22 research outputs found
Nuclear-physical methods of analysis of noble metals and rare-earth elements
A summary of the analysis noble and rare metals by combined methods is presented. The electrodeposition of gold at a carbon film and Rutherford backscattering was used for determination its in ores. The sorbents and particle induced X-ray emission was used for determination rare and noble metals in ores. The minimum detectable concentration for ores was 0.1 mg/g
Use of electron linac for study of fission product and actynide diffusion through glass ceramic matrices
The diffusion of cerium and uranium was investigated in glass ceramic matrices obtained in the gasostat. For activation of isotopes ¹⁴⁰´¹⁴²Се and ²³⁸U the brake radiation from electrons of the linear accelerator was used. The
threshold of detectability of elements was reached from 5 to 15 µg/g for a sample of the area 1 cm². The coefficients
of diffusion in the grain material and at grain boundaries were measured, and their values for the pressing temperature of 910°С and pressure 100~МPa were 3.5⋅10⁻⁹ cm²/s in the grain and 1.2⋅10⁻⁸ cm²/s at grain boundaries.Методом зняття шарів вивчена дифузія церію й урану в синтезовані за допомогою газостатического
пресування склокерамічної матриці. Для активації ізотопів ¹⁴⁰´¹⁴²Се і ²³⁸U використовувалося гальмове
випромінювання від електронів лінійного прискорювача. Межа виявлення ізотопів церію й урану становила
10⁻⁵ г/г. Були вимірювані коефіцієнти дифузії в матеріалі зерна і по границях, що при температурі
пресування 910°С і тиску 100 МПа склали 3,5⋅10⁻⁹ см²/с у зерні і 1,2⋅10⁻⁸ см²/с по границях зерен.Методом снятия слоев изучена диффузия церия и урана в синтезированные посредством газостатического прессования стеклокерамические матрицы. Для активации изотопов ¹⁴⁰´¹⁴²Се и ²³⁸U использовалось тормозное излучение от электронов линейного ускорителя. Предел обнаружения изотопов церия и урана составил
10⁻⁵ г/г. Были измерены коэффициенты диффузии в материале зерна и по границам, которые при температуре прессования 910°С и давлении 100 МПа составили 3,5⋅10⁻⁹ см²/с в зерне и 1,2⋅10⁻⁸ см²/с по границам зерен
The dynamics of element content in patients with lung cancer during radiotherapy
Determination of the element contents in the biological samples (blood, serum of blood, hair) of patients with the
diagnosis of lung cancer III degree is carried out during beam therapy. The method of PIXE excited by protons on
the accelerator with energy 3 MeV has been used. During radiotherapy the difference in the element contents in hair
of patients has not been detected. Trustworthy reduction of Fe, Cu, Mn, Ca, Sr, Rb etc is marked during treatment.
The obtained results can be used as the additional test at carrying out adequate treatment in radiotherapy.Проведено визначення вмiсту мiкроелементiв в бiологiчних зразках (кров, сироватка кровi, волосся)
пацiєнтiв з дiагнозом раку легенi III ступеня в процесi променевої терапiї. Використовувався метод характеристичного рентгенiвського випромiнювання, яке збуджувалось протонами прискорювача з енергiєю 3 МеВ. Протягом радiотерапiї вiдмiнностей у вмiстi елементiв у волоссях пацiєнтiв виявлено не
було. У процесi лiкування вiрогiдно виявлене зменшення Fe, Cu, Mn, Ca, Sr, Rb i т.д. в кровi i сироватцi
кровi. Отриманi результати можуть бути використанi як додатковий тест при проведеннi адекватної
терапiї в курсi променевого лiкування.Проведено определение содержания микроэлементов в биологических образцах (кровь, сыворотка крови, волосы) пациентов с диагнозом рака легкого III степени в процессе лучевой терапии. Использован
метод характеристического рентгеновского излучения, возбуждаемого протонами на ускорителе с энергией 3 МэВ. В течение радиотерапии отличий в содержании элементов в волосах пациентов обнаружено
не было. В процессе лечения достоверно обнаружено уменьшение Fe, Cu, Mn, Ca, Sr, Rb и т.д. в крови и
сыворотке крови. Полученные результаты могут быть использованы в качестве дополнительного теста
при проведении адекватной терапии в курсе лучевого лечения
Application of gamma activation analysis for research of Cs and I diffusion into a glassceramic matrix
Nuclear reactions ¹³³Cs(γ,n)¹³²Cs, ¹²⁷I(γ,n)¹²⁶I were utilized for research of Cs and I diffusion in glassceramic matrices. The glassceramic matrix was manufactured with the help of hot isostatic pressing at 910°C and pressure 100 MPa. Diffusivities of cesium and iodine in a grain and through interphase boundary at 600°C were equal 10⁻¹¹ and 7.9⋅10⁻⁹ sm²/s, accordingly. The decrease of iodine diffusivity in a grain was observed at 750°C. A method of manufacture of glassceramic matrix for long-lived storage and nuclear-waste disposal ¹²⁹I is proposed.Ядерные реакции ¹³³Cs(γ,n)¹³²Cs, ¹²⁷I(γ,n)¹²⁶I использовались для исследования диффузии Cs и I в стеклокерамической матрице. Стеклокерамическая матрица изготовлена при помощи газостатического прессования при 910°С и давлении 100 МПа. Коэффициенты диффузии цезия и йода в зерне и по границам зерен при 600°С составили 10⁻¹¹ и 7,9⋅10⁻⁹ см²/с, соответственно. Обнаружено уменьшение коэффициента диффузии йода в зерне при 750°С. Предложен способ создания матрицы для захоронения ¹²⁹I.Ядерні реакції ¹³³Cs(γ,n)¹³²Cs, ¹²⁷I(γ,n)¹²⁶I використовувалися для дослідження дифузії Cs та I у склокерамічній матриці. Склокерамічна матриця виготовлена за допомогою газостатичного пресування при 910°С і тиску 100 МПа. Коефіцієнти дифузії цезію і йоду в зерні і по границях зерен при 600° С склали 10⁻¹¹ та 7,9⋅10⁻⁹ см²/с, відповідно. Виявлено зменшення коефіцієнта дифузії йоду в зерні при 750°С. Запропоновано спосіб створення матриці для поховання ¹²⁹I
LiMoO Scintillating Bolometers for Rare-Event Search Experiments
International audienceWe report on the development of scintillating bolometers based on lithium molybdate crystals containing molybdenum depleted in the double- active isotope Mo (LiMoO). We used two LiMoO cubic samples, 45 mm side and 0.28 kg each, produced following purification and crystallization protocols developed for double- search experiments with Mo-enriched LiMoO crystals. Bolometric Ge detectors were utilized to register scintillation photons emitted by the LiMoO crystal scintillators. The measurements were performed in the CROSS cryogenic set-up at the Canfranc underground laboratory (Spain). We observed that the LiMoO scintillating bolometers are characterized by excellent spectrometric performance (3--6 keV FWHM at 0.24--2.6 MeV 's), moderate scintillation signal (0.3--0.6 keV/MeV depending on light collection conditions) and high radiopurity (Th and Ra activities are below a few Bq/kg), comparable to the best reported results of low-temperature detectors based on LiMoO with natural or Mo-enriched molybdenum content. Prospects of LiMoO bolometers for use in rare-event search experiments are briefly discussed
LiMoO Scintillating Bolometers for Rare-Event Search Experiments
International audienceWe report on the development of scintillating bolometers based on lithium molybdate crystals containing molybdenum depleted in the double- active isotope Mo (LiMoO). We used two LiMoO cubic samples, 45 mm side and 0.28 kg each, produced following purification and crystallization protocols developed for double- search experiments with Mo-enriched LiMoO crystals. Bolometric Ge detectors were utilized to register scintillation photons emitted by the LiMoO crystal scintillators. The measurements were performed in the CROSS cryogenic set-up at the Canfranc underground laboratory (Spain). We observed that the LiMoO scintillating bolometers are characterized by excellent spectrometric performance (3--6 keV FWHM at 0.24--2.6 MeV 's), moderate scintillation signal (0.3--0.6 keV/MeV depending on light collection conditions) and high radiopurity (Th and Ra activities are below a few Bq/kg), comparable to the best reported results of low-temperature detectors based on LiMoO with natural or Mo-enriched molybdenum content. Prospects of LiMoO bolometers for use in rare-event search experiments are briefly discussed
Aboveground test of an advanced LiMoO scintillating bolometer to search for neutrinoless double beta decay of Mo
Large lithium molybdate (Li2MoO4) crystal boules were produced by using the low thermal gradient Czochralski growth technique from deeply purified molybdenum. A small sample from one of the boules was preliminary characterized in terms of X-ray-induced and thermally-excited luminescence. A large cylindrical crystalline element (with a size of circle divide 40 x 40 mm) was used to fabricate a scintillating bolometer, which was operated aboveground at similar to 15 mK by using a pulse-tube cryostat housing a high-power dilution refrigerator. The excellent detector performance in terms of energy resolution and alpha background suppression along with preliminary positive indications on the radiopurity of this material show the potentiality of Li2MoO4 scintillating bolometers for low-counting experiment to search for neutrinoless double beta decay of Mo-100. (C) 2015 Elsevier B.V. All rights reserved
The background model of the CUPID-Mo experiment
International audienceCUPID-Mo, located in the Laboratoire Souterrain de Modane (France), was a demonstrator for the next generation decay experiment, CUPID. It consisted of an array of 20 enriched LiMoO bolometers and 20 Ge light detectors and has demonstrated that the technology of scintillating bolometers with particle identification capabilities is mature. Furthermore, CUPID-Mo can inform and validate the background prediction for CUPID. In this paper, we present a detailed model of the CUPID-Mo backgrounds. This model is able to describe well the features of the experimental data and enables studies of the decay and other processes with high precision. We also measure the radio-purity of the LiMoO crystals which are found to be sufficient for the CUPID goals. Finally, we also obtain a background index in the region of interest of 3.7(stat)(syst)counts/E/mol/yr, the lowest in a bolometric decay experiment
Final results on the decay half-life limit of Mo from the CUPID-Mo experiment
The CUPID-Mo experiment to search for 0 decay in Mo has been recently completed after about 1.5 years of operation at Laboratoire Souterrain de Modane (France). It served as a demonstrator for CUPID, a next generation 0 decay experiment. CUPID-Mo was comprised of 20 enriched LiMoO scintillating calorimeters, each with a mass of 0.2 kg, operated at 20 mK. We present here the final analysis with the full exposure of CUPID-Mo (Mo exposure of 1.47 kgyr) used to search for lepton number violation via 0 decay. We report on various analysis improvements since the previous result on a subset of data, reprocessing all data with these new techniques. We observe zero events in the region of interest and set a new limit on the Mo 0 decay half-life of year (stat.+syst.) at 90% C.I. Under the light Majorana neutrino exchange mechanism this corresponds to an effective Majorana neutrino mass of \left < (0.28-- eV, dependent upon the nuclear matrix element utilized
New measurement of double beta decays of Mo to excited states of Ru with the CUPID-Mo experiment
The CUPID-Mo experiment, located at Laboratoire Souterrain de Modane (France), was a demonstrator experiment for CUPID. It consisted of an array of 20 LiMoO (LMO) calorimeters each equipped with a Ge light detector (LD) for particle identification. In this work, we present the result of a search for two-neutrino and neutrinoless double beta decays of Mo to the first 0 and excited states of Ru using the full CUPID-Mo exposure (2.71 kgyr of LMO). We measure the half-life of decay to the state as . The bolometric technique enables measurement of the electron energies as well as the gamma rays from nuclear de-excitation and this allows us to set new limits on the two-neutrino decay to the state of T^{2\nu \rightarrow 2_1^+}_{1/2}>4.4\times 10^{21} \ \mathrm{yr} \ \text{(90 % c.i.)} and on the neutrinoless modes of T_{1/2}^{0\nu\rightarrow 2_1^+}>2.1\times10^{23} \ \mathrm{yr}\ \text{(90 % c.i.)}, T_{1/2}^{0\nu\rightarrow 0_1^+}>1.2\times10^{23} \ \mathrm{yr}\ \text{(90 % c.i.)}. Information on the electrons spectral shape is obtained which allows us to make the first comparison of the single state (SSD) and higher state (HSD) decay models for the excited state of Ru