believe that the co

  5. Determination of the cis-trans isomerization barriers of L-alanyl-L-proline in aqueous solutions and at water/hydrophobic interfaces by on-line temperature-jump relaxation HPLC and dynamic on-column reaction HPLC.

    PubMed

    Shibukawa, Masami; Miyake, Ayaka; Eda, Sayaka; Saito, Shingo

    2015-09-15

    Proline cis-trans isomerization is known to play a key role in the rate-determining steps of protein folding. It is thus very important to understand the influence of environments, not only bulk solutions but also microenvironments such as interfaces, on the isomerization reaction of proline peptides. Here we present two HPLC methods for measurements of kinetic and equilibrium parameters for the isomerization reactions in bulk solutions and at liquid/solid interfaces. On-line temperature-jump relaxation HPLC (T-jump HPLC) allows the determination of forward and reverse rate constants of the isomerization in a bulk solution by monitoring the whole time course of conversion of pure isomers from both sides of the reaction, in contrast to other HPLC and capillary zone electrophoresis as well as spectrometric and calorimetric methods, which use a mixture of the isomers. We can then determine cis-trans isomerization barriers of the peptide at liquid/solid interfaces from the kinetic data obtained by dynamic on-column reaction HPLC and T-jump HPLC. We observed that the interconversion around the peptide bond for l-alanyl-l-proline (Ala-Pro) in water is accelerated at the surfaces of an alkyl-bonded silica and a poly(styrene-divinylbenzene) copolymer resin, and this is caused by a remarkable decrease in the enthalpy of activation. The molecular structures of the cis and trans forms of Ala-Pro estimated by quantum mechanics calculation reveal that an equilibrium shift toward the cis form as well as the rapid isomerization of Ala-Pro at the water/hydrophobic interfaces can be attributed to the lower polarity of the interfacial water at the surfaces of the hydrophobic materials compared to that of bulk water. PMID:26320351

  6. Determination of the cis-trans isomerization barriers of L-alanyl-L-proline in aqueous solutions and at water/hydrophobic interfaces by on-line temperature-jump relaxation HPLC and dynamic on-column reaction HPLC.

    PubMed

    Shibukawa, Masami; Miyake, Ayaka; Eda, Sayaka; Saito, Shingo

    2015-09-15

    Proline cis-trans isomerization is known to play a key role in the rate-determining steps of protein folding. It is thus very important to understand the influence of environments, not only bulk solutions but also microenvironments such as interfaces, on the isomerization reaction of proline peptides. Here we present two HPLC methods for measurements of kinetic and equilibrium parameters for the isomerization reactions in bulk solutions and at liquid/solid interfaces. On-line temperature-jump relaxation HPLC (T-jump HPLC) allows the determination of forward and reverse rate constants of the isomerization in a bulk solution by monitoring the whole time course of conversion of pure isomers from both sides of the reaction, in contrast to other HPLC and capillary zone electrophoresis as well as spectrometric and calorimetric methods, which use a mixture of the isomers. We can then determine cis-trans isomerization barriers of the peptide at liquid/solid interfaces from the kinetic data obtained by dynamic on-column reaction HPLC and T-jump HPLC. We observed that the interconversion around the peptide bond for l-alanyl-l-proline (Ala-Pro) in water is accelerated at the surfaces of an alkyl-bonded silica and a poly(styrene-divinylbenzene) copolymer resin, and this is caused by a remarkable decrease in the enthalpy of activation. The molecular structures of the cis and trans forms of Ala-Pro estimated by quantum mechanics calculation reveal that an equilibrium shift toward the cis form as well as the rapid isomerization of Ala-Pro at the water/hydrophobic interfaces can be attributed to the lower polarity of the interfacial water at the surfaces of the hydrophobic materials compared to that of bulk water.

  7. Nucleosome positioning determinants.

    PubMed

    Fernandez, Alfonso G; Anderson, John N

    2007-08-17

    A previous report demonstrated that one site in a nucleosome assembled onto a synthetic positioning sequence known as Fragment 67 is hypersensitive to permanganate. The site is required for positioning activity and is located 1.5 turns from the dyad, which is a region of high DNA curvature in the nucleosome. Here, the permanganate sensitivity of the nucleosome positioning Fragment 601 was examined in order to expand the dataset of nucleosome sequences containing KMnO(4) hypersensitive sites. The hyperreactive T residue in the six sites detected as well as the one in Fragment 67 and three in the 5 S rDNA positioning sequence were contained within a TA step. Seven of the ten sequences were of the form CTAGPuG or the related sequence TTAAPu. These motifs were also found in the binding sites of several transcriptional regulatory proteins that kink DNA. In order to assess the significance of these sites, the 10 bp positioning determinant in Fragment 67 was removed and replaced by the nine sequences from the 5 S rDNA and Fragment 601. The results demonstrated that these derivative fragments promoted high nucleosome stability and positioning as compared to a control sequence that contained an AT step in place of the TA step. The importance of the TA step was further tested by making single base-pair substitutions in Fragment 67 and the results revealed that stability and positioning activity followed the order: TA>TG>TT>/=TC approximately GG approximately GA approximately AT. Sequences flanking the TA step were also shown to be critical for nucleosome stability and positioning. Nucleosome positioning was restored to near wild-type levels with (CTG)(3), which can form slipped stranded structures and with one base bulges that kink DNA. The results of this study suggest that local DNA structures are important for positioning and that single base-pair changes at these sites could have profound effects on those genomic functions that depend on ordered nucleosomes. PMID

  8. Determination of body heat storage: how to select the weighting of rectal and skin temperatures for clothed subjects.

    PubMed

    Aoyagi, Y; McLellan, T M; Shephard, R J

    1996-01-01

    Two methods of estimating body heat storage were compared under differing conditions of clothing and acclimation to heat. Sixteen male subjects underwent 6 consecutive days or two 6-day periods, separated by a 1-day rest period of heat acclimation, exercising 60 min.day-1 at 45%-55% of maximal aerobic power in a hot, dry environment (dry bulb temperature 40 degrees C; relative humidity 30%; and wind speed 0.3 m.s-1). Before and after acclimation, the subjects entered the same environment, wearing either normal light combat clothing or clothing protective against nuclear, biological, and chemical agents; they walked on a treadmill at 1.34 m.s-1, 0% slope continuously (n = 11 for normal clothing) or as repeated 15-min bouts of exercise followed by 15-min sitting rest (n = 5 for normal clothing and n = 16 for protective clothing). Average exposure times were 147 min (preacclimation) and 150 min (postacclimation) for continuous exercise and 150 min (both pre- and postacclimation) for intermittent exercise while wearing normal clothing, and 103 min (preacclimation) and 116 min (postacclimation) for intermittent exercise while wearing protective clothing. Heat storage was determined calorimetrically (from heat gains and heat losses) and thermometrically [using various weightings of rectal temperature (Tre) and mean skin temperature (Tsk)]. There were only minor (<5%) differences in estimated heat storage, whether calculations used a single specific heat (3.47 kJ.kg-1.degree C-1) or a value computed according to the subject's body composition. When wearing normal clothing, a formula with an invariant relative weighting for Tre to Tsk of 4:1 provided the best thermometric estimate of heat storage. When wearing protective clothing, the invariant relative weighting of 4:1 underestimated heat storage by 2%-12%; underestimation was attenuated by using respective relative weightings for a thermoneutral and hot environment of 2:1 and 2:1 or 4:1 and 9:1 before acclimation and 4

  9. Determinants for grading Malaysian rice

    NASA Astrophysics Data System (ADS)

    ChePa, Noraziah; Yusoff, Nooraini; Ahmad, Norhayati

    2016-08-01

    Due to un-uniformity of rice grading practices in Malaysia, zones which actively producing rice in Malaysia are using their own way of grading rice. Rice grading is important in determining rice quality and its subsequent price in the market. It is an important process applied in the rice production industry with the purpose of ensuring that the rice produced for the market meets the quality requirements of consumer. Two important aspects that need to be considered in determining rice grades are grading technique and determinants to be used for grading (usually referred as rice attributes). This article proposes the list of determinants to be used in grading Malaysian rice. Determinants were explored through combination of extensive literature review and series of interview with the domain experts and practitioners. The proposed determinants are believed to be beneficial to BERNAS in improving the current Malaysian rice grading process.

  10. Self-Determination. Feature Issue.

    ERIC Educational Resources Information Center

    IMPACT, 1994

    1994-01-01

    This theme issue explores the relevance of self-determination for persons with developmental disabilities across the life span, ways in which it is or can be expressed, and obstacles to its exercise. The articles show the futility of enhancing self-determination by teaching choice-making skills if environments offer no opportunities to exercise…

  11. The Resurgence of Biological Determinism.

    ERIC Educational Resources Information Center

    Segal, Elizabeth A.; Kilty, Keith M.

    1998-01-01

    Addresses two areas where science has been and still is used to justify policies and attitudes that are discriminatory and oppressive: homosexuality and alcoholism. This article analyzes the debate over whether these correlations are biologically or socially determined. Of particular concern is the potential impact of biological determinism on the…

  12. Precise Orbit Determination for ALOS

    NASA Technical Reports Server (NTRS)

    Nakamura, Ryo; Nakamura, Shinichi; Kudo, Nobuo; Katagiri, Seiji

    2007-01-01

    The Advanced Land Observing Satellite (ALOS) has been developed to contribute to the fields of mapping, precise regional land coverage observation, disaster monitoring, and resource surveying. Because the mounted sensors need high geometrical accuracy, precise orbit determination for ALOS is essential for satisfying the mission objectives. So ALOS mounts a GPS receiver and a Laser Reflector (LR) for Satellite Laser Ranging (SLR). This paper deals with the precise orbit determination experiments for ALOS using Global and High Accuracy Trajectory determination System (GUTS) and the evaluation of the orbit determination accuracy by SLR data. The results show that, even though the GPS receiver loses lock of GPS signals more frequently than expected, GPS-based orbit is consistent with SLR-based orbit. And considering the 1 sigma error, orbit determination accuracy of a few decimeters (peak-to-peak) was achieved.

  13. Method of determining glass durability

    DOEpatents

    Jantzen, Carol Maryanne; Pickett, John Butler; Brown, Kevin George; Edwards, Thomas Barry

    1998-01-01

    A process for determining one or more leachate concentrations of one or more components of a glass composition in an aqueous solution of the glass composition by identifying the components of the glass composition, including associated oxides, determining a preliminary glass dissolution estimator, .DELTA.G.sub.p, based upon the free energies of hydration for the component reactant species, determining an accelerated glass dissolution function, .DELTA.G.sub.a, based upon the free energy associated with weak acid dissociation, .DELTA.G.sub.a.sup.WA, and accelerated matrix dissolution at high pH, .DELTA.G.sub.a.sup.SB associated with solution strong base formation, and determining a final hydration free energy, .DELTA.G.sub.f. This final hydration free energy is then used to determine leachate concentrations for elements of interest using a regression analysis and the formula log.sub.10 (N C.sub.i (g/L))=a.sub.i +b.sub.i .DELTA.G.sub.f. The present invention also includes a method to determine whether a particular glass to be produced will be homogeneous or phase separated. The present invention is also directed to methods of monitoring and controlling processes for making glass using these determinations to modify the feedstock materials until a desired glass durability and homogeneity is obtained.

  14. Method of determining glass durability

    DOEpatents

    Jantzen, C.M.; Pickett, J.B.; Brown, K.G.; Edwards, T.B.

    1998-12-08

    A process is described for determining one or more leachate concentrations of one or more components of a glass composition in an aqueous solution of the glass composition by identifying the components of the glass composition, including associated oxides, determining a preliminary glass dissolution estimator, {Delta}G{sub p}, based upon the free energies of hydration for the component reactant species, determining an accelerated glass dissolution function, {Delta}G{sub a}, based upon the free energy associated with weak acid dissociation, {Delta}G{sub a}{sup WA}, and accelerated matrix dissolution at high pH, {Delta}G{sub a}{sup SB} associated with solution strong base formation, and determining a final hydration free energy, {Delta}G{sub f}. This final hydration free energy is then used to determine leachate concentrations for elements of interest using a regression analysis and the formula log{sub 10}(N C{sub i}(g/L))=a{sub i} + b{sub i}{Delta}G{sub f}. The present invention also includes a method to determine whether a particular glass to be produced will be homogeneous or phase separated. The present invention is also directed to methods of monitoring and controlling processes for making glass using these determinations to modify the feedstock materials until a desired glass durability and homogeneity is obtained. 4 figs.

  15. Erroneous theories of sex determination.

    PubMed Central

    Mittwoch, U

    1985-01-01

    Throughout the major part of history, theories of sex determination had to be formulated in the absence of knowledge of ova and spermatozoa. The most persistent theory postulated that males are associated with the right parental side and females with the left side. At the end of the 19th century, sex was thought to be determined by nutrition. Recent findings regarding bilateral asymmetry in human hermaphrodites and of temperature dependent sex determination in reptiles may restore a small degree of credibility to certain theories predating the discovery of sex chromosomes. Images PMID:3892005

  16. [Mercurimetric determination of cephalosporin antibiotics].

    PubMed

    Pospísilová, B; Kubes, J

    1988-04-01

    The conditions for a potenciometric estimation of cefuroxime, cefsulodin, cefotaxime and ceftriaxon with mercury(II) perchlorate after the previous reaction of the antibiotics with hydroxylamine were established. The mercurimetric determination was well reproducible with the relative error of the mean ranging up to 1% and the results are identical with the spectrometric and microbiological determination. There is no need to use a standard. With this technique only the content of effective antibiotic with an intact beta-lactam ring can be estimated. The method did not provide objective results for cefoperazone and cefoxitin. The direct determination of cephalosporin degradation products was verified for cefalexin, cefalothin, cefuroxime, cefsulodin and ceftriaxon.

  17. Step 4: NCI Funding Determinations

    Cancer.gov

    Funding determinations are made around Oct. 1 each federal fiscal year. These decisions take into account several factors, including Congressional mandates, new scientific opportunities and program priorities when deciding which grants receive funding.

  18. Determination of plutonium metal origins

    SciTech Connect

    Moody, K.J.

    1995-02-01

    Forensic signatures are present in any Pu sample that can determine the sample`s origin: isotopic ratio of Pu, progeny species that grow into the sample, and contaminant species left over from incomplete purification of the Pu in fuel reprocessing. In the context of intelligence information, this can result in attribution of responsibility for the product of clandestine proliferant operations or material smuggled from existing stockpiles. A list of signature elements and what can be determined from them have been developed. Work needs to be done in converting concentrations of signature species into a quantitative forensic analysis, particularly in regard to reactor performance, but this should require only a small effort. A radiochemical analysis scheme has been developed for measuring these nuclides; more work is needed, particularly for determining fission product concentrations. A sample of Pu metal has been analyzed and several parameters determined that are strong indicators of its point of origin.

  19. Concept determination of human dignity.

    PubMed

    Edlund, Margareta; Lindwall, Lillemor; von Post, Iréne; Lindström, Unni Å

    2013-12-01

    This study presents findings from an ontological and contextual determination of the concept of dignity. The study had a caritative and caring science perspective and a hermeneutical design. The aim of this study was to increase caring science knowledge of dignity and to gain a determination of dignity as a concept. Eriksson's model for conceptual determination is made up of five part-studies. The ontological and contextual determination indicates that dignity can be understood as absolute dignity, the spiritual dimension characterized by responsibility, freedom, duty, and service, and relative dignity, characterized by the bodily, external aesthetic dimension and the psychical, inner ethical dimension. Dignity exists in human beings both as absolute and relative dignity.

  20. [Determinants of migration to Warsaw].

    PubMed

    Kucinski, K; Rakowski, W

    1990-01-01

    The authors examine trends and determinants of internal migration to Warsaw, Poland. Consideration is given to occupational and socioeconomic status of migrants, rural-urban migration, and effects of migration on marriage. (SUMMARY IN ENG AND RUS)

  1. Orbit determination in satellite geodesy

    NASA Astrophysics Data System (ADS)

    Beutler, G.; Schildknecht, T.; Hugentobler, U.; Gurtner, W.

    2003-04-01

    For centuries orbit determination in Celestial Mechanics was a synonym for the determination of six so-called Keplerian elements of the orbit of a minor planet or a comet based on a short series of (three or more) astrometric places observed from one or more observatories on the Earth's surface. With the advent of the space age the problem changed considerably in several respects: (1) orbits have to be determined for a new class of celestial objects, namely for artificial Earth satellites; (2) new observation types, in particular topocentric distances and radial velocities, are available for the establishment of highly accurate satellite orbits; (3) even for comparatively short arcs (up to a few revolutions) the orbit model that has to be used is much more complicated than for comparable problems in the planetary system: in addition to the gravitational perturbations due to Moon and planets higher-order terms in the Earth's gravity field have to be taken into account as well as non-gravitational effects like atmospheric drag and/or radiation pressure; (4) the parameter space is often of higher than the sixth dimension, because not only the six osculating elements referring to the initial epoch of an arc, but dynamical parameters defining the (a priori imperfectly known) force field have to be determined, as well. It may even be necessary to account for stochastic velocity changes. Orbit determination is not a well-known task in satellit geodesy. This is mainly due to the fact that orbit determination is often imbedded in a much more general parameter estimation problem, where other parameter types (referred to station positions, Earth rotation, atmosphere, etc.) have to be determined, as well. Three examples of "pure" orbit determination problems will be discussed subsequently: ⊎ The first problem intends to optimize the observation process of one Satellite Laser Ranging (SLR) observatory. It is a filter problem, where the orbit is improved in real time with the

  2. Gender determination of avian embryo

    DOEpatents

    Daum, Keith A.; Atkinson, David A.

    2002-01-01

    Disclosed is a method for gender determination of avian embryos. During the embryo incubation process, the outer hard shells of eggs are drilled and samples of allantoic fluid are removed. The allantoic fluids are directly introduced into an ion mobility spectrometer (IMS) for analysis. The resulting spectra contain the relevant marker peaks in the positive or negative mode which correlate with unique mobilities which are sex-specific. This way, the gender of the embryo can be determined.

  3. Mass Determinations of Star Clusters

    NASA Astrophysics Data System (ADS)

    Meylan, Georges

    Mass determinations are difficult to obtain and still frequently characterised by deceptively large uncertainties. We review below the various mass estimators used for star clusters of all ages and luminosities. We highlight a few recent results related to (i) very massive old star clusters, (ii) the differences and similarities between star clusters and cores of dwarf elliptical galaxies, and (iii) the possible strong biases on mass determination induced by tidal effects.

  4. Lunar Prospector Orbit Determination Results

    NASA Technical Reports Server (NTRS)

    Beckman, Mark; Concha, Marco

    1998-01-01

    The orbit support for Lunar Prospector (LP) consists of three main areas: (1) cislunar orbit determination, (2) rapid maneuver assessment using Doppler residuals, and (3) routine mapping orbit determination. The cislunar phase consisted of two trajectory correction maneuvers during the translunar cruise followed by three lunar orbit insertion burns. This paper will detail the cislunar orbit determination accuracy and the real-time assessment of the cislunar trajectory correction and lunar orbit insertion maneuvers. The non-spherical gravity model of the Moon is the primary influence on the mapping orbit determination accuracy. During the first two months of the mission, the GLGM-2 lunar potential model was used. After one month in the mapping orbit, a new potential model was developed that incorporated LP Doppler data. This paper will compare and contrast the mapping orbit determination accuracy using these two models. LP orbit support also includes a new enhancement - a web page to disseminate all definitive and predictive trajectory and mission planning information. The web site provides definitive mapping orbit ephemerides including moon latitude and longitude, and four week predictive products including: ephemeris, moon latitude/longitude, earth shadow, moon shadow, and ground station view periods. This paper will discuss the specifics of this web site.

  5. Vinyl ethers containing an epoxy group. XVI. Reaction of glycidol vinyloxyethyl ether with acetals

    SciTech Connect

    Nedolya, N.A.; Khil'ko, M.Ya.; Trofimov, B.A.; Sigalov, M.V.

    1988-10-10

    In order to obtain branched acetals with epoxide groups (prospective monomers and intermediates) the authors investigated the reaction of acetaldehyde diethyl and di(1,1,3-trihydrotetrafluoropropyl) acetals with glycidol vinyloxyethyl ether. The addition of acetals to vinyl epoxy ethers was realized, and the first representative of compounds of this type, i.e., 9-glycidyloxy-6-ethoxy-4-methyl-3,7-dioxanonane, was obtained. It was also impossible to add a fluoroacetal to butyl vinyl ether (0.08-1.00 wt. % of catalyst CF/sub 3/COOH, BF/sub 3//times/ OEt/sub 2/, 20-80/degree/C, 0.5-3 h).

  6. Follow-Up Study of 1986 Nursing Graduates. Volume XVI, No. 12.

    ERIC Educational Resources Information Center

    Dincher, J.; Flaherty, A.

    In spring 1987, a follow-up study of nursing program graduates was conducted at William Rainey Harper College (WRHC) to examine employment patterns, further education plans, and graduates' evaluation of particular aspects of their WRHC experience. Questionnaires were mailed to 112 nursing students who graduated with an associate degree in 1986.…

  7. E1 and E2 transitions for Fe XVI, Co XVII and Ni XVIII

    NASA Astrophysics Data System (ADS)

    Çelik, G.; Ateş, Ş.

    2016-07-01

    Electric dipole and electric quadrupole transition data for sodium-like iron, cobalt and nickel have been calculated within the weakest bound electron potential model (WBEPM) theory using experimental energy levels and theoretical expectation values of orbital radii corresponding to those energy levels under the assumption of the {LS} coupling scheme. The results obtained from this study provide theoretical transition probability and oscillator strength data requested in many fields of researches, especially astrophysics. The calculated transition data results have been compared with available data in the literature. The present results are consistent with earlier calculations. Some new electric quadrupole transition probability values not existing in the data bases, especially for iron have been obtained using this method.

  8. Economics of Higher Education. Bulletin, 1962, No. 5. OE-50027. [Chapter XVI - Appendices

    ERIC Educational Resources Information Center

    Mushkin, Selma J., Ed.

    1962-01-01

    In the past few years an important beginning has been made toward defining and exploring the major issues in the economics of higher education. The research of economists covers a wide range of problems, from that of the Nation's requirements for college-trained people, to detailed questions of financing. Perhaps no single area of this work offers…

  9. The Path of Carbon in Photosynthesis XVI. Kinetic Relationships of the Intermediates in Steady State Photosynthesis

    DOE R&D Accomplishments Database

    Benson, A. A.; Kawaguchi, S.; Hayes, P.; Calvin, M.

    1952-06-05

    A kinetic study of the accumulation of C{sup 14} in the intermediates of steady state photosynthesis in C{sup 14}O{sub 2} provides information regarding the sequence of reactions involved. The work described applied the radio-chromatographic technique for analysis of the labeled early products. The simultaneous carboxylation reaction resulting in malic acid as well as phosphoglycerate is demonstrated in experiments at high light intensity. A comparison of radioactivities in a number of phosphorylated sugars as a function of time reveals concurrent synthesis of fructose and sedoheptulose phosphates followed by that of ribulose phosphates and later by that of glucose phosphates. The possibility that the cleavage of C{sub 4} compounds to C{sub 2} carbon dioxide acceptors may involve C{sub 7} and C{sub 5} sugars and evidence for this mechanism is presented.

  10. Oral histories in meteoritics and planetary science—XVI: Donald D. Bogard

    NASA Astrophysics Data System (ADS)

    Sears, Derek W. G.

    2012-03-01

    Donald D. Bogard (Don, Fig. 1) became interested in meteorites after seeing the Fayetteville meteorite in an undergraduate astronomy class at the University of Arkansas. During his graduate studies with Paul Kuroda at Arkansas, Don helped discover the Xe decay products of 244Pu. After a postdoctoral period at Caltech, where he learned much from Jerry Wasserburg, Peter Eberhardt, Don Burnett, and Sam Epstein, Don became one of a number of young Ph.D. scientists hired by NASA's Manned Spacecraft Center to set up the Lunar Receiving Laboratory (LRL) and to perform a preliminary examination of Apollo samples. In collaboration with Oliver Schaeffer (SUNY), Joseph Zähringer (Max Planck, Heidelberg), and Raymond Davis (Brookhaven National Laboratory), he built a gas analysis laboratory at JSC, and the noble gas portion of this laboratory remained operational until he retired in 2010. At NASA, Don worked on the lunar regolith, performed pioneering work on cosmic ray produced noble gas isotopes and Ar-Ar dating, the latter for important insights into the thermal and shock history of meteorites and lunar samples. During this work, he discovered that the trapped gases in SNC meteorites were very similar to those of the Martian atmosphere and thus established their Martian origin. Among Don's many administrative accomplishments are helping to establish the Antarctic meteorite and cosmic dust processing programs at JSC and serving as a NASA-HQ discipline scientist, where he advanced peer review and helped create new programs. Don is a recipient of NASA's Scientific Achievement and Exceptional Service Medals and the Meteoritical Society's Leonard Medal.

  11. Limits to sustained energy intake. XVI. Body temperature and physical activity of female mice during pregnancy.

    PubMed

    Gamo, Yuko; Bernard, Amelie; Mitchell, Sharon E; Hambly, Catherine; Al Jothery, Aqeel; Vaanholt, Lobke M; Król, Elzbieta; Speakman, John R

    2013-06-15

    Lactation is the most energy-demanding phase of mammalian reproduction, and lactation performance may be affected by events during pregnancy. For example, food intake may be limited in late pregnancy by competition for space in the abdomen between the alimentary tract and fetuses. Hence, females may need to compensate their energy budgets during pregnancy by reducing activity and lowering body temperature. We explored the relationships between energy intake, body mass, body temperature and physical activity throughout pregnancy in the MF1 mouse. Food intake and body mass of 26 females were recorded daily throughout pregnancy. Body temperature and physical activity were monitored every minute for 23 h a day by implanted transmitters. Body temperature and physical activity declined as pregnancy advanced, while energy intake and body mass increased. Compared with a pre-mating baseline period, mice increased energy intake by 56% in late pregnancy. Although body temperature declined as pregnancy progressed, this served mostly to reverse an increase between baseline and early pregnancy. Reduced physical activity may compensate the energy budget of pregnant mice but body temperature changes do not. Over the last 3 days of pregnancy, food intake declined. Individual variation in energy intake in the last phase of pregnancy was positively related to litter size at birth. As there was no association between the increase in body mass and the decline in intake, we suggest the decline was not caused by competition for abdominal space. These data suggest overall reproductive performance is probably not constrained by events during pregnancy. PMID:23720802

  12. Chelation in metal intoxication XVI. Influence of chelating agents on chromate poisoned rats

    SciTech Connect

    Tandon, S.K.; Srivastava, L.

    1985-01-01

    The ability of selective polyaminocarboxylic acids and common drugs to reduce the body burden of chromium and restore Cr induced biochemical alterations in chromate intoxicated rats was investigated. 1,2 Cychlohexylene dinitrilotetraacetic acid (CDTA) and triethylenetetramine hexacetic acid (TTHA) were more effective than p-aminosalicylic acid (PAS) and isoniazid (INH) in enhancing urinary excretion of Cr, lowering hepatic and blood levels of Cr and restoring inhibited activity of hepatic aldolase. The chromate antidotal property of chelators seem to be related to the combination of nitrogen and oxygen as the electron donating centres.

  13. Treatment of Wilson's disease with zinc XVI: treatment during the pediatric years.

    PubMed

    Brewer, G J; Dick, R D; Johnson, V D; Fink, J K; Kluin, K J; Daniels, S

    2001-03-01

    The objectives were to evaluate appropriate doses of zinc acetate and its efficacy for the maintenance management of Wilson's disease in pediatric cases. Pediatric patients of 1 to 5 years of age were given 25 mg of zinc twice daily; patients of 6 to 15 years of age, if under 125 pounds body weight, were given 25 mg of zinc three times daily; and patients 16 years of age or older were given 50 mg of zinc three times daily. Patients were followed for efficacy (or over-treatment) until their 19th birthday by measuring levels of urine and plasma copper, urine and plasma zinc and through liver function tests and quantitative speech and neurologic scores. Patients were followed for toxicity by measures of blood counts, blood biochemistries, urinalysis, and clinical follow-up. Thirty-four patients, ranging in ages from 3.2 to 17.7 years of age, were included in the study. All doses met efficacy objectives of copper control, zinc levels, neurologic improvement, and maintenance of liver function except for episodes of poor compliance. No instance of over-treatment was encountered. Four patients exhibited mild and transient gastric disturbance from the zinc. Zinc therapy in pediatric patients appears to have a mildly adverse effect on the high-density lipoprotein/total cholesterol ratio, contrary to results of an earlier large study of primarily adults. In conclusion, zinc is effective and safe for the maintenance management of pediatric cases of Wilson's disease. Our data are strongest in children above 10 years of age. More work needs to be done in very young children, and the cholesterol observations need to be studied further.

  14. 76 FR 56263 - Titles II and XVI: Documenting and Evaluating Disability in Young Adults

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-09-12

    ... cystic fibrosis may cause fatigue because of the physical effort involved in the therapy. The frequency..., and 416.969a. See also SSR 96-8p, 61 FR 34474 (1996), available at: http://www.socialsecurity.gov/OP..., 71 FR 45593 (2006), available at:...

  15. Diffuse idiopathic skeletal hyperostosis in the Medici, Grand Dukes of Florence (XVI century)

    PubMed Central

    Giusiani, Sara; Fornaciari, Antonio; Villari, Natale; Vitiello, Angelica; Fornaciari, Gino

    2009-01-01

    Diffuse idiopathic skeletal hyperostosis (DISH) is a common systemic disorder characterised by the ossification of the anterior longitudinal spinal ligament involving at least three contiguous vertebrae and by diffuse extraspinal enthesopathies. The condition is associated with the male sex and with advanced age; its aetiology is uncertain, but seems to be related to obesity and diabetes. The most recent studies in archaeological series demonstrated a relation between high social status and the incidence of DISH. The present study examines two cases of DISH found amongst the members of the Medici family buried in the Basilica of San Lorenzo in Florence. The skeletons of the Grand Dukes Cosimo I (1519–1574) and his son Ferdinand I (1549–1609) showed the typical features of the condition. This result is related to the obesity of the Grand Dukes, attested by the written and artistic sources, and to the protein-based alimentation demonstrated by a paleonutritional study, thus furnishing further evidence to the significance of DISH as a life style. PMID:19669655

  16. Limits to sustained energy intake. XVI. Body temperature and physical activity of female mice during pregnancy.

    PubMed

    Gamo, Yuko; Bernard, Amelie; Mitchell, Sharon E; Hambly, Catherine; Al Jothery, Aqeel; Vaanholt, Lobke M; Król, Elzbieta; Speakman, John R

    2013-06-15

    Lactation is the most energy-demanding phase of mammalian reproduction, and lactation performance may be affected by events during pregnancy. For example, food intake may be limited in late pregnancy by competition for space in the abdomen between the alimentary tract and fetuses. Hence, females may need to compensate their energy budgets during pregnancy by reducing activity and lowering body temperature. We explored the relationships between energy intake, body mass, body temperature and physical activity throughout pregnancy in the MF1 mouse. Food intake and body mass of 26 females were recorded daily throughout pregnancy. Body temperature and physical activity were monitored every minute for 23 h a day by implanted transmitters. Body temperature and physical activity declined as pregnancy advanced, while energy intake and body mass increased. Compared with a pre-mating baseline period, mice increased energy intake by 56% in late pregnancy. Although body temperature declined as pregnancy progressed, this served mostly to reverse an increase between baseline and early pregnancy. Reduced physical activity may compensate the energy budget of pregnant mice but body temperature changes do not. Over the last 3 days of pregnancy, food intake declined. Individual variation in energy intake in the last phase of pregnancy was positively related to litter size at birth. As there was no association between the increase in body mass and the decline in intake, we suggest the decline was not caused by competition for abdominal space. These data suggest overall reproductive performance is probably not constrained by events during pregnancy.

  17. American Association of Women in Community and Junior Colleges Quarterly; Vol. XVI, Nos. 1-4.

    ERIC Educational Resources Information Center

    AAWCJC Quarterly, 1992

    1992-01-01

    The American Association of Women in Community and Junior Colleges (AAWCJC), an affiliated council of the American Association of Community and Junior Colleges (AACJC), produces the "Quarterly" to disseminate information pertinent to the AAWCJC membership and to provide a forum for the discussion of current issues and events. Each issue of the…

  18. AUTOMOTIVE DIESEL MAINTENANCE 2. UNIT XVI, LEARNING ABOUT AC GENERATOR (ALTERNATOR) PRINCIPLES (PART I).

    ERIC Educational Resources Information Center

    Human Engineering Inst., Cleveland, OH.

    THIS MODULE OF A 25-MODULE COURSE IS DESIGNED TO DEVELOP AN UNDERSTANDING OF THE OPERATING PRINCIPLES OF ALTERNATING CURRENT GENERATORS USED ON DIESEL POWERED EQUIPMENT. TOPICS ARE REVIEWING ELECTRICAL FUNDAMENTALS, AND OPERATING PRINCIPLES OF ALTERNATORS. THE MODULE CONSISTS OF A SELF-INSTRUCTIONAL PROGRAMED TRAINING FILM "AC GENERATORS…

  19. THE MEDICI CHILDREN (FLORENCE, XVI-XVII CENTURIES): ANTHROPOLOGICAL STUDY AND PROPOSAL OF IDENTIFICATION.

    PubMed

    Vitiello, Angelica; Fornaciari, Antonio; Giusiani, Sara; Fornaciari, Gino; Giuffra, Valentina

    2015-01-01

    Exploration of the Medici chapels in San Lorenzo in Florence revealed the burials of nine infantile members of the Medici family. Eight children were found in the intact tomb of the last Grand Duke Giangastone (1671- 1737). The crypt contained several small coffins collapsed to the floor or randomly spread over a raised plank, as a result of the disastrous flood of the Arno river in 1966, which partly upset the tomb and left a layer of dry mould. The children's remains, mostly skeletonised, were found inside the coffins or scattered on the floor or on the plank, probably transported by the water. Another child was exhumed from the chapel of Grand Duke Ferdinand I (1549-1609) and Cristina from Lorena (1565-1636). The infantile remains were submitted to anthropological study, which allowed to establish the number of individuals buried in the crypt, and to estimate the age at death. The anthropological results were compared with information provided by archival documents, related to members of the family who died in infantile age. An identification of the children is proposed.

  20. Raman spectra of gases. XVI - Torsional transitions in ethanol and ethanethiol

    NASA Technical Reports Server (NTRS)

    Durig, J. R.; Bucy, W. E.; Wurrey, C. J.; Carreira, L. A.

    1975-01-01

    The Raman spectra of gaseous ethanol and ethanethiol have been investigated. Thiol torsional fundamentals for the gauche conformer of EtSH and EtSD have been observed and the asymmetric potential function for this vibration has been calculated. Methyl torsional transitions and overtones have also been observed for both of these molecules. Barriers to internal rotation for the methyl top are calculated to be 3.77 and 3.84 kcal/mol for the EtSH and EtSD compounds, respectively. Hydroxyl torsional fundamentals were observed at 207 and 170 per cm in the EtOH and EtOD spectra, respectively. Overtones of the methyl torsion in both molecules yield a barrier to internal rotation of 3.62 kcal/mol for the gauche conformer.

  1. Recombination and Electron Impact Excitation Rate Coefficients for S XV and S XVI

    NASA Astrophysics Data System (ADS)

    Mahmood, S.; Ali, S.; Orban, I.; Tashenov, S.; Lindroth, E.; Schuch, R.

    2012-08-01

    Recombination and electron impact excitation of S14+ and S15+ ions was measured at the Stockholm refrigerated electron beam ion trap. The collision energy range was 1.4-3 keV, in which we covered the KLL, KLM, KLN, and KLO dielectronic recombination resonances resulting in S13+ and S14+ ions. The recombination rates were obtained by detecting the charge state distribution with a newly developed time-of-flight technique. Resonance energies and cross-sections calculated within the relativistic many-body perturbation theory for S15+ agree well with the experimental data. The temperature-dependent rate coefficients were extracted from the measured rates and compared with calculations from the literature used for studies of collisionally ionized astrophysical plasmas. Good agreement for S15+ was obtained, while the plasma rates for S14+ were 23% lower than the current published values. In addition to the time-of-flight spectra, the X-ray spectra, produced mainly by photo-recombination and excitation, were also collected. The combination of these two measurements allowed us to separate the photo-recombination and the excitation spectra, and the excitation rate coefficients for summed intensities with known fractions of S14+ and S15+ ions were extracted.

  2. Panchromatic Hubble Andromeda Treasury. XVI. Star Cluster Formation Efficiency and the Clustered Fraction of Young Stars

    NASA Astrophysics Data System (ADS)

    Johnson, L. Clifton; Seth, Anil C.; Dalcanton, Julianne J.; Beerman, Lori C.; Fouesneau, Morgan; Lewis, Alexia R.; Weisz, Daniel R.; Williams, Benjamin F.; Bell, Eric F.; Dolphin, Andrew E.; Larsen, Søren S.; Sandstrom, Karin; Skillman, Evan D.

    2016-08-01

    We use the Panchromatic Hubble Andromeda Treasury survey data set to perform spatially resolved measurements of star cluster formation efficiency (Γ), the fraction of stellar mass formed in long-lived star clusters. We use robust star formation history and cluster parameter constraints, obtained through color–magnitude diagram analysis of resolved stellar populations, to study Andromeda’s cluster and field populations over the last ˜300 Myr. We measure Γ of 4%–8% for young, 10–100 Myr-old populations in M31. We find that cluster formation efficiency varies systematically across the M31 disk, consistent with variations in mid-plane pressure. These Γ measurements expand the range of well-studied galactic environments, providing precise constraints in an H i-dominated, low-intensity star formation environment. Spatially resolved results from M31 are broadly consistent with previous trends observed on galaxy-integrated scales, where Γ increases with increasing star formation rate surface density (ΣSFR). However, we can explain observed scatter in the relation and attain better agreement between observations and theoretical models if we account for environmental variations in gas depletion time (τ dep) when modeling Γ, accounting for the qualitative shift in star formation behavior when transitioning from a H2-dominated to a H i-dominated interstellar medium. We also demonstrate that Γ measurements in high ΣSFR starburst systems are well-explained by τ dep-dependent fiducial Γ models.

  3. VizieR Online Data Catalog: VMC survey. XVI. (Piatti+, 2015)

    NASA Astrophysics Data System (ADS)

    Piatti, A. E.; de Grijs, R.; Ripepi, V.; Ivanov, V. D.; Cioni, M.-R. L.; Marconi, M.; Rubele, S.; Bekki, K.; For, B.-Q.

    2016-06-01

    The VMC and its initial data are thoroughly described in Cioni et al. (2011A&A...527A.116C), to which we refer the reader for details. Here, we used data of two VMC tiles located in the central part of the LMC bar (LMC 6_4) and in a region covering the 30 Doradus star-forming region (LMC 6_6), for which the VISTA imaging campaign has been completed. (2 data files).

  4. Panchromatic Hubble Andromeda Treasury. XVI. Star Cluster Formation Efficiency and the Clustered Fraction of Young Stars

    NASA Astrophysics Data System (ADS)

    Johnson, L. Clifton; Seth, Anil C.; Dalcanton, Julianne J.; Beerman, Lori C.; Fouesneau, Morgan; Lewis, Alexia R.; Weisz, Daniel R.; Williams, Benjamin F.; Bell, Eric F.; Dolphin, Andrew E.; Larsen, Søren S.; Sandstrom, Karin; Skillman, Evan D.

    2016-08-01

    We use the Panchromatic Hubble Andromeda Treasury survey data set to perform spatially resolved measurements of star cluster formation efficiency (Γ), the fraction of stellar mass formed in long-lived star clusters. We use robust star formation history and cluster parameter constraints, obtained through color-magnitude diagram analysis of resolved stellar populations, to study Andromeda’s cluster and field populations over the last ˜300 Myr. We measure Γ of 4%-8% for young, 10-100 Myr-old populations in M31. We find that cluster formation efficiency varies systematically across the M31 disk, consistent with variations in mid-plane pressure. These Γ measurements expand the range of well-studied galactic environments, providing precise constraints in an H i-dominated, low-intensity star formation environment. Spatially resolved results from M31 are broadly consistent with previous trends observed on galaxy-integrated scales, where Γ increases with increasing star formation rate surface density (ΣSFR). However, we can explain observed scatter in the relation and attain better agreement between observations and theoretical models if we account for environmental variations in gas depletion time (τ dep) when modeling Γ, accounting for the qualitative shift in star formation behavior when transitioning from a H2-dominated to a H i-dominated interstellar medium. We also demonstrate that Γ measurements in high ΣSFR starburst systems are well-explained by τ dep-dependent fiducial Γ models.

  5. Nutrition and somatomedin. XVI: Somatomedins and somatomedin inhibitors in fasted and refed rats.

    PubMed

    Phillips, L S; Goldstein, S; Gavin, J R

    1988-03-01

    Nutritional deprivation is associated with poor growth and decreased levels of net circulating somatomedin activity, as measured by bioassay. Since somatomedin activity reflects the contributions both of somatomedins (which stimulate cartilage) and of somatomedin inhibitors (which antagonize the ability of the somatomedins to stimulate cartilage), we asked if changes in net somatomedin activity could involve progressive underlying alterations in levels of both somatomedins and somatomedin inhibitors. Groups of rats were killed during three days of fasting and 24 hours of refeeding. Fasting was associated with a rise in serum beta-hydroxybutyrate from 1.6 to 12.6 mmol/L after one day, followed by a decline to 4 mmol/L at three days. Somatomedins (low-MW) were separated from somatomedin inhibitors (high-MW) by gel permeation chromatography at acid pH on Sephadex G-50 and TSK-2000 HPLC. Somatomedins fell 35% after one day of fasting, and decreased to 59% below control levels after three days (P less than .05). Somatomedins did not change with six hours of refeeding, but then rose rapidly, reaching control levels after 24 hours. Somatomedins were correlated with change in weight (r = .41, P less than .05), but not with glucose or beta-hydroxybutyrate. Inhibitors rose to 195% above control-levels after one day of fasting, and continued to rise to 375% above control after three days (P less than .01). In contrast to the delayed change in somatomedins with refeeding, there was an abrupt fall in inhibitors (41% below three-day fasted levels after six hours), returning to control levels after 24 hours.(ABSTRACT TRUNCATED AT 250 WORDS)

  6. Proceedings of Workshop XVI; The dynamic characteristics of faulting inferred from recordings of strong ground motion

    USGS Publications Warehouse

    Boatwright, John; Jacobson, Muriel L.

    1982-01-01

    The strong ground motions radiated by earthquake faulting are controlled by the dynamic characteristics of the faulting process. Although this assertion seems self-evident, seismologists have only recently begun to derive and test quantitative relations between common measures of strong ground motion and the dynamic characteristics of faulting. Interest in this problem has increased dramatically in past several years, however, resulting in a number of important advances. The research presented in this workshop is a significant part of this scientific development. Watching this development occur through the work of many scientists is exciting; to be able to gather a number of these scientists together in one workshop is a remarkable opportunity.

  7. A Predictive Framework for Determining How Journalists Determine News.

    ERIC Educational Resources Information Center

    Gaudino, James L.

    To determine how to articulate a concrete definition of the substance of the journalist's occupation, this paper offers a propositional framework of news value based on Kurt Lewin's gatekeeper model. First, the paper follows the established suggestion that news decisions are best studied from a gatekeeping perspective or that "news is whatever…

  8. Ecotoxicological Perspectives of Sex Determination.

    PubMed

    Mizoguchi, Beatriz A; Valenzuela, Nicole

    2016-01-01

    Sex determination or the commitment of the embryo to its sexual fate is a fundamental developmental process with paramount consequences in ecology and evolution. This process, whether triggered by environmental factors or genotypic constitution, can be derailed by environmental contaminants that alter the endocrine system, which is a key component of the regulatory network underlying vertebrate sex determination. Here, we review the molecular basis of sex determination, the endocrine components of its regulation, the maternal and endogenous sources of hormones to the developing embryo, and the routes through which endocrine disrupting chemicals (EDCs) affect gonadal development in reptiles, especially turtles. Among EDCs, we focus on PCBs, BPA, pesticides like atrazine, nitrates, and heavy metals. We also consider whether adaptation might be possible in the face of persistent chemical insult and conclude that, while plausible, contemporary environmental change may outpace adaptive evolution, particularly for many species that are already endangered and suffer from small population sizes. PMID:27022970

  9. Determination of radium in water

    USGS Publications Warehouse

    Barker, Franklin Butt; Johnson, J.O.

    1964-01-01

    Radium isotopes are common radioactive constituents of natural waters. The concentration of radium-226 in potable water is of particular significance because this isotope is generally considered the most hazardous of all radionuclides with respect to ingestion. The approximate concentration of radium-226 is determined after coprecipitating radium with barium sulfate. The short-lived daughters of radium are allowed to grow for 10-12 days, then the alpha activity of the precipitate is measured and compared with that of a precipitate containing a known amount of radium-226. Concentrations of the individual alpha-emitting isotopes of radium-223, radium-224, and radium-226, are determined by coprecipitating radium first with lead sulfate, then with barium chloride, and finally with barium sulfate. This final precipitate is initially free of other alpha-emitting nuclides, thus permitting the isotopic composition to be determined by measuring the growth and decay of the alpha activity of the precipitate.

  10. Lessons for Inductive Germline Determination

    PubMed Central

    Seervai, Riyad N.H.; Wessel, Gary M.

    2015-01-01

    SUMMARY Formation of the germline in an embryo marks a fresh round of reproductive potential, yet the developmental stage and location within the embryo where the primordial germ cells (PGCs) form differs wildly among species. In most animals, the germline is formed either by an inherited mechanism, in which maternal provisions within the oocyte drive localized germ-cell fate once acquired in the embryo, or an inductive mechanism that involves signaling between cells that directs germ-cell fate. The inherited mechanism has been widely studied in model organisms such as Drosophila melanogaster, Caenorhabditis elegans, Xenopus laevis, and Danio rerio. Given the rapid generation time and the effective adaptation for laboratory research of these organisms, it is not coincidental that research on these organisms has led the field in elucidating mechanisms for germline specification. The inductive mechanism, however, is less well understood and is studied primarily in the mouse (Mus musculus). In this review, we compare and contrast these two fundamental mechanisms for germline determination, beginning with the key molecular determinants that play a role in the formation of germ cells across all animal taxa. We next explore the current understanding of the inductive mechanism of germ-cell determination in mice, and evaluate the hypotheses for selective pressures on these contrasting mechanisms. We then discuss the hypothesis that the transition between these determination mechanisms, which has happened many times in phylogeny, is more of a continuum than a binary change. Finally, we propose an analogy between germline determination and sex determination in vertebrates—two of the milestones of reproduction and development—in which animals use contrasting strategies to activate similar pathways. PMID:23450642

  11. MEANS FOR DETERMINING CENTRIFUGE ALIGNMENT

    DOEpatents

    Smith, W.Q.

    1958-08-26

    An apparatus is presented for remotely determining the alignment of a centrifuge. The centrifage shaft is provided with a shoulder, upon which two followers ride, one for detecting radial movements, and one upon the shoulder face for determining the axial motion. The followers are attached to separate liquid filled bellows, and a tube connects each bellows to its respective indicating gage at a remote location. Vibrations produced by misalignment of the centrifuge shaft are transmitted to the bellows, and tbence through the tubing to the indicator gage. This apparatus is particularly useful for operation in a hot cell where the materials handled are dangerous to the operating personnel.

  12. Determination of pyrotechnic functional margin

    NASA Technical Reports Server (NTRS)

    Bement, Laurence J.; Schimmel, Morry L.

    1993-01-01

    Following the failure of a previously qualified pyrotechnically actuated pin puller design, an investigation led to a redesign and requalification. The emphasis of the second qualification was placed on determining the functional margin of the pin puller by comparing the energy deliverable by the pyrotechnic cartridge to the energy required to accomplish the function. Also determined were the effects of functional variables. This paper describes the failure investigation, the test methods employed and the results of the evaluation, and provides a recommended approach to assure the successful functioning of pyrotechnic devices.

  13. Decoherence, determinism and chaos revisited

    SciTech Connect

    Noyes, H.P.

    1994-11-15

    We suggest that the derivation of the free space Maxwell Equations for classical electromagnetism, using a discrete ordered calculus developed by L.H. Kauffman and T. Etter, necessarily pushes the discussion of determinism in natural science down to the level of relativistic quantum mechanics and hence renders the mathematical phenomena studied in deterministic chaos research irrelevant to the question of whether the world investigated by physics is deterministic. We believe that this argument reinforces Suppes` contention that the issue of determinism versus indeterminism should be viewed as a Kantian antinomy incapable of investigation using currently available scientific tools.

  14. Time domain period determination techniques

    NASA Technical Reports Server (NTRS)

    Stellingwerf, R. F.

    1980-01-01

    Two simple period determination schemes are discussed. They are well suited to problems involving non-sinusoidal periodic phenomena sampled at a few irregularly spaced points. Statistical properties are discussed. The techniques are applied to the double mode Cepheids BK Cen and TU Cas as test cases.

  15. Videos Determine the Moon's "g"

    ERIC Educational Resources Information Center

    Persson, J. R.; Hagen, J. E.

    2011-01-01

    Determining the acceleration of a free-falling object due to gravity is a standard experiment in physics. Different methods to do this have been developed over the years. This article discusses the use of video-analysis tools as another method. If there is a video available and a known scale it is possible to analyse the motion. The use of video…

  16. Cesium Eluate Physical Property Determination

    SciTech Connect

    Baich, M.A.

    2001-02-13

    Two bench-scale process simulations of the proposed cesium eluate evaporation process of concentrating eluate produced in the Hanford Site Waste Treatment Plant were conducted. The primary objective of these experiments was to determine the physical properties and the saturation concentration of the eluate evaporator bottoms while producing condensate approximately 0.50 molar HN03.

  17. Determining Learning Disabilities in Mathematics.

    ERIC Educational Resources Information Center

    Dunlap, William P.; And Others

    1979-01-01

    To determine the generalizability of reading expectancy formulas in ascertaining mathematics expectancy levels, correlation coefficients were computed between the scores of 150 Ss (7 to 12 years old) with learning problems on standardized mathematics and reading tests and expectancy scores. Formulas correlated higher with Ss' actual mathematics…

  18. Inulin determination for food labeling.

    PubMed

    Zuleta, A; Sambucetti, M E

    2001-10-01

    Inulin and oligofructose exhibit valuable nutritional and functional attributes, so they are used as supplements as soluble fiber or as macronutrient substitutes. As classic analytical methods for dietary fiber measurement are not effective, several specific methods have been proposed. These methods measure total fructans and are based on one or more enzymatic sample treatments and determination of released sugars. To determine inulin for labeling purposes, we developed an easy and rapid anion-exchange high-performance liquid chromatography (HPLC) method following water extraction of inulin. HPLC conditions included an Aminex HPX- 87C column (Bio-Rad), deionized water at 85 degrees C as the mobile phase and a refractive index detector. The tested foods included tailor-made food products containing known amounts of inulin and commercial products (cookies, milk, ice creams, cheese, and cereal bars). The average recovery was 97%, and the coefficient of variation ranged from 1.1 to 5% in the food matrixes. The obtained results showed that this method provides an easier, faster and cheaper alternative than previous techniques for determining inulin with enough accuracy and precision for routine labeling purposes by direct determination of inulin by HPLC with refractive index detection. PMID:11599989

  19. Processing Determinants of Reading Speed.

    ERIC Educational Resources Information Center

    Jackson, Mark D.; McClelland, James L.

    1979-01-01

    Two groups of undergraduates differing in reading ability were tested on a number of reaction-time tasks designed to determine the speed of encoding visual information at several different levels, tests of sensory functions, verbal and quantitative reasoning ability, short-term auditory memory span, and ability to comprehend spoken text.…

  20. Self-Determination and Bilingualism

    ERIC Educational Resources Information Center

    Landry, Rodrigue; Allard, Real; Deveau, Kenneth

    2009-01-01

    This article focuses on additive bilingualism for minority group children, more specifically the development of strong literacy skills in English and in the children's language. The personal autonomization language learning (PALL) model is presented. It specifies eight testable hypotheses. Self-determination theory (SDT) is central in the PALL…

  1. Determinants of Elementary School Grading.

    ERIC Educational Resources Information Center

    Leiter, Jeffrey; Brown, James S.

    1985-01-01

    Grades given by primary school teachers were found to reflect classroom-specific achievement more than widely valued achievement measured by standardized test scores. The strongest determinant of grading, however, was found to be the effect that a grade in one subject has on the grade in a second subject. (Author/RM)

  2. Cohesin in determining chromosome architecture

    SciTech Connect

    Haering, Christian H.; Jessberger, Rolf

    2012-07-15

    Cells use ring-like structured protein complexes for various tasks in DNA dynamics. The tripartite cohesin ring is particularly suited to determine chromosome architecture, for it is large and dynamic, may acquire different forms, and is involved in several distinct nuclear processes. This review focuses on cohesin's role in structuring chromosomes during mitotic and meiotic cell divisions and during interphase.

  3. Plasma digital density determining device

    DOEpatents

    Sprott, Julien C.; Lovell, Thomas W.; Holly, Donald J.

    1976-01-01

    The density of a decaying plasma in an electrically conducting enclosure is determined by applying an excitation to the cavity formed by the enclosure and counting digitally the number of resonant frequencies traversed by the combination of the cavity and the decaying plasma.

  4. Determinants and Polynomial Root Structure

    ERIC Educational Resources Information Center

    De Pillis, L. G.

    2005-01-01

    A little known property of determinants is developed in a manner accessible to beginning undergraduates in linear algebra. Using the language of matrix theory, a classical result by Sylvester that describes when two polynomials have a common root is recaptured. Among results concerning the structure of polynomial roots, polynomials with pairs of…

  5. Self-Determination and Choice

    ERIC Educational Resources Information Center

    Wehmeyer, Michael L.; Abery, Brian H.

    2013-01-01

    Promoting self-determination and choice opportunities for people with intellectual and developmental disabilities has become best practice in the field. This article reviews the research and development activities conducted by the authors over the past several decades and provides a synthesis of the knowledge in the field pertaining to efforts to…

  6. Determining Salinity by Simple Means.

    ERIC Educational Resources Information Center

    Schlenker, Richard M.

    This paper describes the construction and use of a simple salinometer. The salinometer is composed, mainly, of a milliammeter and a battery and uses the measurement of current flow to determine the salinity of water. A complete list of materials is given, as are details of construction and operation of the equipment. The use of the salinometer in…

  7. Low thrust orbit determination program

    NASA Technical Reports Server (NTRS)

    Hong, P. E.; Shults, G. L.; Huling, K. R.; Ratliff, C. W.

    1972-01-01

    Logical flow and guidelines are provided for the construction of a low thrust orbit determination computer program. The program, tentatively called FRACAS (filter response analysis for continuously accelerating spacecraft), is capable of generating a reference low thrust trajectory, performing a linear covariance analysis of guidance and navigation processes, and analyzing trajectory nonlinearities in Monte Carlo fashion. The choice of trajectory, guidance and navigation models has been made after extensive literature surveys and investigation of previous software. A key part of program design relied upon experience gained in developing and using Martin Marietta Aerospace programs: TOPSEP (Targeting/Optimization for Solar Electric Propulsion), GODSEP (Guidance and Orbit Determination for SEP) and SIMSEP (Simulation of SEP).

  8. System for determining aerodynamic imbalance

    NASA Technical Reports Server (NTRS)

    Churchill, Gary B. (Inventor); Cheung, Benny K. (Inventor)

    1994-01-01

    A system is provided for determining tracking error in a propeller or rotor driven aircraft by determining differences in the aerodynamic loading on the propeller or rotor blades of the aircraft. The system includes a microphone disposed relative to the blades during the rotation thereof so as to receive separate pressure pulses produced by each of the blades during the passage thereof by the microphone. A low pass filter filters the output signal produced by the microphone, the low pass filter having an upper cut-off frequency set below the frequency at which the blades pass by the microphone. A sensor produces an output signal after each complete revolution of the blades, and a recording display device displays the outputs of the low pass filter and sensor so as to enable evaluation of the relative magnitudes of the pressure pulses produced by passage of the blades by the microphone during each complete revolution of the blades.

  9. Method for determining gene knockouts

    DOEpatents

    Maranas, Costa D; Burgard, Anthony R; Pharkya, Priti

    2013-06-04

    A method for determining candidates for gene deletions and additions using a model of a metabolic network associated with an organism, the model includes a plurality of metabolic reactions defining metabolite relationships, the method includes selecting a bioengineering objective for the organism, selecting at least one cellular objective, forming an optimization problem that couples the at least one cellular objective with the bioengineering objective, and solving the optimization problem to yield at least one candidate.

  10. System for determining biofuel concentration

    DOEpatents

    Huff, Shean P.; Janke, Christopher James; Kass, Michael D.; Lewis, Sr, Samuel Arthur; Pawel, Steven J; Theiss, Timothy J.

    2016-09-13

    A measurement device or system configured to measure the content of biofuels within a fuel blend. By measuring a state of a responsive material within a fuel blend, a biofuel content of the fuel blend may be measured. For example, the solubility of a responsive material to biofuel content within a fuel blend, may affect a property of the responsive material, such as shape, dimensional size, or electrical impedance, which may be measured and used as a basis for determining biofuel content.

  11. Range determination for scannerless imaging

    DOEpatents

    Muguira, Maritza Rosa; Sackos, John Theodore; Bradley, Bart Davis; Nellums, Robert

    2000-01-01

    A new method of operating a scannerless range imaging system (e.g., a scannerless laser radar) has been developed. This method is designed to compensate for nonlinear effects which appear in many real-world components. The system operates by determining the phase shift of the laser modulation, which is a physical quantity related physically to the path length between the laser source and the detector, for each pixel of an image.

  12. In-flight thrust determination

    NASA Technical Reports Server (NTRS)

    Abernethy, Robert B.; Adams, Gary R.; Ascough, John C.; Baer-Riedhart, Jennifer L.; Balkcom, George H.; Biesiadny, Thomas

    1986-01-01

    The major aspects of processes that may be used for the determination of in-flight thrust are reviewed. Basic definitions are presented as well as analytical and ground-test methods for gathering data and calculating the thrust of the propulsion system during the flight development program of the aircraft. Test analysis examples include a single-exhaust turbofan, an intermediate-cowl turbofan, and a mixed-flow afterburning turbofan.

  13. Method for determining gene knockouts

    DOEpatents

    Maranas, Costas D.; Burgard, Anthony R.; Pharkya, Priti

    2011-09-27

    A method for determining candidates for gene deletions and additions using a model of a metabolic network associated with an organism, the model includes a plurality of metabolic reactions defining metabolite relationships, the method includes selecting a bioengineering objective for the organism, selecting at least one cellular objective, forming an optimization problem that couples the at least one cellular objective with the bioengineering objective, and solving the optimization problem to yield at least one candidate.

  14. Determination of lipolytic enzyme activities.

    PubMed

    Jaeger, Karl-Erich; Kovacic, Filip

    2014-01-01

    Pseudomonas aeruginosa is a versatile human opportunistic pathogen that produces and secretes an arsenal of enzymes, proteins and small molecules many of which serve as virulence factors. Notably, about 40 % of P. aeruginosa genes code for proteins of unknown function, among them more than 80 encoding putative, but still unknown lipolytic enzymes. This group of hydrolases (EC 3.1.1) is known already for decades, but only recently, several of these enzymes have attracted attention as potential virulence factors. Reliable and reproducible enzymatic activity assays are crucial to determine their physiological function and particularly assess their contribution to pathogenicity. As a consequence of the unique biochemical properties of lipids resulting in the formation of micellar structures in water, the reproducible preparation of substrate emulsions is strongly dependent on the method used. Furthermore, the physicochemical properties of the respective substrate emulsion may drastically affect the activities of the tested lipolytic enzymes. Here, we describe common methods for the activity determination of lipase, esterase, phospholipase, and lysophospholipase. These methods cover lipolytic activity assays carried out in vitro, with cell extracts or separated subcellular compartments and with purified enzymes. We have attempted to describe standardized protocols, allowing the determination and comparison of enzymatic activities of lipolytic enzymes from different sources. These methods should also encourage the Pseudomonas community to address the wealth of still unexplored lipolytic enzymes encoded and produced by P. aeruginosa.

  15. Gender determination from pulpal tissue

    PubMed Central

    Khorate, Manisha M.; Dhupar, Anita; Ahmed, Junaid; Dinkar, Ajit D.

    2014-01-01

    Objective: To evaluate the diagnostic performance of X (Barr body [BB]) and Y (F body [FB]) chromosomes observed in dental pulp tissue for gender determination of an individual. Materials and Methods: The study was carried out on 100 teeth (50 male and 50 female), which were indicated for extraction. The teeth were sectioned at various intervals (within 12 h to 49 days post-extraction), and the pulpal tissue was obtained. Two slides for each pulp tissue were prepared, one for 5% Quinacrine dihydrochloride stain (FB) and the other for Hemotoxylin and Eosin stain (BB). The slides were then observed under the fluorescent microscope for FB and under the light microscope for the BB respectively. Results: Gender determination from human pulp is possible up to 7 weeks. The percentage of FB and BB decrease gradually as the time interval increases. Further, an equation was derived from the data based on the canonical discriminant function coefficients. Conclusion: The determination of gender based on a joint search for the presence or absence of X (BB) and Y (FB) Chromosome is a reliable and cost-effective technique. PMID:25125918

  16. Meteorological determinants of air quality

    NASA Astrophysics Data System (ADS)

    Turoldo, F.; Del Frate, S.; Gallai, I.; Giaiotti, D. B.; Montanari, F.; Stel, F.; Goi, D.

    2010-09-01

    Air quality is the result of complex phenomena, among which the major role is played by human emissions of pollutants. Atmospheric processes act as determinants, e.g., modulating, dumping or amplifying the effects of emissions as an orchestra's director does with musical instruments. In this work, a series of small-scale and meso-scale meteorological determinants of air-quality are presented as they are observed in an area characterized by complex orography (Friuli Venezia Giulia, in the north-eastern side of Italy). In particular, attention is devoted to: i) meso-scale flows favouring the persistence of high concentrations of particulate matter; ii) meso-scale periodic flows (breezes) favouring high values of particulate matter; iii) local-scale thermodynamic behaviour favouring high atmospheric values of nitrogen oxides. The effects of these different classes of determinants are shown through comparisons between anthropic emissions (mainly traffic) and ground-based measurements. The relevance of complex orography (relatively steep relieves near to the sea) is shown for the meso-scale flows and, in particular, for local-scale periodic flows, which favour the increase of high pollutants concentrations mainly in summer, when the breezes regime is particularly relevant. Part of these results have been achieved through the ETS - Alpine Space EU project iMONITRAF!

  17. Determinism, indeterminism, and explanatory bias.

    PubMed

    Targett, M

    1997-12-01

    Actions are a subclass of human behaviours which are distinguished, on a modest view, by certain antecedent mental and neural processes and events, including desires and beliefs. Libertarian philosophies have taken a less modest view, according to which some actions come under the influence of individual persons in a way distinct from being the necessary effect of a sequence of psychoneural events. Determinism claims necessary connections between sequences of events and conditions, including those sequences that involve desires and beliefs and subsequent actions. Even if a certain interpretation of modern physics shows determinism to be false, the sense of personal influence over action which libertarians have remains obscure. It is not enlightened by the physicist's idea of inexplicable fluctuations between courses of events with greater or lesser probabilities. If libertarianism remains obscure, so do the grounds for an approach to explaining behaviour which might be called "explanatory individualism". According to the latter stance, the local outcomes of actions and larger social tendencies are only properly explained in terms of the choices of individuals, rather than, for example, their neural or environmental antecedents. Again, bare indeterminism will not help to supply the required grounds. A more justifiable stance is "explanatory pluralism", a doctrine which denies the intrinsic priority of individualistic modes of explanation over those which focus on psychoneural, environmental, social or genetic conditions. It is stressed that on a sensible pluralism, any determinism which correctly describes the history of actions would be no more "genetic", than indeterminism could be "individualistic".

  18. [Do hormones determine our fate?].

    PubMed

    Vermeulen, A

    1994-01-01

    The hormonal system is a communication system between cells and organs. Hence it is not surprising that it influences almost all physiological functions and, at least partially, our behaviour and fate. The sexual phenotype is determined by the sex hormones. Normally, the phenotype is in accordance with gonadal and genetic sex, but occasionally, as a consequence of enzymatic defects in the biosynthesis of sex hormones or of androgen resistance, gonadal and genetic sex are in discordance with the phenotype, the latter determining generally the civil sex and the sex of rearing. Whereas the gender role is generally determined by the sex of rearing and the phenotype, itself under hormonal influence, homo- and transsexuality constitute notorious exceptions to this rule. Although several authors consider homo- and transsexuality to be the consequence of an impairment in androgenic impregnation in the perinatal period, there are at present no convincing arguments for an hormonal origin for either homo- or transsexuality, although such a possibility can't be excluded either. Besides their role in psychosexual behaviour, sex hormones play also a role in our life expectancy. Indeed, although maximal life expectancy of man is genetically determined, a major determinant of individual life expectancy is cardiovascular pathology. The latter is partly responsible for the difference in life expectancy between men and women, cardiovascular mortality increasing rapidly at menopause and being halved by oestrogen replacement therapy. Also atherogenesis as such is, to a large extend, under hormonal control. Indeed insulin resistance and hyperinsulinism, which develop as a corollary of the aging process, is an important cause of atherosclerosis as well as of hypertension. Other hormones also play an important role in our behaviour. We can mention here the role of the thyroid hormones in the physical and mental development of children as well as in the regression of the intellectual

  19. Effects of cyclosporine A on biomembranes. Vibrational spectroscopic, calorimetric and hemolysis studies.

    PubMed

    O'Leary, T J; Ross, P D; Lieber, M R; Levin, I W

    1986-04-01

    Cyclosporine A (CSA)-dipalmitoylphosphatidylcholine (DPPC) interactions were investigated using scanning calorimetry, infrared spectroscopy, and Raman spectroscopy. CSA reduced both the temperature and the maximum heat capacity of the lipid bilayer gel-to-liquid crystalline phase transition; the relationship between the shift in transition temperature and CSA concentration indicates that the peptide does not partition ideally between DPPC gel and liquid crystalline phases. This nonideality can be accounted for by excluded volume interactions between peptide molecules. CSA exhibited a similar but much more pronounced effect on the pretransition; at concentrations of 1 mol % CSA the amplitude of the pretransition was less than 20% of its value in the pure lipid. Raman spectroscopy confirmed that the effects of CSA on the phase transitions are not accompanied by major structural alterations in either the lipid headgroup or acyl chain regions at temperatures away from the phase changes. Both infrared and Raman spectroscopic results demonstrated that CSA in the lipid bilayer exists largely in a beta-turn conformation, as expected from single crystal x-ray data; the lipid phase transition does not induce structural alterations in CSA. Although the polypeptide significantly affects DPPC model membrane bilayers, CSA neither inhibited hypotonic hemolysis nor caused erythrocyte hemolysis, in contrast to many chemical agents that are believed to act through membrane-mediated pathways. Thus, agents, such as CSA, that perturb phospholipid phase transitions do not necessarily cause functional changes in cell membranes.

  20. High-precision, automated integration of multiple isothermal titration calorimetric thermograms: new features of NITPIC

    PubMed Central

    Scheuermann, Thomas H.; Brautigam, Chad A.

    2014-01-01

    Isothermal titration calorimetry (ITC) has become a standard and widely available tool to measure the thermodynamic parameters of macromolecular associations. Modern applications of the method, including global analysis and drug screening, require the acquisition of multiple sets of data; sometimes these data sets number in the hundreds. Therefore, there is a need for quick, precise, and automated means to process the data, particularly at the first step of data analysis, which is commonly the integration of the raw data to yield an interpretable isotherm. Herein, we describe enhancements to an algorithm that previously has been shown to provide an automated, unbiased, and high-precision means to integrate ITC data. These improvements allow for the speedy and precise serial integration of an unlimited number of ITC data sets, and they have been implemented in the freeware program NITPIC, version 1.1.0. We present a comprehensive comparison of the performance of this software against an older version of NITPIC and a current version of Origin, which is commonly used for integration. The new methods recapitulate the excellent performance of the previous versions of NITPIC while speeding it up substantially, and their precision is significantly better than that of Origin. This new version of NITPIC is therefore well suited to the serial integration of many ITC data sets. PMID:25524420

  1. Estimation of protein folding free energy barriers from calorimetric data by multi-model Bayesian analysis.

    PubMed

    Naganathan, Athi N; Perez-Jimenez, Raul; Muñoz, Victor; Sanchez-Ruiz, Jose M

    2011-10-14

    The realization that folding free energy barriers can be small enough to result in significant population of the species at the barrier top has sprouted in several methods to estimate folding barriers from equilibrium experiments. Some of these approaches are based on fitting the experimental thermogram measured by differential scanning calorimetry (DSC) to a one-dimensional representation of the folding free-energy surface (FES). Different physical models have been used to represent the FES: (1) a Landau quartic polynomial as a function of the total enthalpy, which acts as an order parameter; (2) the projection onto a structural order parameter (i.e. number of native residues or native contacts) of the free energy of all the conformations generated by Ising-like statistical mechanical models; and (3) mean-field models that define conformational entropy and stabilization energy as functions of a continuous local order parameter. The fundamental question that emerges is how can we obtain robust, model-independent estimates of the thermodynamic folding barrier from the analysis of DSC experiments. Here we address this issue by comparing the performance of various FES models in interpreting the thermogram of a protein with a marginal folding barrier. We chose the small α-helical protein PDD, which folds-unfolds in microseconds crossing a free energy barrier previously estimated as ~1 RT. The fits of the PDD thermogram to the various models and assumptions produce FES with a consistently small free energy barrier separating the folded and unfolded ensembles. However, the fits vary in quality as well as in the estimated barrier. Applying Bayesian probabilistic analysis we rank the fit performance using a statistically rigorous criterion that leads to a global estimate of the folding barrier and its precision, which for PDD is 1.3 ± 0.4 kJ mol(-1). This result confirms that PDD folds over a minor barrier consistent with the downhill folding regime. We have further validated the multi-model Bayesian approach through the analysis of two additional protein systems: gpW, a midsize single-domain with α + β topology that also folds in microseconds and has been previously catalogued as a downhill folder, and α-spectrin SH3, a domain of similar size but with a β-barrel fold, slow-folding kinetics and two-state-like thermodynamics. From a general viewpoint, the Bayesian analysis developed here results in a statistically robust, virtually model-independent, method to estimate the thermodynamic free-energy barriers to protein folding from DSC thermograms. Our method appears to be sufficiently accurate to consistently detect small differences in the barrier height, and thus opens up the possibility of characterizing experimentally the changes in thermodynamic folding barriers induced by single-point mutations on proteins within the downhill regime.

  2. Plate stamping of masterplates for the Tile-Cal hadronic calorimetric for ATLAS detector at CERN

    SciTech Connect

    Hill, N.F.; Petereit, E.; Wood, K.; Proudfoot, J.

    1996-05-16

    Various methods have been explored for the fabrication of the large trapezoidal plates used in the construction of the Tile-Cal hadronic calorimeter for ATLAS. The options include die stamping, laser cutting, waterjet cutting, plasma arc cutting, and a combination of machining and laser cutting. Very early in the program, the Argonne group began investigating the possibility of die stamping the master plates. At that time it was felt that two dies would be necessary to achieve the accuracy required. Quotations were received for dies for both the master and spacer plates. Concern was expressed by many members of the collaboration that due to the very precise tolerances required, die stamping, using standard dies, would not be adequate. Fine blanking techniques were felt to be adequate, but were cost prohibitive. Two methods were finally used for the initial cutting of prototype plates, laser cutting and die stamping. Only the die stamping, will be reviewed here.

  3. Calorimetric evidence of interaction of brominated flame retardants with membrane model.

    PubMed

    Librando, Vito; Accolla, Maria Lorena; Minniti, Zelica; Pappalardo, Matteo; Castelli, Francesco; Cascio, Orazio; Sarpietro, Maria Grazia

    2015-05-01

    The presence of polybrominated flame retardants in the environment seems to be increasing in the past decade. Considering the toxic effects of these pollutants, it is important evaluating the potential interaction with biological membranes for a risk assessment. In this study low and high brominated biphenyls and biphenyl ethers were used to investigate their interaction with biological membrane models constituted by liposomes, using differential scanning calorimetry (DSC) technique. The medium influence on membrane absorption was also assessed. The findings indicate that membrane interaction is controlled by compound structural characteristics. The membrane absorption is allowed by lipophilic medium; instead hydrophilic medium prevents membrane permeation.

  4. Differential scanning calorimetric study of acrylic resin powders used in dentistry.

    PubMed

    Ohyama, A; Imai, Y

    2000-12-01

    The thermal behavior of eight dental acrylic resin powders was studied using differential scanning calorimetry (DSC). In addition, high performance liquid chromatography was performed to supplement the DSC analysis. The HPLC analysis revealed that the contents of residual monomers and benzoyl peroxide (BPO) in the powders were 0.01-0.97 mass% and 0.25-1.28 mass%, respectively. All the resin powders produced one broad exothermic peak, while a mixture of BPO and PMMA powders generated two peaks. One peak pattern was assigned to the decomposition of BPO included within the polymer particles. The results suggested that BPO was present inside the particles and little BPO was mixed into the resin powders. Moreover, the present study demonstrated a unique useability of DSC in characterizing resin powders.

  5. Calorimetric Quantification of Cyclodextrin-Mediated Detergent Extraction for Membrane-Protein Reconstitution.

    PubMed

    Textor, Martin; Keller, Sandro

    2016-01-01

    For many in vitro studies, purified membrane proteins need to be reconstituted from detergent micelles into lipid bilayers to regain their native structures and functions. Stoichiometric complexation of detergent by cyclodextrin provides a tightly controllable strategy for detergent extraction. Here, we describe a practical approach making use of isothermal titration calorimetry to obtain a complete set of thermodynamic parameters that allows for quantitative prediction of the transition from micelles to bilayer membranes during reconstitution. These parameters include the dissociation constant of the cyclodextrin/detergent inclusion complex, the critical micellar concentration of the detergent, and the phase boundaries of the lipid/detergent phase diagram. The underlying theoretical framework involves linked equilibria among all pseudophases, as described previously (Textor, Vargas, & Keller, 2015). This chapter focuses on practical aspects of the approach and discusses caveats and calorimetry-specific details of data analysis. With the entire parameter set at hand, exploration of different reconstitution trajectories within the lipid/detergent phase diagram is possible. Together with the straightforward control over the rate of detergent extraction offered by cyclodextrin complexation, this opens the possibility of systematically tuning and optimizing the reconstitution process of membrane proteins. Provided some particular precautions are taken, the approach can be adapted to many other combinations of proteins, lipids, detergents, and cyclodextrins.

  6. The CALorimetric Electron Telescope (CALET) Launch and Early On-Orbit Performance

    NASA Astrophysics Data System (ADS)

    Guzik, T. Gregory; Calet Collaboration

    2016-03-01

    The CALET space experiment, has been developed by collaborators in Japan, Italy and the United States, will study electrons to 20 TeV, gamma rays above 10 GeV and nuclei with Z =1 to 40 up to 1,000 TeV during a five-year mission on the International Space Station. The instrument consists of a particle charge identification module, a thin imaging calorimeter (3 r.l. in total) with tungsten plates interleaving scintillating fiber planes, and a thick calorimeter (27 r.l.) composed of lead tungstate logs. CALET has the depth, imaging capabilities and energy resolution for excellent separation between hadrons, electrons and gamma rays. The instrument was launched into orbit on August 19, 2015 and on August 25, 2015 was mounted as an attached payload on the International Space Station (ISS) Japanese Experiment Module - Exposed Facility (JEM-EF). The experiment has successfully completed on-orbit checkout and has now been transitioned to normal science operations. This presentation summarizes the instrument design, science goals and early on-orbit performance. This effort is supported by NASA in the United States, by JAXA in Japan, and ASI in Italy.

  7. Dipolar magnets and glasses: Neutron-scattering, dynamical, and calorimetric studies of randomly distributed Ising spins

    SciTech Connect

    Reich, D.H.; Ellman, B.; Yang, J.; Rosenbaum, T.F. . James Franck Institute University of Chicago, Chicago, IL . Department of Physics); Aeppli, G. ); Belanger, D.P. )

    1990-09-01

    We have measured the magnetic correlations, susceptibility, specific heat, and thermal relaxation in the dipolar-coupled Ising system LiHo{sub {ital x}}Y{sub 1{minus}{ital x}}F{sub 4}. The material is ferromagnetic for spin concentrations at least as low as {ital x}=0.46, with a Curie temperature obeying mean-field scaling relative to that of pure LiHoF{sub 4}. In contrast, an {ital x}=0.167 sample behaves as a spin glass above its transition temperature, while an {ital x}=0.045 crystal shows very different glassy properties characterized by decreasing barriers to relaxation and nonexponential thermal relaxation as {ital T}{r arrow}0. We find the properties of the {ital x}=0.045 system to be consistent with a single low-degeneracy ground state with a large gap for excitations. The {ital x}=0.167 sample, however, supports a complex ground state with no appreciable gap, in accordance with prevailing theories of spin glasses. The underlying causes of such disparate behavior are discussed in terms of random clusters as probed by neutron studies of the {ital x}=0.167 sample.

  8. Calorimetric study on human erythrocyte glycolysis. Heat production in various metabolic conditions.

    PubMed

    Minakami, S; de Verdier, C H

    1976-06-01

    The heat production of human erythrocytes was measured on a flow microcalorimeter with simultaneous analyses of lactate and other metabolites. The heat production connected with the lactate formation was about 17 kcal (71 kJ) per mol lactate formed which corresponded to the sum of heat production due to the formation of lactate from glucose and the heat production due to neutralization. The heat production rate increased as the pH of the suspension increased, corresponding to the increase in lactate formation. Glycolytic inhibitors such as fluoride and monoiodoacetate caused a decrease in the rate of heat production, whereas arsenate induced a large transient increase in heat production associated with a transient increase in lactate formation. Decrease in pyruvate concentration was usually associated with increase in heat production, although the decreased pyruvate concentration was coupled with formation of 2,3-bisphosphoglycerate. When inosine, dihydroxyacetone or D-glyceraldehyde was used as a substrate, an increase in the heat production rate was observed. Addition of methylene blue caused an oxygen uptake which was accompanied by a remarkable increase in heat production rate corresponding to about 160 kcal (670 kJ) per mol oxygen consumed. The value for heat production in red cells in the above-mentioned metabolic conditions was considered in relation to earlier known data on free energy and enthalpy changes of the different metabolic steps in the glycolytic pathway.

  9. Multispectroscopic and calorimetric studies on the binding of the food colorant tartrazine with human hemoglobin.

    PubMed

    Basu, Anirban; Suresh Kumar, Gopinatha

    2016-11-15

    Interaction of the food colorant tartrazine with human hemoglobin was studied using multispectroscopic and microcalorimetric techniques to gain insights into the binding mechanism and thereby the toxicity aspects. Hemoglobin spectrum showed hypochromic changes in the presence of tartrazine. Quenching of the fluorescence of hemoglobin occurred and the quenching mechanism was through a static mode as revealed from temperature dependent and time-resolved fluorescence studies. According to the FRET theory the distance between β-Trp37 of hemoglobin and bound tartrazine was evaluated to be 3.44nm. Synchronous fluorescence studies showed that tartrazine binding led to alteration of the microenvironment around the tryptophans more in comparison to tyrosines. 3D fluorescence and FTIR data provided evidence for conformational changes in the protein on binding. Circular dichroism studies revealed that the binding led to significant loss in the helicity of hemoglobin. The esterase activity assay further complemented the circular dichroism data. Microcalorimetric study using isothermal titration calorimetry revealed the binding to be exothermic and driven largely by positive entropic contribution. Dissection of the Gibbs energy change proposed the protein-dye complexation to be dominated by non-polyelectrolytic forces. Negative heat capacity change also corroborated the involvement of hydrophobic forces in the binding process. PMID:27450339

  10. Calorimetric study on mechanically milled aluminum and multiwall carbon nanotube composites

    SciTech Connect

    Nayan, Niraj Murty, S.V.S.N.; Sharma, S.C.; Kumar, K. Sree; Sinha, P.P.

    2011-11-15

    Pure aluminum reinforced with carbon nanotube (CNT) composites have been prepared by high energy attritor milling up to 48 hrs. Differential Scanning Calorimetry (DSC) has been carried out to investigate apparent activation energy and order of the reaction between carbon nanotubes and aluminum by Kissinger equation and Crane equation under non-isothermal conditions. The DSC results clearly reveal that an exothermic reaction occurs before the melting of aluminum. The effect of milling time on the initiation of this exothermic reaction has been studied. The peak temperature of the reaction of carbon nanotubes and aluminum is found to depend on the heating rate during the continuous heating. Apparent activation energy was found to get doubled after milling for 36 hrs compared to 24 hrs milled samples. The mechanism of the reaction kinetics which depends on reaction order is instantaneous nucleation and one dimensional growth for both samples. Formation of Al{sub 4}C{sub 3} was confirmed by X-ray diffraction (XRD) of as-milled powders and after performing DSC of the milled powders. Highlights: {yields} Attritor milling used for processing Al-CNT composites. {yields} Powder morphology as a function of time studied. {yields} Apparent activation energy and order of the reaction calculated for Al{sub 4}C{sub 3} formation. {yields} Apparent activation energy increases two fold with increase in milling time from 24 to 36 hours.

  11. Crystallization kinetics of poly-(lactic acid) with and without talc: Optical microscopy and calorimetric analysis

    NASA Astrophysics Data System (ADS)

    Refaa, Z.; Boutaous, M.; Rousset, F.; Fulchiron, R.; Zinet, M.; Xin, S.; Bourgin, P.

    2014-05-01

    Poly-(lactic acid) or PLA is a biodegradable polymer synthesized from renewable resources. Recently, the discovery of new polymerization routes has allowed increasing the produced volumes. As a consequence, PLA is becoming of great interest for reducing the dependence on petroleum-based plastics. Because of its interesting mechanical properties, PLA is seen as a potential substitute for some usual polymers. However, its relatively slow crystallization kinetics can be a disadvantage with regard to industrial applications. The crystallization kinetics of PLA can be enhanced by adding nucleating agents, which also influences on crystalline morphology and rheological behavior. In the present work, the isothermal quiescent crystallization kinetics of both neat PLA and PLA/talc composite (5 wt% talc) are investigated. The effects of talc on the overall crystallization kinetics and on the crystalline morphology are analyzed using both optical microscopy measurements and thermal analysis by differential scanning calorimetry.

  12. Second vital coefficients of aqueous alcohols at elevated temperatures: A calorimetric study

    SciTech Connect

    Archer, D.G. )

    1989-06-29

    Enthalpies of dilution of cyclohexanol (aq) to 448 K and of myo-inositol (aq) and of cyclohexanol + myo-inositol (aq) to 398 K are reported. These results, along with enthalpies of dilution for 1-butanol (aq) to 448 K and for 2-methyl-2-propanol (aq) to 423 K, were combined with freezing point depression measurements and ambient-temperature enthalpy of dilution and heat capacity measurements in order to provide the excess Gibbs energy for the aqueous solutes from 273 to 523 K. These excess Gibbs energies were then used to provide parameters for an additivity scheme that permits an approximation of the excess Gibbs energy, and thus the solute and solvent activity coefficients, for dilute aqueous alcohols for which high-temperature data do not exist. These excess Gibbs energies were also used to estimate the aqueous-solution second virial coefficients of the alcohols and of cyclohexane (aq), 1-butane (aq), and 2-methylpropane (aq) in the McMillan-Mayer convention. These virial coefficients for the aqueous hydrocarbons, when compared to gas-phase virial coefficients for the hydrocarbons, suggest that the effect of low-temperature (298 K) water is to lessen the pairwise attraction of aqueous hydrocarbon over that found in the gas phase at the same temperature and that this lessening of the pairwise attraction diminishes at higher temperatures.

  13. Calorimetric and computational study of 2- and 3-acetyl-1-methylpyrrole isomers.

    PubMed

    Ribeiro da Silva, Manuel A V; Santos, Ana Filipa L O M

    2010-03-01

    This work reports the enthalpies of formation in the condensed and gas phases of 2-acetyl-1-methylpyrrole and 3-acetyl-1-methylpyrrole, derived from the standard (p(o) = 0.1 MPa) molar enthalpies of combustion, in oxygen, Delta(c)H(m)(o), measured by static bomb combustion calorimetry and the standard molar enthalpies of vaporization, Delta(l)(g)H(m)(o), at T = 298.15 K, obtained by high-temperature Calvet microcalorimetry. The theoretically estimated gas-phase enthalpies of formation were calculated from high-level ab initio molecular orbital calculations at the G3(MP2)//B3LYP level; the computed values compare very well with the experimental results obtained in this work and show that the 2-acetyl-1-methylpyrrole is thermodynamically more stable than the 3-isomer. Furthermore, this composite method was also applied in the calculation of bond dissociation enthalpies, gas-phase basicities, proton and electron affinities, and adiabatic ionization enthalpies. PMID:20141148

  14. Space-time development of electromagnetic and hadronic showers and perspectives for novel calorimetric techniques

    DOE PAGESBeta

    Benaglia, Andrea; Auffray, Etiennette; Lecoq, Paul; Wenzel, Hans; Para, Adam

    2016-04-20

    The performance of hadronic calorimeters will be a key parameter at the next generation of High Energy Physics accelerators. A detector combining fine granularity with excellent timing information would prove beneficial for the reconstruction of both jets and electromagnetic particles with high energy resolution. In this work, the space and time structure of high energy showers is studied by means of a Geant4-based simulation toolkit. In particular, the relevant time scales of the different physics phenomena contributing to the energy loss are investigated. A correlation between the fluctuations of the energy deposition of high energy hadrons and the time developmentmore » of the showers is observed, which allows for an event-by-event correction to be computed to improve the energy resolution of the calorimeter. Lastly, these studies are intended to set the basic requirements for the development of a new-concept, total absorption time-imaging calorimeter, which seems now within reach thanks to major technological advancements in the production of fast scintillating materials and compact photodetectors.« less

  15. A Simple Calorimetric Experiment that Highlights Aspects of Global Heat Retention and Global Warming

    ERIC Educational Resources Information Center

    Burley, Joel D.; Johnston, Harold S.

    2007-01-01

    In this laboratory experiment, general chemistry students measure the heating curves for three different systems: (i) 500 g of room-temperature water heated by a small desk lamp, (ii) 500 g of an ice-water mixture warmed by conduction with room-temperature surroundings, and (iii) 500 g of an ice-water mixture heated by a small desk lamp and by…

  16. Thermodynamic model for calorimetric and phase coexistence properties of coal derived fluids. Annual report

    SciTech Connect

    Kabadi, V.N.

    1991-10-01

    On September 1, 1989 work was initiated on a project to extend the available vapor-liquid equilibrium (VLE) model for coal fluids to allow satisfactory predictions of excess enthalpies of coal liquids at high pressures. The available vapor liquid equilibrium model was developed with support from previous grant from DOE-PETC (Grant no. DE-FG22-89PC90541). The current project also involves measurement of some model compound VLE data and chromatographic characterization of coal liquids for distribution of heteroatoms. A computational thermodynamic model for VLE, excess enthalpies and heat capacities of coal derived liquids has been developed. The model uses the modified UNIFAC correlation for the liquid phase. Some unavailable UNIFAC interactions parameters have been regressed from experimental VLE and excess enthalpy data. The computations are carried out using the method of continuous thermodynamics. Mode is used to derive interesting conclusions on the effect of oxygen, nitrogen, and sulfur heteroatoms on the thermodynamic properties of coal liquids. When compared with limited experimental data available for coal liquids the model shows good agreement. Some progress has been made on binary VLE measurements and size exclusion chromatography of coal liquids.

  17. Thermodynamic model for calorimetric and phase coexistence properties of coal derived fluids

    SciTech Connect

    Kabadi, V.N.

    1991-10-01

    On September 1, 1989 work was initiated on a project to extend the available vapor-liquid equilibrium (VLE) model for coal fluids to allow satisfactory predictions of excess enthalpies of coal liquids at high pressures. The available vapor liquid equilibrium model was developed with support from previous grant from DOE-PETC (Grant no. DE-FG22-89PC90541). The current project also involves measurement of some model compound VLE data and chromatographic characterization of coal liquids for distribution of heteroatoms. A computational thermodynamic model for VLE, excess enthalpies and heat capacities of coal derived liquids has been developed. The model uses the modified UNIFAC correlation for the liquid phase. Some unavailable UNIFAC interactions parameters have been regressed from experimental VLE and excess enthalpy data. The computations are carried out using the method of continuous thermodynamics. Mode is used to derive interesting conclusions on the effect of oxygen, nitrogen, and sulfur heteroatoms on the thermodynamic properties of coal liquids. When compared with limited experimental data available for coal liquids the model shows good agreement. Some progress has been made on binary VLE measurements and size exclusion chromatography of coal liquids.

  18. Fitting two- and three-site binding models to isothermal titration calorimetric data

    PubMed Central

    Brautigam, Chad A.

    2014-01-01

    As isothermal titration calorimetry (ITC) gains popularity for the characterization of enthalpies and equilibrium association constants of simple 1:1 biomolecular interactions, its use for more complex systems is growing. The method is increasingly used to study interactions in which a single binding partner (molecule “A”) interacts with multiple copies of a second partner (“B”); thus examinations of ABB and ABBB interactions are not uncommon. The structure of ITC data (commonly formatted as isotherms) has a strong bearing on the ability of the researcher to extract the necessary parameters from them. Usually, only 10-30 injections are recorded in a single ITC experiment. Even if replicates are performed, the data must support the extraction of up to twelve parameters from an ABBB system conducted in triplicate. Further, the refinement of some of the parameters is largely driven by only a subset of the data. The ability of ITC data to guide the deterministic estimation of these parameters may therefore be questioned. This work assesses the ability of both empirical and simulated ITC data of ABB and ABBB systems to support the simultaneous estimation of the desired thermodynamic parameters. The results demonstrate that multiphasic isotherms tend to (but do not always) support the estimation of multiple parameters. On the other hand, uniphasic data obtained from multi-site binding systems are more problematic. In all cases, a thorough exploration of how precisely the estimated parameters are specified by the data is justified. PMID:25484338

  19. Possible calorimetric effects at Mercury due to solar wind-magnetosphere interactions

    NASA Astrophysics Data System (ADS)

    Baker, D. N.; Borovsky, J. E.; Burns, J. O.; Gisler, G. R.; Zeilik, M.

    1987-05-01

    As a result of the solar wind interaction with the magnetosphere of Mercury, the authors expect several effects which may be observable with ground-based and/or near-earth radio and infrared telescopes: (1) there may be direct interaction of the solar wind with the surface of Mercury which could produce measurable heating effects; (2) substormlike magnetotail processes within Mercury's magnetosphere may precipitate particles carrying from 1010 to 1012W (or more) of power into narrow latitudinal bands on the cold (⪉130K) darkside of Mercury, producing surface-heated "auroral" zones; and (3) the presence of Jovian electrons within the inner Hermean magnetosphere may produce transient, very low frequency synchrotron-emitting radiation belts. Hence remote radio and infrared observations hold substantial promise for providing information about the intrinsic properties of Mercury's magnetic field, about the planetary surface, and about the dynamical interaction of the Hermean magnetosphere with the solar wind at ≡0.4 AU.

  20. Temperature-dependent infrared and calorimetric studies on arsenicals adsorption from solution to hematite nanoparticles

    Technology Transfer Automated Retrieval System (TEKTRAN)

    To address the lack of systematic and surface sensitive studies on the adsorption energetics of arsenic compounds on metal (oxyhydr)oxides, we conducted temperature-dependent ATR-FTIR studies for the adsorption of arsenate, monomethylarsonic acid, and dimethylarsinic acid on hematite nanoparticles a...