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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Kashkina L. V., Stebeleva O. P., Emelyanova T. Y., Petrakovskaya E. A., Bayukov O. A.
Заглавие : Hydrodynamic dispersion of calcium aluminosilicate from technogenic and nonmetallic material
Место публикации : J. Sib. Fed. Univ. Eng. Technol. - 2014. - Vol. 7, Is. 1. - P.3-12; Журн. СФУ. Сер. "Техника и технологии"
Ключевые слова (''Своб.индексиров.''): hydrodynamic dispersion--cavitation--crystal ceramic foam--porous glass material--гидродинамическое диспергирование--кавитация--зола--пеноматериал--пористая стеклокерамика
Аннотация: Physicochemical properties of two calcium aluminosilicate materials after reducing in the hydrodynamic rotary generator in supercavitation mode were studied. The samples are the crystal ceramic foam based on Kansko-Achinsk lignite-ash and the porous glass material obtained from low-manganese nonmetallic feed. X-ray phase analysis, EPR-method, NPR-method (the Mossbauer Effect) and optical microscopy were used. It was found that the material is changing its stucrure in a hydrodynamic dispersion process caused by high-cavitation. The nature of the changes depends on its initial state.Изучены физико-химические свойства двух кальций-алюмосиликатных материалов после измельчения в гидродинамическом генераторе роторного типа в режиме суперкавитации. Исследованы образцы – кристаллическая пенокерамика на основе зол бурых Канско-Ачинских углей и пористый стекломатериал, полученный из нерудного сырья с низким содержанием марганца. Для анализа были использованы методы РФА, ЭМР, ЯГР (эффект Мёссбауэра), оптическая микроскопия. Показано, что в процессе гидродинамического диспергирования за счет высокоэнергетического кавитационного воздействия в материалах происходят глубокие структурные изменения. Получено, что характер изменений зависит от исходного состояния исследуемого материала.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Aleksandrov K. S., Vasil'ev A. D., Zvegintsev A. G., Lepeshev A. A., Петров, Михаил Иванович, Khabarov V. I., Khrustalev B. P.
Заглавие : Superconducting ceramic coating obtained by plasma spraying
Место публикации : Zhurnal Tek. Fiz. - 1989. - Vol. 59, Is. 8. - P.157-159. - ISSN 0044-4642
Примечания : Cited References: 3
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Sysoev A. M., Parshikov S. A., Zaitsev A. I., Zamkov A. V., Aleksandrov K. S.
Заглавие : Piezoelectric properties of glassceramic based on lithium tetraborate
Место публикации : Ferroelectrics. - 1996. - Vol. 186, Is. 1. - P.277-280. - ISSN 0015-0193, DOI 10.1080/00150199608218083
Примечания : Cited References: 4
Ключевые слова (''Своб.индексиров.''): ceramic materials--crystal growth--dielectric properties--electroacoustic transducers--glass--hydrophones--lithium compounds--single crystals--acoustoelectric transducer--glass ceramic--lithium tetraborate--microcomposite materials--piezoelectric materials
Аннотация: The preparation and study of a glassceramic based on lithium tetraborate was carried out. It was shown that due to favourable piezoelectric properties this material has good prospects for use as acoustoelectric transducer in devices such as hydrophones.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Aleksandrov K. S., Khrustalev B. P., Krivomazov S. N., Петров, Михаил Иванович, Vasilyev A. D., Zwegintsev S. A.
Заглавие : Superconductivity near liquid nitrogen temperature in the Sn-Ba-Sr-Y-Cu-O system
Место публикации : Physica C-Superconductivity and its Applications. - 1989. - Vol. 161, Is. 4. - P.493-496. - ISSN 0921-4534, DOI 10.1016/0921-4534(89)90087-7
Ключевые слова (''Своб.индексиров.''): ceramic materials--tin compounds--bulk superconductivity--high temperature superconductors--oxide superconductors--tin barium strontium yttrium copper oxide--superconducting materials
Аннотация: A high-Tc phase was found in the Sn-Ba-Sr-Y-Cu-O system. DC susceptibility data of Sn2Ba2Sr0.5Y0.5Cu3Ox show a single transition to bulk superconductivity with an onset temperature of 86 K. В© 1989.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Aleksandrov K. S., Vasilyev A. D., Zwegintsev S. A., Петров, Михаил Иванович, Khrustalev B. P.
Заглавие : Peculiarities of the resistive state of the (Y,Lu)1Ba2Cu3O7-δ superconducting ceramics
Место публикации : Physica C. - 1988. - Vol. 156, Is. 2. - P.249-250. - ISSN 0921-4534
Ключевые слова (''Своб.индексиров.''): ceramic materials--oxides--current voltage characteristics--yttrium barium copper oxides--superconducting materials
Аннотация: The resistive state of the high-Tc superconducting ceramics (Y, Lu)1Ba2Cu3O7-δ has been investigated, a hysteresis instability has been discovered in the current-voltage characteristics (CVC) under a current density j ≈ 1.7 kA cm-2. © 1988.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Chechin G. M., Sakhnenko V. P., Misyul S. V., Aleksandrov K. S.
Заглавие : Improper ferroelectric phase due to condensation of two order parameters in crystals of high-temperature superconductors
Место публикации : Ferroelectrics. - 1992. - Vol. 130, Is. 1. - P.155-162. - ISSN 0015-0193
Примечания : Cited References: 21
Предметные рубрики: TRANSITIONS
FERROELASTICS
RB3CD2CL7
Ключевые слова (''Своб.индексиров.''): ceramic materials--crystals--ferroelectricity--phase diagrams--order parameters--oxide superconductors--high temperature superconductors
Аннотация: Using group-theoretical methods it is shown that improper ferroelectric phase may arise in high-temperature superconductors (HTSC) where high-symmetry phases have space groups D4h1 or D4h17. Their appearance is caused by condensation of order parameters (OP's) transforming two irreducible representations (IR's). The most typical phase diagrams are considered, as well as temperature dependence of OP's and the basic structural mechanism of the ferroelectricity arising in the HTSC.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Guan, Ming, Zheng, Hong, Mei, Lefu, Molokeev M. S., Xie, Jing, Yang, Tao, Wu, Xiaowen, Huang, Saifang, Huang, Zhaohui
Заглавие : Preparation, structure, and up-conversion luminescence of Yb3+/Er3+ codoped SrIn2O4 phosphors
Место публикации : J. Am. Ceram. Soc.: Wiley-Blackwell, 2015. - Vol. 98, Is. 4. - P.1182-1187. - ISSN 0002, DOI 10.1111/jace.13415. - ISSN 15512916(eISSN)
Примечания : Cited References:26. - This present work was supported by the National Natural Science Foundations of China (grant no. 51202226), the Fundamental Research Funds for the Central Universities (grant nos. 292014125,2652013128, 2652013043), and the Research Fund for the Doctoral Program of Higher Education of China (grant no. 20130022110006).
Предметные рубрики: CORE-SHELL NANOPARTICLES
DOPED CaIn2O4
GREEN
Er3+
EMISSION
GLASSES
Аннотация: SrIn2O4, which shows lower phonon energy than CaIn2O4, is not only a good photocatalyst but also can be an excellent up-conversion (UC) host to exhibits UC luminescence. In this work, Yb3+ and/or Er3+ doped SrIn2O4 phosphors were synthesized, and their UC luminescence properties were studied and compared with those in the CaIn2O4 host. The structure of SrIn2O4: 0.01Er3+ and SrIn2O4: 0.1Yb3+/0.01Er3+ samples were refined by the Rietveld method and found to that SrIn2O4: 0.1Yb3+/0.01Er3+ showed increasing unit cell parameters and cell volume, indicating In3+ sites were substituted successfully by Yb3+ and/or Er3+ ions. From the UC luminescence spectra and diffuse reflection spectra, Er3+-doped SrIn2O4 showed very weak luminescence due to ground state absorption of Er3+; Yb3+/Er3+ codoped SrIn2O4 presented strong green (550 nm) and red (663 nm) UC emissions which were assigned to energy transfer from Yb3+ transition 2F7/2→2F5/2 to the Er3+ transition 4S3/2 → 4I15/2 and 4F9/2 → 4I15/2. Comparing with CaIn2O4, Yb3+/Er3+ codoped SrIn2O4 showed obvious advantages with higher UC luminescent intensity. The pumping powers study showed that UC emissions in Yb3+/Er3+ codoped SrIn2O4 were attributed to energy transfer of Yb3+→Er3+ with a two-photon process. The possible UC luminescent mechanism of Yb3+/Er3+-doped SrIn2O4 was discussed.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Liu, Chengyin, Xia, Zhiguo, Molokeev M. S., Liu, Quanlin
Заглавие : Synthesis, crystal structure, and enhanced luminescence of garnet-type Ca3Ga2Ge3O12:Cr3+ by codoping Bi3+
Место публикации : J. Am. Ceram. Soc.: Wiley-Blackwell, 2015. - Vol. 98, Is. 6. - P.1870-1876. - ISSN 0002, DOI 10.1111/jace.13553. - ISSN 15512916(eISSN)
Примечания : Cited References:24. - This work was supported by the National Natural Science Foundations of China (grant nos. 51002146, 51272242), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in University of Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), Beijing Youth Excellent Talent Program (YETP0635), the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306) and Fundamental Research Funds for the Central Universities (FRF-TP-14-005A1).
Предметные рубрики: LIGHT-EMITTING-DIODES
INFRARED PERSISTENT LUMINESCENCE
ENERGY-TRANSFER
PHOSPHOR
RED
NANOPARTICLES
EFFICIENCY
Аннотация: Garnet-type compound Ca3Ga2Ge3O12 and Cr3+-doped or Cr3+/Bi3+ codped Ca3Ga2Ge3O12 phosphors were prepared by a solid-state reaction. The crystal structure of Ca3Ga2Ge3O12 host was studied by X-ray diffraction (XRD) analysis and further determined by the Rietveld refinement. Near-infrared (NIR) photoluminescence (PL) and long-lasting phosphorescence (LLP) emission can be observed from the Cr3+-doped Ca3Ga2Ge3O12 sample, and the enhanced NIR PL emission intensity and LLP decay time can be realized in Cr3+/Bi3+ codped samples. The optimum concentration of Cr3+ in Ca3Ga2Ge3O12 phosphor was about 6 mol%, and optimum Bi3+ concentration induced the energy-transfer (ET) process between Bi3+ and Cr3+ ions was about 30 mol%. Under different excitation wavelength from 280 to 453 nm, all the samples exhibit a broadband emission peaking at 739 nm and the intensity of NIR emission increases owing to the ET behavior from Bi3+ to Cr3+ ions. The critical ET distance has been calculated by the concentration-quenching method. The thermally stable luminescence properties were also studied and the introduction of Bi3+ can also improve the thermal stability of the NIR emission.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Ji H., Huang Z., Xia, Zhiguo, Molokeev M. S., Chen M., Atuchin V. V., Fang M., Liu Y., Wu, Xiaowen
Заглавие : Phase transformation in Ca3(PO4)2:Eu2+ via the controlled quenching and increased Eu2+ content: Identification of new cyan-emitting α-Ca3(PO4)2:Eu2+ phosphor
Место публикации : J. Am. Ceram. Soc. - 2015. - Vol. 98, Is. 10. - P.3280-3284. - ISSN 0002-7820, DOI 10.1111/jace.13787
Примечания : Cited References: 23. - This work was partly supported by the National Natural Science Foundations of China (grant nos. 51272242, 51472222, 51511130035), the Research Fund for the Doctoral Program of Higher Education of China (grant no. 20130022110006), and the Russian Foundation for Basic Research (grant no. 15-52-53080 GFEN_a). VVA was partly supported by the Ministry of Education and Science of the Russian Federation.
Предметные рубрики: NEUTRON POWDER DIFFRACTION
SOLID-SOLUTION PHOSPHORS
CRYSTAL-STRUCTURE
DIODES
PHOTOLUMINESCENCE
LUMINESCENCE
TRANSITION
ALPHA
Аннотация: A case of phosphor is reported where the cooling rate parameter significantly influences the luminescence property. By quenching the sample after the higherature solid-state reaction at 1250°C, we successfully prepared the Eu2+-doped α form Ca3(PO4)2 (α-TCP:Eu2+) as a new kind of bright cyan-emitting phosphor. The unusual emission color variation (from cyan to blue) depends on the cooling rate after sintering and Eu2+ doping level as it was observed in the TCP-based phosphors. By the Rietveld analysis, it is revealed that the cyan- and blue-emitting phosphors are two different TCP forms crystallizing in the monoclinic (space group P21/a, α-TCP) and the rhombohedral structure (space group R3c, β-TCP), respectively. Upon 365 nm UV light excitation, α-TCP:Eu2+ exhibits an asymmetric broad-band cyan emission peaking at 480 nm, while β-TCP:Eu2+ displays a relatively narrow-band blue emission peaking at 416 nm. The Eu2+-doping in Ca3(PO4)2 shifts the upper temperature limit of the stable structural range of β form from 1125°C to ≥1250°C. Moreover, the crystal structures of α/β-TCP:Eu2+ were compared in the aspects of compactness and cation site sets. The emission thermal stability of α/β-TCP:Eu2+ was comparatively characterized and the difference was related to the specific host structural features. © 2015 The American Ceramic Society.
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10.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Lim, Chang Sung, Atuchin V. V., Aleksandrovsky A. S., Molokeev M. S., Oreshonkov A. S.
Заглавие : Microwave sol–gel synthesis of CaGd2(MoO4)4:Er3+/Yb3+ phosphors and their upconversion photoluminescence properties
Место публикации : J. Am. Ceram. Soc.: Wiley-Blackwell, 2015. - Vol. 98, Is. 10. - P.3223-3230. - ISSN 0002, DOI 10.1111/jace.13739. - ISSN 15512916(eISSN)
Примечания : Cited References:69. - This study was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (2014-046024). VVA and ASA are partially supported by the Ministry of Education and Science of the Russian Federation.
Предметные рубрики: RED-EMITTING PHOSPHORS
VIBRATIONAL PROPERTIES
LUMINESCENCE PROPERTIES
WHITE LEDS
SPECTROSCOPIC PROPERTIES
HYDROTHERMAL SYNTHESIS
CRYSTAL-STRUCTURE
ROOM-TEMPERATURE
ENERGY-TRANSFER
SR
Аннотация: CaGd2(MoO4)4:Er3+/Yb3+ phosphors with the doping concentrations of Er3+ and Yb3+ (x = Er3+ + Yb3+, Er3+ = 0.05, 0.1, 0.2, and Yb3+ = 0.2, 0.45) have been successfully synthesized by the microwave sol–gel method, and the crystal structure refinement and upconversion photoluminescence properties have been investigated. The synthesized particles, being formed after heat-treatment at 900°C for 16 h, showed a well-crystallized morphology. Under the excitation at 980 nm, CaGd2(MoO4)4:Er3+/Yb3+ particles exhibited strong 525 and 550-nm emission bands in the green region and a weak 655-nm emission band in the red region. The Raman spectrum of undoped CaGd2(MoO4)4 revealed about 15 narrow lines. The strongest band observed at 903 cm−1 was assigned to the ν1 symmetric stretching vibration of MoO4 tetrahedrons. The spectra of the samples doped with Er and Yb obtained under 514.5 nm excitation were dominated by Er3+ luminescence preventing the recording Raman spectra of these samples. Concentration quenching of the erbium luminescence at 2H11/2→4I15/2 and 4S3/2→4I15/2 transitions in the CaGd2(MoO4)4:Er3+/Yb3+ crystal structure was established to be approximately at the 10 at.% doping level.
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